Ribonucleoside reductase transcription inhibition factor mutant, mutation gene and application of ribonucleoside reductase transcription inhibition factor mutant and mutation gene to preparation of vitamin B2
A technology of transcriptional inhibitors and ribonucleotides, which is applied in the biological field, can solve problems such as ribonucleotide reductase transcriptional inhibitors mutants, and achieve great application value and improve the effect of ability
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Embodiment 1
[0029] Embodiment 1: bacterial strain CGMCC NO.16132 and BS168 ribC m Perform comparative genomic analysis
[0030] strain BS168 ribC m (For the specific construction process, please refer to Chinese patent application 201910604170.3), the genome was used as the reference genome, and the strain CGMCC NO. 16132 was sent to Jinweizhi Biotechnology Co., Ltd. for whole-genome resequencing and differential analysis to find out the effect on vitamin B production. 2 Ability-affected genes. Through sequence comparison analysis, it was found that the strain CGMCC NO. 16132 had a large number of mutations, including a total of 338 mutation sites: after mutation 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 involv...
Embodiment 2
[0032] Embodiment 2: Construct containing wxya mutant strain
[0033] by Bacillus subtilis Chromosome 168 was used as a template, primers UPnrdR-F and UPnrdR-R (including DR) were used to amplify the UPnrdR (including DR) fragment with adapter, and primers araR-F and araR-R (including DR) were used to amplify the araR with adapter ( DR) fragment; use the pC194 plasmid as a template, use primers cat-F, cat-R to amplify the cat fragment with linker; use the chromosome of strain CGMCC NO. 16132 as a template, use primer nrdR m -F, nrdR m -R amplifies nrdR with a point mutation m Fragment, wherein the mutated wxya The nucleotide sequence is shown in SEQ ID No.2, and the encoded amino acid sequence is shown in SEQ ID No.4.
[0034] Take UPnrdR fragment, cat fragment, araR fragment and nrdR m Fragment as template, use primers UPnrdR-F, nrdR m -R for fusion PCR to obtain the assembly fragment UCR-nrdR m , was detected correctly by nucleic acid electrophoresis, and purified...
Embodiment 3
[0043] Example 3: Evaluation of B vitamins in different strains 2 production capacity
[0044] 1. Strain culture conditions:
[0045] Will start strain BS168 ribC m , and engineering strain BS168 nrdR 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 OD 600 and vitamin B 2 Yield.
[0046] , OD of different strains 600 and vitamin B 2 Yield Comparison
[0047] with th...
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