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首页> 外文期刊>Molecular Microbiology >Transcriptome analysis of cyclic AMP-dependent protein kinase A-regulated genes reveals the production of the novel natural compound fumipyrrole by Aspergillus fumigatus
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Transcriptome analysis of cyclic AMP-dependent protein kinase A-regulated genes reveals the production of the novel natural compound fumipyrrole by Aspergillus fumigatus

机译:循环AMP依赖性蛋白激酶A调节基因的转录组分析揭示了通过曲霉(Aspergillus fumigatus)的新型天然复合FumiPyrol的产生

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摘要

Aspergillus fumigatus is an opportunistic human pathogenic fungus causing life-threatening infections in immunocompromised patients. Adaptation to different habitats and also virulence of the fungus depends on signal perception and transduction by modules such as the cyclic AMP-dependent protein kinase A (PKA) pathway. Here, by transcriptome analysis, 632 differentially regulated genes of this important signaling cascade were identified, including 23 putative transcriptional regulators. The highest upregulated transcription factor gene was located in a previously unknown secondary metabolite gene cluster, which we named fmp, encoding an incomplete non-ribosomal peptide synthetase, FmpE. Overexpression of the regulatory gene fmpR using the Tet(On) system led to the specific expression of the other six genes of the fmp cluster. Metabolic profiling of wild type and fmpR overexpressing strain by HPLC-DAD and HPLC-HRESI-MS and structure elucidation by NMR led to identification of 5-benzyl-1H-pyrrole-2-carboxylic acid, which we named fumipyrrole. Fumipyrrole was not described as natural product yet. Chemical synthesis of fumipyrrole confirmed its structure. Interestingly, deletion of fmpR or fmpE led to reduced growth and sporulation of the mutant strains. Although fmp cluster genes were transcribed in infected mouse lungs, deletion of fmpR resulted in wild-type virulence in a murine infection model.
机译:曲霉菌是一种机会主义的人类致病性真菌,导致免疫造成免疫造成患者的危及生命的感染。适应不同的栖息地以及真菌的毒力取决于通过诸如循环AMP依赖性蛋白激酶A(PKA)途径的模块的信号感知和转导。这里,通过转录组分析,鉴定了这种重要信号传导级联的632个差异调节基因,包括23个推定的转录调节剂。最高上调的转录因子基因位于先前未知的次级代谢物基因簇中,我们将FMP命名为FMP,编码不完全的非核糖体肽合成酶FMPE。使用TET(ON)系统的调节基因FMPR的过度表达导致FMP簇的其他六个基因的特异性表达。通过HPLC-DAD和HPLC-HRESI-MS的野生型和FMPR过表达应变的代谢分析和NMR的结构阐明,鉴定为5-苄基-1H-吡咯-2-羧酸,我们命名为FumiProlole。 FumipyRrole尚未描述为天然产品。 FumipyRROLE的化学合成证实了其结构。有趣的是,FMPR或FMPE缺失导致突变菌株的生长和孢子率降低。尽管在感染的小鼠肺中转录FMP群集基因,但缺失FMPR导致小鼠感染模型中的野生型毒力。

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  • 来源
    《Molecular Microbiology》 |2015年第1期|共15页
  • 作者单位

    Leibniz Inst Nat Prod Res &

    Infect Biol HKI Mol &

    Appl Microbiol D-07745 Jena Germany;

    Leibniz Inst Nat Prod Res &

    Infect Biol HKI Biomol Chem D-07745 Jena Germany;

    Leibniz Inst Nat Prod Res &

    Infect Biol HKI Biomol Chem D-07745 Jena Germany;

    Leibniz Inst Nat Prod Res &

    Infect Biol HKI Syst Biol Bioinformat D-07745 Jena Germany;

    Leibniz Inst Nat Prod Res &

    Infect Biol HKI Mol &

    Appl Microbiol D-07745 Jena Germany;

    Univ Wisconsin Plant Pathol Madison WI 53706 USA;

    Cornell Univ Boyce Thompson Inst Ithaca NY 14853 USA;

    Cornell Univ Boyce Thompson Inst Ithaca NY 14853 USA;

    Univ Wisconsin Med Microbiol &

    Immunol Madison WI 53706 USA;

    Leibniz Inst Nat Prod Res &

    Infect Biol HKI Biomol Chem D-07745 Jena Germany;

    Leibniz Inst Nat Prod Res &

    Infect Biol HKI Mol &

    Appl Microbiol D-07745 Jena Germany;

    Leibniz Inst Nat Prod Res &

    Infect Biol HKI Mol &

    Appl Microbiol D-07745 Jena Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 细胞生物学;
  • 关键词

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