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A Review on Platensimycin: A Selective FabF Inhibitor
Emerging resistance to existing antibiotics is an inevitable matter of concern in the treatment of bacterial infection. Naturally occurring unique class of natural antibiotic, platensimycin, a secondary metabolite from Streptomyces platensis, is an excellent breakthrough in recent antibiotic researc...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749828/ https://www.ncbi.nlm.nih.gov/pubmed/26942008 http://dx.doi.org/10.1155/2016/9706753 |
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author | Das, Manik Sakha Ghosh, Partha Manna, Kuntal |
author_facet | Das, Manik Sakha Ghosh, Partha Manna, Kuntal |
author_sort | Das, Manik |
collection | PubMed |
description | Emerging resistance to existing antibiotics is an inevitable matter of concern in the treatment of bacterial infection. Naturally occurring unique class of natural antibiotic, platensimycin, a secondary metabolite from Streptomyces platensis, is an excellent breakthrough in recent antibiotic research with unique structural pattern and significant antibacterial activity. β-Ketoacyl-(acyl-carrier-protein (ACP)) synthase (FabF) whose Gram-positive bacteria need to biosynthesize cell membranes is the target of inhibition of platensimycin. So, isolation, retrosynthetic analysis, synthesis of platensimycin, and analogues of platensimycin synthesized till today are the objectives of this review which may be helpful to further investigate and to reveal untouched area on this molecule and to obtain a potential antibacterial lead with enhanced significant antibacterial activity. |
format | Online Article Text |
id | pubmed-4749828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-47498282016-03-03 A Review on Platensimycin: A Selective FabF Inhibitor Das, Manik Sakha Ghosh, Partha Manna, Kuntal Int J Med Chem Review Article Emerging resistance to existing antibiotics is an inevitable matter of concern in the treatment of bacterial infection. Naturally occurring unique class of natural antibiotic, platensimycin, a secondary metabolite from Streptomyces platensis, is an excellent breakthrough in recent antibiotic research with unique structural pattern and significant antibacterial activity. β-Ketoacyl-(acyl-carrier-protein (ACP)) synthase (FabF) whose Gram-positive bacteria need to biosynthesize cell membranes is the target of inhibition of platensimycin. So, isolation, retrosynthetic analysis, synthesis of platensimycin, and analogues of platensimycin synthesized till today are the objectives of this review which may be helpful to further investigate and to reveal untouched area on this molecule and to obtain a potential antibacterial lead with enhanced significant antibacterial activity. Hindawi Publishing Corporation 2016 2016-01-28 /pmc/articles/PMC4749828/ /pubmed/26942008 http://dx.doi.org/10.1155/2016/9706753 Text en Copyright © 2016 Manik Das et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Das, Manik Sakha Ghosh, Partha Manna, Kuntal A Review on Platensimycin: A Selective FabF Inhibitor |
title | A Review on Platensimycin: A Selective FabF Inhibitor |
title_full | A Review on Platensimycin: A Selective FabF Inhibitor |
title_fullStr | A Review on Platensimycin: A Selective FabF Inhibitor |
title_full_unstemmed | A Review on Platensimycin: A Selective FabF Inhibitor |
title_short | A Review on Platensimycin: A Selective FabF Inhibitor |
title_sort | review on platensimycin: a selective fabf inhibitor |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4749828/ https://www.ncbi.nlm.nih.gov/pubmed/26942008 http://dx.doi.org/10.1155/2016/9706753 |
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