Preparation method and application of flavobacterium and flavobacterium secreta
A technology of flavonoids and secretions, applied in the field of microorganisms, can solve the problems of insufficient control of red tide and low number of algae-lytic bacteria.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0021] The invention provides a method for preparing the secretion of Flavobacterium, the method comprising:
[0022] Step 1. Cultivate the Flavobacterium in the medium for at least 24 hours, centrifuge the medium, take the supernatant, filter, and sterilize the filtered supernatant at 110-120°C;
[0023] Preferably, the culture time is 24-72 hours. The sterilization temperature is 121°C. The formula of the medium is: 5-6g / L peptone, 1-1.5g / L yeast extract, 0.1-0.2g / L ferric phosphate and 10-12g / L agar powder, wherein the solvent is old sea water. The pH value of the medium is 7.6-7.8.
[0024] Step 2: removing polysaccharides in the sterilized supernatant, desalting, separating, and evaporating to dryness to obtain secretions.
[0025] Further, step two specifically includes:
[0026] Inoculate the Flavobacterium species into the sterile liquid medium, and culture it for at least 48 hours at 23-26° C. with a shaker speed of 150-200 rpm.
[0027] Collect the fermentation ...
Embodiment
[0032] 1. Isolation of Flavobacterium
[0033] 1) Akashiwo sanguinea (Akashiwo sanguinea) was cultured for 30 days under continuous light at 22°C with a light intensity of 3000 Lx using the culture medium to obtain algae liquid with a cell concentration of 2×104cells / mL.
[0034] Among them, the composition of the medium is 5 mg of NaH 2 PO 4 .H 2 O, 75mg NaNO3 , 0.22mg ZnSO 4 .7H 2 O, 0.01 mg CoCl 2 .6H 2 O, 0.18 mg MnCl 2 .4H 2 O, 0.006mg NaMoO 4 .2H 2 O, 4.36 mg Na 2 EDTA.2H 2 O, 3.15 mg FeCl 2 .6H 2 O, 0.01 mg CuSO 4 .5H 2 O, 0.1mg of vitamin B 1 , 0.5ug of vitamin B 12 , 0.1ug of Biotin (H) was dissolved in aged sea water to a volume of 1L. Hakata algae was provided by the Marine Algae Species Laboratory of Jinan University.
[0035] 2) Water samples were collected from the sea area of Dongshan, Shenzhen, where the red tide broke out, using high-temperature sterilized glass bottles with blue caps, and transferred to a refrigerator at 4°C within 2 hour...
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