Huertas-González M D, Ruiz-Roldán M C, García Maceira F I, Roncero M I, Di Pietro A
Departamento de Genética, Facultad de Ciencias, Avda. de S. Alberto Magno S/N, 14071 Córdoba, Spain.
Curr Genet. 1999 Feb;35(1):36-40. doi: 10.1007/s002940050430.
A pectate lyase (PL1) from the tomato vascular wilt pathogen Fusarium oxysporum f.sp. lycopersici was previously characterized, and evidence was obtained for its production in planta. The gene encoding PL1 was isolated from a genomic library of F. oxysporum f. sp. lycopersici. Pl1 encodes a 240 amino-acid polypeptide with one putative N-glycosylation site and a 15 amino-acid N-terminal signal peptide. PL1 showed 89%, 67%, 55% and 56% identity with the products of the Fusarium solani f.sp. pisi pelA, pelB, pelC and pelD genes, respectively. A single copy of the gene was detected in different formae speciales of F. oxysporum. The pl1 transcript was observed during growth on polygalacturonic acid sodium salt and tomato vascular tissue, but not on pectin or glucose. RT-PCR showed pl1 expression in roots and stems of tomato plants infected by F. oxysporum f.sp. lycopersici.
先前已对番茄维管束萎蔫病原菌尖孢镰刀菌番茄专化型中的一种果胶酸裂解酶(PL1)进行了表征,并获得了其在植物中产生的证据。编码PL1的基因是从尖孢镰刀菌番茄专化型的基因组文库中分离出来的。Pl1编码一个含有一个推定的N-糖基化位点和一个15个氨基酸的N端信号肽的240个氨基酸的多肽。PL1与豌豆枯萎病菌pelA、pelB、pelC和pelD基因的产物分别具有89%、67%、55%和56%的同一性。在尖孢镰刀菌的不同专化型中检测到该基因的单拷贝。在以聚半乳糖醛酸钠盐和番茄维管束组织为生长基质时观察到pl1转录本,但在果胶或葡萄糖上未观察到。RT-PCR显示pl1在被尖孢镰刀菌番茄专化型感染的番茄植株的根和茎中表达。