乳酸乳球菌亚种dnaK基因区克隆及序列分析。lactis。

T Eaton, C Shearman, M Gasson
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引用次数: 68

摘要

乳酸乳球菌亚种的一个5.4 kb的HindIII片段。利用PCR方法获得的同源dna ak探针对lactis进行鉴定,并在大肠杆菌中克隆。反向PCR生成上游序列。两个克隆片段部分重叠,测序结果为5915bp,显示存在4个开放阅读框,顺序为orf1-grpE-dnaK-orf4。orf1编码一个39 kDa的功能未知蛋白,其序列与枯草芽孢杆菌Orf39和乙酰丁酸梭菌Orfa蛋白具有相当的同源性。下游ORFs与其他原核生物的grpE和dnaK基因具有较高的同源性。与革兰氏阳性物种的所有已知DnaK蛋白一样,DnaK蛋白具有24个氨基酸缺失的特征。在许多细菌中,dnaK和dnaJ基因被发现是同一个操纵子的一部分。乳酸菌的dnaK操纵子是不寻常的,因为dnaK基因后面有一个假定的转录终止子和第四个大的ORF,它与其他细菌的dnaJ基因没有同源性,但与各种膜蛋白有一定程度的同源性。营养启动子序列位于orf1和orf4的上游。在orf1启动子的上游发现了一个12bp的反向重复序列,在该启动子和orf1起始密码子之间发现了一个8bp的反向重复序列。这些重复序列被认为与热休克基因的调控有关。DnaK同源物在42℃的热休克中被诱导约3倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cloning and sequence analysis of the dnaK gene region of Lactococcus lactis subsp. lactis.

A 5.4 kb HindIII fragment of Lactococcus lactis subsp. lactis was identified using a homologous dnaK probe generated by PCR and cloned in Escherichia coli. Upstream sequences were generated by inverse PCR. The two cloned fragments partially overlapped, and sequencing of 5915 bp revealed the presence of four open reading frames in the order orf1-grpE-dnaK-orf4. orf1 encodes a 39 kDa protein of unknown function which shows considerable sequence homology with the Orf39 and Orfa proteins of Bacillus subtilis and Clostridium acetobutylicum, respectively. The downstream ORFs showed high homology to the grpE and dnaK genes of other prokaryotes. The DnaK protein has a characteristic 24-amino-acid deletion exhibited by all the known DnaK proteins of Gram-positive species. In many bacteria the dnaK and dnaJ genes are found as part of the same operon. The L. lactis dnaK operon is unusual in that the dnaK gene is followed by a putative transcription terminator and a fourth large ORF which shares no homology with the dnaJ genes of other bacteria but has a small degree of homology with various membrane proteins. Vegetative promoter sequences are found upstream of both orf1 and orf4. A 12 bp inverted repeat is found upstream of the putative promoter of orf1 and an 8 bp inverted repeat is found between this promoter and the orf1 initiation codon. These repeats are thought to be involved in regulation of the heat-shock genes. The DnaK homologue is induced approximately 3-fold on heat shock at 42 degrees C.

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