Acid-resistant saccharomyces cerevisiae and application thereof in high-acidity fruit fermented wine
A technology of Saccharomyces cerevisiae and main fermentation, applied in the field of brewing engineering, which can solve the problems of lack of Saccharomyces cerevisiae, low pH during fermentation, insufficient flavor, etc., and achieve the effects of shortened brewing cycle, high acid tolerance and rich aroma
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0059] Example 1: Screening and Identification of Saccharomyces cerevisiae ET005-c54 Starting Strains
[0060] Specific steps are as follows:
[0061] 1. Screening and identification of wild Saccharomyces cerevisiae
[0062] Saccharomyces cerevisiae was screened from green plums and soil samples from different geographical locations in the green plum production area of Zhaoan County, Fujian Province. The colonies were initially classified and identified by observing the shape and color, and further tested through alcohol production, gas production, test tube fermentation, and acid resistance. The strains were screened, and finally 10 strains of S. cerevisiae with relatively good fermentation performance were selected for further screening and preserved in our laboratory, named YT012, YT018, YT021, ET005, ET016, ET023, SM003, SM007, SM008, SM012.
[0063] 2. The 10 strains of Saccharomyces cerevisiae obtained in step 1 and the purchased 10 strains of commercial Saccharomyces...
Embodiment 2
[0074] Example 2: Obtaining of Saccharomyces cerevisiae ET005-c54
[0075] 1. Mutagenesis of Saccharomyces cerevisiae starting strain ET005 using an atmospheric pressure and room temperature plasma mutagenesis instrument
[0076] Specific steps are as follows:
[0077] (1) Pick a ring from the plate and inoculate the starting strain ET005 of Saccharomyces cerevisiae obtained in Example 1 into a 250mL Erlenmeyer flask containing 50mL liquid seed medium, and culture it statically at 30°C for 10-12h, so that the bacteria grow logarithmically Expect. Take 1mL logarithmic growth phase bacteria solution to measure its OD 600 , according to OD 600 and the general relationship between the number of colonies to estimate the bacterial concentration, at this time OD 600 0.8, take 1 mL of the bacterial solution and centrifuge at 12000r / min for 2min, collect the bacterial cells, wash with sterile saline 2 to 3 times, and dilute it to 10 7 cfu / mL bacterial suspension.
[0078] (2) Tak...
Embodiment 3
[0095] Embodiment 3: Saccharomyces cerevisiae (Saccharomyces cerevisiae) ET005-c54 performance verification
[0096] 1. Acid resistance test:
[0097] Place ET005-c54 in the selection medium of pH 1.5, pH 2.0, and pH 2.5 respectively, culture on a shaker at 30°C for 72 hours, and measure its OD with a microplate reader 600 . Such as Figure 6 As shown, ET005-c54 has good growth performance in the environment of pH 2.5, therefore, it proves that it has better acid resistance.
[0098] The mutant strain ET005-c54 and the starting strain ET005 were inoculated into the pH 2.5 selection medium and cultivated to OD 600 was about 0.8, and the bacterial cells were collected and observed using a cold field emission scanning electron microscope (cFE-SEM). Such as Figure 7 As shown, at pH 2.5, the mutant strain ET005-c54 was oval and round, with smooth surface without wrinkles, obvious budding and bud scars, most of them were single cells, and there was no adhesion between cells; w...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com