Pichia kudriavzevii and multifunctional complex microbial inoculant and use thereof

Abstract

The present disclosure discloses a Pichia kudriavzevii and a multifunctional complex microbial inoculant and use thereof, and belongs to the technical field of bioengineering. The Pichia kudriavzevii of the present disclosure has a degrading ability of lactic acid as high as 12.69 g.Math.L.sup.−1, which is 2.04 times that of a type strain. At the same time, the strain can also metabolize ethanol and has an OD.sub.600 of 4.48 after fermentation in a sorghum juice medium at 30° C. and 200 rpm for 3 d. The Pichia kudriavzevii could completely consume 58 g.Math.L.sup.−1 of glucose in the sorghum juice medium after 60 h of fermentation and produce 13.06 g.Math.L.sup.−1 of ethanol. The Pichia kudriavzevii degrades lactic acid and can relieve a lactic acid pressure of a fermentation system and enable Saccharomyces cerevisiae to grow and metabolize to produce wine. In addition, the strain and the microbial inoculant thereof can inhibit the production of filamentous fungi and geosmin and have important use prospects for maintaining homeostasis of a fermentation system and food preservation.

Claims

1. A method for degrading lactic acid, comprising using a Pichia kudriavzevii DC-16 or a microbial preparation containing the Pichia kudriavzevii DC-16 as a fermentation agent to degrade lactic acid in a fermentation process; and wherein the Pichia kudriavzevii DC-16 has been deposited in the China General Microbiological Culture Collection Center on Jan. 13, 2020 and has a deposit number of CGMCC NO. 19337.

2. The method according to claim 1, wherein fermentation in the fermentation process is conducted by using a sorghum juice medium as a fermentation medium.

3. The method according to claim 1, wherein the Pichia kudriavzevii DC-16 is inoculated into lactic acid-containing sorghum juice medium and cultured at 28-32° C. and 180-220 rpm for 60-100 h.

4. A method for degrading lactic acid, comprising using a Pichia kudriavzevii DC-16 and a Saccharomyces cerevisiae DC-3, or a microbial preparation containing the Pichia kudriavzevii DC-16 and the Saccharomyces cerevisiae DC-3 as a fermentation agent to degrade lactic acid in a fermentation process; wherein the Pichia kudriavzevii DC-16 has been deposited in the China General Microbiological Culture Collection Center on Jan. 13, 2020 and has a deposit number of CGMCC NO. 19337; and the Saccharomyces cerevisiae DC-3 has been deposited in the China General Microbiological Culture Collection Center on Jan. 13, 2020 and has a deposit number of CGMCC NO. 19336.

5. The method according to claim 4, wherein the fermentation agent is inoculated into the culture medium, lactic acid is added, and culture is conducted at 28-32° C. and 180-220 rpm for 60-100 h.

6. The method according to claim 5, wherein the medium is a sorghum juice medium.

7. The method according to claim 4, wherein the Pichia kudriavzevii DC-16 and the Saccharomyces cerevisiae DC-3 both have an initial inoculation concentration of 10.sup.7-10.sup.8.Math.mL.sup.−1.

8. The method according to claim 4, wherein the Pichia kudriavzevii DC-16 and the Saccharomyces cerevisiae DC-3 have an inoculation concentration ratio of 1:1.

9. Use of a Pichia kudriavzevii DC-16 or a microbial preparation containing the Pichia kudriavzevii DC-16, comprising adding Pichia kudriavzevii DC-16 or a microbial preparation containing the Pichia kudriavzevii DC-16 in preparing food fermentation, food preservation, ecological restoration or odor suppression; and the Pichia kudriavzevii DC-16 has been deposited in the China General Microbiological Culture Collection Center on Jan. 13, 2020 and has a deposit number of CGMCC NO. 19337.

10. The use according to claim 9, wherein the food fermentation or food preservation comprises the processes of wine brewing, sake fermentation, cheese production, dough fermentation and soybean sauce preparation.

11. The use according to claim 9, wherein the ecological restoration or ordor suppression is inhibiting odorin or Streptomyces in the environment.

12. The use according to claim 9, wherein the food fermentation or food preservation comprises maintaining yeast homeostasis or pH stability in an industrial fermentation process.

Description

BRIEF DESCRIPTION OF FIGURES

[0028] FIG. 1A shows growth curves of an experimental strain and a type strain under 20 g L.sup.−1 lactic acid;

[0029] FIG. 1B shows growth curves of an experimental strain and a type strain under 30 g L.sup.−1 lactic acid;

[0030] FIG. 1C shows growth curves of an experimental strain and a type strain under 40 g L.sup.−1 lactic acid;

[0031] FIG. 1D shows specific growth rates of an experimental strain and a type strain under different concentrations of lactic acid;

[0032] FIG. 2A shows a comparison of lactic acid consumption of an experimental strain and a type strain under 20 g L.sup.−1 lactic acid;

[0033] FIG. 2B shows a comparison of lactic acid consumption of an experimental strain and a type strain under 30 g L.sup.−1 lactic acid;

[0034] FIG. 2C shows a comparison of lactic acid consumption of an experimental strain and a type strain under 40 g L.sup.−1 lactic acid;

[0035] FIG. 2D shows lactic acid consumption amount of an experimental strain and a type strain under different concentrations of lactic acid;

[0036] FIG. 3A shows a comparison of lactic acid consumption rates of an experimental strain and a type strain under 20 g L.sup.−1 lactic acid;

[0037] FIG. 3B shows a comparison of lactic acid consumption rates of an experimental strain and a type strain under 30 g L.sup.−1 lactic acid;

[0038] FIG. 3C shows a comparison of lactic acid consumption rates of an experimental strain and a type strain under 40 g L.sup.−1 lactic acid;

[0039] FIG. 4 shows a growth curve of a Pichia kudriavzevii DC-16;

[0040] FIG. 5A shows glucose consumption amount of a strain DC-16 under different times;

[0041] FIG. 5B shows ethanol production amount of a strain DC-16 under different times;

[0042] FIG. 6 shows a comparison of biomass of mono-culture (Pichia kudriavzevii DC-16) and co-culture (Pichia kudriavzevii DC-16 and Saccharomyces cerevisiae DC-3) under lactic acid stress;

[0043] FIG. 7A shows a comparison of ethanol production amount of mono-culture (Pichia kudriavzevii DC-16) and co-culture (Pichia kudriavzevii DC-16 and Saccharomyces cerevisiae DC-3) under lactic acid stress;

[0044] FIG. 7B shows a comparison of ethanol production rates of mono-culture (Pichia kudriavzevii DC-16) and co-culture (Pichia kudriavzevii DC-16 and Saccharomyces cerevisiae DC-3) under lactic acid stress;

[0045] FIG. 8A shows a comparison of lactic acid consumption of mono-culture (Pichia kudriavzevii DC-16) and co-culture (Pichia kudriavzevii DC-16 and Saccharomyces cerevisiae DC-3) under lactic acid stress;

[0046] FIG. 8B shows a comparison of lactic acid consumption rates of mono-culture (Pichia kudriavzevii DC-16) and co-culture (Pichia kudriavzevii DC-16 and Saccharomyces cerevisiae DC-3) under lactic acid stress;

[0047] FIG. 9 shows use of a Pichia kudriavzevii DC-16 and a microbial inoculant thereof in a production process of soy sauce-aroma baijiu;

[0048] FIG. 10 shows an effective inhibitory effect of Pichia kudriavzevii DC-16 on mold outbreak during a baijiu fermentation process;

[0049] FIG. 11 shows an inhibitory effect of a Pichia kudriavzevii DC-16 on Streptomyces albus;

[0050] FIG. 12A shows an effect of a Pichia kudriavzevii DC-16 inoculant on geosmin (the content of geosmin in rind and core of Daqu) in a cultivation process of Daqu;

[0051] FIG. 12B shows an effect of a Pichia kudriavzevii DC-16 inoculant on Streptomyces albus (the content of Streptomyces albus in rind and core of Daqu) in a cultivation process of Daqu;

[0052] FIG. 13 shows an inhibitory effect of a Pichia kudriavzevii DC-16 on common filamentous fungi;

[0053] FIG. 14A shows an antifungal activity of volatile organic compounds produced by a Pichia kudriavzevii DC-16 inoculant; Pichia and Monascus are inoculated to prepare a double-dish system; and a dispersal distance of the Monascus on no-control sorghum extract agar and on a sorghum medium with the Pichia (+Pichia) in the double-dish system is determined daily;

[0054] FIG. 14B shows an antifungal activity of volatile organic compounds produced by a Pichia kudriavzevii DC-16 inoculant; effects of the Pichia on a radial growth and a growth rate of Monascus; and a dispersal distance of the Monascus on no-control sorghum extract agar and on a sorghum medium with the Pichia (+Pichia) in the double-dish system is determined daily; and

[0055] FIG. 15 shows effects of Pichia kudriavzevii on ethanol metabolism during a fermentation process; and Control (normal fermentation group): Pichia kudriavzevii as a dominant microorganism; and defect (abnormal fermentation group): filamentous fungi as a dominant microorganism.

DETAILED DESCRIPTION

[0056] (I) Medium

[0057] Enrichment medium: 40 g L.sup.−1 of lactic acid, 50 g L.sup.−1 of glucose, 20 g L.sup.−1 of peptone, 10 g L.sup.−1 of yeast extract, 2 g L.sup.−1 of dipotassium hydrogen phosphate, 1 g L.sup.−1 of sodium chloride, 0.1 g L.sup.−1 of magnesium sulfate and 0.05 g L.sup.−1 of manganese sulfate.

[0058] Screening medium: 40 g L.sup.−1 of lactic acid, 50 g L.sup.−1 of glucose, 20 g L.sup.−1 of peptone and 10 g L.sup.−1 of yeast extract.

[0059] Sorghum juice medium: adding amylase into sorghum and water at a ratio of 1:4 (M:V) for cooking and liquefaction, adding a saccharifying enzyme for saccharification at 60° C., filtering and centrifuging, and adjusting the sugar content to 7° Bx.

[0060] (II) Method for Detecting Content of Lactic Acid

[0061] A fermentation broth is filtered through a 0.22-μm organic-phase syringe filter and a filtrate is transferred to a liquid-phase vial. Chromatographic column: Bio-Rad Aminex HPX-87H Ion Exclusion Column and column temperature: 60° C.; detector: UV detector (PDA) and detection wavelength: 210 nm; and mobile phase: 5 mmol L.sup.−1 H.sub.2SO.sub.4 and flow rate: 0.6 mL.min.sup.−1.

[0062] (III) Method for Detecting Content of Ethanol

[0063] A fermentation broth is filtered through a 0.22-μm organic-phase syringe filter and a filtrate is transferred to a liquid-phase vial. Chromatographic column: Bio-Rad Aminex HPX-87H Ion Exclusion Column and column temperature: 60° C.; detector: differential refractive index detector (RID); and mobile phase: 5 mmol L.sup.−1 H.sub.2SO.sub.4 and flow rate: 0.6 mL.min.sup.−1.

Example 1

Screening of Strain

[0064] During a fermentation process of soy sauce-aroma baijiu, a strain of lactic acid-resistant Pichia kudriavzevii was obtained. A process was as follows.

[0065] A sample of fermented grains of a soy sauce-aroma baijiu was collected. 10 g of the sample was weighed and put into a 250-mL conical flask, 90 mL of sterile normal saline was added, glass beads were added and even shaking was conducted. 0.1 mL of a supernatant was pipetted into 100 mL of an enrichment medium, culture was conducted at 30° C. and 200 rpm for 2-4 d, and whether the culture medium was turbid or not was observed; if the culture medium was obviously turbid, 0.1 mL of the enrichment medium was pipetted to 100 mL of a new liquid screening medium, culture was conducted at 30° C. and 200 rpm for 2 d, after culturing for 3-4 times, the medium was diluted on YPD solid medium in a gradient manner, and after culturing for 3-4 d, single colonies were a target strain with an anti-lactic acid property.

[0066] Seven single colonies were randomly selected from a plate and inoculated into a sorghum juice liquid medium containing 40 g.Math.L.sup.−1 of lactic acid and a pH was adjusted to 3.5. Fermentation was conducted at 30° C. and 200 rpm for 3 d. The lactic acid concentration in the fermentation broth was determined and one strain had the highest amount of degrading lactic acid at 12.69 g.Math.L.sup.−1. The strain was streaked into a slant medium, stored in a glycerol tube and named DC-16.

Example 2

Identification of Strain

[0067] (1) Colony Characteristics and Cell Morphology

[0068] The colony was white, had a rough surface and uniform texture, and was easy to pick. Morphological results by microscopic observation showed that isolated and screened cells were oval and some cells were budding and dividing.

[0069] (2) Physiological and Biochemical Characteristics

[0070] DC-16 was inoculated in a sorghum juice medium, fermented at 30° C. and 200 rpm for 1 d, and entered a stationary phase. As shown in FIG. 4, the biomass OD.sub.600 of the DC-16 could reach 4.48 when fermentation for 3 d.

[0071] The glucose content in the sorghum juice medium was 58 g.Math.L.sup.−1. As shown in FIG. 5A and FIG. 5B, the DC-16 could completely consume 58 g.Math.L.sup.−1 of glucose in the sorghum juice medium after 60 h of fermentation and produce 13.06 g.Math.L.sup.−1 of ethanol.

[0072] (3) Molecular Biological Identification

[0073] The strain DC-16 was inoculated into the YPD medium and cultured for 1 d, and the total DNA of the strain was extracted as a PCR template. Yeast ITS universal primers were used for PCR amplification and the selected universal primers were ITS1 and ITS4. PCR amplification conditions: 94° C. for 5 min, 94° C. for 30 s, 55° C. for 30 s and 72° C. for 1 min, a total of 30 cycles; and 72° C. for 10 min. After passing a 1% agarose gel inspection, a PCR amplification product was sent to Suzhou JGENEWIZ Biotechnology Co., Ltd. for sequencing. The sequencing results were uploaded to the National Center for Biotechnology Information (NCBI) database for a BLAST comparison and the strain was found to be Pichia kudriavzevii.

[0074] The strain DC-16 was preliminarily identified as a Pichia kudriavzevii DC-16 by comprehensive colony morphological characteristics, physiological and biochemical characteristics and ITS sequence analysis. The strain has been deposited in the China General Microbiological Culture Collection Center whose address is No. 3, Courtyard 1, West Beichen Road, Chaoyang District, Beijing and has a deposit number of CGMCC NO. 19337.

Example 3

Degradation of Lactic Acid by Yeast of the Present Disclosure

[0075] A sorghum juice medium containing lactic acid of different concentrations was used as a fermentation medium, and an experimental strain Pichia kudriavzevii DC-16 (P.k. DC-16) and a type strain Pichia kudriavzevii ATCC 24210 (P.k. ATCC 24210) were used for a lactic acid metabolic experiment. According to detection results of lactic acid in fermented grains during a screening process, the amount of the lactic acid in the designed metabolic experiment was 20, 30, and 40 g.Math.L.sup.−1 separately.

[0076] Experimental groups and control groups were arranged as follows:

[0077] Control group 1: inoculating P.k. ATCC 24210 into a sorghum juice medium containing 20 g.Math.L.sup.−1 lactic acid at an inoculum size of 7% (v:v);

[0078] Experimental group 1: inoculating P.k. DC-16 into a sorghum juice medium containing 20 g.Math.L.sup.−1 lactic acid at an inoculum size of 7% (v:v);

[0079] Control group 2: inoculating P.k. ATCC 24210 into a sorghum juice medium containing 30 g.Math.L.sup.−1 lactic acid at an inoculum size of 7% (v:v);

[0080] Experimental group 2: inoculating P.k. DC-16 into a sorghum juice medium containing 30 g.Math.L.sup.−1 lactic acid at an inoculum size of 7% (v:v);

[0081] Control group 3: inoculating P.k. ATCC 24210 into a sorghum juice medium containing 40 g.Math.L.sup.−1 lactic acid at an inoculum size of 7% (v:v); and

[0082] Experimental group 3: inoculating P.k. DC-16 into a sorghum juice medium containing 40 g.Math.L.sup.−1 lactic acid at an inoculum size of 7% (v:v).

[0083] The type strain P.k. ATCC 24210 was purchased from the China General Microbiological Culture Collection Center and has a deposit number of CGMCC 2.1465. The sorghum juice medium containing lactic acid was adjusted to a pH of 3.5 (a pH of real fermented grains) with 5 M NaOH and the strains were inoculated into the medium at an inoculum size of 7% (v:v) and cultured at 30° C. and 200 rpm for 72 h. Samples were taken every 12 h to determine the content of lactic acid and OD.sub.600 in the fermentation broth.

[0084] The results showed that compared with the type strain P.k. ATCC 24210, the experimental strain P.k. DC-16 had a higher biomass at an end point and a faster specific growth rate. The specific results were as shown in FIG. 1A-FIG. 1C. The type strain P.k. ATCC 24210 had an end-point OD.sub.600 of 3.32, 2.90 and 2.74 separately under 20, 30, and 40 g.Math.L.sup.−1 lactic acid stress; and the experimental strain P.k. DC-16 had an end-point OD.sub.600 of 3.81, 3.49 and 3.18 separately under 20, 30, and 40 g.Math.L.sup.−1 lactic acid stress, which was 1.14, 1.20 and 1.16 times that of the type strain separately. The type strain P.k. ATCC 24210 had a specific growth rate of 0.2074, 0.1956 and 0.1936 t.sup.−1 separately under 20, 30, and 40 g.Math.L.sup.−1 lactic acid stress; and the experimental strain P.k. DC-16 had a specific growth rate of 0.2207, 0.2139 and 0.2035 t.sup.−1 separately under 20, 30, and 40 g.Math.L.sup.−1 lactic acid stress, which was 1.06, 1.09 and 1.05 times that of the type strain separately (FIG. 1D). The above results indicated that the P.k. DC-16 had a higher lactic acid tolerance and was more suitable for a production process of high-lactic acid environment.

[0085] Compared with the type strain P.k. ATCC 24210, the experimental strain P.k. DC-16 could degrade more lactic acid. The specific results were as shown in FIG. 2A-FIG. 2D. When the sorghum juice medium separately contained 20, 30, and 40 g.Math.L.sup.−1 lactic acid, the type strain P.k. ATCC 24210 could degrade 7.62, 3.80 and 6.21 g.Math.L.sup.−1 lactic acid separately; and the experimental strain P.k. DC-16 could degrade 10.48, 10.73 and 12.69 g.Math.L.sup.−1 lactic acid separately, which was 1.37, 2.83 and 2.04 times that of the type strain separately.

[0086] Compared with the type strain P.k. ATCC 24210, the experimental strain P.k. DC-16 had a higher rate for degrading lactic acid. The specific results were as shown in FIG. 3A-FIG. 3C. After 12 h of fermentation, a consumption rate of lactic acid was the highest. When the sorghum juice medium separately contained 20, 30 and 40 g.Math.L.sup.−1 lactic acid, the type strain P.k. ATCC 24210 had a lactic acid consumption rate of 0.31, 0.08 and 0.27 g.Math.L.sup.−1h.sup.'1 separately; and the experimental strain P.k. DC-16 had a lactic acid consumption rate of 0.38, 0.22 and 0.43 g.Math.L.sup.−1h.sup.−1, which was 1.24, 2.70 and 1.57 times that of the type strain separately.

Example 4

Complex Microbial Inoculant for Degrading Lactic Acid

[0087] A sorghum juice medium containing 40 g.Math.L.sup.−1 lactic acid was used as a fermentation medium and an independent or combined fermentation experiment was conducted on an experimental strain P.k. DC-16 and Saccharomyces cerevisiae DC-3 (S.c. DC-3). The Saccharomyces cerevisiae DC-3 had deposited in the China General Microbiological Culture Collection Center on Jan.13, 2020 and had a deposit number of CGMCC NO. 19336.

[0088] Control group 1: Seed liquid of P.k. DC-16 was inoculated into a sorghum juice medium with an inoculum size of a final concentration of 2×10.sup.7 cells.Math.mL.sup.−1 and 40 g.Math.L.sup.−1 lactic acid was added.

[0089] Control group 2: Seed liquid of S.c. DC-3 was inoculated into a sorghum juice medium with an inoculum size of a final concentration of 2×10.sup.7 cells.Math.mL.sup.−1 and 40 g.Math.L.sup.−1 lactic acid was added.

[0090] Experimental group: Seed liquids of P.k. DC-16 and S.c. DC-3 were inoculated into a sorghum juice medium with an inoculum size of 10′ cells.Math.mL.sup.−1 separately and 40 g.Math.L.sup.−1 lactic acid was added.

[0091] The fermentation culture was conducted at 30° C. and 200 rpm for 72 h. Samples were taken every 12 h to determine the biomass and the ethanol and lactic acid content of the two yeasts in the fermentation broth were determined.

[0092] The biomass of the P.k. DC-16 and the S.c. DC-3 during mono-culture and co-culture was shown in FIG. 6. Due to a toxic effect of high-concentration lactic acid on yeast, the biomass of the P.k. DC-16 and the S.c. DC-3 decreased in both mono-culture and co-culture at an early stage of fermentation.

[0093] When fermentation for 12 h, the P.k. DC-16 decreased from 2.0×10.sup.7 cells.Math.mL.sup.−1to 3.8×10.sup.6 cells.Math.mL.sup.−1 during mono-culture and decreased from 1.0×10.sup.7 cells.Math.mL.sup.−1 to 2.8×10.sup.6 cells.Math.mL.sup.−1 during co-culture; and the biomass of the P.k. DC-16 slowly increased and reached a highest value at 72 h, where the end-point biomass of the mono-culture was 5.7×10.sup.7 cells.Math.mL.sup.−1 and the end-point biomass of the co-culture was 5.0×10.sup.7 cells.Math.mL.sup.−1. The biomass of the P.k. DC-16 did not vary significantly between mono-culture and co-culture (P<0.05).

[0094] The S.c. DC-3 reached a minimum biomass of 7.1×10.sup.4 cells.Math.mL.sup.−1 at 48 h during the mono-culture, while reached a minimum biomass of 5.0×10.sup.5 cells.Math.mL.sup.−1 at 12 h during the co-culture due to a shortened lag phase, and the biomass remained stable afterwards. At 48 h, the S.c. DC-3 had a biomass (9.6×10.sup.5 cells.Math.mL.sup.−1) in the co-culture, which was 13 times that in the mono-culture. The above results showed that the P.k. DC-16 utilized lactic acid, thus could relieve a stress effect of the lactic acid on wine-producing yeast in a brewing system, and could better conduct subsequent alcoholic fermentation.

[0095] The S.c. DC-3 had a severely inhibited ethanol-producing ability under 40 g.Math.L.sup.−1 lactic acid stress. As shown in FIG. 7A, at the end of the fermentation, the P.k. DC-16 had the ethanol yield of 16.23 g.Math.L.sup.−1, while the S.c. DC-3 had the ethanol yield of only 4.66 g.Math.L.sup.−1. When the P.k. DC-16 and the S.c. DC-3 were co-cultured, the ethanol yield was 18.08 g.Math.L.sup.−1, which was increased compared to that in the mono-culture. As shown in FIG. 7B, an ethanol production rate of the P.k. DC-16 in the mono-culture was 0.26 g.Math.L.sup.−1h.sup.−1 at 12 h of fermentation and the ethanol production rate of the S.c. DC-3 in the mono-culture was 0.21 g.Math.L.sup.−1h.sup.−1 at 12 h of the mono-culture. The ethanol production rate was 0.42 g.Math.L.sup.−1h.sup.−1 in the co-culture, which was 1.64 and 3.64 times that of the P.k. DC-16 in the mono-culture and the S.c. DC-3 in the mono-culture separately. The co-culture of the P.k. DC-16 and S.c. DC-3 could improve the yield and the production rate of ethanol compared with the mono-culture of the single strain.

[0096] As shown in FIG. 8A, at the end of the fermentation, the P.k. DC-16 could utilize 7.20 g.Math.L.sup.−1 of lactic acid in the medium and the S.c. DC-3 could utilize 4.44 g.Math.L.sup.−1 of lactic acid. However, when the P.k. DC-16 and S.c. DC-3 were co-cultured, the content of lactic acid in the medium decreased by 13.71 g.Math.L.sup.−1 and the degrading amount of lactic acid increased significantly (P<0.01). As shown in FIG. 8B, the P.k. DC-16 had a maximum consumption rate of lactic acid at 0.16 g.Math.L.sup.−1h.sup.−1 and the S.c. DC-3 had a maximum consumption rate of lactic acid at 0.15 g.Math.L.sup.−1h.sup.−1. However, the maximum consumption rate of lactic acid was significantly increased during co-culture (0.32 g.Math.L.sup.−1h.sup.−1). This indicated that the co-culture of the P.k. DC-16 and the S.c. DC-3 could enhance the ability of the yeast to utilize the lactic acid compared with the mono-culture.

[0097] A gene IIdD encodes a lactate dehydrogenase capable of degrading lactic acid to pyruvate and is a key gene involved in degrading lactic acid. Transcription of the gene IIdD of the P.k. DC-16 and the S.c. DC-3 in the co-culture was shown in Table 1. When cultured for 12 h, only the P.k. DC-16 transcribed the gene IIdD, while the S.c. DC-3 did not transcribe the gene IIdD, indicating that when the lactic acid concentration was high, only the P.k. DC-16 was involved in degrading lactic acid. When culture was conducted for 24 h, the concentration of lactic acid in the medium decreased to 35.46 g.Math.L.sup.−1 and both the P.k. DC-16 and the S.c. DC-3 transcribed the gene IIdD, indicating that at a low concentration of lactic acid, the P.k. DC-16 and the S.c. DC-3 participated in degrading lactic acid together.

TABLE-US-00001 TABLE 1 Transcription of gene IldD of two yeast strains in co-culture Culturing time (h) P.k. DC-16 S.c. DC-3 12 + − 24 + + Note: “+” indicated that the transcription of the gene IldD was detected in the sample, while “−” indicated that the transcription of the gene was not detected.

Example 5

Use of Complex Microbial Inoculant in Reducing Lactic Acid in Fermentation Process of Baijiu

[0098] A Pichia kudriavzevii DC-16 was inoculated into a sorghum juice liquid medium and incubated at a constant temperature of 30° C. for 48 h under shaking. The strain-containing liquid medium was centrifuged at 12,000 r/min for 10 min, a supernatant was discarded, a cell precipitate of the strain was obtained and washed with sterile water for several times, and the concentration of yeast liquid was calculated by using a hemocytometer for standby use.

[0099] An experiment of use of the strain in one round of soy sauce-aroma baijiu fermentation was shown in FIG. 9. When Daqu was added into fermented grains, the strain liquid was added with the amount of 10.sup.6 CFU/kg of the fermented grains; and the same amount of distilled water was added as a control group. Each group was tested in triplets. Two groups of the fermented grains were loaded into enamel jars and buried in fermented grains subjected to stacking fermentation for in-situ fermentation, sampling was conducted at the end of the stacking fermentation, and the lactic acid content of the fermented grains was detected.

[0100] After testing, the lactic acid content in the fermented grains of the control group was 12.01 g/kg fermented grains and the lactic acid content in the fermented grains containing the Pichia kudriavzevii DC-16 was 7.55 g/kg fermented grains, and a degradation rate of lactic acid was 37.09%. At the same time, the ethanol content in the fermented grains of the control group was 15.12 g/kg fermented grains, which was not significantly different from that in the fermented grains containing the Pichia kudriavzevii DC-16. Therefore, the Pichia kudriavzevii DC-16 can tolerate and reduce the lactic acid content during a fermentation process without affecting a metabolic function of ethanol.

Example 6

Inhibition on Growth of Undesired Microorganisms by Pichia kudriavzevii DC-16 and Complex Microbial Inoculant Thereof

[0101] In order to verify an ecological regulation effect of Pichia on imbalanced flora, use of functional flora in production was further conducted. A Pichia kudriavzevii DC-16, a Saccharomyces cerevisiae DC-3 and a complex microbial inoculant with an equal proportion of the two strains were selected as compound inoculants. A team with low alcohol yield historically was selected for an adding experiment. When Daqu was added to fermented grains, the yeast strain liquid was evenly sprayed on surfaces of the fermented grains with a final amount of 10.sup.6 CFU/kg of the fermented grains; and the same amount of distilled water was added as a control group. Each group was tested in triplets. Two groups of the fermented grains were loaded into enamel jars and buried in fermented grains subjected to stacking fermentation for in-situ fermentation, sampling was conducted at the end of the stacking fermentation, and comparative analysis of a microbial structure of the fermented grains was conducted.

[0102] The results showed that the team in the experiment was abnormal and the in-situ fermented grains agglomerated more seriously. The fermented grains in an experimental group not containing Pichia also agglomerated in the enamel jar; the fermented grains in an experimental group containing Saccharomyces cerevisiae alone did not show a significant effect; while the fermented grains in an experimental group containing Pichia were loose and did not agglomerate (FIG. 10). The analysis of the microbial structure showed that the Pichia contained in the experimental group could significantly inhibit growth of filamentous fungi. The main microorganism in the fermented grains was the Pichia and had a structure similar to the microorganism in the normal fermented grains. The fermented grains in the agglomeration group were mainly composed of Monascus and showed obvious mildew and agglomeration. Combined with analysis of physical and chemical indicators, there was no significant difference in the ethanol content between the group containing Pichia and the control group, while the content of acetic acid and lactic acid could be significantly reduced, which is important for maintaining proliferation of Saccharomyces cerevisiae in fermentation of baijiu.

Example 7

Use of Complex Microbial Inoculant in Maintenance of Ecological Restoration

[0103] A complex microbial inoculant in inhibiting Streptomyces and geosmin was used as an example.

[0104] Inhibition on growth of the Streptomyces by a Pichia kudriavzevii DC-16 was determined. The growth inhibition was quantified as size of zone of inhibition, that is, a diameter ratio of zone of inhibition to colony (R zone of inhibition/R colony). The size of zone of inhibition was observed by a filter paper method of a Kirby-Bauer (K-B) test and an inhibitory effect of the Pichia kudriavzevii was preliminarily determined. As shown in FIG. 11, 100 mL of 10.sup.6 CFU/L Streptomyces was evenly spread on a plate and 10 mL of 10.sup.6 CFU/L yeast liquid was inoculated on filter paper. A result preliminarily showed that the Pichia kudriavzevii DC-16 had an inhibitory effect on Streptomyces albus in traditional Xifeng aroma Daqu.

[0105] In production of the Daqu, 6 strains of Pichia fermentans, Pichia kudriavzevii DC-16, Saccharomyces cerevisiae, Issatchenkia orientalis and Bacillus subtilis with a significant anti-microbial effect were selected and separately prepared into an anti-microbial agent with the same concentration. When raw materials of the Daqu were blended, a complex microbial inoculant was added to a final concentration of 10.sup.6 CFU/kg of the Daqu material, the material was pressed into blocks and labeled, and the blocks were put into a Daqu room for fermentation. Samples were collected on the day 0, 3, 5, 10, 15 and 20. The content of geosmin in a control group and an experimental group showed similar dynamic characteristics in rind and core of the Daqu. In the rind of the Daqu, the content of the geosmin increased rapidly in both groups in an early stage and a middle stage, fluctuated and decreased around the 15th day. But the content of the geosmin fluctuated slightly in the experimental group compared with that in the control group. The content of the geosmin was the highest in the control group on the 20th day and reached 9.75 μg/kg; and the content of the geosmin was 6.23 μg/kg in the experimental group, which is significantly lower than that of the control group (FIG. 12A). The microorganism had an average inhibitory rate of the geosmin of 14.4% in rind of Daqu and a final inhibitory rate of 36.1%.

[0106] A real-time quantitative PCR (qPCR) analysis was used to monitor the dynamic biomass of Streptomyces albus during a fermentation process. The dynamic changes of the biomass of all Streptomyces albus during the Daqu fermentation process were shown in FIG. 12B. In the rind of the Daqu, the biomass of the Streptomyces albus in the control group was 5.46 log.sub.10 (spore counts/g) at the end of the cultivation. In the experimental group, the biomass of the Streptomyces albus was 5.03 log.sub.10 (spore counts/g) at the end of the cultivation. In the core of the Daqu, the biomass of the Streptomyces albus was 4.08 log.sub.10 (spore counts/g) in the control group at the end of the cultivation. In the experimental group, the biomass of the Streptomyces albus was 4.21 log.sub.10 (spore counts/g) at the end of the cultivation. It can be seen that the geosmin-inhibiting inoculant had a better inhibitory effect on geosmin-producing Streptomyces albus in the rind of the Daqu than in the core of the Daqu, and a better inhibitory effect in the early and middle stages of the Daqu making than in the late stage of the Daqu making.

Example 8

Use of Pichia kudriavzevii DC-16 in Field of Food Preservation

[0107] Filamentous fungi are common contaminating microorganisms in a process of food preservation and can produce mycotoxins such as ochratoxin A, which are harmful to human health. A relationship between a Pichia kudriavzevii DC-16 and filamentous fungi was detected by an agar diffusion method. A piece of 5-mm sterile filter paper was placed in a middle of a PDA plate and the plate was evenly covered with 100 μL of the Pichia kudriavzevii (10.sup.6 CFU/mL). 10 μL of culture liquid of filamentous fungi was dropped onto the filter paper. In a negative control, sterile filter paper and isolated microorganisms were placed in a middle of a blank PDA plate. After incubation at 30° C. for 120 h, it was confirmed that the Pichia kudriavzevii had a strong inhibitory effect on growth of the filamentous fungi (FIG. 13).

[0108] Further analysis showed that the Pichia kudriavzevii DC-16 could produce a volatile substance (VOC)-mediated antifungal property. A double-dish system (DDS) of sorghum extract agar was used to determine whether yeast can produce VOCs to affect growth of Monascus (FIG. 14A). The antagonism was reflected in a significant reduced growth of mycelia cultured at 30° C. (P0.05). The results were shown in FIG. 14B, a growth rate of Monascus in a control group on the sorghum extract agar plate was 11.26±0.67 mmd.sup.−1; and the Pichia significantly reduced a growth rate of Monascus (4.80±1.07 mmd.sup.−1).

Example 9

Use of Pichia kudriavzevii DC-16 in Maintaining Homeostasis of Yeast

[0109] During normal baijiu fermentation, a Pichia kudriavzevii DC-16 was dominated. Abnormally fermented grains showed agglomeration and mildew. A metatranscriptome analysis was used to compare ethanol-producing enzymes and genes to verify effects of the Pichia kudriavzevii DC-16 on functions and homeostasis of yeast flora during a baijiu fermentation process (FIG. 15). In a control group, yeasts (including P. kudriavzevii, Z. bailii, Saccharomyces cerevisiae, Schizosaccharomyces cryophilus and Brettanomyces bruxellensis) were major functional contributors to produce ethanol (FPKM >100). Meanwhile, in the abnormal fermentation group, Zygosaccharomyces bailii and filamentous fungi (Aspergillus fumigatus, Aspergillus calidoustus and Penicillium expansum) had abundant ADH gene expressions (FPKM >100). ADH in different microorganisms exhibited different metabolic abilities to form ethanol, which explained variation in ethanol content between samples during production. This indicated that a Pichia-driven community was beneficial to maintain yeast diversity and ethanol metabolism.

[0110] Although the disclosure has been disclosed as above in the preferred examples, it is not intended to limit the disclosure. Any person skilled in the art can make various changes and modifications without departing from the spirit and scope of the disclosure. Therefore, the protection scope of the disclosure should be as defined in the claims.