Literature DB >> 19903476

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.

Soo-Jin Yeom1, Jung-Kul Lee, Deok-Kun Oh.   

Abstract

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.

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Year:  2010        PMID: 19903476     DOI: 10.1016/j.febslet.2009.11.008

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  3 in total

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Authors:  Shubhangi Kaushik; Utpal Mohan; Uc Banerjee
Journal:  Int J Biochem Mol Biol       Date:  2012-12-24

2.  Conversion of sterically demanding α,α-disubstituted phenylacetonitriles by the arylacetonitrilase from Pseudomonas fluorescens EBC191.

Authors:  Stefanie Baum; Dael S Williamson; Trevor Sewell; Andreas Stolz
Journal:  Appl Environ Microbiol       Date:  2011-10-21       Impact factor: 4.792

3.  The Important Role of Halogen Bond in Substrate Selectivity of Enzymatic Catalysis.

Authors:  Shuiqin Jiang; Lujia Zhang; Dongbin Cui; Zhiqiang Yao; Bei Gao; Jinping Lin; Dongzhi Wei
Journal:  Sci Rep       Date:  2016-10-06       Impact factor: 4.379

  3 in total

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