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导致大肠杆菌温度敏感生长的nusA琥珀突变。

nusA amber mutation that causes temperature-sensitive growth of Escherichia coli.

作者信息

Tsugawa A, Saito M, Court D L, Nakamura Y

机构信息

Department of Tumor Biology, University of Tokyo, Japan.

出版信息

J Bacteriol. 1988 Feb;170(2):908-15. doi: 10.1128/jb.170.2.908-915.1988.

Abstract

The nusA134 mutation was isolated from a sup0 strain as a temperature-sensitive mutant which grew at 32 degrees C but not at 42 degrees C. Immunoblot analysis showed that this mutant produced a 31,000-dalton nusA-encoded protein instead of the full-size 54,500-dalton product. Sequence and genetic analyses of the mutant nusA gene revealed a substitution of T for C at the PstI site (i.e., CTGCAG to CTGTAG), thereby creating a nonsense UAG codon. These results indicate that nusA134 is an amber mutation and that the 31,000-dalton amber fragment is active for Escherichia coli growth at 32 degrees C but not at 42 degrees C. Most lambda bacteriophage variants tested grew normally on the nusA134 mutant both at permissive and at nonpermissive temperatures. However, lambda r32, which carries an IS2 insertion beyond the tR1 terminator, was restricted at 42 degrees C. Defects in the transcriptional antitermination process, but not in transcription termination, were observed. A comparative study of nusA134 protein and a PstI-truncated protein suggests that truncation of the peptide chain at the PstI site by the amber mutation, rather than the loss of the glutamine residue, is primarily responsible for the defect in antitermination. The mode of the involvement of mutant nusA proteins in the N-mediated antitermination reaction is discussed.

摘要

nusA134突变体是从一个sup0菌株中分离得到的温度敏感型突变体,它在32℃时能够生长,但在42℃时不能生长。免疫印迹分析表明,该突变体产生的是一种31,000道尔顿由nusA编码的蛋白质,而非全长的54,500道尔顿产物。对突变的nusA基因进行序列和遗传分析发现,在PstI位点处C被T取代(即CTGCAG变为CTGTAG),从而产生了一个无义UAG密码子。这些结果表明,nusA134是一个琥珀突变,并且31,000道尔顿的琥珀片段在32℃时对大肠杆菌生长有活性,但在42℃时无活性。大多数测试的λ噬菌体变体在nusA134突变体上,无论是在允许温度还是非允许温度下都能正常生长。然而,携带IS2插入在tR1终止子下游的λr32在42℃时受到限制。观察到转录抗终止过程存在缺陷,但转录终止过程无缺陷。对nusA134蛋白和PstI截短蛋白的比较研究表明,琥珀突变导致的肽链在PstI位点处截短,而非谷氨酰胺残基的缺失,是抗终止缺陷的主要原因。文中还讨论了突变的nusA蛋白参与N介导的抗终止反应的方式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e8a/210741/849b7d4ab753/jbacter00180-0434-a.jpg

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