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Catechol Oxidase versus Tyrosinase Classification Revisited by Site‐Directed Mutagenesis Studies.

Authors :
Prexler, Sarah M.
Frassek, Martin
Moerschbacher, Bruno M.
Dirks‐Hofmeister, Mareike E.
Source :
Angewandte Chemie. 6/24/2019, Vol. 131 Issue 26, p8849-8853. 5p.
Publication Year :
2019

Abstract

Catechol oxidases (COs) and tyrosinases (TYRs) are both polyphenol oxidases (PPOs) that catalyze the oxidation of ortho‐diphenols to the corresponding quinones. By the official classification, only TYRs can also catalyze the hydroxylation of monophenols to ortho‐diphenols. Researchers have been trying to find the molecular reason for the mono‐/diphenolase specificity for decades. However, the hypotheses for the lack of monophenolase activity of plant COs are only based on crystal structures so far. To test these hypotheses, we performed site‐directed mutagenesis studies and phylogenetic analyses with dandelion PPOs offering high phylogenetic diversity, the results of which refute the structure‐based hypotheses. While plant PPOs of phylogenetic group 2 solely exhibit diphenolase activity, plant PPOs of phylogenetic group 1 unexpectedly also show monophenolase activity. This finding sheds new light upon the molecular basis for mono‐/diphenol substrate specificity and challenges the current practice of generally naming plant PPOs as COs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00448249
Volume :
131
Issue :
26
Database :
Academic Search Index
Journal :
Angewandte Chemie
Publication Type :
Academic Journal
Accession number :
137000160
Full Text :
https://doi.org/10.1002/ange.201902846