| Literature DB >> 18362960 |
Laurence Marmuse1, Michèle Asther, Emeline Fabre, David Navarro, Laurence Lesage-Meessen, Marcel Asther, Michael O'Donohue, Sébastien Fort, Hugues Driguez.
Abstract
Indolyl and nitrophenyl 5-O-hydroxycinnamoyl-alpha-L-arabinofuranosides were prepared by chemo-enzymatic syntheses. These probes were designed as substrates to be used in assays of feruloyl esterase activity (EC 3.1.1.77). Color development in the assays only occurs when feruloyl esterase activity releases an intermediate chromogenic arabinoside that is a suitable substrate for alpha-L-arabinofuranosidase (EC 3.2.1.55), which in turn releases the free chromogenic group. The usefulness of these compounds was evaluated in both qualitative solid media-based assays and quantitative liquid assays that can be performed in microtiter plates using feruloyl esterases and arabinofuranosidases from various origins.Mesh:
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Year: 2008 PMID: 18362960 DOI: 10.1039/b717742a
Source DB: PubMed Journal: Org Biomol Chem ISSN: 1477-0520 Impact factor: 3.876