The metabolism of trinitrobenzene by a Pseudomonas consortium was stud
ied. The Pseudomonas consortium used trinitrobenzene as a sole source
of nitrogen, but not as a sole source of carbon. Trinitrobenzene was m
etabolized within 60 h of incubation. The main intermediates produced
were dinitroaniline, 1,5 dinitrobenzene, nitroaniline, 5-nitrobenzene,
and ammonia. The ammonia concentration in the culture medium increase
d during the course of incubation. Nearly stoichiometric amounts of 1,
5-dinitrobenzene and 5-nitrobenzene were produced by the consortium. D
uring trinitrobenzene metabolism by this bacterial consortium, the tri
nitrobenzene was first reduced to an amino compound, dinitroaniline. T
his intermediate was reductively deaminated with the release of ammoni
a into the culture medium and production of 1,5-dinitrobenzene. By the
same mechanism, 1,5-dinitrobenzene was further converted to 5-nitrobe
nzene, which was not metabolized further, even after 60 days of incuba
tion. This pathway is believed to be novel in that an aerobic bacteria
l consortium uses the nitroaromatic compound as its nitrogen source bu
t leaves the ring intact. The bacterial consortium studied could be us
ed in a syntrophic culture system with other 5-nitrobenzene-degrading
bacteria to remove trinitrobenzene completely from soil and water at c
ontaminated sites.