We examined the ability of yellow poplar (Liriodendron tulipifera) tis
sue cultures and plantlets to express modified mercuric reductase (mer
A) gene constructs. Mercury-resistant bacteria express merA to convert
highly toxic, ionic mercury, Hg(II), to much less toxic, elemental me
rcury, Hg(0). Expression of merA in transgenic plants might provide an
ecologically compatible approach for the remediation of mercury pollu
tion. Because the alteration of the bacterial merA gene sequence is ne
cessary for high-level expression in Arabidopsis thaliana, yellow popl
ar proembryogenic masses (PEMs) were transformed with three modified m
erA constructs via microprojectile bombardment. Each construct was syn
thesized to have altered flanking regions with increasing amounts of m
odified coding sequence. All merA constructs conferred resistance to t
oxic, ionic mercury in independently transformed PEM colonies. Stabili
ty of merA transgene expression increased in parallel with the extent
of gene coding sequence modification. Regenerated plantlets containing
the most modified merA gene (merA18) germinated and grew vigorously i
n media containing normally toxic levels of ionic mercury. The merA18
plantlets released elemental mercury at approximately 10 times the rat
e of untransformed plantlets. These results indicate that plants expre
ssing modified merA constructs may provide a means for the phytoremedi
ation of mercury pollution.