A strain of Saccharomyces cerevisiae with low fusel oil production and its application
A technology of Saccharomyces cerevisiae and fusel oil, which is applied in the field of microorganisms, can solve problems such as easy to get on the head and large reaction, and achieve the effect of improving the quality of liquor, improving the reaction after drinking, and improving the quality of liquor
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Embodiment 1
[0017] Example 1 Screening of Saccharomyces cerevisiae strains with low fusel oil production
[0018] 1. Separation and screening of high-yielding wine yeast from fermented grains of Jinpai Maotai Town Liquor Industry
[0019] Material: Jin brand Moutai Town Liquor Industry's down to six rounds of fermented fermented grains
[0020] YPD medium: 10g of yeast powder; 20g of glucose; 20g of peptone; 20g of sodium propionate; 1g of penicillin; Put the bottle in a 121°C sterilizer for 30 minutes and cool it down for later use.
[0021] TTC upper medium: liquid A: glucose 5g; agar 15g; water 900mL. Solution B: 100 mL of 0.5% TTC aqueous solution. Liquid A and liquid B were sterilized in a 121°C autoclave for 30 minutes, cooled to 60°C, mixed and used immediately.
[0022] Separation and purification of yeast: Take 5g of fermented grains sample and add 95ml of sterilized distilled water, put it in a shaker at 150r / min and shake it for 30min, put the shaken bacterial suspension in...
Embodiment 2
[0054] Example 2 Identification of Saccharomyces cerevisiae Y267 strain
[0055] 1.18S rDNA sequence analysis
[0056] (1) DNA extraction
[0057] collect bacteria, Soil Genome DNA Extraction Kit for DNA extraction.
[0058] (2) 18S rDNA fragment amplification of Saccharomyces cerevisiae Y267
[0059] Using the extracted Saccharomyces cerevisiae DNA as a template, the fungal 18S rDNA universal primers 18S-P1 and 18S-P2 were used to amplify 18S rDNA fragments. The amplification reaction system is 30 μl, in which Premix Taq TM (TaKaRa Taq TM Version 2.0plusdye) 15 μl, ddH2O 13 μl, primers 18S-P1 and 18S-P2 each 0.5 μl, DNA template 1 μl. Amplification reaction conditions: 94°C for 5min; 94°C for 30s; 55°C for 50s, 72°C for 30s, 32 cycles; 72°C extension for 10mim, 4°C storage.
[0060] (3) 18S rDNA sequence analysis
[0061] The amplified 18S rDNA fragment was sent to Wuhan BGI for sequencing, and the corresponding 18S rDNA amplification sequence results were obtained ...
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