A method for efficiently inhibiting photosynthetic bacteria from phototaxis and adherent liquid to cultivate photosynthetic bacteria
A technology for photosynthetic bacteria and liquid culture, applied in the field of microbiology, can solve problems such as unfavorable large-scale and high-efficiency liquid culture, serious phototaxis adherence, etc., and achieve the effects of inhibiting phototaxis adherence, improving light transmittance, and simple operation.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0050] Adopt formula 1 to add xanthan gum to prepare, refer to above-mentioned " containing 0.3% xanthan gum photosynthetic bacteria medium preparation " method, add reagent from formula 2 to formula 1, adjust the consumption of xanthan gum to prepare containing 0.05% (w / v), 0.25% (w / v), 0.35% (w / v) and 0.50% (w / v) xanthan gum purple sulfur bacteria culture medium, correspondingly subpackaged to the blue cap culture bottle of 500mL (blue Cover culture bottles filled with liquid (the total volume is 530mL), each bottle is filled with 500mL medium, sterilized and cooled to room temperature; In the blue cap bottle, the inoculum amount accounts for 3.0% (v / v) of the total volume (530mL), and then fill up the blue cap culture bottle with the same medium, seal it with a cap, shake well, and its total volume is 530mL. Each treatment was repeated in 3 bottles, and the culture medium without xanthan gum (ie, the culture medium prepared in Formula 1) was used as a control.
[0051] Th...
Embodiment 2
[0054] Use formula 1 to add gelatin to prepare, with reference to the above-mentioned " containing 0.3% carrageenan photosynthetic bacteria culture medium preparation " method, fixation medium changes gelatin from carrageenan, adjusts the consumption preparation of gelatin containing 0.05% (w / v), 0.3% ( w / v) and the purple sulfur bacteria culture medium of 0.50% (w / v) gelatin;
[0055] Inoculate the suspension of marine pigmented bacteria YL28, and use the culture bottle without gelatin as the control. Inoculum size, culture temperature, time and light intensity are carried out according to the corresponding method of embodiment one, the mensuration of adherent biomass, suspended biomass and total biomass, and adherent rate (r%), suspension rate (r%) and The calculation method of the percentage (r%) of the total biomass is carried out according to the method described in Example 1.
[0056] Effects of gelatin on the adherence, suspension and total biomass of the marine chromo...
Embodiment 3
[0058] Formula 1 is prepared by adding carrageenan, referring to the method of "preparation of photosynthetic bacteria medium containing 0.3% carrageenan", adjusting the amount of carrageenan, and preparing a mixture containing 0.05% (w / v), 0.10% (w / v), 0.25% (w / v), 0.3% (w / v) and 0.50% (w / v) carrageenan culture medium for purple sulfur bacteria;
[0059] Inoculate the suspension of YL28 bacteria of marine pigmented bacteria, and use the culture bottle without carrageenan as the control. Inoculum size, culture temperature, time and light intensity are carried out according to the corresponding method of embodiment one, the mensuration of adherent biomass, suspended biomass and total biomass, and adherent rate (r%), suspension rate (r%) and The calculation method of the percentage (r%) of the total biomass is carried out according to the method described in Example 1.
[0060] Effects of carrageenan on the adherence, suspension and total biomass of the marine chromogener YL28 ...
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