Gutiérrez Jorge, Bourque Denis, Criado Raquel, Choi Young J, Cintas Luis M, Hernández Pablo E, Míguez Carlos B
Departamento de Nutrición, Bromatología y Tecnología de los Alimentos, Facultad de Veterinaria, Universidad Complutense de Madrid, 28040 Madrid, Spain.
FEMS Microbiol Lett. 2005 Jul 1;248(1):125-31. doi: 10.1016/j.femsle.2005.05.029.
Enterocin P (EntP), a strong antilisterial pediocin-like bacteriocin from Enterococcus faecium P13, was produced by Methylobacterium extorquens. For heterologous expression of EntP in the methylotrophic bacterium M. extorquens, a recombinant plasmid was constructed. The gene encoding the EntP structural gene (entP) was cloned into the plasmid vector pCM80, under control of the methanol dehydrogenase promoter (P(mxaF)), to generate plasmid pS25. When M. extorquens ATCC 55366 was transformed with pS25, EntP was detected and quantified in supernatants of the recombinant M. extorquens S25 strain by using specific anti-EntP antibodies and a non-competitive indirect enzyme-linked immunosorbent assay (NCI-ELISA). Purification of EntP by hydrophobic adsorption and reverse-phase (RP-FPLC) chromatographies, permitted recovery of active EntP from the supernatants of M. extorquens S25 grown in a synthetic defined medium.
肠球菌素P(EntP)是一种来自粪肠球菌P13的具有强抗李斯特菌活性的类片球菌素细菌素,由扭脱甲基杆菌产生。为了在甲基营养型细菌扭脱甲基杆菌中进行EntP的异源表达,构建了一个重组质粒。将编码EntP结构基因(entP)的基因克隆到质粒载体pCM80中,置于甲醇脱氢酶启动子(P(mxaF))的控制下,以产生质粒pS25。当用pS25转化扭脱甲基杆菌ATCC 55366时,通过使用特异性抗EntP抗体和非竞争性间接酶联免疫吸附测定(NCI-ELISA),在重组扭脱甲基杆菌S25菌株的上清液中检测并定量了EntP。通过疏水吸附和反相(RP-FPLC)色谱法对EntP进行纯化,使得能够从在合成限定培养基中生长的扭脱甲基杆菌S25的上清液中回收活性EntP。