Eaton T, Shearman C, Gasson M
AFRC Institute of Food Research, Norwich Research Park, Colney, UK.
J Gen Microbiol. 1993 Dec;139(12):3253-64. doi: 10.1099/00221287-139-12-3253.
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.
利用通过PCR产生的同源dnaK探针鉴定了乳酸乳球菌乳酸亚种的一个5.4 kb HindIII片段,并将其克隆到大肠杆菌中。通过反向PCR产生上游序列。两个克隆片段部分重叠,对5915 bp进行测序后发现存在四个开放阅读框,顺序为orf1-grpE-dnaK-orf4。orf1编码一种功能未知的39 kDa蛋白质,该蛋白质分别与枯草芽孢杆菌和丙酮丁醇梭菌的Orf39和Orfa蛋白质具有相当程度的序列同源性。下游的开放阅读框与其他原核生物的grpE和dnaK基因具有高度同源性。DnaK蛋白具有革兰氏阳性菌所有已知DnaK蛋白特有的24个氨基酸缺失。在许多细菌中,dnaK和dnaJ基因是同一操纵子的一部分。乳酸乳球菌的dnaK操纵子不同寻常之处在于,dnaK基因后面跟着一个假定的转录终止子和第四个大的开放阅读框,该开放阅读框与其他细菌的dnaJ基因没有同源性,但与各种膜蛋白有一定程度的同源性。在orf1和orf4上游均发现了营养型启动子序列。在orf1假定启动子上游发现一个12 bp的反向重复序列,在该启动子与orf1起始密码子之间发现一个8 bp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℃热休克时诱导约3倍。