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Activation studies with amines and amino acids of the β-carbonic anhydrase encoded by the Rv3273 gene from the pathogenic bacterium Mycobacterium tuberculosis
The activation of a β-class carbonic anhydrase (CAs, EC 4.2.1.1) from Mycobacterium tuberculosis, encoded by the gene Rv3273 (mtCA 3), was investigated using a panel of natural and non-natural amino acids and amines. mtCA 3 was effectively activated by D-DOPA, L-Trp, dopamine and serotonin, with K(A...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009870/ https://www.ncbi.nlm.nih.gov/pubmed/29322836 http://dx.doi.org/10.1080/14756366.2017.1422250 |
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author | Angeli, Andrea Del Prete, Sonia Osman, Sameh M. Alasmary, Fatmah A. S. AlOthman, Zeid Donald, William A. Capasso, Clemente Supuran, Claudiu T. |
author_facet | Angeli, Andrea Del Prete, Sonia Osman, Sameh M. Alasmary, Fatmah A. S. AlOthman, Zeid Donald, William A. Capasso, Clemente Supuran, Claudiu T. |
author_sort | Angeli, Andrea |
collection | PubMed |
description | The activation of a β-class carbonic anhydrase (CAs, EC 4.2.1.1) from Mycobacterium tuberculosis, encoded by the gene Rv3273 (mtCA 3), was investigated using a panel of natural and non-natural amino acids and amines. mtCA 3 was effectively activated by D-DOPA, L-Trp, dopamine and serotonin, with K(A)s ranging between 8.98 and 12.1 µM. L-His and D-Tyr showed medium potency activating effects, with K(A)s in the range of 17.6–18.2 µM, whereas other amines and amino acids were relatively ineffective activators, with K(A)s in the range of 28.9–52.2 µM. As the physiological roles of the three mtCAs present in this pathogen are currently poorly understood and considering that inhibition of these enzymes has strong antibacterial effects, discovering molecules that modulate their enzymatic activity may lead to a better understanding of the factors related to the invasion and colonisation of the host during Mycobacterium tuberculosis infection. |
format | Online Article Text |
id | pubmed-6009870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-60098702018-07-11 Activation studies with amines and amino acids of the β-carbonic anhydrase encoded by the Rv3273 gene from the pathogenic bacterium Mycobacterium tuberculosis Angeli, Andrea Del Prete, Sonia Osman, Sameh M. Alasmary, Fatmah A. S. AlOthman, Zeid Donald, William A. Capasso, Clemente Supuran, Claudiu T. J Enzyme Inhib Med Chem Short Communication The activation of a β-class carbonic anhydrase (CAs, EC 4.2.1.1) from Mycobacterium tuberculosis, encoded by the gene Rv3273 (mtCA 3), was investigated using a panel of natural and non-natural amino acids and amines. mtCA 3 was effectively activated by D-DOPA, L-Trp, dopamine and serotonin, with K(A)s ranging between 8.98 and 12.1 µM. L-His and D-Tyr showed medium potency activating effects, with K(A)s in the range of 17.6–18.2 µM, whereas other amines and amino acids were relatively ineffective activators, with K(A)s in the range of 28.9–52.2 µM. As the physiological roles of the three mtCAs present in this pathogen are currently poorly understood and considering that inhibition of these enzymes has strong antibacterial effects, discovering molecules that modulate their enzymatic activity may lead to a better understanding of the factors related to the invasion and colonisation of the host during Mycobacterium tuberculosis infection. Taylor & Francis 2018-01-11 /pmc/articles/PMC6009870/ /pubmed/29322836 http://dx.doi.org/10.1080/14756366.2017.1422250 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 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 work is properly cited. |
spellingShingle | Short Communication Angeli, Andrea Del Prete, Sonia Osman, Sameh M. Alasmary, Fatmah A. S. AlOthman, Zeid Donald, William A. Capasso, Clemente Supuran, Claudiu T. Activation studies with amines and amino acids of the β-carbonic anhydrase encoded by the Rv3273 gene from the pathogenic bacterium Mycobacterium tuberculosis |
title | Activation studies with amines and amino acids of the β-carbonic anhydrase encoded by the Rv3273 gene from the pathogenic bacterium Mycobacterium tuberculosis |
title_full | Activation studies with amines and amino acids of the β-carbonic anhydrase encoded by the Rv3273 gene from the pathogenic bacterium Mycobacterium tuberculosis |
title_fullStr | Activation studies with amines and amino acids of the β-carbonic anhydrase encoded by the Rv3273 gene from the pathogenic bacterium Mycobacterium tuberculosis |
title_full_unstemmed | Activation studies with amines and amino acids of the β-carbonic anhydrase encoded by the Rv3273 gene from the pathogenic bacterium Mycobacterium tuberculosis |
title_short | Activation studies with amines and amino acids of the β-carbonic anhydrase encoded by the Rv3273 gene from the pathogenic bacterium Mycobacterium tuberculosis |
title_sort | activation studies with amines and amino acids of the β-carbonic anhydrase encoded by the rv3273 gene from the pathogenic bacterium mycobacterium tuberculosis |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6009870/ https://www.ncbi.nlm.nih.gov/pubmed/29322836 http://dx.doi.org/10.1080/14756366.2017.1422250 |
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