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Inhibitory Effects of Diketopiperazines from Marine-Derived Streptomyces puniceus on the Isocitrate Lyase of Candida albicans

机译:Diketopiperazines从海洋衍生的链霉菌对念珠菌蛋白酶裂解酶的抑制作用

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摘要

The glyoxylate cycle is a sequence of anaplerotic reactions catalyzed by the key enzymes isocitrate lyase (ICL) and malate synthase, and plays an important role in the pathogenesis of microorganisms during infection. An icl-deletion mutant of Candida albicans exhibited reduced virulence in mice compared with the wild type. Five diketopiperazines, which are small and stable cyclic peptides, isolated from the marine-derived Streptomyces puniceus Act1085, were evaluated for their inhibitory effects on C. albicans ICL. The structures of these compounds were elucidated based on spectroscopic data and comparisons with previously reported data. Cyclo(L-Phe-L-Val) was identified as a potent ICL inhibitor, with a half maximal inhibitory concentration of 27 μg/mL. Based on the growth phenotype of the icl-deletion mutants and icl expression analyses, we demonstrated that cyclo(L-Phe-L-Val) inhibits the gene transcription of ICL in C. albicans under C2-carbon-utilizing conditions.
机译:乙醛酸循环是由关键酶异柠檬酸裂解酶(ICL)和雄性合成酶催化的促进反应序列,并且在感染期间微生物发病机制起着重要作用。与野生型相比,Candida albicans的ICL缺失突变体表现出小鼠的毒力。从海洋衍生的链霉菌对Punysus ACT1085中分离的循环肽中分离的五个二酮哌嗪,用于对C. albicans ICL的抑制作用评价。基于与先前报告的数据的光谱数据和比较,阐明了这些化合物的结构。将Cyclo(L-Phe-L-Val)鉴定为有效的ICL抑制剂,其半最大抑制浓度为27μg/ mL。基于ICL - 缺失突变体和ICL表达分析的生长表型,我们证明了Cyclo(L-Phe-L-Val)在C2-碳利用条件下抑制了C.醛糖型蛋白酶C.醛糖的基因转录。

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