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Aili Fan
fanaili@bjmu.edu.cn
Chinese, German, English
Beijing
Peking University
Pharmaceutical Sciences
  • 2011.9-2015.7 PhD in Pharmacy and Biotechnology: University of Marburg, Germany
  • 2009.9-2011.7 Master's in Natural Product Chemistry: Peking University
  • 2005.9-2009.7 Bachelor's in Pharmacy: Peking University
  • 2020.12- Associate Researcher - Peking University
  • 2015.9-2020.11 Associate Professor - Beijing University of Chemical Technology
  • 2015.10-2017.8 Assistant Researcher - Institute of Microbiology, Chinese Academy of Sciences
Discovery of marine natural products based on biosynthesis and synthetic biology
Analysis of biosynthetic pathways and catalytic mechanisms of key enzymes in marine natural products
Biomanufacturing of active drug source molecules based on heterologous expression/metabolic regulation
  • Biosynthesis of epipyrone A reveals a highly specific membrane-bound fungal C-glycosyltransferase for pyrone galactosylation, Fan, Aili; Zhong, B.; Liu, D.; Lu, Y.; Wu, M.; Jin, H.; Shi, X.-M.; Ren, J.; Zhang, B.; Su, X.-d.; Ma, M.; Li, S.-M.; and Lin, W., 2024
  • Brominated depsidones with antibacterial effects from a deep-sea-derived fungus Spiromastix sp., Huang, Z.; Liu, D.; Chen, S.; Ren, J.; Gao, C.; Li, Z.; Fan, A.; and Lin, W., 2024
  • Concise biosynthesis of tropone-containing spiromaterpenes by a sesquiterpene cyclase and a multifunctional P450 from a deep-sea-derived Spiromastix sp. fungus, Liu, J.; Guo, X.; Guo, X.; Zhong, B.; Wang, T.; Liu, D.; Jin, H.; Ren, J.; Liu, Z.; Gao, J.; Li, S. M.; Fan, A.; Lin, W., 2022
  • Sclerotiamides C–H, notoamides from a marine gorgonian-derived fungus with cytotoxic activities, Guo, X.; Meng, Q.; Liu, J.; Wu, J.; Jia, H.; Liu, D.; Gu, Y.; Liu, J.; Huang, J.; Fan, A.; Lin, W., 2022
  • ThpacC acts as a positive regulator of homodimericin A biosynthesis and antifungal activities of Trichoderma harzianum 3.9236, Wu, M.; Wei, H.; Ma, K.; Cui, P.; Zhu, S.; Lai, D.; Ren, J.; Wang, W.; Fan, A.; Lin, W.; Su, H., 2021
  • Rapid colonization and biodegradation of untreated commercial polyethylene wrap by a new strain of Bacillus velezensis C5, Liu, X.; Zhang, Y.; Sun, Q.; Liu, Z.; Zhao, Y.; Fan, A.; Su, H., 2021
  • Epigenetic manipulation to trigger production of guaiane-type sesquiterpenes from a marine-derived Spiromastix sp. fungus with antineuroinflammatory effects, Guo, X.; Meng, Q.; Niu, S.; Liu, J.; Guo, X.; Sun, Z.; Liu, D.; Gu, Y.; Huang, J.; Fan, A.; Lin, W., 2021
  • Recombinant protein production in the filamentous fungus Trichoderma, Wei, H.; Wu, M.; Fan, A.; Su, H., 2021
  • Enhanced resistance of Trichoderma harzianum LZDX-32-08 to hygromycin B induced by sea salt, Yu, X.; Wei, H.; Liu, X.; Liu, D.; Fan, A.; Su, H., 2020
  • Enhancing robustness of aerobic granule sludge under low C/N ratios with addition of kitchen wastewater, Wang, L.; Yu, X.; Xiong, W.; Li, P.; Wang, S.; Fan, A.; Su, H., 2020
  • Reinvestigation of the substrate specificity of a reverse prenyltransferase NotF from Aspergillus sp. MF297-2, Yang, K.; Li, S.-M.; Liu, X.; Fan, A., 2020
  • Unequivocal identification of two-bond heteronuclear correlations in natural products at nanomole scale by i-HMBC, Wang, Y.; Fan, A.; Cohen, R.D.; Dal Poggetto, G.; Huang, Z.; Yang, H.; Martin, G.E.; Sherer, E.C.; Reibarkh, M.; and Wang, X., 2023
  • Oxepinamide F biosynthesis involves enzymatic D-aminoacyl epimerization, 3H-oxepin formation, and hydroxylation induced double bond migration, Zheng, L.; Wang, H.; Fan, A.; Li, S. M., 2020
  • Asperphenamate biosynthesis reveals a novel two-module NRPS system to synthesize amino acid esters in fungi, Li, W.; Fan, A.; Wang, L.; Zhang, P.; Liu, Z.; An, Z.; Yin, W.-B., 2018
  • Deletion of a histone acetyltransferase leads to the pleiotropic activation of natural products in Metarhizium robertsii, Fan, A.; Mi, W.; Liu, Z.; Zeng, G.; Zhang, P.; Hu, Y.; Fang, W.; Yin, W.-B., 2017
Marine Natural Products Biosynthesis Synthetic Biology Key Enzymes Catalytic Mechanisms Heterologous Expression Metabolic Regulation Biomanufacturing Drug Source Molecules Active Compounds

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