Discovery of an ultraspecific triuret hydrolase (TrtA) establishes the triuret biodegradation pathway

• Published in: The Journal of biological chemistry Vol. 296; p. 100055
• Main Authors: Tassoulas, Lambros J., Elias, Mikael H., Wackett, Lawrence P.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.01.2021; American Society for Biochemistry and Molecular Biology
• Subjects: BASIC BIOLOGICAL SCIENCES; BiuH; biuret; cysteine hydrolase; enzyme evolution; IHL protein family; MATERIALS SCIENCE; nitrogen-containing compound; substrate discrimination; triuret; TrtA; urea pyrolysis; uric acid oxidation; FPLC; CD; IHL protein family; BiuH; substrate discrimination; nitrogen-containing compound; VDW; biuret; enzyme evolution; TrtA; IHL; cysteine hydrolase; triuret; uric acid oxidation; LB; urea pyrolysis; BME
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.RA120.015631

Triuret (carbonyldiurea) is an impurity found in industrial urea fertilizer (<0.1% w/w) that is applied, worldwide, around 300 million pounds each year on agricultural lands. In addition to anthropogenic sources, endogenous triuret has been identified in amoeba and human urine, the latter being diagnostic for hypokalemia. The present study is the first to describe the metabolic breakdown of triuret, which funnels into biuret metabolism. We identified the gene responsible for triuret decomposition (trtA) in bacterial genomes, clustered with biuH, which encodes biuret hydrolase and has close protein sequence homology. TrtA is a member of the isochorismatase-like hydrolase (IHL) protein family, similarly to BiuH, and has a catalytic efficiency (kcat/KM) of 6 x 105 M−1s−1, a KM for triuret of 20 μM, and exquisite substrate specificity. Indeed, TrtA has four orders of magnitude less activity with biuret. Crystal structures of TrtA in apo and holo form were solved and compared with the BiuH structure. The high substrate selectivity was found to be conveyed by second shell residues around each active site. Mutagenesis of residues conserved in TrtA to the alternate consensus found in BiuHs revealed residues critical to triuret hydrolase activity but no single mutant evolved more biuret activity, and likely a combination of mutations is required to interconvert between TrtA, BiuH functions. TrtA-mediated triuret metabolism is relatively rare in recorded genomes (1–2%), but is largely found in plant-associated, nodulating, and endophytic bacteria. This study suggests functions for triuret hydrolase in certain eukaryotic intermediary processes and prokaryotic intermediary or biodegradative metabolism