Meberg B M, Sailer F C, Nelson D E, Young K D
Department of Microbiology and Immunology, University of North Dakota School of Medicine, Grand Forks, North Dakota 58202-9037, USA.
J Bacteriol. 2001 Oct;183(20):6148-9. doi: 10.1128/JB.183.20.6148-6149.2001.
Previously, we constructed a set of mutants from which eight penicillin binding protein (PBP) genes were deleted in 192 combinations from Escherichia coli (S. A. Denome, P. K. Elf, T. A. Henderson, D. E. Nelson, and K. D. Young, J. Bacteriol. 181:3981-3993, 1999). Although these mutants were constructed correctly as determined by restriction mapping and the absence of relevant protein products, we recently discovered by PCR mapping that strains from which mrcA (PBP 1a) was deleted were also missing two neighboring genes of unknown function (yrfE and yrfF). We created a new deletion mutation in mrcA and reconstructed 63 strains lacking PBP 1a and other PBP mutant combinations. The new mrcA mutants do not exhibit mucoidy, phage resistance, temperature sensitivity, growth rate defects, or antibiotic resistance, suggesting that these phenotypes require the loss of either yrfE or yrfF alone or in combination with the absence of multiple PBPs.
此前,我们构建了一组突变体,从大肠杆菌中以192种组合方式缺失了8个青霉素结合蛋白(PBP)基因(S. A. 德诺姆、P. K. 埃尔夫、T. A. 亨德森、D. E. 尼尔森和K. D. 杨,《细菌学杂志》181:3981 - 3993,1999年)。尽管通过限制性酶切图谱分析以及相关蛋白质产物的缺失确定这些突变体构建正确,但我们最近通过PCR图谱分析发现,缺失mrcA(PBP 1a)的菌株也缺失了两个功能未知的相邻基因(yrfE和yrfF)。我们在mrcA中创建了一个新的缺失突变,并重建了63株缺失PBP 1a和其他PBP突变组合的菌株。新的mrcA突变体不表现出黏液样、噬菌体抗性、温度敏感性、生长速率缺陷或抗生素抗性,这表明这些表型单独需要yrfE或yrfF的缺失,或者与多个PBP的缺失相结合。