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反硝化副球菌电子传递黄素蛋白亚基编码基因的克隆、测序及表达

Cloning, sequencing, and expression of the genes encoding subunits of Paracoccus denitrificans electron transfer flavoprotein.

作者信息

Bedzyk L A, Escudero K W, Gill R E, Griffin K J, Frerman F E

机构信息

Department of Pediatrics, University of Colorado School of Medicine, Denver 80262.

出版信息

J Biol Chem. 1993 Sep 25;268(27):20211-7.

PMID:8376381
Abstract

The genes encoding the two subunits of Paracoccus denitrificans electron transfer flavoprotein (ETF) were identified by screening a genomic library constructed in pBluescript II SK+ with probes generated by amplification of genomic sequences by the polymerase chain reaction. Primers for the polymerase chain reaction were designed based on peptide sequences from purified Paracoccus ETF subunits. The genes are arranged in tandem in the genomic DNA with the deoxyadenylic acid residue in the TGA termination codon of the small subunit providing the deoxyadenylic acid residue for the ATG initiating codon of the large subunit. The deduced amino acid sequences of the ETF subunits exhibits extensive sequence identity with the human ETF subunits. The Paracoccus ETF is expressed from the pBluescript vector in Escherichia coli, yielding 30 mg of purified, catalytically active protein per liter of culture.

摘要

通过用聚合酶链反应扩增基因组序列所产生的探针筛选构建于pBluescript II SK+中的基因组文库,鉴定出了编码反硝化副球菌电子传递黄素蛋白(ETF)两个亚基的基因。基于纯化的反硝化副球菌ETF亚基的肽序列设计了聚合酶链反应的引物。这些基因在基因组DNA中串联排列,小亚基TGA终止密码子中的脱氧腺苷酸残基为大亚基的ATG起始密码子提供脱氧腺苷酸残基。ETF亚基的推导氨基酸序列与人类ETF亚基具有广泛的序列同一性。反硝化副球菌ETF在大肠杆菌中从pBluescript载体表达,每升培养物产生30毫克纯化的、具有催化活性的蛋白质。

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