Physiological responses of transgenic merA-tobacco (Nicotiana tabacum) to foliar and root mercury exposure

Plants expressing a modified bacterial mercury reductase, merA, are highly resistant to Hg(II) toxicity as a result of the enzymatically catalyzed electrochemical reduction of Hg(II) to the much less toxic and volatile Hg(0). merA expression may allow plants to manifest a suite of responses to mercury exposure, making them more capable than wild-type plants of interacting with and removing mercury from contaminated soil or water. We have engineered merA-expressing Nicotiana tabacum (tobacco) as a model plant for examining these responses. Mercury resistance was demonstrated by germinating and growing merA tobacco seeds on semi-solid medium spiked with a HgCl(2) concentration acutely toxic to wild-type plants. On similar growth medium, merA plant roots penetrated a highly concentrated, localized Hg(II) zone of HgS (cinnibar) more readily than wild-type roots. In hydroponic medium spiked with HgCl(2), merA plants maintained higher evapotranspiration activity than wild-type plants. The ability of merA Hg(II)-reductive activity to counter typical plant-catalyzed Hg(0) oxidation to Hg(II) was demonstrated by a lower net foliar absorption of atmospheric Hg(0) than wild-type plants. Mercury translocation through merA plants was examined through reciprocally grafted merA and wild-type tobacco grown on HgCl(2)-spiked hydroponic medium. Elevated mercury concentrations in wild-type shoots grafted to merA roots suggest the vertical movement of mercury within merA tissues or plants may be facilitated by dynamic balance between native Hg(0) oxidation and MerA-catalyzed Hg(II) reduction. These experiments demonstrate that merA-engineered tobacco plants display an array of tissue-level and whole-plant attributes which should allow for more efficient mercury extraction and processing compared to the wild-type.