A strain of Ormer Kodak yeast degrading patulin and its application
A patulin and yeast technology, applied in the field of microorganisms, can solve the problems of unsatisfactory control effect of patulin and great influence of environmental factors, etc.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0010] Embodiment 1: Omer Kodak yeast ( K. ohmeri ) Screening method for HYJM34
[0011] A total of 58 strains of yeasts collected from seabed silt, seawater and some marine organisms in the vast sea area of China were preserved in this laboratory for cultivation. Inoculate 100 μL of activated yeast fermentation broth into 10 mL of YPD liquid medium containing 10 μg / mL of patulin (add hydrochloric acid to adjust the pH to 4.0), add 100 μL of sterile water to the blank, and culture on a shaking table at 28 °C. After 24 h, it was centrifuged at 4000 r / min for 10 min, and the content of patulin in the supernatant was determined by high performance liquid chromatography.
[0012] By comparing the degradation rate of patulin by various marine yeasts, a strain with strong degradation ability to patulin was screened out, and the degradation rate of patulin could reach 95.19% after 24 hours. According to the 26S rRNA sequence analysis, the strain was Saccharomyces americana.
Embodiment 2
[0013] Embodiment 2: Affect Omer Kodak yeast ( K. ohmeri ) HYJM34 degrading factors of patulin
[0014] For the preserved Omer Kodak yeast ( K. ohmeri ) HYJM34 were cultured, and the cells were collected by centrifugation (4000 r / min, 10 min, 4 ℃). (1) Resuspend the bacteria in 5 mL of citric acid-disodium hydrogen phosphate buffer (pH 4.0) containing 10 μg / mL of patulin, and adjust the concentration of the bacteria suspension to 1.0×10 8 CFU / mL. Cultivate at different temperatures (20°C, 25°C, 28°C, 30°C, 35°C, 40°C) at 100 r / min for 18 h; (2) Resuspend the bacteria in 5 mL of In citric acid-disodium hydrogen phosphate buffer (pH 2.0, 3.0, 4.0, 5.0, 6.0, 7.0, 8.0), adjust the concentration of the bacterial suspension to 1.0×10 8 CFU / mL. Cultivate at 35°C and 100 r / min for 18 h; (3) Resuspend the bacteria in 5 mL of citric acid-disodium hydrogen phosphate buffer (pH 4.0) containing 10 μg / mL of patulin, and adjust the concentration of the bacteria suspension respective...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More