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Bailey Miller

Bailey Miller, PhD

Academic Office Information

bailey.miller@utah.edu

Research Interests

  • Antibiotics discovery from marine shipworm symbionts

RESEARCH INTERESTS

Antibiotics discovery from marine shipworm symbionts

Shipworms are wood-eating marine bivalves that host symbiotic bacteria in their gill tissues. These microbes provide the animal enzymes to help digest the lignocellulose from their woody diet and are also prolific producers of complex secondary metabolites. These molecules may play a role in protecting their host from infection by pathogens or in protecting their shared food resources from pathogens. My research focuses on isolating and characterizing these molecules as antibiotics that could be used for human health. Recent advances include the discovery of the turnercyclamycins, a new family of cyclic lipodepsipeptides with in vivo efficacy against Acinetobacter baumannii

Education History

University of California Santa Barbara
Biopsychology
BS
University of California San Diego
Marine Chemical Biology
PhD

Selected Publications

Journal Article

  1. Miller, B.W., Schmidt, E.W, Concepcion, G.P., Haygood, M.G. Halogenated metal-binding compounds from shipworm symbionts. Journal of Natural Products. 2022

  2. Miller, B.W., Lim, A.L., Lin, Z., Bailey, J., Aoyagi, K.L., Fisher, M.A., Barrows, L.R., Manoil, C., Haygood, M.G., Schmidt, E.W. Shipworm symbiosis ecology-guided discovery of an antibiotic the kills colistin-resistant AcinetobacterCell Chemical Biology. 2021

  3. Lacerna, N. M., Ramones, C.M.V., Robes, J.M.D., Picart, M.R.D., Tun, J.O., Miller, B.W., Haygood, M.G., Schmidt, E.W., Salvador-Reyes, L.A., Concepcion, G.P. Inhibition of biofilm formation by modified oxylipins from the shipworm symbiont Teredinibacter turneraeMarine Drugs. 2020

  4. Miller, B.W.*, Torres, J.P.*, Tun, J.O.*, Flores, M.S., Forteza, I., Rosenberg, G., Haygood, M.G., Schmidt, E.W., Concepcion, G.P. Synergistic anti-methicillin-resistant Staphylococcus aureus (MRSA) activity and absolute stereochemistry of 7,8-dideoxygriseorhodin C. J. Antibiotics. 2020, 73(5), 290-298 *Indicates co-first authors

  5. Boudraeu, P.D.*, Miller, B.W.*, McCall, L, Almaliti, J., Reher, R., Hirata, K., Le, T., Siqueira-Neto, J., Hook, V., Gerwick, W.H. Design of Gallinamide A Analogs as Potent Inhibitors of the Cysteine Porteases Human Cathepsin L and Trypanosoma cruzi Cruzain. Journal of Medicinal Chemistry. 2019

  6. Lacerna II, N., Miller, B.W., Lim, A. L., Tun, J.O., Robes, J.M.D., Cleofas, M.J.B., Lin, Z., Salvador-Reyes, L., Haygood, M.G., Schmidt, E.W., Concepcion, G.P. Mindapyrroles A-C, Pyoluteorin Analogs from A Shipworm-Associated Bacterium. Journal of Natural Products. 2019, 82 (4), 1024-1028

  7. Almaliti, J., Miller, B. W., Pietraszkiewicz, H., Glukhov, E., Naman, C. B., Kline, T., Hanson, J., Li, X., Zhou, S., Valeriote, F. A., et al. Exploration of the Carmaphycins as Payloads in Antibody Drug Conjugate Anticancer Agents. European Journal of Medicinal Chemistry 2019, 161, 416–432.

  8. Naman, C.B., Rattan, R., Nikoulina, S.E., Lee, J., Miller, B.W., Moss, N.A., Armstrong, L., Boudreau, P.D., Debonsi, H.M., Valeriote, F.A., et al. Integrating Molecular Networking and Biological Assays to Target the Isolation of a Cytotoxic Cyclic Octapeptide, Samoamide A, from an American Samoan Marine Cyanobacterium. J. Nat. Prod. 2017, 80 (3), 625–633.

  9. Miller, B., Friedman, A.J., Choi, H., Hogan, J., McCammon, J.A., Hook, V., Gerwick, W.H. The Marine Cyanobacterial Metabolite Gallinamide A Is a Potent and Selective Inhibitor of Human Cathepsin L. J. Nat. Prod. 2014, 77 (1), 92–99.

    More Selected Publications