Michio Kurosu, Ph.D.
Professor at University of Tennessee health Science Center
CEO of MK Consulting
Graduate school of pharmaceutical Sciences
Osaka University, PHD
Pharmaceutical Sciences | Organic Chemistry | Medicinal Chemistry
Harvard University, Postdoctoral Fellow
Department of Chemistry and Chemical Biology
Chemical Biology | Organic Chemistry
Dr. Kurosu has a long-term interest in identifying new drug targets for bacterial infections and in the development of new antibacterial agents. Tuberculosis (TB) treatment that is applicable in the context of HIV co-infection through host-directed therapies by enhancing immunologic reactions is believed to be an ultimate approach. Humoral markers to identify M. tuberculosis as vaccine targets and inducers that produce pivotal cytokines (e.g. IL-12, INF-gamma) need further investigations. It is my long-term goal to understand immune pathology of TB and identify selective immune-modulatory small molecules for the treatment of replicating and non-replicating M. tuberculosis. He has over 25 years of experience as a synthetic/medicinal chemist and has engaged in a wide range of research projects associated with infectious diseases. He has developed concise syntheses of complex natural and unnatural molecules, and design/synthesize chiral small molecules and generates small optimized libraries in solution or on polymer-supports. He also develops convenient assays against target proteins. These efforts have resulted in the discovery of several new drug leads effective against multidrug-resistant (MDR)-M. tuberculosis and dormant form of M. tuberculosis, and Gram-positive (e.g. Clostridioides difficile) and Gram-negative bacteria (e.g. Acinetobacter baumannii, Pseudomonas aeruginosa, and Klebsiella pneumoniae). Our lab. has set up bacterial growth inhibitory assays against a battery of pathogens including BSL3 bacteria. These assays will be performed at the UTHS RBL facility. Over the last 10 years, he has studied electron transport systems, menaquinone biosynthesis, unexploited peptidoglycan biosynthesis (MurX, MraY, WecA, MurG), protein biosynthesis, membrane disruption, and bacterial kinases. New inhibitor molecules identified in these programs will apply for structural elucidation and functional characterization of bacterial transmembrane enzymes. He has had experience in anti-cancer drug developments in industrial and academic settings. Generated small molecule libraries have been screened against batteries of human cancer cell lines in his lab and spectrum of anticancer activity of identified molecules is determined by assaying against the National Cancer Institute (NCI) 60 human tumor cell line. His lab is primarily interested in phosphotransferase which is overexpressed in certain cancer cells.