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枯草芽孢杆菌tms和prs基因的一级结构。

Primary structure of the tms and prs genes of Bacillus subtilis.

作者信息

Nilsson D, Hove-Jensen B, Arnvig K

机构信息

Enzyme Division, University Institute of Biological Chemistry B, Copenhagen, Denmark.

出版信息

Mol Gen Genet. 1989 Sep;218(3):565-71. doi: 10.1007/BF00332425.

Abstract

The nucleotide sequence was determined of a 3211 nucleotide pair EcoRI-PvuII DNA fragment containing the tms and prs genes as well as a part of the ctc gene of Bacillus subtilis. The prs gene encodes phosphoribosylpyrophosphate (PRPP) synthetase, whereas the functioning of the tms and ctc gene products remains to be established. The prs gene contains an open reading frame of 317 codons resulting in a subunit Mr of 34828. An open reading frame comprising the tms gene contained 456 codons resulting in a putative translation product with an Mr of 49,554. Comparison of the deduced B. subtilis PRPP synthetase amino acid sequence with PRPP synthetases from Escherichia coli and rat liver showed extensive similarity. The deduced Tms amino acid sequence was found to be 43% similar to the deduced amino acid sequence of ecourfl, a gene of E. coli with unknown function.

摘要

测定了枯草芽孢杆菌一个3211核苷酸对的EcoRI - PvuII DNA片段的核苷酸序列,该片段包含tms和prs基因以及ctc基因的一部分。prs基因编码磷酸核糖焦磷酸(PRPP)合成酶,而tms和ctc基因产物的功能尚待确定。prs基因包含一个由317个密码子组成的开放阅读框,产生的亚基分子量为34828。包含tms基因的一个开放阅读框有456个密码子,产生一个推测的翻译产物,分子量为49554。将推导的枯草芽孢杆菌PRPP合成酶氨基酸序列与来自大肠杆菌和大鼠肝脏的PRPP合成酶进行比较,发现有广泛的相似性。发现推导的Tms氨基酸序列与大肠杆菌中功能未知的ecourfl基因的推导氨基酸序列有43%的相似性。

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