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编码tRNA加工酶RNase BN的大肠杆菌rbn基因的鉴定与特性分析。

Identification and characterization of the Escherichia coli rbn gene encoding the tRNA processing enzyme RNase BN.

作者信息

Callahan C, Deutscher M P

机构信息

Department of Biochemistry, University of Connecticut Health Center, Farmington 06030, USA.

出版信息

J Bacteriol. 1996 Dec;178(24):7329-32. doi: 10.1128/jb.178.24.7329-7332.1996.

Abstract

The gene encoding RNase BN was localized to 88 min on the Escherichia coli chromosome by a novel suppressor assay and conjugational and transductional analysis. Assay of subclones derived from lambda phage 543 of the Kohara library, which encompasses this region of the chromosome, for elevated RNase BN activity identified o290, a previously reported open reading frame, as the gene encoding RNase BN. Interruption of this gene with a Kan(r) cassette and introduction into the chromosome eliminated cellular RNase BN activity but had no effect on cell growth. On the basis of these data, we suggest that o290 be renamed rbn. Potential homologs of rbn in other organisms also were identified.

摘要

通过一种新型抑制子检测以及接合和转导分析,将编码核糖核酸酶BN(RNase BN)的基因定位到大肠杆菌染色体上88分钟处。对源自小原文库λ噬菌体543(该文库涵盖染色体的这一区域)的亚克隆进行检测,以寻找核糖核酸酶BN活性升高的情况,结果确定了o290(一个先前报道的开放阅读框)为编码核糖核酸酶BN的基因。用卡那霉素抗性(Kan(r))盒中断该基因并导入染色体后,消除了细胞中的核糖核酸酶BN活性,但对细胞生长没有影响。基于这些数据,我们建议将o290重新命名为rbn。还鉴定出了其他生物体中rbn的潜在同源物。

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