A kind of Saccharomyces cerevisiae with high production of c6-c10 ethyl ester and its construction method and use

A technology of C6-C10 and Saccharomyces cerevisiae, which is applied in the breeding of industrial microorganisms, Saccharomyces cerevisiae producing C6-C10 ethyl ester and its construction, can solve the problems of high grain consumption, affecting the yield of raw materials, and low efficiency of high-grade wine

A technology of C6-C10 and Saccharomyces cerevisiae, which is applied in the breeding of industrial microorganisms, Saccharomyces cerevisiae producing C6-C10 ethyl ester and its construction, can solve the problems of high grain consumption, affecting the yield of raw materials, and low efficiency of high-grade wine

CN110804561BActive Publication Date: 2021-04-09TIANJIN UNIV OF SCI & TECH
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  • A kind of Saccharomyces cerevisiae with high production of c6-c10 ethyl ester and its construction method and use
  • A kind of Saccharomyces cerevisiae with high production of c6-c10 ethyl ester and its construction method and use
  • A kind of Saccharomyces cerevisiae with high production of c6-c10 ethyl ester and its construction method and use

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0102] Example 1: Construction of high-yielding C6-C10 ethyl ester Saccharomyces cerevisiae strain

[0103]The starting strain used in this example is Saccharomyces cerevisiae CA in Angelia yeast, and the strain preservation number is CGMCCNo.18670. The Escherichia coli DH5a was purchased from Takara Company. The YPD medium is a general complete medium, and the solid medium contains 2% imported agar powder.

[0104] The main construction process of the strain is as follows:

[0105] (1) Enhancing the synthesis of acetyl-CoA to produce C6-C10 ethyl ester Saccharomyces cerevisiae strain

[0106] Using the genome of yeast strain CA as a template and Gal80 as an integration site, PCR amplification with a primer pair of GA-U (SEQ ID NO:9) and GA-D (SEQ ID NO:10) yielded a 549bp TEF1 with a promoter P The upper homology arm GA segment of the homology region; use the primer pair GB-U (SEQ ID NO: 11) and GB-D (SEQ ID NO: 12) PCR amplification to obtain a size of 502bp with the scre...

Embodiment 2

[0148] Embodiment 2: Corn mash fermentation experiment of producing C6-C10 ethyl ester Saccharomyces cerevisiae strain

[0149] 1) The specific fermentation process is: corn flour→soaking→liquefaction→saccharification→cooling→inoculation→fermentation→steaming wine→determining indicators;

[0150] 2) Process conditions

[0151] Soaking conditions: 60-70°C, soaking for 20 minutes; liquefaction conditions: 85-90°C, adding high-temperature-resistant α-amylase, liquefying for 90 minutes; saccharification conditions: 55-60°C, adding glucoamylase, saccharifying for 20 hours;

[0152] 3) Ingredients: 1500g corn flour, 4500mL water, let stand for 20min, high temperature resistant α-amylase 2×10 4 U / mL, 0.9ml, glucoamylase 1×10 5 U / mL, 3mL.

[0153] 4) Culture medium configuration

[0154] Primary seed medium: 8°Brix corn hydrolyzate, add 0.5% yeast extract powder, aliquot 5mL into test tubes, boil for 10min to sterilize.

[0155] Secondary seed medium: 12°Brix corn hydrolyzate, ad...

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Abstract

The invention discloses a Saccharomyces cerevisiae with high yield of C6-C10 ethyl ester, its construction method and application, and belongs to the technical field of bioengineering. The present invention strengthens the synthesis of acetyl-CoA by overexpressing acetaldehyde dehydrogenase ALD6 and acetyl-CoA synthetase ASC1 in the starting strain, overexpressing acetyl-CoA carboxylase ACC1** strengthens malonyl-CoA, overexpression Expression of fatty acid synthases FAS1 and FAS2 strengthened medium-chain acyl-CoA, making the metabolic flow more to medium-chain acyl-CoA, and further exogenously introduced the alcohol acyltransferase gene SAAT in strawberry to obtain the modified strain C‑ald6acs1A*F1F2S, which in Under fermentation conditions, the yield of ethyl hexanoate was 7.53mg / L, which was 2.72 times that of the starting strain C-ald6acs1A*F1F2, and 26.89 times (only 0.27mg / L) that of the original starting strain CA ethyl hexanoate. The yields of ethyl caprylate and ethyl caprate were 13.65mg / L and 13.89mg / L respectively, 9.11 times and 7.27 times higher than that of the original starting strain CA, which has potential application in improving the flavor and quality of wine prospect.

Description

Technical field: [0001] The invention belongs to the technical field of bioengineering and relates to the breeding of industrial microorganisms, in particular to a C6-C10 ethyl ester producing Saccharomyces cerevisiae and its construction method and application. Background technique: [0002] Ester aroma substances are the main flavor substances in wine. The higher ester content not only endows it with an important ester aroma, but also can effectively expand and relax nerves and reduce the side effects caused by drinking. C6-C10 ethyl ester refers to ethyl caproate, ethyl caprylate and ethyl caprate. C6-C10 ethyl esters are the important aroma substances of all aroma-type Chinese liquors, especially the characteristic aroma substances of Luzhou-flavor liquors and wines. Ethyl caproate, ethyl caprylate, and ethyl caprate had pineapple, apple, and fatty acid odors, respectively. Because Saccharomyces cerevisiae lacks the corresponding acyl-CoA and lacks specific alcohol acy...

Claims

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Application Information

Patent Timeline
09 Apr 2021
Publication
CN110804561B
IPC
C12N1/19; C12N15/81; C12G3/021; C12G1/022; C12J1/04; A23L27/50; C12R1/865
CPC
A23L27/50; C12G1/0203; C12G2200/11; C12J1/04; C12N9/0008; C12N9/1029; C12N9/93; C12N15/52
Inventors
陈叶福; 李洁