Literature DB >> 11749956

Bicyclic triterpenes as new main products of squalene-hopene cyclase by mutation at conserved tyrosine residues.

C Füll1.   

Abstract

The catalytic cavity of the Alicyclobacillus acidocaldarius squalene-hopene cyclase is predominantly lined by aromatic amino acids. In mutant cyclases, the four tyrosine residues in the catalytic cavity were replaced by different amino acids. The mutants showed significant differences in catalytic behavior compared to the wild-type and to each other. Mutants Y609L, Y609C and Y609S produced the bicyclic main product gamma-polypodatetraene, while Y495L and Y612L showed a wild-type product pattern and produced hopene as the main product. Altered product patterns were also found with Y420 mutations.

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Year:  2001        PMID: 11749956     DOI: 10.1016/s0014-5793(01)03153-2

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


  2 in total

Review 1.  Protein engineering towards natural product synthesis and diversification.

Authors:  Angelica O Zabala; Ralph A Cacho; Yi Tang
Journal:  J Ind Microbiol Biotechnol       Date:  2011-10-18       Impact factor: 3.346

2.  Predicting the functions and specificity of triterpenoid synthases: a mechanism-based multi-intermediate docking approach.

Authors:  Bo-Xue Tian; Frank H Wallrapp; Gemma L Holiday; Jeng-Yeong Chow; Patricia C Babbitt; C Dale Poulter; Matthew P Jacobson
Journal:  PLoS Comput Biol       Date:  2014-10-09       Impact factor: 4.475

  2 in total

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