Literature DB >> 31037807

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

Sarah M Prexler1, Martin Frassek1, Bruno M Moerschbacher1, Mareike E Dirks-Hofmeister2.   

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.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  enzyme engineering; metalloenzymes; mutagenesis; oxidoreductases; substrate specificity

Year:  2019        PMID: 31037807     DOI: 10.1002/anie.201902846

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  6 in total

1.  Evidence for H-bonding interactions to the μ-η22-peroxide of oxy-tyrosinase that activate its coupled binuclear copper site.

Authors:  Ioannis Kipouros; Agnieszka Stańczak; Martin Culka; Erik Andris; Timothy R Machonkin; Lubomír Rulíšek; Edward I Solomon
Journal:  Chem Commun (Camb)       Date:  2022-03-22       Impact factor: 6.222

2.  Conversion of walnut tyrosinase into a catechol oxidase by site directed mutagenesis.

Authors:  Felix Panis; Ioannis Kampatsikas; Aleksandar Bijelic; Annette Rompel
Journal:  Sci Rep       Date:  2020-02-03       Impact factor: 4.379

3.  Identification of Amino Acid Residues Responsible for C-H Activation in Type-III Copper Enzymes by Generating Tyrosinase Activity in a Catechol Oxidase.

Authors:  Ioannis Kampatsikas; Matthias Pretzler; Annette Rompel
Journal:  Angew Chem Int Ed Engl       Date:  2020-09-09       Impact factor: 15.336

Review 4.  Plant Copper Metalloenzymes As Prospects for New Metabolism Involving Aromatic Compounds.

Authors:  Lisa S Mydy; Desnor N Chigumba; Roland D Kersten
Journal:  Front Plant Sci       Date:  2021-11-29       Impact factor: 5.753

5.  Investigation of Enzymes in the Phthalide Biosynthetic Pathway in Angelica sinensis Using Integrative Metabolite Profiles and Transcriptome Analysis.

Authors:  Wei-Meng Feng; Pei Liu; Hui Yan; Guang Yu; Sen Zhang; Shu Jiang; Er-Xin Shang; Da-Wei Qian; Jin-Ao Duan
Journal:  Front Plant Sci       Date:  2022-07-01       Impact factor: 6.627

Review 6.  Similar but Still Different: Which Amino Acid Residues Are Responsible for Varying Activities in Type-III Copper Enzymes?

Authors:  Ioannis Kampatsikas; Annette Rompel
Journal:  Chembiochem       Date:  2020-12-11       Impact factor: 3.164

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.