Degradation of the Ferric Chelate of EDTA by a Pure Culture of an Agrobacterium sp

Author:

Lauff John J.1,Steele D. Bernie1,Coogan Louise A.1,Breitfeller James M.1

Affiliation:

1. Genencor International, 1870 Winton Road, South, Rochester, New York 14618, and Department of Botany and Microbiology, Auburn University, Auburn, Alabama 368992

Abstract

A pure culture of an Agrobacterium sp. (deposited as ATCC 55002) that mineralizes the ferric chelate of EDTA (ferric-EDTA) was isolated by selective enrichment from a treatment facility receiving industrial waste containing ferric-EDTA. The isolate grew on ferric-EDTA as the sole carbon source at concentrations exceeding 100 mM. As the degradation proceeded, carbon dioxide, ammonia, and an unidentified metabolite(s) were produced; the pH increased, and iron was precipitated from solution. The maximum rate of degradation observed with sodium ferric-EDTA as the substrate was 24 mM/day. At a substrate concentration of 35 mM, 90% of the substrate was degraded in 3 days and 70% of the associated chemical oxygen demand was removed from solution. Less than 15% of the carbon initially present was incorporated into the cell mass. Significant growth of this strain was not observed with uncomplexed EDTA as the sole carbon source at comparable concentrations; however, the ferric chelate of propylenediaminetetraacetic acid (ferric-PDTA) did support growth.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

Reference18 articles.

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3. Drucker D. B. 1976. Gas-liquid chromatographic chemotaxonomy p. 51-125. In J. R. Norris (ed.) Methods in microbiology vol. 9. Academic Press Inc. (London) Ltd. London.

4. A correlation study of biodegradability determinations with various chemicals in various tests;Gerike P.;Ecotoxicol. Environ. Safety,1975

5. (An)aerobic breakdown of chelating agents used in household detergents;Egli T.;Microbiol. Sci.,1988

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