Dominy Clifford N, Deane Shelly M, Rawlings Douglas E
Department of Microbiology, University of Cape Town, Private Bag Rondebosch, Cape Town 7700, South Africa.
Microbiology (Reading). 1997 Oct;143 ( Pt 10):3123-3136. doi: 10.1099/00221287-143-10-3123.
During a search for genes encoding electron transport proteins from a Thiobacillus ferroxidans ATCC 33020 gene bank, a 19.8 kb plasmid, pTF5, which conferred increased sensitivity to the antimicrobial agent metronidazole upon an Escherichia coli mutant, was isolated and cloned in E. coli. The plasmid had an identical restriction enzyme map to a plasmid which has been found in T. ferrooxidans strains isolated from many different parts of the world. The plasmid was present at between two and four copies per genome and contained a region of approximately 5-6 kb which was also found on the chromosome. This region was sequenced and found to have four complete ORFs, which when translated had high percentage amino acid similarity to [3Fe-4S,4Fe-4S] ferredoxins, proteins of the FNR regulator family, prismane-like proteins and the NADH oxidoreductase subunit of a methane monooxygenase. In vitro protein analysis using an E. coli-derived transcription-translation system indicated that three of the four products (FdxA, PsmA and RedA) were expressed in the heterologous system. Ferredoxins, prismane-like proteins and NADH oxidoreductases are redox-active proteins and it is likely that the proteins on pTF5 represent an electron transport system of as yet unknown function. Surprisingly, although genes for redox-active proteins have been isolated from other bacteria by screening gene banks for increased sensitivity to metronidazole, the region of pTF5 containing the genes for these proteins was not responsible for the increase in metronidazole sensitivity conferred by the plasmid. The region of pTF5 which did confer increased metronidazole sensitivity to an E. coli metronidazole-resistant mutant was a 319 bp region of DNA close to the origin of plasmid replication. This region contained no ORFs and was identical to that previously reported for the replicon of a 9.8 kb T. ferrooxidans plasmid, pTF191.
在从氧化亚铁硫杆菌ATCC 33020基因库中搜寻编码电子传递蛋白的基因时,分离出了一个19.8 kb的质粒pTF5,并将其克隆到大肠杆菌中。该质粒赋予大肠杆菌突变体对抗菌剂甲硝唑更高的敏感性。该质粒的限制性酶切图谱与在从世界许多不同地区分离出的氧化亚铁硫杆菌菌株中发现的一个质粒相同。该质粒在每个基因组中以2至4个拷贝的数量存在,并且包含一个约5 - 6 kb的区域,该区域也存在于染色体上。对该区域进行测序后发现有四个完整的开放阅读框(ORF),翻译后的氨基酸序列与[3Fe - 4S,4Fe - 4S]铁氧化还原蛋白、FNR调节因子家族的蛋白、棱柱烷样蛋白以及甲烷单加氧酶的NADH氧化还原酶亚基具有高度的氨基酸相似性。使用大肠杆菌来源的转录 - 翻译系统进行的体外蛋白质分析表明,四个产物中的三个(FdxA、PsmA和RedA)在异源系统中表达。铁氧化还原蛋白、棱柱烷样蛋白和NADH氧化还原酶都是具有氧化还原活性的蛋白质,pTF5上的这些蛋白质可能代表一个功能未知的电子传递系统。令人惊讶的是,尽管通过筛选基因库以寻找对甲硝唑敏感性增加的基因,已经从其他细菌中分离出了具有氧化还原活性的蛋白质的基因,但pTF5中包含这些蛋白质基因的区域并不是质粒赋予甲硝唑敏感性增加的原因。pTF5中确实赋予大肠杆菌甲硝唑抗性突变体更高甲硝唑敏感性的区域是靠近质粒复制起点的一个319 bp的DNA区域。该区域不包含开放阅读框,并且与先前报道的9.8 kb氧化亚铁硫杆菌质粒pTF191的复制子相同。