Suppr超能文献

汞操纵子的结构。

The structure of the mer operon.

作者信息

Barrineau P, Gilbert P, Jackson W J, Jones C S, Summers A O, Wisdom S

出版信息

Basic Life Sci. 1985;30:707-18. doi: 10.1007/978-1-4613-2447-8_49.

Abstract

The DNA sequence has been determined for a 3.8-kb region which encodes the mercury-resistance (mer) operon of the IncFII plasmid NR1. The sequence reveals 4 open reading frames which could encode proteins of 12,522, 9,429, 14,965, and 58,912 d corresponding to the 4 previously described Hg-inducible proteins detected in minicells carrying mer+ plasmids. The Hg(II) reductase protein sequence is about 90% homologous to that of Tn501, but the DNA sequence shows a homology of 60-70% to that of Tn501 except for short regions of very high homology. The entire mer region is 63.4% G-C overall. The region encoding the merR (positive regulatory) function has 3 possible open reading frames, 2 of which overlap in one direction and the third of which reads in the opposite direction. Attempts to visualize the polypeptide(s) encoded by the merR cistron were unsuccessful.

摘要

已测定了一个3.8千碱基区域的DNA序列,该区域编码IncFII质粒NR1的汞抗性(mer)操纵子。该序列显示有4个开放阅读框,它们可能编码分子量分别为12,522、9,429、14,965和58,912道尔顿的蛋白质,这与在携带mer +质粒的小细胞中检测到的4种先前描述的汞诱导蛋白相对应。汞(II)还原酶的蛋白质序列与Tn501的序列约90%同源,但DNA序列与Tn501的序列同源性为60 - 70%,除了非常高同源性的短区域。整个mer区域的G - C含量总体为63.4%。编码merR(正向调节)功能的区域有3个可能的开放阅读框,其中2个在一个方向上重叠,第3个在相反方向上阅读。可视化由merR顺反子编码的多肽的尝试未成功。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验