JPH10500024A - 無毒、非毒素原性、非病原性の発現系、並びにその中で利用するためのプロモーター及びターミネーター - Google Patents
無毒、非毒素原性、非病原性の発現系、並びにその中で利用するためのプロモーター及びターミネーターInfo
- Publication number
- JPH10500024A JPH10500024A JP8503267A JP50326796A JPH10500024A JP H10500024 A JPH10500024 A JP H10500024A JP 8503267 A JP8503267 A JP 8503267A JP 50326796 A JP50326796 A JP 50326796A JP H10500024 A JPH10500024 A JP H10500024A
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- Prior art keywords
- host cell
- promoter
- sequence
- cell according
- fusarium
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P21/00—Preparation of peptides or proteins
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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
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/80—Vectors or expression systems specially adapted for eukaryotic hosts for fungi
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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)
- C12N9/16—Hydrolases (3) acting on ester bonds (3.1)
- C12N9/18—Carboxylic ester hydrolases (3.1.1)
- C12N9/20—Triglyceride splitting, e.g. by means of lipase
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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)
- C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
- C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
- C12N9/58—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from fungi
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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)
- C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
- C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
- C12N9/64—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue
- C12N9/6421—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue from mammals
- C12N9/6424—Serine endopeptidases (3.4.21)
- C12N9/6427—Chymotrypsins (3.4.21.1; 3.4.21.2); Trypsin (3.4.21.4)
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P21/00—Preparation of peptides or proteins
- C12P21/02—Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/911—Microorganisms using fungi
- Y10S435/929—Fusarium
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Genetics & Genomics (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mycology (AREA)
- Physics & Mathematics (AREA)
- Biophysics (AREA)
- Plant Pathology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Enzymes And Modification Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.プロモーターに作用可能式に連結された異種タンパク質をコードする核酸 配列を含んで成る無毒、非毒素原性、非病原性組換フサリウム宿主細胞。 2.前記フサリウムがフサリウム・グラミネアルムである、請求項1記載の宿 主細胞。 3.前記フサリウム・グラミネアルムがATCC 20334の認定表示を有する請求項 1記載の宿主細胞。 4.前記異種タンパク質が菌類タンパク質である、請求項1記載の宿主細胞。 5.前記異種タンパク質が分泌タンパク質である、請求項1記載の宿主細胞。 6.前記異種タンパク質が菌類酵素である、請求項1記載の宿主細胞。 7.前記菌類酵素が、カタラーゼ、ラッカーゼ、フェノールオキシダーゼ、オ キシダーゼ、オキシドリダクターゼ、セルラーゼ、キシラナーゼ、ペルオキシダ ーゼ、リパーゼ、ヒドロラーゼ、エステラーゼ、キュチナーゼ、タンパク分解酵 素、アミノペプチダーゼ、カルボキシペプチダーゼ、フィターゼ、リアーゼ、ペ クチン分解酵素、アミラーゼ、グルコアミラーゼ、α−ガラクトシダーゼ、β− ガラクトシダーゼ、α−グルコシダーゼ、β−グルコシダーゼ、マンノシダーゼ 、イソメラーゼ、インベルターゼ、トランスフェラーゼ、リボヌクレアーゼ、キ チナーゼ及びデオキシリボヌクレアーゼより成る群から選ばれる、請求項6記載 の宿主細胞。 8.前記菌類酵素がプロテアーゼである、請求項6記載の宿主細胞。 9.前記菌類酵素がアルカリ性プロテアーゼである、請求項6記載の宿主細胞 。 10.前記アルカリ性プロテアーゼがフサリウム・オキシスポルム・トリプシン 様プロテアーゼである、請求項9記載の宿主細胞。 11.前記フサリウム・オキシスポルム・トリプシン様プロテアーゼがSEQ ID N O:4に示すアミノ酸配列を有する、請求項10記載の宿主細胞。 12.前記菌類酵素がエンドグルカナーゼ又はその変異体である、請求項6記載 の宿主細胞。 13.前記エンドグルカナーゼがSEQ ID NO:8に示すアミノ酸配列を有する、 請求項14記載の宿主細胞。 14.前記菌類酵素が1,3リパーゼ又はその変異体である、請求項6記載の宿 主細胞。 15.前記1,3リパーゼがSEQ ID NO:1に示すアミノ酸配列を有する、請求 項12記載の宿主細胞。 16.前記異種タンパク質がホルモン、成長因子及びレセプターより成る群から 選ばれる、請求項1記載の宿主細胞。 17.前記プロモーターが菌類プロモーターである、請求項1記載の宿主細胞。 18.前記プロモーターがA.ニドゥランス amdS由来のプロモーターより成る 群から選ばれる、請求項17記載の宿主細胞。 19.前記菌類プロモーターがフサリウム・オキシスポルム・トリプシン様プロ テアーゼをコードする遺伝子に由来するものであるか又はこの配列と実質的に同 じプロモーター活性を有するそのフラグメントである、請求項17記載の宿主細胞 。 20.前記プロモーター配列がSEQ ID NO:5に示すものである、請求項19記載 の宿主細胞。 21.選択マーカーも含んで成る、請求項1記載の宿主細胞。 22.前記マーカーがargB,trpC,pyrG,amdS,niaD及びhygBより成る群 から選ばれる、請求項13記載の宿主細胞。 23.ターミネーターも含んで成る、請求項1記載の宿主細胞。 24.前記ターミネーターがフサリウム・オキシスポルム・トリプシン様プロテ アーゼをコードする遺伝子に由来するものであるか又はこの配列と実質的に同じ ターミネーター活性を有するそのフラグメントである、請求項23記載の宿主細胞 。 25.前記ターミネーター配列がSEQ ID NO:6に示すものである、請求項24記 載の宿主細胞。 26.注目のタンパク質を製造するための方法であって、プロモーターに作用可 能式に連結された前記タンパク質をコードする核酸配列を含んで成る無毒、非毒 素原性、非病原性組換宿主細胞を培養し、そしてそのタンパク質を単離すること を含んで成る方法。 27.フサリウム・オキシスポルム・トリプシン様プロテアーゼをコードする遺 伝子に由来するプロモーター配列又はその配列と実質的に同じプロモーター活性 を有するそのフラグメントであって、ここで前記プロモーターがSEQ ID NO:5 に示す配列を有するものである、前記配列。 28.フサリウム・オキシスポルム・トリプシン様プロテアーゼをコードする遺 伝子に由来するターミネーター配列又はその配列と実質的に同じターミネーター 活性を有するそのフラグメントであって、ここで前記ターミネーターがSEQ ID N O:6に示す配列を有するものである、前記配列。
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US26944994A | 1994-06-30 | 1994-06-30 | |
US08/269,449 | 1994-06-30 | ||
US40467895A | 1995-03-15 | 1995-03-15 | |
US08/404,678 | 1995-03-15 | ||
US404,678 | 1995-03-15 | ||
US269,449 | 1995-03-15 | ||
PCT/US1995/007743 WO1996000787A1 (en) | 1994-06-30 | 1995-06-15 | Non-toxic, non-toxigenic, non-pathogenic fusarium expression system and promoters and terminators for use therein |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2000349977A Division JP3511005B2 (ja) | 1994-06-30 | 2000-11-16 | 無毒、非毒素原性、非病原性の発現系、並びにその中で利用するためのプロモーター及びターミネーター |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH10500024A true JPH10500024A (ja) | 1998-01-06 |
JP3167729B2 JP3167729B2 (ja) | 2001-05-21 |
Family
ID=26953701
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP50326796A Expired - Lifetime JP3167729B2 (ja) | 1994-06-30 | 1995-06-15 | 無毒、非毒素原性、非病原性の発現系、並びにその中で利用するためのプロモーター及びターミネーター |
JP2000349977A Expired - Lifetime JP3511005B2 (ja) | 1994-06-30 | 2000-11-16 | 無毒、非毒素原性、非病原性の発現系、並びにその中で利用するためのプロモーター及びターミネーター |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2000349977A Expired - Lifetime JP3511005B2 (ja) | 1994-06-30 | 2000-11-16 | 無毒、非毒素原性、非病原性の発現系、並びにその中で利用するためのプロモーター及びターミネーター |
Country Status (9)
Country | Link |
---|---|
US (1) | US5837847A (ja) |
EP (2) | EP1559776A3 (ja) |
JP (2) | JP3167729B2 (ja) |
CN (2) | CN1151762A (ja) |
AT (1) | ATE294871T1 (ja) |
AU (1) | AU2705895A (ja) |
DE (1) | DE69534185T2 (ja) |
FI (1) | FI119437B (ja) |
WO (1) | WO1996000787A1 (ja) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2002539793A (ja) * | 1999-03-22 | 2002-11-26 | ノボザイムス バイオテック,インコーポレイティド | 菌類細胞中で遺伝子を発現させるためのプロモーター |
JP2003502011A (ja) * | 1999-01-13 | 2003-01-21 | ノボザイムス バイオテック,インコーポレイティド | シクロヘキサデプシペプチド欠損細胞におけるポリペプチドの産生方法 |
JP2006500069A (ja) * | 2002-09-24 | 2006-01-05 | ノボザイムス,インコーポレイティド | キモトリプシン活性を有する微生物トリプシン変異体及びそれをコードする核酸 |
JP2009291207A (ja) * | 1998-05-20 | 2009-12-17 | Novozymes Inc | トリコテセン−欠失糸状菌変異体細胞において異種ポリベプチドを生成するための方法 |
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AU3634797A (en) * | 1996-07-24 | 1998-02-10 | Meiji Seika Kaisha Ltd. | Enzyme endoglucanase and cellulase preparations containing the same |
US7883872B2 (en) * | 1996-10-10 | 2011-02-08 | Dyadic International (Usa), Inc. | Construction of highly efficient cellulase compositions for enzymatic hydrolysis of cellulose |
US5811381A (en) * | 1996-10-10 | 1998-09-22 | Mark A. Emalfarb | Cellulase compositions and methods of use |
AU7381098A (en) | 1997-05-16 | 1998-12-08 | Novo Nordisk Biotech, Inc. | Polypeptides having prolyl pipeptidyl aminopeptidase activity and nucleic acids encoding same |
EP1117808B1 (en) * | 1998-10-06 | 2004-12-29 | Mark Aaron Emalfarb | Transformation system in the field of filamentous fungal hosts: in chrysosporium |
CN1197965C (zh) | 1998-10-26 | 2005-04-20 | 诺维信公司 | 在丝状真菌细胞内构建和筛选目的dna文库 |
US6361973B1 (en) | 1999-03-22 | 2002-03-26 | Novozymes Biotech, Inc. | Promoters for expressing genes in a fungal cell |
EP1214426A2 (en) | 1999-08-31 | 2002-06-19 | Novozymes A/S | Novel proteases and variants thereof |
AR027509A1 (es) | 2000-01-10 | 2003-04-02 | Maxygen Aps | Conjugados g-csf |
RU2278123C2 (ru) | 2000-02-11 | 2006-06-20 | Максиджен Холдингз Лтд. | Молекулы, подобные фактору vii или viia |
ATE469223T1 (de) | 2000-03-14 | 2010-06-15 | Novozymes As | Pilz transkriptionsaktivator zur verwendung in verfahren zur herstellung von polypeptiden |
EP2287296A1 (en) | 2000-06-26 | 2011-02-23 | Novozymes A/S | Lipolytic enzyme |
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CA2419577A1 (en) | 2000-09-05 | 2002-03-14 | Novozymes A/S | Manganese lipoxygenase |
HUP0303251A2 (hu) | 2001-02-27 | 2003-12-29 | Maxygen Aps | Béta-interferon-szerű molekulák |
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DE10207702C1 (de) * | 2002-02-22 | 2003-08-28 | Albrecht Gmbh | Einstellbare Gelenkorthese |
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- 1995-06-15 AU AU27058/95A patent/AU2705895A/en not_active Abandoned
- 1995-06-15 DE DE69534185T patent/DE69534185T2/de not_active Expired - Lifetime
- 1995-06-15 WO PCT/US1995/007743 patent/WO1996000787A1/en active IP Right Grant
- 1995-06-15 EP EP05103695A patent/EP1559776A3/en not_active Withdrawn
- 1995-06-15 EP EP95922334A patent/EP0777737B1/en not_active Expired - Lifetime
- 1995-06-15 AT AT95922334T patent/ATE294871T1/de not_active IP Right Cessation
- 1995-06-15 CN CN200710096070A patent/CN101659926A/zh active Pending
- 1995-06-15 JP JP50326796A patent/JP3167729B2/ja not_active Expired - Lifetime
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1996
- 1996-12-27 FI FI965220A patent/FI119437B/fi not_active IP Right Cessation
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1997
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JP2009291207A (ja) * | 1998-05-20 | 2009-12-17 | Novozymes Inc | トリコテセン−欠失糸状菌変異体細胞において異種ポリベプチドを生成するための方法 |
JP2003502011A (ja) * | 1999-01-13 | 2003-01-21 | ノボザイムス バイオテック,インコーポレイティド | シクロヘキサデプシペプチド欠損細胞におけるポリペプチドの産生方法 |
JP2002539793A (ja) * | 1999-03-22 | 2002-11-26 | ノボザイムス バイオテック,インコーポレイティド | 菌類細胞中で遺伝子を発現させるためのプロモーター |
JP2010227108A (ja) * | 1999-03-22 | 2010-10-14 | Novozymes Inc | 菌類細胞中で遺伝子を発現させるためのプロモーター |
JP2013121361A (ja) * | 1999-03-22 | 2013-06-20 | Novozymes Inc | 菌類細胞中で遺伝子を発現させるためのプロモーター |
JP2013121360A (ja) * | 1999-03-22 | 2013-06-20 | Novozymes Inc | 菌類細胞中で遺伝子を発現させるためのプロモーター |
JP2006500069A (ja) * | 2002-09-24 | 2006-01-05 | ノボザイムス,インコーポレイティド | キモトリプシン活性を有する微生物トリプシン変異体及びそれをコードする核酸 |
Also Published As
Publication number | Publication date |
---|---|
FI119437B (fi) | 2008-11-14 |
FI965220A0 (fi) | 1996-12-27 |
AU2705895A (en) | 1996-01-25 |
JP3511005B2 (ja) | 2004-03-29 |
EP0777737B1 (en) | 2005-05-04 |
US5837847A (en) | 1998-11-17 |
EP1559776A3 (en) | 2006-01-11 |
FI965220A (fi) | 1997-02-25 |
DE69534185T2 (de) | 2006-02-23 |
JP3167729B2 (ja) | 2001-05-21 |
EP1559776A2 (en) | 2005-08-03 |
CN101659926A (zh) | 2010-03-03 |
CN1151762A (zh) | 1997-06-11 |
ATE294871T1 (de) | 2005-05-15 |
JP2001169791A (ja) | 2001-06-26 |
DE69534185D1 (de) | 2005-06-09 |
WO1996000787A1 (en) | 1996-01-11 |
EP0777737A1 (en) | 1997-06-11 |
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