High-resistant yeast strain and preparation method thereof
A yeast strain, high-tolerance technology, applied in the field of bioengineering, can solve problems such as blanks, achieve good resistance to high sugar, improve the level of production technology, and promote the effect of popularization and application
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Embodiment 1
[0037] Example 1: Construction of High Temperature Resistance, High Sugar Resistance, Freezing Resistance Baker's Yeast Strain
[0038] (1) Construction of recombinant plasmid Yep-KPS
[0039] The construction process of the recombinant plasmid Yep-KPS is as follows: figure 1 shown;
[0040] Using the total DNA of yeast strain CICC31616 as a template, PCR amplified the complete sequence of the SNR84 gene;
[0041] Upstream primer S1: 5'-GGA AGATCT ATTGCACAACTTAAGTTTGTCGAGG-3' (SEQ ID NO: 2);
[0042] Downstream primer S2: 5'-GGA AGATCT TAATGTGTCTCTTTGAGTCATGTTCCTT-3' (SEQ ID NO: 3); the underlined part is the restriction site;
[0043] PCR reaction conditions: 95°C for 5min; 94°C for 40s, 54°C for 1min, 72°C for 40s, 30 cycles; 72°C for 10min, 0.8% agarose gel electrophoresis to identify the amplified product;
[0044] The PCR product was connected to the pUC-PGK1 vector containing a strong promoter to obtain pUC-PGKS; using pUC-PGKS as a template, PCR amplification obta...
Embodiment 2
[0053] Example 2: Fermentation experiment of high temperature resistant, high sugar resistant, and freezing resistant baker's yeast strains
[0054] (1) High temperature tolerance experiment of recombinant strains and starting strains
[0055] A ring of yeast cells was picked and cultured in YEPD liquid medium to exponential phase (OD 660 =1–1.5); cells were transferred into 5mL fresh YEPD liquid medium, and the cell OD was adjusted with YEPD liquid medium 600 After = 1.0, take 200 μL of cell culture solution into a 1.5 mL centrifuge tube, heat shock in a water bath at 52°C for 2 min, and immediately ice-bath. After the cells are cooled, take 50 μL of the cell culture and dilute to a certain concentration, and at the same time, dilute the unheated yeast cells to the same multiple, spread them on the YEPD plate and culture them for 2 days, count the number of single colonies, and record them as u 1 , u 2 . Cell survival rate at high temperature (%) = (u 1 / u 2 )×100%.
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