Literature DB >> 17975855

Oxidation of a laccase mediator ABTS as studied by ESI-FTICR mass spectrometry.

Asse Marjasvaara1, Janne Jänis, Pirjo Vainiotalo.   

Abstract

The oxidation reaction of a laccase mediator ABTS (2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) was studied by electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI-FTICRMS). Oxidation products of ABTS were measured after reaction times that varied from a few minutes up to several days and both positive and negative ionization modes were employed. Exact mass measurements and collision-induced dissociation (CID) experiments were used to characterize the structures of the ions formed. After reacting with Trametes versicolor laccase (TvL), the radical cation form of ABTS was the main product observed by the positive ionization mode. Negative ionization mode experiments revealed that a degradation product from ABTS was formed. John Wiley & Sons, Ltd

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Year:  2008        PMID: 17975855     DOI: 10.1002/jms.1332

Source DB:  PubMed          Journal:  J Mass Spectrom        ISSN: 1076-5174            Impact factor:   1.982


  2 in total

1.  Biomimetic synthesis of galantamine via laccase/TEMPO mediated oxidative coupling.

Authors:  Claudio Zippilli; Lorenzo Botta; Bruno Mattia Bizzarri; Maria Camilla Baratto; Rebecca Pogni; Raffaele Saladino
Journal:  RSC Adv       Date:  2020-03-17       Impact factor: 4.036

2.  Laccase catalyzed synthesis of iodinated phenolic compounds with antifungal activity.

Authors:  Julian Ihssen; Mark Schubert; Linda Thöny-Meyer; Michael Richter
Journal:  PLoS One       Date:  2014-03-03       Impact factor: 3.240

  2 in total

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