Preparation and application of ribonucleic acid (RNA) polymerase mutant for highly yielding antifungal substance Iturin A
A technology of RNA polymerase and mutants, applied in the field of screening of RNA polymerase mutants, can solve the problems of restricting the production and promotion of microbial pesticides, and low content of active ingredients
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[0029] 1. Screening of RNA polymerase mutants
[0030] Activation of the strain
[0031] The wild-type Acinetobacter baumannii LCH0606 (WT) and its RNA polymerase mutant were inoculated in 4 mL / tube of LB liquid medium with a 1% inoculum amount, activated at 37°C and 120 rpm for 48 hours, and then inoculated with the same Quantity and culture conditions for secondary activation in 8 LB liquid medium, cultivated for 24h.
[0032] Preparation of rifampicin-containing plates
[0033] Add the rifampicin solution to the LB solid medium at 50-60°C to a final concentration of 50 μg / mL, which is the rifampicin-containing plate.
[0034] Will The secondary activation seed solution (8 test tubes) prepared in , was evenly spread on the plate containing rifampicin according to the amount of 200 μL / dish, cultured in the dark at 37°C for 2 days, and the colonies were observed after 2 days, which was the possible mutation of RNA polymerase A total of 78 mutants were screened.
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