Durairaj M, Doran J L, Jensen S E
Department of Microbiology, University of Alberta, Edmonton, Canada.
Appl Environ Microbiol. 1992 Dec;58(12):4038-41. doi: 10.1128/aem.58.12.4038-4041.1992.
The pcbC gene, which encodes isopenicillin N synthase (IPNS), was subcloned from Streptomyces clavuligerus into Escherichia coli by using the pT7 series of plasmid vectors. The polymerase chain reaction was used to introduce an NdeI site at the translation initiation codon of pcbC, allowing the gene to be inserted behind an E. coli type of ribosome binding site. This construction directed high-level expression of IPNS, but the IPNS was in an inactive form in inclusion bodies. Active IPNS was recovered by solubilizing and renaturing the protein.
编码异青霉素N合成酶(IPNS)的pcbC基因,通过使用pT7系列质粒载体从棒状链霉菌亚克隆到大肠杆菌中。利用聚合酶链反应在pcbC的翻译起始密码子处引入一个NdeI位点,使该基因能够插入到大肠杆菌型核糖体结合位点之后。这种构建方式指导了IPNS的高水平表达,但IPNS以无活性形式存在于包涵体中。通过使蛋白质溶解和复性回收了活性IPNS。