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CN112852667A - A kind of method for improving the content of flavor substances in soy sauce - Google Patents

A kind of method for improving the content of flavor substances in soy sauce Download PDF

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CN112852667A
CN112852667A CN202110078955.9A CN202110078955A CN112852667A CN 112852667 A CN112852667 A CN 112852667A CN 202110078955 A CN202110078955 A CN 202110078955A CN 112852667 A CN112852667 A CN 112852667A
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方芳
胡光耀
堵国成
陈坚
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Abstract

本发明公开了一种提高酱油风味物质含量的方法,属于生物工程技术领域。本发明从酱醪中筛选分离菌株,筛选获得一株具有增加酱油风味物质含量的类肠膜魏斯氏菌,以通用的高盐稀态酱油发酵体系考察了共同强化类肠膜魏斯氏菌与鲁氏接合酵母对酱油风味物质含量的影响,发现共同强化两菌可以显著提高酱油风味物质含量。在高盐稀态酱油发酵过程中,与不强化任何菌株对照相比,共同强化魏斯氏菌与鲁氏接合酵母可使体系内风味物质含量的生成量增加2.1倍,有机酸总含量提高了72.76%,游离氨基酸总含量提高了33.15%。

Figure 202110078955

The invention discloses a method for increasing the content of flavor substances in soy sauce, and belongs to the technical field of biological engineering. In the present invention, isolated strains are screened from soy sauce mash, and a strain of Weissella enterica that increases the content of soy sauce flavor substances is obtained by screening, and a common high-salt dilute soy sauce fermentation system is used to investigate the co-strengthening Weisseria enterica. The effect of Zygosaccharomyces ruotii on the content of flavor substances in soy sauce, it was found that co-enhancing the two bacteria can significantly increase the content of flavor substances in soy sauce. In the fermentation process of high-salt dilute soy sauce, compared with the control without any strain, co-enhancing Weissella and Zygosaccharomyces ruckeri increased the content of flavor substances in the system by 2.1 times, and the total content of organic acids increased. 72.76%, and the total free amino acid content increased by 33.15%.

Figure 202110078955

Description

Method for improving content of flavor substances of soy sauce
Technical Field
The invention relates to a method for improving the content of flavor substances of soy sauce, belonging to the technical field of bioengineering.
Background
The main components of the soy sauce comprise free amino acids, polypeptides, organic acids and volatile flavor substances, wherein the free amino acids and the volatile flavor substances influence the taste and the flavor of the soy sauce and are key substances influencing the quality of the soy sauce. The variety and content of volatile flavor substances have important influence on the flavor of the soy sauce, and the unique flavor of the soy sauce is derived from succession of microbial communities and metabolic regulation. By summarizing research reports related to soy sauce aroma substances, 1038 volatile compounds are identified and arranged together. These compounds fall into two main categories: aromatic compounds and aliphatic compounds, further subdivided to include alcohols, acids, esters, phenols, aldehydes, ketones, furans, pyrazines, and the like.
The flavor substances of the soy sauce are improved mainly from two aspects: 1. the fermentation process is improved. The soy sauce flavor substances are influenced by fermentation factors and fermentation processes, wherein the content of the flavor substances can be effectively improved by regulating and controlling multiple factors such as fermentation temperature, fermentation time, carbon-nitrogen ratio, fermentation capacity, saccharification capacity and the like; in addition, the fermentation conditions such as temperature, pH, oxygen content, etc. of the fermentation process also have an effect. The defects of the method are that the workload is large, the time and the labor are consumed, and the efficiency is low due to excessive influence factors; 2. a microbial means. The screening of aroma-enhancing microorganisms is the most important means for improving the content of flavor substances at present, and the multi-strain fermentation can improve the diversity and activity of enzymes and can better improve the flavor substances of the soy sauce, but the strain screening process is slow, so that the quality improvement of the soy sauce is influenced. Therefore, strengthening functional microorganisms in soy sauce fermentation is currently the safest and most effective method.
The soy sauce mash is one of main environments where important functional microorganisms inhabit in the soy sauce fermentation process, free amino acids and organic acids generated by bacterial metabolism of the soy sauce mash are main precursors of main fragrances HEMF and 4-EG of soy sauce, and have important influence on the quality and flavor of the soy sauce. In the continuous acclimation and dynamic flora replacement process of the soy sauce fermentation high-salt environment, the functional microbial flora adapted to the soy sauce mash environment is gradually enriched, and the generation of flavor substances in the soy sauce fermentation process can be improved. Therefore, the strengthening of the functional microbial flora in the high-salt dilute soy sauce mash has important significance for promoting the application of improving the content of the flavor substances in the soy sauce fermentation process.
Disclosure of Invention
The invention aims to overcome the defects in the prior art and provide a method for improving the content of soy sauce flavor substances.
The first purpose of the invention is to provide a Weissella mesenteroides (Weissellaparameteroides) LCW-28 which is preserved in China center for type culture Collection at 11-27 months in 2020 with the preservation number of CCTCCM 2020778.
The second purpose of the invention is to provide a culture method of Weissella mesenteroides LCW-28, which is to inoculate Weissella mesenteroides LCW-28 to MRS culture medium and culture the Weissella mesenteroides LCW-28 statically at 37 ℃.
The third purpose of the invention is to provide a starter which contains Weissella mesenteroides LCW-28.
In one embodiment of the present invention, the preparation method of the leavening agent is: inoculating 200-600 mu L of Weissella mesenteroides LCW-28 into 10-30 mLMRS liquid culture medium, activating for 2-3 generations at 37 ℃, and waiting until Weissella mesenteroides LCW-28 reaches 1.0 multiplied by 107When the number of viable bacteria is more than CFU/mL, centrifuging for 15min at 6000-10000 rpm, removing supernatant, sequentially adding buffer solution and cryoprotectant in a sterile environment until the cell concentration is not less than 1.0 multiplied by 107And (5) performing vacuum freeze drying treatment at CFU/mL to obtain the leaven.
In one embodiment of the present invention, the buffer solution is 0.1-0.3M phosphate buffer solution with pH 6-7 and/or 0.5-1% physiological saline and/or double distilled water, and the cryoprotectant is 10-20% glycerol and/or 8-12% trehalose.
The fourth purpose of the invention is to provide a method for improving the content of flavor substances of soy sauce, which is to add the Weissella mesenteroides LCW-28 or the leavening agent in the soy sauce fermentation process.
In one embodiment of the invention, the Weissella mesenteroides LCW-28 or starter culture has a final concentration of 1.0X 10 in the fermentation system6~1.0×108CFU/g。
In one embodiment of the invention, the Weissella mesenteroides LCW-28 is present in a mash environment having a mash concentration of 18% of at least 1.0 x 107CFU/g。
In one embodiment of the present invention, yeast is also added during the soy sauce fermentation.
In one embodiment of the invention, the weissella mesenteroides LCW-28 or starter is added simultaneously with the yeast during soy sauce fermentation.
In one embodiment of the invention, the yeast is added to the Weissella mesenteroides LCW-28 or the leavening agent in a ratio of 1:1 during soy sauce fermentation.
In one embodiment of the present invention, the yeast is ZQ-01, Zygosaccharomyces rouxii.
The fifth purpose of the invention is to provide the application of the Weissella mesenteroides LCW-28 or the leavening agent or the method for improving the content of the flavor substances in the preparation of soy sauce.
Has the advantages that:
the Weissella mesenteroides LCW-28 strain capable of remarkably improving the generation of flavor substances in the soy sauce fermentation process is obtained by separating and purifying soy sauce mash microorganisms. The strain and the strain ZQ-01 are strengthened together, so that the content of flavor substances generated in a system can be well improved, and the content of the flavor substances can be improved by 2.1 times compared with a Control group without the added strain. Meanwhile, compared with a Control group without adding the bacterial strains, the total content of the organic acid of the two bacteria is increased by 72.76%, and the total content of the free amino acid is increased by 33.15%. The amino nitrogen of the two-bacterium reinforced group is improved by 97.4 percent compared with the Control group without the added strain on the 40 th day of fermentation. Therefore, the Weissella mesenteroides LCW-28 is a strain which is suitable for the soy sauce fermentation production environment and can obviously improve the content of flavor substances in the fermentation process, and the content of the flavor substances in the soy sauce can be well controlled within a proper range by adjusting the addition amount of the strain, so that the Weissella mesenteroides LCW-28 has important significance for improving the flavor substances in the soy sauce fermentation production.
Biological material preservation
The Weissella mesenteroides provided by the invention is classified and named as Weissellaparameteroides LCW-28, is preserved in China center for type culture Collection at 11/27 of 2020, has the preservation number of CCTCCM2020778, and has the preservation address of Wuhan university in China.
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FIG. 1 shows the dynamic changes of the amounts of Weissella mesenteroides (a) and Zygosaccharomyces rouxii (b) in the fermentation process of high-salt dilute soy sauce.
FIG. 2 shows the changes of physicochemical indexes (a is the change of reducing sugar, b is the change of pH, c is the change of total acid, and d is the change of amino nitrogen) of singly reinforced Weissella mesenteroides LCW-28 and singly reinforced zygosaccharomyces rouxii ZQ-01.
FIG. 3 shows the changes in organic acid content for the individual enrichment of Weissella mesenteroides LCW-28, the individual enrichment of ZQ-01, and the joint enrichment of both bacteria.
Detailed Description
ZQ-01: the mechanism of production of ethyl carbamate in soy sauce and elimination strategy described in sarean, study [ D ]. university of south of the river, 2016.
MRS culture medium: 10g/L of peptone, 8g/L of beef extract powder, 4g/L of yeast extract powder, 20g/L of glucose, 2g/L of dipotassium phosphate, 2g/L of diammonium hydrogen citrate, 5g/L of sodium acetate, 0.2g/L of magnesium sulfate, 0.04g/L of manganese sulfate and 801g/L of tween.
Bengal red medium: 5g/L of peptone, 10g/L of glucose, 1g/L of dipotassium phosphate, 0.5g/L of magnesium sulfate, 20g/L of agar and 100mL/L of 1/3000 Bengal solution.
YPD medium: 10g/L of yeast extract, 20g/L of peptone and 20g/L of glucose.
Example 1: screening of strains
With vancomycin (0.2 g. L)-1) And natamycin (0.1 g.L)-1) The MRS medium of (1) was isolated and screened from the moromia. Selecting sauce mash samples fermented for 5, 15 and 25 days, taking 15g of sauce mash and placing the sauce mash into a beaker, adding 135mL of sterile normal saline and adding a proper amount of glass beads, and stirring at 100 r.min-1Oscillating for 5min, standing at room temperature for 5min, taking 1mL of bacterial suspension, diluting the bacterial suspension in gradient, and coating on vancomycin (0.2 g. L)-1) And natamycin (0.1 g.L)-1) MRS medium of (5), inversion at 37 ℃Culturing for 1-3 days. Single colonies were picked from the plates and inoculated into 50mL of a suspension containing vancomycin (0.2 g. L)-1) And natamycin (0.1 g.L)-1) The MRS liquid culture medium is kept still for 24 hours at 37 ℃ and 8000r/min, and thalli are collected by centrifugation.
Extracting the genome of the strain by using a commercial gene extraction kit, respectively amplifying the 16SrRNA gene sequence and the recN gene sequence of the strain by using a 16SrRNA general primer and a recN gene specific primer (table 1) as templates, sending the amplified products to Shanghai bioengineering company Limited for sequencing, and comparing and analyzing the sequencing result with the sequence in an NCBI database.
TABLE 1PCR primers
Figure BDA0002908405440000041
Example 2: soy sauce preparation using Weissella mesenteroides LCW-28 and ZQ-01
(1) Strain culture:
culturing Weissella mesenteroides LCW-28: selecting Weissella mesenteroides single colony from a microorganism activation plate, inoculating the Weissella mesenteroides single colony into a liquid MRS culture medium, standing and culturing at 37 ℃ for 24h, inoculating the Weissella mesenteroides single colony into a fresh MRS culture medium according to the proportion of 1% (v/v), and culturing until OD is obtained600To 3.0.
Culture of ZQ-01 of ZQ-Lu's yeast: respectively picking single yeast colony from microorganism activation plate, inoculating into liquid YPD medium, culturing at 37 deg.C and 220r min-1Culturing for 30h, inoculating to fresh YPD medium at a ratio of 1% (v/v), and culturing to OD600To 4.0.
(2) The fermentation process of the high-salt dilute soy sauce comprises the following steps:
a starter propagation process: soaking bean cake in 1.2 times of water for 2 hr, sterilizing at 121 deg.C for 15min, and cooling to room temperature. Mixing soy sauce koji (1.5 ‰ (w/w) of total weight of raw materials) with appropriate amount of parched wheat grains, and mixing with soybean meal and wheat grains (w/w is 6: 4). Culturing at 30 deg.C in biochemical incubator, turning over at appropriate time, making starter for 48h, and collecting yeast material with yellow-green mycelium on surface.
The fermentation process comprises the following steps: mixing the finished koji with a mixture containing 200 g.L-1NaCl brine was mixed in a volume ratio of 1: 1.8. And (3) filling the uniformly mixed sauce mash into 500mL beakers, and fermenting for 30 days at 30 ℃. The fermentation was stirred once daily for week 1, and every two days thereafter. Samples were taken on days 0, 5, 10, 15, 20, 25, 30.
The strengthening mode is as follows: the adding mode of the bacterial strain in the fermentation process of the high-salt dilute soy sauce is as follows: adding 10 at 0 day of fermentation7CFU·g-1ZQ-01 of ZQ-01 and simultaneously adding 107CFU·g-1Weissella mesenteroides LCW-28.
Five experimental groups are arranged in total, the specific implementation mode is as above,
control group: no strain is added;
rouxii group: zygosaccharomyces rouxii alone is fortified;
parametenteroides group: strengthening Weissella mesenteroides alone;
co-encapsulation group: simultaneously strengthening Weissella mesenteroides and zygosaccharomyces rouxii;
sequentialinocilation: is to inoculate Weissella mesenteroides and the like at first and then inoculate zygosaccharomyces rouxii when the pH value is reduced to 5.
Example 3: determination of quantities of Weissella mesenteroides LCW-28 and ZQ-01
In order to confirm that Weissella mesenteroides and Zygosaccharomyces rouxii can be enhanced by adding strains during soy sauce fermentation, a plate counting method is adopted for measuring the quantity of Weissella mesenteroides and yeast. Weighing 1g of fresh soy sauce mash or co-culture bacteria liquid, pouring into a conical flask containing sterilized glass beads and 99mL of physiological saline, mixing uniformly, and diluting in a gradient manner (respectively diluting to 10)-1、10-2、10-3、10-4、10-5、10-6) Diluted and spread on MRS medium and Bengal medium, and cultured at 37 ℃ for 1 day, and counted. Weissella mesenteroides is facultative anaerobe, and bacterial colony appears in plate culture for 1-2 days. The predominant salt-tolerant bacteria in the sauce mash is the halophilic tetragenococcus, and bacterial colonies appear after 4-6 days of plate culture. Therefore, the MRS plate can be used for mixing sauce during countingDominant salt-tolerant bacteria (including Weissella, Bacillus, Staphylococcus) in mash. The yeast amount calculated by the method comprises the added zygosaccharomyces rouxii and salt-tolerant yeast (such as torulopsis, candida and the like) in the sauce mash. The latter are less numerous and negligible compared to the former.
The result shows that the addition of Weissella mesenteroides LCW-28 can increase the number of Weissella mesenteroides in the sauce mash by 1.9-3.0 orders of magnitude compared with the Weissella mesenteroides contrast which is not added, and the maximum value reaches 1.0 multiplied by 108CFU·g-1Gradually decreases in the later stage and stabilizes at 1.0 × 107CFU·g-1. Therefore, the addition of Weissella mesenteroides LCW-28 can increase the concentration of the Weissella mesenteroides LCW-28 in the soy sauce fermentation process and strengthen the strain (figure 1).
Example 4: the reinforced influence of Weissella mesenteroides LCW-28 and ZQ-01 on the physicochemical indexes of the soy sauce mash sample
The moromi of example 1 was sampled on days 0, 5, 10, 15, 20, 25, 30, 35 and 40. Taking 100g of sauce mash in a centrifuge tube, and carrying out 12000 r.min-1Centrifuging for 30min, collecting supernatant, and filtering with filter membrane with pore diameter of 0.22 μm for physicochemical index determination. The pH of the soy sauce mash is directly measured by a precise pH meter. The total acid content was determined by acidimetry. The content of amino acid nitrogen is measured by adopting a formaldehyde titration method. The content of reducing sugar is determined by 3, 5-dinitrosalicylic acid method (DNS).
Analysis of physicochemical indexes such as pH, total acid, reducing sugar and amino acid nitrogen of the moromi mash in the high-salt dilute soy sauce fermentation process shows that the pH of the moromi mash is slightly reduced by adding Weissella mesenteroides, the total acid content is slightly increased, the content of the amino acid nitrogen is obviously increased, as shown in figure 2, at the 40 th day, compared with a Control group, the pH of the moromi mash is reduced by 15% by strengthening two bacteria (Co-infection group), the total acid is increased by 41.28%, the reducing sugar is decreased by 132.8%, and the amino nitrogen is increased by 97.4%. The amino nitrogen is used as the main judgment standard of the national soy sauce quality, and the content of the amino nitrogen can be obviously improved by jointly strengthening the two bacteria.
Example 5: effect of enhanced Weissella mesenteroides LCW-28 and ZQ-01 on free amino acids
The free amino acid is measured by high performance liquid chromatography, and is subjected to in-column derivatization by adopting o-xylene (OPA), and the specific measurement method is referred to documents. Diluting the soy sauce filtrate by 20 times with 5% trichloroacetic acid, treating in dark for 30min, filtering with water system filter membrane with pore diameter of 0.22 μm, and collecting 1mL sample. This operation can remove the interference of the protein on the measurement result. Chromatographic conditions are as follows: chromatograph Agilent1260, column ODSYPERSIL (250 mm. times.4.6 mm. times.5 μm). The mobile phase A and the mobile phase B are prepared as before, and are filtered and subjected to ultrasonic treatment for more than 30min before use. Mobile phase a phase: 5 g.L-1Sodium acetate solution (containing 0.2 mL. L)-1 Triethylamine 5 mL. L-1Tetrahydrofuran), pH adjusted to 7.2 with acetic acid. Mobile phase B phase: 5 g.L-1Sodium acetate-methanol-acetonitrile solution with the volume ratio of 1:2: 2.
The free amino acid has important contribution to the formation of unique taste and aroma of fermented foods, particularly the fermented soybean foods taking protein as a main fermentation substrate. The content of free amino acid is one of the main physicochemical indexes for measuring the quality of soy sauce. Glutamic acid is umami amino acid and is main free amino acid in the umami taste of the soy sauce. Glycine and threonine are sweet amino acids. Compared with the Control group, the total content of free amino acid of the two reinforced bacteria (Co-inoculation group) is improved by 33.15 percent. Wherein glutamic acid is improved by 50%, lysine is improved by 56.39%, glycine is improved by 38.62%, and threonine is improved by 70.79%.
TABLE 2 Change in free amino acids of enhanced Weissella mesenteroides and Zygosaccharomyces rouxii (mg. mL)-1)
Figure BDA0002908405440000061
Example 6: effect of enhanced Weissella mesenteroides LCW-28 and ZQ-01 on organic acid content
The organic acid is determined by high performance liquid chromatography, and the specific method is referred to in the literature. The filtrate of the moromi mash was diluted 10 times with ultrapure water, and then filtered through a water-based filter membrane having a pore size of 0.22 μm, and 1mL of a sample was sampled and measured. Chromatographic conditions are as follows: liquid phase system: agilent 1260; a chromatographic column: an organic acid column;an ultraviolet detector: 210 nm; sample introduction volume: 10 mu L of the solution; mobile phase: 5 mmol. L-1 dilute sulfuric acid; column temperature: 40 ℃; elution speed: 0.5 mL/min-1(ii) a Separation time: and (3) 30 min.
The organic acid generated by lactic acid bacteria in the soy sauce is not only an important component of soy sauce flavor substances, but also plays a role in inhibiting the growth of putrefying bacteria or mixed bacteria in soy sauce mash, and the total content of organic acid for strengthening two bacteria (Co-inoculation group) is improved by 72.76 percent compared with the Control group at the 40 th day. In which propionic acid, which is a short chain saturated fatty acid, was increased by 1.43 fold (fig. 3).
Example 7: effect of enhanced Weissella mesenteroides LCW-28 and ZQ-01 on flavor content
The volatile flavor substances are determined by adopting a solid phase microextraction combined gas chromatography-mass spectrometry (SPME-GC-MS) technology, and the specific method is referred to in the literature. Taking three parallel samples from each sample at the end of fermentation, filtering, mixing uniformly, accurately measuring 5mL of soy sauce sample, placing in a 20mL headspace sample injection bottle, adding 83.36 μ g.L-1The 2-octanol as internal standard, mixed evenly and sealed immediately for determination. And (3) comparing and identifying the mass spectrogram of the sample with a NIST2.0 standard spectrum library after determination. Volatile substances were characterized according to Retention Index (RI). The volatile substances were quantitatively analyzed according to the area of the internal standard 2-octanol.
The reinforced Weissella mesenteroides or the Zygosaccharomyces rouxii can obviously increase the content of main flavor substances (alcohol, acid, ester, phenol, aldehyde and the like) in the soy sauce fermentation process, and particularly, the content of the flavor substances is increased most when the two bacteria are added together. Compared with the Control group, the total content of volatile flavor substances is increased by 2.12 times when the two bacteria are enhanced. Wherein the alcohol is increased by 1.39 times, the acid is increased by 2.39 times, and the aldehyde is increased by 2 times. Wherein the characteristic flavor substance of the soy sauce is 4-ethylguaiacol is improved by 1.58 times, and the HEMF is improved by 2.73 times.
TABLE 3 Main differential volatile substance content (g/kg) in different soy sauce samples
Figure BDA0002908405440000071
Figure BDA0002908405440000081
TABLE 4 content of major volatile substances (g/kg) in different soy sauce samples
Figure BDA0002908405440000082
Comparative example: the influence of the joint reinforcement of different Weissella bacteria and ZQ-01 on the flavor substance content of the sauce mash sample
Soy sauce was prepared by fortifying the other Weissella bacteria selected in example 1, such as Weissellactonusa fusi (panel 1) and Weissella civora Weissellacia Weissellaspora (panel 2), with ZQ-01, respectively, in the same manner as in examples 2 and 7. As shown in Table 5, the other two Weissella strains screened in example 1 were selected for co-fortification with ZQ-01, which was a zygosaccharomyces rouxii strain with a flavor content about 50% less than the co-fortification of Weissella mesenteroides LCW-28 with ZQ-01.
TABLE 5 content of major volatile substances (g/kg) in different soy sauce samples
Figure BDA0002908405440000083
Although the present invention has been described with reference to the preferred embodiments, it should be understood that various changes and modifications can be made therein by those skilled in the art without departing from the spirit and scope of the invention as defined in the appended claims.

Claims (10)

1.一株类肠膜魏斯氏菌(Weissellaparamesenteroides)LCW-28,已于2020年11月27日保藏于中国典型培养物保藏中心,保藏编号为CCTCC M 2020778,保藏地址为中国,武汉,武汉大学。1. A strain of Weissella paramesenteroides LCW-28 has been deposited in the China Center for Type Culture Collection on November 27, 2020, with the deposit number CCTCC M 2020778, and the deposit address is Wuhan, Wuhan, China the University. 2.一种发酵剂,其特征在于,含有权利要求1所述类肠膜魏斯氏菌LCW-28。2 . A starter, characterized in that it contains Weisseria enterica LCW-28 according to claim 1 . 3 . 3.一种提高酱油风味物质含量的方法,其特征在于,所述方法是在酱油发酵过程中添加权利要求1所述类肠膜魏斯氏菌LCW-28或权利要求2所述发酵剂。3. A method for improving the content of flavoring substances in soy sauce, characterized in that the method is to add the Weissella enterica LCW-28 described in claim 1 or the starter described in claim 2 in the fermentation process of soy sauce. 4.根据权利要求3所述方法,其特征在于,权利要求1所述类肠膜魏斯氏菌LCW-28或权利要求2所述发酵剂在发酵体系中的终浓度为1.0×106~1.0×108CFU/g。4 . The method according to claim 3 , wherein the final concentration of the Weissella enterica LCW-28 according to claim 1 or the starter according to claim 2 in the fermentation system is 1.0×10 6 ~ 4 . 1.0×10 8 CFU/g. 5.根据权利要求3所述方法,其特征在于,酱油发酵过程中还添加了酵母。5. The method according to claim 3, wherein yeast is also added in the soy sauce fermentation process. 6.根据权利要求5所述方法,其特征在于,所述酵母与权利要求1所述类肠膜魏斯氏菌或权利要求2所述发酵剂的添加数量比为1:1。6 . The method according to claim 5 , wherein the ratio of the added quantity of the yeast to the Weisseria enterobacterium of claim 1 or the starter of claim 2 is 1:1. 7 . 7.根据权利要求6所述方法,其特征在于,所述酵母为鲁氏接合酵母ZQ-01。7 . The method according to claim 6 , wherein the yeast is Zygosaccharomyces rouge ZQ-01. 8 . 8.制备权利要求2所述发酵剂的方法,其特征在于,将权利要求1所述的类肠膜魏斯氏菌LCW-28活化,将活化后得到的菌液经离心、收集沉淀后,在沉淀中加入缓冲液和冷冻保护剂得到重悬液,将重悬液经真空冷冻干燥处理得到发酵剂。8. the method for preparing the described starter of claim 2, it is characterised in that the described Weisseria enteroides LCW-28 of claim 1 is activated, the bacterium liquid obtained after activation is centrifuged, collects precipitation, A buffer solution and a cryoprotectant are added to the precipitation to obtain a re-suspension, and the re-suspension is subjected to vacuum freeze-drying to obtain a starter. 9.根据权利要求8所述的方法,其特征在于,所述缓冲液为0.1~0.3M磷酸盐缓冲液和/或0.5~1%的生理盐水和/或双蒸水,冷冻保护剂为10~20%的甘油和/或8~12%的海藻糖。9. The method according to claim 8, wherein the buffer is 0.1~0.3M phosphate buffer and/or 0.5~1% normal saline and/or double distilled water, and the cryoprotectant is 10 ~20% glycerol and/or 8-12% trehalose. 10.权利要求1所述类肠膜魏斯氏菌或权利要求2所述发酵剂,或权利要求3~6任一所述方法在发酵酱油中的应用。10 . The Weissella enterica of claim 1 , the starter of claim 2 , or the application of any one of the methods of claims 3 to 6 in fermented soy sauce. 11 .
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