[Objective] Cloning of a new gene possessing a function of Echinocandin B (ECB) side-chain deacylation from a wild type Streptomyces strain NCPC-1020 of soil source. [Methods] Using degenerate PCR and TAIL PCR strategy, we successfully cloned the target gene, which was heterologously expressed in S. lividans TK24, then a whole-cell catalysis method was developed to dectect the deacylation activity of ECB deacylase by LC-MS. [Results] The ECB deacylase gene was cloned and its function was confirmed. [Conclusion] Combined the two PCR techniques, degenerate and TAIL PCR, a new gene could be cloned quickly. The obtain of the new ECB deacylase gene lays a good foundation for the researches on semibiosynthetic of ECB related drugs.
XU Dong-Mei, KE Ai-Bing, LU Xin-Hua, CHEN Wen-Qing, DENG Zi-Xin. Molecular cloning and functional analysis of a gene encoding echinocandin B deacylase from Streptomyces sp. NCPC-1020[J]. Microbiology China, 2014, 41(8): 1564-1573
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