Chlorella preservation method
A technology for chlorella and culture containers, which is applied in the field of chlorella preservation, can solve the problems of increased labor costs and pollution risks, degradation of good properties of algae species, and harsh storage conditions, so as to facilitate batch preservation, facilitate management and The effect of maintenance and long storage time
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0024] Take Chlorella minutissima as the test algae strain, add it to the Erlenmeyer flask containing 100mL of growth medium, illuminance 6000lx, 24h continuous light, temperature 26℃, shaking culture under the conditions of 150rpm, the color of the culture solution can be observed Gradually turn green to dark green, and enter the logarithmic growth phase after 5 days.
[0025] Take the algae liquid of Chlorella minutis in the logarithmic growth phase for microscopic examination, and after confirming that there is no miscellaneous bacteria, draw 5 μL of the algae liquid and drop it on the middle position of the agar plate medium in the corresponding well of the 96-well culture plate (the same 96-well plate Different wells of the culture plate can store different chlorella species at the same time, just mark it with a marking pen on the front or back culture plate corresponding to the well). Place the 96-well culture plate filled with agar plate medium on a shaker for 3 minutes...
Embodiment 2
[0035] Take Chlorella pyrenoidosa as the test algae strain, add it to the Erlenmeyer flask filled with 100mL growth medium, and shake it under the conditions of 4000lx illumination, 24h continuous illumination, temperature 22°C, and 180rpm, and the culture medium can be observed The color gradually turns green to dark green, and it enters the logarithmic growth phase after 7 days.
[0036]Take the algae liquid of Chlorella pyrenoidosa in the logarithmic growth phase for microscopic examination. After confirming that there is no miscellaneous bacteria, draw 5 μL of algae liquid and drop it on the middle position of the agar plate medium in the corresponding well of the 96-well culture plate (the same 96-well culture plate). Different wells of the well culture plate can preserve different chlorella species at the same time, and can be marked with a marking pen on the front or back culture plate corresponding to the well). Place the 96-well culture plate filled with agar plate me...
experiment example 3
[0046] The number of live algae cells of Chlorella microella preserved by the method of Example 1 and the biomass of algae cells in the activated algae liquid were used as indicators to evaluate the preservation effect of the preservation method of Example 1 on Chlorella microminis.
[0047] Under aseptic conditions, the Chlorella microella preserved for 3 months, 6 months, 9 months and 12 months by the preservation method of Example 1 was scraped, added to sterile water, and made into algae liquid, and the flat algae was used to The counting method was used to measure the density of living algae in the algae liquid, and three parallel control groups were set up for each experiment. Calculate the average value of the algal cell survival rate, and the determination method refers to "Industrial Microbiology Experimental Technology Manual" (China Light Industry Press, 1997). Adopt the preservation method of embodiment 1 to preserve Chlorella microella after 3 months, 6 months, 9 ...
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