Naoka Katayama, Kotone Kume, Rina Terada, Tatsuya Goi, Kenji Kai
{"title":"Characterization of Collimonin Biosynthesis in the Fungus-Feeding Bacterium Collimonas fungivorans Ter331","authors":"Naoka Katayama, Kotone Kume, Rina Terada, Tatsuya Goi, Kenji Kai","doi":"10.1021/acschembio.6c00065","DOIUrl":null,"url":null,"abstract":"<p>Collimonins A–D are bacterial polyynes produced by the fungus-feeding bacterium <em>Collimonas fungivorans</em> Ter331. The <em>col</em> biosynthetic gene cluster (BGC) is implicated in collimonin biosynthesis, but their gene functions remain unclear. In this study, the biosynthetic pathway of collimonins in <em>C. fungivorans</em> Ter331 was elucidated through genetic and chemical characterization of each <em>col</em> gene’s function. The biosynthetic intermediates (namely, CBIs-1–4) were isolated from gene-deletion mutants (or with gene overexpression), and their structures were elucidated by spectroscopic analyses. The conversion of these intermediates to other intermediates or collimonins was analyzed by mutant coculturing, gene overexpression, and feeding experiments. CBI-1, which is the first detectable intermediate, was converted into collimonins A–D through desaturation, oxidation, and lactonization. Results indicated that the Rieske oxygenase ColK, the fatty acid desaturase ColJ, the possible cyclase ColM, and the flavin-dependent monooxygenase ColI were involved in the conversion of CBI-1 to collimonins A and B, whereas only ColK was responsible for its conversion to collimonins C and D. The <em>mas</em> BGC of <em>Massilia armeniaca</em> ZMN-3, which has a similar gene set to the <em>col</em> BGC but lacks a homologue of <em>colI</em>, can produce collimonins A–D when coexpressed with <em>colI</em>. A comparison of the antifungal activity between Ter331 and its <em>col</em> mutants suggested the importance of the latter lactonization in collimonin biosynthesis for the activity. This study represents the first comprehensive description of the biosynthetic pathway for collimonins and establishes an important basis for future biochemical analyses of each conversion step.</p>","PeriodicalId":11,"journal":{"name":"ACS Chemical Biology","volume":"21 9","pages":"2143–2156"},"PeriodicalIF":3.6000,"publicationDate":"2026-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Chemical Biology","FirstCategoryId":"99","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acschembio.6c00065","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/11 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Collimonins A–D are bacterial polyynes produced by the fungus-feeding bacterium Collimonas fungivorans Ter331. The col biosynthetic gene cluster (BGC) is implicated in collimonin biosynthesis, but their gene functions remain unclear. In this study, the biosynthetic pathway of collimonins in C. fungivorans Ter331 was elucidated through genetic and chemical characterization of each col gene’s function. The biosynthetic intermediates (namely, CBIs-1–4) were isolated from gene-deletion mutants (or with gene overexpression), and their structures were elucidated by spectroscopic analyses. The conversion of these intermediates to other intermediates or collimonins was analyzed by mutant coculturing, gene overexpression, and feeding experiments. CBI-1, which is the first detectable intermediate, was converted into collimonins A–D through desaturation, oxidation, and lactonization. Results indicated that the Rieske oxygenase ColK, the fatty acid desaturase ColJ, the possible cyclase ColM, and the flavin-dependent monooxygenase ColI were involved in the conversion of CBI-1 to collimonins A and B, whereas only ColK was responsible for its conversion to collimonins C and D. The mas BGC of Massilia armeniaca ZMN-3, which has a similar gene set to the col BGC but lacks a homologue of colI, can produce collimonins A–D when coexpressed with colI. A comparison of the antifungal activity between Ter331 and its col mutants suggested the importance of the latter lactonization in collimonin biosynthesis for the activity. This study represents the first comprehensive description of the biosynthetic pathway for collimonins and establishes an important basis for future biochemical analyses of each conversion step.
期刊介绍:
ACS Chemical Biology provides an international forum for the rapid communication of research that broadly embraces the interface between chemistry and biology.
The journal also serves as a forum to facilitate the communication between biologists and chemists that will translate into new research opportunities and discoveries. Results will be published in which molecular reasoning has been used to probe questions through in vitro investigations, cell biological methods, or organismic studies.
We welcome mechanistic studies on proteins, nucleic acids, sugars, lipids, and nonbiological polymers. The journal serves a large scientific community, exploring cellular function from both chemical and biological perspectives. It is understood that submitted work is based upon original results and has not been published previously.