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两种转录因子CabA和CabR独立参与编码新型氨基香豆素卡西比星的生物合成基因簇的多级调控。

Two transcription factors, CabA and CabR, are independently involved in multilevel regulation of the biosynthetic gene cluster encoding the novel aminocoumarin, cacibiocin.

作者信息

Wolański Marcin, Łebkowski Tomasz, Kois-Ostrowska Agnieszka, Zettler Judith, Apel Alexander K, Jakimowicz Dagmara, Zakrzewska-Czerwińska Jolanta

机构信息

Faculty of Biotechnology, University of Wrocław, ul. Joliot-Curie 14A, 50-383, Wrocław, Poland.

Pharmazeutische Biologie, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 8, 72076, Tübingen, Germany.

出版信息

Appl Microbiol Biotechnol. 2016 Apr;100(7):3147-64. doi: 10.1007/s00253-015-7196-7. Epub 2015 Dec 5.

Abstract

Aminocoumarins are potent antibiotics belonging to a relatively small group of secondary metabolites produced by actinomycetes. Genome mining of Catenulispora acidiphila has recently led to the discovery of a gene cluster responsible for biosynthesis of novel aminocoumarins, cacibiocins. However, regulation of the expression of this novel gene cluster has not yet been analyzed. In this study, we identify transcriptional regulators of the cacibiocin gene cluster. Using a heterologous expression system, we show that the CabA and CabR proteins encoded by cabA and cabR genes in the cacibiocin gene cluster control the expression of genes involved in the biosynthesis, modification, regulation, and potentially, efflux/resistance of cacibiocins. CabA positively regulates the expression of cabH (the first gene in the cabHIYJKL operon) and cabhal genes encoding key enzymes responsible for the biosynthesis and halogenation of the aminocoumarin moiety, respectively. We provide evidence that CabA is a direct inducer of cacibiocin production, whereas the second transcriptional factor, CabR, is involved in the negative regulation of its own gene and cabT-the latter of which encodes a putative cacibiocin transporter. We also demonstrate that CabR activity is negatively regulated in vitro by aminocoumarin compounds, suggesting the existence of analogous regulation in vivo. Finally, we propose a model of multilevel regulation of gene transcription in the cacibiocin gene cluster by CabA and CabR.

摘要

氨基香豆素是一类强效抗生素,属于放线菌产生的相对较少的次级代谢产物。最近,对嗜酸链状孢菌的基因组挖掘发现了一个负责新型氨基香豆素——卡西比菌素生物合成的基因簇。然而,这个新型基因簇的表达调控尚未得到分析。在本研究中,我们鉴定了卡西比菌素基因簇的转录调节因子。利用异源表达系统,我们表明卡西比菌素基因簇中cabA和cabR基因编码的CabA和CabR蛋白控制着参与卡西比菌素生物合成、修饰、调控以及可能的外排/抗性相关基因的表达。CabA正向调节cabH(cabHIYJKL操纵子中的第一个基因)和cabhal基因的表达,这两个基因分别编码负责氨基香豆素部分生物合成和卤化的关键酶。我们提供的证据表明,CabA是卡西比菌素产生的直接诱导剂,而第二个转录因子CabR参与对其自身基因和cabT的负调控,后者编码一种假定的卡西比菌素转运蛋白。我们还证明,CabR的活性在体外受到氨基香豆素化合物的负调控,这表明体内可能存在类似的调控。最后,我们提出了一个由CabA和CabR对卡西比菌素基因簇中的基因转录进行多级调控的模型。

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