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Article Dans Une Revue Organic & Biomolecular Chemistry Année : 2008

New chromogenic substrates for feruloyl esterases

Résumé

Indolyl and nitrophenyl 5-O-hydroxycinnamoyl-α-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 α-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.

Domaines

Chimie organique

Dates et versions

hal-02655815 , version 1 (29-05-2020)

Identifiants

Citer

Laurence Marmuse, Michèle Asther, Emeline Fabre, David Navarro, Laurence Lesage-Meessen, et al.. New chromogenic substrates for feruloyl esterases. Organic & Biomolecular Chemistry, 2008, 6 (7), pp.1208. ⟨10.1039/b717742a⟩. ⟨hal-02655815⟩
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