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西方烟曲霉聚酮合酶基因“aoks1”参与赭曲霉毒素A的生物合成。

Aspergillus westerdijkiae polyketide synthase gene "aoks1" is involved in the biosynthesis of ochratoxin A.

作者信息

Bacha Nafees, Atoui Ali, Mathieu Florence, Liboz Thierry, Lebrihi Ahmed

机构信息

Laboratoire de Génie Chimique UMR5503 (CNRS/INPT/UPS), Ecole Nationale Supérieure Agronomique de Toulouse, Institut National Polytechnique de Toulouse, 1, Avenue de l'Agrobiopôle, BP32607, 31326 Castanet Tolosan, France.

出版信息

Fungal Genet Biol. 2009 Jan;46(1):77-84. doi: 10.1016/j.fgb.2008.09.015. Epub 2008 Oct 12.

Abstract

Ochratoxin A (OTA) is a potential nephrotoxic, teratogenic, immunogenic, hepatotoxic and carcinogenic mycotoxin, produced by Aspergillus westerdijkiae NRRL 3174. Herein we describe the characterization of a putative OTA-polyketide synthase gene "aoks1", cloned by using gene walking approach. The predicted amino acid sequence of the 2kb clone display 34-60% similarities to different polyketide synthase genes including lovastatine biosynthesis gene "lovb" in A. terreus, compactin biosynthesis gene "mlcA" in Penicillium citrinum and OTA biosynthesis gene "otapksPN" in P. nordicum. Based on the reverse transcription PCR and kinetic secondary metabolites production studies, aoks1 expression was found to be associated with OTA biosynthesis. Further a mutant, in which the aoks1 gene was inactivated by Escherichia coli hygromycin B phosphotransferase gene, lost the capacity to produce OTA, but still producing mellein. To our knowledge this report describes for the first time characterization of a gene involved in OTA biosynthesis, with the information about mellein which was proposed in the literature to be an intermediate OTA. This study also suggests that aoks1 may be the second polyketide synthase gene required for OTA biosynthesis in A. westerdijkiae NRRL 3174.

摘要

赭曲霉毒素A(OTA)是一种潜在的具有肾毒性、致畸性、免疫原性、肝毒性和致癌性的霉菌毒素,由西氏曲霉NRRL 3174产生。在此,我们描述了通过基因步移法克隆的一个假定的OTA - 聚酮合酶基因“aoks1”的特性。该2kb克隆的预测氨基酸序列与不同的聚酮合酶基因显示出34 - 60%的相似性,这些基因包括土曲霉中洛伐他汀生物合成基因“lovb”、桔青霉中康帕丁生物合成基因“mlcA”以及北欧青霉中OTA生物合成基因“otapksPN”。基于逆转录PCR和动力学次级代谢产物产生研究,发现aoks1的表达与OTA生物合成相关。此外,一个突变体,其中aoks1基因被大肠杆菌潮霉素B磷酸转移酶基因失活,失去了产生OTA的能力,但仍能产生蜜色菌素。据我们所知,本报告首次描述了一个参与OTA生物合成的基因的特性,以及文献中提出的作为OTA中间体的蜜色菌素的相关信息。本研究还表明,aoks1可能是西氏曲霉NRRL 3174中OTA生物合成所需的第二个聚酮合酶基因。

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