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Biosynthesis of coelulatin for the methylation of anthraquinone featuring HemN-like radical S-adenosyl-L-methionine enzyme

Bacterial aromatic polyketides are usually biosynthesized by the type II polyketide synthase (PKS-II) system. Advances in deoxyribonucleic acid (DNA) sequencing, informatics, and biotechnologies have broadened opportunities for the discovery of aromatic polyketides. Meanwhile, metagenomics is a biot...

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Autores principales: Nie, Lishuang, Wei, Tianyi, Cao, Mingming, Lyu, Yunbin, Wang, Shaochen, Feng, Zhiyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9714029/
https://www.ncbi.nlm.nih.gov/pubmed/36466681
http://dx.doi.org/10.3389/fmicb.2022.1040900
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author Nie, Lishuang
Wei, Tianyi
Cao, Mingming
Lyu, Yunbin
Wang, Shaochen
Feng, Zhiyang
author_facet Nie, Lishuang
Wei, Tianyi
Cao, Mingming
Lyu, Yunbin
Wang, Shaochen
Feng, Zhiyang
author_sort Nie, Lishuang
collection PubMed
description Bacterial aromatic polyketides are usually biosynthesized by the type II polyketide synthase (PKS-II) system. Advances in deoxyribonucleic acid (DNA) sequencing, informatics, and biotechnologies have broadened opportunities for the discovery of aromatic polyketides. Meanwhile, metagenomics is a biotechnology that has been considered as a promising approach for the discovery of novel natural products from uncultured bacteria. Here, we cloned a type II polyketide biosynthetic gene cluster (BGC) from the soil metagenome, and the heterologous expression of this gene cluster in Streptomyces coelicolor M1146 resulted in the production of three anthraquinones, two of which (coelulatins 2 and 3) had special hydroxymethyl and methyloxymethyl modifications at C2 of the polyketide scaffold. Gene deletion and in vitro biochemical characterization indicated that the HemN-like radical S-adenosyl-L-methionine (SAM) enzyme CoeI exhibits methylation and is involved in C2 modification.
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spelling pubmed-97140292022-12-02 Biosynthesis of coelulatin for the methylation of anthraquinone featuring HemN-like radical S-adenosyl-L-methionine enzyme Nie, Lishuang Wei, Tianyi Cao, Mingming Lyu, Yunbin Wang, Shaochen Feng, Zhiyang Front Microbiol Microbiology Bacterial aromatic polyketides are usually biosynthesized by the type II polyketide synthase (PKS-II) system. Advances in deoxyribonucleic acid (DNA) sequencing, informatics, and biotechnologies have broadened opportunities for the discovery of aromatic polyketides. Meanwhile, metagenomics is a biotechnology that has been considered as a promising approach for the discovery of novel natural products from uncultured bacteria. Here, we cloned a type II polyketide biosynthetic gene cluster (BGC) from the soil metagenome, and the heterologous expression of this gene cluster in Streptomyces coelicolor M1146 resulted in the production of three anthraquinones, two of which (coelulatins 2 and 3) had special hydroxymethyl and methyloxymethyl modifications at C2 of the polyketide scaffold. Gene deletion and in vitro biochemical characterization indicated that the HemN-like radical S-adenosyl-L-methionine (SAM) enzyme CoeI exhibits methylation and is involved in C2 modification. Frontiers Media S.A. 2022-11-17 /pmc/articles/PMC9714029/ /pubmed/36466681 http://dx.doi.org/10.3389/fmicb.2022.1040900 Text en Copyright © 2022 Nie, Wei, Cao, Lyu, Wang and Feng. https://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 Microbiology
Nie, Lishuang
Wei, Tianyi
Cao, Mingming
Lyu, Yunbin
Wang, Shaochen
Feng, Zhiyang
Biosynthesis of coelulatin for the methylation of anthraquinone featuring HemN-like radical S-adenosyl-L-methionine enzyme
title Biosynthesis of coelulatin for the methylation of anthraquinone featuring HemN-like radical S-adenosyl-L-methionine enzyme
title_full Biosynthesis of coelulatin for the methylation of anthraquinone featuring HemN-like radical S-adenosyl-L-methionine enzyme
title_fullStr Biosynthesis of coelulatin for the methylation of anthraquinone featuring HemN-like radical S-adenosyl-L-methionine enzyme
title_full_unstemmed Biosynthesis of coelulatin for the methylation of anthraquinone featuring HemN-like radical S-adenosyl-L-methionine enzyme
title_short Biosynthesis of coelulatin for the methylation of anthraquinone featuring HemN-like radical S-adenosyl-L-methionine enzyme
title_sort biosynthesis of coelulatin for the methylation of anthraquinone featuring hemn-like radical s-adenosyl-l-methionine enzyme
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9714029/
https://www.ncbi.nlm.nih.gov/pubmed/36466681
http://dx.doi.org/10.3389/fmicb.2022.1040900
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