Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/117641
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorGuo, S-
dc.creatorPardeshi, L-
dc.creatorQin, L-
dc.creatorCheung, CY-
dc.creatorLiu, X-
dc.creatorFan, L-
dc.creatorMok, CC-
dc.creatorParsania, C-
dc.creatorDong, Z-
dc.creatorKo, BCB-
dc.creatorTan, K-
dc.creatorWong, KH-
dc.date.accessioned2026-02-26T03:47:40Z-
dc.date.available2026-02-26T03:47:40Z-
dc.identifier.urihttp://hdl.handle.net/10397/117641-
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.rightsOpen Access 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.en_US
dc.rights© The Author(s) 2025en_US
dc.rightsThe following publication Guo, S., Pardeshi, L., Qin, L. et al. Systematic over-expression of secondary metabolism transcription factors to reveal the pharmaceutical potential of Aspergillus nidulans. Commun Biol 8, 1444 (2025) is available at https://doi.org/10.1038/s42003-025-08840-z.en_US
dc.titleSystematic over-expression of secondary metabolism transcription factors to reveal the pharmaceutical potential of aspergillus nidulansen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume8-
dc.identifier.doi10.1038/s42003-025-08840-z-
dcterms.abstractMany life-saving drugs are derived from fungal secondary metabolites, and the rich diversity of these metabolites is a gold mine of bioactive compounds for drug discovery. However, the biosynthetic genes for most secondary metabolites remain transcriptionally silent in fungi, posing a significant bottleneck in their discovery. Here, we apply a systematic approach to separately over-express 51 secondary metabolism-related transcription factors using the strong inducible promoter of the xylP gene from Penicillium chrysogenum. Growing the individual secondary metabolism transcription factor over-expression strains under inducible conditions leads to the production of a collection of diverse metabolites with anti-bacterial, anti-fungal and anti-cancer activities. The overall approach and the over-expression system established in this study are broadly-applicable, providing a valuable means to revealing the pharmaceutical potentials of fungi.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationCommunications biology, 2025, v. 8, 1444-
dcterms.isPartOfCommunications biology-
dcterms.issued2025-
dc.identifier.scopus2-s2.0-105018274262-
dc.identifier.pmid41068425-
dc.identifier.eissn2399-3642-
dc.identifier.artn1444-
dc.description.validate202602 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextWe thank the members of the Wong laboratory for their valuable comments and discussions, and Prof. Yit-Heng Chooi and Prof. Zhou (Alex) Shang for their advice and suggestions. We acknowledge the services and technical support provided by the Genomics and Single Cell Analysis Core, as well as the Drug and Development Core of the Faculty of Health Sciences at the University of Macau. This work was partially conducted on the High-Performance Computing Cluster (HPC), supported by the Information and Communication Technology Office (ICTO) of the University of Macau. We gratefully acknowledge funding support from the Science and Technology Development Fund, Macao S.A.R. (FDCT, project no. 0099/2022/A2), the Research Services and Knowledge Transfer Office (project nos. MYRG2022-00107-FHS and MYRG-GRG2023-00084-FHS-UMDF), and the Faculty of Health Sciences, University of Macau, awarded to K.H.W. and Research Grants Council, HK. (C5012-15E) to B.C.B.K.en_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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