铅锌矿区耐砷细菌的分离、鉴定及性质研究

旨在从湖南康家湾铅锌矿区的重金属污染土壤样品中筛选出耐高浓度砷的细菌菌株。用稀释涂布法分离耐砷细菌;根据16S r RNA基因系统发育分析鉴定分离得到的砷高耐受性菌株并检测菌株内含有的砷耐受性相关基因;用砷钼蓝法测定耐砷细菌的砷氧化还原能力;并通过吲哚乙酸(IAA)定量实验检测优势菌株产IAA的能力。结果显示,从土壤样品中共分离出152株耐砷细菌,其中6株细菌对As5+和As3+的耐受性值分别高达800 mmol/L和20 mmol/L;并且这6株耐砷细菌分属于5个不同的属:假单胞菌属、苍白杆菌属、芽孢杆菌属、威廉氏菌属和节细菌属;菌株Tw31、Tw133、Sw149和Tw222中存在砷还原酶基因ars C,Bw218和Tw222中存在砷离子外排基因ars B/ACR3(2);在72 h之内,菌株Tw133和Tw222的As3+氧化率(约17%)和As5+还原率(约35%)均高于其他菌株;尤其是菌株Tw133在144 h具有48.66%的As5+还原率;且这两株菌分别能产生42.86μg/m L和24.36μg/m L的IAA。筛选出的Tw133和Tw222菌株在砷耐受性、砷氧还能力和产IAA能力等方面展现出了较明显的优势,为深入研究细菌的砷耐受性机制提供了实验材料。     

紫色非硫细菌的砷代谢机制

[目的]系统阐述紫色非硫细菌(PNSB)砷代谢机制和砷代谢基因簇的进化关系.[方法]通过生物信息学方法分析了PNSB砷代谢基因簇的分布、组成、排布方式.采用UV-Vis和HPLC-ICP-MS方法,研究了3个PNSB种类对砷的抗性、砷形态及价态的转化、砷在细胞中的积累和分布以及磷酸盐对As细胞毒性的影响.[结果]砷基因簇分析表明:已公布全基因组序列的17个PNSB菌株基因组中均含有以ars operon为核心的砷代谢基因簇,由1-4个操纵子组成,主要含有与细胞质砷还原和砷甲基化代谢相关的基因,但基因的组成和排列方式因种和菌株而异,尤其是arsM和两类进化来源不同的arsC.实验结果表明:光照厌氧条件下,3个PNSB种类对As(V)和As(Ⅲ)均具有抗性,As(V)和As(Ⅲ)均能进入细胞 ;在胞内As(V)能够还原为As(Ⅲ)并被排出胞外,但不能将As(Ⅲ)氧化为As(V),也未检测到甲基砷化物 ;磷酸盐浓度升高,能够抑制As(V)进入细胞,降低As(V)对细胞的毒性,而不能抑制As(Ⅲ)进入细胞.[结论]PNSB砷代谢机制主体为细胞质As(V)还原,也还有砷甲基化途径.通过对砷代谢基因簇结构多样性特点和进化方式分析,提出了与Rosen不同的ars operon进化途径.这对深入开展PNSB砷代谢和基因之间的相互作用研究奠定基础.     

胡杨根际细菌提高木本植物对重金属胁迫的耐受性

胡杨是我国西北荒漠地区特有的、对多种非生物逆境具有高抗逆性的树种,但其相关微生物的生态和生理功能研究还比较缺乏.本文从新疆沙雅地区原始胡杨林根际土壤中分离出重金属抗性细菌共72株.其中具有单一重金属(Cu²⁺、Ni²⁺、Pb²⁺或Zn²⁺)抗性的细菌菌株50株,有三重以上重金属抗性的菌株9株.将其中5株多重重金属抗性细菌接种至生根的竹柳插条,进行重金属胁迫下的盆栽培养.结果表明: 在铜或锌胁迫下,5株多重重金属抗性细菌对竹柳的生长抑制有不同程度的缓解,其中假单胞菌Z30和贪铜菌N8菌对铜和锌两种胁迫下竹柳生物量的增长与不接菌对照相比均达到显著差异水平.说明在非重金属污染区生长的胡杨根际存在多样性的重金属抗性细菌,其中一些多重重金属抗性菌对改善重金属胁迫下植物的生长有显著作用,具有应用于木本植物-微生物联合修复环境重金属污染的价值.     

肠道菌分泌的抑菌肽——小菌素

小菌素是由肠道菌分泌的一类小分子抑菌肽,分子量小于10kDa,由细菌质粒或基因组上相关基因簇编码,小菌素的抑菌谱较窄,仅对肠道菌中部分亲缘较近的菌种发挥有效的抑菌效应。编码小菌素的基因簇一般包括几个部分:前体基因,自身免疫基因,分泌基因,转录后修饰基因。与很多微生物通过非核糖体途径分泌抑菌物质不同,小菌素前体通过核糖体途径分泌。目前已发现的小菌素有15种,它们的结构和抑菌机制具有多样性。     

畜禽养殖废物中抗生素和重金属抗性基因的产生机制和控制方法研究进展

动物饲料中常混有抗生素和重金属,导致外排的动物粪便中携带有抗生素和重金属,引发细菌产生耐药性和重金属抗性,继而产生抗生素抗性基因和重金属抗性基因。抗生素和重金属抗性基因污染已成为威胁人类身体健康及破坏生态环境的重大问题。本文从细菌进化的角度,明确了细菌的抗生素和重金属长期进化试验对抗性机制研究的重要性;抗生素抗性基因与重金属抗性基因间存在复杂的协同选择抗性,两者间相互影响,共同决定着细菌环境行为;抗性基因的水平转移增加了细菌在环境中的可变性,可移动遗传元件在抗性基因水平转移中发挥着重要作用。在抗性基因污染控制方面,高级氧化技术具有很好的抗性基因去除效果,尤其是UV/TiO₂氧化技术,能使抗生素抗性基因丰度减少4.7～5.8 log,减少率大于99.99%。其他的控制策略,如抗生素替代品博落回提取物以及噬菌体与抗生素结合使用,对于抗性基因的控制也具有重要意义。     

一株新的砷还原菌分离鉴定及其对天然矿物臭葱石的溶解作用

【目的】探究江汉平原土著砷还原微生物如何介导臭葱石的溶解和释放过程,以及硝酸盐和硫酸盐对该过程的影响。【方法】采集江汉平原高砷沉积物,利用多轮传代富集方法筛选出一株兼性厌氧砷还原菌;克隆其16S rRNA基因、砷还原酶基因(arsC)、硫代硫酸盐还原酶基因(phsA)、硝酸盐还原酶基因(nar)以获得其分类地位;分析该细菌的As(V)、NO3–、Fe(III)、S_2O_3~(2–)还原功能;利用microcosm技术分析该菌株催化臭葱石中不可溶砷和铁的溶解和释放作用及硝酸盐和硫酸盐对此过程的影响;采用X-射线衍射(XRD)和扫描电镜(SEM)等方法对细菌作用前后的矿物表面形貌进行分析。【结果】16S rRNA基因测序结果表明该细菌为柠檬酸杆菌属(Citrobacter sp.),故命名为Citrobacter sp. A11;在Citrobacter sp. A11作用下,0.45 mmol/L As(V)在4 d内被还原成As(III),2.0 mmol/L S_2O_3~(2–)在6 d内被还原成S~(2–),1.0 mmol/L Fe(III)在3 d内被还原成Fe(II),140.0 mg/L NO_3~–在28 h内被还原成NO_2~–;经过28 d该细菌的催化作用使得体系中不可溶砷和铁的释放量分别为33.68μmol/L、51.93μmol/L;硫酸根的加入使得砷和铁的释放量分别增长了41.04%和34.30%,硝酸根的加入则使砷和铁释放量分别降低了35.07%和53.46%。XRD、SEM-EDS分析表明,细菌作用后的臭葱石表面形貌发生明显改变,并出现细小且分散的溶解性颗粒。【结论】本次研究从江汉平原高砷沉积物中富集分离得到一株兼性厌氧砷还原细菌Citrobacter sp. A11,能有效还原As(V)、S_2O_3~(2–)、NO_3~–、Fe(III);砷还原细菌Citrobacter sp. A11能显著促进臭葱石中砷和铁的溶解和释放,硫酸根离子的存在会促进细菌介导臭葱石中固态砷、铁的释放,而硝酸根离子的存在则对此过程起明显抑制作用。     

万顺铅锌矿区蜈蚣草内生细菌砷氧化基因(aoxB)的多样性分析

【背景】近年来,由于金属矿的开采和冶炼、砷产品的加工与使用、煤的燃烧等各种因素,导致土壤环境中的砷污染越来越严重,导致许多人暴露于极度危险的砷毒毒害之下。【目的】研究四川的万顺铅锌矿区蜈蚣草根组织内生细菌aoxB基因的多样性,为提高土壤重金属污染生态修复效率提供理论依据。【方法】利用实时荧光定量PCR (Real-time quantitative PCR,qPCR)和限制性片段长度多态性(Restriction fragment length polymorphism,RFLP)技术,对四川省汉源县万顺铅锌矿区蜈蚣草根组织内生细菌aoxB基因表达量及多样性进行研究。【结果】qPCR结果表明,不同采样点间的蜈蚣草根组织内生细菌aoxB基因表达量存在明显差异,表现为选矿区进山口弃渣场尾矿区矿口。酶切图谱结果表明,不同采样点蜈蚣草根组织内生细菌aoxB基因多样性存在明显差异,多样性指数表现为尾矿矿口弃渣场进山口选矿区。Pearson相关分析显示,aoxB基因的表达量与重金属As之间呈显著负相关(P0.05),多样性指数则与重金属Pb和As之间呈极显著正相关(P0.01)。系统发育分析显示,aoxB基因的优势菌群为α-变形菌门(Alphaproteobacteria)。【结论】蜈蚣草根组织中存在丰富的含aoxB基因内生细菌种群,这些内生细菌表现出潜在的应用价值。     

铜矿厂区土壤中耐铜菌株的筛选及其生长特性初探

为了筛选和开发能够治理重金属污染的微生物资源,运用梯度驯化筛选法和单因素变量法分别对铜矿厂区土壤中的耐铜微生物进行了筛选及其生产培养条件的研究。结果表明,一株耐铜微生物Cladosporium sp.能耐受Cu2+的浓度达15 000 mg/L。在优化的培养时间96 h,转速150r/min,温度28℃,p H 6.0下该菌的耐铜性可提高3.62倍,达到54 300 mg/L,对环境中铜离子的吸附能力可提高2.27倍,达到38.19 mg/g。该菌对重金属Cu2+有非常高的耐受和吸附特性,可作为今后微生物治理重金属污染的优良备选菌种,其耐重金属基因也可作为基因工程的实验研究材料。     

大蒜植物络合素合酶基因转化对酵母重金属抗性的提高

重金属污染是全球面临的亟待解决的生态问题。利用植物对重金属的富集作用来清除环境重金属污染即植物修复已成为重要的环境生物技术之一。这一技术的长远发展有赖于在重金属富集或耐受中起关键作用的基因的克隆和应用。植物络合素是植物体内一类重要的对重金属起螯合作用的多肽, 其合成受植物络合素合酶的催化。该文取得了如下研究结果:1)通过原子吸收测定表明,在大蒜(Allium sativum)的根部可以积累3 000 mg·kg^-1的重金属镉;2)将克隆的大蒜植物络合素合酶基因(AsPCS)置于酵母表达启动子之下,构建酵母表达载体,并将其分别转入了因CUP1和acr3基因缺失而对重金属镉和砷敏感的酵母突变体菌株后,发现来自大蒜的AsPCS基因的表达使酵母CUP1缺失菌株对镉的耐受性提高了4倍, acr3缺失菌株对砷的耐受性提高了两倍;3)表达AsPCS基因酵母的生长模式证实了AsPCS基因的表达是酵母对重金属耐受性提高的原因。这些结果暗示, 大蒜植物络合素合酶基因在大蒜对重金属的抗性及大蒜根部对镉的积累中起关键作用,可作为重要的基因元件应用到修复污染的植物基因工程中。     

4种蚯蚓肠道微生物对砷毒性的响应差异研究

蚯蚓肠道是微生物多样性的一个潜在存储库。砷对蚯蚓肠道微生物群落的影响已被证实,但砷在不同蚯蚓肠道菌群中生物转化的差异仍不清楚。为了进一步阐述土壤中广泛存在的低浓度砷(浓度为5,15,25 mg/kg)对不同种类蚯蚓肠道微生物影响的差异,将4种典型蚯蚓暴露于砷污染土壤后,测定其肠道微生物组成变化,并分析砷对不同蚯蚓肠道内砷富集、形态和砷生物转化基因的影响。结果显示,所有蚯蚓组织内均存在明显的砷富集,其富集系数由高到低依次为:安德爱胜蚓(1.93)>加州腔蚓(0.80)>通俗腔蚓(0.78)>湖北远盲蚓(0.52),蚯蚓组织和肠道内砷形态主要以无机砷为主,其中As(III)含量比例> 80%,部分蚯蚓组织内还发现少量有机砷。4种蚯蚓肠道微生物群落在门水平上主要以变形菌、厚壁菌和放线菌为主,并与周围土壤细菌群落组成存在显著差异。同时,在土壤和肠道内共检测到17个砷转化基因,其中蚯蚓肠道内As(V)还原和砷转运相关基因相对丰度较高,而砷(去)甲基化基因丰度较低。此外,低浓度砷污染对蚯蚓生长无显著影响,却能引起蚯蚓肠道微生物群落的紊乱。蚯蚓种类和砷污染是引起蚯蚓肠道微生物...     

Arsenic-resistant bacteria isolated from agricultural soils of Bangladesh and characterization of arsenate-reducing strains

Aims:  To analyse the arsenic-resistant bacterial communities of two agricultural soils of Bangladesh, to isolate arsenic-resistant bacteria, to study their potential role in arsenic transformation and to investigate the genetic determinants for arsenic resistance among the isolates.
Methods and Results:  Enrichment cultures were performed in a minimal medium in the presence of As(III) and As(V) to isolate resistant bacteria. Twenty-one arsenic-resistant bacteria belonging to different genera of Gram-positive and Gram-negative bacteria were isolated. The isolates, with the exception of Oceanimonas doudoroffii Dhal Rw, reduced 2 mmol l⁻¹ As(V) completely to As(III) in aerobic conditions. Putative gene fragments for arsenite efflux pumps were amplified in isolates from Dhal soil and a putative arsenate reductase gene fragment was amplified from a Bacillus sp. from Rice soil.
Conclusions:  Phylogenetically diverse arsenic-resistant bacteria present in agricultural soils of Bangladesh are capable of reducing arsenate to arsenite under aerobic conditions apparently for detoxification purpose.
Significance and Impact of the Study:  This study provides results on identification, levels of arsenic resistance and reduction of arsenate by the bacterial isolates which could play an important role in arsenic cycling in the two arsenic-contaminated soils in Bangladesh.     

The <Emphasis Type="Italic">ars</Emphasis> genotype characterization of arsenic-resistant bacteria from arsenic-contaminated gold–silver mines in the Republic of Korea

The isolates were identified on the basis of ars genotype characteristics as well as arsenic oxidation/reduction analysis based on the molecular detection characterization. Diversity, pH range (4.0 to 7.0), location, and ars features were assessed for four arsenic-contaminated pond sites and six arsenic tailings located in the Duck-um mine and Myoung-bong mine areas. The presence of ars genes in the genomes of each bacterial strain was evaluated using polymerase chain reaction. Batch experiment results showed that Pseudomonas putida strains OS-3 and -18 completely oxidized 1 mM of arsenite(III) to arsenate(V) within 35-40 h. In contrast, two arsenate-reducing bacteria isolated from mines, P. putida RS-4 and RS-5, were capable of growing aerobically in growth medium supplemented with up to 66.7 mM arsenate(V), which are significantly higher concentration than those tolerated by other arsenic-resistant bacteria. These results suggest that newly isolated indigenous arsenic-resistant bacteria may provide a better understanding of the molecular geomicrobiology and may be applied to the bioremediation of arsenic-contaminated mines in Korea. Ecologically, the redox potential plays an important role in arsenic toxicity and mobility in As-contaminated mine areas, as it facilitates the biogeochemical cycling activity of Pseudomonas sp. groups.     

Rhizosphere colonization and arsenic translocation in sunflower (Helianthus annuus L.) by arsenate reducing Alcaligenes sp. strain Dhal-L

In the present study, six arsenic-resistant strains previously isolated were tested for their plant growth promoting characteristics and heavy metal resistance, in order to choose one model strain as an inoculum for sunflower plants in pot experiments. The aim was to investigate the effect of arsenic-resistant strain on sunflower growth and on arsenic uptake from arsenic contaminated soil. Based on plant growth promoting characteristics and heavy metal resistance, Alcaligenes sp. strain Dhal-L was chosen as an inoculum. Beside the ability to reduce arsenate to arsenite via an Ars operon, the strain exhibited 1-amino-cyclopropane-1-carboxylic acid deaminase activity and it was also able to produce siderophore and indole acetic acid. Pot experiments were conducted with an agricultural soil contaminated with arsenic (214 mg kg^?1). A real time PCR method was set up based on the quantification of ACR3(2) type of arsenite efflux pump carried by Alcaligenes sp. strain Dhal-L, in order to monitor presence and colonisation of the strain in the bulk and rhizospheric soil. As a result of strain inoculation, arsenic uptake by plants was increased by 53 %, whereas ACR3(2) gene copy number in rhizospheric soil was 100 times higher in inoculated than in control pots, indicating the colonisation of strain. The results indicated that the presence of arsenate reducing strains in the rhizosphere of sunflower influences arsenic mobilization and promotes arsenic uptake by plant.     

Identification of an arsenic tolerant double mutant with a thiol-mediated component and increased arsenic tolerance in phyA mutants

A genetic screen was performed to isolate mutants showing increased arsenic tolerance using an Arabidopsis thaliana population of activation tagged lines. The most arsenic-resistant mutant shows increased arsenate and arsenite tolerance. Genetic analyses of the mutant indicate that the mutant contains two loci that contribute to arsenic tolerance, designated ars4 and ars5. The ars4ars5 double mutant contains a single T-DNA insertion, ars4, which co-segregates with arsenic tolerance and is inserted in the Phytochrome A (PHYA) gene, strongly reducing the expression of PHYA. When grown under far-red light conditions ars4ars5 shows the same elongated hypocotyl phenotype as the previously described strong phyA-211 allele. Three independent phyA alleles, ars4, phyA-211 and a new T-DNA insertion allele (phyA-t) show increased tolerance to arsenate, although to a lesser degree than the ars4ars5 double mutant. Analyses of the ars5 single mutant show that ars5 exhibits stronger arsenic tolerance than ars4, and that ars5 is not linked to ars4. Arsenic tolerance assays with phyB-9 and phot1/phot2 mutants show that these photoreceptor mutants do not exhibit phyA-like arsenic tolerance. Fluorescence HPLC analyses show that elevated levels of phytochelatins were not detected in ars4, ars5 or ars4ars5, however increases in the thiols cysteine, gamma-glutamylcysteine and glutathione were observed. Compared with wild type, the total thiol levels in ars4, ars5 and ars4ars5 mutants were increased up to 80% with combined buthionine sulfoximine and arsenic treatments, suggesting the enhancement of mechanisms that mediate thiol synthesis in the mutants. The presented findings show that PHYA negatively regulates a pathway conferring arsenic tolerance, and that an enhanced thiol synthesis mechanism contributes to the arsenic tolerance of ars4ars5.     

Arsenic-resistant proteobacterium from the phyllosphere of arsenic-hyperaccumulating fern (Pteris vittata L.) reduces arsenate to arsenite

An arsenic-resistant bacterium, AsRB1, was isolated from the fronds of Pteris vittata grown in a site contaminated with copper chromium arsenate. The bacterium exhibited resistance to arsenate, arsenite, and antimony in the culture medium. AsRB1, like Pseudomonas putida, grew on MacConkey and xylose-lactose-desoxycholate agars and utilized citrate but, unlike P. putida, was positive for indole test and negative for oxidase test. A phylogenetic analysis of the 16S rRNA gene showed that AsRB1 is a proteobacterium of the beta subclass, related to Pseudomonas saccharophila and Variovorax paradoxus. Following an exogenous supply of arsenate, most arsenic occurred as arsenite in the medium and the cell extracts, suggesting reduction and extrusion of arsenic as the mechanism for arsenic resistance in AsRB1.     

Arsenic-resistant bacteria isolated from contaminated sediments of the Orbetello Lagoon, Italy, and their characterization

AIMS: The aim of this study was to isolate arsenic-resistant bacteria from contaminated sediment of the Orbetello Lagoon, Italy, to characterize isolates for As(III), As(V), heavy metals resistance, and from the phylogenetic point of view. METHODS AND RESULTS: Enrichment cultures were carried out in the presence of 6.75 mmol l(-1) of As(III), allowing isolation of ten bacterial strains. Four isolates, ORAs1, ORAs2, ORAs5 and ORAs6, showed minimum inhibitory concentration values equal or superior to 16.68 mmol l(-1) and 133.47 mmol l(-1) in the presence of As(III) and As(V), respectively. Isolate ORAs2 showed values of 1.8 mmol l(-1) in the presence of Cd(II) and 7.7 mmol l(-1) of Zn(II), and isolate ORAs1 pointed out a value of 8.0 mmol l(-1) in the presence of Cu(II). Analysis of 16S rRNA gene sequences revealed that they can be grouped in the three genera Aeromonas, Bacillus and Pseudomonas. Phylogenetic analysis of the four more arsenic-resistant strains was also performed. CONCLUSION: Isolates are highly resistant to both As(III) and As(V) and they could represent good candidates for bioremediation processes of native polluted sediments. SIGNIFICANCE AND IMPACT OF THE STUDY: This study provides original results on levels of resistance to arsenic and to assigning genera of bacterial strains isolated from arsenic-polluted sediments.     

Arsenic-resistant bacteria solubilized arsenic in the growth media and increased growth of arsenic hyperaccumulator Pteris vittata L

The role of arsenic-resistant bacteria (ARB) in arsenic solubilization from growth media and growth enhancement of arsenic-hyperaccumulator Pteris vittata L. was examined. Seven ARB (tolerant to 10 mM arsenate) were isolated from the P. vittata rhizosphere and identified by 16S rRNA sequencing as Pseudomonas sp., Comamonas sp. and Stenotrophomonas sp. During 7-d hydroponic experiments, these bacteria effectively solubilized arsenic from the growth media spiked with insoluble FeAsO? and AlAsO? minerals (from < 5 μg L?1 to 5.04-7.37 mg L?1 As) and enhanced plant arsenic uptake (from 18.1-21.9 to 35.3-236 mg kg?1 As in the fronds). Production of (1) pyochelin-type siderophores by ARB (fluorescent under ultraviolet illumination and characterized with thin layer chromatography) and (2) root exudate (dissolved organic C) by P. vittata may be responsible for As solubilization. Increase in P. vittata root biomass from 1.5-2.2 to 3.4-4.2 g/plant dw by ARB and by arsenic was associated with arsenic-induced plant P uptake. Arsenic resistant bacteria may have potential to enhance phytoremediation of arsenic-contaminated soils by P. vittata.     

Isolation and Characterization of A Metal-resistant Pseudomonas Aeruginosa Strain

Summary The use of microorganisms to remove heavy metals from industrial effluent is an area of extensive research and development. Attempts have been made to isolate and characterize metal-resistant microorganisms from treated oil mill industry effluent wastewater samples. The metal-resistant organisms that showed values of minimum inhibitory concentration towards metals (Cd, Cr, Ni and Pb) ranging from 100 to 800 ppm level were screened. A potent metal-resistant organism, isolate BC15 from the wastewater samples was tentatively identified as Pseudomonas sp. Detailed analysis of morphological, biochemical and 16S rDNA sequence of the isolate revealed that it is closely related to Pseudomonas aeruginosa (94%). Pseudomonas BC15 was capable of absorbing 93% Ni, 65% Pb, 50% Cd and 30% Cr within 48 h from the medium containing 100 mg of each heavy metal per liter. The multiple metal tolerance of this strain was also associated with resistance to antibiotics such as ampicillin, tetracycline, chloramphenicol, erythromycin, kanamycin and streptomycin.     

arsRBOCT arsenic resistance system encoded by linear plasmid pHZ227 in Streptomyces sp. strain FR-008

In the arsenic resistance gene cluster from the large linear plasmid pHZ227, two novel genes, arsO (for a putative flavin-binding monooxygenase) and arsT (for a putative thioredoxin reductase), were coactivated and cotranscribed with arsR1-arsB and arsC, respectively. Deletion of the ars gene cluster on pHZ227 in Streptomyces sp. strain FR-008 resulted in sensitivity to arsenic, and heterologous expression of the ars gene cluster in the arsenic-sensitive Streptomyces strains conferred resistance on the new hosts. The pHZ227 ArsB protein showed homology to the yeast arsenite transporter Acr3p. The pHZ227 ArsC appears to be a bacterial thioredoxin-dependent ArsC-type arsenate reductase with four conserved cysteine thioredoxin-requiring motifs.