4.5 Article

A positively charged amino acid at position 129 in nitrilase from Rhodococcus rhodochrous ATCC 33278 is an essential residue for the activity with meta-substituted benzonitriles

Journal

FEBS LETTERS
Volume 584, Issue 1, Pages 106-110

Publisher

WILEY
DOI: 10.1016/j.febslet.2009.11.008

Keywords

Mutational analysis; Nitrilase; Rhodococcus rhodochrous ATCC 33278; Selective activity; Substituted benzonitrile

Funding

  1. Korean Government (MOEHRD) [KRF-2008-D00133]

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A positively charged amino acid (Arg, Lys, or His) at position 129 in Rhodococcus rhodochrous ATCC 33278 nitrilase is essential for the activity of aromatic nitriles. The wild-type enzyme containing Arg129 was active only for meta-and para-substituted benzonitriles with a methyl or amino group, but the R129K and R129H mutant enzymes were active only for meta-substituted benzonitriles. The lack of activity of the mutants for para-substituted benzonitriles may be attributable to steric hindrance between the para-substituent and the side chain of Lys or His. Crown Copyright (C) 2009 Published by Elsevier B. V. on behalf of Federation of European Biochemical society. All rights reserved.

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