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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...

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Detalles Bibliográficos
Autores principales: Yu, Yi, Zhang, Qi, Deng, Zixin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2017
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.
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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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