Literature DB >> 18362960

New chromogenic substrates for feruloyl esterases.

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.

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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


  3 in total

1.  Synthesis of Indoxyl-glycosides for Detection of Glycosidase Activities.

Authors:  Stephan Böttcher; Joachim Thiem
Journal:  J Vis Exp       Date:  2015-05-27       Impact factor: 1.355

2.  Synthesis of a 1,2-cis-indoxyl galactoside as a chromogenic glycosidase substrate.

Authors:  Sakuto Nagata; Hirotaka Tomida; Haruka Iwai-Hirose; Hide-Nori Tanaka; Hiromune Ando; Akihiro Imamura; Hideharu Ishida
Journal:  RSC Adv       Date:  2019-09-09       Impact factor: 3.361

3.  Regioselective chemoenzymatic syntheses of ferulate conjugates as chromogenic substrates for feruloyl esterases.

Authors:  Olga Gherbovet; Fernando Ferreira; Apolline Clément; Mélanie Ragon; Julien Durand; Sophie Bozonnet; Michael J O'Donohue; Régis Fauré
Journal:  Beilstein J Org Chem       Date:  2021-02-01       Impact factor: 2.883

  3 in total

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