Liu Guohua, Feng Kai, Guo Daosen, Li Ronggui
Department of Biology, Qingdao University, Qingdao, 266071, People's Republic of China.
Folia Microbiol (Praha). 2015 Sep;60(5):443-50. doi: 10.1007/s12223-015-0380-4. Epub 2015 Feb 27.
Peroxiredoxins (Prxs) are enzymatic antioxidants widely distributed in biological kingdoms, which constitute a family of heme-free peroxidases that reduce alkyl hydroperoxides and hydrogen peroxide. In this paper, an open reading frame (ORF) of 639 bp, which encoded a protein of 213 amino acid residues, was cloned from Pseudomonas fluorescens GcM5-1A carried by pine wood nematode. Amino acid sequence alignment showed that the encoded protein shared 99, 97, and 97 % identity with the thiol-specific antioxidant protein LsfA of P. fluorescens Q2-87, the peroxiredoxin of Pseudomonas sp. GM17 and 1-Cys peroxiredoxin of P. fluorescens Pf 0-1, respectively. The ORF was cloned into expressing vector pET-15b and introduced into Escherichia coli BL21 (DE3). Overexpression of a 27-kDa protein was achieved by IPTG induction. The recombinant protein was purified by affinity chromatography on a Ni(2+) matrix column. Non-reducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis indicated that part of the recombinant appeared in dimer form. Bioassay results showed that purified recombinant protein had both peroxidase and thioredoxin activity. Furthermore, E. coli expressing the ORF showed tolerance to hydrogen peroxide stress, which indicated that the gene might help P. fluorescens GcM5-1A resist hydrogen peroxide generated by host pines after pine wood nematode associated with this bacterium infected pine trees.
过氧化物酶(Prxs)是广泛分布于生物界的酶促抗氧化剂,它们构成了一类无血红素的过氧化物酶家族,可还原烷基过氧化氢和过氧化氢。本文从松材线虫携带的荧光假单胞菌GcM5-1A中克隆了一个639 bp的开放阅读框(ORF),该阅读框编码一个由213个氨基酸残基组成的蛋白质。氨基酸序列比对表明,所编码的蛋白质与荧光假单胞菌Q2-87的硫醇特异性抗氧化蛋白LsfA、假单胞菌GM17的过氧化物酶和荧光假单胞菌Pf 0-1的1-半胱氨酸过氧化物酶的同源性分别为99%、97%和97%。将该ORF克隆到表达载体pET-15b中,并导入大肠杆菌BL21(DE3)。通过IPTG诱导实现了27 kDa蛋白的过表达。重组蛋白通过镍(2+)基质柱上的亲和层析进行纯化。非还原十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)分析表明,部分重组蛋白以二聚体形式出现。生物测定结果表明,纯化的重组蛋白具有过氧化物酶和硫氧还蛋白活性。此外,表达该ORF的大肠杆菌对过氧化氢胁迫具有耐受性,这表明该基因可能有助于荧光假单胞菌GcM5-1A抵抗松材线虫与该细菌感染松树后宿主松树产生的过氧化氢。