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Avermectin C5-O-甲基转移酶基因的克隆、序列分析及其基因置换

Study on C5-O-methyltransferase gene cloning, sequencing and replacement

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【作者】 朱浩君郑应华

【Author】 Zhu Hao jun 1 and Zheng Ying hua 2 (1 Institute of life Science and Technology, Huazhong Agriculture University, Wuhan 430070; 2 Beijing Institute of Biomedicine, Beijing 100091)

【机构】 华中农业大学生命科学院北京生物医药研究所 武汉430070北京100091

【摘要】 C5 O 甲基转移酶基因 (aveD)位于阿维链霉菌 (Streptomycesavermitilis)染色体 3 4kbBamHI的片段上 ,通过构建avermectin基因组约 3 4kbBamHI片段的亚基因文库 ,用PCR的方法获得该基因的连锁基因C5 酮基还原酶基因 (aveF) ,并作为探针筛出aveD的克隆子。测序后和GenBank做同源比较 ,结果一致。构建基因置换穿梭载体 pHJ5 80 3 (pHZ13 5 8∷aveD&Amr) ,通过ET12 5 67::pUZ80 0 2属间接合转移导入S .avermitilis。放松培养后筛选出双交换重组菌株 ,并用PCR验证重组菌株的aveD已经破坏 ,将重组菌株摇瓶发酵液提取avermectin进行色谱质谱联机分析 ,发现重组菌株仅产生 4个组分 ,与出发菌株的 4个B组分完全一致。

【Abstract】 C5 O methyltransferase gene is a key gene that is involved in biosynthesis of avermectin A. C5 O methyltransferase gene was cloned from the sub library constructed by the pool of 3 4kb Bam HI DNA fragment of Streptomyces avermitilis chromosome by using C5 ketoreductase gene as the probe.The sequence analysis indicated that the cloned gene was identical to the C5 O methyltransferase gene in S.avermitilis . The gene replacement vector, pHJ5803 (apra+), was constructed and introduced into S.avermitilis by conjugation. The gene replacement strain Bjbm0006, which no longer produce the avermectin A, was obtained and confirmed.

  • 【文献出处】 中国抗生素杂志 ,Chinese Journal of Antibiotics , 编辑部邮箱 ,2003年01期
  • 【分类号】Q78
  • 【被引频次】18
  • 【下载频次】181
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