4.6 Article

Identification of a Desaturase Involved in Mycolic Acid Biosynthesis in Mycobacterium smegmatis

期刊

PLOS ONE
卷 11, 期 10, 页码 -

出版社

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0164253

关键词

-

资金

  1. Medical Research Council (UK)
  2. BBSRC [BB/N01314X/1] Funding Source: UKRI
  3. MRC [MR/K00042X/1, G0600105, MR/K012118/1] Funding Source: UKRI
  4. Biotechnology and Biological Sciences Research Council [BB/N01314X/1] Funding Source: researchfish
  5. Medical Research Council [MR/K00042X/1, MR/K012118/1, G0600105] Funding Source: researchfish

向作者/读者索取更多资源

Mycolic acids are unique long chain fatty acids found in the cell walls of mycobacteria including the tubercle bacillus, Mycobacterium tuberculosis. The introduction of double bonds in mycolic acids remains poorly understood, however, genes encoding two potential aerobic desaturases have been proposed to be involved in this process. Here we show that one of these genes, desA1, is essential for growth of the saprophytic Mycobacterium smegmatis. Depletion of desA1 in a M. smegmatis conditional mutant led to reduction of mycolic acid biosynthesis and loss of viability. The DesA1-depleted cells exhibited two other phenotypes: using (14)[C]-labelling, we detected the accumulation of minor mycolic acid-related species that migrated faster in a silver TLC plate. Spiral Time of Flight Mass Spectroscopic analysis suggested the presence of species with sizes corresponding to what were likely monoenoic derivatives of alpha-mycolic acids. Additionally, conditional depletion led to the presence of free fatty acyl species of lengths similar to C-26-C-48 in the lysing cells. Cell viability could be rescued in the conditional mutant by Mycobacterium tuberculosis desA1, highlighting the potential of desA1 as a new drug target in pathogenic mycobacteria.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据