RESEARCH EXPERIENCE
Laboratory of Professor
A.C. Matin
· Investigating bacterial magnetite genes for an MRI reporter, in collaboration with the Gambhir Lab and members of the Molecular Imaging Program at Stanford (MIPS).
· Developing a high-throughput method for screening flow-cell biofilms with a microfluidic device, in collaboration with Fluxion Biosciences.
Post-doctoral Scholar, Stanford University,
Department of Microbiology &
Immunology, 2006 - 2009
Primary Advisor: Professor A.C. Matin; Co-advisor: Professor Sanjiv Sam Gambhir.
· Investigated MRI contrast enhancement and tumor targeting ability of magnetotactic bacteria, in collaboration with the Gambhir Lab and members of the Molecular Imaging Program at Stanford (MIPS).
· Discovered a gene involved in biofilm-specific antibiotic resistance. Demonstrated the role of the gene in regulating a multi-drug efflux pump and reducing penetration of antibiotics through the biofilm polymeric matrix.
· Examined the effect of low-shear simulated microgravity on bacterial biofilm resistance to stress, and validated the experimental fluid dynamics with a numerical model.
Doctoral Research, University of
Colorado, 1999 - 2005
BioServe Space Technologies, Aerospace Engineering Sciences Dept.
(Advisor: Assoc. Prof. David M.
Klaus)
· Investigated bacterial antibiotic production in space with a space flight experiment onboard the International Space Station. Helped design, build, and integrate an automated bioreactor developed uniquely for this experiment, in collaboration with Bristol-Myers Squibb. See NASA Mission Description
· Created a numerical model for studying the effects of gravity on extracellular mass transport.
· Developed a novel system to simulate microgravity by bacterial production of gas vesicles to generate neutral buoyancy.
· Tested and developed a prototype instrument for spaceflight experiments that uses digital holography to measure small changes in fluid density for cell biology experiments.
· Studied host-pathogen interactions between opportunistic pathogens (Listeria monocytogenes and Legionella pneumophila) and murine macrophages.