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Complete reconstitution of the diverse pathways of gentamicin B biosynthesis

Gentamicin B (GB), a valuable starting material for the preparation of the semisynthetic aminoglycoside antibiotic isepamicin, is produced in trace amounts by the wild-type Micromonospora echinospora. While the biosynthetic pathway to GB has remained obscure for decades, we have now identified three...

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Autores principales: Ban, Yeon Hee, Song, Myoung Chong, Hwang, Jae-yeon, Shin, Hea-lyung, Kim, Hak Joong, Hong, Seung Kon, Lee, Na Joon, Park, Je Won, Cha, Sun-Shin, Liu, Hung-wen, Yoon, Yeo Joon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488028/
https://www.ncbi.nlm.nih.gov/pubmed/30643280
http://dx.doi.org/10.1038/s41589-018-0203-4
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author Ban, Yeon Hee
Song, Myoung Chong
Hwang, Jae-yeon
Shin, Hea-lyung
Kim, Hak Joong
Hong, Seung Kon
Lee, Na Joon
Park, Je Won
Cha, Sun-Shin
Liu, Hung-wen
Yoon, Yeo Joon
author_facet Ban, Yeon Hee
Song, Myoung Chong
Hwang, Jae-yeon
Shin, Hea-lyung
Kim, Hak Joong
Hong, Seung Kon
Lee, Na Joon
Park, Je Won
Cha, Sun-Shin
Liu, Hung-wen
Yoon, Yeo Joon
author_sort Ban, Yeon Hee
collection PubMed
description Gentamicin B (GB), a valuable starting material for the preparation of the semisynthetic aminoglycoside antibiotic isepamicin, is produced in trace amounts by the wild-type Micromonospora echinospora. While the biosynthetic pathway to GB has remained obscure for decades, we have now identified three hidden pathways to GB production via seven hitherto unknown intermediates in M. echinospora. The narrow substrate specificity of a key glycosyltransferase and the C6′-amination enzymes, in combination with the weak and unsynchronized gene expression of the 2′-deamination enzymes, limit GB production in M. echinospora. The crystal structure of the aminotransferase involved in C6′-amination explains its substrate specificity. Some of the new intermediates displayed similar premature termination codon readthrough activity but with reduced toxicity compared to the natural aminoglycoside G418. This work not only led to the discovery of unknown biosynthetic routes to GB, but also demonstrated the potential to mine new aminoglycosides from nature for drug discovery.
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spelling pubmed-64880282019-07-14 Complete reconstitution of the diverse pathways of gentamicin B biosynthesis Ban, Yeon Hee Song, Myoung Chong Hwang, Jae-yeon Shin, Hea-lyung Kim, Hak Joong Hong, Seung Kon Lee, Na Joon Park, Je Won Cha, Sun-Shin Liu, Hung-wen Yoon, Yeo Joon Nat Chem Biol Article Gentamicin B (GB), a valuable starting material for the preparation of the semisynthetic aminoglycoside antibiotic isepamicin, is produced in trace amounts by the wild-type Micromonospora echinospora. While the biosynthetic pathway to GB has remained obscure for decades, we have now identified three hidden pathways to GB production via seven hitherto unknown intermediates in M. echinospora. The narrow substrate specificity of a key glycosyltransferase and the C6′-amination enzymes, in combination with the weak and unsynchronized gene expression of the 2′-deamination enzymes, limit GB production in M. echinospora. The crystal structure of the aminotransferase involved in C6′-amination explains its substrate specificity. Some of the new intermediates displayed similar premature termination codon readthrough activity but with reduced toxicity compared to the natural aminoglycoside G418. This work not only led to the discovery of unknown biosynthetic routes to GB, but also demonstrated the potential to mine new aminoglycosides from nature for drug discovery. 2019-01-14 2019-03 /pmc/articles/PMC6488028/ /pubmed/30643280 http://dx.doi.org/10.1038/s41589-018-0203-4 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Ban, Yeon Hee
Song, Myoung Chong
Hwang, Jae-yeon
Shin, Hea-lyung
Kim, Hak Joong
Hong, Seung Kon
Lee, Na Joon
Park, Je Won
Cha, Sun-Shin
Liu, Hung-wen
Yoon, Yeo Joon
Complete reconstitution of the diverse pathways of gentamicin B biosynthesis
title Complete reconstitution of the diverse pathways of gentamicin B biosynthesis
title_full Complete reconstitution of the diverse pathways of gentamicin B biosynthesis
title_fullStr Complete reconstitution of the diverse pathways of gentamicin B biosynthesis
title_full_unstemmed Complete reconstitution of the diverse pathways of gentamicin B biosynthesis
title_short Complete reconstitution of the diverse pathways of gentamicin B biosynthesis
title_sort complete reconstitution of the diverse pathways of gentamicin b biosynthesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488028/
https://www.ncbi.nlm.nih.gov/pubmed/30643280
http://dx.doi.org/10.1038/s41589-018-0203-4
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