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苏云金芽孢杆菌mel基因在大肠杆菌中的克隆与表达。

Cloning and expression of mel gene from Bacillus thuringiensis in Escherichia coli.

作者信息

Ruan L, He W, He J, Sun M, Yu Z

机构信息

State Key Laboratory of Agricultural Microbiology, Huazhong Agriculture University, Wuhan 430070, China.

出版信息

Antonie Van Leeuwenhoek. 2005 May;87(4):283-8. doi: 10.1007/s10482-004-4775-5.

Abstract

Previous work from our laboratory has shown that most of Bacillus thuringiensis strains possess the ability to produce melanin in the presence of L -tyrosine at elevated temperatures (42 degrees C). Furthermore, it was shown that the melanin produced by B. thuringiensis was synthesized by the action of tyrosinase, which catalyzed the conversion of L -tyrosine, via L -DOPA, to melanin. In this study, the tyrosinase-encoding gene (mel) from B. thuringiensis 4D11 was cloned using PCR techniques and expressed in Escherichia coli DH5 alpha. A DNA fragment with 1179 bp which contained the intact mel gene in the recombinant plasmid pGEM1179 imparted the ability to synthesize melanin to the E. coli recipient strain. The nucleotide sequence of this DNA fragment revealed an open reading frame of 744 bp, encoding a protein of 248 amino acids. The novel mel gene from B.thuringiensis expressed in E. coli DH5 alpha conferred UV protection on the recipient strain.

摘要

我们实验室之前的研究表明,大多数苏云金芽孢杆菌菌株在高温(42摄氏度)及L-酪氨酸存在的情况下具备产生黑色素的能力。此外,研究表明苏云金芽孢杆菌产生的黑色素是由酪氨酸酶作用合成的,酪氨酸酶催化L-酪氨酸经L-多巴转化为黑色素。在本研究中,利用PCR技术克隆了苏云金芽孢杆菌4D11的酪氨酸酶编码基因(mel),并在大肠杆菌DH5α中进行表达。重组质粒pGEM1179中一个含有完整mel基因的1179 bp DNA片段赋予了大肠杆菌受体菌株合成黑色素的能力。该DNA片段的核苷酸序列显示有一个744 bp的开放阅读框,编码一个248个氨基酸的蛋白质。在大肠杆菌DH5α中表达的来自苏云金芽孢杆菌的新mel基因赋予了受体菌株紫外线防护能力。

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