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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...

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Autores principales: Jiang, Lin, Pu, Hong, Xiang, Jingxi, Su, Meng, Yan, Xiaohui, Yang, Dong, Zhu, Xiangcheng, Shen, Ben, Duan, Yanwen, Huang, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
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.
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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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