Chauhan Nar Singh, Nain Sonam, Sharma Rakesh
CSIR-Institute of Genomics and Integrative Biology, Council of Scientific and Industrial Research, Sukhdev Vihar, Mathura Road, Delhi, 110020 India.
Department of Biochemistry, Present Address: Maharishi Dayanand University, Rohtak, Haryana India.
Indian J Microbiol. 2017 Sep;57(3):299-306. doi: 10.1007/s12088-017-0658-0. Epub 2017 Jul 5.
A metagenomic library of sea sediment metagenome containing 245,000 recombinant clones representing ~ 2.45 Gb of sea sediment microbial DNA was constructed. Two unique arsenic resistance clones, A7 and A12, were identified by selection on sodium arsenite containing medium. Clone A7 showed a six-fold higher resistance to arsenate [As(V)], a three-fold higher resistance to arsenite [As(III)] and significantly increased resistance to antimony [Sb(III)], while clone A12 showed increased resistance only to sodium arsenite and not to the other two metalloids. The clones harbored inserts of 8.848 Kb and 6.771 Kb, respectively. Both the clones possess A + T rich nucleotide sequence with similarity to sequences from marine psychrophilic bacteria. Sequence and transposon-mutagenesis based analysis revealed the presence of a putative arsenate reductase (ArsC), a putative arsenite efflux pump (ArsB/ACR) and a putative NADPH-dependent FMN reductase (ArsH) in both the clones and also a putative transcriptional regulatory protein (ArsR) in pA7. The increased resistance of clone A7 to As(V), As(III) and Sb(III) indicates functional expression of ArsC and ArsB proteins from pA7. The absence of increased As(V) resistance in clone A12 may be due to the expression of a possible inactive ArsC, as conserved Arg60 residue in this protein was replaced by Glu60, while the absence of Sb(III) resistance may be due to the presence of an ACR3p-type arsenite pump, which is known to lack antimony transport ability.
构建了一个海洋沉积物宏基因组文库,该文库包含245,000个重组克隆,代表约2.45 Gb的海洋沉积物微生物DNA。通过在含亚砷酸钠的培养基上筛选,鉴定出两个独特的抗砷克隆A7和A12。克隆A7对砷酸盐[As(V)]的抗性高6倍,对亚砷酸盐[As(III)]的抗性高3倍,对锑[Sb(III)]的抗性显著增加,而克隆A12仅对亚砷酸钠的抗性增加,对其他两种类金属没有抗性。这些克隆分别含有8.848 Kb和6.771 Kb的插入片段。两个克隆都具有富含A + T的核苷酸序列,与海洋嗜冷细菌的序列相似。基于序列和转座子诱变的分析表明,两个克隆中都存在一个假定的砷酸盐还原酶(ArsC)、一个假定的亚砷酸盐外排泵(ArsB/ACR)和一个假定的NADPH依赖性FMN还原酶(ArsH),并且在pA7中还存在一个假定的转录调节蛋白(ArsR)。克隆A7对As(V)、As(III)和Sb(III)抗性的增加表明来自pA7的ArsC和ArsB蛋白具有功能表达。克隆A12中As(V)抗性没有增加可能是由于可能无活性的ArsC的表达,因为该蛋白中保守的Arg60残基被Glu60取代,而Sb(III)抗性的缺乏可能是由于存在ACR3p型亚砷酸盐泵,已知该泵缺乏锑转运能力。