Patent Application
20110123673
The present invention relates to methods and compositions for initiation of as well as to methods of fermentation in a liquid composition comprising a fermentable compound. In particular the invention relates to methods and compositions for initiation of malo-lactic fermentation during wine production.
Wine contain L-malic acid in the range of 1 to 10 g/L. The amount of malic acid depends largely on the climatic conditions. Hence, wines produced in colder areas tend to have a relative higher concentration. From a taste and flavour point of view, malic acid is considered undesirable in most red wines and in several types of white wines and sparkling wines and from a practically/economically point of view malic acid is undesirable as it can support growth of bacteria in the wine after it has been bottled.
During the alcoholic fermentation only a small part of the present malic acid is degraded by the yeast. However, the content of malic acid in a wine may be effectively reduced by the so-called malolactic fermentation (MLF) which normally occurs after completion of the alcoholic fermentation. The MLF results from the catabolic activity of various lactic acid bacteria, including species belonging to the genera of Lactobaccilus, Pediococcus and Oenococcus.
The bacteria may be present in the wine as part of the indigenous microbial flora, or they may have been added as a bacterial starter culture. The most preferable bacteria species by winemakers is Oenococcus oeni, formerly known as Leuconostoc oenos. The catabolic phase is usually entered when the malolactically active bacteria during the growth phase has reached a population density of about 106 colony forming units (CFU) per ml in the wine. During the MLF the bacteria degrade the malic acid, a dicarboxylic acid, to lactic acid, a monocarboxylic acid. As a result of this the acidity of the wine decreases and the pH increases, resulting in a wine with softer palate. Within the field the malolactic fermentation is considered completed when the concentration of malic acid in the wine is less than 30 mg/l (Zoecklein at al., in Wine Analysis and Production, Chapman and Hall, p 296).
However, during the malolactic fermentation Oenococcus oeni also degrade the citric acid, which normally is present in the wine at a concentration of 0.3-0.9 g/L The catabolism of malic acid and citric acid is in general not concomitant, but sequential, i.e. the citric acid degradation is delayed compared to the malic acid fermentation (see for example Nielsen et al., 1999, Appl. Environ. Microbiol., 65:740-745 and Viljakainen and Laakso, 2000, Eur. Food Res. Technol., 211:438-442). The degree of delay is dependent on the specific bacteria and the wine. The degradation of citric acid is often undesired as the wine looses some of its fruitiness which is appreciated in most wines. Another undesired and unavoidable effect of the citric acid degradation by Oenococcus oeni during MLF is the production of acetic acid, which is one of the end products from the citric acid degradation. The acetic acid concentration in the wine may increase with 0.1-0.3 g/L during the MLF. Acetic acid is highly undesired as it gives the wine an unpleasant vinegar flavour at higher concentration and the winemaker use much attention to keep the acetic acid concentration in the wine as low as possible during the different winemaking steps. Besides the lactic acid bacteria the other sources of acetic acid in winemaking is yeast and acetic acid bacteria. An important intermediary compound in the metabolism of citric acid by Oenococcus oeni is diacetyl. When present at concentration above the sensory threshold, diacetyl gives the wine a buttery aroma which is undesired in most red wines. However, in some white wines, e.g. Chardonnay the aroma may be appreciated.
Because the winemaker often prefer to exercise a greater degree of control over the malolactic fermentation process it has become increasingly common practice in the wine industry to induce the fermentation by use of commercially available concentrated frozen or freeze dried starter cultures of Oenococcus oeni, which are inoculated directly into the wine without any prior re-hydration and activation steps. The usefulness of a concentrated frozen or freeze dried culture which are inoculated direct into wine depends very much on the survival rate of the bacteria culture after the inoculation. The transition of the bacteria from a friendly propagation medium with high pH and high nutrition level to the hostile condition in wine with high ethanol concentration, low pH, low nutrition level, and presence of SO2 is very stressful for the bacteria and may result in survival rates below 1% in the inoculated wine.
Typically, the described propagation medium for lactic acid bacteria, including Oenococcus oeni, contain various nutrients such as vitamins, minerals, yeast extract and sugars. The amount of sugars in the media are normally within 20-50 g/L as higher concentrations of sugars are considered to strongly reduce or inhibit the growth of lactic acid bacteria. In the prior art higher concentrations of sugars in the propagation medium have therefore been considered to be of no practically use or economically interest.
Freeze dried cultures of a strain of Oenococcus oeni, which do not ferment the citric acid in the wine during the malolactic fermentation, are commercially available. There are several advantages in using this strain for malolactic fermentation in wine. The fruitiness of the wine is conserved, there is no production of acetic acid during the malolactic fermentation and there is no production of the buttery flavour, diacetyl. However, the commercial cultures of this strain on the market can not be used for direct inoculation into wine as this results in a survival rate which is of no practical use. According to the commercial application manuals of the products the freeze dried cultures needs re-hydration and an adaptation procedure involving several steps before the bacteria can be inoculated into wine. The first step may involve dissolving the freeze dried product in 5 L of half water, half grape juice or wine added different nutrition. After 5-7 days incubation the pre-culture is diluted with 20-200 L wine which is incubated for another 2-12 days before the final inoculation into the production tank with wine. The adaptation steps are very time and labour consuming for the winemaker as he has to follow the adaptation steps carefully, and there is a high risk for contamination with spoilage bacteria and yeast as the adaptation steps under the practical conditions in the wineries can not be conducted under sterile conditions.
WO 9320180 discloses a method for inducing malolactic fermentation in wine or fruit juice by the direct inoculation of a concentrate of a starter culture containing a selected malolactically active bacteria strain having a survival rate of at least 80% when introduced into a wine having a pH of 3.2 or lower and containing at least 25 mg SO2 per L and at least 12 vol % ethanol, and capable of starting malolactic fermentation when added directly to the wine or fruit juice at a concentration of less than 107 colony forming units per ml. Said bacteria strain is also capable of degrading citric acid. The document clearly indicates that the bacteria strains ability to survive the direct inoculation into wine is linked to the genetic of the strain selected. According to the disclosure the selected bacteria strains are propagated according to processes which are well-known in the art.
U.S. Pat. No. 6,284,518 B1 discloses a media for propagation of different lactic acid bacteria species, including Oenococcus oeni. According to the disclosure a key feature of the invention is the use of a fructose/glucose mixture where fructose is the primary carbohydrate source. Fructose/glucose mixtures containing between 3% to about 45% glucose can be employed, preferably the amount is between 5% and about 40% glucose. Most preferable, the amount is less then 20% of the mixture. In the disclosed media, as biomass growth occurs, the pH is allowed to drop. The amount of carbohydrate source in the disclosed medium is between 30 g/L to 60 g/L. They document describes that 106-107 bacteria/ml are inoculated into the medium and the bacteria are then propagated for 6-8 days before the bacteria can be inoculated into wine.
In U.S. Pat. No. 4,562,077 is disclosed a method for the reduction of malic acid to lactic acid in wine which comprises the inoculation of a culture concentrate into non-sterile fruit juice containing a nitrogen source to provide about 107 to 1010 bacteria per nil. After this activation step the mixture of fruit juice and bacteria are introduced into wine or grape must to produce wine having a reduced malic acid content. The activation conditions disclosed are an activation period of 48 to 72 hours at 18° C. to 25° C.
Carrié at al., 2002, Revue des OEnologues 103: 16-18 describes various malic acid fermenting bacteria, some of which can be inoculated directly into wine. The document furthermore describes the citric acid concentration in wine after/during malolactic fermentation with these bacteria. It appears from
Nielsen et al., 1996 Am. J. Enol. Vitic. 47:42-48 describes Leuconostoc oenos bacterial cultures capable of fermenting malic acid to lactic acid. The bacteria can be inoculated directly into wine. The bacteria are capable of degrading citric acid.
Nielsen and Richelieu, 1999, Appl. Environ. Microbiol. 65:740-745 describes malolactic fermention and describes that citric acid degradation is delayed compared to degradation of malic acid.
U.S. Pat. No. 5,460,837 describes a method of initiating malolactic fermentation by cultivating malolactically active bacteria in a medium comprising 0.05 to 0.5% glucose, separation of biomass and optionally freeze drying. The freeze dried cultures may be inoculated directly in wine.
It is therefore an object of the present invention to provide improved methods of inducing specific fermentation processes in a liquid composition.
Hence, in one aspect the present invention relates to induction of specific fermentation processes in a liquid composition comprising at least one fermentable compound as well as to microbial organisms for use in said methods.
In particular the present invention provides, compared to known methods, a significant improved method of inducing malolactic fermentation in wine or fruit juice without the concomitant degradation of citric acid, production of acetic acid, and production of diacetyl herein within a short period of time by inoculation wine or a fruit juice directly with a concentrated culture composition of malolactically active and non, citric acid fermenting bacteria at an economically feasible concentration and accordingly, to avoid the tediously, risky and costly processes of re-hydration, activation, and adaptation which are currently required with commercial malolactically non-citric acid fermenting starter cultures.
Also, the present invention provides, compared to known methods, a significant improved method of inducing malolactic fermentation in wine or fruit juice within a short period of time by inoculation wine or a fruit juice with a specially activated concentrated culture solution of malolactically active and citric acid or non-citric acid fermenting bacteria at an economically feasible concentration and accordingly, to avoid the lag and dead phase observed when commercial dry malolactic starter cultures are inoculated directly into wine and also to significantly improve the tediously, risky and costly processes of re-hydration, activation, and adaptation which are currently required with commercial malolactic starter cultures not suitable for direct inoculation into wine.
It is therefore a first objective of the present invention to provide isolated and purified microbial organisms, wherein said microbial organisms are capable of fermenting malic acid to lactic acid,
Hence, said microbial organism may be added directly into for example a fermented fruit juice during wine production without any previous adaptation. It is in general laborious to adapt bacteria to growth in fermented fruit juice and there is a high risk of contamination using the conventional adaptation procedure, in particular in a normal winery where the adaptation frequently cannot be done under sterile conditions.
It is also an objective of the present invention to provide a concentrate comprising or consisting of said microbial organism(s), wherein said concentrate has a content of colony forming units being in the range of 109 to 1012 per g.
It is a second objective of the present invention to provide methods of preferentially degrading malic acid over citric acid in a liquid composition comprising malic acid and citric acid, said methods comprising the steps of
Preferably said microbial organism has at least one of the characteristics outlined herein above.
It is a third objective of the present invention to provide methods of inducing malolactic fermentation during wine production, comprising the steps of
Preferably said microbial organism has at least one of the characteristics outlined herein above.
It is another objective of the present invention to provide methods of producing the microbial organism described herein above, wherein said method comprises the steps of
It is a further objective of the present invention to provide methods of preparing a freeze-dried microbial organism capable of fermenting malic acid to lactic acid, which has reduced citric acid degrading activity and which is capable of survival after direct inoculation into fermented fruit juice, said method comprising the steps of
It is a still further objective of the present invention to provide an activation solution comprising
Said activation solution is useful for adapting freeze-dried or frozen microbial organisms to growth in liquid solutions with a pH below 5 and/or an alcohol content above 10%. When using this adaptation solution, the adaptation procedure is much faster and easier to handle compared to conventional adaptation procedures.
It is an even further objective of the present invention to provide a dry activation composition, wherein in the range of 80 to 200 g of said dry activation composition comprises
It is yet another objective of the present invention to provide methods of inducing fermentation in a liquid composition comprising a fermentable compound comprising the steps of
Table 1. Data for sample A, B, C, and D sampled during the propagation of the selected non-citric acid fermenting mutant strain Oenococcus oeni DSM 16571 in the cultivation and adaptation medium shown in
Table 2. Survival rates of the selected non-citric acid fermenting mutant strain Oenococcus oeni DSM 15571 in the experimental wine measured 2 days after inoculation of the freeze dried samples A, B, C, and D (
Table 3. Data for sample 1, 2, 3, and 4 sampled during the activation of the normal citric acid fermenting strain Oenococcus oeni DSM 15568 in the activation composition solution (
Table 4. Survival rates of the normal citric acid fermenting strain Oenococcus oeni DSM 15568 in the experimental wine measured 2 days after inoculation of the activated bacteria samples 1, 2, 3, and 4 (
Activation or adaptation of microbial organisms: Both terms refer to methods involving placing a microbial organism under conditions that allow for the physiological changes necessary in order for said microbial organism to survive and grow in a new liquid composition with harsh conditions. In particular, activation or adaptation cover placing a freeze-dried, frozen or otherwise preserved microbial organism in a medium for a specific time period that allow said physiological changes, before said microbial organism is placed in a new liquid composition with harsh conditions. Harsh conditions may for example be low pH, high ethanol content or a mixture of both.
Directly: The term “added directly to” is meant to encompass that the compound, i.e. the frozen or freeze-dried microbial organism is added directly to the liquid composition in the frozen or freeze-dried state without any preceding adaptation, activation and/or expansion.
Ethanol content: the ethanol content is always indicated as volume percent (vol %) unless otherwise specifically indicated, hence an ethanol content of x % refers to x vol % ethanol.
Frozen: The microbial organism is frozen when it is stored at a temperature below 0° C. The microbial organism may be frozen according to any conventional protocol. In general the microbial organism is frozen by mixing said microbial organism with suitable cryoprotectants such as glycerol, gelatine or Na-caseinate and incubating the mixture at a temperature below 18° C.
Freeze dried: Freeze-drying a microbial organism involves freezing said microbial organism generally in the presence of a suitable cryoprotectant, and subsequently removing trapped ice by reducing the pressure and causing it to sublime. The microbial organism according to the present invention may be freeze dried using any conventional method known to the person skilled in the art. For example any of the methods described in “Fundamentals of Freeze Drying, J. D. Mellor, 1978, Academic Press.
In one aspect the present invention relates to microbial organism capable of fermenting malic acid to lactic acid. Preferably, said microbial organism when placed in a medium containing a predetermined amount of citric acid is only capable of degrading at the most 80% of said citric acid. Even more preferably, the microbial organism is only capable of degrading at the most 70%, such as 60%, for example 50%, such as 40%, for example 30%, such as 25%, for example 20%, such as 15%, for example 12%, such as 10% of said citric acid. Hence, it is preferred that the microbial organism is only capable of degrading in the range of 0 to 50%, more preferably 0 to 40%, even more preferably 0 to 30%, yet more preferably 0 to 20% of said citric acid. It is furthermore preferred that the microbial organism is only capable of degrading at the most 50%, more preferably at the most 40%, even more preferably at the most 30%, yet more preferably at the most 20%, even more preferably at the most 10% of said citric acid within for example 3 weeks, more preferably within 2 weeks, such as within 13, for example 12, such as 11, for example 10 days. In a preferred embodiment of the invention the microbial organism is only capable of degrading at the most 50%, more preferably at the most 40%, even more preferably at the most 30%, yet more preferably at the most 20%, even more preferably at the most 15% of the initial citric acid even during long term incubation, such as storage for 30 days, for example for 40 days, for example for 50 days, such as for 60 days, for example for 80 days, such as for 100 days, preferably for at least 40 days, more preferably for at least 50 days.
Because the citric acid degradation in general is delayed compared to the malic acid degradation (see for example
In a very preferred embodiment of the invention the microbial organism is not capable of degrading more than 50%, preferably not more than 40%, more preferably not more than 30%, even more preferably not more than 20% of the initial citric acid, for as long as said microbial organism is metabolically active.
Preferably, the microbial organism when placed in a liquid composition comprising a predetermined amount of malic acid is capable of degrading at least 30%, such as 50%, for example 70%, such as 80%, at least 90%, for example at least 95% of said malic acid. Preferably, the microbial organism is capable of degrading in the range of 70 to 100%, more preferably in the range of 80% to 100%, even more preferably in the range of 90 to 100% of said malic acid.
More preferably, the microbial organism when placed in a liquid composition comprising a predetermined amount of malic acid is capable of fermenting at least 30%, such as 50%, for example 70%, such as 80%, at least 90%, for example at least 95% of said malic acid to lactic acid.
In a very preferred embodiment, the microbial organism when placed in a liquid composition comprising a predetermined amount of malic acid is capable of completing malolactic fermentation, i.e. is capable of fermenting malic acid to an end concentration of malic acid of at the most 30 mg/L, more preferably at the most 15 mg/L.
Said degradation of malic acid preferably is completed within at the most 1 month, preferably within at the most 3 weeks, more preferably within at the most 2 weeks, such as 13, for example 12, such as 11, for example 10, such as 9 days.
The liquid composition comprising said predetermined amount of malic acid and/or citric acid furthermore preferably comprises one or more of the following parameters
It is preferred that said microorganism is incubated with said fermented fruit juice at a temperature of in the range of 15 to 30° C., such as in the range of 20 to 25° C., for example around 23° C.
Preferably, the microbial organism is capable of degrading malic acid and/or citric acid as indicated herein above when said organism is present at a concentration of CFUs (colony forming units) in the range of 1×103 to 5×1012 per ml, preferably in the range of 1×104 to 5×1010 per ml, more preferably in the range of 1×106 to 5×106 per ml, for example in the range of 1×106 to 5×107 per ml.
In one preferred embodiment of the present invention the microbial organism is capable of reducing malic acid within 9 days to less than 1 g/L, such as less than 0.5 g/L, for example less than 0.1 g/L, such as less than 30 mg/L, for example less than 15 mg/L, when incubated at a temperature of approximately 23° C., when said microbial organism is added directly in a frozen or freeze dried state to a fermented fruit juice at a concentration of CFUs in the range of 1×106 to 5×107, wherein said fermented fruit juice is prepared by yeasting a sterile fruit juice without added sulphite resulting in a fermented fruit juice having an ethanol content of 12.0 vol %, pH 3.4, below 5 g/L residual sugar, 3.3 g/L of malic acid, and 450 mg/L of citric acid.
Furthermore, it is preferred that the microbial organism reduces the citric acid content by less than 50%, such as less than 20%, for example less than 10% within 10 days, preferably within 20 days, more preferably within 40 days, for example within 50 days, such as within 100 dayS, when incubated at a temperature of approximately 23° C., when said microbial organism is added directly in a frozen or freeze dried state to a fermented fruit juice at a concentration of CFUs in the range of 1×106 to 5×107 per ml, wherein said fermented fruit juice is prepared by yeasting a sterile fruit juice without added sulphite resulting in a fermented fruit juice having an ethanol content of 12.0 vol %, pH 3.4, below 5 g/L residual sugar, 3.3 g/L of malic acid, and 450 mg/L of citric acid.
The microbial organism according to the present invention preferably has at least one of the following characteristics, when said microbial organism in a frozen or freeze dried state is added directly into a fermented fruit juice:
Preferably, the survival rate is at least 5%, such as at least 10%, for example at least 15%, such as at least 20%, for example at least 25%, such as at least 30%, for example at least 35%, such as at least 40%, for example at least 45%, such as at least 50%, for example at least 55%, such as at least 60%, for example at least 65%, such as at least 70%, for example at least 75%, such as at least 80% after two days at 23° C. in a fermented sterile fruit juice with a pH of less than 4, preferably in the range of 3 to 4, for example in the range of 3.1 to 3.8, such as in the range of 3.2 to 3.6, for example around 3.4 and comprising at least 12 vol % ethanol, preferably around 12 vol % ethanol.
In one embodiment of the invention the microbial organism has a survival rate which is at least 1%, for example at least 5%, such as at least 10%©, for example at least 15%, such as at least 20%, for example at least 25%, such as at least 30%, for example at least 35%, such as at least 40%, for example at least 45%, such as at least 50%, for example at least 55%, such as at least 60%, for example at least 65%, such as at least 70%, for example at least 75%, such as at least 80% after two days at 23° C., when added directly to a wine prepared by yeasting a sterile grape fruit juice without added sulphite, said wine having an ethanol content of 12.0 vol %, pH 3.4, below 5 g/L residual sugar, 3.3 g/L of malic acid, and 450 mg/L of citric acid.
In another embodiment of the present invention the survival rate is preferably at least 70%, more preferably at least 75%, for example at least 80%, such as at least 85%, for example at least 90% after two days at 17° C. in a fermented sterile fruit juice with a pH of less than 4, preferably in the range of 3 to 4, for example in the range of 3.1 to 3.8, such as in the range of 3.2 to 3.6, for example around 3.4, wherein the fermented sterile fruit juice comprises at least 13.9 vol % ethanol, preferably around 13.9 vol % ethanol.
In another embodiment of the invention the microbial organism has a survival rate which is in the range of 70% to 100%, more preferably at least 75%, for example at least 80%, such as at least 85%, for example at least 90% after two days at 18° C., when added directly into a wine prepared with 30 ppm SO2 added before the alcoholic fermentation, said wine having an ethanol content of 13.8 vol %, pH 3.5, 1.3 g/L malic acid, and 340 mg/L of citric acid.
In yet another embodiment of the present invention the microbial organism has a survival rate which is at least 80%, such as at least 85%, for example at least 90% after two days at 17° C., when added directly to a wine prepared without SO2 added, said wine having an ethanol content of 13.9 vol %, pH 3.6, 1.7 g/L malic acid, and 320 mg/L of citric acid.
The microbial organism according to the present invention is preferably resistant to one or more different bacteriophages, more preferably the organism is in general resistant to bacteriophages.
Furthermore it is preferred that the microbial organism retains its characteristics during propagation and concentration, i.e. it is preferred that the microbial organism retains its capability of survival, of degrading malic acid and/or citric acid as described herein above during propagation and concentration. Preferably, the microbial organism retains it characteristics after 10, such as after 20, for example after 30, such as after 40, such as after 50, for example after 60, such as after 70, for example after 80, such as after 90, for example after 100 population doublings. It is preferred that the microbial organism retains it characteristics after concentration as described herein below.
In one preferred embodiment of the present invention the microbial organism is a bacterial strain, more preferably the microbial organism is a bacterial strain belonging to the Oenococcus family, even more preferably, the microbial organism is an Oenococcus oeni strain. For example the microbial organism may be selected from the group consisting of strains deposited under the accession numbers DMS 15569, DMS 15570, and DSM 15571.
In one aspect the present invention relates to a concentrate of microbial organisms comprising or consisting of any of the above mentioned microbial organisms, wherein said concentrate has a content of colony forming units being in the range of 109 to 1012 per g.
The concentrate may be prepared by any conventional method, for example the concentrate may be prepared by centrifugation, such as by centrifugation of a liquid composition comprising the microbial organisms according to any protocol known to the person skilled in the art. For example the liquid composition may be centrifuged at in the range of centrifugation 2000 to 10,000 g, such as in the range of 3000 to 9000 m for example in the range of 4000 to 8000, such as in the range of 5000 to 7000, for example around 6000 g for in the range of 1 to 120 minutes, for example for in the range of 5 to 60 minutes, such as for around 20 minutes. It is also comprised within the present invention that the concentrate may be prepared using more advanced centrifugation methods, for example methods involving use of different centrifugational forces or by using centrifuges allowing the liquid composition to be added continuously and the eluate to be harvested continuously, Said liquid composition is in general a cultivation medium.
Prior to preparation of the concentrate the microbial organisms may have been cultivated in any conventional medium known to the person skilled in the art.
However, in one preferred embodiment of the invention, the microbial organism has been cultivated in any of the adaptation media described herein below, said adaptation medium comprising at least 6% sugar. Preferably, said adaptation medium comprises at least 5% glucose and/or 5% fructose or at least 3% glucose and at least 3% fructose. Preferably microbial organism has been incubated in said adaptation medium for at least 12 hours, such as at least 24 hours, for example around 48 hours prior to harvest by for example centrifugation.
The harvested microbial organisms may in one embodiment of the invention be mixed with any suitable cryoprotectants, for example glycerol, gelatine, Na-caseinate or sucrose and stored frozen at a temperature in the range of −90° C. to 0° C., for example at around −80° C. or around −20° C. Hence, the concentrate may in one embodiment comprise frozen microbial organisms.
It is also comprised within the present invention that the harvested microbial organisms may be dried by for example air drying, spray drying, freeze drying, drum drying or dried using a tray drier, ring-dryer, fluid-bed dryer or vacuum-band dryer. Drying may be done using any suitable protocol known to the person skilled in the art. Hence, the concentrate may in one embodiment comprise dried microbial organisms, such as freeze-dried microbial organisms.
In one embodiment the harvested microbial organisms are freeze dried. Freeze drying may be done according to any suitable protocol known to the person skilled in the art, for example according to any of the protocols described in “Fundamentals of Freeze Drying”, J. D. Mellor, 1978, Academic Press.
In one aspect the present invention relates to methods of preferentially degrading malic acid over citric acid in a liquid composition comprising malic acid and citric acid, said method comprising the steps of
The liquid composition may in one preferred embodiment of the invention be fruit juice or fermented fruit juice, preferably grape juice or fermented grape juice, such as wine, for example red wine, white wine, rosé or sparkling wine.
Furthermore, the liquid composition preferably comprises in the range of 5 to 15 vol % ethanol, such as 10 to 14 vol % ethanol, for example 11 to 14 vol %, such as 12 to 14 vol %, for example at least 12 vol % ethanol.
It is also preferred that the liquid composition comprises in the range of 0.1 to 30 g/L sugar, more preferably in the range of 0.5 to 25 g/L, even more preferably in the range of 1 to 20 g/L, such as in the range of 1 to 15 g/L, for example in the range of 1 to 10, such as in the range of 2 to 9, such as in the range of 3 to 8, such as in the range of 4 to 6, for example around 5 g/L sugar. More preferably, the liquid composition comprises less than 10 g/L, such as less than 7 g/L, for example less than 5 g/L sugar.
It is furthermore preferred that the liquid composition comprises in the range of 1 to 50 g/L, preferably 1 to 25 g/L, even more preferably in the range of 1 to 10 g/L, for example in the range of 2 to 8 g/L, such as in the range of 2 to 5 g/L, for example in the ramie of 3 to 4 g/L, such as around 3.3 g/L malic acid.
It is also preferred that the liquid composition comprises in the range of 1 to 5000 mg/L, more preferably in the range of 10 to 2500 mg/L, even more preferably in the range of 100 to 1000 mg/L, for example in the range of 200 to 800 mg/L, such as in the range of 300 to 600 mg/L, for example in the range of 400 to 500 mg/L, such as around 450 mg/L of citric acid. Preferably, the liquid composition comprises in the range of 50 to 2000 mg/L, such as 100 to 1000 mg/L, for example 200 to 800 mg/L, such as 400 to 500 mg/L citric acid.
It is preferred that the final liquid composition comprises at least 50%, preferably at least 60%, more preferably at least 70%, for example at least 75%, such as at least 80% of the initial citric acid.
It is furthermore preferred that the finial liquid composition comprises less than 20%, preferably less than 15%, such as less than 10%, for example less than 5% of the initial malic acid.
The microbial organism is preferably added at a concentration of CFUs in the range of 1×103 to 5×1012 per ml, preferably in the range of 1×104 to 5×1016 per ml, more preferably in the range of 1×105 to 5×108 per ml, for example in the range of 1×106 to 5×107 per ml. More preferably, the microbial organism is added at a concentration less than 5×107 CFU per ml of the liquid composition, such as at a concentration of in the range of 1×106 to 5×107 CFUs per ml of the liquid composition.
The conditions comprises incubation at a temperature in the range of 5 to 40° C., for example 15 to 30° C., such as in the range of 17 to 23° C.
In a preferred embodiment, the method comprises incubation of said liquid composition for at least the time required to obtain the desired fermentation of malic acid, however it is preferred that the incubation is longer, for example at least 5 days, such as at least 10 days, for example at least 15 days, such as at least 20 days, for example at least 30 days, such as at least 40 days more than the time required to obtain the desired malic acid concentration.
In a very preferred embodiment, the method comprises incubation of said liquid composition for a longer period of time than required for completion of malolactic fermentation, for example for at least 5 days, such as at least 10 days, for example at least 15 days, such as at least 20 days, for example at least 30 days, such as at least 40 days more than required for completion of malolactic fermentation.
The present invention also relates to methods of inducing malolactic fermentation, comprising the steps of
The liquid composition is in one preferred embodiment a fruit juice, such as a fermented fruit juice. For example, the liquid composition may be a grape fruit juice, a fermented grape fruit juice or a wine. The wine may for example be selected from the group consisting of red wines, white wines and sparkling wines.
Preferably, the microbial organism is in a frozen or freeze-dried state. The methods thus preferably comprises that the microbial organism in a frozen or freeze-dried state is added directly to the liquid composition, for example to the grape juice or a fermented grape juice.
The microbial organism is preferably added to the liquid composition at a concentration of CFUs in the range of 1×103 to 5×1012 per ml, preferably in the range of 1×104 to 5×1010 per ml, more preferably in the range of 1×106 to 5×108 per ml, for example in the range of 1×106 to 5×107 per mi. More preferably, the microbial organism is added at a concentration less than 5×107 CFU per ml of the liquid composition, such as at a concentration of in the range of 1×106 to 5×107 CFUs per ml of the liquid composition.
The liquid composition, for example the grape juice or a fermented grape juice preferably has a pH in the range of 2 to 5, such as 3 to 4, for example around 3.4.
Furthermore, the liquid composition such as the grape juice or a fermented grape juice preferably comprises in the range of 5 to 15 vol % ethanol, such as 10 to 14 vol % ethanol, for example 11 to 14 vol %, such as 12 to 14 vol %, for example at least 12 vol % ethanol.
It is also preferred that the liquid composition, such as the grape juice or a fermented grape juice comprises in the range of 0.1 to 30 g/L sugar, more preferably in the range of 0.5 to 25 g/L, even more preferably in the range of 1 to 20 g/L, such as in the range of 1 to 15 g/L, for example in the range of 1 to 10, such as in the range of 2 to 9, such as in the range of 3 to 8, such as in the range of 4 to 6, for example around 5 g/L sugar. More preferably, the liquid composition comprises less than 10 g/L, such as less than 7 g/L, for example less than 5 g/L sugar.
It is furthermore preferred that the liquid composition such as the grape juice or a fermented grape juice comprises in the range of 1 to 50 g/L, preferably 1 to 25 g/L, even more preferably in the range of 1 to 10 g/L, for example in the range of 2 to 8 g/L, such as in the range of 2 to 5 g/L, for example in the range of 3 to 4 g/L, such as around 3.3 g/L malic acid.
It is also preferred that the liquid composition such as the grape juice or fermented grape juice comprises in the range of 1 to 5000 mg/L, more preferably in the range of 10 to 2500 mg/L, even more preferably in the range of 100 to 1000 mg/L, for example in the range of 200 to 800 mg/L, such as in the range of 300 to 600 mg/L, for example in the range of 400 to 500 mg/L, such as around 450 mg/L of citric acid. Preferably, the liquid composition comprises in the range of 50 to 2000 mg/L, such as 100 to 1000 mg/L, for example 200 to 800 mg/L, such as 400 to 500 mg/L citric acid.
In one embodiment of the invention the Malolactic fermentation may for example be induced according to the protocols described in example 3 or 4.
The present invention also describes methods of producing the microbial organism described herein above. The methods comprise the steps of
The starting microbial organism is preferably capable of fermenting malic acid, more preferably, the starting microbial organism is capable of fermenting malic acid to lactic acid.
The starting microbial organism is preferably resistant to low pH, i.e. to pH below 5, preferably said organism is resistant to pH around 4.5 or lower, more preferably around 4.0 or lower, for example around 3.6 or lower, such as 3.4 or lower, for example said microbial organism is resistant to pH 3.2.
The starting microbial organism is furthermore preferably resistant to high ethanol concentration, i.e. to an ethanol concentration of at least 8 vol %, preferably said organism is resistant to an ethanol concentration of around 9 vol % or higher, more preferably around 10 vol % or higher, for example around ii vol % or higher, such as 12.5 vol % or higher, for example said microbial organism is resistant to an ethanol concentration of around 13%.
In one preferred embodiment of the present invention the starting microbial organism is a bacterial strain, more preferably the starting microbial organism is a bacterial strain belonging to the Oenococcus family, even more preferably, the starting microbial organism is an Oenococcus oeni strain.
The starting microbial organism may be obtained from any suitable source, it may for example be purchased commercially or isolated from any suitable source known to the skilled person. In one embodiment the starting microbial organism is isolated from a fermented fruit juice, for example from a wine, preferably from a wine with completed spontaneous malolactic fermentation.
Mutagenesis may be done by any conventional method known to the person skilled in the art. In one embodiment mutagenisis comprises incubating the microbial organism in the presence of a mutagenising agent. Said mutagenising agent may for example be selected from the group consisting of ethylmethanesulfunate, N-ethyl-N′-nitro-N-nitrosoguanidine and 1-(2-hydroxyethyl)-1-nitrosourea.
Incubation with the mutagenising agent may be done for any suitable time, for example for in the range of 5 min. to 24 hours, such as in the range of 10 minutes to 12 hours, for example in the range of 15 minutes to 6 hours, such as in the range of 30 minutes to 4 hours, for example in the range of 1 hour to 3 hours, such as in the range of 1.5 hours to 2.5 hours, for example around 2 hours
After mutagenisis, mutated microbial organisms with the desired characteristic may be selected, for example mutated microbial organisms with any of the characteristics outlined herein above may be selected.
In one embodiment of the invention microbial organisms with reduced citric acid degradation activity are selected. The selection may for example be performed based on the methods described by G. M. Kempler and L. L. McKay (Appl. Environ. Microbiol.; 1980, 39, 926-927) as described in example 1 herein below.
One non-limiting example of how to prepare a microbial organism according to the present invention is described in example 1.
Surprisingly, the present invention discloses that freeze dried microbial organisms have an increased survival rate after direct inoculation into wine, if the microbial organisms have been cultivated in the adaptation medium described herein below.
Hence, the present invention also relates to methods of preparing a dried microbial organism capable of fermenting malic acid to lactic acid, which has reduced citric acid degrading activity and which is capable of survival after direct inoculation into fermented fruit juice, said method comprising the steps of
Preferably microbial organism is incubated in said adaptation medium for at least 12 hours, such as at least 24 hours, for example around 48 hours prior to harvest. The incubation is preferably at a temperature in the range of 15 to 40° C., such as in the range of 20° C. to 37° C., for example in the range of 25° C. to 35° C., preferably around 30° C. Furthermore, during incubation the pH is preferably kept constant in the range of pH 3.5 to 6.0, such as in the range of pH 4 to 5, preferable around pH 4.5.
The microbial organism may be harvested by any conventional technique known to the person skilled in the art. In general, harvesting said microbial organism comprises centrifugation.
Drying said microbial organism may be done by a number of different methods including, but not limited to air drying, spray drying, freeze drying, drum drying or drying using a tray drier, ring-dryer, fluid-bed dryer or vacuum-band dryer.
Preferably however, the microbial organism is freeze-dried. Freeze-drying may be done according to any protocol known to the skilled person as for example as described in Fundamentals of Freeze Drying, J. D. Mellor, 1978, Academic Press. In general the microbial organism is mixed with a suitable cryoprotective, for example gelatine and/or sucrose and freeze dried using any suitable freeze drier.
The adaptation medium according to the present invention comprises at least 6%, preferably at least 7%, more preferably at least 8%, such as at least 9%, for example at least 10%, such as at least 11% sugar by weight. The sugar may be any suitable sugar for example the sugar may be selected from the group consisting of glucose, fructose, sucrose and maltose. Preferably the sugar is glucose and/or fructose.
In one preferred embodiment the adaptation medium comprises at least 3%, preferably at least 4%, more preferably at least 5%, such as at least 6%, for example at least 7%, such as at least 8%, for example at least 9%, such as at least 10%, for example in the range of 3 to 10%, such as in the range of 4 to 8%, for example in the range of 5 to 6% glucose.
It is also comprised within the present invention that the adaptation medium comprises at least 3%, preferably at least 4%, more preferably at least 5%, such as at least 6%, for example at least 7%, such as at least 8%, for example at least 9%, such as at least 10%, for example in the range of 3 to 10%, such as in the range of 4 to 8%, for example in the range of 5 to 6% fructose.
In a preferred embodiment the adaptation medium comprises at least 3%, preferably at least 4%, more preferably at least 5%, such as at least 6%, for example at least 7% glucose and at least 3%, preferably at least 4%, more preferably at least 5%, such as at least 6%, for example at least 7% fructose.
The adaptation medium furthermore preferably comprises one or more selected from the group consisting of nitrogen sources, salts, detergents and buffers.
The nitrogen source may be any suitable nitrogen source known to the skilled person. Preferably the nitrogen source comprises amino acids, for example free amino acids or amino acids comprised within a polypeptide or a peptide, It is preferred that the nitrogen source comprises free amino acids and/or short peptides. Short peptides may be prepared by hydrolysing a protein source. In one embodiment of the invention the nitrogen source is selected from the group consisting of yeast extracts, Casein hydrolysate (hydrolysed milk protein) and Bacto peptone (hydrolysed meat).
The salt may for example be MnSO4 or MgSO4, NaCl, MgCl2 or any other suitable salt.
The pH of the adaptation medium is preferably in the range of 2 to 8, more preferably in the range of 3 to 7, even more preferably in the range of 3.5 to 6, even more preferably in the range of 4 to 5, for example around 4.5. The buffer is therefore preferably a buffer capable of buffering the medium to said pH.
The detergent may be any suitable detergent, preferably a detergent containing derivates of unsaturated fatty acids, for example, Tween 80.
In one embodiment of the invention, the adaptation medium is the adaptation medium described in example 2 herein below.
In one aspect the present invention relates to an activation composition and an activation solution, wherein said activation solution may be prepared from the activation composition by addition of water. The activation solution is useful for fast and safe activation of microbial organisms prior to inoculation of said microbial organisms into a liquid solution. In particular, freeze dried bacteria can frequently not survive to be inoculated directly into a liquid composition with harsh conditions, such as low pH and/or high ethanol content. Thus prior to inoculation, the microbial organisms must be adapted to survival and growth in said liquid composition. The conventional adaptation procedures are complex and time and labour consuming. They involve one or several steps of propagation and growth in a suitable medium for several days. However, the conventional media are also suitable for the growth of many other microbial organisms. There is therefore a high risk for contamination with spoilage bacteria and yeast as the propagation and adaptation steps under the practical conditions in the wineries can not be conducted under sterile conditions. The risk is especially high because the growth of useful microbial organisms, such as microbial organisms capable of fermenting malic acid to lactic acid, for example Oenococcus oeni is much slower compared to the growth of other microbial organisms. The number of bacteria in the activation solution according to the present invention, is very high from the beginning and there is only limited growth or preferably almost no growth of increase in the bacteria population during the activation time. The initial high bacteria number results in a fast drop in the pH and a fast production of large amount of lactic acid from the very high sugar content in the activation solution. Low pH and lactic acid at high concentrations are toxic to most other microbial organisms and thereby greatly reduce the risk for growth of contaminants in the activation solution according to the present invention. The short time of activation also contributes to strongly reduce the risk of contamination. The present inventor has interestingly discovered that a large drop in pH and a large increase in the lactic acid concentration are factors, which aids adaptation of bacteria to survive direct inoculation into a liquid composition with harsh conditions, for example wine and to initiate the growth in the liquid immediately. In the activation solution according to the present invention, where all the bacteria are present from the beginning, the bacteria adapt to the wine conditions much faster and more effectively than with the conventional adaptation procedures because of the fast drop in pH and fast production of high concentration of lactic acid from the initial high sugar concentration.
Hence, the invention in one aspect relates to an activation solution comprising
In particular, said activation solution may be useful as an activator of starter cultures, for example malolactic starter cultures. The term starter culture is meant to encompass a composition comprising a microbial organism capable of fermenting a fermentable compound. The activation solution according to the present invention, comprises a very high concentration of sugar, which previously has been thought to inhibit growth of microbial organisms.
The invention also relates to a dry activation composition, wherein in the range of 80 to 200 g of said dry activation composition comprises
The fermentable compound may be any compound desirable to ferment. In one preferred embodiment of the present invention, the fermentable compound is malic acid. It is thus preferred that the microbial organism is capable of fermenting malic acid, in particular it is preferred that the microbial organism is capable of fermenting malic acid to lactic acid.
The microbial organism is capable of fermenting malic acid to lactic acid, when said microbial organism when placed in a liquid composition comprising a predetermined amount of malic acid it is capable of fermenting at least 30%, preferably at least 50%, more preferably at least 70%, such as at least 80%, at least at least 90%, for example at least at least 95% of said malic acid to lactic acid.
Said degradation of malic acid preferably is completed within at the most 1 month, preferably within at the most 3 weeks, more preferably within at the most 2 weeks, such as 13, for example 12, such as 11, for example 10, such as 9 clays. In one embodiment of the present invention the microbial organism has reduced citric acid degradation activity. For example, said microbial organism, when placed in a medium containing a predetermined amount of citric acid is only capable of degrading at the most 80% of said citric acid. Even more preferably, the microbial organism is only capable of degrading at the most 70%, such as 60%, for example 50%, such as 40%, for example 30%, such as 25%, for example 20%, such as 15%, for example 12%, such as 10% of said citric acid. Hence, it is preferred that the microbial organism is only capable of degrading in the range of 0 to 50%, more preferably 0 to 40%, even more preferably 0 to 30%, yet more preferably 0 to 20% of said citric acid. It is furthermore preferred that the microbial organism is only capable of degrading at the most 50%, more preferably at the most 40%, even more preferably at the most 30%, yet more preferably at the most 20%, even more preferably at the most 10% of said citric acid within for example 3 weeks, more preferably within 2 weeks, such as within 13, for example 12, such as 11, for example 10 days.
The liquid composition comprising said predetermined amount of malic acid and/or citric acid furthermore preferably comprises one or more of the following parameters preferably a pH in the range of 2 to 7, preferably in the range of 3 to 6, more preferably in the range of 3 to 5, even more preferably in the range of 3 to 4, for example in the range of 3.1 to 3.8, such as in the range of 3.2 to 3.6, for example around 3.4; and/or
It is preferred that said microorganism is incubated with said liquid composition at a temperature of in the range of 15 to 30° C., such as in the range of 20 to 25° C., for example around 23° C.
Preferably, the microbial organism is capable of degrading malic acid and/or citric acid as indicated herein above when said organism is present in a concentration in the range of 1×103 to 5×1012 per ml, preferably in the range of 1×104 to 5×1010 per ml, more preferably in the range of 1×106 to 5×106 per ml, for example in the range of 1×106 to 5×107 per ml.
In one preferred embodiment of the present invention the microbial organism is capable of reducing malic acid within 9 days to less than 1 g/L, such as less than 0.5 g/L, for example less than 0.1 g/L, when incubated at a temperature of approximately 23° C., when said microbial organism is added directly in a frozen or freeze dried state to a fermented fruit juice at a concentration of CFUs in the range of 1×106 to 5×107 per ml, wherein said fermented fruit juice is prepared by yeasting a sterile fruit juice without added sulphite resulting in a fermented fruit juice having an ethanol content of 12.0 vol %, pH 3.4, below 5 g/L residual sugar, 3.3 g/L of malic acid, and 450 mg/L of citric acid.
In another embodiment, it is preferred that the microbial organism reduces the citric acid content by less than 50%, such as less than 20%, for example less than 10% within 10 days, when incubated at a temperature of approximately 23° C., when said microbial organism is added directly in a frozen or freeze dried state to a fermented fruit juice at a concentration of CFUs in the range of 1×106 to 5×107 per ml, wherein said fermented fruit juice is prepared by yeasting a sterile fruit juice without added sulphite resulting in a fermented fruit juice having an ethanol content of 12.0 vol %, pH 3.4, below 5 g/L residual sugar, 3.3 g/L of malic acid, and 450 mg/L of citric acid.
In one preferred embodiment of the present invention, the freeze-dried or frozen microbial organism have a low surviving rate or is not capable of surviving at all when directly inoculated into a fermented fruit juice, i.e. the microbial organism does not have one or more of the characteristics mentioned herein below. In a preferred embodiment the microbial organism does not have any of the characteristics mentioned herein below. It is however comprised within the invention that the freeze-dried or frozen microbial organism may have a high survival rate when directly inoculation into a fermented fruit juice. Such microbial organisms may however in general survive better and start growth faster when inoculated into fermented fruit juice if they have been pre-incubated in the activation solution according to the invention.
Hence, the microbial organism may or may not have one or more of the following characteristics, when said microbial organism in a frozen or freeze dried state is added directly into a fermented fruit juice:
For example, the survival rate may be at least 15%, such as at least 20%, for example at least 25%, such as at least 30%, for example at least 35%, such as at least 40%, for example at least 45%, such as at least 50%, for example at least 55%, such as at least 60%, for example at least 65%, such as at least 70%, for example at least 75%, such as at least 80% after two days at 23° C. in a fermented sterile fruit juice with a pH of less than 4, preferably in the range of 3 to 4, for example in the range of 3.1 to 3.8, such as in the range of 3.2 to 3.6, for example around 3.4 and comprising at least 12 vol % ethanol, preferably around 12 vol % ethanol.
Preferably, the microbial organism after activation for more than 4 hours, preferably for more than 5 hours, for example for in the range of 5 hours to 2 weeks, such as in the range of 6 hours to 1 week, for example for in the range of 6 hours to 5 days, such as in the range of 7 hours to 3 days, for example for in the range of 7 hours to 2 days, such as in the range of 8 hours to 48 hours, for example for in the range of 8 hours to 46 hours, such as around 4 hours, for example around 8 hours, such as around 19 hours, for example around 46 hours in the activation solution has a survival rate which is at least 3%, preferably at least 5%, more preferably at least 10%, even more preferably at least 20%, yet more preferably at least 30%, even more preferably at least 33%, yet even more preferably at least 40%, such as at least 50%, for example at least 60%, such as at least 70%, for example at least 80%, such as at least 90%, preferably at least 94%, for example at least 95%, such as around 100% after two days at 23° C. when inoculated into a fermented fruit juice having an ethanol content of at least 12.0 vol %.
More preferably, the microbial organism after activation for more than 4 hours, preferably for more than 5 hours, for example for in the range of 5 hours to 2 weeks, such as in the range of 6 hours to 1 week, for example for in the range of 6 hours to 5 days, such as in the range of 7 hours to 3 days, for example for in the range of 7 hours to 2 days, such as in the range of 8 hours to 48 hours, for example for in the range of 8 hours to 46 hours, such as around 4 hours, for example around 8 hours, such as around 19 hours, for example around 46 hours in the activation solution has a survival rate which is at least 3%, preferably at least 5%, more preferably at least 10%, even more preferably at least 20%, yet more preferably at least 30%, even more preferably at feast 33%, yet even more preferably at least 40%, such as at least 50%, for example at least 60%, such as at least 70%, for example at least 80%, such as at least 90%, preferably at least 94%, for example at least 95%, such as around 100% after two days at 23° C. when inoculated into a fermented fruit juice prepared by yeasting a sterile grape fruit juice without added sulphite, said fermented fruit juice having an ethanol content of 12.0 vol %, pH 3.4, below 5 g/L residual sugar, 3.3 g/L of malic acid, and 450 mg/L of citric acid
The microbial organism according to the present invention is preferably resistant to one or more different bacteriophages, more preferably the organism is in general resistant to bacteriophages.
Furthermore it is preferred that the microbial organism retains its characteristics during propagation and concentration, i.e. it is preferred that the microbial organism retains its capability of survival, of degrading malic acid and/or citric acid as described herein above during propagation and concentration. Preferably, the microbial organism retains it characteristics after 10, such as after 20, for example after 30, such as after 40, such as after 50, for example after 60, such as after 70, for example after 80, such as after 90, for example after 100 population doublings. It is preferred that the microbial organism retains it characteristics after concentration as described herein below.
In one preferred embodiment of the present invention the microbial organism is a bacterial strain, preferably the microbial organism is selected from the group consisting of bacteria belonging to the Oenococcus family and the Lactobacillus family. More preferably, the microbial organism is selected from the group consisting Oenococcus oeni, Lactobacillus hilgardii, Lactobacillus brevis Lactobacillus casei and Lactobacillus plantarum. Even more preferably the microbial organism is selected from the group consisting Oenococcus oen, and Lactobacillus plantarum.
For example, the microbial organism may be selected from the group consisting of the bacterial strains MBR Alpha, MBR Beta, MBR 31, MBR 41 and MBR OSU available from Lallemand Inc., Montreal, Canada. Said strains may survive direct inoculation into wine. The microbial organism may also be selected from the group consisting of Inobacter (IB), OSU, ProVino, MCW, 3X, and MT01 available from Lallemand Inc., Montréal, Canada. Said strains require adaptation prior to inoculation into wine. In one preferred embodiment of the invention the microbial organism is MT01 available from Lallemand Inc., Montreal, Canada, which has reduced citric acid degradation activity. The microbial organism may also be selected from the group consisting of Viniflora oenos and Viniflora CH35 available from Chr. Hansen A/S, Hoersholm, Denmark. These strains may be inoculated directly into wine.
In one embodiment the microbial organism may be any of the microbial organisms described in international patent application WO 93/20180, which is hereby incorporated herein in its entirety.
In one preferred embodiment of the invention, the microbial organism is a bacteria belonging to the Oenococcus family, more preferably the microbial organism is an Oenococcus oeni. For example, the microbial organism may selected from the group consisting of microbial organisms deposited under the accession numbers DSM 15568, DSM 7008, DMS 15569, DMS 15570, and DSM 15571.
In one embodiment of the present invention the microbial organism is any of the microbial organisms described herein above in the section “Microbial organisms capable of fermenting malic acid”.
The sugar in the dry activation composition and in the activation solution according to the present invention may be any suitable sugar. For example the sugar may be selected from the group consisting of glucose, fructose, sucrose and maltose. Preferably the sugar is glucose and/or fructose.
The activation solution according to the present invention comprises in the range of 60 to 140 g sugar per L, preferably in the range of 70 to 130 g sugar per L, more preferably in the range of 80 to 120 g sugar per L, for example in the range of 90 to 110 g sugar per L, such as around 100 g sugar per L.
Accordingly, the activation composition preferably comprises in the range of 60 to 140 g sugar, preferably in the range of 70 to 130 g sugar, more preferably in the range of 80 to 120 g sugar, for example in the range of 90 to 110 g sugar, such as around 100 g sugar per 80 to 200 g of said dry activation composition. For example, in the range of 110 to 150 g of said dry activation composition comprises in the range of 80 to 110 g, such as 90 to 110 g, for example 95 to 105 g sugar
The activation solution may for example comprise in the range of 30 g to 100 g, such as in the range of 30 to 90 g, for example in the range of 30 to 80 g, such as in the range of 35 to 70 g, such as 40 to 80 g, for example in the range of 40 to 60 g, such as in the range of 45 to 55 g, for example around 50 g glucose per L.
Thus the dry activation composition may comprise in the range of 30 g to 100 g, such as in the range of 30 to 90 g, for example in the range of 30 to 80 g, such as in the range of 35 to 70 g, such as 40 to 80 g, for example in the range of 40 to 60 g, such as in the range of 45 to 55 g, for example around 50 g glucose per 80 to 200 g of said dry activation composition.
The activation solution may for example comprise in the range of 30 g to 100 g, such as in the range of 30 to 90 g, for example in the range of 30 to 80 g, such as 40 to 80 g, such as in the range of 35 to 70 g, for example in the range of 40 to 60 g, such as in the range of 45 to 55 g, for example around 50 g fructose per L.
Thus the dry activation composition may comprise in the range of 30 g to 100 g, such as in the range of 30 to 90 g, for example in the range of 30 to 80 g, such as 40 to 80 g, such as in the range of 35 to 70 g, for example in the range of 40 to 60 g, such as in the range of 45 to 55 g, for example around 50 g fructose per 80 to 200 g of said dry activation composition.
Preferably, the activation solution or the activation composition comprises both glucose and fructose, for in the range of 30 to 80 g, such as 40 to 80 g, such as in the range of 35 to 70 g, for example in the range of 40 to 60 g, such as in the range of 45 to 55 g, for example around 50 g glucose and in the range of 30 to 80 g, such as 40 to 80 g, such as in the range of 35 to 70 g, for example in the range of 40 to 60 g, such as in the range of 45 to 55 g, for example around 50 g fructose per L or per 80 to 200 g of said dry activation composition.
The activation solution and/or the activation composition furthermore preferably comprises one or more selected from the group consisting of nitrogen sources, salts and chemical compound with buffering capacity (buffer). Preferably the activation solution and/or the activation composition comprises all.
The nitrogen source may be any suitable nitrogen source known to the skilled person. Preferably the nitrogen source comprises amino acids, for example free amino acids and/or amino acids comprised within a polypeptide or a peptide, It is preferred that the nitrogen source comprises free amino acids and/or short peptides. Short peptides are usually prepared by hydrolysing a protein source. In one embodiment of the invention the nitrogen source is selected from the group consisting of yeast extracts, Casein hydrolysate (hydrolysed milk protein), Bacto peptone (hydrolysed meat) and other hydrolysed proteins.
The salt may for example be MnSO4 or MgSO4, NaCl, MgCl2 or any other suitable salt.
The pH of the adaptation medium is preferably in the range of 2 to 8, more preferably in the range of 3 to 7, even more preferably in the range of 4 to 6, for example around 4.9. The chemical compound with buffering capacity is therefore preferably a buffer capable of buffering the medium to said pH. For example the chemical compound may be selected from the group consisting of tartaric acid, malic acid, lactic acid, phosphate and citrate.
In one embodiment of the present invention the dry activation composition is the dry activation composition described in example 5, wherein the freeze dried bacteria (DSM 15568) used in example 5 optionally may be substituted with any of the microbial organisms mentioned above in this section.
The present invention also relates to methods of inducing fermentation in a liquid composition comprising a fermentable compound comprising the steps of
The liquid composition may be any suitable liquid composition in which it is desirable to induce a fermentation process, for example the liquid composition may be a fruit juice or a fermented fruit juice, such as a grape fruit juice or fermented grape fruit juice. A fermented grape fruit juice may for example be a wine, such as a red wine, white wine, sparkling wine or rose wine.
The activation time may be selected according to the specific embodiment. In general a longer activation time results in better survival after inoculation up to an activation time of approximately 2 days. Preferably, the activation time is thus more than 4 hours, preferably for more than 5 hours, for example for in the range of 5 hours to 2 weeks, such as in the range of 6 hours to 1 week, for example for in the range of 6 hours to 5 days, such as in the range of 7 hours to 3 days, for example for in the range of 7 hours to 2 days, such as in the range of 8 hours to 48 hours, for example for in the range of 8 hours to 46 hours, such as around 4 hours, for example around 8 hours, such as around 19 hours, for example around 46 hours.
Preferably, the activation time is selected so that the microbial organism has a survival rate which is at least 3%, preferably at least 5%, more preferably at least 10%, even more preferably at least 20%, yet more preferably at least 30%, even more preferably at least 33%, yet even more preferably at least 40%, such as at least 50%, for example at least 60%, such as at least 70%, for example at least 80%, such as at least 90%, preferably at least 94%, for example at least 95%, such as around 100% after two days at 23° C. when inoculated into a fermented fruit juice having an ethanol content of at least 12.0 vol %.
The activation conditions preferably comprises incubation at a temperature in the range of 10° C. to 40° C., for example 15° C. to 35° C., such as 15° C. to 30° C., for example 18° C. to 25° C., such as 20° C. to 25° C., for example around 23° C.
The fermentable compound may be any compound desirable to ferment. In one preferred embodiment of the present invention, the fermentable compound is malic acid.
Preferably around 1 L of water is added to in the range of 80 to 200 g of the dry activation composition comprising in the range of 60 to 140 g sugar. Water may for example be tap water, distilled water or sterile water.
The present invention refers to microbial organisms deposited under the accession numbers DSM 15568, DSM 15569, DSM 15570, and DSM 15571 at DSMZ Deutsche Sammlung von Mlkroorganismen and Zellkulturen GmbH, Mascheroder Weg 1b, 38124 Braunschweig, GERMANY. Details regarding the deposited microbial organisms are given in the table below.
Oenococcus oeni
Oenococcus oeni
Oenococcus oeni
Oenococcus oeni
The deposits were made under the provisions of the Budapest Treaty on the International recognition of the Deposit of Microorganisms for the Purpose of Patent Procedure and Regulations thereunder.
Strains of Oenococcus oeni with resistance to pH below 3.2 and more than 13 vol % ethanol were isolated from different wines with completed spontaneously malolactic fermentation using techniques known in the art.
The objective of the mutagenesis of the Oenococcus oeni strains was to obtain mutants where the citric acid metabolism, depicted in
2% glucose
2% fructose
2% yeast extract (Oxoid Ltd., England)
pH, adjusted to 5.0 with 20% NaOH. From the stationary phase culture, spread plates were made using the methods described by G. M. Kempler and L. L. McKay (Appl. Environ. Microbiol.; 1980, 39, 926-927) except that the agar used had the following composition:
1% glucose
1% fructose
1% yeast extract (Oxoid Ltd., England)
pH adjusted to 5.5 with 20% HCl
The plates were incubated for 10 days at 30° C. On the plates white colonies containing mutated non-citric acid fermenting bacteria could be differentiated from blue colonies containing normal citric acid fermenting bacteria.
A 5 litre sterile glass container was added 4 litre of sterile Biota grape juice (Biotta A G, Switzerland) adjusted with sucrose to a total sugar concentration of 212 g/l and inoculated with 1.5 g of active dry yeast (Saccharomyces cerevisiae, Saint George S101, Fould-Springer, France). The juice was incubated at 23° C. After 14 days the alcoholic fermentation was completed and the wine was adjusted to pH 3.4 with 20% HCl. The concentration of total glucose and fructose in the wine was below 5 g/litre, the ethanol concentration was 12.0% (v/v), and the L-malic acid and citric acid concentration was 3.3 g/litre and 0.45 g/liter respectively. The glucose, fructose, ethanol, malic acid, and citric acid concentrations were determined by the enzymatic test kits of Boehringer Mannheim, Germany.
Examination of Selected Non-Citric Acid Fermenting Oenococcus oeni Mutants.
For unknown reason the growth of the selected mutants in commercially available cultivation media for lactic acid bacteria (MRS Broth from Oxoid Ltd.) were slow compared to the non-mutated strains. Also when pre-cultivated in MRS Broth for 48 hours at 30° C. and inoculated directly from the cultivation broth into the experimental wine, the survival rate of the inoculated mutants in the wine measured 2 days after inoculation were 20-50 times lower compared to the non-mutated strains. Clearly, the mutation in the selected strains somehow effect the growth and the ability to survive direct inoculation into wine.
Examination of new cultivation and adaptation medium for the production of non-citric acid fermenting Oenococcus oeni mutants.
The selected non-citric acid fermenting Oenococcus oeni strain DSM 15571 were grown in the cultivation and adaptation medium of the following composition by weight:
5.5% glucose
5.5% fructose
3.9% yeast extract (Oxoid Ltd., England)
pH adjusted to 4.5 with 20% HCl.
The cultivation and adaptation medium was sterilized at 121° C. for ID minutes and cooled to 30° C.
The medium was inoculated with the non-citric acid fermenting Oenococcus oeni strain DSM 15571 which had been pre-cultured in a medium with the same composition for 46 hours at 30° C.
The inoculated medium was held at 30° C. and at constant pH 4.5 by addition of 20% NaOH.
At different times during the fermentation, 200 ml samples were removed. The name and time of the sampling, the OD600, the total concentration of sugar, and the calculated amount of fermented sugar in the samples are shown in Table 1. The bacteria were harvested from the sample by centrifugation. The bacteria concentrate from the centrifugation was re-suspended in sterile water containing 4% gelatine as cryoprotective and freeze dried using techniques known in the art.
The enumeration of viable bacteria in the freeze dried product and in inoculated wine was performed after appropriate dilution in water containing 0.1% peptone and 0.9% NaCl, followed by pour plate seeding in agar. The composition of the agar used was by weight:
2% glucose
2% fructose
2% yeast extract (Oxoid Ltd., England)
pH adjusted to 5.0 with 20% HCl.
The agar was autoclaved at 125° C. for 10 minutes and cooled to 45° C. before use. Viable counts were obtained as the number of colony forming units (CFU) after incubation at 30° C. for 7 days
Based on the determination of the CFU/g in the freeze dried samples, 4 L experimental wine was inoculated directly with the freeze dried samples of Oenococcus oeni DSM 15571 to an initial concentration of 5×106 CFU/ml wine. The wine was incubated at 23° C.
The results in
The malolactic fermentation induced by freeze dried preparation of the non-citric acid fermenting strain Oenococcus oeni DSM 15571, prepared as described for sample D in Example 2, was examined in 4 L experimental wine inoculated directly with the freeze dried sample to an initial concentration of 2×106 CFU/ml wine.
The results of this experiment are shown in
Freeze dried preparation of three non-citric acid fermenting mutants of Oenococcus oeni, DSM 15570, DSM 15569, and DSM 15571 were tested by direct inoculation into 250 L oak barrels containing different wines form Russian River and Sonoma, California (see description of the figures for further details) or by direct inoculation into the experimental wine described in example 2. All freeze dried preparations were prepared as previously described for sample D in Example 2. For comparison, a freeze dried commercial culture (Viniflora oenos from Chr. Hansen A/S, Denmark) of Oenococcus oeni (strain DSM 7008) with a normal citric acid metabolism was included.
The results from the experiments are shown in
A dry activation composition was produced by blending the following components:
50 g glucose
50 g fructose
10 g yeast extract (Oxoid Ltd., England)
0.45 g tartaric acid
20 g freeze dried Oenococcus oeni strain DSM 15568 (normal citric acid fermenting strain)
Tartaric acid is an organic acid with buffer capacity. The amount of tartaric acid in the above composition was chosen so that the dry composition, when water was added to a total of 1 L, resulted in a pH of 4.9 in the solution. The freeze dried Oenococcus oeni strain DSM 15568 in the composition contained 4×1011 CFU/g and was prepared as described for sample A in Example 2.
The blended dry activation composition was re-hydrated by addition of water to a total of 1 L followed by incubation of the activation composition solution at 23° C. The activation composition solution, which from start contained a total of 100 g sugar/L and 8×109 CFU/ml of Oenococcus oeni strain DSM 15568 was followed by the determination of total sugar/L, pH and CFU/ml. The results are shown in
At different time during the activation four samples, named 1, 2, 3, and 4 were removed from the solution. The name and time of the sampling, the pH, the amount of total sugar, and the calculated amount of sugar fermented in the samples are shown in Table 3.
1 ml of the samples 1, 2, 3, and 4 were inoculated directly into 2.5 L experimental wine in a 5 L container which resulted in an initial bacteria number of 3.2×106 CFU/ml. The number of viable bacteria and the malic acid concentration in the wine was followed and the results are shown in
A dry activation composition was produced as described in Example 5 except for the bacteria strain where 15 g freeze dried product of the selected non-citric acid fermenting mutant strain Oenococcus oeni DSM 15569 was used and that the amount of sugar was changed to 55 g glucose and 55 g fructose. The freeze dried strain was prepared as described for sample A in Example 2 and the product contained 3.5×1011 CFU/g.
The dry activation composition was re-hydrated by addition of water to a total of 1 L which resulted in a bacteria concentration of 5.3×109 CFU/ml. The activation solution was incubated at 23° C. After 8, 16, 24 and 38 hours incubation respectively, a sample of 1 ml of the activated bacteria solution was inoculated directly into 2.5 L experimental wine in a 5 L container resulting in an initial bacteria number of 2.1×106 CFU/ml. The samples was named 1, 2, 3, and 4 respectively. Also included in the examination was the direct inoculation of the wine with freeze dried Oenococcus oeni strain DSM 15569 to a concentration of 2.1×106 CFU/mL. The freeze dried strain was prepared as described for sample A in Example 2. The wine was kept at 20° C. and followed by the determination of CFU/ml and malic acid concentration.
A dry activation composition was produced as described in example 5 except for the bacteria strain where 15 g freeze dried product of the commercial culture Viniflora oenos from Chr. Hansen A/S, Denmark, was used. The product contain Oenococcus oeni, strain DSM 7008 and it is recommended by the producer for direct inoculation into wine at a concentration of 15 g per 2500 L wine.
The dry activation composition was re-hydrated by addition of water to a total of 1 L which resulted in a bacteria concentration of 1.2×1010 CFU/ml. The activation solution was incubated at 23° C. and after 24 hours the number of bacteria in the activation solution was determined to be 1.1×1010 CFU/mL indicating that no bacteria growth had occurred. After the 24 hours a sample of the activated bacteria solution was inoculated into 2.5 L Chardonnay wine from California with 12.5 vol % ethanol, pH 3.3 and with 20 ppm SO2 added at crush. The inoculation resulted in an initial bacteria concentration of 5×106 CFU/ml in the wine. 2.5 l of the wine was also inoculated directly with the freeze dried product according to instruction of the manufacture which also resulted in an initial bacteria concentration of 5×106 CFU/ml. The wine was kept at 24° C. and followed by the determination of CFU/ml and malic acid concentration.
For all deposited microbial organisms mentioned in the present patent application the following applies.
In respect to those designations in which a European Patent is sought a sample of the deposited microorganism will be made available until the publication of the mention of the grant of the European patent or until the date on which application has been refused or withdrawn or is deemed to be withdrawn, only by the issue of such a sample to an expert nominated by the person requesting the sample, and approved either i) by the Applicant and/or ii) by the European Patent Office, whichever applies. (Rule 28 (4) EPC).
The applicant requests that, until either a Canadian patent has been issued on the basis of an application or the application has been refused, or is abandoned and no longer subject to reinstatement, or is withdrawn, the Commissioner of Patents only authorizes the furnishing of a sample of the deposited biological material referred to in the application to an independent expert nominated by the Commissioner, the applicant must, by a written statement, inform the international Bureau accordingly before completion of technical preparations for publication of the international application.
The applicant hereby requests that, until the application has been laid open to public inspection (by the Norwegian Patent Office), or has been finally decided upon by the Norwegian Patent Office without having been laid open inspection, the furnishing of a sample shall only be effected to an expert in the art. The request to this effect shall be filed by the applicant with the Norwegian Patent Office not later than at the time when the application is made available to the public under Sections 22 and 33(3) of the Norwegian Patents Act. If such a request has been filed by the applicant, any request made by a third party for the furnishing of a sample shall indicate the expert to be used. That expert may be any person entered on the list of recognized experts drawn up by the Norwegian Patent Office or any person approved by the applicant in the individual case.
The applicant hereby gives notice that the furnishing of a sample of a microorganism shall only be effected prior to the grant of a patent, or prior to the lapsing, refusal or withdrawal of the application, to a person who is a skilled addressee without an interest in the invention (Regulation 3.25(3) of the Australian Patents Regulations).
The applicant hereby requests that, until the application has been laid open to public inspection (by the National Board of Patents and Regulations), or has been finally decided upon by the National Board of Patents and Registration without having been laid open to public inspection, the furnishing of a sample shall only be effected to an expert in the art.
The applicant hereby requests that the furnishing of a sample of a microorganism shall only be made available to an expert. The request to this effect must be filed by the applicant with the International Bureau before the completion of the technical preparations for the international publication of the application.
The applicant hereby requests that, until the application has been laid open to public inspection (by the Danish Patent Office), or has been finally decided upon by the Danish Patent office without having been laid open to public inspection, the furnishing of a sample shall only be effected to an expert in the art. The request to this effect shall be filed by the applicant with the Danish Patent Office not later that at the time when the application is made available to the public under Sections 22 and 33(3) of the Danish Patents Act. If such a request has been filed by the applicant, any request made by a third party for the furnishing of a sample shall indicate the expert to be used. That expert may be any person entered on a list of recognized experts drawn up by the Danish Patent Office or any person by the applicant in the individual case.
The applicant hereby requests that, until the application has been laid open to public inspection (by the Swedish Patent Office), or has been finally decided upon by the Swedish Patent Office without having been laid open to public inspection, the furnishing of a sample shall only be effected to an expert in the art. The request to this effect shall be filed by the applicant with the International Bureau before the expiration of 16 months from the priority date (preferably on the Form PCT/RO/134 reproduced in annex Z of Volume I of the PCT Applicant's Guide). If such a request has been filed by the applicant any request made by a third party for the furnishing of a sample shall indicate the expert to be used. That expert may be any person entered on a list of recognized experts drawn up by the Swedish Patent Office or any person approved by a applicant in the individual case.
The applicant hereby requests that until the date of a grant of a Netherlands patent or until the date on which the application is refused or withdrawn or lapsed, the microorganism shall be made available as provided in the 3 IF(1) of the Patent Rules only by the issue of a sample to an expert. The request to this effect must be furnished by the applicant with the Netherlands industrial Property Office before the date on which the application is made available to the public under Section 22C or Section 25 of the Patents Act of the Kingdom of the Netherlands, whichever of the two dates occurs earlier.
| Number | Date | Country | Kind |
|---|---|---|---|
| PA 2003 00977 | Jun 2003 | DK | national |
| Number | Date | Country | |
|---|---|---|---|
| 60483139 | Jun 2003 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10562421 | May 2006 | US |
| Child | 13017332 | US |
