Non-enzymatic pyridine ring formation in the biosynthesis of the rubrolone tropolone alkaloids

The biosynthesis of pyridine rings is still poorly understood. Here the authors propose a biosynthetic pathway for pyridine-containing rubrolones, which is characterized by a non-enzymatic condensation and cyclization of the pyridine moiety.

Bibliographic Details
Main Authors: Yijun Yan, Jing Yang, Zhiyin Yu, Mingming Yu, Ya-Tuan Ma, Li Wang, Can Su, Jianying Luo, Geoffrey P. Horsman, Sheng-Xiong Huang
Format: Article
Language:English
Published: Nature Publishing Group 2016-10-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/ncomms13083
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spelling doaj-31b58558e98149e0865282c772e6c8b22021-05-11T11:20:24ZengNature Publishing GroupNature Communications2041-17232016-10-017111010.1038/ncomms13083Non-enzymatic pyridine ring formation in the biosynthesis of the rubrolone tropolone alkaloidsYijun Yan0Jing Yang1Zhiyin Yu2Mingming Yu3Ya-Tuan Ma4Li Wang5Can Su6Jianying Luo7Geoffrey P. Horsman8Sheng-Xiong Huang9State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of SciencesState Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of SciencesState Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of SciencesState Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of SciencesState Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of SciencesState Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of SciencesState Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of SciencesState Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of SciencesDepartment of Chemistry & Biochemistry, Wilfrid Laurier UniversityState Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of SciencesThe biosynthesis of pyridine rings is still poorly understood. Here the authors propose a biosynthetic pathway for pyridine-containing rubrolones, which is characterized by a non-enzymatic condensation and cyclization of the pyridine moiety.https://doi.org/10.1038/ncomms13083
collection DOAJ
language English
format Article
sources DOAJ
author Yijun Yan
Jing Yang
Zhiyin Yu
Mingming Yu
Ya-Tuan Ma
Li Wang
Can Su
Jianying Luo
Geoffrey P. Horsman
Sheng-Xiong Huang
spellingShingle Yijun Yan
Jing Yang
Zhiyin Yu
Mingming Yu
Ya-Tuan Ma
Li Wang
Can Su
Jianying Luo
Geoffrey P. Horsman
Sheng-Xiong Huang
Non-enzymatic pyridine ring formation in the biosynthesis of the rubrolone tropolone alkaloids
Nature Communications
author_facet Yijun Yan
Jing Yang
Zhiyin Yu
Mingming Yu
Ya-Tuan Ma
Li Wang
Can Su
Jianying Luo
Geoffrey P. Horsman
Sheng-Xiong Huang
author_sort Yijun Yan
title Non-enzymatic pyridine ring formation in the biosynthesis of the rubrolone tropolone alkaloids
title_short Non-enzymatic pyridine ring formation in the biosynthesis of the rubrolone tropolone alkaloids
title_full Non-enzymatic pyridine ring formation in the biosynthesis of the rubrolone tropolone alkaloids
title_fullStr Non-enzymatic pyridine ring formation in the biosynthesis of the rubrolone tropolone alkaloids
title_full_unstemmed Non-enzymatic pyridine ring formation in the biosynthesis of the rubrolone tropolone alkaloids
title_sort non-enzymatic pyridine ring formation in the biosynthesis of the rubrolone tropolone alkaloids
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2016-10-01
description The biosynthesis of pyridine rings is still poorly understood. Here the authors propose a biosynthetic pathway for pyridine-containing rubrolones, which is characterized by a non-enzymatic condensation and cyclization of the pyridine moiety.
url https://doi.org/10.1038/ncomms13083
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