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Enzymatic halogenation of the phenolic monoterpenes thymol and carvacrol with chloroperoxidase†
Laura Getrey,Thomas Krieg,Frank Hollmann,Jens Schrader,Dirk Holtmann
Green Chemistry Pub Date : 11/28/2013 00:00:00 , DOI:10.1039/C3GC42269K
Abstract

The conversion of the phenolic monoterpenes thymol and carvacrol into antimicrobials by (electro)-chemoenzymatic halogenation was investigated using a chloroperoxidase (CPO) catalyzed process. The CPO catalysed process enables for the first time the biotechnological production of chlorothymol, chlorocarvacrol and bromothymol as well as a dichlorothymol with high conversion rates, total turnover numbers and space time yields of up to 90%, 164 000 and 4.6 mM h−1, respectively.

Graphical abstract: Enzymatic halogenation of the phenolic monoterpenes thymol and carvacrol with chloroperoxidase
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