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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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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. |
format | Online Article Text |
id | pubmed-6488028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
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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