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本文引用的文献

1
Nucleotide sequence of plasmid pCNB1 from comamonas strain CNB-1 reveals novel genetic organization and evolution for 4-chloronitrobenzene degradation.来自丛毛单胞菌菌株CNB-1的质粒pCNB1的核苷酸序列揭示了4-氯硝基苯降解的新遗传组织和进化。
Appl Environ Microbiol. 2007 Jul;73(14):4477-83. doi: 10.1128/AEM.00616-07. Epub 2007 May 25.
2
Causes of DNA single-strand breaks during reduction of chromate by glutathione in vitro and in cells.谷胱甘肽在体外和细胞内还原铬酸盐过程中导致DNA单链断裂的原因。
Free Radic Biol Med. 2006 Jun 1;40(11):1981-92. doi: 10.1016/j.freeradbiomed.2006.01.028. Epub 2006 Feb 20.
3
Effect of chromate stress on Escherichia coli K-12.铬酸盐胁迫对大肠杆菌K-12的影响。
J Bacteriol. 2006 May;188(9):3371-81. doi: 10.1128/JB.188.9.3371-3381.2006.
4
Resistance determinants of a highly arsenic-resistant strain of Leptospirillum ferriphilum isolated from a commercial biooxidation tank.从一个商业生物氧化罐中分离出的嗜铁钩端螺旋菌的高抗砷菌株的抗性决定因素。
Appl Environ Microbiol. 2006 Mar;72(3):2247-53. doi: 10.1128/AEM.72.3.2247-2253.2006.
5
Nei deficient Escherichia coli are sensitive to chromate and accumulate the oxidized guanine lesion spiroiminodihydantoin.内源性缺陷型大肠杆菌对铬酸盐敏感,并积累氧化鸟嘌呤损伤产物螺环亚氨基二氢尿嘧啶。
Chem Res Toxicol. 2005 Sep;18(9):1378-83. doi: 10.1021/tx0501379.
6
An unusual Tn21-like transposon containing an ars operon is present in highly arsenic-resistant strains of the biomining bacterium Acidithiobacillus caldus.一种含有抗砷操纵子的不寻常的类Tn21转座子存在于生物采矿细菌嗜酸氧化硫硫杆菌的高耐砷菌株中。
Microbiology (Reading). 2005 Sep;151(Pt 9):3027-3039. doi: 10.1099/mic.0.28131-0.
7
Importance of chromium-DNA adducts in mutagenicity and toxicity of chromium(VI).铬-DNA加合物在六价铬的致突变性和毒性中的重要性。
Chem Res Toxicol. 2005 Jan;18(1):3-11. doi: 10.1021/tx049774+.
8
Ochrobactrum tritici strain 5bvl1 - characterization of a Cr(VI)-resistant and Cr(VI)-reducing strain.小麦苍白杆菌5bvl1菌株——一种耐六价铬和还原六价铬菌株的特性
Can J Microbiol. 2004 Sep;50(9):697-703. doi: 10.1139/w04-048.
9
The bzd gene cluster, coding for anaerobic benzoate catabolism, in Azoarcus sp. strain CIB.偶氮螺菌属菌株CIB中编码厌氧苯甲酸分解代谢的bzd基因簇。
J Bacteriol. 2004 Sep;186(17):5762-74. doi: 10.1128/JB.186.17.5762-5774.2004.
10
Human nucleotide excision repair efficiently removes chromium-DNA phosphate adducts and protects cells against chromate toxicity.人类核苷酸切除修复可有效去除铬 - DNA 磷酸加合物,并保护细胞免受铬酸盐毒性的影响。
J Biol Chem. 2004 Jul 16;279(29):30419-24. doi: 10.1074/jbc.M402486200. Epub 2004 Apr 15.

来自转座元件TnOtChr的铬酸盐诱导型chrBACF操纵子赋予对铬(VI)和超氧化物的抗性。

The chromate-inducible chrBACF operon from the transposable element TnOtChr confers resistance to chromium(VI) and superoxide.

作者信息

Branco Rita, Chung Ana Paula, Johnston Tatiana, Gurel Volkan, Morais Paula, Zhitkovich Anatoly

机构信息

Laboratorio de Microbiologia, Departmento de Bioquimica, Universidade de Coimbra, 3001-517 Coimbra, Portugal.

出版信息

J Bacteriol. 2008 Nov;190(21):6996-7003. doi: 10.1128/JB.00289-08. Epub 2008 Sep 5.

DOI:10.1128/JB.00289-08
PMID:18776016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2580707/
Abstract

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.

摘要

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。