Ghim S Y, Switzer R L
Department of Biochemistry, University of Illinois, Urbana 61801, USA.
FEMS Microbiol Lett. 1996 Mar 15;137(1):13-8. doi: 10.1111/j.1574-6968.1996.tb08075.x.
The pyrimidine nucleotide biosynthetic (pyr) operon in Bacillus subtilis is regulated by a transcriptional attenuation mechanism in which PyrR, a bifunctional pyr RNA-binding attenuation protein/uracil phosphoribosyltransferase, plays a crucial role. A convenient procedure for isolation of pyrR mutants with defects in the regulation of pyr operon expression is described. The selection is based on the selection of spontaneous mutations that convert the pyrimidine-sensitive growth of cpa strain (lacking arginine-repressible carbamyl phosphate synthetase) to pyrimidine resistance. Twelve such mutants were isolated and sequenced. All resulted from point mutations in the pyrR gene.
枯草芽孢杆菌中的嘧啶核苷酸生物合成(pyr)操纵子受转录衰减机制调控,其中双功能的pyr RNA结合衰减蛋白/尿嘧啶磷酸核糖转移酶PyrR发挥着关键作用。本文描述了一种分离在pyr操纵子表达调控方面存在缺陷的pyrR突变体的简便方法。该筛选基于对自发突变的选择,这些突变可将cpa菌株(缺乏精氨酸可阻遏的氨甲酰磷酸合成酶)对嘧啶敏感的生长特性转变为对嘧啶的抗性。分离出了12个这样的突变体并进行了测序。所有突变均源于pyrR基因中的点突变。