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dc.contributor.author | Tsukada, Kento | en |
dc.contributor.author | Shinki, Shono | en |
dc.contributor.author | Kaneko, Akiho | en |
dc.contributor.author | Murakami, Kazuma | en |
dc.contributor.author | Irie, Kazuhiro | en |
dc.contributor.author | Murai, Masatoshi | en |
dc.contributor.author | Miyoshi, Hideto | en |
dc.contributor.author | Dan, Shingo | en |
dc.contributor.author | Kawaji, Kumi | en |
dc.contributor.author | Hayashi, Hironori | en |
dc.contributor.author | Kodama, Eiichi N. | en |
dc.contributor.author | Hori, Aki | en |
dc.contributor.author | Salim, Emil | en |
dc.contributor.author | Kuraishi, Takayuki | en |
dc.contributor.author | Hirata, Naoya | en |
dc.contributor.author | Kanda, Yasunari | en |
dc.contributor.author | Asai, Teigo | en |
dc.contributor.alternative | 塚田, 健人 | ja |
dc.contributor.alternative | 新木, 翔之 | ja |
dc.contributor.alternative | 金子, 秋穂 | ja |
dc.contributor.alternative | 村上, 一馬 | ja |
dc.contributor.alternative | 入江, 一浩 | ja |
dc.contributor.alternative | 村井, 正俊 | ja |
dc.contributor.alternative | 三芳, 秀人 | ja |
dc.contributor.alternative | 旦, 慎吾 | ja |
dc.contributor.alternative | 河治, 久実 | ja |
dc.contributor.alternative | 林, 宏典 | ja |
dc.contributor.alternative | 児玉, 栄一 | ja |
dc.contributor.alternative | 堀, 亜紀 | ja |
dc.contributor.alternative | 倉石, 貴透 | ja |
dc.contributor.alternative | 平田, 尚也 | ja |
dc.contributor.alternative | 諫田, 泰成 | ja |
dc.contributor.alternative | 浅井, 禎吾 | ja |
dc.date.accessioned | 2020-05-20T04:18:18Z | - |
dc.date.available | 2020-05-20T04:18:18Z | - |
dc.date.issued | 2020-04-14 | - |
dc.identifier.issn | 2041-1723 | - |
dc.identifier.uri | http://hdl.handle.net/2433/250909 | - |
dc.description.abstract | A synthetic biology method based on heterologous biosynthesis coupled with genome mining is a promising approach for increasing the opportunities to rationally access natural product with novel structures and biological activities through total biosynthesis and combinatorial biosynthesis. Here, we demonstrate the advantage of the synthetic biology method to explore biological activity-related chemical space through the comprehensive heterologous biosynthesis of fungal decalin-containing diterpenoid pyrones (DDPs). Genome mining reveals putative DDP biosynthetic gene clusters distributed in five fungal genera. In addition, we design extended DDP pathways by combinatorial biosynthesis. In total, ten DDP pathways, including five native pathways, four extended pathways and one shunt pathway, are heterologously reconstituted in a genetically tractable heterologous host, Aspergillus oryzae, resulting in the production of 22 DDPs, including 15 new analogues. We also demonstrate the advantage of expanding the diversity of DDPs to probe various bioactive molecules through a wide range of biological evaluations. | en |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | Springer Nature | en |
dc.rights | © The Author(s) 2020. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. | en |
dc.subject | Combinatorial libraries | en |
dc.subject | Genetic engineering | en |
dc.subject | Metabolic engineering | en |
dc.subject | Natural product synthesis | en |
dc.title | Synthetic biology based construction of biological activity-related library of fungal decalin-containing diterpenoid pyrones | en |
dc.type | journal article | - |
dc.type.niitype | Journal Article | - |
dc.identifier.jtitle | Nature Communications | en |
dc.identifier.volume | 11 | - |
dc.relation.doi | 10.1038/s41467-020-15664-4 | - |
dc.textversion | publisher | - |
dc.identifier.artnum | 1830 | - |
dc.identifier.pmid | 32286350 | - |
dcterms.accessRights | open access | - |
datacite.awardNumber | 16H06276 | - |
datacite.awardNumber | 17H05055 | - |
datacite.awardNumber | 17H05428 | - |
datacite.awardNumber | 18K19388 | - |
datacite.awardNumber | 19H04642 | - |
datacite.awardNumber | 16H06194 | - |
datacite.awardNumber | 17H04107 | - |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName.alternative | Japan Society for the Promotion of Science (JSPS) | en |
jpcoar.funderName.alternative | Japan Society for the Promotion of Science (JSPS) | en |
jpcoar.funderName.alternative | Japan Society for the Promotion of Science (JSPS) | en |
jpcoar.funderName.alternative | Japan Society for the Promotion of Science (JSPS) | en |
jpcoar.funderName.alternative | Japan Society for the Promotion of Science (JSPS) | en |
jpcoar.funderName.alternative | Japan Society for the Promotion of Science (JSPS) | en |
jpcoar.funderName.alternative | Japan Society for the Promotion of Science (JSPS) | en |
出現コレクション: | 学術雑誌掲載論文等 |
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