COMPRESSED YEAST FOR DIRECT INOCULATION OF A FRUIT OR VEGETABLE SUBSTRATE
20180179479 ยท 2018-06-28
Assignee
Inventors
- Kristine BJERRE (Virum, DK)
- Jan Hendrik Swiegers (Fredensborg, DK)
- Mansour Badaki (Vanloese, DK)
- Katja Sander JENSEN (Hvidovre, DK)
Cpc classification
C12G1/02
CHEMISTRY; METALLURGY
C12G2200/05
CHEMISTRY; METALLURGY
C12N1/04
CHEMISTRY; METALLURGY
International classification
Abstract
The present invention relates to a novel form of compressed yeast for direct inoculation in the fermentation of a fruit or vegetable substrate, e.g. for the fermentation of beverages, such as wine or beer. Especially, the present invention relates to compressed yeast with a dry matter content of between 35% and 90% (w/w), preferably in a frozen form, a method for producing a fermented beverage by direct inoculation of a fruit or vegetable substrate with the compressed yeast and a container comprising the compressed yeast.
Claims
1-12. (canceled)
13. A method for producing a fermented beverage, comprising: (a) providing a fruit or vegetable substrate for production of the beverage; (b) adding a frozen compressed yeast with a dry matter content of between 35% and 90% (w/w) to the fruit or vegetable substrate without any re-hydration or re-activating steps; and (c) fermenting the fruit or vegetable substrate with the compressed yeast to obtain the fermented beverage.
14. The method according to claim 13, wherein the dry matter content of the frozen compressed yeast is between 45% and 75% (w/w).
15. The method according to claim 13, wherein the compressed yeast does not comprise any added additives.
16. The method according to claim 13, wherein the compressed yeast is frozen in the absence of any added additives added to the liquid yeast concentrate in order to stabilize the yeast cells during and after freezing.
17. The method according to claim 13, wherein the viability of the frozen yeast is at least 20% based on the concentration of CFU (colony forming units) of the compressed yeast before freezing and the concentration of CFU of the compressed yeast after freezing.
18. The method according to claim 13, wherein the viability of the yeast is at least 60% after step (b) as calculated based on the concentration of CFU (colony forming units) of the compressed yeast and the concentration of CFU of the material resulting from step (b).
19. The method according to claim 13, wherein the viability of the yeast is at least 80% after storage for five months at a temperature of ?20? C. followed by step (b) as calculated based on the concentration of CFU (colony forming units) of the compressed yeast before freezing and the concentration of CFU of the material resulting from step (b).
20. The method according to claim 13, wherein the yeast is selected from Saccharomyces, Kluyveromyces, Lachancea, Torulaspora, Brettanomyces, Pichia, Metschnikowia, Candida, Hanseniaspora, Saccharomycodes, Zygosaccharomyces, Cryptococcus, Issatchenkia, Schizosaccharomyces, Wickerhamomyces and Debaryomyces.
21. The method according to claim 20, wherein the yeast is a Saccharomyces yeast.
22. The method according to claim 13, wherein the fermented beverage is selected from wine, beer, cider, sake and soft drinks.
23. The method according to claim 13, wherein the substrate is a fruit juice.
24. The method according to claim 23, wherein the fruit juice is grape juice and the fermented beverage is wine.
Description
DETAILED DESCRIPTION OF THE INVENTION
[0012]
[0013] As can be seen in
[0014] The present invention in a first aspect relates to the provision of a compressed yeast for direct inoculation of a fruit or vegetable substrate with a dry matter content of between 35% and 90% (w/w). In some embodiments, the dry matter content is between 30% and 45%, such as between 30% and 40% or between 35% and 45%.
[0015] In another embodiment, the dry matter content of the compressed yeast is between 45% and 75% (w/w).
[0016] The dry matter content of the sample is measured by heating at 105? C.+/?5? C. in order to evaporate water content. The sample is measured before and after drying and the below calculations are carried out to get dry-matter content expressed as % (w/w):
[0017] The dry matter (W.sub.dm) content expressed as a percentage of mass or grams per kilogram is calculated using the following equations:
[0018] where:
[0019] W.sub.dm is the dry matter of the sample, in percentages or grams per kilogram;
[0020] m.sub.a is the mass of the empty dish or crucible in grams;
[0021] m.sub.b is the mass of the dish or crucible containing the sample in grams;
[0022] m.sub.c is the mass of the dish or crucible containing the sample in grams after complete dehydration and removal of all water;
[0023] f is a conversion factor, f=100 for expression of results as a percentage and factor f=1000 for expression in grams per kilogram.
[0024] Values should be rounded to the nearest 0.1% (w/w) or alternatively to the nearest 1 g/kg.
[0025] In a preferred embodiment the compressed yeast according to the invention does not comprise any added additives.
[0026] In a preferred embodiment, the viability of the compressed yeast is at least 20% after freezing as calculated based on the concentration of CFU (colony forming units) of the compressed yeast before freezing and the concentration of CFU of the compressed yeast after freezing. Preferably, the viability of the yeast is at least 25%, such as at least 30%, such as at least 35%, such as at least 40%, such as at least 45%, such as at least 50%, such as at least 55%, such as at least 60%, at least 65%, such as at least 70%, such as at least 75%, such as at least 80%, such as at least 85%, such as at least 90%, such as at least 91%, such as at least 92%, such as at least 93%, such as at least 94%, such as at least 95%, such as at least 96%, such as at least 97%, such as at least 98%, such as at least 99%. Most preferably, the viability is 100%.
[0027] In a preferred embodiment the viability of the compressed yeast is at least 60% after direct inoculation of a fruit or vegetable substrate as calculated based on the concentration of CFU (colony forming units) of the compressed yeast and the concentration of CFU of the inoculated material. Preferably, the viability of the yeast is at least 65%, such as at least 70%, such as at least 75%, such as at least 80%, such as at least 85%, such as at least 90%, such as at least 95%.
[0028] In another preferred embodiment the viability of the compressed yeast is at least 80% after storage for five months at a temperature of ?20? C. followed by direct inoculation of a fruit or vegetable substrate as calculated based on the concentration of CFU (colony forming units) of the compressed yeast before storage and the concentration of CFU of the inoculated material. Preferably, the viability of the yeast is at least 85%, such as at least 90%, such as at least 95%.
[0029] In a preferred embodiment, the compressed yeast is frozen at a temperature below 0? C. Preferably, the compressed yeast is frozen at a temperature significantly below 0? C., such as at ?5? C., such as at ?20? C., such as at ?50? C.
[0030] In a preferred embodiment, the frozen compressed yeast according to the present invention is frozen in the absence of any additives added to the liquid yeast concentrate in order to stabilize the yeast cells during and after freezing.
[0031] In a preferred embodiment, the viability of the frozen compressed yeast is at least 20% after freezing as calculated based on the concentration of CFU (colony forming units) of the compressed yeast before freezing and the concentration of CFU of the compressed yeast after freezing. Preferably, the viability of the yeast is at least 25%, at least 30%, such as at least 35%, such as at least 40%, such as at least 45%, such as at least 50%, such as at least 55%, such as at least 60%, at least 65%, such as at least 70%, such as at least 75%, such as at least 80%, such as at least 85%, such as at least 90%, such as at least 91%, such as at least 92%, such as at least 93%, such as at least 94%, such as at least 95%, such as at least 96%, such as at least 97%, such as at least 98%, such as at least 99%. Most preferably, the viability is 100%.
[0032] The determination of the viability of yeast can be carried out by any suitable method known to the skilled person. In a preferred embodiment the determination of CFU/g and CFU/ml cell counts is performed as set out by OIV in chapter II of the International Oenological Codex, 2013 Issue.
[0033] In a preferred embodiment the viability of the frozen compressed yeast is at least 60% after direct inoculation of a fruit or vegetable substrate as calculated based on the concentration of CFU (colony forming units) of the compressed yeast and the concentration of CFU of the inoculated material. Preferably, the viability of the yeast is at least 65%, such as at least 70%, such as at least 75%, such as at least 80%, such as at least 85%, such as at least 90%, such as at least 95%.
[0034] In another preferred embodiment the viability of the frozen compressed yeast is at least 80% after storage for five months at a temperature of ?20? C. followed by direct inoculation of a fruit or vegetable substrate as calculated based on the concentration of CFU (colony forming units) of the compressed yeast before freezing and storage and the concentration of CFU of the inoculated material. Preferably, the viability of the yeast is at least 85%, such as at least 90%, such as at least 95%.
[0035] The compressed yeast according to the present invention is preferably present in a concentrated form.
[0036] In a preferred embodiment the compressed yeast contains at least 10.sup.9 CFU/g of yeast, such as at least 5?10.sup.9 CFU/g of yeast, such as at least 10.sup.10 CFU/g of yeast, such as at least 5?10.sup.10 CFU/g of yeast, such as at least 10.sup.11 CFU/g of yeast, such as at least 5?10.sup.11 CFU/g of yeast, such as at least 10.sup.12 CFU/g of yeast.
[0037] In a preferred embodiment the compressed yeast is selected from the genera of the group consisting of Saccharomyces, Kluyveromyces, Lachancea, Torulaspora, Brettanomyces, Pichia, Metschnikowla, Candida, Hanseniaspora, Saccharomycodes, Zygosaccharomyces, Cryptococcus, Issatchenkia, Schizosaccharomyces, Wickerhamomyces and Debaryomyces.
[0038] In a preferred embodiment the compressed yeast is a Saccharomyces yeast, preferably a Saccharomyces cerevisiae yeast
[0039] In another preferred embodiment the yeast is a wine yeast or a brewer's yeast, preferably the wine yeast or brewer's yeast is a yeast selected from the group consisting of Saccharomyces. Kluyveromyces, Lachancea, Torulaspora, Brettanomyces, Pichia and Metschnikowia yeast.
[0040] The invention further provides a method for producing a fermented beverage comprising the steps:
[0041] a) providing a fruit or vegetable substrate for production of the beverage;
[0042] b) directly inoculating the substrate with the compressed yeast according to the invention; and
[0043] c) fermenting the substrate with the compressed yeast to obtain the fermented beverage. As known to the skilled person directly inoculating means that the compressed yeast is added directly to the fruit or vegetable substrate without any re-hydration or re-activating steps.
[0044] The fermentation may be carried out under aerobic or anaerobic conditions or it may be carried out under a sequence of aerobic and anaerobic conditions.
[0045] In a preferred embodiment the fermented beverage is selected from the group consisting of wine, beer, cider, sake and soft-drinks. Preferably, the fermented beverage is wine.
[0046] In another preferred embodiment the fruit or vegetable substrate for production of the beverage is a fruit or vegetable juice. Preferably, the fruit juice is grape juice and the fermented beverage is wine.
[0047] It is contemplated that the compressed yeast according to the present invention will be equally suitable for use in a similar method of direct inoculation of an aqueous fruit or vegetable substrate for ethanol fermentation under anaerobic conditions. Suitable fruit or vegetable substrates are carbohydrate-rich substrates including but not limited to aqueous solutions based on corn syrup, cane sugar/molasses.
[0048] Another aspect of the present invention is related to a container comprising the compressed yeast according to the invention. In a preferred embodiment, the container is selected from the group consisting of a carton or a sealed plastic container.
Definitions
[0049] The term cream yeast herein refers to liquid yeast with a dry matter content of below 28% (w/w) conventionally produced by propagation of yeast in a fermentor followed by concentration by centrifugation.
[0050] The term compressed yeast refers herein to a yeast with a dry matter content of between 35% and 90% (w/w) conventionally produced by propagation of yeast in a fermentor followed by concentration, filtration, extrusion and optionally partial drying on a drier, such as a fluid bed drier. In some embodiments, the dry matter content is between 30% and 45%, such as between 30% and 40% or between 35% and 45%.
[0051] Thus, the term partially dried compressed yeast refers herein to a yeast with a dry matter content of between 45% to 90% (w/w) produced by propagation of yeast in a fermentor followed by concentration, filtration, extrusion and partial drying on a drier, such as a fluid bed drier.
[0052] The term active dried yeast or ADY refers herein to yeast with a dry matter content of more than 90% (w/w) conventionally produced by propagation of yeast in a fermentor followed by concentration, filtration, extrusion and drying on a fluid bed drier.
[0053] The term vegetable refers herein to any plant. Preferably, the term vegetable herein refers to edible plants or edible plant parts.
[0054] The term fruit refers herein to the edible part of a plant developed from a flower. Fruit may include any accessory tissues of the edible part, such as the skin, peel or pod.
[0055] The term yeast enhancer herein refers to supplementary nutrients, such as vitamins, nitrogen, phosphate or minerals, added prior to or during propagation of the yeast.
[0056] The term additives herein refers to food-grade agents which are added to the yeast concentrate at any time point during production of the yeast formulation after propagation of the yeast, e.g. to assist in the extrusion and cutting of the yeast concentrate, e.g. emulsifiers, including, but not limited to, glycerol, glucose, sucrose and trehalose, and oil, to improve the stability of the yeast cells during freezing and/or cold storage, to change the melting point of the frozen yeast formulation, e.g. water-activity modifying agents, etc.
[0057] The term added when referring to additives herein refers to that the additives are introduced into the yeast concentrate during production of the compressed yeast in an amount efficient to give the desired effect.
BRIEF DESCRIPTION OF THE FIGURES
[0058]
[0059]
[0060]
[0061]
[0062]
[0063]
EXAMPLES
Example 1
[0064] During the production of a conventional Saccharomyces cerevisiae strain, samples were taken out at three different stages during production; 1) as liquid (cream) yeast after centrifugation; 2) as compressed yeast (fresh yeast) with a dry matter content of 40% alter extrusion, and 3) as active dry yeast (ADY) with a dry matter content of 92% after fluid bed drying:
[0065] These samples were analysed according to cell count, survival after either keeping the concentrate at 4? C. or freezing the concentrate at ?20? C., at ?50? C. in the freezer or in liquid nitrogen and storing for 1 month at the indicated temperature (
Survival of Treatment and Over Time
[0066] The liquid yeast was frozen with 200 ml sample in a ?20? C. freezer as untreated or with 20% trehalose. Cell counts were measured before and then again one month after freezing and followed over time.
[0067] The compressed yeast was frozen in different sizes and at different temperatures in order to verify the effect of the freezing rate on the survival of yeast cells. The sizes of the samples were 200 ml bottles (big) and 50 ml falcon tubes (small). The temperatures of the freezers were ?20? C. and ?50? C. respectively.
[0068] Also the compressed yeast was frozen in liquid nitrogen as pellets (1-2 ml long (small) and as 5 g clumps (big)).
[0069] For determination of yeast survival (in percentages), cell counts were measured before freezing and again one month after freezing (
Survival in Direct Inoculation
[0070] All samples were also used for direct inoculation after 1 month of storage in order to see the survival when the yeast cells were exposed to water and high osmotic pressure in the grape juice. 1.0 g of samples was added to 200 mL Riesling juice (Table 1). The samples were dissolved by gentle stirring and after approximately 10-15 min. the dilution series was performed and for determination of yeast survival (in percentages), CFU/g was calculated after direct inoculation (
TABLE-US-00001 TABLE 1 Parameters of grape juice used for direct inoculation experiments after 1 month Grape juice Sugar (g/l) Malic acid (g/l) TSO.sub.2 (mg/l) Riesling (Germany) 180 6.6 0
Comparison of Survival by Direct Inoculation and Reactivation of the Yeast
[0071] Survival of inoculation by use of two different methods was compared. In both methods the inoculation volume was 0.2 g/l. For direct inoculation, the sample was added directly to the Chardonnay juice (Table 2). For standard inoculation, the sample was first rehydrated 1:10 in unchlorinated water for approximately half an hour. Un-sulphured grape juice was then added to the water in the ratio (1:3) and the suspension was then left to activate for approximately another 20 minutes. The final activated suspension was then added to the juice to reach a final inoculation level of 0.2 g/l. All inoculations were performed in duplicates.
[0072] CFU/g of the products were calculated before inoculation and after inoculation and the survival was then calculated as percentages (
TABLE-US-00002 TABLE 2 Parameters of grape juice used for direct inoculation experiments after 8 months Grape juice Sugar (g/l) Malic acid (g/l) TSO.sub.2 (mg/l) Chardonnay (Germany) 180 6.7 0
Determination of Colony Forming Units (CFU)
[0073] For determination of CFU/g and CFU/ml cell counts from samples taken from either inoculated grape juice or yeast dissolved in peptone water were performed by pour-plating on YGC media (prepared as set out by OIV in appendix VI of the International Oenological Codex, 2013 Issue). 1 ml of the sample from the dilution series (peptone water) was added to the plate and on top of that the liquid YGC agar (45? C.) was poured over the sample and mixed. After setting, the plates were incubated at 30? C. for 2-3 days. Determinations of CFU were in all cases performed in triplicates.
Conclusion:
[0074] The results show that the survival of the yeast in direct inoculation (
[0075] The survival of the yeast after different treatments and storage of the samples for 1 month at this temperature shows high variations (
[0076] The overall survival shows that the compressed yeast, even when frozen, shows the highest survival (
[0077] Stability of the different formats is measured over 5 months and results are shown in (
[0078] The compressed yeast stored at 4? C. was only followed for 4 months as the sample was not packed in a proper sanitary way to be kept for a longer period of time.
[0079] The active dry yeast (ADY) products show lower survival when directly inoculated compared to when inoculated after rehydration and reactivation (
REFERENCES
[0080] Roger Boulton, Vernon Singleton, Linda Bisson and Ralph Kunkee. 1996. Principles and Practices of Winemaking. pp. 124. [0081] Karien O'Kennedy. (2008). How to avoid stuck fermentations, The Australian & New Zealand Grapegrower & Winemaker. November, Issue 538, 103-105. [0082] Virginie Soubeyrand, Anne Jullen and Jean-Marie Sablayrolles (2006) Rehydration Protocols for Active Dry Wine Yeasts and the Search for Early Indicators of Yeast Activity American Journal of Enolology and Viticulture. 57(4)474-480.