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首页> 外文期刊>International Journal of Food Microbiology >The gene PatG involved in the biosynthesis pathway of patulin, a food-borne mycotoxin, encodes a 6-methylsalicylic acid decarboxylase.
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The gene PatG involved in the biosynthesis pathway of patulin, a food-borne mycotoxin, encodes a 6-methylsalicylic acid decarboxylase.

机译:涉及生物合成途径的Patulin途径,一种食品传播的霉菌毒素,编码了6-甲基羟基丙酸脱羧酶。

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摘要

Patulin is a mycotoxin produced by fungal genera such as Aspergillus, Penicillium and Byssochlamys. It induces neurological, gastrointestinal and immunological effects, which is why patulin belongs to a short list of mycotoxins whose level in food is regulated in many countries around the world. Recently, a cluster gathering 15 genes involved in the biosynthesis of patulin has been identified in Aspergillus clavatus, but so far, only 4 genes encoding 6-methylsalicylic acid synthase, m-cresol hydroxylase, m-hydroxybenzyl alcohol hydroxylase and isoepoxydon dehydrogenase have been characterized. Previous studies have shown the involvement of a decarboxylase in the transformation of 6-methylsalicylic acid, the first stable patulin precursor, into m-cresol. In this study a putative decarboxylase gene, PatG, was identified in the genome sequence of A. clavatus. This gene is located near two P450 cytochrome genes PatH and PatI responsible respectively for the hydroxylation of m-cresol and m-hydroxybenzyl alcohol. This decarboxylase encoded by PatG (ACLA_093620) consists of 325 amino acids. The search for putative conserved domain revealed that the gene product belongs to the AminoCarboxyMuconate Semialdehyde Decarboxylase (ACMSD) related protein family. This family includes decarboxylases such as the gamma -resorcylate decarboxylase or o-pyrocatechuate decarboxylase. The substrates of these enzymes display strong structural similarities with 6-methylsalicylic acid. PatG was strongly expressed during patulin production whereas it was very weakly expressed in non-patulin permissive conditions. The coding sequence was used to enable heterologous expression of functional enzymes in Saccharomyces cerevisiae. The presence of decarboxylase was confirmed by Western blot. The bioconversion assays showed that PATG catalyzed the decarboxylation of 6-methylsalicylic acid into m-cresol. These results confirm for the first time that 6-methylsalicylic acid is the substrate for PATG, the 6-methylsalicylic acid decarboxylase. With this study, the four genes involved in the four first steps of patulin biosynthesis pathway (acetate -> gentisyl alcohol) are now identified.
机译:Patulin是一种由真菌属,如曲霉,青霉素和Byssochlamys生产的霉菌毒素。它诱导神经系统,胃肠道和免疫效应,这就是为什么帕卢林属于霉菌毒素的简短列表,其食物水平在全球许多国家/地区受到监管。最近,在Aspergillus clavatus中鉴定了涉及参与鉴定生物合成的15个基因的聚类,但到目前为止,已经表现了仅编码6-甲基羟基丙烯酸合酶,M-甲酚羟基苄基醇羟基羟化酶和异己酸钠脱氢酶的4个基因。以前的研究表明,脱羧酶参与在6-甲基仲丙烯酸,第一稳定鉴定前体的转化中,进入M-甲酚。在这项研究中,在A.Clavatus的基因组序列中鉴定了推​​定的脱羧酶基因帕特。该基因位于两种P450细胞色素基因和Pati附近,分别用于M-甲酚和M-羟基苄醇的羟基化。由PATG(ACLA_093620)编码的这种脱羧酶由325个氨基酸组成。寻求推定的保守域显示基因产物属于氨基羧酸氨酸氨丁基脱羧酶(ACMSD)相关蛋白质。该系列包括脱羧酶,例如γ-甲酸酯脱羧酶或O-发球菌脱羧酶。这些酶的底物与6-甲基胱二甲酸显示出强的结构相似性。在竞争期间强烈表达Patg,而在非鉴定允许条件下,它非常弱。编码序列用于在酿酒酵母中能够使官能酶的异源表达。通过蛋白质印迹确认脱羧酶的存在。生物转化测定表明,PATG催化了6-甲基仲丙酸的脱羧剂至m-甲酚。这些结果首次证实了6-甲基仲丙烯酸是帕格,6-甲基山酸脱羧酶的基材。通过该研究,现在鉴定了参与鉴定生物合成途径(乙酸酯 - >乙酸醇)的四个第一步骤的四个基因。

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