Kaur Sukhvinder, Kamli Majid Rasool, Ali Arif
Gene Expression Laboratory, Department of Biosciences, Jamia Millia Islamia, New Delhi, 110025, India.
Curr Microbiol. 2009 Sep;59(3):288-94. doi: 10.1007/s00284-009-9432-9. Epub 2009 May 30.
A polymerase chain reaction (PCR) approach was used to assess the occurrence and diversity of arsenate reductase gene (arsC gene) in arsenic-resistant environmental E. coli strains. For this purpose, two different sets of primers were designed for the specific amplification of approximately 370-bp fragments from the arsC gene. These primers were used to screen a collection of 25 environmental arsenic-resistant strains isolated from different geographical regions of India, as well as Bangladesh. The PCR results showed that 17 out of the 25 environmental isolates (68%) contained a gene related to the arsC family. Phylogenetic analysis of the protein sequences deduced from the amplicons indicated a prevalence of arsC genes in the isolated strains. A significant divergence in the DNA sequence was found in the arsC genes among As-resistant environmental E. coli strains from this study, and arsenic resistance, a genetic character, arose from a common ancestral background.
采用聚合酶链反应(PCR)方法评估抗砷环境大肠杆菌菌株中砷酸盐还原酶基因(arsC基因)的存在情况和多样性。为此,设计了两组不同的引物,用于从arsC基因特异性扩增约370 bp的片段。这些引物用于筛选从印度以及孟加拉国不同地理区域分离出的25株环境抗砷菌株。PCR结果显示,25株环境分离株中有17株(68%)含有与arsC家族相关的基因。对扩增子推导的蛋白质序列进行系统发育分析表明,分离菌株中arsC基因普遍存在。在本研究的抗砷环境大肠杆菌菌株中,arsC基因的DNA序列存在显著差异,并且抗砷这一遗传特性源自共同的祖先背景。