The ability of plants to metabolize the xenobiotic nitrate ester, glyc
erol trinitrate (GTN, nitroglycerin), was examined using cultured plan
t cells and plant cell extracts. Intact cells rapidly degrade GTN with
the initial formation of glycerol dinitrate (GDN) and the later forma
tion of glycerol mononitrate (GMN). A material balance analysis of the
se intermediates indicates little, if any, formation of reduced, conju
gated or cell-bound carbonaceous metabolites. Cell extracts were shown
to be capable of degrading GTN with the simultaneous formation of GDN
in stoichiometric amounts. The intermediates observed, and the timing
of their appearance, are consistent with a sequential denitration pat
hway that has been reported for the microbial degradation of nitrate e
sters. The degradative activities of plant cells are only tenfold less
than those reported for bacterial GTN degradation. These results sugg
est that plants may serve a direct degradative function for the phytor
emediation of sites contaminated by organic nitrate esters.