3.8 Article

Evolution of an organophosphate-degrading enzyme: a comparison of natural and directed evolution

Journal

PROTEIN ENGINEERING
Volume 16, Issue 2, Pages 135-145

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/proeng/gzg013

Keywords

Agrobacterium; bioremediation; carboxylated lysine; directed evolution; organophosphates; phosphotriesterase

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Organophosphate-degrading enzyme from Agrobacterium radiobacter P230 (OPDA) is a recently discovered enzyme that degrades a broad range of organophosphates. It is very similar to OPH first isolated from Pseudomonas diminuta MG. Despite a high level of sequence identity, OPH and OPDA exhibit different substrate specificities. We report here the structure of OPDA and identify regions of the protein that are likely to give it a preference for substrates that have shorter alkyl substituents. Directed evolution was used to evolve a series of OPH mutants that had activities similar to those of OPDA. Mutants were selected for on the basis of their ability to degrade a number of substrates. The mutations tended to cluster in particular regions of the protein and in most cases, these regions were where OPH and OPDA had significant differences in their sequences.

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