Saccharomyces strain for degrading organic acids and application of saccharomyces strain
A technology of yeast strains and organic acids, applied in the direction of yeast-containing food ingredients, fungi, and methods based on microorganisms, which can solve problems such as poor taste
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Embodiment 1
[0024] Example 1 Screening and Identification of a Yeast Strain Degrading Organic Acids
[0025] The gene sequence of the dominant strain that efficiently degrades organic acids in berries is shown in the sequence table SEQ ID NO.1; the dominant strain is similar to Zygosaccharomyces ( Zygosaccharomyces bisporus ) has the closest genetic distance and the best homology, combined with the strain's morphological characteristics and physiological and biochemical tests, it can be judged that the strain is Zygomyces dispora ( Zygosaccharomyces bisporus ); the dominant strain was deposited in the China Center for Type Culture Collection in Wuhan, Hubei Province on December 16, 2020, with the preservation number CCTCC M 2020912. The screening and identification methods of strains are as follows:
[0026] 1. Separation and purification of bacteria
[0027] Take 4.9g of yeast extract powder peptone glucose agar medium and dissolve it in 100mL of distilled water, put it in an autocl...
Embodiment 2
[0059] Example 2 Degradation of Organic Acids in Berries by Dominant Strains
[0060] Determination conditions of high performance liquid chromatography for degrading the organic acids of L. indigo and Seabuckthorn by dominant strains: chromatographic column Agilent ZORBAX Extend-C18 (250 mm × 4.6 mm), gradient elution with methanol-0.1% phosphoric acid aqueous solution (see Table 2), volume The mobile phase with a ratio of 97.5:2.5 was eluted for 10 minutes, and then the methanol phase reached 100% with a short time gradient and equilibrated for 5 minutes, and then the mobile phase was adjusted to 0.1% phosphoric acid solution-methanol volume ratio of 97.5: 2.5, equilibrate for 5 min. The flow rate was 0.7 mL / min, the injection volume was 20 μL, the column temperature was 40 °C, and the detection wavelength was 210 nm. Measure the standard series and samples in turn.
[0061] Draw a standard curve with the concentration of the standard sample versus the peak area, and calcu...
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