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Myrosinase-dependent and –independent formation and control of isothiocyanate products of glucosinolate hydrolysis

Brassicales contain a myrosinase enzyme that hydrolyzes glucosinolates to form toxic isothiocyanates (ITC), as a defense against bacteria, fungi, insects and herbivores including man. Low levels of ITC trigger a host defense system in mammals that protects them against chronic diseases. Because huma...

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Autores principales: Angelino, Donato, Dosz, Edward B., Sun, Jianghao, Hoeflinger, Jennifer L., Van Tassell, Maxwell L., Chen, Pei, Harnly, James M., Miller, Michael J., Jeffery, Elizabeth H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4593958/
https://www.ncbi.nlm.nih.gov/pubmed/26500669
http://dx.doi.org/10.3389/fpls.2015.00831
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author Angelino, Donato
Dosz, Edward B.
Sun, Jianghao
Hoeflinger, Jennifer L.
Van Tassell, Maxwell L.
Chen, Pei
Harnly, James M.
Miller, Michael J.
Jeffery, Elizabeth H.
author_facet Angelino, Donato
Dosz, Edward B.
Sun, Jianghao
Hoeflinger, Jennifer L.
Van Tassell, Maxwell L.
Chen, Pei
Harnly, James M.
Miller, Michael J.
Jeffery, Elizabeth H.
author_sort Angelino, Donato
collection PubMed
description Brassicales contain a myrosinase enzyme that hydrolyzes glucosinolates to form toxic isothiocyanates (ITC), as a defense against bacteria, fungi, insects and herbivores including man. Low levels of ITC trigger a host defense system in mammals that protects them against chronic diseases. Because humans typically cook their brassica vegetables, destroying myrosinase, there is a great interest in determining how human microbiota can hydrolyze glucosinolates and release them, to provide the health benefits of ITC. ITC are highly reactive electrophiles, binding reversibly to thiols, but accumulating and causing damage when free thiols are not available. We found that addition of excess thiols released protein-thiol-bound ITC, but that the microbiome supports only poor hydrolysis unless exposed to dietary glucosinolates for a period of days. These findings explain why 3–5 servings a week of brassica vegetables may provide health effects, even if they are cooked.
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spelling pubmed-45939582015-10-23 Myrosinase-dependent and –independent formation and control of isothiocyanate products of glucosinolate hydrolysis Angelino, Donato Dosz, Edward B. Sun, Jianghao Hoeflinger, Jennifer L. Van Tassell, Maxwell L. Chen, Pei Harnly, James M. Miller, Michael J. Jeffery, Elizabeth H. Front Plant Sci Plant Science Brassicales contain a myrosinase enzyme that hydrolyzes glucosinolates to form toxic isothiocyanates (ITC), as a defense against bacteria, fungi, insects and herbivores including man. Low levels of ITC trigger a host defense system in mammals that protects them against chronic diseases. Because humans typically cook their brassica vegetables, destroying myrosinase, there is a great interest in determining how human microbiota can hydrolyze glucosinolates and release them, to provide the health benefits of ITC. ITC are highly reactive electrophiles, binding reversibly to thiols, but accumulating and causing damage when free thiols are not available. We found that addition of excess thiols released protein-thiol-bound ITC, but that the microbiome supports only poor hydrolysis unless exposed to dietary glucosinolates for a period of days. These findings explain why 3–5 servings a week of brassica vegetables may provide health effects, even if they are cooked. Frontiers Media S.A. 2015-10-06 /pmc/articles/PMC4593958/ /pubmed/26500669 http://dx.doi.org/10.3389/fpls.2015.00831 Text en Copyright © 2015 Angelino, Dosz, Sun, Hoeflinger, Van Tassell, Chen, Harnly, Miller and Jeffery. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Angelino, Donato
Dosz, Edward B.
Sun, Jianghao
Hoeflinger, Jennifer L.
Van Tassell, Maxwell L.
Chen, Pei
Harnly, James M.
Miller, Michael J.
Jeffery, Elizabeth H.
Myrosinase-dependent and –independent formation and control of isothiocyanate products of glucosinolate hydrolysis
title Myrosinase-dependent and –independent formation and control of isothiocyanate products of glucosinolate hydrolysis
title_full Myrosinase-dependent and –independent formation and control of isothiocyanate products of glucosinolate hydrolysis
title_fullStr Myrosinase-dependent and –independent formation and control of isothiocyanate products of glucosinolate hydrolysis
title_full_unstemmed Myrosinase-dependent and –independent formation and control of isothiocyanate products of glucosinolate hydrolysis
title_short Myrosinase-dependent and –independent formation and control of isothiocyanate products of glucosinolate hydrolysis
title_sort myrosinase-dependent and –independent formation and control of isothiocyanate products of glucosinolate hydrolysis
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4593958/
https://www.ncbi.nlm.nih.gov/pubmed/26500669
http://dx.doi.org/10.3389/fpls.2015.00831
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