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Isolation and characterization of unsaturated fatty acid auxotrophs of Streptococcus pneumoniae and Streptococcus mutans

机译:肺炎链球菌和变形链球菌的不饱和脂肪酸营养缺陷型的分离和鉴定

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摘要

Unsaturated fatty acid (UFA) biosynthesis is essential for the maintenance of membrane structure and function in many groups of anaerobic bacteria. Like Escherichia coli, the human pathogen Streptococcus pneumoniae produces straight-chain saturated fatty acids (SFA) and monounsaturated fatty acids. In E. coli UFA synthesis requires the action of two gene products, the essential isomerase/dehydratase encoded by fabA and an elongation condensing enzyme encoded by fabB. S. pneumoniae lacks both genes and instead employs a single enzyme with only an isomerase function encoded by the fabM gene. In this paper we report the construction and characterization of an S. pneumoniae 708 fabM mutant. This mutant failed to grow in complex medium, and the defect was overcome by addition of UFAs to the growth medium. S. pneumoniae fabM mutants did not produce detectable levels of monounsaturated fatty acids as determined by gas chromatography-mass spectrometry and thin-layer chromatography analysis of the radiolabeled phospholipids. We also demonstrate that a fabM null mutant of the cariogenic organism Streptococcus mutants is a UFA auxotroph, indicating that FabM is the only enzyme involved in the control of membrane fluidity in streptococci. Finally we report that the fabN gene of Enterococcus faecalis, coding for a dehydratase/isomerase, complements the growth of S. pneumoniae fabM mutants. Taken together, these results suggest that FabM is a potential target for chemotherapeutic agents against streptococci and that S. pneumoniae UFA auxotrophs could help identify novel genes encoding enzymes involved in UFA biosynthesis.
机译:不饱和脂肪酸(UFA)的生物合成对于维持许多厌氧菌群的膜结构和功能至关重要。与大肠杆菌一样,人类病原体肺炎链球菌也会产生直链饱和脂肪酸(SFA)和单不饱和脂肪酸。在大肠杆菌中,UFA合成需要两个基因产物的作用,即fabA编码的必需异构酶/脱水酶和fabB编码的延伸缩合酶。肺炎链球菌缺乏这两个基因,而是使用一种仅具有由fabM基因编码的异构酶功能的酶。在本文中,我们报告了肺炎链球菌708 fabM突变体的构建和表征。该突变体不能在复杂的培养基中生长,并且通过向生长培养基中添加UFA克服了该缺陷。肺炎链球菌fabM突变体未产生可检测水平的单不饱和脂肪酸,这是通过放射性同位素标记的磷脂的气相色谱-质谱和薄层色谱分析确定的。我们还证明了,致癌生物链球菌突变体的fabM空突变体是UFA营养缺陷型,表明FabM是参与链球菌膜流动性控制的唯一酶。最后,我们报告粪肠球菌的fabN基因编码脱水酶/异构酶,补充了肺炎链球菌fabM突变体的生长。综上所述,这些结果表明,FabM是抗链球菌的化学治疗剂的潜在靶标,并且肺炎链球菌UFA营养缺陷型可以帮助鉴定编码涉及UFA生物合成的酶的新基因。

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