CN104673703B - Bacillus and its application of saccharomyces cerevisiae production alcohol and flavor substance can be promoted simultaneously - Google Patents

Bacillus and its application of saccharomyces cerevisiae production alcohol and flavor substance can be promoted simultaneously Download PDF

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CN104673703B
CN104673703B CN201410747485.0A CN201410747485A CN104673703B CN 104673703 B CN104673703 B CN 104673703B CN 201410747485 A CN201410747485 A CN 201410747485A CN 104673703 B CN104673703 B CN 104673703B
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bacillus
saccharomyces cerevisiae
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acid
flavor substance
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徐岩
吴群
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Jiangsu King's Luck Brewery Co., Ltd.
Jiangnan University
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    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12GWINE; PREPARATION THEREOF; ALCOHOLIC BEVERAGES; PREPARATION OF ALCOHOLIC BEVERAGES NOT PROVIDED FOR IN SUBCLASSES C12C OR C12H
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Abstract

The present invention relates to bacillus and its application that can promote saccharomyces cerevisiae production alcohol and flavor substance simultaneously, belong to technical field of bioengineering.The bacillus of the present invention includes bacillus licheniformis Bacillus licheniformis CGMCC NO.3963, bacillus cereus Bacillus cereus CCTCC NO:M 2013369, bacillus lentus Bacillus lentus CCTCC NO:M 2013370;Methylotrophic bacillus methylotrophicus CCTCC NO:2013371.After these bacillus are mixed with saccharomyces cerevisiae, it is possible to increase alcohol output more than 20%, while improve saccharomyces cerevisiae metabolism aldehydes, alcohols, esters, acids and other flavor substances.These bacillus are applied in brewed wine production, distillation yield can be improved, while the flavor quality of brewed wine significantly improves.

Description

Bacillus and its application of saccharomyces cerevisiae production alcohol and flavor substance can be promoted simultaneously
Technical field
The present invention relates to bacillus and its application that can promote saccharomyces cerevisiae production alcohol and flavor substance simultaneously, belong to raw Thing field of engineering technology.
Background technology
Brewed wine industry is the advantage national tradition manufacturing industry in China, and the important component of food industry.2013 Year total output value accounts for food industry total value about 6-7% up to more than 600,000,000,000 yuan.Therefore the development of brewed wine industry is eaten for China The development of conduct industry even national economy all has great importance.
China white wine is the Typical Representative of brewed wine.But compared with international brewed wine manufacturing, exist and ask as follows Topic:First, production efficiency is relatively low, i.e., yeast of white wine is low.Ethanol maximum concentration is only 7% or so in white wine solid-state fermented grain, most High liquor ratio of raw material only 50% (Chinese yeast delicate fragrance), minimum only 35% or so (giving off a strong fragrance), far below theoretical distillation yield (65%);Its Secondary, liquor flavor metabolism is uncontrollable, and important flavor substance anabolism is weaker, causes quality percentage relatively low, at present annual production High quality liquor only account for the 5~10% of national white wine yield.For example, (the representative enterprise of the quality percentage of fen-flavor type white spirit only 6% Internal data), consumption demand of the people to quality product can not be met.Therefore, the distillation yield of white wine and high-quality is improved Product rate is the inevitable requirement of liquor industry sustainable development.
Saccharomyces cerevisiae is the important microbe of liquor production, provide not only alcohol, and provides important flavor substances Matter, therefore it is that liquor fermentation needs the important content of regulation and control to improve the alcohol metabolism of saccharomyces cerevisiae and flavor metabolism.But due to Liquor production belongs to open type spontaneous fermentation, and Wine brewing yeast strain and its metabolism are all unmanageable, although being adopted in liquor production With certain method, but all produce little effect.For example, the stronger yeast of metabolic activity is added in liquor production, but both Disclosure satisfy that alcohol vigor height, disclosure satisfy that the high yeast of flavor metabolic activity is less again, and many yeast be all difficult in adapt to it is white The adverse circumstances of wine fermentation, also, the saccharomyces cerevisiae strengthened is not quantitatively advantageous, can not substitute the wine brewing ferment in native country Mother, therefore, directly strengthen the mode effect and unobvious of high-quality saccharomyces cerevisiae.If it is possible to direct regulation and control actual production The metabolism of saccharomyces cerevisiae is a kind of more efficiently approach in environment.But unlike that controlling fermentation, the natural hair of liquor production Ferment determines the difficulty of its metabolic regulation.In addition, at present in liquor production, distillation yield is difficult that can expire simultaneously with flavor lifting Foot, flavor can then decline when general distillation yield improves, and during flavor raising, distillation yield can then decline.More than in addition to difficulty, also It is difficult to improve yeast-alcohol and flavor metabolism simultaneously.
Present invention finds 4 bacillus, it is capable of the alcohol metabolism and flavor metabolic capability of Effective Regulation saccharomyces cerevisiae, Because above-mentioned bacterial strains come from brewed spirit, therefore it is suitable for brewed spirit environment, is applied in liquor production, can be same When to effectively improve the alcohol of saccharomyces cerevisiae and flavor metabolic capability in production system, the final distillation yield for improving white wine simultaneously with Quality, solves the difficulty that distillation yield present in current liquor production and flavor quality are difficult to improve simultaneously.Meet liquor industry The requirement of sustainable development.Meanwhile present invention could apply to other fermentation food fields, for promoting the efficient of fermentation food There is important practice significance with fine quality production.
The content of the invention
The present invention provides the bacillus for improving saccharomyces cerevisiae metabolism alcohol and flavor substance, and its applied to liquor production The middle method for improving yeast of white wine and quality.
First purpose of the present invention is to provide 4 plants of gemma bars that can promote saccharomyces cerevisiae production alcohol and flavor substance simultaneously Bacterium.
The bacillus is bacillus licheniformis Bacillus licheniformis CGMCC NO.3963;Waxy bud Spore bacillus Bacillus cereus BC-1, i.e. B.cereus CCTCC NO:M 2013369;Bacillus lentus Bacillus Lentus BL-1, i.e. B.lentus CCTCC NO:M 2013370;Methylotrophic bacillus Methylotrophicus BM-1, i.e. B.methylotrophicusCCTCC NO:M 2013371.
The bacillus licheniformis B.licheniformis CGMCC NO.3963, on June 28th, 2010 is preserved in State's General Microbiological Culture preservation administrative center, deposit number are CGMCC NO.3963;The bacillus cereus B.cereus CCTCC NO:M 2013369, China typical culture collection center, deposit number CCTCC are preserved within 8th in August in 2013 NO:M 2013369;The bacillus lentus B.lentus CCTCC NO:M 2013370, it is preserved within 8th in August in 2013 China typical culture collection center, deposit number are CCTCC NO:M 2013370;The Methylotrophic bacillus B.methylotrophicus CCTCC NO:M 2013371, China typical culture collection is preserved within 8th in August in 2013 Center, deposit number are CCTCC NO:M 2013371.
The flavor substance includes:Acetaldehyde, 2 methyl propanal, the 3- tert-butyl group -4- metoxyphenols of aldehydes, the 2- of alcohols Methylpropanol, 3- methyl butanols, the benzaldehyde of the fragrant same clan, phenylacetaldehyde, ethyl phenylacetate, phenethyl acetate, caproic acid phenethyl ester, 2, the 3- Dihydrobenzofuranes of phenethyl isobutyrate,phenylethyl isobutyrate, ketone and furans, acids 2 Methylpropionic acid, caproic acid, octanoic acid, capric acid, and Farnesol, β-citronellol.
The bacillus licheniformis B.licheniformis CGMCC NO.3963, it is characterised in that by itself and ferment of making wine Female mixed fermentation, saccharomyces cerevisiae alcohol metabolism ability can be improved;Increase the ability of saccharomyces cerevisiae metabolism flavor substance, bag simultaneously Include acetaldehyde, the 3- tert-butyl group -4- metoxyphenols, 3- methyl butanols, benzaldehyde, phenylacetaldehyde, benzyl carbinol, phenethyl acetate, caproic acid Phenethyl ester, phenethyl isobutyrate,phenylethyl isobutyrate, 2,3- Dihydrobenzofuranes, 2 Methylpropionic acid, caproic acid, octanoic acid, capric acid, trans-nerolidol, Farnesol, Tetramethylpyrazine.
Described bacillus cereus B.cereus CCTCC NO:M 2013369, it is characterised in that by itself and ferment of making wine Female mixed fermentation, saccharomyces cerevisiae alcohol metabolism ability can be improved;Increase the ability of saccharomyces cerevisiae metabolism flavor substance, bag simultaneously Include acetaldehyde, 2 methyl propanal, the 3- tert-butyl group -4- metoxyphenols, 2,4- DI-tert-butylphenol compounds, 2- methylpropanols, 3- methyl fourths Alcohol, benzaldehyde, phenylacetaldehyde, benzyl carbinol, ethyl phenylacetate, phenethyl acetate, caproic acid phenethyl ester, phenethyl isobutyrate,phenylethyl isobutyrate, sad second Ester, ethyl caprate, 3- hydroxy-2-butanones, 2,3- Dihydrobenzofuranes, 2 Methylpropionic acid, caproic acid, octanoic acid, capric acid, trans-orange The flower tertiary alcohol, farnesol, β-citronellol, dorinone.
Described bacillus lentus B.lentus CCTCC NO:M 2013370, it is characterised in that by itself and ferment of making wine Female mixed fermentation, saccharomyces cerevisiae alcohol metabolism ability can be improved;Increase the ability of saccharomyces cerevisiae metabolism flavor substance, bag simultaneously Include acetaldehyde, guaiacol, 4- vinyl guaiacols, the 3- tert-butyl group -4- metoxyphenols, 2,4- DI-tert-butylphenol compounds, 2- first Base propyl alcohol, 3- methyl butanols, benzaldehyde, benzyl carbinol, ethyl phenylacetate, phenethyl acetate, caproic acid phenethyl ester, isobutyric acid benzene second Ester, ethyl caprate, 3- hydroxy-2-butanones, 2,3- Dihydrobenzofuranes, 2 Methylpropionic acid, caproic acid, octanoic acid, capric acid, trans-orange The flower tertiary alcohol, farnesol, β-citronellol.
Described Methylotrophic bacillus B.Methylotrophicus CCTCC NO:M 2013371, its feature It is, by itself and saccharomyces cerevisiae mixed fermentation, saccharomyces cerevisiae alcohol metabolism ability can be improved;Increase saccharomyces cerevisiae metabolism simultaneously The ability of flavor substance, including acetaldehyde, guaiacol, 4- vinyl guaiacols, 2- methylpropanols, 2- methyl -4- amylenes -1- Alcohol, benzaldehyde, phenylacetaldehyde, ethyl phenylacetate, phenethyl acetate, phenethyl isobutyrate,phenylethyl isobutyrate, ethyl caprilate, ethyl caprate, 3- hydroxyls- 2- butanone, 2,3- Dihydrobenzofuranes, 2 Methylpropionic acid, caproic acid, octanoic acid, capric acid, farnesol, dorinone.
4 described bacillus all have following microbial characteristic:Gram-positive, amphimicrobian, hydrolyzable junket Albumen, gelatin and starch;Directly it can be grown in sorghum solid medium, its feature is need not be to sorghum solid medium Saccharification processing is carried out, directly can grow and be metabolized using sorghum starch;60 DEG C of high growth temperatures are resistant to, tolerance 15~18% It NaCl and KCl, can be grown in pH3.8~4,10~12% ethanol can be resistant to.Features above can survive in white Liquor brewing complex environment, and saccharomyces cerevisiae is metabolized to form facilitation.Simultaneously as the bacterium is for a long time in brewed spirit environment In can produce interaction with saccharomyces cerevisiae mutual survival, evolution with yeast, and promote growth and the generation of saccharomyces cerevisiae Thank.
Second object of the present invention is to provide method that is a kind of while promoting saccharomyces cerevisiae production alcohol and flavor substance, is Saccharomyces cerevisiae and following at least one bacillus are mixed:Bacillus licheniformis B.licheniformis CGMCC NO.3963, bacillus cereus B.cereus CCTCC NO:M 2013369, bacillus lentus B.lentus CCTCC NO:M 2013370, Methylotrophic bacillus B.methylotrophicus CCTCC NO:M 2013371.
The saccharomyces cerevisiae is any one saccharomyces cerevisiae.
Methods described is specifically:By saccharomyces cerevisiae and bacillus seed liquor, it is according to thalline quantity ratio after inoculation 0.001:1000 to 1000:0.001 is inoculated in culture medium, in 25 DEG C to 40 DEG C, 0rpm to 200rpm cultures 16h to 72h.
Methods described, to culture medium no requirement (NR).In one embodiment of the invention, the culture medium is sorghum liquid Culture medium.
Third object of the present invention is to provide application of the bacillus in terms of wine brewing.
The application is to be applied to bacillus to improve brewed wine distillation yield and quality in brewed wine production.
The application be by bacillus liquid microbial inoculum or solid fungicide, with wine brewing distiller's yeast kind or after fermentation raw material mixes, Fermented, the distillation yield and quality of brewed wine significantly improve.
The application, it is that reinforcing of the bacillus in brewed wine production should in one embodiment of the invention With being inoculated in by the way of liquid bacterial agent or solid fungicide in production system, improve distillation yield and product special flavour substance classes With content.
The liquid bacterial agent production method, in one embodiment of the invention, be by the seed liquor of activation by 1~ 5% (w/w) inoculum concentration is inoculated in the liquid culture medium of sterilizing, 25 (i.e. per 100g liquid culture mediums inoculation seed liquor 1-5g) ~40 DEG C of culture 24h~72h.
The liquid culture medium, it is sorghum fluid nutrient medium in one embodiment of the invention, preparation method is: 20~200g sorghums sample after crushed, the water for adding mL/g to count 1~4 times, boiling 1-5h, in the pasty state, adds 10~50 after cooling Unit/g carbohydrase, 2~10h is kept in 40~100 DEG C, filtering, centrifugation gained filtrate, pol is 10~15 ° of Bx.
The production method of the solid fungicide, it is by the seed liquor inoculation of activation in one embodiment of the invention In (first order seed) sorghum solid medium (inoculum concentration is 1~5%, w/w), in 25~40 DEG C of environment solid state fermentation 32~ 72h, solid-state bacteria preparation is made.Sorghum solid medium production method:Sorghum is crushed, by 1:1~1:After 2 ratio adds water, Boiling 30-60min.
The bacillus of the present invention brewages screening in environment from Chinese Maotai-flavor liquor and obtained, due to Maotai-flavor liquor Brewage and with features such as high temperature, peracid, high ethano concentration, impart the bacillus that above bacillus is different from routine, tool Have tolerance high temperature, the feature of peracid and high ethano concentration of uniqueness, be adapted to brewed wine it is severe brewage environment, and promote to make The metabolism of brewer yeast.Meanwhile the raising that yeast flavor is metabolized in mixed fermentation is not by bacillus own metabolism After material, first mixed fermentation, the growth of bacillus receives certain suppression, while the metabolite that yeast improves is big absolutely Part is not that therefore, the bacillus mixes with yeast can improve saccharomyces cerevisiae caused by bacillus institute energy metabolism Metabolic capability.
Present invention finds 4 bacillus, the alcohol and wind of saccharomyces cerevisiae in production system can be effectively improved simultaneously Taste metabolic capability, the final distillation yield and quality for improving white wine simultaneously, solves distillation yield present in current liquor production and wind Flavor quality is difficult to the difficulty improved simultaneously, meets the requirement of liquor industry sustainable development.
Biomaterial preservation
Bacillus licheniformis B.licheniformis CGMCC NO.3963, it is general that China is preserved on June 28th, 2010 Logical Microbiological Culture Collection administrative center, preservation address are Institute of Micro-biology of the Chinese Academy of Sciences of BeiJing, China, deposit number CGMCC NO.3963;
Bacillus cereus Bacillus cereus BC-1, it is preserved within 8th Chinese Typical Representative culture in August in 2013 and protects Tibetan center, preservation address are Wuhan, China Wuhan University, and deposit number is CCTCC NO:M 2013369;
Bacillus lentus Bacillus lentus BL-1, it is preserved within 8th Chinese Typical Representative culture in August in 2013 and protects Tibetan center, preservation address are Wuhan, China Wuhan University, and deposit number is CCTCC NO:M 2013370;
Methylotrophic bacillus methylotrophicus BM-1, it is preserved within 8th in August in 2013 China typical culture collection center, preservation address are Wuhan, China Wuhan University, and deposit number is CCTCC NO:M 2013371。
Brief description of the drawings
Fig. 1:Individually culture and the growth of saccharomyces cerevisiae after mixed culture, A, saccharomyces cerevisiae,, single culture;●, addition ground Clothing bacillus;△, add bacillus cereus;▼, add bacillus lentus;◇, add Methylotrophic bacillus.
Embodiment
Flavor substance detects:With headspace solid-phase microextraction technology (HS-SPME) and gas chromatography-mass spectrum (GC-MS) side Method is analyzed volatile products, takes 8mL samples, is put into the headspace sampling bottle equipped with 3g NaCl, is added 10 μ L concentration and is 42.60mg·L-14- methyl -2- amylalcohols be internal standard.By ml headspace bottle in 50 DEG C of constant temperature extracting 45min.GC- is carried out after having extracted MS is analyzed.
The saccharomyces cerevisiae of embodiment 1 and the mixed culture of bacillus
Saccharomyces cerevisiae seed liquor:The ring saccharomyces cerevisiae bacterium mud of picking one is inoculated in YEPD fluid nutrient mediums, and 30 DEG C, 200rpm is trained Support 16h.Bacillus seed liquor:The ring bacillus bacterium mud of picking one is inoculated in LB fluid nutrient mediums, and 37 DEG C, 200rpm is cultivated 16h.Prepare sorghum diffusion juice, inoculation saccharomyces cerevisiae seed liquor and bacillus seed liquor, both final concentrations are 1 × 106cfu/mL.At 30 DEG C, 200rpm is cultivated.The method that sampling is coated with by flat board determines cell concentration;Cultivate 24~48h, bacterium Liquid centrifuges 10min, measure concentration of alcohol and flavor substance composition and content in 8000rpm.Saccharomyces cerevisiae cell concentration is with the time Change curve see Fig. 1, concentration of alcohol change is shown in Table 1, and flavor components change is shown in Table 2 to table 3.
By determining the cell concentration of bacillus and saccharomycete in fermentation process, finding the growth of bacillus can drop Low, the growth of saccharomyces cerevisiae changes less compared with individually culture.
As it can be seen from table 1 after being mixed with bacillus, the producing and ethanol ability of saccharomyces cerevisiae improves 17%- 40.2%.
From table 2 to table 3 as can be seen that bacillus and the bag that after yeast mixed culture, flavor substance content is all improved Include:The flavor substance includes:Acetaldehyde, 2 methyl propanal, the 3- tert-butyl group -4- metoxyphenols of aldehydes, the 2- methyl of alcohols Propyl alcohol, 3- methyl butanols, benzaldehyde, phenylacetaldehyde, ethyl phenylacetate, phenethyl acetate, caproic acid phenethyl ester, the isobutyl of the fragrant same clan 2, the 3- Dihydrobenzofuranes of sour phenethyl ester, ketone and furans, acids 2 Methylpropionic acid, caproic acid, octanoic acid, capric acid, and method Alcohol, β-citronellol.
It is demonstrated experimentally that bacillus be do not produce or it is extremely low production alcohol, acid, ester.Bacillus grows during due to mixed culture Reduce, yeast growth, and the species of flavor substance and its concentration can improve, indicating not bacillus itself has high yield second Alcohol and important alcohol, acid, the metabolic capability of esters flavor substance, but bacillus promotes the metabolic capability of saccharomyces cerevisiae.
Table 1 adds different bacillus saccharomyces cerevisiaes and produces concentration of alcohol (g/l)
Table 2 adds the change (μ g/L) of aldehydes, alcohols and aromatic series flavor substance after different bacillus
Table 3 adds the change (μ g/L) of esters, acids and other flavor substances after different bacillus
The bacillus of embodiment 2 is applied to improve brewed wine distillation yield and quality in brewed wine production
By the bacillus CCTCC NO of the present invention:M 2013369 and CCTCC NO:Liquid is respectively prepared in M 2013370 Microbial inoculum or solid fungicide, fermented after being mixed with wine brewing distiller's yeast kind or fermentation raw material.
The liquid bacterial agent production method:By the seed liquor of activation by 1~5% (w/w) inoculum concentration (i.e. per 100g liquid Culture medium inoculated seed liquor 1-5g) it is inoculated in the liquid culture medium of sterilizing, 25~40 DEG C of culture 24h~72h.
The liquid culture medium is sorghum extract culture medium, and preparation method is:20~200g sorghums sample after crushed, The water for adding mL/g to count 1~4 times, boiling 1-5h, in the pasty state, 10~50 units/g carbohydrase is added after cooling, in 40~100 DEG C 2~10h is kept, filtering, centrifugation gained filtrate, pol is 10~15 ° of Bx.
The production method of the solid fungicide is in seed liquor inoculation (first order seed) sorghum solid medium by activation (inoculum concentration is 1~5%, w/w), 32~72h of solid state fermentation in 25~40 DEG C of environment, is made solid-state bacteria preparation.
Sorghum solid medium production method:Sorghum is crushed, by 1:1~1:After 2 ratio adds water, boiling 30- 60min.
Both bacillus are applied respectively in Maotai-flavor liquor production, and sense organ product are carried out to the white wine of application production Comment, as a result as shown in table 4, it can be seen that be improved using quality of white spirit after bacillus.Wherein, according to bacillus with Yeast flavor metabolic characteristics, bacillus production acid, alcohol, the ability of ester are very low, the mellowness that is improved in white wine, sugariness, sour master To be alcohols thing and the acid contribution of yeast metabolism, it is mainly that Ester caused by yeast metabolism is contributed to put fragrant intensity. As a result show, the important flavor such as acid, alcohol, ester is that have bacillus to promote saccharomyces cerevisiae metabolism to produce in white wine.
The key application bacteria combination of table 4 produces Liquor Tasting result
Comment wine personnel:National white wine judging panel 1;Provincial white wine judging panel 5;Brewery judging panel 2.
Point system:Made number one by sequence and weight 3 points, second weights 2 points, and the 3rd weights 1 point.
The application of bacillus has been carried out in 1~4 round for going out wine of Maotai-flavor liquor production, it is equal to produce white wine quality It is improved and distillation yield is improved, as a result as shown in table 5.
The distillation yield (%) of the application bacillus bacterium production white wine of table 5
The saccharomyces cerevisiae of embodiment 3 and the mixed culture of bacillus
By saccharomyces cerevisiae and B.licheniformis CGMCC NO.3963, B.lentus CCTCC NO:M 2013370 Seed liquor is respectively prepared.Will be by B.licheniformis CGMCC3963, B.lentus CCTCC NO:M 2013370 presses bacterium Number 1:After 1 ratio mixing, it is inoculated in together with saccharomyces cerevisiae in YPD culture mediums, makes the bacterium of yeast and bacillus after inoculation Number is respectively 104Individual/mL, 1010Individual/mL, with 30 DEG C of quiescent culture 72h.As a result find, compared with individually culture, acetaldehyde, 2- first Base propionic aldehyde, the 3- tert-butyl group -4- metoxyphenols, 2- methylpropanols, 3- methyl butanols, benzaldehyde, phenylacetaldehyde, ethyl phenylacetate, Phenethyl acetate, caproic acid phenethyl ester, phenethyl isobutyrate,phenylethyl isobutyrate, 2,3- Dihydrobenzofuranes, 2 Methylpropionic acid, caproic acid, octanoic acid, the last of the ten Heavenly stems The content of material such as acid, farnesol, β-citronellol have a certain degree of rise.
The saccharomyces cerevisiae of embodiment 4 and the mixed culture of bacillus
By saccharomyces cerevisiae and B.cereus CCTCC NO:M 2013369、B.lentus CCTCC NO:M 2013370、 B.methylotrophicus CCTCC NO:Seed liquor is respectively prepared in M 2013371.Will be by B.cereus CCTCC NO: M2013369、B.lentus CCTCC NO:M 2013370、B.methylotrophicus CCTCC NO:M 2013371 is pressed Bacterium number 1:2:After 2 ratio mixing, it is inoculated in together with saccharomyces cerevisiae in culture medium, makes the bacterium of yeast and bacillus after inoculation Number is respectively 108Individual/mL, 103Individual/mL, 16h is cultivated with 40 DEG C of 100rpm.As a result find, compared with individually culture, acetaldehyde, 2- Butylic aldehyde, the 3- tert-butyl group -4- metoxyphenols, 2- methylpropanols, 3- methyl butanols, benzaldehyde, phenylacetaldehyde, phenylacetic acid second Ester, phenethyl acetate, caproic acid phenethyl ester, phenethyl isobutyrate,phenylethyl isobutyrate, 2,3- Dihydrobenzofuranes, 2 Methylpropionic acid, caproic acid, octanoic acid, The content of material such as capric acid, farnesol, β-citronellol have a certain degree of rise.Meanwhile the liquor output rate of yeast also improves 22.3%.
Although the present invention is disclosed as above with preferred embodiment, it is not limited to the present invention, any to be familiar with this skill The people of art, without departing from the spirit and scope of the present invention, it can all do various change and modification, therefore the protection model of the present invention Enclose being defined of being defined by claims.

Claims (7)

1. the bacillus of saccharomyces cerevisiae production alcohol and flavor substance can be promoted simultaneously, it is characterised in that the bacillus is Bacillus cereus Bacillus cereus BC-1, China typical culture collection center was preserved in 8th in August in 2013, Preservation address is Wuhan, China Wuhan University, and deposit number is CCTCC NO:M 2013369.
2. bacillus according to claim 1, it is characterised in that the flavor substance includes:Acetaldehyde, 2- methyl-props Aldehyde, the 3- tert-butyl group -4- metoxyphenols, 2- methylpropanols, 3- methyl butanols, benzaldehyde, phenylacetaldehyde, ethyl phenylacetate, acetic acid Phenethyl ester, caproic acid phenethyl ester, phenethyl isobutyrate,phenylethyl isobutyrate, 2,3- Dihydrobenzofuranes, 2 Methylpropionic acid, caproic acid, octanoic acid, capric acid, with And farnesol, β-citronellol.
3. bacillus according to claim 1, it is characterised in that the bacillus and saccharomyces cerevisiae mixed fermentation When, it is possible to increase saccharomyces cerevisiae produces alcohol ability and increases the ability of saccharomyces cerevisiae metabolism flavor substance;The waxy gemma bar Bacterium CCTCC NO:The flavor substance that M 2013369 can be improved includes acetaldehyde, 2 methyl propanal, the 3- tert-butyl group -4- methoxybenzenes Phenol, 2,4- DI-tert-butylphenol compounds, 2- methylpropanols, 3- methyl butanols, benzaldehyde, phenylacetaldehyde, benzyl carbinol, ethyl phenylacetate, second Sour phenethyl ester, caproic acid phenethyl ester, phenethyl isobutyrate,phenylethyl isobutyrate, ethyl caprilate, ethyl caprate, 3- hydroxy-2-butanones, 2,3- dihydrobenzos Furans, 2 Methylpropionic acid, caproic acid, octanoic acid, capric acid, trans-nerolidol, farnesol, β-citronellol, dorinone.
4. it is a kind of at the same promote saccharomyces cerevisiae production alcohol and flavor substance method, it is characterised in that be by saccharomyces cerevisiae with B.cereus CCTCC NO:M 2013369 is mixed;Either by saccharomyces cerevisiae, B.cereus CCTCC NO:M 2013369 are mixed with any one or more following bacillus:B.licheniformis CGMCC NO.3963、B.lentus CCTCC NO:M 2013370、B.methylotrophicus CCTCC NO:M 2013371。
5. application of the bacillus described in claim 1 in terms of wine brewing.
6. application according to claim 5, it is characterised in that the application is by bacillus liquid microbial inoculum or solid bacterium Agent, after being mixed with wine brewing distiller's yeast kind or fermentation raw material, fermented.
7. application according to claim 6, it is characterised in that the liquid bacterial agent production method:By seed liquor by every 100g liquid culture mediums inoculation seed liquor 1-5g inoculum concentration is inoculated in the liquid culture medium of sterilizing, 25~40 DEG C of culture 24h ~72h, the preparation method of the liquid culture medium are:20~200g sorghums after crushed, add the water of 1~4 times of quality, boiling 1-5h, press the carbohydrase that 10~50U is added per g sorghums in the pasty state, after cooling, keep 2~10h in 40~100 DEG C, filtering, from Filtrate obtained by the heart, pol is 10~15 ° of Bx;The production method of the solid fungicide:Seed liquor is pressed per 100g solid mediums Seed liquor 1-5g inoculum concentration inoculation sorghum solid medium is inoculated with, 32~72h of solid state fermentation, is made in 25~40 DEG C of environment Solid-state microbial inoculum.
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