An important activity of the complex and numerous microbial population which resides in the human colon is the catabolism of dietary and host-produced polysaccharides. Products of this catabolism are thought to contribute to human nutrition and may have other effects on the health of the human host. Some information is available about the utilization of polysaccharides by colon bacteria growing in laboratory culture, but at present there is no way of determining what these same organisms are actually doing in the colon. The long range goal of this project is to develop specific probes which can be used to detect and measure bacterial activities in complex mixtures such as colon contents. The project will focus on the genus Bacteroides. This genus accounts for at least 20% of all colon isolates and contains the most versatile polysaccharide utilizers. We will first characterize proteins which are associated with growth of Bacteroides on polysaccharides such as the tissue mucopolysaccharide chondroitin sulfate (CS). These proteins include not only degradative enzymes but also membrane proteins. Specific antiserum to these proteins will be obtained. Antisera will be used to determine the effect of very slow growth rates and carbohydrate limitation, conditions encountered by the bacteria in their natural habitat, on production of these proteins. The antisera will also be used to determine whether these proteins are actually produced in the colon. Since the antibodies will distinguish polysaccharide-associated proteins produced by different species, they can be used to determine which species is (are) utilizing a particular polysacchraide in the colon. If successful, this approach can be used to answer such questions as how the host's diet affects the activities of colonic bacteria.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI017876-07
Application #
3127476
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1981-04-01
Project End
1989-03-31
Budget Start
1987-04-01
Budget End
1988-03-31
Support Year
7
Fiscal Year
1987
Total Cost
Indirect Cost
Name
University of Illinois Urbana-Champaign
Department
Type
Schools of Arts and Sciences
DUNS #
041544081
City
Champaign
State
IL
Country
United States
Zip Code
61820
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Cho, K H; Salyers, A A (2001) Biochemical analysis of interactions between outer membrane proteins that contribute to starch utilization by Bacteroides thetaiotaomicron. J Bacteriol 183:7224-30
Salyers, A A; Bonheyo, G; Shoemaker, N B (2000) Starting a new genetic system: lessons from bacteroides. Methods 20:35-46
Shipman, J A; Cho, K H; Siegel, H A et al. (1999) Physiological characterization of SusG, an outer membrane protein essential for starch utilization by Bacteroides thetaiotaomicron. J Bacteriol 181:7206-11
D'Elia, J N; Salyers, A A (1996) Contribution of a neopullulanase, a pullulanase, and an alpha-glucosidase to growth of Bacteroides thetaiotaomicron on starch. J Bacteriol 178:7173-9
D'Elia, J N; Salyers, A A (1996) Effect of regulatory protein levels on utilization of starch by Bacteroides thetaiotaomicron. J Bacteriol 178:7180-6
Reeves, A R; D'Elia, J N; Frias, J et al. (1996) A Bacteroides thetaiotaomicron outer membrane protein that is essential for utilization of maltooligosaccharides and starch. J Bacteriol 178:823-30
Cheng, Q; Salyers, A A (1995) Use of suppressor analysis to find genes involved in the colonization deficiency of a Bacteroides thetaiotaomicron mutant unable to grow on the host-derived mucopolysaccharides chondroitin sulfate and heparin. Appl Environ Microbiol 61:734-40
Cheng, Q; Yu, M C; Reeves, A R et al. (1995) Identification and characterization of a Bacteroides gene, csuF, which encodes an outer membrane protein that is essential for growth on chondroitin sulfate. J Bacteriol 177:3721-7
Hwa, V; Salyers, A A (1992) Evidence for differential regulation of genes in the chondroitin sulfate utilization pathway of Bacteroides thetaiotaomicron. J Bacteriol 174:342-4

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