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Identification of a gene required for the formation of lyso-ornithine lipid, an intermediate in the biosynthesis of ornithine-containing lipids

机译:鉴定溶血鸟氨酸脂质形成所需的基因,溶血鸟氨酸脂质是含鸟氨酸脂质生物合成的中间体

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Under phosphate-limiting conditions, some bacteria replace their membrane phospholipids by lipids not containing any phosphorus. One of these phosphorus-free lipids is an ornithine-containing lipid (OL) that is widespread among eubacteria. In earlier work, we had identified a gene (olsA) required for OL biosynthesis that probably encodes an O-acyltransferase using acyl-acyl carrier protein (acyl-AcpP) as an acyl donor and that converts lyso-ornithine lipid into OL. We now report on a second gene (olsB) required for OL biosynthesis that is needed for the incorporation of radiolabelled ornithine into OL. Overexpression of OlsB in an olsA-deficient mutant of Sinorhizobium (Rhizobium) meliloti leads to the transient accumulation of lyso-ornithine lipid, the biosynthetic intermediate of OL biosynthesis. Overexpression of OlsB in Escherichia coli is sufficient to cause the in vivo formation of lyso-ornithine lipid in this organism and is the cause for a 3-hydroxyacyl-AcpP-dependent acyltransferase activity forming lyso-ornithine lipid from ornithine. These results demonstrate that OlsB is required for the first step of OL biosynthesis, in which ornithine is N-acylated with a 3-hydroxy-fatty acyl residue in order to obtain lyso-ornithine lipid. OL formation in a wild-type S. meliloti is increased upon growth under phosphate-limiting conditions. Expression of OlsB from a broad host range vector leads to the constitutive formation of relatively high amounts of OL (12-14% of total membrane lipids) independently of whether strains are grown in the presence of low or high concentrations of phosphate, suggesting that in S. meliloti the formation of OlsB is usually limiting for the amount of OL formed in this organism. Open reading frames homologous to OlsA and OlsB were identified in many eubacteria and although in S. meliloti the olsB and olsA gene are 14 kb apart, in numerous other bacteria they form an operon.
机译:在限制磷酸盐的条件下,某些细菌用不含任何磷的脂质代替其膜磷脂。这些无磷脂质中的一种是在鸟细菌中广泛分布的含鸟氨酸的脂质(OL)。在较早的工作中,我们已经鉴定了OL生物合成所需的基因(olsA),该基因可能使用酰基载体蛋白(acyl-AcpP)作为酰基供体编码O-酰基转移酶,并将溶血鸟氨酸脂质转化为OL。现在,我们报告了OL生物合成所需的第二个基因(olsB),这是将放射性标记鸟氨酸掺入OL所需的。苜蓿根瘤菌(Rhizobium)的olsA缺陷型突变体中过表达OlsB会导致溶血鸟氨酸脂质(OL生物合成的生物合成中间体)的瞬时积累。大肠杆菌中OlsB的过表达足以引起该生物体内溶血鸟氨酸脂质的体内形成,并且是由鸟氨酸形成溶血鸟氨酸脂质的3-羟酰基-AcpP依赖性酰基转移酶活性的原因。这些结果表明,OlsB是OL生物合成第一步所必需的,其中鸟氨酸被3-羟基脂肪酰基残基N-酰化以获得溶血鸟氨酸脂质。在磷酸盐限制条件下生长时,野生型苜蓿链球菌中OL的形成增加。从广泛的宿主范围载体表达OlsB会导致组成相对较高量的OL(占总膜脂的12-14%)的组成形成,而与菌株在低浓度或高浓度磷酸盐存在下生长无关,这表明苜蓿链球菌OlsB的形成通常限制了该生物中形成的OL的数量。在许多真细菌中鉴定出与OlsA和OlsB同源的开放阅读框,尽管在苜蓿链球菌中,olsB和olsA基因相距14 kb,但在许多其他细菌中它们形成操纵子。

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