Laboratório de Genética Molecular de Microrganismos, Departamento de Microbiologia/Instituto de Biotecnologia Aplicada à Agropecuária (BIOAGRO), Universidade Federal de Viçosa, Viçosa, Brazil.
Laboratório de Biotecnologia Molecular, Departamento de Bioquímica e Biologia Molecular, Universidade Federal de Viçosa, Viçosa, Brazil.
J Appl Microbiol. 2022 Sep;133(3):1857-1871. doi: 10.1111/jam.15692. Epub 2022 Jul 13.
To identify and analyse genes that encode pectinases in the genome of the fungus Colletotrichum lindemuthianum, evaluate the expression of these genes, and compare putative pectinases found in C. lindemuthianum with pectinases produced by other fungi and oomycetes with different lifestyles.
Genes encoding pectinases in the genome of C. lindemuthianum were identified and analysed. The expression of these genes was analysed. Pectinases from C. lindemuthianum were compared with pectinases from other fungi that have different lifestyles, and the pectinase activity in some of these fungi was quantified. Fifty-eight genes encoding pectinases were identified in C. lindemuthianum. At least six types of enzymes involved in pectin degradation were identified, with pectate lyases and polygalacturonases being the most abundant. Twenty-seven genes encoding pectinases were differentially expressed at some point in C. lindemuthianum during their interactions with their host. For each type of pectinase, there were at least three isoenzyme groups. The number of pectinases present in fungi with different lifestyles seemed to be related more to the lifestyle than to the taxonomic relationship between them. Only phytopathogenic fungi showed pectate lyase activity.
The collective results demonstrate the pectinolytic arsenal of C. lindemuthianum, with many and diverse genes encoding pectinases more than that found in other phytopathogens, which suggests that at least part of these pectinases must be important for the pathogenicity of the fungus C. lindemuthianum.
Knowledge of these pectinases could further the understanding of the importance of this broad pectinolytic arsenal in the common bean infection and could be exploited for biotechnological purposes.
鉴定和分析蔓枯病菌基因组中编码果胶酶的基因,评估这些基因的表达情况,并将在蔓枯病菌中发现的推测性果胶酶与其他具有不同生活方式的真菌和卵菌纲生物产生的果胶酶进行比较。
鉴定和分析了蔓枯病菌基因组中编码果胶酶的基因。分析了这些基因的表达情况。将蔓枯病菌的果胶酶与具有不同生活方式的其他真菌的果胶酶进行了比较,并对其中一些真菌的果胶酶活性进行了定量。在蔓枯病菌中鉴定出 58 个编码果胶酶的基因。至少鉴定出 6 种参与果胶降解的酶,其中果胶酸裂解酶和多聚半乳糖醛酸酶最为丰富。在蔓枯病菌与宿主相互作用的某些时候,有 27 个基因编码的果胶酶表现出差异表达。对于每一种果胶酶,至少有 3 个同工酶组。具有不同生活方式的真菌中存在的果胶酶数量似乎与其生活方式有关,而与它们之间的分类关系关系不大。只有植物病原真菌表现出果胶酸裂解酶活性。
综合结果表明,蔓枯病菌具有丰富多样的果胶酶分解武器库,其编码果胶酶的基因数量多于其他植物病原菌,这表明至少部分果胶酶对蔓枯病菌的致病性很重要。
了解这些果胶酶可以进一步了解这个广泛的果胶酶分解武器库在感染普通豆中的重要性,并可用于生物技术目的。