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Applied and Environmental Microbiology, April 2006, p. 2491-2495, Vol. 72, No. 4
0099-2240/06/$08.00+0 doi:10.1128/AEM.72.4.2491-2495.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Gang Cheng,2,3,4,
Michael J. Sadowsky,2,3,4 and
Lawrence P. Wackett1,2,3*
Department of Biochemistry, Molecular Biology and Biophysics,1 BioTechnology Institute,2 Center for Microbial and Plant Genomics,3 Department of Soil, Water and Climate, University of Minnesota, St. Paul, Minnesota 551084
Received 1 November 2005/ Accepted 21 January 2006
TrzF, the allophanate hydrolase from Enterobacter cloacae strain 99, was cloned, overexpressed in the presence of a chaperone protein, and purified to homogeneity. Native TrzF had a subunit molecular weight of 65,401 and a subunit stoichiometry of
2 and did not contain significant levels of metals. TrzF showed time-dependent inhibition by phenyl phosphorodiamidate and is a member of the amidase signature protein family. TrzF was highly active in the hydrolysis of allophanate but was not active with urea, despite having been previously considered a urea amidolyase. TrzF showed lower activity with malonamate, malonamide, and biuret. The allophanate hydrolase from Pseudomonas sp. strain ADP, AtzF, was also shown to hydrolyze biuret slowly. Since biuret and allophanate are consecutive metabolites in cyanuric acid metabolism, the low level of biuret hydrolase activity can have physiological significance. A recombinant Escherichia coli strain containing atzD, encoding cyanuric acid hydrolase that produces biuret, and atzF grew slowly on cyanuric acid as a source of nitrogen. The amount of growth produced was consistent with the liberation of 3 mol of ammonia from cyanuric acid. In vitro, TrzF was shown to hydrolyze biuret to liberate 3 mol of ammonia. The biuret hydrolyzing activity of TrzF might also be physiologically relevant in native strains. E. cloacae strain 99 grows on cyanuric acid with a significant accumulation of biuret.
N.S. and G.C. contributed equally to this work.
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