Suárez M Belén, Vizcaíno J Antonio, Llobell Antonio, Monte Enrique
Centro Hispano-Luso de Investigaciones Agrarias, Departamento de Microbiología y Genética, Campus Miguel de Unamuno, Universidad de Salamanca, 37007 Salamanca, Spain.
Curr Genet. 2007 May;51(5):331-42. doi: 10.1007/s00294-007-0130-5. Epub 2007 Apr 6.
Proteolytic enzymes (EC 3.4) secreted by Trichoderma strains are receiving increasing attention because of their potential implication in the Trichoderma biocontrol abilities. We have used an expressed sequence tag (EST) approach to identify genes encoding extracellular peptidases in T. harzianum CECT 2413 grown under several biocontrol-related conditions. Based on BlastX results and Gene Ontology annotation, a total of 61 (among 3478) unique sequences (unisequences) were predicted to encode enzymes with peptidase activity, three corresponding to secreted peptidases already known from this Trichoderma strain (PAPA, PRA1 and P6281). Further manual screening based on the functional identity and cellular location of the best matches revealed ten unisequences encoding novel extracellular peptidases. We report the characterization of the corresponding genes as well as a potential orthologous gene of the intracellular peptidase PAPB from T. asperellum. In each case, full-length coding sequences were obtained, and deduced proteins were compared at phylogenetic level with peptidases from other organisms. T. harzianum CECT 2413 novel peptidases included six serine endopeptidases (EC 3.4.21) belonging to the families S1, S8 and S53, three aspartic endopeptidases (EC 3.4.23) of the family A1, one metallo-endopeptidase (EC 3.4.24) of the family M35, and one aminopeptidase (EC 3.4.11) of the family M28. Results obtained by Northern blot analyses demonstrated that the genes within a family are differentially regulated in response to different culture conditions, suggesting that they have diverse functional roles.
木霉菌株分泌的蛋白水解酶(EC 3.4)因其在木霉菌生物防治能力中的潜在作用而受到越来越多的关注。我们采用表达序列标签(EST)方法,在几种与生物防治相关的条件下培养哈茨木霉CECT 2413,以鉴定编码细胞外肽酶的基因。基于BlastX结果和基因本体注释,预测在3478个独特序列(单序列)中有61个编码具有肽酶活性的酶,其中三个对应于该木霉菌株已知的分泌肽酶(PAPA、PRA1和P6281)。基于最佳匹配的功能特性和细胞定位进行进一步的人工筛选,发现了十个编码新型细胞外肽酶的单序列。我们报告了相应基因以及来自棘孢木霉的细胞内肽酶PAPB的一个潜在直系同源基因的特征。在每种情况下,都获得了全长编码序列,并将推导的蛋白质在系统发育水平上与其他生物的肽酶进行了比较。哈茨木霉CECT 2413的新型肽酶包括六个属于S1、S8和S53家族的丝氨酸内肽酶(EC 3.4.21)、三个属于A1家族的天冬氨酸内肽酶(EC 3.4.23)、一个属于M35家族的金属内肽酶(EC 3.4.24)和一个属于M28家族的氨肽酶(EC 3.4.11)。Northern印迹分析结果表明,一个家族内的基因在不同培养条件下受到差异调节,这表明它们具有不同的功能作用。