Nishijima S, Asami Y, Uetake N, Yamagoe S, Ohta A, Shibuya I
Department of Biochemistry, Saitama University, Urawa, Japan.
J Bacteriol. 1988 Feb;170(2):775-80. doi: 10.1128/jb.170.2.775-780.1988.
The cls gene of Escherichia coli is responsible for the synthesis of a major membrane phospholipid, cardiolipin, and has been proposed to encode cardiolipin synthase. This gene cloned on a pBR322 derivative was disrupted by either insertion of or replacement with a kanamycin-resistant gene followed by exchange with the homologous chromosomal region. The proper genomic disruptions were confirmed by Southern blot hybridization and a transductional linkage analysis. Both types of disruptants had essentially the same properties; cardiolipin synthase activity was not detectable, but the strains grew well, although their growth rates and final culture densities were lower than those of the corresponding wild-type strains and strains with the classical cls-1 mutation. A disruptant harboring a plasmid that carried the intact cls gene grew normally. The results indicate that the cls gene and probably the cardiolipin synthase are dispensable for E. coli but may confer growth or survival advantages. Low but definite levels of cardiolipin were synthesized by all the disruptants. Cardiolipin content of the cls mutants depended on the dosage of the pss gene, and attempts to transfer a null allele of the cls gene into a pss-1 mutant were unsuccessful. We point out the possibilities of minor cardiolipin formation by phosphatidylserine synthase and of the essential nature of cardiolipin for the survival of E. coli cells.
大肠杆菌的cls基因负责合成一种主要的膜磷脂——心磷脂,并被认为编码心磷脂合酶。克隆在pBR322衍生物上的该基因,通过插入或替换卡那霉素抗性基因,随后与同源染色体区域交换而被破坏。通过Southern印迹杂交和转导连锁分析证实了正确的基因组破坏。两种类型的破坏菌株具有基本相同的特性;未检测到心磷脂合酶活性,但菌株生长良好,尽管它们的生长速率和最终培养密度低于相应的野生型菌株和具有经典cls-1突变的菌株。携带完整cls基因质粒的破坏菌株生长正常。结果表明,cls基因以及可能的心磷脂合酶对大肠杆菌来说是可有可无的,但可能赋予生长或生存优势。所有破坏菌株都合成了低但确定水平的心磷脂。cls突变体的心磷脂含量取决于pss基因的剂量,并且将cls基因的无效等位基因转移到pss-1突变体中的尝试未成功。我们指出了磷脂酰丝氨酸合酶形成少量心磷脂的可能性以及心磷脂对大肠杆菌细胞存活的本质重要性。