Strain of saccharomycopsis fibuligera for producing 3-methylthio propanol as well as culture method and application of strain of saccharomycopsis fibuligera
A technology of methylthiopropanol and buckle capsule lamination, which is applied in the field of microorganisms to achieve the effects of increasing production, optimizing ingredients and culture conditions
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0044] Example 1 Separation of Saccharomyces fornicata Y1402
[0045] Yeast strains were isolated from Daqu powder using traditional microbial isolation methods, and the specific method was as follows: Take 1 g of crushed and mixed Daqu powder and dilute it 10 times with sterile water. In a sterile environment, the bacterial solution gradient was diluted to 10 -5 、10 -6 and 10 -7 . Spread 0.1 mL of each serial dilution on a YPD plate and incubate at 30°C for 2 days. Pick a single colony with white protrusions and opaque yeast morphology, and streak it on the YPD plate to obtain pure yeast, and save it in a glycerol tube for future use.
[0046] The yeast screened from Daqu was inoculated in YPD medium and activated at 28°C and 180 r / min for 24 h. According to the inoculum amount of 0.2%, inoculate the seed liquid of the three activated yeast strains into the sterilized 3-methylthiopropanol transformation medium, and put them in a shaker with a temperature of 30 °C and a r...
Embodiment 2
[0050] Example 2 Identification of Saccharomyces fornicata Y1402
[0051] Gained vesicle complex membrane yeast ( Saccharomycopsis fibuligera ) The identification of Y1402 includes the following steps:
[0052] Step 1: Morphological Characterization
[0053] In order to identify the yeast strains involved, the following morphological characteristics were observed:
[0054] Yeast colony morphology observation: Inoculate the yeast in YPD liquid medium and culture for 24-48 h, inoculate the activated strain into the WL differential medium with a three-section line, and place it in a constant temperature and humidity incubator at 30°C for static After culturing for 48 h, the colony morphology was observed at the end of the culture. The colony morphology of strain Y1402 on WL differential medium is as follows: figure 1 As shown in a, the colony is white, with circular protrusions, and the colony is small. The color of the medium where the strain grows changes from blue-green t...
Embodiment 4
[0096] Example 4 Growth characteristics of yeast Y1402
[0097] The present invention relates to the growth characteristics of the vesicle complex membrane yeast, which is characterized in that the steps are as follows:
[0098] Step 1: Temperature Tolerance
[0099] Using YPD medium as the base medium, the activated bacterial solution was inoculated into YPD medium at an inoculum amount of 0.2%, at temperatures of 20°C, 25°C, 30°C, 35°C, 40°C, 45°C, OD was measured by turbidity method after cultured at 50°C and 180 r / min for 48 hours 560 . Turbidity method: Put the fermentation broth in a cuvette, use a spectrophotometer to detect the optical density of the fermentation broth at a wavelength of 560nm, and the measured OD value can be used to reflect the concentration of bacteria. The result is as image 3 As shown in a, the strain involved in the present invention cannot grow when the temperature is higher than 40°C, and its optimum growth temperature is 25°C.
[0100] S...
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