Gntr family transcriptional repressor mutants, mutant genes and their role in the production of vitamin b 2 application in
A technology of transcriptional repressors and mutants, which is applied in the field of preparation of vitamin B2, can solve the problems that there are no GntR family transcriptional repressor mutant genes, etc., and achieve great application value and the effect of improving ability
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Embodiment 1
[0029] Example 1: Strains CGMCC NO.16132 and BS168 ribC m Perform comparative genomic analysis
[0030] strain BS168 ribC m (Refer to Chinese patent application 201910604170.3 for the specific construction process) The genome is used as the reference genome, and the strain CGMCC NO.16132 is sent to Jinweizhi Biotechnology Co., Ltd. for whole-genome resequencing and differential analysis, in order to find out the ability to produce vitamin B2. Gene. Through sequence comparison analysis, it was found that a large number of mutations occurred in the strain CGMCC NO.16132, which contained a total of 338 mutation sites: after mutation data statistics, a total of 72 genes were involved in the mutation. Mutations in the coding region involved a total of 59 genes, including 8 synonymous mutations, 41 non-synonymous mutations, 2 nonsense mutations, 5 frameshift mutations, and 3 non-frameshift mutations; mutations in non-coding regions A total of 13 genes were involved.
[0031] Rem...
Embodiment 2
[0032] Embodiment 2: construct the bacterial strain containing ytrA mutant
[0033] Using Bacillus subtilis 168 chromosome as template, primer UPytrA m -F, UPytrA m -R (with DR) to amplify UPytrA with adapter and point mutation m (DR-containing) fragment, use primers araR-F, araR-R (containing DR) to amplify the araR (containing DR) fragment with adapter; use pC194 plasmid as template, use primers cat-F, cat-R to amplify the fragment with adapter The cat fragment of the bacterial strain CGMCC NO.16132 is used as a template, and the downstream homology arm fragment DNytrA is amplified with primers DNytrA-F and DNytrA-R, wherein the nucleotide sequence of the mutated ytrA is as SEQ ID No.2 As shown, the encoded amino acid sequence is shown in SEQID No.4.
[0034] with UPytrA m Fragment, cat fragment, araR fragment and DNytrA fragment as templates, use primer UPytrA m -F, DNytrA-R fusion PCR, get the assembly fragment UCR-ytrA m , was detected correctly by nucleic acid elec...
Embodiment 3
[0042] Example 3: Evaluation of B vitamins in different strains 2 production capacity
[0043] 1. Strain culture conditions:
[0044] Will start strain BS168 ribC m , and engineering strain BS168 ytrA m Under sterile conditions, the LB solid plate containing 25 mg / L erythromycin was streaked with an inoculation needle, and cultured upside down in a 37°C incubator for 24 hours to obtain freshly activated single colonies. Pick a single colony with an inoculation needle and streak the LB solid slope containing 25 mg / L erythromycin, and culture it in a 37°C incubator for 48 hours. Scrape 1 / 3 of the bacterial lawn on the inclined surface and inoculate it into a 500mL baffled Erlenmeyer flask containing 70mL of fermentation medium (3 parallels for each strain of bacteria), shake culture at 37°C and 200rpm for 41h, then take the fermentation broth to measure OD600 and vitamin B 2 Yield.
[0045] 2. OD600 and vitamin B of different strains 2 Yield Comparison
[0046] with the s...
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