Taizong Wu

Mr. Taizong Wu

orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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25 July 2023 in Bioorganic Chemistry
Verified
Journal Article
Closed access
ZHZhi-Hui He
Zhi-Hui He
CXChun-Lan Xie
Chun-Lan Xie
TWTaizong Wu
Taizong Wu
YZYong Zhang
Yong Zhang
ZZZheng-Biao Zou
Zheng-Biao Zou
Xian-Wen YangXian-Wen Yang
Xian-Wen Yang

3 September 2021 in Marine Drugs
Verified
Journal Article
Open access
PDF file
ASAngela A Salim
Angela A Salim
Zeinab KhalilZeinab Khalil
Zeinab Khalil
Ahmed ElbannaAhmed Elbanna
Ahmed Elbanna
TWTaizong Wu
Taizong Wu
Rob CaponRob Capon
Rob Capon
This review presents an account of the microbial biodiscovery methodology developed and applied in our laboratory at The University of Queensland, Institute for Molecular Bioscience, with examples drawn from our experiences studying natural products produced by Australian marine-derived (and terrestrial) fungi and bacteria.


19 December 2022 in Molecules
Verified
Journal Article
Open access
PDF file
TWTaizong Wu
Taizong Wu
ASAngela A Salim
Angela A Salim
PBPaul V. Bernhardt
Paul V. Bernhardt
Rob CaponRob Capon
Rob Capon
This study showcases the application of an integrated workflow of molecular networking chemical profiling (GNPS), together with miniaturized microbioreactor cultivation profiling (MATRIX) to successfully detect, dereplicate, prioritize, optimize the production, isolate, characterize, and identify a diverse selection of new chemically labile natural products from the Queensland sheep pasture soil-derived fungus Aspergillus sp. CMB-MRF324. More specifically, we report the new tryptamine enamino tripeptide aspergillamides E–F (7–8), dihydroquinoline-2-one aflaquinolones H–I (11–12), and prenylated phenylbutyrolactone aspulvinone Y (14), along with an array of known co-metabolites, including asterriquinones SU5228 (9) and CT5 (10), terrecyclic acid A (13), and aspulvinones N-CR (15), B (16), D (17), and H (18). Structure elucidation was achieved by a combination of detailed spectroscopic and chemical analysis, biosynthetic considerations, and in the case of 11, an X-ray crystallographic analysis.