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Activation of Human Salivary Aldehyde Dehydrogenase by Sulforaphane: Mechanism and Significance
Cruciferous vegetables contain the bio-active compound sulforaphane (SF) which has been reported to protect individuals against various diseases by a number of mechanisms, including activation of the phase II detoxification enzymes. In this study, we show that the extracts of five cruciferous vegeta...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5172892/ https://www.ncbi.nlm.nih.gov/pubmed/27997560 http://dx.doi.org/10.1371/journal.pone.0168463 |
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author | Alam, Md. Fazle Laskar, Amaj Ahmed Maryam, Lubna Younus, Hina |
author_facet | Alam, Md. Fazle Laskar, Amaj Ahmed Maryam, Lubna Younus, Hina |
author_sort | Alam, Md. Fazle |
collection | PubMed |
description | Cruciferous vegetables contain the bio-active compound sulforaphane (SF) which has been reported to protect individuals against various diseases by a number of mechanisms, including activation of the phase II detoxification enzymes. In this study, we show that the extracts of five cruciferous vegetables that we commonly consume and SF activate human salivary aldehyde dehydrogenase (hsALDH), which is a very important detoxifying enzyme in the mouth. Maximum activation was observed at 1 μg/ml of cabbage extract with 2.6 fold increase in the activity. There was a ~1.9 fold increase in the activity of hsALDH at SF concentration of ≥ 100 nM. The concentration of SF at half the maximum response (EC(50) value) was determined to be 52 ± 2 nM. There was an increase in the V(max) and a decrease in the K(m) of the enzyme in the presence of SF. Hence, SF interacts with the enzyme and increases its affinity for the substrate. UV absorbance, fluorescence and CD studies revealed that SF binds to hsALDH and does not disrupt its native structure. SF binds with the enzyme with a binding constant of 1.23 x 10(7) M(-1). There is one binding site on hsALDH for SF, and the thermodynamic parameters indicate the formation of a spontaneous strong complex between the two. Molecular docking analysis depicted that SF fits into the active site of ALDH3A1, and facilitates the catalytic mechanism of the enzyme. SF being an antioxidant, is very likely to protect the catalytic Cys 243 residue from oxidation, which leads to the increase in the catalytic efficiency and hence the activation of the enzyme. Further, hsALDH which is virtually inactive towards acetaldehyde exhibited significant activity towards it in the presence of SF. It is therefore very likely that consumption of large quantities of cruciferous vegetables or SF supplements, through their activating effect on hsALDH can protect individuals who are alcohol intolerant against acetaldehyde toxicity and also lower the risk of oral cancer development. |
format | Online Article Text |
id | pubmed-5172892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-51728922017-01-04 Activation of Human Salivary Aldehyde Dehydrogenase by Sulforaphane: Mechanism and Significance Alam, Md. Fazle Laskar, Amaj Ahmed Maryam, Lubna Younus, Hina PLoS One Research Article Cruciferous vegetables contain the bio-active compound sulforaphane (SF) which has been reported to protect individuals against various diseases by a number of mechanisms, including activation of the phase II detoxification enzymes. In this study, we show that the extracts of five cruciferous vegetables that we commonly consume and SF activate human salivary aldehyde dehydrogenase (hsALDH), which is a very important detoxifying enzyme in the mouth. Maximum activation was observed at 1 μg/ml of cabbage extract with 2.6 fold increase in the activity. There was a ~1.9 fold increase in the activity of hsALDH at SF concentration of ≥ 100 nM. The concentration of SF at half the maximum response (EC(50) value) was determined to be 52 ± 2 nM. There was an increase in the V(max) and a decrease in the K(m) of the enzyme in the presence of SF. Hence, SF interacts with the enzyme and increases its affinity for the substrate. UV absorbance, fluorescence and CD studies revealed that SF binds to hsALDH and does not disrupt its native structure. SF binds with the enzyme with a binding constant of 1.23 x 10(7) M(-1). There is one binding site on hsALDH for SF, and the thermodynamic parameters indicate the formation of a spontaneous strong complex between the two. Molecular docking analysis depicted that SF fits into the active site of ALDH3A1, and facilitates the catalytic mechanism of the enzyme. SF being an antioxidant, is very likely to protect the catalytic Cys 243 residue from oxidation, which leads to the increase in the catalytic efficiency and hence the activation of the enzyme. Further, hsALDH which is virtually inactive towards acetaldehyde exhibited significant activity towards it in the presence of SF. It is therefore very likely that consumption of large quantities of cruciferous vegetables or SF supplements, through their activating effect on hsALDH can protect individuals who are alcohol intolerant against acetaldehyde toxicity and also lower the risk of oral cancer development. Public Library of Science 2016-12-20 /pmc/articles/PMC5172892/ /pubmed/27997560 http://dx.doi.org/10.1371/journal.pone.0168463 Text en © 2016 Alam et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Alam, Md. Fazle Laskar, Amaj Ahmed Maryam, Lubna Younus, Hina Activation of Human Salivary Aldehyde Dehydrogenase by Sulforaphane: Mechanism and Significance |
title | Activation of Human Salivary Aldehyde Dehydrogenase by Sulforaphane: Mechanism and Significance |
title_full | Activation of Human Salivary Aldehyde Dehydrogenase by Sulforaphane: Mechanism and Significance |
title_fullStr | Activation of Human Salivary Aldehyde Dehydrogenase by Sulforaphane: Mechanism and Significance |
title_full_unstemmed | Activation of Human Salivary Aldehyde Dehydrogenase by Sulforaphane: Mechanism and Significance |
title_short | Activation of Human Salivary Aldehyde Dehydrogenase by Sulforaphane: Mechanism and Significance |
title_sort | activation of human salivary aldehyde dehydrogenase by sulforaphane: mechanism and significance |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5172892/ https://www.ncbi.nlm.nih.gov/pubmed/27997560 http://dx.doi.org/10.1371/journal.pone.0168463 |
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