WO2006136161A2 - Amylases for pharmaceutical use - Google Patents
Amylases for pharmaceutical use Download PDFInfo
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- WO2006136161A2 WO2006136161A2 PCT/DK2006/000354 DK2006000354W WO2006136161A2 WO 2006136161 A2 WO2006136161 A2 WO 2006136161A2 DK 2006000354 W DK2006000354 W DK 2006000354W WO 2006136161 A2 WO2006136161 A2 WO 2006136161A2
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- amino acids
- amylase
- protease
- lipase
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/43—Enzymes; Proenzymes; Derivatives thereof
- A61K38/46—Hydrolases (3)
- A61K38/47—Hydrolases (3) acting on glycosyl compounds (3.2), e.g. cellulases, lactases
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
- C12N9/24—Hydrolases (3) acting on glycosyl compounds (3.2)
- C12N9/2402—Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
- C12N9/2405—Glucanases
- C12N9/2408—Glucanases acting on alpha -1,4-glucosidic bonds
- C12N9/2411—Amylases
- C12N9/2414—Alpha-amylase (3.2.1.1.)
- C12N9/2417—Alpha-amylase (3.2.1.1.) from microbiological source
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/43—Enzymes; Proenzymes; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/43—Enzymes; Proenzymes; Derivatives thereof
- A61K38/54—Mixtures of enzymes or proenzymes covered by more than a single one of groups A61K38/44 - A61K38/46 or A61K38/51 - A61K38/53
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- the present invention relates to the pharmaceutical use of amylases related to certain Bacillus alpha-amylases (SEQ ID NOs: 1-3), optionally in combination with a lipase and/or a protease.
- SEQ ID NOs: 1-3 Bacillus alpha-amylases
- Examples of medical indications are: Treatment of digestive disorders, pancreatic exocrine insufficiency (PEI), pancreatitis, cystic fibrosis, diabetes type I, and/or diabetes type
- pancreatic enzyme supplements for the treatment of pancreatic exocrine insufficiency.
- the active ingredients of these products are digestive enzymes, mainly amylase, lipase and protease, which are normally produced in the pancreas and excreted to the upper part of the small intestine (the duodenum).
- the enzymes used in such medicaments derive from bovine or swine pancreas, however there are also products on the market with microbial enzymes, e.g. the product Nortase® which contains a lipase from Rhizopus oryzae, a protease from Aspergillus oryzae, and an amylase from Aspergillus oryzae.
- US 5614189 (EP 600868) describes the use of, i.a., a lipase derived from Humicola lanuginosa in pancreatic enzyme replacement therapy, for example in the treatment of patients suffering from cystic fibrosis.
- This lipase is from Humicola lanuginosa DSM 4109 and has the amino acid sequence of amino acids 1-269 of SEQ ID NO: 9 herein.
- WO 00/54799 describes the use of physiologically acceptable enzyme mixtures having lipolytic, proteolytic and amylolytic activity in the treatment of diabetes mellitus type I and II.
- WO 02/060474 describes the use of a concentrated lipase from Rhizopus delemar, a neutral protease from Aspergillus melleus, and an amylase from Aspergillus oryzae in the treatment of maldigestion.
- WO 01/62280 describes the use of a non-fungal lipase crystal crosslinked with a multifunctional crosslinking agent, a protease, and an amylase, wherein the lipase crystal is active at a pH range from about 2.0 to 9.0, for treating or preventing a gastrointestinal disorder in a mammal.
- a preferred lipase is from Pseudomonas, preferred amylases are from
- preferred proteases are bromelain, papain or ficin.
- EP 0828509 describes the use of certain acid-stable amylases, optionally in combination with certain acid-stable lipases and/or proteases, in the treatment of exocrine pancreas insufficiency.
- a preferred amylase is from Aspergillus niger, and preferred lipases are from Rhizopus arrhizus or Rhizopus javanicus.
- WO 99/19467 describes certain variants of alpha-amylases derived from Bacillus stearothermophilus, Bacillus licheniformis, and Bacillus amyloliquefaciens, as well as various industrial uses thereof, however not the pharmaceutical use. The sequences of these wildtype
- Bacillus alpha-amylases designated SEQ ID NOs: 3-5 in WO 99/19467 are included herein as SEQ ID NOs: 10-12, respectively.
- EP 0594235 describes a method for preparing purified amylase from a fermentation broth.
- a pharmaceutical composition is also claimed, and a potential use as digestive aid is mentioned, along with other potential uses.
- the examples illustrate the claimed purification method for a Bacillus licheniformis alpha-amylase.
- WO 2004/078960 discloses a method for identifying at least one T-cell epitope of an amylase and variant amylases comprising at least one alteration in at least one epitope. Many potential uses are enumerated, including the pharmaceutical use.
- An amylase from Bacillus licheniformis is referred to.
- EP 0828509 describes the use of certain acid-stable amylases, optionally in combination with certain acid-stable lipases and/or proteases, in the treatment of exocrine pancreas insufficiency.
- a preferred amylase is from Aspergillus niger, and preferred lipases are from Rhizopus arrhizus or Rhizopus javanicus.
- the present invention provides alternative, preferably improved, enzymes for pharmaceutical use, in particular for the treatment of digestive disorders, pancreatic exocrine insufficiency (PEI), pancreatitis, cystic fibrosis, diabetes type I, and/or diabetes type II.
- the new enzymes are proteases, amylases, and lipases.
- the enzymes for use according to the invention have an improved efficacy in vivo and/or in vitro; an improved pH- activity profile; an improved specific activity; an improved degradation profile; are active in the presence of bile salts; and/or have a reduced allergenicity.
- the present invention relates to an amylase of at least 50% identity to (i) amino acids 1-481 of SEQ ID NO: 1 , (ii) amino acids 1-481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3; for use as a medicament, optionally in combination with a lipase, and/or a protease.
- the invention also relates to the use of such amylases for the manufacture of a medicament for the treatment of digestive disorders, PEI, pancreatitis, cystic fibrosis, diabetes type I, and/or diabetes type II, these uses optionally further comprising the use of a lipase, and/or a protease.
- the invention furthermore relates to a pharmaceutical composition comprising such amylases, together with at least one pharmaceutically acceptable auxiliary material, optionally including a lipase and/or a protease.
- the invention also relates to a method for the treatment of digestive disorders, PEI, pancreatitis (acute and/or chronic), cystic fibrosis, diabetes type I, and/or diabetes type II, by administering a therapeutically effective amount of such amylases, optionally together with a lipase and/or a protease.
- FIG. 1 shows a chromatogram representing the degradation profile of an amylase having the amino acid sequence of amino acids 1-486 of SEQ ID NO: 1 (a Bacillus stearothermophilus amylase variant);
- Fig. 2 shows a chromatogram representing the degradation profile of an amylase from Aspergillus oryzae
- Fig. 3 shows a chromatogram representing the degradation profile of Pancreatin
- Fig. 4 shows a chromatogram representing the degradation profile of an amylase having the amino acid sequence of amino acids 1-483 of SEQ ID NO: 3 (a Bacillus sp. amylase variant);
- Fig. 5 shows a chromatogram representing the degradation profile of an amylase having the amino acid sequence of amino acids 1-481 of SEQ ID NO: 2 (a Bacillus licheniformis amylase variant).
- Enzymes The present invention relates to the pharmaceutical use of amylases having at least
- the invention also relates to the use of such amylases for the manufacture of a medicament for the treatment of digestive disorders, PEI, pancreatitis (acute and/or chronic), cystic fibrosis, diabetes type I, and/or diabetes type II.
- the invention furthermore relates to a pharmaceutical composition comprising such amylases, together with at least one pharmaceutically acceptable auxiliary material.
- the invention furthermore relates to a method for the treatment of the diseases mentioned above by administering a therapeutically effective amount of such amylases.
- amylase for use in the compositions, methods and uses of the invention is referred to as the "amylase of the invention.”
- an amylase is an enzyme that catalyzes the endo-hydrolysis of starch and other linear and branched oligo- and polysaccharides.
- the amylase for use according to the invention has alpha-amylase activity, viz. catalyzes the endohydrolysis of 1 ,4-alpha-glucosidic linkages in oligosaccharides and polysaccharides.
- Alpha-amylases act, e.g., on starch, glycogen and related polysaccharides and oligosaccharides in a random manner, liberating reducing groups in the alpha-configuration.
- the amylase of the invention is an alpha-amylase
- the amylase of the invention belongs to the EC 3.2.1.- group of amylases, such as EC 3.2.1.1 (alpha-amylase), EC 3.2.1.2 (beta-amylase), EC 3.2.1.3 (glucan 1 ,4-alpha-glucosidase, amyloglucosidase, or glucoamylase), EC 3.2.1.20 (alpha-glucosidase), EC 3.2.1.60 (glucan 1 ,4-alpha-maltotetraohydrolase), EC 3.2.1.68 (isoamylase), EC 3.2.1.98 (glucan 1 ,4-alpha- maltohexosidase), or EC 3.2.1.133 (glucan 1 ,4-alpha-maltohydrolase).
- EC 3.2.1.- group of amylases such as EC 3.2.1.1 (alpha-amylase), EC 3.2.1.2 (beta-amylase), EC 3.2.
- the amylase for use according to the invention can be, or is, classified as belonging to the EC 3.2.1.1 group.
- the EC numbers refer to Enzyme Nomenclature 1992 from NC-IUBMB, Academic Press, San Diego, California, including supplements 1-5 published in Eur. J. Biochem. 1994, 223, 1-5; Eur. J. Biochem. 1995, 232, 1-6; Eur. J. Biochem. 1996, 237, 1-5; Eur. J. Biochem. 1997, 250, 1-6; and Eur. J. Biochem. 1999, 264, 610-650; respectively.
- the nomenclature is regularly supplemented and updated; see e.g. the World Wide Web at http://www.chem.qmw.ac.uk/iubmb/enzyme/index.html.
- the amylase of the invention has a degree of identity to any one of (i) amino acids 1-481 of SEQ ID NO: 1 , (ii) amino acids 1-481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3 of at least 51%, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, or at least 60%.
- the amylase of the invention has a degree of identity to any one of (i) amino acids 1-481 of SEQ ID NO: 1 , (ii) amino acids 1-481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3 of at least 61%, 62%, 63%, 64%, 65%, 66%, 67%, 68%, 69%, or at least 70%.
- the amylase of the invention has a degree of identity to any one of (i) amino acids 1-481 of SEQ ID NO: 1 , (ii) amino acids 1-481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3 of at least 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, or at least 80%.
- the amylase of the invention has a degree of identity to any one of (i) amino acids 1-481 of SEQ ID NO: 1 , (ii) amino acids 1-481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3 of at least 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, or at least 90%.
- the amylase of the invention has a degree of identity to any one of (i) amino acids 1-481 of SEQ ID NO: 1 , (ii) amino acids 1-481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3 of at least 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or at least 99%.
- the amylase of the invention comprises at least one substitution, deletion, and/or insertion of one or more amino acids in any one of the sequences of (i) amino acids 1-481 of SEQ ID NO: 1 , (ii) amino acids 1-481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3.
- the amino acid changes are of a minor nature, that is conservative amino acid substitutions or insertions that do not significantly affect the folding and/or activity of the protein; small deletions; small amino- or carboxyl-terminal extensions, such as an amino-terminal methionine residue; a small linker peptide; or a small extension that facilitates purification by changing net charge or another function, such as a poly-histidine tract, an antigenic epitope or a binding domain.
- the term "small” independently designates a number of up to 25 amino acid residues. In preferred embodiments, the term “small” designates up to 24, 23, 22, 21 , or up to 20 amino acid residues.
- the term “small” independently designates up to 19, 18, 17, 16, 15, 14, 13, 12, 11 , or up to 10 amino acid residues. In further preferred embodiments, the term “small” independently designates up to 9, 8, 7, 6, 5, 4, 3, 2, or up to 1 amino acid residue. In alternative embodiments, the term “small” independently designates up to 40, 39, 38, 37, 36, 35, 34, 33, 32, 31 , 30, 29, 28, 27, 26, or up to 25 amino acid residues. Examples of conservative substitutions are within the group of basic amino acids
- amino acids (arginine, lysine and histidine), acidic amino acids (glutamic acid and aspartic acid), polar amino acids (serine, threonine, glutamine and asparagine), hydrophobic amino acids (leucine, isoleucine, valine and alanine), aromatic amino acids (phenylalanine, tryptophan and tyrosine), and small amino acids (glycine, alanine, proline, serine, threonine, cysteine and methionine).
- conservative substitutions are within the group of basic amino acids (arginine, lysine and histidine), acidic amino acids (glutamic acid and aspartic acid), polar amino acids (glutamine and asparagine), hydrophobic amino acids (leucine, isoleucine and valine), aromatic amino acids (phenylalanine, tryptophan and tyrosine), and small amino acids (glycine, alanine, serine, threonine and methionine).
- Amino acid substitutions which do not generally alter specific activity are known in the art and are described, for example, by H. Neurath and R.L. Hill, 1979, In, The Proteins, Academic Press, New York.
- the most commonly occurring exchanges are Ala/Ser, Val/lle, Asp/Glu, Thr/Ser, Ala/Gly, Ala/Thr, Ser/Asn, Ala/Val, Ser/Gly, Tyr/Phe, Ala/Pro, Lys/Arg, Asp/Asn, Leu/lle, Leu/Val, Ala/Glu, and Asp/Gly.
- the amylase of the invention has an amino acid sequence which differs by no more than 25, 24, 23, 22, 21 , 20, 19, 18, 17, 16, 15, 14, 13, 12, or no more than 11 amino acids from any one of (i) amino acids 1-481 of SEQ ID NO: 1 , (ii) amino acids 1- 481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3; or, it differs from any one of (i) amino acids 1-481 of SEQ ID NO: 1, (ii) amino acids 1-481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3 by no more than 10, 9, 8, 7, 6, 5, 4, 3, 2, or by no more than 1 amino acid.
- the amylase of the invention has an amino acid sequence which differs by no more than 40, 39, 38, 37, 36, 35, 34, 33, 32, 31 , 30, 29, 28, 27, or no more than 26 amino acids from any one of (i) amino acids 1-481 of SEQ ID NO: 1 , (ii) amino acids 1-481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3.
- the amylase of the invention is an allelic variant of any one of the amylases having (i) amino acids 1-481 of SEQ ID NO: 1 , (ii) amino acids 1- 481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3, or a fragment thereof that has amylase activity.
- the amylase of the invention may also be an allelic variant of any one of the amylases having the amino acid sequences of SEQ ID NO: 10, SEQ ID NO: 11 , and SEQ ID NO: 12.
- allelic variant denotes any of two or more alternative forms of a gene occupying the same chromosomal locus.
- allelic variation arises naturally through mutation, and may result in polymorphism within populations. Gene mutations can be silent (no change in the encoded polypeptide) or may encode polypeptides having altered amino acid sequences.
- An allelic variant of a polypeptide is a polypeptide encoded by an allelic variant of a gene.
- fragment is defined herein as a polypeptide having one or more amino acids deleted from the amino and/or carboxyl terminus of SEQ ID NO: 1 , SEQ ID NO: 2 or SEQ ID NO: 3, preferably having one or more amino acids deleted from the amino and/or carboxyl terminus of amino acids 1-481 , 1-484, 1-486, or 1-513 of SEQ ID NO: 1 ; of amino acids 1-481 of SEQ ID NO: 2, or of amino acids 1-483 of SEQ ID NO: 3.
- a small number of amino acids has been deleted, small being defined as explained above.
- a fragment contains at least 440, 441 , 442, 443, 444, 445, 446, 447, 448, 449, 450, 451 , 452, 453, or at least 454 amino acid residues. Most preferably, a fragment contains at least 452, 453 454, 455, 456, 457, 458, 459, 460, 461 , 462, 463, 464, 465, 466, 467, 468, 469, or at least 470 amino acid residues. Even more preferably, a fragment contains at least 471, 472, 473, 474, 475, 476, 477, 478, 479, or at least 480 amino acid residues.
- one embodiment of the present invention relates to an amylase for pharmaceutical use, wherein a) the amylase comprises an amino acid sequence selected from the group consisting of (i) amino acids 1-481 of SEQ ID NO: 1 , (ii) amino acids 1-481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3; and/or b) the amylase is a variant of an amino acid sequence selected from the group consisting of (i) amino acids 1-481 of SEQ ID NO: 1, (ii) amino acids 1-481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3, wherein the variant differs from the respective amino acid sequence by no more than twenty- five amino acids, and wherein: (i) the variant comprises at least one substitution, deletion and/or insertion of one or more amino acids as compared to the respective amino acid sequence; and/or (ii) the variant comprises at least one small deletion as compared to the respective amino acid sequence
- the present invention relates to an amylase for pharmaceutical use, wherein the amylase has an amino acid sequence selected from the group consisting of (i) amino acids 1-481 , 1-484, 1-486, or 1-513 of SEQ ID NO: 1 , (ii) amino acids 1-481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3.
- the amylase is derived from a microorganism, for example from a fungus, or from a bacterium.
- bacteria are strains of Bacillus, such as strains of Bacillus amyloliquefaciens, Bacillus circulans, Bacillus halmapalus, Bacillus licheniformis, Bacillus megaterium, Bacillus sp., Bacillus stearother- mophilus, and Bacillus subtilis; preferably from strains of Bacillus amyloliquefaciens, Bacillus circulans, Bacillus halmapalus, Bacillus licheniformis, Bacillus megaterium, Bacillus sp., and Bacillus stearothermophilus; most preferably from strains of Bacillus stearothermophilus, Bacillus licheniformis, or Bacillus sp.
- the term "derived from” includes enzymes obtainable, or obtained, from wildtype strains; as well as, preferably, variants thereof having at least one substitution, insertion, and/or deletion of at least one amino acid residue.
- the term variant also includes shufflants, hybrids, chimeric enzymes and consensus enzymes.
- the variants may have been produced by any method known in the art, such as site-directed mutagenesis, random mutagenesis, consensus derivation processes (EP 897985), and gene shuffling (WO 95/22625, WO 96/00343), etc.
- Non-limiting examples of wildtype amylases of the invention are those derived from Bacillus licheniformis, such as Swissprot entry name AMY_BACLI, primary accession number P06278; Bacillus amyloliquefaciens, such as Swissprot entry name AMY-BACAM, primary accession number P00692; Bacillus megaterium, such as Swissprot entry name AMY-BACME, primary accession number P20845; Bacillus circulans, such as Swissprot entry name AMY_BACCI, primary accession number P08137; Bacillus stearothermophilus, such as Swissprot entry name AMY-BACST, primary accession number P06279.
- Bacillus licheniformis such as Swissprot entry name AMY_BACLI, primary accession number P06278
- Bacillus amyloliquefaciens such as Swissprot entry name AMY-BACAM, primary accession number P00692
- Bacillus megaterium such as Swissprot entry name AM
- Another example is from Bacillus subtilis, such as Swissprot entry name AMY_BACSU, primary accession number P00691.
- a still further example is the amylase derived from Bacillus halmapalus, amino acids 1-485 of SEQ ID NO: 4.
- Non-limiting examples of amylase variants for use according to the invention are disclosed in WO 96/23873, WO 99/19467, US patent no. 4,933,279, EP 722490, and EP 904360.
- the amylase of the invention (i) is not Swissprot entry name AMY_BACLI, primary accession number P06278; and/or (ii) is not Swissprot entry name AMY_BACST, primary accession number P06279.
- amylases of the invention are the amylases contained in the following commercial products: Clarase, DexLo, GC 262 SP, G-Zyme G990, G-Zyme G995, G-Zyme G997, G-Zyme G998, HTAA, Optimax 7525, Purastar OxAm, Purastar ST, Spezyme AA, Spezyme Alpha, Spezyme BBA, Spezyme Delta AA, Spezyme DBA, Spezyme Ethyl, Spezyme Fred (GC521), Spezyme HPA, and Ultraphlow (all from Genencor); Validase BAA, Validase FAA, Validase HT340L, Valley Thin 340L (all from Valley Research); Avizyme 1500, Dextro 300 L, Kleistase, Maltazyme, Maxamyl, Thermozyme, Thermatex, Starzyme HT 120 L, Starzyme Super Cone, and Ultraphlo.
- amylases of the invention are the following: An amylase comprising amino acids 1-481 of SEQ ID NO: 1 , such as amylases having amino acids 1-481 of SEQ ID NO: 1 , amino acids 1-484 of SEQ ID NO: 1 , amino acids 1-486 of SEQ ID NO: 1 , or amino acids 1-513 of SEQ ID NO: 1 ; an amylase having amino acids 1-481 of SEQ ID NO: 2; and an amylase having amino acids 1-483 of SEQ ID NO: 3.
- an additional amylase may be used.
- additional amylases are mammalian amylases, and microbial proteases.
- a preferred mammalian amylase is pancreas extract, e.g. from swine or ox, such as pancreatin.
- the pancreatin may be used in the form of an uncoated (raw) product, or in the form of a formulated product (enteric coated (to provide resistance against gastric acid), or non- functionally coated (coated, but not to provide resistance against gastric acid)).
- Pancreatin potentially comprises still further enzymatic active constituents like pancreatic lipase, BSSL (Bile Salt Stimulated Lipase), and/or pancreatic protease.
- the microbial amylase may, for example, derive from bacterial or fungal strains, such as Bacillus, Pseudomonas, Aspergillus, or Rhizopus.
- the amylase may in particular be derived from a strain of Aspergillus, such as Aspergillus niger, Aspergillus oryzae or Aspergillus melleus, for example either of the products Amylase A1TM derived from Aspergillus oryzae which is commercially available from Amano Pharmaceuticals, Japan, or Amylase ECTM derived from Aspergillus melleus which is commercially available from Extract-Chemie, Germany.
- Aspergillus such as Aspergillus niger, Aspergillus oryzae or Aspergillus melleus
- Amylase A1TM derived from Aspergillus oryzae which is commercially available from Amano Pharmaceuticals, Japan
- Amylase ECTM derived from Aspergillus melleus which is commercially available from Extract-Chemie, Germany.
- amylase of the invention may be used, with or without a lipase as described below, in combination with a protease.
- protease is defined herein as an enzyme that hydrolyses peptide bonds. It includes any enzyme belonging to the EC 3.4 enzyme group (including each of the thirteen subclasses thereof, these enzymes being in the following referred to as "belonging to the EC 3.4.-.- group”).
- the protease may be a mammalian proteases, or a microbial proteases.
- a preferred mammalian protease is pancreas extract, e.g. from swine or ox, such as pancreatin.
- the pancreatin may be used in the form of an uncoated (raw) product, or in the form of a formulated product (enteric coated, or non-functionally coated). Pancreatin potentially comprises still further enzymatic active constituents like pancreatic lipase, BSSL, and/or pancreatic amylase.
- the microbial protease may be, e.g., based on or derived from bacterial or fungal strains.
- the protease may in particular be derived from a strain of Aspergillus, such as Aspergillus oryzae or Aspergillus melleus, in particular the product Prozyme 6TM (neutral, alkaline protease EC 3.4.21.63) which is commercially available from Amano Pharmaceuticals, Japan.
- bacterial proteases are proteases from Bacillus and Nocardiopsis, such as the Bacillus licheniformis protease having the amino acid sequence of amino acids 1-274 of SEQ ID NO: 5, the Nocardiopsis sp. protease having the amino acid sequence of amino acids 1-188 of SEQ ID NO: 6, or the Nocardiopsis ensembleonviellei subsp.
- the protease of amino acids 1-274 of SEQ ID NO: 5 may, e.g., be prepared as described in DK patent application no. 2005 00930 entitled “Proteases for Pharmaceutical Use” and filed on June 24, 2005 by Solvay Pharmaceuticals GmbH and Novozymes A/S.
- the proteases of amino acids 1-188 of SEQ ID NO: 6-7 may, e.g., be prepared as described in WO 2001/58276, or in WO 2004/111224.
- the protease is at least 70% identical to either of (i) amino acids 1-274 of SEQ ID NO: 5, (ii) amino acids 1-188 of SEQ ID NO: 6, and/or (iii) amino acids 1-188 of SEQ ID NO: 7.
- the degrees of identity is at least 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or at least 99%.
- the degrees of identity is at least about 50%, 51 %, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%, 64%, 65%, 66%, 67%, 68%, or at least 69%.
- the amylase of the invention may be used, with or without a protease as mentioned above, in combination with a lipase.
- a lipase means a carboxylic ester hydrolase EC 3.1.1.-, which includes activities such as EC 3.1.1.3 triacylglycerol lipase, EC 3.1.1.4 phospholipase A1 , EC 3.1.1.5 lysophospholipase, EC 3.1.1.26 galactolipase, EC 3.1.1.32 phospholipase A1 , EC 3.1.1.73 feruloyl esterase.
- the lipase is an EC 3.1.1.3 triacylglycerol lipase.
- the lipase may be a mammalian lipase, or a microbial lipase.
- a preferred mammalian lipase is pancreas extract, e.g. from swine or ox, such as pancreatin.
- the pancreatin may be used in the form of an uncoated (raw) product, or in the form of a formulated product (enteric coated, or non-functionally coated). Pancreatin potentially comprises still further enzymatic active constituents like pancreatic protease, BSSL, and/or pancreatic amylase.
- the microbial lipase may, for example, be derived from bacterial or fungal strains, such as Bacillus, Pseudomonas, Aspergillus, or Rhizopus.
- the lipase may in particular be derived from a strain of Rhizopus, such as Rhizopus javanicus, Rhizopus oryzae, or Rhizopus delemar, for example the product Lipase D Amano 2000TM (also designated Lipase D2TM) which is commercially available from Amano Pharmaceuticals, Japan.
- the lipase is a recombinantly produced microbial lipase, for example derived from a fungus such as Humicola or Rhizomucor, from a yeast such as Candida, or from a bacterium such as Pseudomonas.
- the lipase is derived from a strain of Humicola lanuginosa or Rhizomucor miehei.
- the Humicola lanuginosa (synonym Thermomyces lanuginosus) lipase (SEQ ID NO: 9) is described in EP 305216, and particular lipase variants are described in, for example, WO 92/05249, WO 92/19726, WO 94/25577, WO 95/22615, WO 97/04079, WO 97/07202, WO 99/42566, WO 00/32758, WO 00/60063, WO 01/83770, WO 02/055679, and WO 02/066622.
- a preferred lipase variant is a lipase comprising amino acids 1-269, or 2-269, of SEQ ID NO: 8, such as the following: (i) amino acids +1 to +269 of SEQ ID NO: 8, (ii) amino acids -5 to +269 of SEQ ID NO: 8, (iii) amino acids -4 to +269 of SEQ ID NO: 8; (iv) amino acids -3 to +269 of SEQ ID NO: 8; (v) amino acids -2 to +269 of SEQ ID NO: 8; (vi) amino acids -1 to +269 of SEQ ID NO: 8, (vii) amino acids +2 to +269 of SEQ ID NO: 1 , as well as (viii) any mixture of two or more of the lipases of (i)-(vii) - and variants thereof.
- the lipase for use according to the invention is selected from the lipases of (i), (ii), and any mixture of (i) and (ii).
- Preferred mixtures of (i) and (ii) comprise at least 5%, preferably at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or at least 95% of lipase (i), the percentages being determined by N-terminal sequencing using the Edman method, as described in Example 5 of the PCT application that claims priority from DK patent application no. 2005 00929.
- compositions comprising 35-75%, preferably 40-70%, more preferably 45-65% of lipase (ii);
- the lipases of SEQ ID NO: 8 and 9 may, e.g., be prepared on the basis of the basis of the teaching in US patent no. 5,869,438 (in which SEQ ID NO: 1 is a DNA sequence encoding the lipase of SEQ ID NO: 9).
- the lipase of SEQ ID NO: 8 can, e.g., be prepared by recombinant expression in a suitable host cell of a DNA sequence which is a modification of SEQ ID NO:1 of the US patent, the modification reflecting the amino acid differences between SEQ ID NO: 8 and 9 herein. Such modifications can be made by site-directed mutagenesis, as is known in the art.
- fungal lipases are the cutinase from Humicola insolens which is described in EP 785994, and the phospholipase from Fusarium oxysporum which is described in EP 869167.
- yeast lipases are lipase A and B from Candida antarctica of which lipase A is described in EP 652945, and lipase B is described by, for example, Uppenberg et al in Structure, 2 (1994), 293.
- An example of a bacterial lipase is the lipase derived from Pseudomonas cepacia, which is described in EP 214761.
- the lipase is at least 70% identical to the lipase of SEQ ID NO: 8, or to amino acids 1-269 thereof.
- the degree of identity to SEQ ID NO: 8, or to amino acids 1-269 thereof is at least 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or at least 99%.
- the degree of identity to SEQ ID NO: 8, or to amino acids 1-269 thereof is at least about 50%, 51%, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%, 64%, 65%, 66%, 67%, 68%, or at least 69%.
- the lipase like the mammalian pancreatic lipase, is a 1 ,3-position specific lipase.
- particularly preferred combinations of enzymes are the following: (i) The protease of amino acids 1-274 of SEQ ID NO: 5 in combination with an amylase comprising amino acids 1-481 of SEQ ID NO: 1 (such as amino acids 1-481 , 1-484, 1-486, or 1-513 thereof); (ii) the protease of amino acids 1-274 of SEQ ID NO: 5 in combination with the amylase of SEQ ID NO: 2; (iii) the protease of amino acids 1- 274 of SEQ ID NO: 5 in combination with the amylase of SEQ ID NO: 3; (iv) the protease of amino acids 1-188 of SEQ ID NO: 6 in combination with an amylase comprising amino acids 1- 481 of SEQ ID NO: 1 (such as amino acids 1-481 , 1-484, 1-486, or 1-513 thereof); (v) the protease of amino acids 1-188 of SEQ ID NO: 6 in combination with the amylase of SEQ ID NO: 5 in combination with
- one embodiment of the present invention relates to an amylase in combination with a lipase and/or a protease according to claim 4 or 5, wherein the amylase is an amylase selected from the group consisting of a) an amylase comprising amino acids 1-481 of SEQ ID NO: 1 , b) an amylase having amino acids 1-481 of SEQ ID NO: 2, and c) an amylase having amino acids 1-483 of SEQ ID NO: 3; (ii) the lipase comprises amino acids 2- 269 of SEQ ID NO: 8; (iii) the protease is a protease selected from the group consisting of a) a protease having amino acids 1-274 of SEQ ID NO: 5, b) a protease having amino acids 1-188 of SEQ ID NO: 6, and c) a protease having amino acids 1-188 of SEQ ID NO: 7.
- the amylase is an amylase selected from the group consisting of a) an
- enzymes are the following: (i) A protease having at least 50% identity to amino acids 1-274 of SEQ ID NO: 5 in combination with an amylase having at least 50% identity to amino acids 1-481 of SEQ ID NO: 1 ; (ii) a protease having at least 50% identity to amino acids 1-274 of SEQ ID NO: 5 in combination with an amylase having at least 50% identity to amino acids 1-481 of SEQ ID NO: 2; (iii) a protease having at least 50% identity to amino acids 1-274 of SEQ ID NO: 5 in combination with an amylase having at least 50% identity to amino acids 1-483 of SEQ ID NO: 3; (iv) a protease having at least 50% identity to amino acids 1-188 of SEQ ID NO: 6 in combination with an amylase having at least 50% identity to amino acids 1-481 of SEQ ID NO: 1 ; (v) a protease having at least 50% identity to amino acids 1-188 of SEQ ID NO: 6 in combination with an amy
- each degree of identity is, independently, at least 51 %, 52%, 53%, 54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%, 64%, 65%, 66%, 67%, 68%, 69%, 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or at least 99%.
- one embodiment of the invention relates to an amylase in combination with a lipase and/or a protease according to claim 4 or 5, wherein (i) the amylase is an amylase as defined herein; (ii) the lipase has at least 70% identity to a lipase having amino acids 1-269 of SEQ ID NO: 8; (ii) the protease has at least 70% identity to a protease selected from the group consisting of a) a protease having amino acids 1-274 of SEQ ID NO: 5, b) a protease having amino acids 1-188 of SEQ ID NO: 6, and c) a protease having amino acids 1- 188 of SEQ ID NO: 7.
- the amylase, protease, and lipase enzymes (hereinafter “the enzyme(s)”) of the invention may be natural or wild-type enzymes obtained from animals, in particular mammals, for example human or swine enzymes; from plants, or from microorganisms, but also any mutants, variants, fragments etc. thereof exhibiting the desired enzyme activity, as well as synthetic enzymes, such as shuffled, hybrid, or chimeric enzymes, and consensus enzymes.
- the enzyme(s) are low-allergenic variants, designed to invoke a reduced immunological response when exposed to animals, including man.
- the term immunological response is to be understood as any reaction by the immune system of an animal exposed to the enzyme(s).
- One type of immunological response is an allergic response leading to increased levels of IgE in the exposed animal.
- Low-allergenic variants may be prepared using techniques known in the art.
- the enzyme(s) may be conjugated with polymer moieties shielding portions or epitopes of the enzyme(s) involved in an immunological response. Conjugation with polymers may involve in vitro chemical coupling of polymer to the enzyme(s), e.g.
- Conjugation may in addition or alternatively thereto involve in vivo coupling of polymers to the enzyme(s). Such conjugation may be achieved by genetic engineering of the nucleotide sequence encoding the enzyme(s), inserting consensus sequences encoding additional glycosylation sites in the enzyme(s) and expressing the enzyme(s) in a host capable of glycosylating the enzyme(s), see e.g. WO 00/26354.
- Another way of providing low-allergenic variants is genetic engineering of the nucleotide sequence encoding the enzyme(s) so as to cause the enzymes to self-oligomerize, effecting that enzyme monomers may shield the epitopes of other enzyme monomers and thereby lowering the antigenicity of the oligomers.
- Such products and their preparation is described e.g. in WO 96/16177.
- Epitopes involved in an immunological response may be identified by various methods such as the phage display method described in WO 00/26230 and WO 01/83559, or the random approach described in EP 561907.
- an epitope Once an epitope has been identified, its amino acid sequence may be altered to produce altered immunological properties of the enzyme(s) by known gene manipulation techniques such as site directed mutagenesis (see e.g. WO 00/26230, WO 00/26354 and/or WO 00/22103) and/or conjugation of a polymer may be done in sufficient proximity to the epitope for the polymer to shield the epitope.
- gene manipulation techniques such as site directed mutagenesis (see e.g. WO 00/26230, WO 00/26354 and/or WO 00/22103) and/or conjugation of a polymer may be done in sufficient proximity to the epitope for the polymer to shield the epitope.
- the enzyme(s) are (i) stable at pH 2-8, preferably also at pH 3-7, more preferably at pH 4-6; (ii) active at pH 4-9, preferably 4-8; (iii) stable against degradation by pepsin and other digestive proteases (such as pancreas proteases, i.e., mainly trypsin and chymotrypsin); and/or (iv) stable and/or active in the presence of bile salts.
- the amylase of the invention has an activity at pH 7.0 and
- the activity at pH 7.0 and 37°C is at least 40, 45, 50, 55, 60, 65, 70, or at least 75% of the activity at the pH-optimum and 37°C (cf. Table 2 of Example 3).
- the amylase of the invention has an activity at pH 7.0 and 37°C and in the presence of 5mM bile salts of at least 25% relative to the activity at the pH-optimum and 37°C in the absence of bile salts. More preferably, the activity at pH 7.0 and 37 0 C and in the presence of 5mM bile salts is at least 30, 35, 40, 45, 50, 55, 60, or at least 65% of the activity at the pH-optimum and 37 0 C in the absence of bile salts (cf.
- the specific activity of the amylase of the invention, at pH 7.0 and 37°C, is at least 10%, more preferably at least 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, or at least 70%, relative to the specific activity of the amylase of SEQ ID NO: 1 at pH 5.0 and 37°C (cf. Table 4 of Example 3).
- the specific activity of the amylase of the invention, at pH 7.0 and 37°C and in the presence of 5mM bile salts is at least 10%, more preferably at least 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, or at least 75%, relative to the specific activity of the amylase of SEQ ID NO: 1 at pH 5.0 and 37°C and in the presence of 5mM bile salts (cf. Table 5 of Example 3).
- the activities referred to in the above preferred embodiments may suitably be determined using a reducing sugar assay, e.g. as described in Example 3, using preferably waxy corn as a substrate. A detailed procedure is described in Example 3.
- the amylase of the invention has a starch degradation profile with one or more of the following characteristic features: (i) DP1 is detected as a degradation product; (i) the DP4 amount is lower than the amount of DP5; (iii) the DP4 amount is lower than the amount of DP6; and/or (iv) the amount of DP5 and/or DP6 is higher than the amount of DP1.
- the monomer DP1 is preferably glucose, and the DP2-DP6 products are dimers-hexamers, respectively, of glucose.
- the degradation profile may be determined using HPLC as described in Example 4, i.e. after having incubated for 24 hours at a temperature of 60 or 37 0 C, at a pH of 6.0 or 5.5, preferably using waxy corn as a substrate, more preferably in the presence of Ca 2+ .
- the term "in combination with” refers to the combined use according to the invention of the protease, lipase, and/or amylase.
- the combined use can be simultaneous, overlapping, or sequential, these three terms being generally interpreted in the light of the prescription made by the physician.
- the term “simultaneous” refers to circumstances under which the enzymes are active at the same time, for example when they are administered at the same time as one or more separate pharmaceutical products, or if they are administered in one and the same pharmaceutical composition.
- sequential refers to such instances where one and/or two of the enzymes are acting first, and the second and/or third enzyme subsequently.
- a sequential action can be obtained by administering the enzymes in question as separate pharmaceutical formulations with desired intervals, or as one pharmaceutical composition in which the enzymes in question are differently formulated (compartmentalized), for example with a view to obtaining a different release time, providing an improved product stability, or to optimizing the enzyme dosage.
- overlapping refers to such instances where the enzyme activity periods are neither completely simultaneous nor completely sequential, viz. there is a certain period in which the enzymes are both, or all, active.
- a for example when used in the context of the enzyme(s) of the invention, means at least one.
- “a” means “one or more,” or “at least one”, which again means one, two, three, four, five etc.
- the alignment of two amino acid sequences is determined by using the Needle program from the EMBOSS package (http://emboss.org) version 2.8.0.
- the Needle program implements the global alignment algorithm described in
- invention sequence e.g. amino acids 1-481 of SEQ ID NO: 1
- foreign sequence e.g. amino acids 1-514 of SEQ ID NO: 12
- the length of a sequence is the number of amino acid residues in the sequence (e.g. the length of SEQ ID NO: 1 is 481).
- the percentage of identity of an amino acid sequence of a polypeptide with, or to, amino acids 1-481 of SEQ ID NO: 1 is determined by i) aligning the two amino acid sequences using the Needle program, with the BLOSUM62 substitution matrix, a gap opening penalty of 10, and a gap extension penalty of 0.5; ii) counting the number of exact matches in the alignment; iii) dividing the number of exact matches by the length of the shortest of the two amino acid sequences, and iv) converting the result of the division of iii) into percentage.
- the percentage of identity to, or with, other sequences of the invention such as amino acids 1-481 of SEQ ID NO: 2, or 1-483 of SEQ ID NO: 3, is calculated in an analogous way.
- the degree of identity between two amino acid sequences may be determined by the program "align" which is a Needleman-Wunsch alignment (i.e. a global alignment).
- the sequences are aligned by the program, using the default scoring matrix BLOSUM50.
- the penalty for the first residue of a gap is 12, and for further residues of a gap the penalties are 2.
- the Needleman-Wunsch algorithm is described in Needleman, S.B. and Wunsch, CD., (1970), Journal of Molecular Biology, 48: 443-453, and the align program by Myers and W.
- the degree of identity between a sample, or test, sequence of any of the enzyme(s) of the invention and a specified sequence may be determined as follows: The two sequences are aligned using the program "align.” The number of perfect matches ("N-perfect-match") in the alignment is determined (a perfect match means same amino acid residue in same position of the alignment). The common length of the two aligned sequences is also determined, viz. the total number of amino acids in the alignment (the overlap), including trailing and leading gaps created by the alignment, if any ("N-overlap"). The degree of identity is calculated as the ratio between "N-perfect-match" and "N-overlap” (for conversion to percentage identity, multiply by 100).
- the degree of identity between the sample, or test, sequence and a specified sequence may be determined as follows: The sequences are aligned using the program "align.” The number of perfect matches ("N-perfect-match”) in the alignment is determined (a perfect match means same amino acid residue in same position of the alignment). The length of the sample sequence (the number of amino acid residues) is determined ("N-sample”). The degree of identity is calculated as the ratio between "N-perfect- match” and "N-sample” (for conversion to percentage identity, multiply by 100).
- the degree of identity between the sample, or test, sequence and a specified sequence may be determined as follows: The sequences are aligned using the program "align.” The number of perfect matches ("N-perfect-match”) in the alignment is determined (a perfect match means same amino acid residue in same position of the alignment). The length of the specified sequence (the number of amino acid residues) is determined (“N-specified”). The degree of identity is calculated as the ratio between "N-perfect- match” and "N-specified” (for conversion to percentage identity, multiply by 100).
- the overlap is at least 20% of the specified sequence ("N-overlap" as defined above, divided by the number of the amino acids in the specified sequence ("N- specified"), and multiplied by 100), more preferably at least 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, or at least 95%.
- N-overlap as defined above, divided by the number of the amino acids in the specified sequence
- N- specified the specified sequence
- the overlap is at least 20% of the specified sequence (N-overlap" as defined above, divided by the number of the amino acids in the specified sequence ("N- specified"), and multiplied by 100), more preferably at least 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, or at least 95%.
- at least 20% (preferably 25-95%) of the amino acids of the specified sequence end up being included in the overlap, when the sample sequence is aligned to the specified sequence.
- the overlap is at least 20% of the specified sequence ("N-overlap” as defined above, divided by "N-sample” as defined above, and multiplied by 100), more preferably at least 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, or at least 95%.
- the activity of the enzyme(s) of the invention can be measured using any suitable assay.
- assay-pH and assay-temperature may be adapted to the enzyme in question.
- assay-pH-values are pH 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 , or 12.
- assay-temperatures are 30, 35, 37, 40, 45, 50, 55, 60, 65, 70, 80, 90, or 95 0 C.
- Preferred pH values and temperatures are in the physiological range, such as pH values of 4, 5, 6, 7, or 8, and temperatures of 30, 35, 37, or 40 0 C.
- Suitable assays are described in the experimental part, and in DK patent application no. 2005 00929 and 2005 00930 as well as the corresponding PCT-applications. Other examples are the Ph. Eur. assays for protease, lipase and amylase activity.
- the term "medicament” means a compound, or mixture of compounds, that treats, prevents and/or alleviates the symptoms of disease, preferably treats and/or alleviates.
- the medicament may be prescribed by a physician, or it may be an over-the- counter product.
- Isolation, purification, and concentration of the enzyme(s) of the invention may be carried out by conventional means.
- they may be recovered from a fermentation broth by conventional procedures including, but not limited to, centrifugation, filtration, extraction, spray-drying, evaporation, or precipitation, and further purified by a variety of procedures known in the art including, but not limited to, chromatography (e.g., ion exchange, affinity, hydrophobic, chromatofocusing, and size exclusion), electrophoretic procedures (e.g., preparative isoelectric focusing), differential solubility (e.g., ammonium sulphate precipitation), SDS-PAGE, or extraction (see, e.g., Protein Purification, J.-C. Janson and Lars Ryden, editors, VCH Publishers, New York, 1989).
- chromatography e.g., ion exchange, affinity, hydrophobic, chromatofocusing, and size exclusion
- electrophoretic procedures e.g., preparative isoelectric
- DNA encoding the amylase of the invention may be recombinant ⁇ expressed in a Bacillus host cell as is known in the art, and purified from the fermentation liquid by process steps like centrifugation, filtration, ultrafiltration and, if desired, germ-filtration. Additional, optional, process steps include various kinds of chromatography like, e.g., ion-exchange chromatograhpy and hydrophobic interaction chromatography.
- a suitable hydrophobic column material is butyl or phenyl, and such columns are commercially aviable, e.g. from Pharmacia.
- the pi of the amylases of SEQ ID NO: 1, 2, and 3 are 5.7, 7.3, and 8.8, respectively, and the molecular weights approximately 55 kDa by SDS-PAGE for all three amylases.
- concentrated solid or liquid preparations of each of the enzyme(s) are prepared separately. These concentrates may also, at least in part, be separately formulated, as explained in more detail below.
- the enzyme(s) are incorporated in the pharmaceutical compositions of the invention in the form of solid concentrates.
- the enzyme(s) can be brought into the solid state by various methods as is known in the art.
- the solid state can be either crystalline, where the enzyme molecules are arranged in a highly ordered form, or a precipitate, where the enzyme molecules are arranged in a less ordered, or disordered, form.
- Crystallization may, for example, be carried out at a pH close to the pi of the enzyme(s) and at low conductivity, for example 10 mS/cm or less, as described in EP 691982.
- precipitation methods including precipitation with salts, such as ammonium sulphate, and/or sodium sulphate; with organic solvents, such as ethanol, and/or isopropanol; or with polymers, such as PEG (Poly Ethylene Glycol).
- the enzyme(s) can be precipitated from a solution by removing the solvent (typically water) by various methods known in the art, e.g. lyophilization, evaporation (for example at reduced pressure), and/or spray drying.
- the solid concentrate of the enzyme(s) has a content of active enzyme protein of at least 50% (w/w) by reference to the total protein content of the solid concentrate.
- the content of active enzyme protein, relative to the total protein content of the solid concentrate is at least 55, 60, 65, 70, 75, 80, 85, 90, or at least 95% (w/w).
- the protein content can be measured as is known in the art, for example by densitometer scanning of coomassie-stained SDS-PAGE gels, e.g. using a GS-800 calibrated densitometer from BIO-RAD; by using a commercial kit, such as Protein Assay ESL, order no. 1767003, which is commercially available from Roche, or on the basis of the method described in Example 8 of WO 01/58276.
- the amylase enzyme protein constitutes at least 50%, more preferably at least 55, 60, 65, 70, 75, 80, 85, 90, 92, 94, 95, 96, or at least 97% of the protein spectrum of the solid lipase concentrate for use according to the invention, as measured by densitometer scanning of a coomassie-stained SDS-PAGE gel.
- a pharmaceutical composition of the invention comprises the enzyme(s), preferably in the form of concentrated enzyme preparations, more preferably solid concentrates, together with at least one pharmaceutically acceptable auxiliary, or subsidiary, material such as (i) at least one carrier and/or excipient; or (ii) at least one carrier, excipient, diluent, and/or adjuvant.
- Non-limiting examples of, optional, other ingredients, all pharmaceutically acceptable are disintegrators, lubricants, buffering agents, moisturizing agents, preservatives, flavouring agents, solvents, solubilizing agents, suspending agents, emulsifiers, stabilizers, propellants, and vehicles.
- the composition of the invention may be designed for all manners of administration known in the art, preferably including enteral administration (through the alimentary canal).
- the composition may be in solid, semi-solid, liquid, or gaseous form, such as tablets, capsules, powders, granules, microspheres, ointments, creams, foams, solutions, suppositories, injections, inhalants, gels, microspheres, lotions, and aerosols.
- the medical practitioner will know to select the most suitable route of administration and of course avoid potentially dangerous or otherwise disadvantageous administration routes.
- the enzyme(s) can be used alone or in combination with appropriate additives to make pellets, micropellets, tablets, microtablets, powders, granules or capsules, for example, with conventional carriers, such as lactose, mannitol, corn starch, or potato starch; with excipients or binders, such as crystalline, or microcrystalline, cellulose, cellulose derivatives, acacia, corn starch, or gelatins; with disintegrators, such as corn starch, potato starch, or sodium carboxymethylcellulose; with lubricants, such as carnauba wax, white wax, shellac, waterless colloid silica, polyethylene glycol (PEGs, also known under the term macrogol) from 1500 to 20000, in particular PEG 4000, PEG 6000, PEG 8000, povidone, talc, monolein, or magnesium stearate; and if desired, with diluents, adjuvants, buffering agents, moistening
- conventional carriers such
- the enzyme(s) can also, quite generally, be formulated into liquid oral preparations, by dissolving, suspending, or emulsifying them in an aqueous solvent such as water, or in nonaqueous solvents such as vegetable or other similar oils, synthetic aliphatic acid glycerides, esters of higher aliphatic acids, propylene glycol, polyethylene glycol such as PEG 4000, or lower alcohols such as linear or ramified C1-C4 alcohols, for example 2-propanol; and if desired, with conventional subsidiary materials or additives such as solubilizers, adjuvants, diluents, isotonic agents, suspending agents, emulsifying agents, stabilizers, and preservatives.
- an aqueous solvent such as water, or in nonaqueous solvents such as vegetable or other similar oils, synthetic aliphatic acid glycerides, esters of higher aliphatic acids, propylene glycol, polyethylene glycol such as PEG 4000,
- the enzyme(s) can generally be made into suppositories for rectal administration by mixing with a variety of bases such as emulsifying bases or water-soluble bases.
- bases such as emulsifying bases or water-soluble bases.
- the suppository can include vehicles such as cocoa butter, carbowaxes and polyethylene glycols, which melt at body temperature, yet are solidified at room temperature.
- the use of liposomes as a delivery vehicle is another method of possible general interest.
- the lipids may be any useful combination of known liposome forming lipids, including cationic or zwitterionic lipids, such as phosphatidylcholine.
- the remaining lipid will normally be neutral or acidic lipids, such as cholesterol, phosphatidyl serine, phosphatidyl glycerol, and the like.
- the procedure described by Kato et al. (1991) J. Biol. Chem. 266:3361 may be used.
- Unit dosage forms for oral or rectal administration such as syrups, elixirs, powders, and suspensions may be provided wherein each dosage unit, for example, teaspoonful, tablespoonful, capsule, tablet or suppository, contains a predetermined amount of the enzyme(s).
- unit dosage forms for injection or intravenous administration may comprise the enzyme(s) in a composition as a solution in sterile water, normal saline, or another pharmaceutically acceptable carrier.
- unit dosage form refers to physically discrete units suitable as unitary dosages for human and animal subjects, each unit containing a predetermined quantity of enzyme(s) in an amount sufficient to produce the desired effect.
- the pharmaceutical composition of the invention is for enteral, preferably oral, administration.
- the oral composition is (i) a liquid composition containing crystals of the enzyme(s); (ii) a liquid suspension of sediments of (highly) purified enzyme(s); (iii) a gel containing the enzyme(s) in solid or solubilized form; (iv) a liquid suspension of immobilized enzyme(s) or of enzymes adsorbed to particles and the like; or (v) a solid composition in the form of enzyme(s)-containing powder, pellets, granules, or microspheres, if desired in the form of tablets, capsules, or the like, that are optionally coated, for example with an acid-stable coating.
- the enzyme(s) are compartmentalized, viz. separated from each other, for example by means of separate coatings.
- the protease is separated from other enzyme components of the composition, such as the lipase, and/or the amylase.
- the dosage of the enzyme(s) will vary widely, depending on the specific enzyme(s) to be administered, the frequency of administration, the manner of administration, the severity of the symptoms, and the susceptibility of the subject to side effects, and the like. Some of the specific enzymes may be more potent than others.
- Examples of solid oral preparations of the enzyme(s) of the invention comprise: (i) an amylase of at least 50% identity to (i) amino acids 1-481 of SEQ ID NO: 1 , (ii) amino acids 1- 481 of SEQ ID NO: 2, and/or (iii) amino acids 1-483 of SEQ ID NO: 3; (ii) a protease having at least 70% identity to a protease selected from the group consisting of a) a protease having amino acids 1-274 of SEQ ID NO: 5, b) a protease having amino acids 1-188 of SEQ ID NO: 6, and c) a protease having amino acids 1-188 of SEQ ID NO: 7; and/or (iii) a lipase having at least 70% identity to a lipase having amino acids 1-269 of SEQ ID NO: 8; wherein preferably the anticipated daily clinical dosages of the enzymes of (i), (ii), and (iii) are as follows (all in mg
- a preferred example of solid oral preparations of the enzyme(s) of the invention comprise: (i) an amylase comprising amino acids 1-481 of SEQ ID NO: 1, (ii) a protease comprising amino acids 1-274 of SEQ ID NO: 5, and/or (i) a lipase comprising amino acids 2- 269 of SEQ ID NO: 8.
- Examples of anticipated daily clinical dosages of the enzymes of (i), (ii), and (iii) are as follows (all in mg enzyme protein per kg of bodyweight (bw)): For the amylase of (i): 0.01-50, 0.05-10, or 0.1-5 mg/kg bw; for the protease of (ii): 0.05-100, 0.1-50, or 0.5-25 mg/kg bw; for the lipase of (iii): 0.1-250, 0.5-100, or 1-50 mg/kg bw.
- the amide (peptide) bonds, as well as the amino and carboxy termini, may be modified for greater stability on oral administration.
- the carboxy terminus may be amidated.
- compositions of the invention suitable for the treatment of digestive disorders, PEI, pancreatitis, cystic fibrosis, diabetes type I, and/or diabetes type II, may be prepared by incorporating the enzyme(s) of the invention into pellets.
- the pellets may generally comprise from 10-90% (w/w, relative to the dry weight of the resulting pellets) of a physiologically acceptable organic polymer, from 10-90% (w/w, relative to the dry weight of the resulting pellets) of cellulose or a cellulose derivative, and from 80-20% (w/w, relative to the dry weight of the resulting pellets) of the enzyme(s), the total amount of organic polymer, cellulose or cellulose derivative and enzyme(s) making up to 100% in each case.
- the physiologically acceptable organic polymer can be selected from the group consisting of polyethylene glycol 1500, polyethylene glycol 2000, polyethylene glycol 3000, polyethylene glycol 4000, polyethylene glycol 6000, polyethylene glycol 8000, polyethylene glycol 10000, polyethylene glycol 20000, hydroxypropyl methylcellulose, polyoxyethylen, copolymers of polyoxyethylen-polyoxypropylen and mixtures of said organic polymers.
- Polyethylene glycol 4000 is preferred as physiologically acceptable organic polymer.
- the cellulose or a cellulose derivative can e.g. be selected from cellulose, cellulose acetate, cellulose fatty acid ester, cellulose nitrates, cellulose ether, carboxymethyl cellulose, ethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, methyl cellulose, methyl ethylcellulose and methylhydroxypropyl cellulose.
- Cellulose, in particular microcrystalline cellulose is preferred as cellulose or cellulose derivative.
- the resulting pellets may be coated with a suitable enteric coating, other non functional coating or be used directly without such coating. Further, the resulting pellets may be filled in capsules like hard gelatin capsules or gelatin free capsules of a suitable size for therapy of a disorder or disease as described in more detail above.
- pellets produced from different enzyme types in particular from lipase, protease and/or amylase may be filled into said capsules. While filling the capsules with the different enzyme types, the dosing of the single enzyme types (viz.
- lipase, protease or amylase may be adapted to specific needs of a certain indication group or a certain patient subgroup by adding a specified amount of any of lipase, protease and/or amylase to the capsules, i.e. capsules may be produced which vary in their specific ratios of lipase:protease:amylase.
- the pharmaceutical composition comprises a macrogolglyceride mixture of mono-, di- and tri-acylglycerides and polyethylene glycol (PEG) mono- and di-esters of aliphatic C6-C22 carboxylic acids, and also possibly small proportions of glycerol and free polyethylene glycol.
- PEG polyethylene glycol
- the polyethylene glycol (PEG) contained in the macrogolglyceride mixtures is preferably PEG which has on average 6 to at most 40 ethylene oxide units per molecule or a molecular weight of between 200 and 2000.
- One further aspect of the invention provides for the pharmaceutical composition of the enzyme(s) of the invention to comprise a system consisting of surfactant, co-surfactant and lipophilic phase, the system having an HLB value (Hydrophilic-Lipophilic Balance) greater than or equal to 10 and a melting point greater than or equal to 3O 0 C.
- the system has an HLB value of 10 to 16, preferably of 12 to 15, and has a melting point of between 30 and 600°C, preferably between 40 and 500 0 C.
- the system characterised by HLB value and melting point is a mixture of mono-, di- and triacylgylcerides and mono- and diesters of polyethylene glycol (PEG) with aliphatic carboxylic acids with 8 to 20, preferably 8 to 18, carbon atoms, whereby the polyethylene glycol preferably has about 6 to about 32 ethylene oxide units per molecule, and the system optionally contains free glycerin and/or free polyethylene glycol.
- PEG polyethylene glycol
- the HLB value of such a system is preferably regulated by the chain length of the PEG.
- the melting point of such a system is regulated by the chain length of the fatty acids, the chain length of the PEG and the degree of saturation of the fatty-acid chains, and hence the starting oil for the preparation of the macrogolglyceride mixture.
- “Aliphatic C8-C18 carboxylic acids” designates mixtures in which caprylic acid (C8), capric acid (C10), lauric acid (C12), myristic acid (C14), palmitic acid (C16) and stearic acid (C18) are contained in a significant and variable proportion, if these acids are saturated, and the corresponding unsaturated C8-C18 carboxylic acids. The proportions of these fatty acids may vary according to the starting oils.
- Such a mixture of mono-, di- and triacylgylcerides and mono- and diesters of polyethylene glycol (PEG) with aliphatic carboxylic acids with 8 to 18 carbon atoms can for example be obtained by a reaction between a polyethylene glycol with a molecular weight of between 200 and 1500 and a starting oil, the starting oil consisting of a triglyceride mixture with fatty acids which are selected from the group containing caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid and linolenic acid, individually or as a mixture.
- the product of such a reaction may also contain small proportions of glycerin and free polyethylene glycol.
- Ge- lucire® Such mixtures are commercially available for example under the trade name Ge- lucire®.
- One advantageous embodiment of the invention provides that, of the products known under the trade name Gelucire ®, in particular "Gelucire ® 50/13" and/or “Gelucire® 44/14" represent suitable mixtures for use in the pharmaceutical preparations according to the invention.
- Gelucire® 50/13 is a mixture with mono-, di- and triacylglycerides and mono- and diesters of polyethylene glycol, with palmitic acid (C16) and stearic acid (C18) at 40% to 50% and 48% to 58%, respectively making up the major proportion of bound fatty acids.
- the proportion of caprylic acid (C8) and capric acid (C10) is less than 3% in each case, and the proportion of lauric acid (C12) and myristic acid (C14) in each case is less than 5%.
- Gelucire® 44/14 is a mixture with mono-, di- and triacylgylcerides and mono- and diesters of polyethylene glycol, the respective proportions of palmitic acid (C16) being 4 to 25%, stearic acid (C18) 5 to 35%, caprylic acid (C8) less than 15%, capric acid (C10) less than 12%, lauric acid (C12) 30 to 50% and myristic acid (C14) 5 to 25%.
- Gelucire® 44/14 can for example be prepared by an alcoholysis/esterification reaction using palm kernel oil and polyethylene glycol 1500.
- a preferred embodiment of the present invention provides for a pharmaceutical composition of the enzyme(s) of the invention which comprises a system containing a mixture of mono-, di- and triacyl- glycerides and polyethylene glycol mono- and diesters of aliphatic C8-C18 carboxylic acids and also possibly small proportions of glycerin and free polyethylene glycol, the system having a melting point between 40 0 C and 55°C and an HLB value in the range between 12 and 15. More preferred, the system has a melting point between 44°C and 50 0 C and an HLB value in the range from 13 - 14. Alternatively, the system has a melting point around 44 0 C and an HLB value of 14, or the system has a melting point around 50 0 C and an HLB value of 13.
- amylase of the invention optionally in combination with a lipase, and/or a protease
- animal includes all animals, and in particular human beings. Examples of animals are non-ruminants, and ruminants, such as sheep, goat, and cattle, e.g. beef cattle, and cow. In a particular embodiment, the animal is a non-ruminant animal.
- Non-ruminant animals include mono-gastric animals, e.g.
- pig including, but not limited to, piglets, growing pigs, and sows
- poultry such as turkey, duck and chicken (including but not limited to broiler chicks, layers); young calves; pets such as cat, and dog; and fish (including but not limited to salmon, trout, tilapia, catfish and carps); and crustaceans (including but not limited to shrimps and prawns).
- the animal is a mammal, more in particular a human being.
- the enzyme(s) are useful in the treatment of digestive disorders like maldigestion or dyspepsia that are often caused by a deficient production and/or secretion into the gastrointestinal tract of digestive enzymes normally secreted from, i.a., the stomach, and the pancreas.
- PEI can be verified using, i.a., the Borgstrom test (JOP. J Pancreas (Online) 2002; 3(5):116-125), and it may be caused by diseases and conditions such as pancreatic cancer, pancreatic and/or gastric surgery, e.g. total or partial resection of the pancreas, gastrectomy, post gastrointestinal bypass surgery (e.g. Billroth Il gastroenterostomy); chronic pancreatitis; Shwachman Diamond Syndrome; ductal obstruction of the pancreas or common bile duct (e.g.
- the enzyme(s) may also be useful in the treatment of acute pancreatitis.
- the effect of the enzyme(s) on digestive disorders can be measured as generally described in EP 0600868, in which Example 2 describes an in vitro digestibility test for measuring lipase stability test under gastric conditions, and Example 3 an in vitro digestibility test for lipase activity in the presence of bile salts. Corresponding tests can be set up for the protease and amylase.
- WO 02/060474 discloses suitable tests, for example (1) an in vitro test for measuring lipid digestion in a swine test feed, and (2) an in vivo trial with pancreas insufficient swine in which the digestibility of fat, protein and starch is measured.
- the effect of the amylase of the invention is measured using the in vivo screening test for amylase efficacy of Example 2.
- the enzyme(s) are useful in the treatment of Diabetes mellitus type I, and/or type II, in particular for adjuvant treatment in a diabetes therapy of digestive disorders usually accompanying this disease, with a view to diminishing late complications.
- the effect on Diabetes mellitus of the enzyme(s) may be determined by one or more of the methods described in WO 00/54799, for example by controlling the level of glycosylated haemoglobin, the blood glucose level, hypoglycaemic attacks, the status of fat-soluble vitamins like vitamins A, D and E, the required daily dosage of insulin, the body-weight index, and hyper glycaemic periods.
- the invention described and claimed herein is not to be limited in scope by the specific embodiments herein disclosed, since these embodiments are intended as illustrations of several aspects of the invention. Any equivalent embodiments are intended to be within the scope of this invention. Indeed, various modifications of the invention in addition to those shown and described herein will become apparent to those skilled in the art from the foregoing description. Such modifications are also intended to fall within the scope of the appended claims. In the case of conflict, the present disclosure including definitions will control.
- Enzyme standards can be procured from the International Commission on
- Amylase FIP assay The amylolytic activity of pancreatin was analyzed according to the method published in the European Pharmacopoeia 5.1 against the pancreatin standard supplied by the FIP.
- the assay for amylolytic activity of microbial amylases described by the FIP was modified.
- starch is hydrolysed by amylase at pH 5.8 and at constant temperature (37.0 +/- 0.1 0 C) in the presence of sodium chloride and calcium chloride.
- the reducing groups resulting from the hydrolysis react with iodine in alkaline solution and the excess of iodine are titrated with thiosulphate.
- One unit of amylase is defined as the amount of enzyme, which, under the defined conditions and substrate, hydrolyzes 1 micromol of glycosidic bond per minute.
- Substrate solution The substrate is soluble starch (e.g. Merck, No. 101252).
- the water content of each batch of soluble starch is determined upon opening of the container.
- soluble starch e.g. Merck, No. 101252
- Buffer (acetate) solution pH 5.8 (0.2 mol/L): Dissolve 12 g of acetic acid, 1 g of sodium chloride and 544 mg calcium chloride in about 800 mL of water. Adjust the pH to 5.8 with a sodium hydroxide solution (about 10 N). Dilute to 1000 mL.
- 0.1 N iodine solution e.g. Titrisol (Merck 9910), diluted with pure water
- 0.1 N sodium thiosulphate solution e.g. 0.1 N iodine solution (e.g. Titrisol (Merck 9910), diluted with pure water)
- 0.1 N sodium thiosulphate solution e.g. Titrisol (Merck 9910), diluted with pure water
- Sulphuric acid (p.a.) 20 %: to 4 volume parts water add 1 volume part sulphuric acid 96 % carefully.
- Fungal amylase reference standard FIP Batch No. 2; 55310 FIP-U/g, Condition 25 0 C without calcium chloride.
- Quality control suspension (Fungal Amylase reference standard): Dissolve an accurately weighed quantity of the reference standard so that the solution gives a titration volume of thiosulfate, that is between 2 and 4 mL (e.g. weigh about 12 - 15 mg of the fungal amylase standard and dissolve in 100 ml buffer solution). The quality control suspension is used only for day to day monitoring of the test system.
- Test suspension Dissolve an accurately weighed quantity of the test sample so that the solution gives a titration volume of thiosulfate, that is between 2 and 4 mL.
- Test sample For each determination prepare a reaction solution containing 25.0 mL of substrate solution and 10.0 mL of 0.2 M acetate buffer solution in a 300 mL Erlenmeyer flask. Stopper it with a rubber stopper and place it in a water bath at a constant temperature (37.0 +/- 0.1 0 C). As soon as the substrate mixture has reached a constant temperature, start the reaction by adding 2.0 mL of the test suspension. Shake briefly and incubate for exactly 10 minutes at 37°C. Stop the reaction immediately by adding 4 mL of hydrochloric acid.
- Quality control sample Determine the activity of the quality control suspension as described for the test sample in duplicate. Use 2.0 mL of the reference suspension. Blank values: Prepare blank values of the test and reference suspensions. Repeat the procedure as described above but add the 4 mL of 1 N hydrochloric acid before addition of the test and the reference solution.
- the measured activity of the monitoring sample is 97500 U/g, with a Range of Mean +/- 3 x SD, in particular with a Range of +/- 6000 U/g .
- amylase assay can be used:
- Substrate Phadebas tablets (Pharmacia Diagnostics; cross-linked, insoluble, blue-coloured starch polymer, which is mixed with bovine serum albumin and a buffer substance, and manufactured into tablets)
- APTSMYQI-3207 is available on request from Novozymes A/S, Krogshoejvej 36, DK-2880
- the digested product with yellow colour has a characteristic absorbance at 405nm. Its quantity is determined by spectrophotometry.
- One lipase unit is the amount of enzyme which releases 1 micromole titratable butyric acid per minute under the given assay conditions.
- a more detailed assay description, AF95/6-GB, is available on request from Novozymes A/S,
- Substrate Suc-AAPF-pNA (Sigma ® S-7388).
- Assay buffer 10OmM succinic acid, 10OmM HEPES (Sigma H-3375), 10OmM CHES (Sigma C-2885), 10OmM CABS (Sigma C-5580), 1mM CaCI 2 , 15OmM KCI, 0.01% Triton ® X-100 adjusted to pH 9.0 with HCI or NaOH.
- Assay temperature 25°C.
- 300 ⁇ l diluted protease sample was mixed with 1.5ml of the assay buffer and the activity reaction was started by adding 1.5ml pNA substrate (50mg dissolved in 1.0ml DMSO and further diluted 45x with 0.01% Triton ® X-100) and, after mixing, the increase in A 405 WaS monitored by a spectrophotometer as a measurement of the protease activity.
- the protease samples were diluted prior to the activity measurement in order to ensure that all activity measurements fell within the linear part of the dose-response curve for the assay.
- Example 2 In vivo screening test for amylase efficacy
- PEI ileo-caecal re-entrant cannula
- the test meal containing 15.4% protein, 69% starch, and 2.1% fat, had the following composition in g/100 g dry matter: Poultrymeat meal 7.1 ; fishmeal 2.45; casein 4.1 ; wheat flour 20.65; shelled rice 9.8; potato starch 7.7; maize starch 39.8; cellulose powder 3.0; vitamins 5.3 (as per the nutritional requirements).
- the pigs were fed 250 g of this test meal mixed with 1 litre water, 0.625 g Cr 2 O 3 and into which differing amounts of amylases (0, 7500, 18750, 90000 FIP U amylase/meal, see Example 1 ) were mixed immediately before feeding.
- Ileal chyme collected for a total of 6h after first appearance of the meal marker in the ileum (green chyme) was frozen at -20 0 C immediately after collection, to avoid any bacterial fermentation of the samples. At least one day washout was allowed between separate determinations.
- DM dry matter
- starch was analysed polarimetrically after acid hydrolysis and sugar was estimated gravimetrically.
- Cr 2 O 3 was oxidized to chromate and chromium content was calculated via extinction at 365 nm (spectrophotometer), as described by Petry and Rapp in Japanese fur Tierphysiologie (1970), vol. 27, p. 181-189.
- amylases of the invention perform much better than the known Aspergillus oryzae amylase and better than known pancreatin preparations.
- the amylases of the invention caused a strong and dose dependent improvement on starch digestibility, already showing a highly efficient improvement at the lowest dosage tested.
- Example 3 Amylase pH profiles, with and without bile salts
- pancreatic replacement enzymes For use in the treatment of PEI and related diseases it is preferable for pancreatic replacement enzymes to have a high activity around pH 6-7 (typical conditions of the upper small intestines). This experiment serves to determine the pH profiles of four alpha-amylases, three bacterial amylases of the invention and a prior art fungal Aspergillus oryzae amylase, with and without added bile salts.
- the amylases used for this study were the purified Bacillus amylases of amino acids 1- 486 of SEQ ID NO: 1 (“SEQ 1”) , amino acids 1-481 of SEQ ID NO: 2 (“SEQ 2”) and amino acids 1-483 of SEQ ID NO: 3 (“SEQ 3"), and, for comparison, a purified fungal amylase derived from Aspergillus oryzae ("A. oryzae”), the amylase of the commercial FungamylTM amylase product, which is available from Novozymes A/S, Krogshoejvej 36, DK-2880 Bagsvaerd, Denmark.
- Enzyme buffer 50 mM acetate, 50 mM imidazole, 50 mM malonic acid, 1 mM CaCI 2 , 0.01% Triton X-100. Adjust to pH 2.0, 3.0, 4.0, 5.0, 6.0, or 7.0 with HCI/NaOH.
- Substrate buffer 1.5 mg/ml amylopectin (waxy corn, e.g. Waxy corn 04201 from Cerestar, batch WM5671 ), 50 mM acetate, 50 mM imidazole, 50 mM malonic acid, 1 mM CaCI 2 . Adjust to the desired pH (as above) with HCI/NaOH. Incubate for 5 min at 100 0 C.
- the substrate buffer was made with or without 5 mM bile salts (i.e. Sodium taurocholate BRP, lot 2, from the Ph.Eur or FIP, also commercially available from e.g. LGC promochem, 500g/mol).
- the amylase activity was detected by reducing sugar assay. Briefly, 50 ⁇ l enzyme (diluted in enzyme buffer so as to fall within the linear range of the assay) was mixed with 100 ⁇ l substrate buffer in PCR-MTP (Thermo-Fast® 96, ABgene, cat. no. AB-0600). The MTP's were incubated at 37°C for 15 min, following which 75 ⁇ l stop solution (100 mM p-hydroxy- benzoic acid hydrazide, 180 mM K-Na-tartrate, 2% NaOH) was added, and the plates were incubated at 95°C for 10 min. Then 150 ⁇ l from each well was transferred to 96-well MTP, and the absorbance at 410 nm was monitored as a measure of amylase activity. Results
- Table 2 shows the activity of each enzyme at the pH indicated in the absence of bile salts. For each enzyme, the maximum activity was set to 100%.
- Table 3 shows the same as Table 2, but in the presence of 5mM bile salts.
- Table 4 shows the activity of each enzyme per mg enzyme protein at the pH indicated in the absence of bile salts, relative to the maximum enzyme activity measured in this experiment, which was the activity of the SEQ 1 enzyme at pH 5.0 (100%). The activity of each enzyme has accordingly been normalized relative to this activity. The amount of enzyme protein for each enzyme was determined on the basis of the specific activity.
- Table 5 shows the same as Table 4, but in the presence of 5mM bile salts.
- the activity of the SEQ 1 enzyme at pH 5.0 in the presence of 5mM bile salts is the reference value (100%).
- Tables 4 and 5 demonstrate that, at least under these conditions, the amylase having amino acids 1-486 of SEQ ID NO: 1 has a significantly higher activity per mg enzyme than all the other amylases tested.
- the degradation profile (DP1-10 qualitative fingerprint) of five alpha-amylases was determined by degradation of waxy maize starch followed by analysis on HPLC.
- the enzymes were purified Bacillus amylases of amino acids 1-486 of SEQ ID NO: 1 ( 11 SEQ 1") , amino acids 1-481 of SEQ ID NO: 2 ("SEQ 2") and amino acids 1-483 of SEQ ID NO: 3 ( 11 SEQ 3"), and, for comparison, a purified fungal amylase derived from Aspergillus oryzae ("A. oryzae"), the amylase of the commercial FungamylTM amylase product, which is available from Novozymes A/S, Krogshoejvej 36, DK-2880 Bagsvaerd, Denmark. Pancreatin was from Solvay Pharmaceuticals.
- a slurry of 50 mg/mL waxy maize starch (e.g. Waxy corn 04201 from Cerestar, Batch: WM5671 ) was made in 50 mM Na-acetate buffer pH 6.0, 40 ppm Ca 2+ .
- Purified enzymes were dosed at a concentration of 0.0073 mg enzyme protein per g of dry substance of the reaction mixture.
- the amount of amylase enzyme protein was calculated on the basis of the A 2 eo values and the amino acid sequences (amino acid compositions) using the principles outlined in S.C.Gill & P.H. von Hippel, Analytical Biochemistry 182, 319-326, (1989). After dosing the enzyme, the reaction was incubated at 60 0 C.
- pancreatin 100 mg was dissolved in 10 mL 50 mM Na-acetate buffer pH 5.5. 20 ul of this solution was added to 1 mL substrate slurry (50 mg/mL waxy corn starch in 50 mM Na- acetate pH 5.5) and incubated at 37 0 C for 24 hours, and then inactivated and filtered as described above prior to application on the HPLC. In a separate experiment (not shown), the "SEQ 1" amylase was also tested at 37°C which gave rise to the same degradation profile as at 6O 0 C.
- Pancreatin As far as Pancreatin is concerned, it appears to behave like a mixture of the fungal and bacterial amylases described above, i.e. generating small DP products (DP1 , DP2 and DP3), almost nothing of DP4, DP5 and DP6, and only leaving a small non-hydrolysed substrate peak.
- a liquid concentrate was prepared as described in DK 2005 00931 (a germ-filtered ultrafiltrate) of the amylase having amino acids 1-486 of SEQ ID NO: 1.
- the liquid concentrate was spray-dried.
- the measured amylase protein content of the spray-dried amylase powder was 37%.
- 1125 g of the spray-dried amylase powder was dry pre-mixed together with microcrystalline cellulose (450 g) and polyethylene glycol 4000 (MacrogolTM 4000; 675 g) in a commercially available mixer, lsopropyl alcohol 100 % (460 g) was added and the resulting wet mass was continued to be thoroughly mixed at room temperature.
- the homogenized mass was then extruded in a commercially available extruder which was fitted with a piercing die having a hole diameter of 0.8 mm to form cylindrical pellets.
- the bead temperature was not exceeding 5O 0 C while extruding.
- the extrudate produced was rounded to spherical pellets with a commercially available spheronizer by adding the necessary amount of isopropyl alcohol 100% (75.5 g).
- the pellets were dried at a supply temperature of approximately 4O 0 C in a commercially available vacuum dryer (from Voetsch). The product temperature did not exceed 45 0 C.
- the dried pellets were then separated by using a mechanical sieving machine with 0.7 and 1.4 mm screens. The sieve fractions of ⁇ 0.7 mm and ⁇ 1.4 mm were collected and can be filled in portions of 200 mg pellets each in capsules of size 2.
- the amylase concentration of the resulting dry pellets was approximately 18.5% (w/w).
- pellets with a lower content of amylase were produced using 562.5 g of the same spray-dried amylase powder, microcrystalline cellulose
- the resulting pellets from examples (A) and (B) were tested for amylolytic activity by applying a modified FIP method for microbial amylases.
- starch is hydrolysed by amylase at pH 5.8 and at a constant temperature (37.0+/-0.1 0 C) in the presence of sodium chloride and calcium chloride.
- the reducing groups resulting from the hydrolysis react with iodine in alkaline solution and the excess of iodine was titrated with thiosulphate.
- One unit of amylase is defined as the amount of enzyme, which, under the defined conditions and substrate, hydrolyzes 1 micromol of glycosidic bond per minute.
- the amylolytic activity in the pellets was found to be approximately 96% relative to the amylolytic activity in the starting powdery amylase material for each of the examples (A) and (B).
- Example 6 Pharmaceutical compositions of amylase and protease
- High-strength pellets containing amylase and protease were prepared as follows: A germ-filtered liquid concentrate of the protease of amino acids 1-274 of SEQ ID NO: 5 was prepared as described in Example 1 of DK patent application no. 2005 00930 and spray-dried. Spray-dried amylase in powder form (398.5 g) prepared as described in Example 5 was dry pre-mixed together with the spray-dried protease powder (746.5 g, having a measured protease protein content of 58.5%), microcrystalline cellulose (458 g) and polyethylene glycol 4000 (MacrogolTM 4000; 687 g) in a commercially available mixer.
- Isopropyl alcohol 100 % (460 g) was added and the resulting wet mass was continued to be thoroughly mixed at room temperature. The homogenized mass was then extruded in a commercially available extruder which was fitted with a piercing die having a hole diameter of 0.8 mm to form cylindrical pellets. The bead temperature was not exceeding 50 0 C while extruding. The extrudate produced was rounded to spherical pellets with a commercially available spheronizer by adding the necessary amount of isopropyl alcohol 100% (58 g). The pellets were dried using a supply temperature of approximately 4O 0 C in a commercially available vacuum dryer (from Voetsch). The product temperature did not exceed 45°C. The dried pellets were then separated by using a mechanical sieving machine with 0.7 and 1.4 mm screens. The sieve fractions of ⁇ 0.7 mm and ⁇ 1.4 mm were collected and can be filled in portions of 200 mg each in capsules of size 2.
- the resulting pellets from were tested for proteolytic and amylolytic activities according to the methods as outlined above. No loss in proteolytic or amylolytic activity was found in the pellets in each case relative to the starting powdery protease or amylase material, respectively.
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Abstract
Description
Claims
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NZ563737A NZ563737A (en) | 2005-06-24 | 2006-06-16 | Amylases derived from Bacillus stearothermophilus optionally in combination with proteases and/or lipases for pharmaceutical use |
US11/917,551 US8017351B2 (en) | 2005-06-24 | 2006-06-16 | Amylases for pharmaceutical use |
CA002612811A CA2612811A1 (en) | 2005-06-24 | 2006-06-16 | Amylases for pharmaceutical use |
EP06742473A EP1896057A2 (en) | 2005-06-24 | 2006-06-16 | Amylases for pharmaceutical use |
MX2007015471A MX2007015471A (en) | 2005-06-24 | 2006-06-16 | Amylases for pharmaceutical use. |
JP2008517320A JP2008546396A (en) | 2005-06-24 | 2006-06-16 | Amylase for pharmaceutical use |
AU2006261444A AU2006261444A1 (en) | 2005-06-24 | 2006-06-16 | Amylases for pharmaceutical use |
BRPI0611932-8A BRPI0611932A2 (en) | 2005-06-24 | 2006-06-16 | amylase, use thereof, pharmaceutical composition, and method for treating a disease |
IL187635A IL187635A0 (en) | 2005-06-24 | 2007-11-26 | Amylases for pharmaceutical use |
NO20080439A NO20080439L (en) | 2005-06-24 | 2008-01-23 | Amylases for pharmaceutical use |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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DKPA200500931 | 2005-06-24 | ||
DKPA200500931 | 2005-06-24 |
Publications (2)
Publication Number | Publication Date |
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WO2006136161A2 true WO2006136161A2 (en) | 2006-12-28 |
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CN (1) | CN101242853A (en) |
AU (1) | AU2006261444A1 (en) |
BR (1) | BRPI0611932A2 (en) |
CA (1) | CA2612811A1 (en) |
IL (1) | IL187635A0 (en) |
MX (1) | MX2007015471A (en) |
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NZ (1) | NZ563737A (en) |
RU (1) | RU2008102650A (en) |
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ZA (1) | ZA200710644B (en) |
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0594235A2 (en) * | 1992-10-20 | 1994-04-27 | Solvay Enzymes, Inc. | Method of purification of amylase, purified amylase so obtained and uses of purified amylase |
EP0828509A1 (en) * | 1995-05-31 | 1998-03-18 | Medzyme N.V. | Composition to improve digestibility and utilisation of nutrients |
WO2000054799A2 (en) * | 1999-03-17 | 2000-09-21 | Solvay Pharmaceuticals Gmbh | Medicament for treating diabetes |
WO2001062280A2 (en) * | 2000-02-24 | 2001-08-30 | Altus Biologics, Inc. | Lipase-containing composition and methods of use thereof |
WO2002060474A2 (en) * | 2001-01-19 | 2002-08-08 | Solvay Pharmaceuticals Gmbh | Mixtures of mushroom enzymes and the use thereof for treating maldigestion |
WO2004078960A1 (en) * | 2003-02-26 | 2004-09-16 | Genencor International, Inc. | Amylases producing an altered immunogenic response and methods of making and using the same |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK173590D0 (en) | 1990-06-06 | 1990-07-19 | Novo Nordisk As | RECOMBINANT THERAPEUTIC LIPASES |
ES2432519T3 (en) * | 1996-04-30 | 2013-12-04 | Novozymes A/S | Alpha-amylase mutants |
JP4358431B2 (en) | 1997-10-13 | 2009-11-04 | ノボザイムス アクティーゼルスカブ | α-Amylase mutant |
US6410295B1 (en) * | 1999-03-30 | 2002-06-25 | Novozymes A/S | Alpha-amylase variants |
RU2201763C1 (en) | 2001-12-29 | 2003-04-10 | Закрытое акционерное общество "Брынцалов-А" | Ferestal polyenzymatic preparation |
DE10260903A1 (en) * | 2002-12-20 | 2004-07-08 | Henkel Kgaa | New perhydrolases |
EP1896577A2 (en) * | 2005-06-24 | 2008-03-12 | Novozymes A/S | Lipases for pharmaceutical use |
EP1896058A2 (en) * | 2005-06-24 | 2008-03-12 | Novozymes A/S | Proteases for pharmaceutical use |
-
2006
- 2006-06-16 US US11/917,551 patent/US8017351B2/en not_active Expired - Fee Related
- 2006-06-16 BR BRPI0611932-8A patent/BRPI0611932A2/en not_active IP Right Cessation
- 2006-06-16 WO PCT/DK2006/000354 patent/WO2006136161A2/en active Application Filing
- 2006-06-16 NZ NZ563737A patent/NZ563737A/en not_active IP Right Cessation
- 2006-06-16 EP EP06742473A patent/EP1896057A2/en not_active Withdrawn
- 2006-06-16 JP JP2008517320A patent/JP2008546396A/en active Pending
- 2006-06-16 AU AU2006261444A patent/AU2006261444A1/en not_active Abandoned
- 2006-06-16 CA CA002612811A patent/CA2612811A1/en not_active Abandoned
- 2006-06-16 RU RU2008102650/13A patent/RU2008102650A/en not_active Application Discontinuation
- 2006-06-16 KR KR1020077029681A patent/KR20080031868A/en not_active Application Discontinuation
- 2006-06-16 MX MX2007015471A patent/MX2007015471A/en not_active Application Discontinuation
- 2006-06-16 CN CNA2006800302221A patent/CN101242853A/en active Pending
-
2007
- 2007-11-26 IL IL187635A patent/IL187635A0/en unknown
- 2007-12-06 ZA ZA200710644A patent/ZA200710644B/en unknown
-
2008
- 2008-01-23 NO NO20080439A patent/NO20080439L/en not_active Application Discontinuation
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0594235A2 (en) * | 1992-10-20 | 1994-04-27 | Solvay Enzymes, Inc. | Method of purification of amylase, purified amylase so obtained and uses of purified amylase |
EP0828509A1 (en) * | 1995-05-31 | 1998-03-18 | Medzyme N.V. | Composition to improve digestibility and utilisation of nutrients |
WO2000054799A2 (en) * | 1999-03-17 | 2000-09-21 | Solvay Pharmaceuticals Gmbh | Medicament for treating diabetes |
WO2001062280A2 (en) * | 2000-02-24 | 2001-08-30 | Altus Biologics, Inc. | Lipase-containing composition and methods of use thereof |
WO2002060474A2 (en) * | 2001-01-19 | 2002-08-08 | Solvay Pharmaceuticals Gmbh | Mixtures of mushroom enzymes and the use thereof for treating maldigestion |
WO2004078960A1 (en) * | 2003-02-26 | 2004-09-16 | Genencor International, Inc. | Amylases producing an altered immunogenic response and methods of making and using the same |
Non-Patent Citations (2)
Title |
---|
DATABASE Geneseq [Online] 11 May 1998 (1998-05-11), "Bacillus stearothermophilus Termamyl-like alpha-amylase." XP002419749 retrieved from EBI accession no. GSP:AAW31406 Database accession no. AAW31406 * |
GRAY G L ET AL: "STRUCTURAL GENES ENCODING THE THERMOPHILIC ALPHA-AMYLASES OF BACILLUS STEAROTHERMOPHILUS AND BACILLUS LICHENIFORMIS" JOURNAL OF BACTERIOLOGY, WASHINGTON, DC, US, vol. 166, no. 2, 1 May 1986 (1986-05-01), pages 635-643, XP002910153 ISSN: 0021-9193 cited in the application * |
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WO2024102698A1 (en) | 2022-11-09 | 2024-05-16 | Danisco Us Inc. | Subtilisin variants and methods of use |
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RU2008102650A (en) | 2009-07-27 |
CA2612811A1 (en) | 2006-12-28 |
IL187635A0 (en) | 2008-03-20 |
US8017351B2 (en) | 2011-09-13 |
US20090035293A1 (en) | 2009-02-05 |
MX2007015471A (en) | 2008-04-04 |
AU2006261444A1 (en) | 2006-12-28 |
WO2006136161A3 (en) | 2007-07-05 |
NO20080439L (en) | 2008-03-04 |
BRPI0611932A2 (en) | 2011-01-04 |
EP1896057A2 (en) | 2008-03-12 |
KR20080031868A (en) | 2008-04-11 |
CN101242853A (en) | 2008-08-13 |
NZ563737A (en) | 2010-08-27 |
JP2008546396A (en) | 2008-12-25 |
ZA200710644B (en) | 2008-11-26 |
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