A SIMPLE WAY TO (+ -)-DIHYDROACTINIDIOLIDE FROM BETA-IONONE RELATED TO THE ENZYMATIC COOXIDATION OF BETA-CAROTENE IN AQUEOUS-SOLUTION/

Authors
BOSSER A PAPLOREY E BELIN JM
Citation
A. Bosser et al., A SIMPLE WAY TO (+ -)-DIHYDROACTINIDIOLIDE FROM BETA-IONONE RELATED TO THE ENZYMATIC COOXIDATION OF BETA-CAROTENE IN AQUEOUS-SOLUTION/, Biotechnology progress, 11(6), 1995, pp. 689-692
Citations number
25
Categorie Soggetti
Biothechnology & Applied Migrobiology","Food Science & Tenology
Journal title
Biotechnology progress → ACNP
ISSN journal
87567938
Volume
11
Issue
6
Year of publication
1995
Pages
689 - 692
Database
ISI
SICI code
8756-7938(1995)11:6<689:ASWT(->2.0.ZU;2-Q
Abstract
In a previous paper (Bosser and Belin, 1994), it was shown that the co -oxidation of beta-carotene (BC) by xanthine olridase in aqueous solut ions at 37 degrees C led to beta-ionone, epoxy-5,6-beta-ionone, and di hydroactinidiolide (DHA). We explain in this article the pathways betw een the ionone derivatives, and the respective places of each volatile compound in the enzymatic bleaching of BC are discussed. We also prop ose a simple synthetic way to DHA from commercially available beta-ion one.