Professor, Medicinal Chemistry
Department of Pharmaceutical Sciences
College of Pharmacy
Oregon State University
203 Pharmacy Building
Corvallis, OR 97331-3507
Phone: 541-737-5774
Mark.Zabriskie@oregonstate.edu
University of Alberta, Killam Foundation Postdoctoral Fellow, 1990-1992
NSF/NATO Postdoctoral Fellow, 1989-1990
University of Utah, Ph.D., 1989; B.S., 1985
Current research in Mark Zabriskie’s laboratory focuses on the biosynthesis of nonribosomal peptide and peptidyl nucleoside antibiotics. All of the compounds being studied are effective in treating various drug resistant bacterial infections and most are produced by Streptomyces spp. soil bacteria. Representative target compounds include the antitubercular agent viomycin, the antibacterial peptide enduracidin and the antifungal compound blasticidin S. Peptide natural products like enduracidin and viomycin are not synthesized by the typical ribosomal mechanism, and a main interest of the group is the biosynthetic enzymes that assemble these complex, amino acid-derived natural products. There is a particular emphasis on enzymes involved in the formation of unusual precursor amino acids and post-assembly modifications of the nascent peptides. The overarching goal in the laboratory is to gain a better understanding of the basic molecular genetics and biochemistry of these processes and then apply this knowledge toward developing novel antimicrobial agents. Our approach involves a combination of genetic and chemical methods to generate analogs that may have improved therapeutic properties.
The group also collaborates with other OSU colleagues and scientists from Indonesia to screen a collection of unique bacteria isolated from a rare Indonesian ecosystem for novel antimicrobial compounds. The bacteria are fermented in our laboratory and the extracts are screened for biological activity. The structures of the active constituents are determined, and promising lead compounds serve as the scaffold for subsequent chemical modifications to improve drug-like properties and expand chemical diversity for additional biological screening. The biosynthetic genes for compounds with exceptional activity, or which have structures suggesting novel biochemistry, may be cloned to facilitate analog development through genetic manipulation and combinatorial biosynthesis.
