Kim S G, Batt C A
Department of Food Science, Cornell University, Ithaca, NY 14853.
Gene. 1993 May 15;127(1):121-6. doi: 10.1016/0378-1119(93)90626-e.
The operon (groESL) coding for the Lactococcus lactis subsp. lactis heat-shock proteins GroEL and GroES, has been isolated and its complete nucleotide (nt) sequence determined. A set of degenerate PCR primers, deduced from amino acids which are conserved in a number of prokaryotic GroELs, were synthesized and used to amplify a 957-bp fragment. This PCR fragment was used as a probe to isolate a 5.0-kb EcoRI chromosomally derived fragment. A region of this 5.0-kb EcoRI fragment was sequenced and revealed that the groES gene was located 5' to groEL. This sequence was then used to design a set of inverse PCR primers and a 2.5-kb HindIII fragment was cloned which contained the region 5' to groEL. The complete nt sequence of the groESL operon was determined from overlapping fragments. It revealed that the groESL operon was preceded by a stem-loop structure and the promoter appears similar to most L. lactis subsp. lactis and other Gram+ bacterial promoters. Northern analysis demonstrated that the groESL operon is under tight regulation and a dramatic induction of mRNA synthesis occurs within 15 min after heat shock.
编码乳酸乳球菌乳酸亚种热休克蛋白GroEL和GroES的操纵子(groESL)已被分离出来,并确定了其完整的核苷酸(nt)序列。根据多种原核GroEL中保守的氨基酸序列合成了一组简并PCR引物,并用于扩增一个957 bp的片段。该PCR片段用作探针,分离出一个5.0 kb的染色体来源的EcoRI片段。对该5.0 kb EcoRI片段的一个区域进行测序,结果显示groES基因位于groEL的5'端。然后利用该序列设计了一组反向PCR引物,并克隆了一个2.5 kb的HindIII片段,该片段包含groEL 5'端的区域。通过重叠片段确定了groESL操纵子的完整nt序列。结果表明,groESL操纵子之前有一个茎环结构,其启动子似乎与大多数乳酸乳球菌乳酸亚种和其他革兰氏阳性菌的启动子相似。Northern分析表明,groESL操纵子受到严格调控,热休克后15分钟内mRNA合成会显著诱导。