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嗜麦芽窄食单胞菌酪氨酸酶基因mel的克隆与过表达

Cloning and overexpression of a tyrosinase gene mel from Pseudomonas maltophila.

作者信息

Wang G, Aazaz A, Peng Z, Shen P

机构信息

Department of Microbiology and Immunology, College of Life Sciences, Wuhan University, Wuhan, PR China.

出版信息

FEMS Microbiol Lett. 2000 Apr 1;185(1):23-7. doi: 10.1111/j.1574-6968.2000.tb09035.x.

Abstract

The tyrosinase gene (mel), which is responsible for melanin formation, was isolated by shotgun cloning of SalI fragments of Pseudomonas maltophila DNA. A 0.7-kb SalI fragment in the recombinant plasmid pWSY8 imparted the ability to synthesize melanin to an Escherichia coli host HB101. The nucleotide sequence of this DNA fragment revealed an open reading frame of 504 bp, encoding a protein of 169 amino acids. The fragment containing the mel gene was then cloned into an expression plasmid pPAS1 under the control of a promoter isolated from the host, P. maltophilia AT18. This strain increased the melanin production by 70.6% compared with the strain HB101/pWSY8, in which the cloned mel gene was under the control of the lac promoter from the vector pUC18.

摘要

负责黑色素形成的酪氨酸酶基因(mel),是通过对嗜麦芽窄食单胞菌DNA的SalI片段进行鸟枪法克隆而分离得到的。重组质粒pWSY8中的一个0.7 kb SalI片段赋予了大肠杆菌宿主HB101合成黑色素的能力。该DNA片段的核苷酸序列显示有一个504 bp的开放阅读框,编码一个由169个氨基酸组成的蛋白质。然后将含有mel基因的片段克隆到表达质粒pPAS1中,该表达质粒受从宿主嗜麦芽窄食单胞菌AT18分离得到的启动子控制。与克隆的mel基因受载体pUC18的lac启动子控制的菌株HB101/pWSY8相比,该菌株的黑色素产量提高了70.6%。

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