...
首页> 外文期刊>Journal of bacteriology >Isolation and Characterization of Unsaturated Fatty Acid Auxotrophs of Streptococcus pneumoniae and Streptococcus mutans
【24h】

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

获取原文
   

获取外文期刊封面封底 >>

       

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细菌群体的膜结构和功能至关重要。像大肠杆菌一样,人类病原体肺炎链球菌会产生直链饱和脂肪酸(SFA)和单不饱和脂肪酸。在 E中。大肠杆菌UFA的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(S. pneumoniae)缺少这两个基因,而是使用一种仅具有 fabM 基因编码的异构酶功能的酶。在本文中,我们报告了 S的构建和表征。肺炎 708 fabM 突变体。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。 S。气相色谱-质谱法和放射性标记的磷脂的薄层色谱分析法测定,肺炎FabM 突变体未产生可检测水平的单不饱和脂肪酸。我们还证明了致癌生物链球菌突变体 fabM 空突变体是UFA营养缺陷型,表明FabM是唯一参与控制链球菌膜流动性的酶。最后,我们报道了粪肠球菌 fabN 基因,编码脱水酶/异构酶,补充了 S的生长。肺炎fabM 突变体。综上所述,这些结果表明,FabM是针对链球菌和 S的化学治疗剂的潜在靶标。肺炎乌发营养缺陷型细菌可以帮助鉴定编码涉及UFA生物合成酶的新基因。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号