State Key Lab of Microbial Technology, Shandong University, Jinan 250100, China.
Microbiol Res. 2011 Oct 20;166(7):515-20. doi: 10.1016/j.micres.2010.10.003. Epub 2011 Jan 15.
A mercury-resistant plasmid of pTMJ212 which was able to shuttle between Acidithiobacillus caldus and Escherichia coli was constructed by inserting the mercury resistant determinants, the mer operon of Acidithiobacillus ferrooxidans, into the IncQ plasmid of pJRD215. pTMJ212 was transferred from Escherichia coli into Acidithiobacillus caldus through conjugation. Furthermore, pTMJ212 was transferred back from Acidithiobacillus caldus into Escherichia coli, thereby confirming the initial transfer of pTMJ212 from Escherichia coli to Acidithiobacillus caldus. Compared to the control, the cell growth of the recombinant Acidithiobacillus caldus increased markedly under mercury (Hg(2+)) stress especially at Hg(2+) concentrations ranging from 2.0 to 4.5 μg/ml.
构建了一种可在嗜酸硫杆菌和大肠杆菌之间穿梭的 pTMJ212 型抗汞质粒,该质粒通过将抗汞决定簇,即氧化亚铁硫杆菌的 mer 操纵子,插入 pJRD215 的 IncQ 质粒中而构建。pTMJ212 通过接合从大肠杆菌转移到嗜酸硫杆菌中。此外,pTMJ212 从嗜酸硫杆菌中转移回大肠杆菌,从而证实了 pTMJ212 最初从大肠杆菌转移到嗜酸硫杆菌。与对照组相比,在汞(Hg(2+))胁迫下,重组嗜酸硫杆菌的细胞生长明显增加,特别是在 Hg(2+)浓度范围为 2.0 至 4.5μg/ml 时。