首页> 外文OA文献 >Cloning and sequence analysis of tryptophan synthetase genes of an extreme thermophile, Thermus thermophilus HB27: plasmid transfer from replica-plated Escherichia coli recombinant colonies to competent T. thermophilus cells.
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Cloning and sequence analysis of tryptophan synthetase genes of an extreme thermophile, Thermus thermophilus HB27: plasmid transfer from replica-plated Escherichia coli recombinant colonies to competent T. thermophilus cells.

机译:嗜高温嗜热菌HB27色氨酸合成酶基因的克隆和序列分析:质粒从复本铺盖的大肠杆菌重组菌落转移至感受态嗜热链球菌细胞。

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摘要

Tryptophan synthetase genes (trpBA) of the extreme thermophile Thermus thermophilus HB27 were cloned by a novel method of direct plasmid transfer from replica-plated Escherichia coli recombinant colonies to competent T. thermophilus HB27 trpB cells. The nucleotide sequences of the trpBA genes were determined. The amino acid sequences deduced from the nucleotide sequences of Thermus trpB and trpA were found to have identities of 54.8 and 28.7%, respectively, with those of E. coli trpB and trpA genes. Low cysteine content (one in trpB; zero in trpA) is a striking feature of these proteins, which may contribute to their thermostability.
机译:嗜热嗜热菌HB27的色氨酸合成酶基因(trpBA)克隆了一种新方法,可将质粒直接从复制板接种的大肠杆菌重组菌落转移到嗜热嗜热菌HB27 trpB细胞中。确定了trpBA基因的核苷酸序列。发现从Thermus trpB和trpA的核苷酸序列推导的氨基酸序列与大肠杆菌trpB和trpA基因的同源性分别为54.8和28.7%。半胱氨酸含量低(trpB中为1; trpA中为0)是这些蛋白质的显着特征,可能有助于它们的热稳定性。

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  • 作者

    Koyama, Y; Furukawa, K;

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  • 年度 1990
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  • 原文格式 PDF
  • 正文语种 en
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