Lipinska B, Fayet O, Baird L, Georgopoulos C
Department of Cellular, Viral, and Molecular Biology, University of Utah Medical Center, Salt Lake City 84132.
J Bacteriol. 1989 Mar;171(3):1574-84. doi: 10.1128/jb.171.3.1574-1584.1989.
We identified and cloned an Escherichia coli gene called htrA (high temperature requirement). The htrA gene was originally discovered because mini-Tn10 transposon insertions in it allowed E. coli growth at 30 degrees C but prevented growth at elevated temperatures (above 42 degrees C). The htrA insertion mutants underwent a block in macromolecular synthesis and eventually lysed at the nonpermissive temperature. The htrA gene was located at approximately 3.7 min (between the fhuA and dapD loci) on the genetic map of E. coli and between 180 and 187.5 kilobases on the physical map. It coded for an unstable, 51-kilodalton protein which was processed by removal of an amino-terminal fragment, resulting in a stable, 48-kilodalton protein.
我们鉴定并克隆了一个名为htrA(高温需求)的大肠杆菌基因。htrA基因最初是因为mini-Tn10转座子插入其中后,能使大肠杆菌在30摄氏度生长,但在高温(42摄氏度以上)时则阻止其生长而被发现的。htrA插入突变体在大分子合成过程中出现阻断,并最终在非允许温度下裂解。htrA基因位于大肠杆菌遗传图谱上约3.7分钟处(在fhuA和dapD基因座之间),在物理图谱上位于180至187.5千碱基之间。它编码一种不稳定的51千道尔顿蛋白质,该蛋白质经去除氨基末端片段后进行加工,产生一种稳定的48千道尔顿蛋白质。