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天蓝色链霉菌A3(2)三个RNA聚合酶sigma因子基因的克隆、破坏及转录分析

Cloning, disruption, and transcriptional analysis of three RNA polymerase sigma factor genes of Streptomyces coelicolor A3(2).

作者信息

Buttner M J, Chater K F, Bibb M J

机构信息

School of Biological Sciences, University of East Anglia, University Plain, Norwich, United Kingdom.

出版信息

J Bacteriol. 1990 Jun;172(6):3367-78. doi: 10.1128/jb.172.6.3367-3378.1990.

Abstract

The rpoD gene of Myxococcus xanthus was used as a probe to isolate three Streptomyces coelicolor genes, hrdB, hrdC, and hrdD, which appear to encode RNA polymerase sigma factors extremely similar to the sigma 70 polypeptide of Escherichia coli. Gene disruption experiments suggested that hrdB is essential in S. coelicolor A3(2) but showed that hrdC and hrdD mutants are viable and are apparently unaffected in differentiation, gross morphology, and antibiotic production. S1 nuclease mapping showed that hrdB and hrdD, but not hrdC, were transcribed in liquid culture. The most upstream of two hrdD promoters is internal to an open reading frame (ORF X) on the opposite strand. The predicted product of this gene is homologous to the phosphinothricin acetyltransferases of Streptomyces hygroscopicus and Streptomyces viridochromogenes. The possible significance of the overlapping and divergent transcription of hrdD and ORF X is discussed. A general method for in vivo gene replacement was developed that allowed a positive selection for the desired mutants even in the absence of a mutant phenotype; it was used to isolate a stable hrdC mutant.

摘要

以黄色黏球菌的rpoD基因作为探针,分离出天蓝色链霉菌的三个基因hrdB、hrdC和hrdD,它们似乎编码与大肠杆菌的σ70多肽极为相似的RNA聚合酶σ因子。基因破坏实验表明,hrdB在天蓝色链霉菌A3(2)中是必需的,但结果显示hrdC和hrdD突变体是可行的,并且在分化、总体形态和抗生素产生方面显然未受影响。S1核酸酶图谱分析表明,hrdB和hrdD(而非hrdC)在液体培养中被转录。hrdD的两个启动子中最上游的启动子位于相反链上一个开放阅读框(ORF X)的内部。该基因的预测产物与吸水链霉菌和绿色产色链霉菌的膦丝菌素乙酰转移酶同源。讨论了hrdD与ORF X重叠和反向转录的可能意义。开发了一种体内基因置换的通用方法,即使在没有突变体表型的情况下也能对所需突变体进行阳性选择;该方法用于分离稳定的hrdC突变体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/781a/209148/a6c2ba60c118/jbacter00160-0567-a.jpg

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