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嗜热解芽孢杆菌的prs基因,其编码磷酸核糖二磷酸合酶。

Bacillus caldolyticus prs gene encoding phosphoribosyl-diphosphate synthase.

作者信息

Krath B N, Hove-Jensen B

机构信息

Center for Enzyme Research, University of Copenhagen, Denmark.

出版信息

Gene. 1996 Oct 17;176(1-2):73-9. doi: 10.1016/0378-1119(96)00222-3.

Abstract

The prs gene, encoding phosphoribosyl-diphosphate (PRPP) synthase, as well as the flanking DNA sequences were cloned and sequenced from the Gram-positive thermophile, Bacillus caldolyticus. Comparison with the homologous sequences from the mesophile, Bacillus subtilis, revealed a gene (gcaD) encoding N-acetylglucosamine-1-phosphate uridyltransferase upstream of prs, and a gene homologous to ctc downstream of prs. cDNA synthesis with a B. caldolyticus gcaD-prs-ctc-specified mRNA as template, followed by amplification utilising the polymerase chain reaction indicated that the three genes are co-transcribed. Comparison of amino acid sequences revealed a high similarity among PRPP synthases across a wide phylogenetic range. An E. coli strain harbouring the B. caldolyticus prs gene in a multicopy plasmid produced PRPP synthase activity 33-fold over the activity of a haploid B. caldolyticus strain. B. caldolyticus PRPP synthase was resistant to heat treatment at 70 degrees C to a much higher extent than PRPP synthase from B. subtilis.

摘要

从革兰氏阳性嗜热菌嗜热解硫胺素芽孢杆菌中克隆并测序了编码磷酸核糖焦磷酸(PRPP)合酶的prs基因及其侧翼DNA序列。与嗜温菌枯草芽孢杆菌的同源序列比较,发现在prs上游有一个编码N-乙酰葡糖胺-1-磷酸尿苷转移酶的基因(gcaD),在prs下游有一个与ctc同源的基因。以嗜热解硫胺素芽孢杆菌gcaD-prs-ctc特定的mRNA为模板进行cDNA合成,随后利用聚合酶链反应进行扩增,结果表明这三个基因是共转录的。氨基酸序列比较显示,在广泛的系统发育范围内,PRPP合酶之间具有高度相似性。在多拷贝质粒中携带嗜热解硫胺素芽孢杆菌prs基因的大肠杆菌菌株产生的PRPP合酶活性比单倍体嗜热解硫胺素芽孢杆菌菌株的活性高33倍。嗜热解硫胺素芽孢杆菌PRPP合酶比枯草芽孢杆菌的PRPP合酶对70℃热处理的抗性要强得多。

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