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Parallel pathways in the biosynthesis of aminoglycoside antibiotics
Despite their inherent toxicity and the global spread of bacterial resistance, aminoglycosides (AGs), an old class of microbial drugs, remain a valuable component of the antibiotic arsenal. Recent studies have continued to reveal the fascinating biochemistry of AG biosynthesis and the rich potential...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461906/ https://www.ncbi.nlm.nih.gov/pubmed/28620453 http://dx.doi.org/10.12688/f1000research.11104.1 |
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author | Yu, Yi Zhang, Qi Deng, Zixin |
author_facet | Yu, Yi Zhang, Qi Deng, Zixin |
author_sort | Yu, Yi |
collection | PubMed |
description | Despite their inherent toxicity and the global spread of bacterial resistance, aminoglycosides (AGs), an old class of microbial drugs, remain a valuable component of the antibiotic arsenal. Recent studies have continued to reveal the fascinating biochemistry of AG biosynthesis and the rich potential in their pathway engineering. In particular, parallel pathways have been shown to be common and widespread in AG biosynthesis, highlighting nature’s ingenuity in accessing diverse natural products from a limited set of genes. In this review, we discuss the parallel biosynthetic pathways of three representative AG antibiotics—kanamycin, gentamicin, and apramycin—as well as future directions towards the discovery and development of novel AGs. |
format | Online Article Text |
id | pubmed-5461906 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-54619062017-06-14 Parallel pathways in the biosynthesis of aminoglycoside antibiotics Yu, Yi Zhang, Qi Deng, Zixin F1000Res Review Despite their inherent toxicity and the global spread of bacterial resistance, aminoglycosides (AGs), an old class of microbial drugs, remain a valuable component of the antibiotic arsenal. Recent studies have continued to reveal the fascinating biochemistry of AG biosynthesis and the rich potential in their pathway engineering. In particular, parallel pathways have been shown to be common and widespread in AG biosynthesis, highlighting nature’s ingenuity in accessing diverse natural products from a limited set of genes. In this review, we discuss the parallel biosynthetic pathways of three representative AG antibiotics—kanamycin, gentamicin, and apramycin—as well as future directions towards the discovery and development of novel AGs. F1000Research 2017-05-18 /pmc/articles/PMC5461906/ /pubmed/28620453 http://dx.doi.org/10.12688/f1000research.11104.1 Text en Copyright: © 2017 Yu Y et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Yu, Yi Zhang, Qi Deng, Zixin Parallel pathways in the biosynthesis of aminoglycoside antibiotics |
title | Parallel pathways in the biosynthesis of aminoglycoside antibiotics |
title_full | Parallel pathways in the biosynthesis of aminoglycoside antibiotics |
title_fullStr | Parallel pathways in the biosynthesis of aminoglycoside antibiotics |
title_full_unstemmed | Parallel pathways in the biosynthesis of aminoglycoside antibiotics |
title_short | Parallel pathways in the biosynthesis of aminoglycoside antibiotics |
title_sort | parallel pathways in the biosynthesis of aminoglycoside antibiotics |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5461906/ https://www.ncbi.nlm.nih.gov/pubmed/28620453 http://dx.doi.org/10.12688/f1000research.11104.1 |
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