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In vitro anaerobic trinitrotoluene (TNT) degradation with rumen fluid ...

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1.3 <strong>TNT</strong> <strong>degradation</strong> under <strong>anaerobic</strong> conditions<br />

The <strong>degradation</strong> of explosives under <strong>anaerobic</strong> conditions has been intensively<br />

studied <strong>with</strong>in past the few years. Various microorganisms, including denitrifing,<br />

sulfate reducing, methanogenic, and specific enzymes, were applied to examine the<br />

feasibility of explosives <strong>degradation</strong> under <strong>anaerobic</strong> conditions. Principal findings are<br />

as summarized below.<br />

McCormick et al. (18) investigated <strong>TNT</strong> reduction by cell-free extracts, resting<br />

cells, and growing cultures. The cell-free extracts and resting cells reduced three nitro<br />

groups to corresponding amino groups under strctly <strong>anaerobic</strong> conditions. Growing<br />

cultures of V. alkalescens and E. colt produced 2,4DA6NT. <strong>In</strong> the case of<br />

nitrotoluene, the reduction of a para-positioned nitro group was followed by the<br />

ortho-positioned group. The nitro reductase separated from V. alkalescens consisted<br />

of hydrogenase and ferredoxin-like materials, but whether the nitro reduction took<br />

place solely via hydrogenase or ferredoxin was not conclusively demonstrated.<br />

Boopathy et al. (5) examined the <strong>anaerobic</strong> removal of <strong>TNT</strong> under different<br />

electron accepting conditions in a soil-bacterial consortium. Under nitrate reducing<br />

conditions, 82% of the <strong>TNT</strong> was removed from contaminants <strong>with</strong> 100 ppm of <strong>TNT</strong>.<br />

Under sulfate reducing conditions, 30% of 100 ppm was removed. Using CO2 as an<br />

electron acceptor, 35 % of 100 ppm <strong>TNT</strong> was removed. <strong>In</strong> these experiments, <strong>TNT</strong><br />

did not serve as a carbon or primarily energy source, but its removal was achieved by<br />

co-metabolism <strong>with</strong> the energy source. The <strong>TNT</strong> intermediate reductions were<br />

4A26DNT and 2A46DNT, wherein the former was predominant.<br />

9

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