A kind of Corynebacterium glutamicum and its application
A technology of Corynebacterium glutamicum and polyhydroxyalkanoate, which is applied in the field of microorganisms and can solve problems such as synthetic limitations
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Embodiment 1
[0020] The identification of embodiment 1 bacterial strain
[0021] Corynebacterium glutamicum was isolated from Wuxi landfill plant. This strain grows well on LBG medium. The composition of LBG medium is 1% peptone, 0.5% yeast powder, 0.5% NaCl, pH 7.0-7.2. The colonies are round, beige, with neat edges. The 16S rDNA gene sequence of this Corynebacterium glutamicum strain was homologously compared with the bacterial 16S rDNA gene sequence in NCBI, and it was found that this strain had the closest similarity to the reported Corynebacterium glutamicum ATCC13869. The bacterium was preserved in the China Center for Type Culture Collection on June 1, 2016, and the preservation number is CCTCC NO: M 2016303.
Embodiment 2
[0022] Example 2 Extraction and determination of intracellular propionyl-CoA and acetyl-CoA of strain CCTCC NO: M 2016303 of the present invention
[0023] 1. Cell culture
[0024] After culturing with the seed medium for 18 hours, transfer to the fermentation medium according to 1% inoculation amount, and after culturing for 24 hours, take the fermentation sample;
[0025] 2. Extraction of Intracellular Propionyl-CoA and Acetyl-CoA
[0026] Take 1mL of mid-log phase fermentation broth, centrifuge at 10,000rpm, 0oC for 30s to collect the cells, wash the cells twice with ice-cold 0.9% saline, wash with 1mL of solution I (methanol: acetonitrile: water = 45:45:10, v / v / v) resuspend the cells, and add 0.1M formic acid to quench; then, the quenched bacterial suspension was sonicated for 5 minutes at 0oC, centrifuged to remove cell debris and other precipitates, and the supernatant was filtered to obtain propionyl-CoA and acetyl-CoA extract for liquid mass spectrometry.
[0027] 3...
Embodiment 3
[0035] Example 3 Application of bacterial strains of the present invention in PHBV synthesis
[0036] 1. Construction of recombinant engineering bacteria WM001 / pDXW-8-phaCAB
[0037] (1) Taking Eutropha rosenbergii genome NC_008313.1 as a template, primers phaCAB-F / phaCAB-R were used to amplify the phaCAB gene cluster, and the sequence of the primer phaCAB-F / phaCAB-R for amplifying the phaCAB gene cluster was
[0038] phaCAB-F: 5'-CTGGAATTCAGAAGGAGAATCAAATCATGGCGACCGG-3'
[0039] phaCAB-R: 5'-CCGCTCGAGAGGTCAGCCCATATGCAGG-3'
[0040] (2) Digest the PCR product with restriction endonucleases EcoRI and XhoI, carrier pDXW-8 (for the construction method of the carrier pDXW-8, refer to the application number 200910233618.1, and the name of the invention is a kind of Escherichia coli-coryneform bacteria shuttle type induction expression carrier pDXW -8 and the patent application for its construction method) were digested with EcoRI and XhoI, and after purification of the digested p...
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