从棒状链霉菌中克隆对克拉维酸具有正调控作用的基因claR。构建了claR的重组质粒pSET152-claR,通过接合转移将重组质粒pSET152-claR转入了野生型S.clavuligerus中,通过pSET152-claR中的attP位点整个质粒插入到S.clavuligerus基因组中的attB位点,实现了S.clavuligerus基因组DNA中增加一个拷贝claR基因的目的,所得突变株S.clavuligerus∷claR通过发酵培养,HPLC检测克拉维酸产量为原产量的1.86倍。

Clavulanic acid positive regulation gene claR of Streptomyces clavuligerus was cloned.claR expression plasmid pSET152-claR was constructed and transformed into S.clavuligerus by conjugation.The attP site in pSET152-claR could inserted into attB site of S.clavuligerus.Thus an extra copy of claR was inserted into the chromosome of S.clavuligerus.The obtained mutant S.clavuligerus: claR was cultured in the shaken flask,and the production of clavulanic acid was analyzed by HPLC,the yield of clavulanic acid was 1.86 times compared with S.clavuligerus.