Faculty of Pharmaceutical Sciences, Setsunan University, 45-1 Nagaotogecho, Hirakata Osaka, 573-0101, Japan.
Appl Microbiol Biotechnol. 2010 Jun;87(2):781-6. doi: 10.1007/s00253-010-2572-9.
To develop the potential of plant for phytoremediation of methylmercury pollution, a genetically engineered tobacco plant that coexpresses organomercurial lyase (MerB) with the ppk-specified polyphosphate (polyP) and merT-encoding mercury transporter was constructed by integrating a bacterial merB gene into ppk/merT-transgenic tobacco. A large number of independent transgenic tobaccos was obtained, in some of which the merB gene was stably integrated in the plant genome and substantially translated to the expected MerB enzyme in the transgenic tobacco. The ppk/merT/merB-transgenic tobacco callus showed more resistance to methylmercury (CH3Hg+) and accumulated more mercury from CH3Hg+-containing medium than the ppk/merT-transgenic and wild-type progenitors. These results suggest that the MerB enzyme encoded by merB degraded the incorporated CH3Hg+ to Hg2+, which then accumulated as a less toxic Hg-polyP complex in the tobacco cells. Phytoremediation of CH3Hg+ and Hg2+ in the environment with this engineered ppk/merT/merB-transgenic plant, which prevents the release mercury vapor (Hg0) into the atmosphere in addition to generating potentially recyclable mercury-rich plant residues, is believed to be more acceptable to the public than other competing technologies, including phytovolatilization.
为了开发植物修复甲基汞污染的潜力,构建了一种通过整合细菌 merB 基因到 ppk/merT 转基因烟草中,共表达有机汞裂解酶(MerB)与 ppk 特异性多聚磷酸盐(polyP)和 merT 编码汞转运蛋白的转基因烟草。获得了大量的独立转基因烟草,其中一些转基因烟草中 merB 基因稳定整合到植物基因组中,并在转基因烟草中大量翻译为预期的 MerB 酶。ppk/merT/merB 转基因烟草愈伤组织对甲基汞(CH3Hg+)的抗性更强,并且从含 CH3Hg+的培养基中积累的汞比 ppk/merT 转基因和野生型亲本更多。这些结果表明,由 merB 编码的 MerB 酶将掺入的 CH3Hg+ 降解为 Hg2+,然后以毒性较低的 Hg-polyP 复合物的形式在烟草细胞中积累。与其他竞争技术相比,包括植物挥发,用这种工程化的 ppk/merT/merB 转基因植物进行 CH3Hg+ 和 Hg2+ 的植物修复,除了产生潜在可回收的富含汞的植物残渣外,还可以防止汞蒸气(Hg0)释放到大气中,预计更能被公众接受。