Strain of saccharomycopsis fibuligera and application thereof
A technology for decapsulating and laminating, yeast, applied in the application, biochemical equipment and methods, organic fertilizers and other directions, can solve the problem of α-amylase activity, protease activity is not disclosed to produce other enzymes and the size of enzyme activity, and the variety of enzymes produced is rich. and high enzyme activity, acid resistance of undisclosed strains, etc., to achieve the effect of improving the quality of fruits and vegetables, high enzyme activity, and vigorous growth.
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[0070] Example 1 Separation, purification, screening and identification of yeast Y-1
[0071] 1) Separation and purification: accurately weigh 10g of the distiller's grain sample taken from the natural accumulation and fermentation of Wuliangye Group in Yibin City, Sichuan Province, and add it to a sterile triangular flask with glass beads containing 100mL of cooled sterile water, and shake it on a 200r / min shaker Mix for 30 minutes, let stand for 5 minutes, draw 1 mL of supernatant, and dilute sequentially to obtain 10 -1 -10 -5 Concentration, select 10 -1 , 10 -2 , 10 -3 , 10 -4 , 10 -5 Use a pipette to draw 100μL of each gradient suspension, and spread it evenly on the YPD plate with streptomycin sulfate. The final concentration of Streptomyces sulfate in the medium is 30μg / mL. Bacterial water control, put the plate upside down in an incubator, culture at 30°C for 7 days, and repeat 3 sets of each treatment setting level. According to the shape, size, surface structure, edge st...
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[0112] Example 2 Low pH Tolerance Test of Saccharomyces cerevisiae Y-1
[0113] (1) Method: Pick an appropriate amount of Sporangium sphaerocephala Y-1 cells into YPD liquid medium, culture with shaking at 30°C and 180rpm for 48h to obtain the seed solution, and then connect the seed solution to different inoculation ratios at 0.5%. pH value (1.5, 2.0, 2.5, 3.0, 3.5, 4.0, 4.5, 5.0, 5.5, 6.0, 6.5) sterilized YPD liquid medium in the Erlenmeyer flask, each pH value is three replicates, and the non-inoculation is Blank control, 30℃, 180r / min shaking culture for 48h, observe whether the bacterial liquid in the Erlenmeyer flask is turbid and turbidity at each pH, and measure the bacterial activity of the turbid bacterial liquid;
[0114] (2) Test results: Except for the pH value of 1.0, 1.5, 2.0 and the CK group bacteria liquid is still clear, other YPD liquid media with different pH (2.5-6.5) are all turbid, indicating that the yeast Y-1 It can grow in the range of pH 2.5-6.5, and t...
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[0115] Example 3 Solid State Fermentation of Spore Spore Y-1
[0116] (1) Strain activation: Use an inoculating loop to pick up an appropriate amount of Dimosporium frondosa Y-1 and streak it on a PDA plate medium, and cultivate at 30°C for 48 hours;
[0117] (2) Preparation of the first-level seed solution: use an inoculating loop to pick up an appropriate amount of activated Sporangium saccharomyces cerevisiae Y-1 and inoculate it in YPD liquid medium, shake culture at 30°C and 200 rpm for 24 hours to obtain the first-level seed solution;
[0118] (3) Preparation of secondary seed liquid: inoculate the primary seed liquid into YPD liquid medium again according to the inoculation amount of 1% (v / v), shake culture at 30°C and 180 rpm for 36 hours to obtain secondary seed liquid;
[0119] (4) Solid-state fermentation research:
[0120] ① Mixing: According to the formula of solid fermentation medium A, first use 500mL tap water to mix glucose, peptone, (NH 4 ) 2 SO 4 , NaH 2 PO 4 , MgSO 4...
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