The overall goal of this project is to study the flux (both in and out) of small molecules across the surface layers of bacteria. As is well-known, multiple resistance in pathogenic microorganisms is becoming a serious threat to human health. Recent studies in our own and other laboratories suggest that in many cases such resistance is the synergistic effect of two factors, the cell surface layer acting as permeability barrier for the influx of drugs (outer membrane of Gram-negative bacteria or mycolate-containing cell wall of mycobacteria) and active, multidrug efflux pumps. In fact, for more advanced antimicrobial agents that resist the enzymatic inactivation of bacteria, such as fluoroquinolones, this mechanism that prevents the access of drugs to the target has become a primary mechanism of resistance. In this study, we plan to continue our characterization of both of these resistance mechanisms. Thus we will characterize the """"""""slow"""""""" porins of organism such as Pseudomonas aeruginosa, the proteins that contribute to the generalized intrinsic resistance of these bacteria by slowing down the influx of antimicrobial agents across their outer membrane. We will study the mechanism in which the cell wall of mycobacteria drastically slows down the entry of most agents by producing an organized layer of mycolic acid and other lipids. At the other end, we will investigate the mechanism of multidrug efflux pumps, especially those pumps that show an incredibly wide range of specificity, such as AcrAB of Escherichia coli that extrudes almost any lipophilic or amphiphilic compounds, including dyes, disinfectants, detergents, solvents, and practically all antibiotic (except aminoglycosides). These pumps appear to become expressed more strongly when the bacteria are under stress, and the pathway of regulation will be defined. Finally, as a prototype of ABC transporter, which includes P-glycoprotein and CFTR, the maltose transporter complex of a hyperthermophile Pyrococcus furiosus will be purified, because proteins from hyperthermophiles tend to produce well-diffracting crystals, and there is great need to obtain crystallographic data on this important class of transporters.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI009644-33
Application #
6510186
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Program Officer
Korpela, Jukka K
Project Start
1976-03-01
Project End
2006-02-28
Budget Start
2002-03-01
Budget End
2003-02-28
Support Year
33
Fiscal Year
2002
Total Cost
$587,750
Indirect Cost
Name
University of California Berkeley
Department
Microbiology/Immun/Virology
Type
Schools of Arts and Sciences
DUNS #
094878337
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Nikaido, Hiroshi (2018) RND transporters in the living world. Res Microbiol 169:363-371
Kinana, Alfred D; Vargiu, Attilio V; May, Thithiwat et al. (2016) Aminoacyl ?-naphthylamides as substrates and modulators of AcrB multidrug efflux pump. Proc Natl Acad Sci U S A 113:1405-10
Kinana, Alfred D; Vargiu, Attilio V; Nikaido, Hiroshi (2016) Effect of site-directed mutations in multidrug efflux pump AcrB examined by quantitative efflux assays. Biochem Biophys Res Commun 480:552-557
Sugawara, Etsuko; Kojima, Seiji; Nikaido, Hiroshi (2016) Klebsiella pneumoniae Major Porins OmpK35 and OmpK36 Allow More Efficient Diffusion of ?-Lactams than Their Escherichia coli Homologs OmpF and OmpC. J Bacteriol 198:3200-3208
Soparkar, Ketaki; Kinana, Alfred D; Weeks, Jon W et al. (2015) Reversal of the Drug Binding Pocket Defects of the AcrB Multidrug Efflux Pump Protein of Escherichia coli. J Bacteriol 197:3255-64
Nobre, Thatyane M; Martynowycz, Michael W; Andreev, Konstantin et al. (2015) Modification of Salmonella Lipopolysaccharides Prevents the Outer Membrane Penetration of Novobiocin. Biophys J 109:2537-2545
Li, Xian-Zhi; Plésiat, Patrick; Nikaido, Hiroshi (2015) The challenge of efflux-mediated antibiotic resistance in Gram-negative bacteria. Clin Microbiol Rev 28:337-418
Vargiu, Attilio V; Ruggerone, Paolo; Opperman, Timothy J et al. (2014) Molecular mechanism of MBX2319 inhibition of Escherichia coli AcrB multidrug efflux pump and comparison with other inhibitors. Antimicrob Agents Chemother 58:6224-34
Bansal-Mutalik, Ritu; Nikaido, Hiroshi (2014) Mycobacterial outer membrane is a lipid bilayer and the inner membrane is unusually rich in diacyl phosphatidylinositol dimannosides. Proc Natl Acad Sci U S A 111:4958-63
Opperman, Timothy J; Kwasny, Steven M; Kim, Hong-Suk et al. (2014) Characterization of a novel pyranopyridine inhibitor of the AcrAB efflux pump of Escherichia coli. Antimicrob Agents Chemother 58:722-33

Showing the most recent 10 out of 35 publications