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Huanglongmycin A-C, Cytotoxic Polyketides Biosynthesized by a Putative Type II Polyketide Synthase From Streptomyces sp. CB09001
Three natural products of nonaketide biosynthetic origin, probably biosynthesized from nine molecules of malonyl-CoA, have been isolated. Herein we described the isolation and structure elucidation of huanglongmycin (HLM) A-C and identification of the putative hlm biosynthetic gene cluster from Stre...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036704/ https://www.ncbi.nlm.nih.gov/pubmed/30013965 http://dx.doi.org/10.3389/fchem.2018.00254 |
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author | Jiang, Lin Pu, Hong Xiang, Jingxi Su, Meng Yan, Xiaohui Yang, Dong Zhu, Xiangcheng Shen, Ben Duan, Yanwen Huang, Yong |
author_facet | Jiang, Lin Pu, Hong Xiang, Jingxi Su, Meng Yan, Xiaohui Yang, Dong Zhu, Xiangcheng Shen, Ben Duan, Yanwen Huang, Yong |
author_sort | Jiang, Lin |
collection | PubMed |
description | Three natural products of nonaketide biosynthetic origin, probably biosynthesized from nine molecules of malonyl-CoA, have been isolated. Herein we described the isolation and structure elucidation of huanglongmycin (HLM) A-C and identification of the putative hlm biosynthetic gene cluster from Streptomyces sp. CB09001, isolated from a karstic cave in Xiangxi, China. Albeit previously isolated, HLM A was reported for the first time to exhibit moderate cytotoxicity against A549 lung cancer cell line (IC(50) = 13.8 ± 1.5 μM) and weak antibacterial activity against gram-negative clinical isolates. A putative biosynthetic pathway for HLM A, featuring a nonaketide-specific type II polyketide synthase, was proposed. It would be consistent with the isolation of HLM B and C, which are two new natural products and likely shunt metabolites during HLM A biosynthesis. |
format | Online Article Text |
id | pubmed-6036704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60367042018-07-16 Huanglongmycin A-C, Cytotoxic Polyketides Biosynthesized by a Putative Type II Polyketide Synthase From Streptomyces sp. CB09001 Jiang, Lin Pu, Hong Xiang, Jingxi Su, Meng Yan, Xiaohui Yang, Dong Zhu, Xiangcheng Shen, Ben Duan, Yanwen Huang, Yong Front Chem Chemistry Three natural products of nonaketide biosynthetic origin, probably biosynthesized from nine molecules of malonyl-CoA, have been isolated. Herein we described the isolation and structure elucidation of huanglongmycin (HLM) A-C and identification of the putative hlm biosynthetic gene cluster from Streptomyces sp. CB09001, isolated from a karstic cave in Xiangxi, China. Albeit previously isolated, HLM A was reported for the first time to exhibit moderate cytotoxicity against A549 lung cancer cell line (IC(50) = 13.8 ± 1.5 μM) and weak antibacterial activity against gram-negative clinical isolates. A putative biosynthetic pathway for HLM A, featuring a nonaketide-specific type II polyketide synthase, was proposed. It would be consistent with the isolation of HLM B and C, which are two new natural products and likely shunt metabolites during HLM A biosynthesis. Frontiers Media S.A. 2018-06-26 /pmc/articles/PMC6036704/ /pubmed/30013965 http://dx.doi.org/10.3389/fchem.2018.00254 Text en Copyright © 2018 Jiang, Pu, Xiang, Su, Yan, Yang, Zhu, Shen, Duan and Huang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Jiang, Lin Pu, Hong Xiang, Jingxi Su, Meng Yan, Xiaohui Yang, Dong Zhu, Xiangcheng Shen, Ben Duan, Yanwen Huang, Yong Huanglongmycin A-C, Cytotoxic Polyketides Biosynthesized by a Putative Type II Polyketide Synthase From Streptomyces sp. CB09001 |
title | Huanglongmycin A-C, Cytotoxic Polyketides Biosynthesized by a Putative Type II Polyketide Synthase From Streptomyces sp. CB09001 |
title_full | Huanglongmycin A-C, Cytotoxic Polyketides Biosynthesized by a Putative Type II Polyketide Synthase From Streptomyces sp. CB09001 |
title_fullStr | Huanglongmycin A-C, Cytotoxic Polyketides Biosynthesized by a Putative Type II Polyketide Synthase From Streptomyces sp. CB09001 |
title_full_unstemmed | Huanglongmycin A-C, Cytotoxic Polyketides Biosynthesized by a Putative Type II Polyketide Synthase From Streptomyces sp. CB09001 |
title_short | Huanglongmycin A-C, Cytotoxic Polyketides Biosynthesized by a Putative Type II Polyketide Synthase From Streptomyces sp. CB09001 |
title_sort | huanglongmycin a-c, cytotoxic polyketides biosynthesized by a putative type ii polyketide synthase from streptomyces sp. cb09001 |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036704/ https://www.ncbi.nlm.nih.gov/pubmed/30013965 http://dx.doi.org/10.3389/fchem.2018.00254 |
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