Fruit wine yeast with high yield of glutathione and application of fruit wine yeast
A technology of glutathione and fruit wine yeast, which is applied in the field of bioengineering, can solve problems such as human health hazards, and achieve the effects of strong tolerance, low browning value, and soft and pure taste
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Embodiment 1
[0045] Embodiment 1: Determination of growth curve of yeast strain
[0046] Add a ring of yeast into 100mL of sterilized YPD liquid medium, culture at 28°C and shake at 150rpm for 24h, sample 5mL every 2h, and measure the absorbance of each tube of bacterial liquid at a wavelength of 600nm with a spectrophotometer (with Uninoculated YPD culture solution for blank test), if the concentration of bacteria is too high, dilute it with distilled water before measuring. Taking culture time as abscissa, OD 600 As the ordinate, draw a growth curve to determine the logarithmic growth period, such as figure 1 shown.
Embodiment 2
[0047] Embodiment 2: yeast mutagenesis
[0048] (1) Determination of mutagenesis time
[0049] The mutagenesis starting strain was activated in YPD medium for 18 hours, inserted into liquid medium, and cultured for 14 hours. Take 5 mL of logarithmic growth phase bacterial liquid, centrifuge and wash twice with sterile saline, restore to the original volume, and transfer to a magnetic field. In a stirred sterile petri dish, irradiate for a certain period of time under a UV lamp with a power of 15W and a distance of 35cm. The irradiated bacterial suspension was properly diluted in a sterile room under the condition of avoiding light (operating under red light), and then coated with 1.0g / L zinc chloride plate. The plates were placed upside down in a 30°C incubator and incubated in the dark for 2 days. After the bacteria grow on the plate, the lethality of ultraviolet mutagenesis at each time is calculated according to the number of bacteria. When the lethality is 70%, the mutag...
Embodiment 3
[0052] Embodiment 3: yeast performance comparison
[0053] The bacterial strain is inoculated into the seed medium, and after 24 hours of shaker culture, it is inoculated into the fermentation medium with 10% inoculation amount, and cultivated for 30 hours at a temperature of 30° C. and a rotational speed of 150-200 r / min. Using the biomass and extracellular GSH content of yeast as indicators, the glutathione-producing ability of different yeast screened after mutagenesis was compared, and the results are shown in Table 1. The number Y-11 is the Saccharomyces cerevisiae of the present invention, and the preservation number is CCTCCNO: M2015544. The total amount of GSH can reach 106mg / L, and the extracellular content reaches 66% of the total amount. The more extracellular secretion, the more the fermentation broth The greater the content in the fermentation broth, the greater the antioxidant effect of glutathione in the fermentation broth.
[0054] Simultaneously, the present ...
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