de Oliveira Ceita Geruza, Vilas-Boas Laurival Antônio, Castilho Marcelo Santos, Carazzolle Marcelo Falsarella, Pirovani Carlos Priminho, Selbach-Schnadelbach Alessandra, Gramacho Karina Peres, Ramos Pablo Ivan Pereira, Barbosa Luciana Veiga, Pereira Gonçalo Amarante Guimarães, Góes-Neto Aristóteles
Laboratório de Pesquisa em Microbiologia , Departamento de Ciências Biológicas , Universidade Estadual de Feira de Santana , Feira de Santana, BA , Brazil . ; Laboratório de Biologia Molecular , Instituto de Biologia , Departamento de Biologia Geral , Universidade Federal da Bahia , Salvador, BA , Brazil .
Centro de Ciências Biológicas , Departamento de Biologia Geral , Universidade Estadual de Londrina , Londrina, PR , Brazil .
Genet Mol Biol. 2014 Oct;37(4):683-93. doi: 10.1590/S1415-47572014005000017. Epub 2014 Nov 3.
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.
可可树扫帚病的病原菌——致病疫霉(Moniliophthora perniciosa (Stahel) Aime & Philips-Mora)给巴西的可可生产造成了巨大损失。分子研究试图鉴定在真菌存活和毒力方面起重要作用的基因。在本研究中,对致病疫霉基因组测序项目数据库中存储的序列进行了分析,以确定潜在的生物学靶点。首次对致病疫霉的麦角甾醇生物合成途径进行了研究,并克隆了编码该途径主要酶且是杀菌剂作用靶点的羊毛甾醇14α-脱甲基酶基因(ERG11),对其进行了分子特征分析并分析了其系统发育。对ERG11基因组DNA和cDNA进行了特征分析,对ERG11蛋白的序列分析确定了该酶典型的高度保守结构域,如SRS1、SRS4、EXXR和血红素结合区域(HBR)。蛋白质序列比较和系统发育分析表明,致病疫霉的该酶与灰盖鬼伞(Coprinopsis cinerea)的酶关系最为密切。