Branco Rita, Chung Ana Paula, Johnston Tatiana, Gurel Volkan, Morais Paula, Zhitkovich Anatoly
Laboratorio de Microbiologia, Departmento de Bioquimica, Universidade de Coimbra, 3001-517 Coimbra, Portugal.
J Bacteriol. 2008 Nov;190(21):6996-7003. doi: 10.1128/JB.00289-08. Epub 2008 Sep 5.
Large-scale industrial use of chromium(VI) has resulted in widespread contamination with carcinogenic chromium(VI). The abilities of microorganisms to survive in these environments and to detoxify chromate require the presence of specific resistance systems. Here we report identification of the transposon-located (TnOtChr) chromate resistance genes from the highly tolerant strain Ochrobactrum tritici 5bvl1 surviving chromate concentrations of >50 mM. The 7,189-bp-long TnOtChr of the mixed Tn21/Tn3 transposon subfamily contains a group of chrB, chrA, chrC, and chrF genes situated between divergently transcribed resolvase and transposase genes. The chrB and chrA genes, but not chrF or chrC, were essential for establishment of high resistance in chromium-sensitive O. tritici. The chr promoter was strongly induced by chromate or dichromate, but it was completely unresponsive to Cr(III), oxidants, sulfate, or other oxyanions. Plasmid reporter experiments identified ChrB as a chromate-sensing regulator of chr expression. Induction of the chr operon suppressed accumulation of cellular Cr through the activity of a chromate efflux pump encoded by chrA. Expression of chrB, chrC, or chrF in an Escherichia coli sodA sodB double mutant restored its aerobic growth in minimal medium and conferred resistance to superoxide-generating agents menadione and paraquat. Nitroblue tetrazolium staining on native gels showed that ChrC protein had superoxide dismutase activity. TnOtChr appears to represent a mobile genetic system for the distribution of the chromate-regulated resistance operon. The presence of three genes protecting against superoxide toxicity should provide an additional survival advantage to TnOtChr-containing cells in the environments with multiple redox-active contaminants.
铬(VI)的大规模工业使用导致了致癌性铬(VI)的广泛污染。微生物在这些环境中生存并解毒铬酸盐的能力需要特定抗性系统的存在。在此,我们报告了从耐铬酸盐浓度>50 mM的高耐受性小麦苍白杆菌5bvl1菌株中鉴定出位于转座子上的(TnOtChr)铬酸盐抗性基因。混合的Tn21/Tn3转座子亚家族的7189 bp长的TnOtChr包含一组位于反向转录的解离酶和转座酶基因之间的chrB、chrA、chrC和chrF基因。chrB和chrA基因,而非chrF或chrC基因,对于铬敏感的小麦苍白杆菌建立高抗性至关重要。chr启动子受到铬酸盐或重铬酸盐的强烈诱导,但对Cr(III)、氧化剂、硫酸盐或其他含氧阴离子完全无反应。质粒报告实验确定ChrB是chr表达的铬酸盐感应调节因子。chr操纵子的诱导通过chrA编码的铬酸盐外排泵的活性抑制细胞内Cr的积累。在大肠杆菌sodA sodB双突变体中chrB、chrC或chrF的表达恢复了其在基本培养基中的有氧生长,并赋予了对产生超氧化物的试剂甲萘醌和百草枯的抗性。天然凝胶上的硝基蓝四唑染色表明ChrC蛋白具有超氧化物歧化酶活性。TnOtChr似乎代表了一个用于分布铬酸盐调节抗性操纵子的可移动遗传系统。存在三个防止超氧化物毒性的基因应该会为含有TnOtChr的细胞在具有多种氧化还原活性污染物的环境中提供额外的生存优势。