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Genome-based discovery and total synthesis of janustatins, potent cytotoxins from a plant-associated bacterium
Host-associated bacteria are increasingly recognized as underexplored sources of bioactive natural products with unprecedented chemical scaffolds. A recently identified example is the plant root-associated marine bacterium Gynuella sunshinyii of the chemically underexplored order Oceanospirillales....
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7613652/ https://www.ncbi.nlm.nih.gov/pubmed/36064972 http://dx.doi.org/10.1038/s41557-022-01020-0 |
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author | Ueoka, Reiko Sondermann, Philipp Leopold-Messer, Stefan Liu, Yizhou Suo, Rei Bhushan, Agneya Vadakumchery, Lida Greczmiel, Ute Yashiroda, Yoko Kimura, Hiromi Nishimura, Shinichi Hoshikawa, Yojiro Yoshida, Minoru Oxenius, Annette Matsunaga, Shigeki Williamson, R. Thomas Carreira, Erick M. Piel, Jörn |
author_facet | Ueoka, Reiko Sondermann, Philipp Leopold-Messer, Stefan Liu, Yizhou Suo, Rei Bhushan, Agneya Vadakumchery, Lida Greczmiel, Ute Yashiroda, Yoko Kimura, Hiromi Nishimura, Shinichi Hoshikawa, Yojiro Yoshida, Minoru Oxenius, Annette Matsunaga, Shigeki Williamson, R. Thomas Carreira, Erick M. Piel, Jörn |
author_sort | Ueoka, Reiko |
collection | PubMed |
description | Host-associated bacteria are increasingly recognized as underexplored sources of bioactive natural products with unprecedented chemical scaffolds. A recently identified example is the plant root-associated marine bacterium Gynuella sunshinyii of the chemically underexplored order Oceanospirillales. Its genome contains at least 22 biosynthetic gene clusters suggesting a rich and mostly uncharacterized specialized metabolism. In this work, in silico chemical prediction of a non-canonical polyketide synthase cluster led to the discovery of janustatins, structurally unprecedented polyketide alkaloids with potent cytotoxicity that are produced at minute quantities. A combination of MS and 2D NMR experiments, density functional theory calculations of (13)C chemical shifts, and semiquantitative interpretation of T-ROESY data were conducted to determine the relative configuration, which enabled the total synthesis of both enantiomers and assignment of the absolute configuration. Janustatins feature a previously unknown pyridodihydropyranone heterocycle and an unusual biological activity consisting of delayed, synchronized cell death at subnanomolar concentrations. |
format | Online Article Text |
id | pubmed-7613652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-76136522023-03-05 Genome-based discovery and total synthesis of janustatins, potent cytotoxins from a plant-associated bacterium Ueoka, Reiko Sondermann, Philipp Leopold-Messer, Stefan Liu, Yizhou Suo, Rei Bhushan, Agneya Vadakumchery, Lida Greczmiel, Ute Yashiroda, Yoko Kimura, Hiromi Nishimura, Shinichi Hoshikawa, Yojiro Yoshida, Minoru Oxenius, Annette Matsunaga, Shigeki Williamson, R. Thomas Carreira, Erick M. Piel, Jörn Nat Chem Article Host-associated bacteria are increasingly recognized as underexplored sources of bioactive natural products with unprecedented chemical scaffolds. A recently identified example is the plant root-associated marine bacterium Gynuella sunshinyii of the chemically underexplored order Oceanospirillales. Its genome contains at least 22 biosynthetic gene clusters suggesting a rich and mostly uncharacterized specialized metabolism. In this work, in silico chemical prediction of a non-canonical polyketide synthase cluster led to the discovery of janustatins, structurally unprecedented polyketide alkaloids with potent cytotoxicity that are produced at minute quantities. A combination of MS and 2D NMR experiments, density functional theory calculations of (13)C chemical shifts, and semiquantitative interpretation of T-ROESY data were conducted to determine the relative configuration, which enabled the total synthesis of both enantiomers and assignment of the absolute configuration. Janustatins feature a previously unknown pyridodihydropyranone heterocycle and an unusual biological activity consisting of delayed, synchronized cell death at subnanomolar concentrations. 2022-09-05 /pmc/articles/PMC7613652/ /pubmed/36064972 http://dx.doi.org/10.1038/s41557-022-01020-0 Text en https://www.springernature.com/gp/open-research/policies/accepted-manuscript-termsUsers 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: https://www.springernature.com/gp/open-research/policies/accepted-manuscript-terms |
spellingShingle | Article Ueoka, Reiko Sondermann, Philipp Leopold-Messer, Stefan Liu, Yizhou Suo, Rei Bhushan, Agneya Vadakumchery, Lida Greczmiel, Ute Yashiroda, Yoko Kimura, Hiromi Nishimura, Shinichi Hoshikawa, Yojiro Yoshida, Minoru Oxenius, Annette Matsunaga, Shigeki Williamson, R. Thomas Carreira, Erick M. Piel, Jörn Genome-based discovery and total synthesis of janustatins, potent cytotoxins from a plant-associated bacterium |
title | Genome-based discovery and total synthesis of janustatins, potent cytotoxins from a plant-associated bacterium |
title_full | Genome-based discovery and total synthesis of janustatins, potent cytotoxins from a plant-associated bacterium |
title_fullStr | Genome-based discovery and total synthesis of janustatins, potent cytotoxins from a plant-associated bacterium |
title_full_unstemmed | Genome-based discovery and total synthesis of janustatins, potent cytotoxins from a plant-associated bacterium |
title_short | Genome-based discovery and total synthesis of janustatins, potent cytotoxins from a plant-associated bacterium |
title_sort | genome-based discovery and total synthesis of janustatins, potent cytotoxins from a plant-associated bacterium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7613652/ https://www.ncbi.nlm.nih.gov/pubmed/36064972 http://dx.doi.org/10.1038/s41557-022-01020-0 |
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