A method for improving alcohol tolerance of yeast by utilizing lactic acid bacteria
A technology of yeast and lactic acid bacteria, applied in the field of bioengineering, can solve problems such as affecting food production efficiency, inhibiting cell survival, growth and fermentation activity, yeast poisoning, etc., to improve alcohol tolerance, improve growth performance, and high survival. rate effect
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example 1
[0014] Example 1: The lactic acid bacteria Tetragenococcus halophilus CGMCC 3792 added to yeast Zygosaccharomyces rouxii Mixed culture in CGMCC 3791 culture system for 4 h. After alcohol treatment, the number of yeast colonies counted on the YPD agar medium with 0.01% chloramphenicol was added, and the survival rate was calculated ( figure 1 ).
[0015] Take the lactic acid bacteria and yeast glycerol tube storage solutions stored at -80 °C respectively, inoculate 5 mL of lactic acid bacteria medium and yeast medium according to 20% of the inoculum, and inoculate them at 30 °C for 24 hours. The inoculum was transferred to 100 mL of lactic acid bacteria medium and yeast medium, and cultured at 30 °C for 24 h. The two cultures were centrifuged at 10,000 rpm and 4°C for 5 min to collect bacteria, and resuspended in 4 mL of sterile water. Take 0.5 mL of yeast suspension to inoculate into the mixed culture medium, and then add 1 mL of lactic acid bacteria suspension to the ...
example 2
[0016] Example 2: Yeast Zygosaccharomyces rouxii CGMCC 3791 pure culture. After alcohol treatment, the number of yeast colonies counted on the YPD agar medium was calculated to calculate the survival rate ( figure 1 ).
[0017] Take the yeast glycerol storage solution stored at -80 °C, inoculate it into 5 mL of yeast medium according to 20% of the inoculum, inoculate it at 30 °C for 24 hours, and then transfer it to 100 mL of yeast according to 5% of the inoculum. Bacteria culture medium, 30 ℃ static culture for 24h. The seed solution was centrifuged at 10,000 rpm and 4 °C for 5 min to collect the bacterial cells, resuspended in 4 mL of sterile water, and 0.5 mL of it was inoculated into 30 mL of mixed culture medium, and cultured at 30 °C for 4 h. . Take 2 mL of culture medium into two 5 mL EP tubes, centrifuge at 10,000 rpm and 4 °C for 5 min, and discard the supernatant. Then, 4 mL of normal saline and 4 mL of normal saline containing 8% (v / v) alcohol were added resp...
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