Cargando…

1-(2-aminophenyl)-1H-1,2,3-triazole-4-carboxylic acid: activity against Gram-positive and Gram-negative pathogens including Vibrio cholerae

We report a new synthetic aromatic ε-amino acid containing a triazole moiety with antimicrobial potential against Gram-positive, Gram-negative and pathogenic bacteria including Vibrio cholerae. Structure–property relationship studies revealed that all the functional groups are essential to enhance t...

Descripción completa

Detalles Bibliográficos
Autores principales: Maji, Krishnendu, Haldar, Debasish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666259/
https://www.ncbi.nlm.nih.gov/pubmed/29134076
http://dx.doi.org/10.1098/rsos.170684
_version_ 1783275272108244992
author Maji, Krishnendu
Haldar, Debasish
author_facet Maji, Krishnendu
Haldar, Debasish
author_sort Maji, Krishnendu
collection PubMed
description We report a new synthetic aromatic ε-amino acid containing a triazole moiety with antimicrobial potential against Gram-positive, Gram-negative and pathogenic bacteria including Vibrio cholerae. Structure–property relationship studies revealed that all the functional groups are essential to enhance the antimicrobial activity. The 1-(2-aminophenyl)-1H-1,2,3-triazole-4-carboxylic acid was synthesized by click chemistry. From X-ray crystallography, the amino acid adopts a kink-like structure where the phenyl and triazole rings are perpendicular to each other and the amine and acid groups maintain an angle of 60°. The agar diffusion test shows that the amino acid has significant antibacterial activity. The liquid culture test exhibits that the minimum inhibitory concentration (MIC) value for Bacillus subtilis and Vibrio cholerae is 59.5 µg ml(−1). FE-SEM experiments were performed to study the morphological changes of bacterial shape after treatment with compound 1. The antimicrobial activity of the amino acid was further studied by DNA binding and degradation study, protein binding, dye-binding assay and morphological analysis. Moreover, the amino acid does not have any harmful effect on eukaryotes.
format Online
Article
Text
id pubmed-5666259
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher The Royal Society Publishing
record_format MEDLINE/PubMed
spelling pubmed-56662592017-11-13 1-(2-aminophenyl)-1H-1,2,3-triazole-4-carboxylic acid: activity against Gram-positive and Gram-negative pathogens including Vibrio cholerae Maji, Krishnendu Haldar, Debasish R Soc Open Sci Chemistry We report a new synthetic aromatic ε-amino acid containing a triazole moiety with antimicrobial potential against Gram-positive, Gram-negative and pathogenic bacteria including Vibrio cholerae. Structure–property relationship studies revealed that all the functional groups are essential to enhance the antimicrobial activity. The 1-(2-aminophenyl)-1H-1,2,3-triazole-4-carboxylic acid was synthesized by click chemistry. From X-ray crystallography, the amino acid adopts a kink-like structure where the phenyl and triazole rings are perpendicular to each other and the amine and acid groups maintain an angle of 60°. The agar diffusion test shows that the amino acid has significant antibacterial activity. The liquid culture test exhibits that the minimum inhibitory concentration (MIC) value for Bacillus subtilis and Vibrio cholerae is 59.5 µg ml(−1). FE-SEM experiments were performed to study the morphological changes of bacterial shape after treatment with compound 1. The antimicrobial activity of the amino acid was further studied by DNA binding and degradation study, protein binding, dye-binding assay and morphological analysis. Moreover, the amino acid does not have any harmful effect on eukaryotes. The Royal Society Publishing 2017-10-18 /pmc/articles/PMC5666259/ /pubmed/29134076 http://dx.doi.org/10.1098/rsos.170684 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Chemistry
Maji, Krishnendu
Haldar, Debasish
1-(2-aminophenyl)-1H-1,2,3-triazole-4-carboxylic acid: activity against Gram-positive and Gram-negative pathogens including Vibrio cholerae
title 1-(2-aminophenyl)-1H-1,2,3-triazole-4-carboxylic acid: activity against Gram-positive and Gram-negative pathogens including Vibrio cholerae
title_full 1-(2-aminophenyl)-1H-1,2,3-triazole-4-carboxylic acid: activity against Gram-positive and Gram-negative pathogens including Vibrio cholerae
title_fullStr 1-(2-aminophenyl)-1H-1,2,3-triazole-4-carboxylic acid: activity against Gram-positive and Gram-negative pathogens including Vibrio cholerae
title_full_unstemmed 1-(2-aminophenyl)-1H-1,2,3-triazole-4-carboxylic acid: activity against Gram-positive and Gram-negative pathogens including Vibrio cholerae
title_short 1-(2-aminophenyl)-1H-1,2,3-triazole-4-carboxylic acid: activity against Gram-positive and Gram-negative pathogens including Vibrio cholerae
title_sort 1-(2-aminophenyl)-1h-1,2,3-triazole-4-carboxylic acid: activity against gram-positive and gram-negative pathogens including vibrio cholerae
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666259/
https://www.ncbi.nlm.nih.gov/pubmed/29134076
http://dx.doi.org/10.1098/rsos.170684
work_keys_str_mv AT majikrishnendu 12aminophenyl1h123triazole4carboxylicacidactivityagainstgrampositiveandgramnegativepathogensincludingvibriocholerae
AT haldardebasish 12aminophenyl1h123triazole4carboxylicacidactivityagainstgrampositiveandgramnegativepathogensincludingvibriocholerae