NZ623863B2 - Preservative combinations - Google Patents

Preservative combinations Download PDF

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Publication number
NZ623863B2
NZ623863B2 NZ623863A NZ62386312A NZ623863B2 NZ 623863 B2 NZ623863 B2 NZ 623863B2 NZ 623863 A NZ623863 A NZ 623863A NZ 62386312 A NZ62386312 A NZ 62386312A NZ 623863 B2 NZ623863 B2 NZ 623863B2
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NZ
New Zealand
Prior art keywords
vanillin
beverage
cinnamate
ppm
preservative
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Application number
NZ623863A
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NZ623863A (en
Inventor
Eelco Anthonius Johannes Heintz
Kumar Saurabh
Original Assignee
Purac Biochem Bv
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Publication date
Priority claimed from EP11185613.4A external-priority patent/EP2583568A1/en
Application filed by Purac Biochem Bv filed Critical Purac Biochem Bv
Publication of NZ623863A publication Critical patent/NZ623863A/en
Publication of NZ623863B2 publication Critical patent/NZ623863B2/en

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Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23FCOFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
    • A23F3/00Tea; Tea substitutes; Preparations thereof
    • A23F3/16Tea extraction; Tea extracts; Treating tea extract; Making instant tea
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23FCOFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
    • A23F3/00Tea; Tea substitutes; Preparations thereof
    • A23F3/16Tea extraction; Tea extracts; Treating tea extract; Making instant tea
    • A23F3/163Liquid or semi-liquid tea extract preparations, e.g. gels, liquid extracts in solid capsules
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/42Preservation of non-alcoholic beverages
    • A23L2/44Preservation of non-alcoholic beverages by adding preservatives
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/52Adding ingredients
    • A23L2/56Flavouring or bittering agents
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L3/00Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
    • A23L3/34Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals
    • A23L3/3454Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals in the form of liquids or solids
    • A23L3/3463Organic compounds; Microorganisms; Enzymes
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L3/00Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
    • A23L3/34Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals
    • A23L3/3454Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals in the form of liquids or solids
    • A23L3/3463Organic compounds; Microorganisms; Enzymes
    • A23L3/3481Organic compounds containing oxygen
    • A23L3/3499Organic compounds containing oxygen with doubly-bound oxygen
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L3/00Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs
    • A23L3/34Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals
    • A23L3/3454Preservation of foods or foodstuffs, in general, e.g. pasteurising, sterilising, specially adapted for foods or foodstuffs by treatment with chemicals in the form of liquids or solids
    • A23L3/3463Organic compounds; Microorganisms; Enzymes
    • A23L3/3481Organic compounds containing oxygen
    • A23L3/3508Organic compounds containing oxygen containing carboxyl groups

Abstract

The present disclosure relates to a preservative system capable of protecting against spoilage by bacteria, yeasts and moulds in carbonated and non-carbonated beverages. In accordance with the disclosure this objective is realized with a preservative system comprising a combination of vanillin and cinnamate. Vanillin is known for its anti mould action. However the dosages that are needed of are too high for most applications. It has been found that potassium cinnamate at low concentrations has a positive effect on the inhibition of moulds in combination with vanillin. Moreover, the present disclosure, using a combination of vanillin cinnamate accomplishes complete inactivation of moulds at manageable sensory levels. Hence the present disclosure provides a preservation system comprising combinations of vanillin and cinnamate as well as applications of such preservation systems in alimentary products, especially carbonated and non-carbonated beverages. innamate. Vanillin is known for its anti mould action. However the dosages that are needed of are too high for most applications. It has been found that potassium cinnamate at low concentrations has a positive effect on the inhibition of moulds in combination with vanillin. Moreover, the present disclosure, using a combination of vanillin cinnamate accomplishes complete inactivation of moulds at manageable sensory levels. Hence the present disclosure provides a preservation system comprising combinations of vanillin and cinnamate as well as applications of such preservation systems in alimentary products, especially carbonated and non-carbonated beverages.

Description

PRESERVATIVE COMBINATIONS Field of the Invention The present invention relates to a preservative system with a broad spectrum of applications. In particular, the invention provides a preservative system capable of protecting against spoilage by yeasts, especially in carbonated and/or juice containing beverages. The invention further provides the use of the preservative system as well as to alimentary products containing the preservative system, ally carbonated and/or juice ning beverages.
Background of the Invention Microbial spoilage of ges is a significant concern in the beverage industry today. Beverages have varying degrees of sensitivity to iological spoilage depending on intrinsic factors of the beverage such as pH, nt content (e.g., juice, n, or micronutrient content), carbonation level, BriX, water quality (e.g., alkalinity and/or hardness), and preservatives. Spoilage events occur when microorganisms are able to overcome the beverage's intrinsic factors and grow.
Microbiological spoilage can result from one or more , ia, and/or . For example, yeasts and ia are capable of spoiling carbonated and non- carbonated beverages such as fruit drinks enhanced waters, etc.
The ability of yeasts and certain bacteria to grow anaerobically enables their growth in carbonated beverages. Typically, bacteria tend to produce off-flavors and odors with associated sedimentation. Spoilage by yeasts usually manifests itself as fermentation with gas and l production, as well as sedimentation, off-flavors and odors, and loss of cloud or emulsion stability. Yeasts such as Saccharomyces, Zygosaccharomyces, Candida, a spp. and Pichia are often responsible for spoilage incidents in common beverages, both carbonated and non-carbonated.
Protection against microbiological spoilage of beverages can be achieved using chemical preservatives and/or processing techniques such as hot filling, tunnel pasteurization, ultra-high temperature ent (UHT) or pasteurization followed by aseptic packaging, and/or pasteurization followed by chilling the beverage.
Current preservation systems for acidic, stable beverages rely on acidic preservatives, especially benzoic acid, benzoates, sorbic acid, sorbates and sulphite.
These preservatives can have an impact on the flavour and the use of these preservatives is restricted in many countries.
It has therefore often been attempted to reduce the amount of sorbic and/or benzoic acid necessary to achieve microbial stability. One such attempt involves the addition of naturally occurring and less potentially toxic agents such as oils of cinnamon and thyme.
US 6,042,861 teaches the use of cinnamic acid in the preservation of carbonated and non-carbonated tea based beverages, so as to e a reduction in the amount of sorbic and/or benzoic acid necessary to inhibit microbial growth. The combination of 0.40 g/l of potassium sorbate and 30 ppm cinnamic acid is tested in a still tea based beverage.
The itions of US 6,042,861 contain substantial amounts of an acidulant in order to achieve preservation stability.
It is an object of the present ion to solve one or more of the aforementioned shortcomings of the existing methods of chemical preservation. It is a particular object of the present invention to provide a preservative system with a improved activity against yeasts in carbonated and/or juice containing beverages. y of the Invention In accordance with the invention this objective is ed with a preservative system comprising a combination of vanillin and ate.
In experiments, the present inventors observed that binary ations of vanillin and cinnamate were ive in inhibiting the growth of certain yeasts often associated with spoilage of carbonated and juice containing beverages, at dosages suitable for this kind of application.
The t invention, using a combination of vanillin and cinnamate accomplishes protection t yeast spoilage at acceptable sensory levels.
Hence the present invention provides a preservation system, relying on the combination of vanillin and cinnamate as well as ations of such preservation systems in alimentary products, especially carbonated and/or juice containing beverages.
Detailed Description of the Invention A first aspect of this invention provides a preservative system comprising (i) more than 0.1 wt.% of vanillin and/or a derivative thereof and (ii) more than 0.1 wt.% of cinnamic acid or a salt thereof, the preservative system being free from preservative agents ed from the group of tes and sorbates. ic acid (3-phenylpropenoic acid) is well known as a food ingredient, which obtained RAS status in 1965. As will be tood by those skilled in the art, any soluble cinnamic acid salt may be used in accordance with the invention.
Typically, the cinnamate is a water soluble salt of cinnamic acid. For convenience, the term mate’ is used herein to refer to any substance containing the cinnamic acid anion, in particular to denote cinnamic acid and the salts thereof. rmore, a number of cinnamic acid derivatives are known and used in the food industry, including p- dimethylaminocinnamate, aldehyde, cinnamyl acetate, cinnamyl alcohol, yl te, cinnamyl cinnamate, cinnamyl formate, cinnamyl isobutyrate, cinnamyl isovalerate and cinnamyl phenylacetate, which may also be referred to herein as ‘cinnamate derivatives’. In accordance with the invention these derivatives are equally suitable for use in the preservative system either alone or in combination with cinnamic acid or other cinnamate salts or derivates. In a ularly preferred embodiment of the invention the preservative system comprises cinnamic acid and/or a cinnamic acid salt selected from the group of sodium cinnamate and potassium cinnamate. In a preferred embodiment, the preservative comprises potassium cinnamate.
In one preferred embodiment, the preservative system ses cinnamate and/or a cinnamate derivative in an amount of less than 50 wt.% based on the total weight of the preservative system, preferably less than 45 wt.%, preferably less than 40 wt.%, preferably less than 35 wt.%, preferably less than 30 wt.%, preferably less than 25 wt.%, preferably less than 20 wt.%, preferably less than 15 wt.%, preferably less than 12 wt.%, preferably less than 11 wt.%, preferably less than 10 wt.%, based on the total weight of the preservative system.
In one preferred embodiment, the preservative system comprises cinnamate and/or cinnamate derivative in an amount of more than 0.1 wt.%, based on the total weight of the preservative system, preferably more than 0.25 wt.%, preferably more than 0. 5 wt.%, preferably more than 1 wt.%, preferably more than 2.5 wt%, preferably more than 4 wt.%, preferably more than 5 wt%, preferably more than 6 wt.%, preferably more than 7 wt.%, preferably more than 8 wt.%, based on the total weight of the preservative system.
Vanillin (4-Hydroxymethoxybenzaldehyde) is approved as a food additive by authorities world wide. Vanillin was given FEMA-GRAS status in 1965. Derivatives of vanillin such as methyl vanillin, ethyl in and vanillin 2,3-butanediol acetal may also suitably used in accordance with this invention, although the use of vanillin is ularly preferred.
In one red embodiment, the preservative system comprises vanillin and/or a in derivative in an amount of less than 25 wt. % based on the total weight of the preservative system, preferably less than 20 wt. %, preferably less than 15 wt. %, preferably less than 12 wt. %, preferably less than wt. %, preferably less than 10 wt. %, preferably less than 9 wt. %, preferably less than 8 wt. %, preferably less than 7 wt. %, preferably less than 6 wt. %, preferably less than 5 wt. %, preferably less than 4 wt. %, preferably less than 3.5 wt. %, preferably less than 3 wt. %, based on the total weight of the preservative system.
In one preferred embodiment, the preservative system comprises vanillin and/or a in derivative in an amount of more than 0.025wt. %, based on the total weight of the preservative system, preferably more than 0.05 wt. %, preferably more than 0.1 wt. %, preferably more than 0.25 wt. %, preferably more than 0.5 wt.%, preferably more than 1 wt. %, preferably more than 1.5 wt%, ably more than 2 wt. %, ably more than 2.5 wt. %, based on the total weight of the preservative system.
In one preferred embodiment, the preservative system is characterized by a (molar) ratio of (i) in and/or derivatives thereof : (ii) cinnamate of less than 10 (1.0:0. 1), preferably less than 4 (100.25), preferably less than 2 (10:05), e.g. around 1.75. In one preferred ment, the preservative system is characterized by a ratio of (i) : (ii) of more than 0.1 (1.0:10), preferably more than 0.5 (1.0:2), preferably more than 1 (1.0:1), preferably more than 1.25 (1.008), most preferably more than 1.5 ).
The preservative system of the present invention can optionally include other preservatives. Weak acid preservatives are preferred for this purpose. As indicated in the foregoing however, an advantage of the present invention resides in the fact that the presence of other preservatives, especially synthetic preservatives such as benzoates and sorbates can be minimized or avoided altogether while achieving the desired level of microbial stability. The preservative system of the t invention typically contains no or only minor s of additional preservative agents, such as, in particular, benzoate and/or sorbate. In a preferred embodiment of the invention the preservative system contains less than 1 wt% of preservative agents selected from the group consisting of sorbates and benzoates, ably less than 0.5 wt%, preferably less than 0.1 wt%. In a particularly preferred embodiment of the invention the preservative system is essentially or tely free from preservative agents selected from the group of benzoates and sorbates.
In one embodiment of the invention the preservative composition further comprises a carrier material, the choice of which will largely depend on the physical form in which the vative system is to be ed. The carrier material is typically used in any amount required to provide a t that has the desired properties relating to production, storage and .
In one embodiment of the invention, a preservative system in the form of a free flowing powder or granulate, which may comprise a r material. In another preferred embodiment a free flowing powder is provided ting essentially of the vative combination. Such a free g powder may be obtained by combining the various components in an aqueous sion or solution followed by drying, e.g. spray-drying.
In another embodiment a liquid preservative system is provided comprising solution or dispersion of the above defined components in an aqueous phase, which for instance may be obtained by concentrating the aqueous dispersion or solution.
As discussed herein the present preservative system is capable of preventing and/or inhibiting the growth of, and/or killing of a organism in a food system. This may be slowing or arresting a micro-organism, or by killing the micro-organism present on contact with the t composition. In a preferred aspect the microbicidal or microbiostatic effect is in respect of an organism associated with food spoilage or food borne disease, especially ge of carbonated and/or fruit juice containing beverages. In a preferred aspect the microbiocidal or microbiostatic effect is in respect of at least one, more preferably at least two, most preferably at least three organism selected from Yeasts, especially from the species of a (e.g. C. krusei, C. parapsilosis, C. utilis, C. valida, C. albicans), a (e.g. D. bruxellensis), Debaryomyces (e.g. D. hansenii), Hanseniaspora (e.g. H. uvarum) Kluyveromyces (e.g. K. loctis), Pichia (P. membranaefaciens), Rhodosporidium, Rhodotorula (Rh mucilaginosa), romyces (e.g. S. bayanus, S. boulardi, S. ergensis, S. cerevisiae, S. exiguus, S. florentinus, S. unisporus), Zygosaccharonmyces (e.g. Z. rouxii, Z baili), more preferably a yeast selected from Candida, Saccharomyces and Zygosaccharomyces, most preferably from Candida albicans, Saccharomyces cerevisiae and Zygosaccharomyces baiii. .
A second aspect of the invention concerns a beverage comprising an effective amount of (i) vanillin and/or a derivative thereof and (ii) cinnamic acid or a salt thereof and less than 10 ppm of preservative agents selected from the group of sorbates and benzoates.
As used herein the term ‘effective amount’ refers to an amount sufficient to preserve the product to which the present preservative system is added, i.e. to keep the product from microbial spoilage. As commonly tood in the art, the definitions of the terms "preserve, preservative," and "preservation" do not provide a standard time period for how long the thing to be preserved is kept from ge, decomposition, or oration. The time period for "preservation" can vary greatly depending on the subject matter. As used herein, the terms "preserve, preservative," and "preservation" refer to the protection against spoilage of a product that is the result of the growth of spoilage microorganisms for a period of at least 1 weeks, preferably at least 2 weeks, preferably at least 5 weeks, preferably at least 10 weeks, preferably at least 15 weeks. This period is in keeping with the time required to transport a beverage product from location of manufacture, through distribution channels, into the hand of the consumer. Typically, the product is preserved under ambient conditions, which include the full range of temperatures experienced during storage, transport, and display (e.g., 00C to 400C, 100C to 300C, 200C to 25°C) without limitation to the length of exposure to any given temperature.
Absence of ge is noted by absence any evidence of growth of ge organisms (turbidity, viable count, direct microscopic count or other standard methods of enumeration) and by the absence of any discernable change in the product attributes that could be routinely attributed to metabolism of spoilage sms.
As noted herein before, the present preservative system is particularly suited for beverages, especially carbonated beverages and/or juice containing ges. Hence in a preferred embodiment an alimentary product as defined above is provided, which is selected from the group consisting of beverages, more preferably from the group of carbonated ges and juice containing beverages. Some examples of carbonated beverages that may suitably be preserved using the present preservative system include cola beverages, flavored waters, tea based beverages, mineral , vitamin waters, fruit juice-containing beverages, etc.
In one preferred embodiment, the beverage ses vanillin and/or vanillin derivative in an amount of less than 700 ppm, preferably less than 600 ppm, preferably less than 500 ppm, preferably less than 450 ppm, preferably less than 425 ppm, preferably less than 400 ppm, preferably less than 375 ppm, preferably less than 350 ppm, preferably less than 340 ppm, preferably less than 330 ppm, preferably less than 325.
In one preferred embodiment, the beverage comprises vanillin and/or in derivative in an amount of more than 1 ppm, preferably more than 5 ppm, preferably more than 10 ppm, preferably more than 50 ppm, ably more than 100 ppm, preferably more than 150 ppm, ably more than 200 ppm, preferably more than 250 ppm, W0 2013/058651 preferably more than 275 ppm, preferably more than 300 ppm, preferably more than 325 ppm.
In one preferred embodiment, the beverage ses cinnamate and/or cinnamate derivative in an amount of less than 1000 ppm, preferably less than 750 ppm, preferably less than 500 ppm, preferably less than 400 ppm, preferably less than 350 ppm, preferably less than ppm, preferably less than 300, preferably less than 275 ppm, preferably less than 250 ppm, preferably less than 225 ppm, ably less than 210 ppm.
In one preferred embodiment, the beverage ses cinnamate and/or cinnamate derivative in an amount of more than 1 ppm, preferably more than 5 ppm, preferably more than 10 ppm, preferably more than 50 ppm, ably more than 100 ppm, preferably more than 125 ppm, preferably more than 150 ppm, preferably more than 175 ppm, preferably more than 185 ppm, preferably more than 190 ppm, preferably more than 195 ppm, preferably more than 200 ppm.
In one embodiment a beverage as defined herein above is provided, which contains less than 250 ppm of preservative agents selected from the group of sorbates and benzoates, preferably less than 200 ppm, more preferably less than 100 ppm, more preferably less than 50 ppm, more preferably less than 10 ppm, more preferably less than 1 ppm and most preferably less than 0.5 ppm. This ensures that no negative taste effects are ed. In a particularly preferred embodiment of the invention the beverage is ially or completely free from preservative agents selected from the group of benzoates and sorbates.
In one preferred embodiment of the invention, the beverage is a carbonated beverage.
Herein, the term "carbonated ge" is any combination of water and ingredient which is ed for human consumption and which possesses more than 0.2 volumes of carbon dioxide. The term "volume of C02" is understood to mean a quantity of carbon dioxide absorbed into the liquid wherein one volume C02 is equal to 1.96 grams of carbon dioxide (C02) per liter of product (0.045 5M) at 25 0C.
Such beverages may be supplemented with flavours, fruit juices, sweeteners, ns, nutrients, minerals, amino acids, etc.
Certain examples of the beverage product of the ion include (carbonated) tea- or fruit- based beverages, especially carbonated ice-teas and ‘flavoured water beverages’.
The term "tea based beverage" bes a beverage that contains the solid extracts of leaf material from Camellia sinensis, Camellia assamica, or Aspalathus is. The tea may be added to the beverage in various forms including an extract, a concentrate, a powder or as granules. Without preservation, tea acts as a nutrient that enhances the potential for microbial ge, at low concentrations, such as 0.01 to 3%.
The term “flavoured water” refers to a beverage essentially consisting of water with added natural or artificial flavors, herbs, and sweeteners. The flavoured water type beverages are usually low in es, as compared to regular soft drinks, and are typically marketed as diet or light drinks. In many cases, flavored waters se fruits or fruit juices, in limited amounts, as a source of the vitamins, minerals and flavours.
Typically, beverages according to the present ion will possess a specified range of acidity. The ion typically can function at a pH within the range of 2-7. In one preferred embodiment of the invention, the pH is at least 2, preferably at least 2.5, preferably at least 2.75, preferably at least 3, preferably at least 3.2, preferably at least 3.3, preferably at least 3.4, preferably at least 3.5. In one preferred embodiment of the invention, the pH of the ge is below 7, preferably below 6, preferably below 5.5, preferably below 5, preferably below 4.75, preferably below 4.6, preferably below 4.5. For highly acidic beverages, the ion is not limited by the type of acidulant employed in acidifying the product. Typically, in accordance with the present invention, acidulants may be inorganic acids, such as phosphoric acids, or organic acids, such as citric, malic, ascorbic, tartaric, lactic, gluconic, and succinic acid, fumaric acid. The various acids can be ed with salts of the same or different acids in order to manage pH or the buffer capacity of the beverage to a specified pH or range of pH. Virtually any organic acid salt can be used so long as it is edible and does not provide an vor. The choice of salt or salt mixture will be ined by the solubility and the taste. Citrate, malate and ascorbate yield ingestible complexes whose flavors are judged to be quite acceptable, particularly in fruit juice beverages. Tartaric acid is acceptable, particularly in grape juice beverages, as is lactic acid. Longer-chain fatty acids may be used but can affect flavor and water solubility.
For essentially all purposes, the malate, gluconate, citrate and ascorbate and lactate moieties are red.
As stated before, a preferred ment of the invention concerns juicecontaining beverages. In a particularly preferred embodiment of the invention the beverage product comprises fruit juice in an amount of less than 10 % (v/v). It is furthermore preferred that the beverage product comprises fruit juice in an amount of more than 5 % v/v. By way of example, juice can be obtained from the fruit of apple, cranberry, pear, peach, plum, apricot, nectarine, grape, , currant, raspberry, goose-berry, blackberry, blueberry, strawberry, lemon, orange, ruit, passionfruit, mandarin, mirabelle, tomato, lettuce, celery, spinach, cabbage, watercress, dandelion, rhubarb, carrot, beet, cucumber, pineapple, custard- apple, t, pomegranate, guava, kiwi, mango, papaya, watermelon, Io han guo, cantaloupe, pineapple, banana or banana puree, lemon, mango, papaya, lime, tangerine, and mixtures thereof. Preferred juices are the citrus juices, and most preferred are the non-citrus juices, apple, pear, cranberry, strawberry, grape, papaya, mango and cherry. Any juice can be used to make the beverage of this invention.
The preservation function of the t invention in beverage formulations typically is not affected by the type of sweeteners t therein. The sweetener may be any sweetener commonly employed for use in beverages. Sweeteners suitable for use in various embodiments of the ges sed here include nutritive and non-nutritive, natural and artificial or synthetic sweeteners. The sweetener can include a monosaccharide or a disaccharide. Peptides possessing sweet taste are also permitted. The most commonly employed saccharides include sucrose, fructose, dextrose, maltose and lactose and invert sugar. Mixtures of these sugars can be used. Other natural carbohydrates can be used if less or more ess is desired. Suitable non-nutritive sweeteners and combinations of such sweeteners include e. g. aspartame, neotame, and alitame, and ptide based sweeteners, for example, sodium saccharin, calcium saccharin, acesulfame potassium, sodium ate, calcium cyclamate, neohesperidin dihydrochalcone, and sucralose.
Beverage products typically contain flavors of various types and nature. In general, the beverage preservative system according to the t ion is ible with beverages formulated to contain artificial flavours, natural flavors, botanical , fruit flavors, aqueous essences, etc. The preservation function of the present invention is typically is not affected by such components. The term "botanical flavor" refers to flavors derived from parts of a plant other than the fruit. Also included within the term "botanical flavor" are tically prepared flavors made to simulate botanical flavors derived from natural sources. Botanical flavors can be derived from natural sources such as essential oils and extracts, or can be synthetically prepared. As used herein, the term "aqueous essence" refers to the water soluble aroma and flavor materials which are derived from fruit juices.
Beverage products typically can be fortified with added nutrients, vitamins, minerals, trace elements and the like. Such onal ents typically do not affect the preservation function of the invention. miting es of such additional ents that may typically be present in the beverages of the invention include vitamins A, B1, B2, B6, B12, C, D, E, K, Biotin, Folic Acid, Pantothenic Acid, Niacin, calcium, magnesium, iron, zinc, potassium, selenium, copper, manganese, etc.
The preservative system of the invention may also function in ge products of the meal substitute type, in which case substantial amounts of protein, carbohydrate, y fibers and/or lipids are lly present. r aspect of the invention concerns the use of the preservative system of this invention, for the preservation of an alimentary product, especially a beverage as defined previously. Yet another aspect of the invention concerns a method of preserving an alimentary product, ally a beverage as defined previously, comprising the step of adding to said product the preservative system of this invention. Preferred embodiments concern uses and methods, wherein the vation comprises inactivation of yeast and/or inhibiting yeast growth. In particularly preferred embodiments the yeast is a yeast selected from the group consisting of Candida (e.g. C. krusei, C. parapsilosz's, C. ulilis, C. valida, C. ns), Dekkera (e.g. D. bruxellensis), Debaryomyces (e. g. D. hansenii), Hanseniaspora (e. g. H. uvarum) Kluyveromyces (e. g. K. locll's), Pichia (P. membranaefaciens), poridium, orula (Rh mucilaginosa), Saccharomyces (e.g. S. baycmus, S. boulardi, S. carlsbergensis, S. cerevisiae, S. exiguus, S. florentinus, S. unisporus), Zygosaccharonmyces (e. g. Z. rouxii, Z baili). The details and preferred embodiments of these s of the invention will be y understood by those skilled in the art based on the foregoing detailed descriptions of the preservative system and products containing them.
Thus, the invention has been described by reference to certain embodiments discussed above. It will be recognized that these embodiments are susceptible to various modifications and alternative forms well known to those of skill in the art.
Many modifications in addition to those described above may be made to the structures and techniques described herein without departing from the spirit and scope of the invention. Accordingly, although specific ments have been described, these are examples only and are not limiting upon the scope of the invention.
Furthermore, for a proper understanding of this document and in its claims, it is to be understood that the verb "to comprise" and its conjugations is used in its non-limiting sense to mean that items following the word are included, but items not specifically mentioned are not excluded. In addition, reference to an element by the indefinite article a or "an" does not exclude the possibility that more than one of the element is present, unless the context y requires that there be one and only one of the elements. The indefinite article "a" or "an" thus usually means "at least one".
All patent and literature references cited in the present specification are hereby incorporated by reference in their entirety.
The following examples are offered for illustrative purposes only, and are not intended to limit the scope of the present invention in any way Examples The efficacy of cinnamate and vanillin in preserving against yeast was screened in a model beverage separate and in combination. After the screening l taste sessions were organized between resulting in potential preservative formulations to be tested in application. ation ments were set up using a model beverage. First the combined efficacy of both components was tested against 3 different yeasts (see table 1), known for their beverage spoiling ies. These tests were carried out in e 96-well microtiter plates. Sterile matrix was prepared (see recipe table 2) with increasing quantities of two ent inhibitors. The concentrations of each inhibitor were presented in 8 equal concentration steps that ranged from O to l — 2 times the (estimated) MIC value of particular yeast for a particular inhibitor ing in 64 different media. 200 ul of each medium was transferred to a panel of a sterile 96-well microtiter plate. ted well plates were stored at 4 0C until further use. For the inoculation of this test Sul of a 72 to 84 hours grown culture (Inoculation 103'4 per ml) was used.
Table l: teste microorganisms organism source Candida albicans Plant environment Saccharomyces cerevisiae Plant environment Zygosaccharomyces bailii Orange concentrate Table 2: recipe of the model drink % juice model drink, pH ~3.5 Water (Vittel) 965 g Citric acid (Sigma) 2.2 g e 40 g Flavour (Givaudan) 0.35 g Apple juice concentrate (Gargill) 8.28 g The data was obtained via OD measurement and the processing of the data was done in excel. Figurea 1-3 shows the results obtained in the form of 3D graphs (Figure l: Zygosaccharomyces bailil'; Figure 2: Saccharomyces cerevisiae; Figure 3: Candida albicans). Points in the graph represent the optical density of the corresponding well (Z aXis). The X and Y axes show increasing percentage of cinnamate and vanillin (A and B respectively).
As can be ed from these results, the model drink containing KCIN and vanillin were protected against yeast spoilage. Amounts of vanillin and cinnamate needed to accomplish this proved to be within the limits considered leptically acceptable in taste experiments.
Partial tion of the growth of molds could be observed in ison to the control without preservatives.

Claims (19)

  1. Claims 1. Preservative system comprising (i) more than 0.1 wt.% of vanillin and derivatives thereof in combination with (ii) more than 0.1 wt.% of cinnamic acid or a salt thereof, the 5 preservative system being free from preservative agents selected from the group of benzoates and sorbates.
  2. 2. Preservative composition according to claim 1, comprising vanillin in an amount within the range of 1-10 wt%.
  3. 3. Preservative composition according to claim 1 or 2, comprising cinnamate in an amount within the range of 5-50 wt%.
  4. 4. Preservative composition according to any one of the preceding claims wherein the ratio 15 of (i) : (ii) is within the range of 1.0 : 1.0 – 1.0 : 0.5.
  5. 5. Beverage comprising an effective amount of (i) vanillin and/or a derivative thereof and (ii) cinnamic acid or a salt thereof and less than 10 ppm of preservative agents selected from the group of sorbates and benzoates.
  6. 6. ge according to claim 5, sing in in an amount within the range of 200-500 ppm; and cinnamate in an amount within the range of 50-400 ppm.
  7. 7. Beverage according to claim 5 or 6, wherein the beverage has a pH of at least 2.
  8. 8. Beverage ing to any one of claims 5 to 7, wherein the beverage has a pH of at least 3.
  9. 9. Beverage according to any one of claims 5 to 8, n the beverage has a pH of at 30 least 3.2.
  10. 10. Use of a preservative composition according to any one of claims 1-4, for the vation of a beverage.
  11. 11. Use of a preservative composition according to any one of claims 1-4 for the inactivation of yeast in a beverage.
  12. 12. Use of a preservative composition according to any one of claims 1-4 for inhibiting 5 yeast growth in a beverage.
  13. 13. Use according to claim 11 or 12, wherein the yeast is selected from the group of a albicans, Saccharomyces cerevisiae and Zygosaccharomyces baiii. 10
  14. 14. A preservative system according to claim 1, substantially as herein described or exemplified.
  15. 15. A ge according to claim 5, substantia lly as herein described or exemplified. 15 19.
  16. Use according to claim 10, substantially as herein described or ified.
  17. 17. Use ing to claim 11, substantially as herein described or exemplified.
  18. 18. Use according to claim 12, substantially as herein described or exemplified.
  19. WO 58651 Maximum
NZ623863A 2011-10-18 2012-10-18 Preservative combinations NZ623863B2 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201161548535P 2011-10-18 2011-10-18
EP11185613.4A EP2583568A1 (en) 2011-10-18 2011-10-18 Preservative combinations comprising vanillin and cinnamic acid
US61/548,535 2011-10-18
EP11185613.4 2011-10-18
PCT/NL2012/050726 WO2013058651A1 (en) 2011-10-18 2012-10-18 Preservative combinations

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NZ623863A NZ623863A (en) 2015-11-27
NZ623863B2 true NZ623863B2 (en) 2016-03-01

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