Pedersen L B, Setlow P
Department of Biochemistry, University of Connecticut Health Center, Farmington, Connecticut 06032, USA.
J Bacteriol. 2000 Mar;182(6):1650-8. doi: 10.1128/JB.182.6.1650-1658.2000.
Previous work has shown that the ponA gene, encoding penicillin-binding protein 1 (PBP1), is in a two-gene operon with prfA (PBP-related factor A) (also called recU), which encodes a putative 206-residue basic protein (pI = 10.1) with no significant sequence homology to proteins with known functions. Inactivation of prfA results in cells that grow slower and vary significantly in length relative to wild-type cells. We now show that prfA mutant cells have a defect in chromosome segregation resulting in the production of approximately 0.9 to 3% anucleate cells in prfA cultures grown at 30 or 37 degrees C in rich medium and that the lack of PrfA exacerbates the chromosome segregation defect in smc and spoOJ mutant cells. In addition, overexpression of prfA was found to be toxic for and cause nucleoid condensation in Escherichia coli.
先前的研究表明,编码青霉素结合蛋白1(PBP1)的ponA基因与prfA(PBP相关因子A,也称为recU)处于一个双基因操纵子中,prfA编码一种推定的206个残基的碱性蛋白(pI = 10.1),与已知功能的蛋白质没有明显的序列同源性。prfA的失活导致细胞生长比野生型细胞慢,且长度差异显著。我们现在表明,prfA突变细胞在染色体分离方面存在缺陷,在富含培养基中于30或37摄氏度培养的prfA培养物中产生约0.9%至3%的无核细胞,并且缺乏PrfA会加剧smc和spoOJ突变细胞中的染色体分离缺陷。此外,发现prfA的过表达对大肠杆菌有毒并导致类核凝聚。