Novel extraction process of coenzyme Q10
A new technology, coenzyme technology, applied in the direction of microorganisms, biochemical equipment and methods, organic chemistry, etc., can solve the problems of low bacterial concentration and product yield, reduced corporate profit margin, high production cost, etc., to achieve yield and purity Improvement, avoid pollution, low cost effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0024] A kind of extracting coenzyme Q from fermented liquid 10 The novel process, it comprises the steps:
[0025] 1) Rhodotorula rubra ATCC74283 (see US5474919A), Rhodobacter sphaeroides ATCC17025 (see Journal of Biological Chemistry2001, V276, No44, P41161-41164) and Paracoccus denitrificans ATCC 19367 (see J.Bacteriol.April 1996V178, No7, p1866-1871) was cultured to a concentration of 1×108 / mL bacteria solution, mixed according to the volume ratio of 1:1:2 to obtain a mixed bacteria solution, and then According to 5% (v / v) inoculum size, inoculate in fermentation medium (glucose 10g, peptone 5g, (NH 4 ) 2 SO 4 5g, KH 2 PO 4 1.0g, Na 2 HPO 4 0.5g, MgSO 4 0.5g, water 1000mL, pH 7.0), culture temperature 29°C, 100rpm shaker culture for 30 hours to obtain fermentation broth, the measured dry cell weight was 120g / L;
[0026] 2) Centrifuge the fermentation broth at 4000rpm for 30min, separate the supernatant and the bacterial cells, wash the bacterial cells until neutr...
Embodiment 2
[0031] A kind of extracting coenzyme Q from fermented liquid 10 The novel process, it comprises the steps:
[0032] 1) Cultivate Rhodotorula rubra ATCC 74283, Rhodobacter sphaeroides ATCC 17025 and Paracoccus denitrificans ATCC 19367 to a concentration of 1×10 8 Each / mL of the bacterial solution was mixed according to the volume ratio of 1:1:2 to obtain the mixed bacterial solution, and then inoculated in the fermentation medium (glucose 10g, peptone 5g, (NH 4 ) 2 SO 4 5g, KH 2 PO 4 1.0g, Na 2 HPO 4 0.5g, MgSO 4 0.5g, water 1000mL, pH 7.0), culture temperature 29°C, 100rpm shaker culture for 30 hours to obtain fermentation broth, the measured dry cell weight was 120g / L;
[0033] 2) Centrifuge the fermentation broth at 5000rpm for 30min, separate the supernatant and the bacterial cells, wash the bacterial cells until neutral, dry them at 60°C and crush them; mix the crushed bacterial cells and n-hexane in a mass ratio of 2:2 Mix, mix and extract with magnetic stirring, a...
Embodiment 3
[0038] Choose 200 piglets of 60 days, be divided into two groups, every group of 100, wherein the experimental group is raised with the feed prepared in this embodiment 1, and the matched group is fed with Tongwei medium and large pigs; same. See Table 1 for the indicators detected after 9 weeks of feeding.
[0039] Table 1
[0040] indicators
[0041] Conclusion: The feed prepared by the invention has better feeding effect, daily gain and feed-to-weight ratio are better than common pig feed in the market, and the cost is lower than that of the commercial feed.
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