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中国生物工程杂志

CHINA BIOTECHNOLOGY
中国生物工程杂志  2007, Vol. 27 Issue (12): 26-30    
研究报告     
天蓝淡红链霉菌SIPI-1482的dauW基因的克隆及在大肠杆菌中的表达
胡鹤 尚珂 胡又佳 朱宝泉 朱春宝
上海医药工业研究院 上海医药工业研究院 上海医药工业研究院 上海医药工业研究院 上海医药工业研究院
Cloning and Expression of dauW Gene from Daunorubicin-producing Streptomyces coeruleorubidus SIPI-1482
以此为准:上海中山北一路1111号创新中心201室200437
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摘要:

克隆得到了柔红霉素产生菌天蓝淡红链霉菌(Streptomyces coeruleorubidus) SIPI-1482位于dnrX下游的新基因dauW,其位于基因组上dnrX和drrB之间,GenBank中Blast发现它与dnrW有较高的同源性,将其命名为dauW,并提交GenBank获得登录号EF523565,根据保守域推测dauW所编码的蛋白属于FAD依赖的氧化还原酶类。将dauW分别克隆至表达载体pET-28a(+)、pET-32a(+),在宿主菌BL21(DE3)中经IPTG诱导后,实现了在大肠杆菌中的表达。初步实验表明dauW在BL21(DE3)中的表达能增加宿主对柔红霉素的抗性,可能与天蓝淡红链霉菌对柔红霉素的自身抗性有关。

Abstract:

A novel gene, located between dnrX and drrB in the genome of daunorubicin-producing strain Streptomyces coeruleorubidus SIPI-1482, was cloned and named as dauW. The full sequence of dauW was submitted to GenBank (Accession No.EF523565). Blast result indicated that it showed high homology with dnrW in GenBank. The exact function of dauW is as yet unknown despite the possibility that it might belong to a family of FAD-dependent oxidoreductases on the basis of conserved domain analysis. dauW was cloned into expression plasmids pET-28a(+) and pET-32a(+), respectively, and was successfully expressed in E.coli DE3 after induction with IPTG. The preliminary results of the expression of dauW suggested that it might be involved in the self resistance in Streptomyces coeruleorubidus due to the increased resistance to daunorubicin in the E.coli host.

收稿日期: 2007-09-19 出版日期: 2007-12-25
通讯作者: 朱春宝   
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引用本文:

胡鹤,尚珂,胡又佳,朱宝泉,朱春宝. 天蓝淡红链霉菌SIPI-1482的dauW基因的克隆及在大肠杆菌中的表达[J]. 中国生物工程杂志, 2007, 27(12): 26-30.

. Cloning and Expression of dauW Gene from Daunorubicin-producing Streptomyces coeruleorubidus SIPI-1482. China Biotechnology, 2007, 27(12): 26-30.

链接本文:

https://manu60.magtech.com.cn/biotech/CN/        https://manu60.magtech.com.cn/biotech/CN/Y2007/V27/I12/26

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