Two-component regulatory system mutant gene yvrH of bacillus subtilis and application thereof
A Bacillus subtilis, mutant gene technology, applied in the field of biotechnology and molecular biology, can solve the problem that there is no high-yielding strain of Bacillus subtilis two-component regulatory system mutant gene riboflavin, so as to improve the ability and genetic background Clear, build-up level effects
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Embodiment 1
[0020] Example 1: Construction of the starting strain B.subtilis BUK and the basic operation plasmid pSS for screening the Bacillus subtilis system without antibiotic markers
[0021] The starting strain B. subtilis BUK used in the present invention is derived from B. subtilis168, and the basic operation plasmid pSS is derived from pUC18. For the detailed construction process of the two, please refer to published document 1.
[0022] The present invention does not limit the construction method of the basic operation plasmid pSS and the selection of the resistance gene.
Embodiment 2
[0023] Embodiment 2: Construction process of engineering bacterial strains B.subtilis RC1 and B.subtilis RC2
[0024] (1) The operation process of introducing the gene mutation ribC* (G596A) into the genome of the strain B. subtilis BUK without trace is as follows:
[0025] Using ribC*-F-U, ribC*-F-L and ribC*-B-U, ribC*-B-L two pairs of primers, using the B. subtilis168 genome as a template, using KOD-plus high-fidelity DNA polymerase to amplify the size of 894bp and 928bp respectively The upstream and downstream homology arms of ribC*-F and ribC*-B. After the PCR fragment of ribC*-F was recovered by gel cutting, it was digested with Thermo Fast digest AatII and XhoI, connected and transformed into plasmid pSS to obtain plasmid pSS-ribC*-F. After the PCR fragment of ribC*-B was recovered by gel cutting, it was double digested with Thermo Fast digest SalI and ScaI, ligated and transformed into plasmid pSS-ribC*-F to obtain the plasmid pSS-ribC*-FB. The plasmid with the corre...
Embodiment 3
[0028] Example 3: Construction of engineering strain B. subtilis RC3 (introduction of Bacillus subtilis two-component regulatory system mutant gene yvrH (G665A))
[0029] Using two pairs of primers yvrH*-F-U, yvrH*-F-L and yvrH*-B-U, yvrH*-B-L, using the B.subtilis168 genome as a template, using KOD-plus high-fidelity DNA polymerase to amplify the size of 1067bp and 849bp respectively The upstream and downstream homology arms of yvrH*-F and yvrH*-B. The PCR fragment of yvrH*-F was recovered by cutting the gel, and was digested with Thermo Fast digest AatII and XhoI. After ligation and transformation of plasmid pSS, plasmid pSS-yvrH*-F was obtained. After the PCR fragment of yvrH*-B was recovered by cutting the gel, it was double digested with Thermo Fast digest SalI and KpnI, ligated and transformed into plasmid pSS-yvrH*-F to obtain plasmid pSS-yvrH*-FB. The plasmid with the correct sequencing result was transformed into Bacillus subtilis B. subtilis RC2 through Spizizen trans...
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