Recombinant streptomyces ansochromogenes, preparation method thereof and use thereof
A technology of Streptomyces chromogenes and recombinant bacteria, applied in biochemical equipment and methods, recombinant DNA technology, microbial-based methods, etc., can solve the problem that it is difficult to obtain full-length gene clusters, and achieve increased yield and increased yield Effect
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Embodiment 1
[0031] Embodiment 1, the construction of the recombinant plasmid pNIK containing nikkomycin biosynthesis gene cluster
[0032] 1. Preparation of recombinant cosmids containing nikkomycin biosynthesis gene cluster fragments
[0033] Streptomyces chromogenes 7100 CGMCC 4.321 (purchased from the General Microorganism Center of China Microbiological Culture Collection Management Committee), its spores are in the shape of silk hooks, or coils, and rarely coils; the spores are spherical or oval.
[0034] Genomic DNA was extracted from Streptomyces chromogenes 7100 CGMCC 4.321, digested with Sau3AI, separated by pulse electrophoresis, and a 40-50kb DNA fragment was recovered. At the same time, the cosmid supercos1 (Stratagene) was digested with BamHI (Sau3AI homologous enzyme), After dephosphorylation and recovered DNA fragments with T 4 DNA ligase linking, transforming Escherichia coli XL 1-blue MR (Stratagene) to obtain a recombinant cosmid library containing a fragment of the nik...
Embodiment 2
[0043] Embodiment 2, the construction of nikkomycin engineering bacteria
[0044] 1. The acquisition of the recombinant Streptomyces ansochromogenes (Streptomyces ansochromogenes) transferred to the recombinant plasmid pNIK
[0045] The recombinant plasmid pNIK containing the entire nikkomycin biosynthetic gene cluster can be used to increase the copy number of the nikkomycin biosynthetic gene cluster on the Streptomyces chromogenes genome, since the recombinant plasmid pNIK can be integrated in the chromogenic The Streptomyces genome replicates along with the chromosome, so the nikkomycin high-yielding engineered bacteria constructed with this plasmid are genetically stable. The specific method is as follows:
[0046] The recombinant plasmid pNIK was transferred into E.coli ET12567 (John Innes Institute, Norwich, UK) to remove the restriction modification, and apramycin was used as a selection marker, and the recombinant plasmid pNIK was transferred into the Streptomyces chr...
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