Biosynthesis of Nonimmunosuppressive FK506 Analogues with Antifungal Activity

Ji Yoon Beom, Jin A. Jung, Kyung Tae Lee, Areum Hwangbo, Myoung Chong Song, Yeonseon Lee, Soo Jung Lee, Ji Hoon Oh, Sang Jun Ha, Sang Jip Nam, Eunji Cheong, Yong Sun Bahn, Yeo Joon Yoon

Research output: Contribution to journalArticlepeer-review

17 Scopus citations


A reduction in the strong immunosuppressive activity of FK506 (1) is essential for developing this compound as an antifungal agent. Seven new FK506 analogues modified at both the FK506-binding protein 12- and the calcineurin-binding regions were biosynthesized. 9-DeoxoFK520 (7) exhibited a >900-fold reduction in the in vitro immunosuppressive activity but maintained significant antifungal activity, indicating that the C-9 and C-21 positions are critical for separation of immunosuppressive and antifungal activities. 7 exhibited robust synergistic antifungal activity with fluconazole. FK506 (1) is a 23-membered macrolide produced by several Streptomyces species and is used as an immunosuppressive drug to prevent the rejection of transplanted organs. FK506 has also exhibited antifungal, neuroprotective, and neuroregenerative activities. In humans, FK506 binds to FK506-binding protein (FKBP) 12, and the resulting FKBP12-FK506 complex interacts with a Ca2+-calmodulin-dependent phosphatase, calcineurin (CaN). Inactivation of CaN by forming the FKBP12-FK506-CaN ternary complex prevents the activation of nuclear factor of activated T cells (NF-AT), inhibiting the production of interleukin-2 and subsequent T-cell proliferation. This CaN signaling pathway also plays a critical role in the growth and pathogenesis of major fungal pathogens such as Cryptococcus neoformans, Candida albicans, and Aspergillus fumigatus. Therefore, the synthesis of FK506 analogues that can discriminate human FKBP12/CaN from its fungal counterparts may separate antifungal activity from the immunosuppressive activity, thereby allowing the development of a novel antifungal agent.

Original languageEnglish
Pages (from-to)2078-2086
Number of pages9
JournalJournal of Natural Products
Issue number8
StatePublished - 23 Aug 2019

Bibliographical note

Funding Information:
This work was supported by National Research Foundation of Korea (NRF) grants funded by the Ministry of Science and ICT (MSIT) (2019R1A2B5B03069338; 2016R1E1A1A01943365; 2018R1A5A1025077; 2017R1A2B3011098; 2017M3C7A1023471), the Bio & Medical Technology Development Program of the NRF funded by the MSIT (2018M3A9F3079662), a grant of the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI) funded by the Ministry of Health & Welfare (HI18C1664), and the Strategic Initiative for Microbiomes in Agriculture and Food funded by Ministry of Agriculture, Food and Rural Affairs (918012-4), Republic of Korea. J.Y.B. was the recipient of the Ewha Womans University scholarship of 2015. K.-T.L. was also supported by the Yonsei University Research Fund (Yonsei Frontier Lab Young Researcher Supporting Program) of 2018.

Publisher Copyright:
Copyright © 2019 American Chemical Society and American Society of Pharmacognosy.


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