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[嗜热栖热菌HB8延伸因子G编码基因fus的克隆及核苷酸序列测定]

[Cloning and nucleotide sequence determination of the fus gene coding for the elongation factor G of Thermus thermophilus HB8].

作者信息

Iakhnin A V, Vorozheĭkina D P, Matvienko N I

出版信息

Biokhimiia. 1990 Sep;55(9):1539-52.

PMID:2078632
Abstract

A clone with the Thermus thermophilus HB8 fus gene coding for elongation factor G has been identified in a genomic library in plasmid pBR 322 by hybridization with labeled oligonucleotide 19 bases that are complementary in length to the 3'-end of the T. thermophilus fus gene. The fragment with the fus gene was recloned into the pTZ 18R plasmid. A restriction map of this fragment has been made. A set of short overlapping fragments of the fus gene has been obtained by nucleotide sequence unspecific linearization of the plasmid and by the restriction fragment subcloning into M13 mp18 and mp19 vectors. The nucleotide sequence of the fus gene was determined by the dideoxy chain termination method. Fus gene codes the elongation factor G 690 amino acids in length (Mr = 76756 Da). The amino acid sequence of EF-G from T. thermophilus has a 59.7% homology with that of E. coli and a 29.0% homology with EF-2 of rat liver.

摘要

通过与长度为19个碱基的标记寡核苷酸杂交,该寡核苷酸与嗜热栖热菌fus基因的3'端长度互补,在质粒pBR 322的基因组文库中鉴定出一个携带编码延伸因子G的嗜热栖热菌HB8 fus基因的克隆。携带fus基因的片段被重新克隆到pTZ 18R质粒中。已绘制出该片段的限制性图谱。通过质粒的核苷酸序列非特异性线性化以及将限制性片段亚克隆到M13 mp18和mp19载体中,获得了一组fus基因的短重叠片段。通过双脱氧链终止法测定了fus基因的核苷酸序列。fus基因编码长度为690个氨基酸的延伸因子G(Mr = 76756 Da)。嗜热栖热菌的EF - G氨基酸序列与大肠杆菌的氨基酸序列具有59.7%的同源性,与大鼠肝脏的EF - 2具有29.0%的同源性。

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