A novel screening assay for hydroxynitrile lyases suitable for high-throughput screening
- PMID: 17157404
- DOI: 10.1016/j.jbiotec.2006.10.004
A novel screening assay for hydroxynitrile lyases suitable for high-throughput screening
Abstract
Hydroxynitrile lyases (Hnls) are important biocatalysts for the synthesis of optically pure cyanohydrins, which are used as precursors and building blocks for a wide range of high price fine chemicals. Although two Hnl enzymes, from the tropical rubber tree Hevea brasiliensis and from the almond tree Prunus amygdalus, are already used for large scale industrial applications, the enzymes still need to be improved and adapted to the special demands of industrial processes. In many cases directed evolution has been the method of choice to improve enzymes, which are applied as industrial biocatalysts. The screening procedure is the most crucial point in every directed evolution experiment. Herein, we describe the successful development of a novel screening assay for Hnls and its application in high-throughput screening of Escherichia coli mutant libraries. The new assay allows rapid screening of mutant libraries and facilitates the discovery of improved enzyme variants. Hnls catalyze the cleavage of cyanohydrins to hydrocyanic acid and the corresponding aldehyde or ketone. The enzyme assay is based on the detection of hydrocyanic acid produced, making it an all-purpose screening assay, without restriction to any kind of substrate. The gaseous HCN liberated within the Hnl reaction is detected by a visible colorimetric reaction. The facile, highly sensitive and reproducible screening method was validated by identifying new enzyme variants with novel substrate specificities.
Similar articles
-
A high-throughput screening assay for hydroxynitrile lyase activity.Chem Commun (Camb). 2006 Oct 28;(40):4201-3. doi: 10.1039/b607863j. Epub 2006 Aug 29. Chem Commun (Camb). 2006. PMID: 17031431
-
Potential and capabilities of hydroxynitrile lyases as biocatalysts in the chemical industry.Appl Microbiol Biotechnol. 2007 Aug;76(2):309-20. doi: 10.1007/s00253-007-1025-6. Epub 2007 Jul 3. Appl Microbiol Biotechnol. 2007. PMID: 17607575 Review.
-
Stereoselective biocatalytic synthesis of (S)-2-hydroxy-2-methylbutyric acid via substrate engineering by using "thio-disguised" precursors and oxynitrilase catalysis.Chemistry. 2007;13(12):3369-76. doi: 10.1002/chem.200601114. Chemistry. 2007. PMID: 17226866
-
High-level intracellular expression of hydroxynitrile lyase from the tropical rubber tree Hevea brasiliensis in microbial hosts.Protein Expr Purif. 1997 Oct;11(1):61-71. doi: 10.1006/prep.1997.0765. Protein Expr Purif. 1997. PMID: 9325140
-
Hydroxynitrile lyases of higher plants.Biol Chem. 1996 Oct;377(10):611-7. Biol Chem. 1996. PMID: 8922588 Review.
Cited by
-
Enzyme discovery beyond homology: a unique hydroxynitrile lyase in the Bet v1 superfamily.Sci Rep. 2017 May 3;7:46738. doi: 10.1038/srep46738. Sci Rep. 2017. PMID: 28466867 Free PMC article.
-
Discovery of a novel (R)-selective bacterial hydroxynitrile lyase from Acidobacterium capsulatum.Comput Struct Biotechnol J. 2014 Jul 8;10(16):58-62. doi: 10.1016/j.csbj.2014.07.002. eCollection 2014 Jun. Comput Struct Biotechnol J. 2014. PMID: 25210600 Free PMC article.
-
Characterization of two bacterial hydroxynitrile lyases with high similarity to cupin superfamily proteins.Appl Environ Microbiol. 2012 Mar;78(6):2053-5. doi: 10.1128/AEM.06899-11. Epub 2012 Jan 6. Appl Environ Microbiol. 2012. PMID: 22226952 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous