Asperpyridone A represents an unusual class of pyridone alkaloids with demonstrated potential for hypoglycemic activity, primarily by promoting glucose consumption in HepG2 cells. Trichodin A, initially isolated from the marine fungus Trichoderma sp. strain MF106, exhibits notable antibiotic activities against . Despite their pharmacological significance, the regulatory mechanisms governing their biosynthesis have remained elusive. In this investigation, we initiated the activation of a latent gene cluster, denoted as "", through the overexpression of the ZnCys transcription factor TopC in . The activation of the cluster led to the biosynthesis of asperpyridone A, pyridoxatin, and trichodin A. Our study also elucidated that the regulator TopC exerts precise control over the biosynthesis of asperpyridone A and trichodin A through the detection of protein-nucleic acid interactions. Moreover, by complementing these findings with gene deletions involving and , we proposed a comprehensive biosynthesis pathway for asperpyridone A and trichodin A in .
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http://dx.doi.org/10.3390/microorganisms11102578 | DOI Listing |
Microorganisms
October 2023
School of Medicine and the Children's Hospital, Zhejiang University, Hangzhou 310058, China.
Asperpyridone A represents an unusual class of pyridone alkaloids with demonstrated potential for hypoglycemic activity, primarily by promoting glucose consumption in HepG2 cells. Trichodin A, initially isolated from the marine fungus Trichoderma sp. strain MF106, exhibits notable antibiotic activities against .
View Article and Find Full Text PDFJ Nat Prod
October 2019
Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, Tongji Medical College , Huazhong University of Science and Technology, Wuhan 430030 , Hubei Province , People's Republic of China.
A pyridone alkaloid, asperpyridone A (), which possesses an unusual pyrano[3,2-]pyridine scaffold, was isolated from solid cultures of the endophytic fungus sp. TJ23. Its structure, including its absolute configuration, was determined using a combination of nuclear magnetic resonance, high-resolution electrospray ionization mass spectrometry, quantum chemical calculations (electronic circular dichroism), and X-ray crystallography.
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