Confirmation of conjugation processes during TNT metabolism by axenic plant roots
- Rice Univ., Houston, TX (United States)
This paper examines processes in plants for the formation of fate products of TNT beyond its animated reduction products, 2-amino-4,6-dinitrotoluene and 4-amino-2,6-dinitrotoluene. TNT metabolites were isolated and characterized in combination with temporal analyses of production profiles and {sup 14}C distribution, in microbe-free, axenic root cultures of Catharanthus roseus. Four unique TNT-derived compounds were isolated. Using evidence from {sup 1}H NMR, mass spectroscopy, HPLC, acid hydrolysis, and enzymatic hydrolysis with {beta}-glucuronidase and {beta}-glucosidase, they were established as conjugates formed by reactions of the amine groups of 2-amino-4,6-dinitrotoluene and 4-amino-2,6-dinitrotoluene. From the mass spectral evidence, at least a six-carbon unit from the plant intracellular milleu was involved in conjugate formation. Mass balance analysis indicated that, by 75 h after TNT amendment of the initial TNT radiolabel, extractable conjugates comprised 22%, bound residues comprised another 29%, 2-amino-4,6-dinitrotoluene was 4%, and the rest remained unidentified. Isolates from TNT-amended roots versus monoamino-dinitrotoluene-amended roots were not identical, suggesting numerous possible outcomes for the plant-based conjugation of 2-amino-2,6-dinitrotoluene or 4-amino-2,6-dinitrotoluene. This study is the first direct evidence for the involvement of the primary reduction products of TNT--2-amino-4,6-dinitrotoluene ad 4-amino--2,6-dinitrotoluene--in conjugation process in plant detoxification of TNT.
- OSTI ID:
- 323809
- Journal Information:
- Environmental Science and Technology, Vol. 33, Issue 3; Other Information: PBD: 1 Feb 1999
- Country of Publication:
- United States
- Language:
- English
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