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Published January 31, 2020 | Version v1
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Prenylated quinolinone alkaloids and prenylated isoindolinone alkaloids from the fungus Aspergillus nidulans

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  • 1. ∗∗ & ∗ & Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and

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Li, Qin, Chen, Chunmei, He, Yan, Wei, Mengsha, Cheng, Li, Kang, Xin, Wang, Jianping, Hao, Xincai, Zhu, Hucheng, Zhang, Yonghui (2020): Prenylated quinolinone alkaloids and prenylated isoindolinone alkaloids from the fungus Aspergillus nidulans. Phytochemistry (112177) 169: 1-5, DOI: 10.1016/j.phytochem.2019.112177, URL: http://dx.doi.org/10.1016/j.phytochem.2019.112177

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urn:lsid:plazi.org:pub:E447C805FF85A204FFBCFFE8FFDAFFA1

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Figure: 10.5281/zenodo.8293643 (DOI)

References

  • Ahuja, M., Chiang, Y.M., Chang, S.L., Praseuth, M.B., Entwistle, R., Sanchez, J.F., Lo, H.C., Yeh, H.H., Oakley, B.R., Wang, C.C.C., 2012. Illuminating the diversity of aromatic polyketide synthases in Aspergillus nidulans. J. Am. Chem. Soc. 134, 8212-8221.
  • An, C.Y., Li, X.M., Luo, H., Li, C.S., Wang, M.H., Xu, G.M., Wang, B.G., 2013. 4-Phenyl- 3,4-dihydroquinolone derivatives from Aspergillus nidulans MA-143, an endophytic fungus isolated from the mangrove plant Rhizophora stylosa. J. Nat. Prod. 76, 1896-1901.
  • Berdy, J., 2012. Thoughts and facts about antibiotics: where we are now and where we are heading. J. Antibiot. 65, 385-395.
  • Chiang, Y.M., Oakley, C.E., Ahuja, M., Entwistle, R., Schultz, A., Chang, S.L., Sung, C.T., Wang, C.C.C., Oakley, B.R., 2013. An efficient system for heterologous expression of secondary metabolite genes in Aspergillus nidulans. J. Am. Chem. Soc. 135, 7720-7731.
  • Chiang, Y.M., Ahuja, M., Oakley, C.E., Entwistle, R., Asokan, A., Zutz, C., Wang, C.C.C., Oakley, B.R., 2016. Development of genetic dereplication strains in Aspergillus nidulans results in the discovery of aspercryptin. Angew. Chem. Int. Ed. 55, 1662-1665.
  • Lo, H.C., Entwistle, R., Guo, C.J., Ahuja, M., Szewczyk, E., Hung, J.H., Chiang, Y.M., Oakley, B.R., Wang, C.C., 2012. Two separate gene clusters encode the biosynthetic pathway for the meroterpenoids austinol and dehydroaustinol in Aspergillus nidulans. J. Am. Chem. Soc. 134, 4709-4720.
  • Nielsen, M.L., Nielsen, J.B., Rank, C., Klejnstrup, M.L., Holm, D.K., Brogaard, K.H., Hansen, B.G., Frisvad, J.C., Larsen, T.O., Mortensen, U.H., 2011. A genome-wide polyketide synthase deletion library uncovers novel genetic links to polyketides and meroterpenoids in Aspergillus nidulans. FEMS Microbiol. Lett. 321, 157-166.
  • Okada, M., Matsuda, Y., Mitsuhashi, T., Hoshino, S., Mori, T., Nakagawa, K., Quan, Z., Qin, B., Zhang, H., Hayashi, F., Kawaide, H., Abe, I., 2016. Genome-based discovery of an unprecedented cyclization mode in fungal sesterterpenoid biosynthesis. J. Am. Chem. Soc. 138, 10011-10018.
  • Qin, B., Matsuda, Y., Mori, T., Okada, M., Quan, Z., Mitsuhashi, T., Wakimoto, T., Abe, I., 2016. An unusual chimeric diterpene synthase from Emericella variecolor and its functional conversion into a sesterterpene synthase by domain swapping. Angew. Chem. Int. Ed. 55, 1658-1661.
  • Sanchez, J.F., Entwistle, R., Hung, J.H., Yaegashi, J., Jain, S., Chiang, Y.M., Wang, C.C.C., Oakley, B.R., 2011. Genome-based deletion analysis reveals the prenyl xanthone biosynthesis pathway in Aspergillus nidulans. J. Am. Chem. Soc. 133, 4010-4017.
  • Scherlach, K., Hertweck, C., 2006. Discovery of aspoquinolones A-D, prenylated quinoline-2-one alkaloids from Aspergillus nidulans, motivated by genome mining. Org. Biomol. Chem. 4, 3517-3520.
  • Scherlach, K., Schuemann, J., Dahse, H.M., Hertweck, C., 2010. Aspernidine A and B, prenylated isoindolinone alkaloids from the model fungus Aspergillus nidulans. J. Antibiot. 63, 375-377.
  • Wu, Z., Tong, Q., Zhang, X., Zhou, P., Dai, C., Wang, J., Chen, C., Zhu, H., Zhang, Y., 2019. Amichalasines A-C: three cytochalasan heterotrimers from Aspergillus micronesiensis PG-1. Org. Lett. 21, 1026-1030.
  • Zang, Y., Genta-Jouve, G., Zheng, Y., Zhang, Q., Chen, C., Zhou, Q., Wang, J., Zhu, H., Zhang, Y., 2018. Griseofamines A and B: two indole-tetramic acid alkaloids with 6/5/ 6/5 and 6/5/7/5 ring systems from Penicillium griseofulvum. Org. Lett. 20, 2046-2050.
  • Zhu, H., Chen, C., Yang, J., Li, X.N., Liu, J., Sun, B., Huang, S.X., Li, D., Yao, G., Luo, Z., Li, Y., Zhang, J., Xue, Y., Zhang, Y., 2014. Bioactive acylphloroglucinols with adamantyl skeleton from Hypericum sampsonii. Org. Lett. 16, 6322-6325.