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Analysis of the ergosterol biosynthesis pathway cloning molecular characterization and phylogeny of lanosterol 14 α-demethylase (ERG11) gene of Moniliophthora perniciosa

机译:多年生念珠菌羊毛甾醇14α-脱甲基酶(ERG11)基因麦角固醇生物合成途径的克隆分子表征和系统发育分析

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摘要

The phytopathogenic fungus Moniliophthora perniciosa (Stahel) Aime & Philips-Mora, causal agent of witches’ broom disease of cocoa, causes countless damage to cocoa production in Brazil. Molecular studies have attempted to identify genes that play important roles in fungal survival and virulence. In this study, sequences deposited in the M. perniciosa Genome Sequencing Project database were analyzed to identify potential biological targets. For the first time, the ergosterol biosynthetic pathway in M. perniciosa was studied and the lanosterol 14α-demethylase gene (ERG11) that encodes the main enzyme of this pathway and is a target for fungicides was cloned, characterized molecularly and its phylogeny analyzed. ERG11 genomic DNA and cDNA were characterized and sequence analysis of the ERG11 protein identified highly conserved domains typical of this enzyme, such as SRS1, SRS4, EXXR and the heme-binding region (HBR). Comparison of the protein sequences and phylogenetic analysis revealed that the M. perniciosa enzyme was most closely related to that of Coprinopsis cinerea.
机译:女巫的可可扫帚病的病原体是植物致病性真菌百日草(Stahel)Aime和飞利浦-莫拉(Philips-Mora),对巴西的可可生产造成了无数损害。分子研究已尝试鉴定在真菌存活和毒力中起重要作用的基因。在这项研究中,分析了多年生支原体基因组测序计划数据库中存储的序列,以鉴定潜在的生物学靶标。首次研究了多年生黑麦草中麦角甾醇的生物合成途径,并克隆了编码该途径主要酶并作为杀真菌剂目标的羊毛甾醇14α-脱甲基酶基因(ERG11),进行了分子表征和系统发育分析。对ERG11基因组DNA和cDNA进行了表征,并对ERG11蛋白进行了序列分析,确定了该酶典型的高度保守结构域,例如SRS1,SRS4,EXXR和血红素结合区(HBR)。蛋白质序列的比较和系统发育分析表明,多年生分支杆菌酶与灰粉菌最密切相关。

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