This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Cho, K. H.
Right arrow Articles by Salyers, A. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cho, K. H.
Right arrow Articles by Salyers, A. A.

 Previous Article  |  Next Article 

Journal of Bacteriology, December 2001, p. 7198-7205, Vol. 183, No. 24
0021-9193/01/$04.00+0   DOI: 10.1128/JB.183.24.7198-7205.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

New Regulatory Gene That Contributes to Control of Bacteroides thetaiotaomicron Starch Utilization Genes

Kyu Hong Cho, Diedre Cho, Gui-Rong Wang, and Abigail A. Salyers*

Department of Microbiology, University of Illinois, Urbana, Illinois 61801

Received 15 June 2001/Accepted 19 September 2001

Bacteroides thetaiotaomicron uses starch as a source of carbon and energy. Early steps in the pathway of starch utilization, such as starch binding and starch hydrolysis, are encoded by sus genes, which have been characterized previously. The sus structural genes are expressed only if cells are grown in medium containing maltose or higher oligomers of glucose. Regulation of the sus structural genes is mediated by SusR, an activator that is encoded by a gene located next to the sus structural genes. A strain with a disruption in susR cannot grow on starch but can still grow on maltose and maltotriose. A search for transposon-generated mutants that could not grow on maltose and maltotriose unexpectedly located a gene, designated malR, which regulates expression of an alpha -glucosidase not controlled by SusR. Although a disruption in susR did not affect expression of the malR controlled gene, a disruption in malR reduced expression of the sus structural genes. Thus, MalR appears to participate with SusR in regulation of the sus genes. Results of transcriptional fusion assays and reverse transcription-PCR experiments showed that malR is expressed constitutively. Moreover, multiple copies of malR provided on a plasmid (5 to 10 copies per cell) more than doubled the amount of alpha -glucosidase activity in cell extracts. Our results demonstrate that the starch utilization system of B. thetaiotaomicron is controlled on at least two levels by the regulatory proteins SusR and MalR.


* Corresponding author. Mailing address: Department of Microbiology, 601 S. Goodwin Ave., CLSL 103, University of Illinois, Urbana, IL 61801. Phone: (217) 333-7378. Fax: (217) 244-8485. E-mail: abigails{at}uiuc.edu.


Journal of Bacteriology, December 2001, p. 7198-7205, Vol. 183, No. 24
0021-9193/01/$04.00+0   DOI: 10.1128/JB.183.24.7198-7205.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Kitamura, M., Okuyama, M., Tanzawa, F., Mori, H., Kitago, Y., Watanabe, N., Kimura, A., Tanaka, I., Yao, M. (2008). Structural and Functional Analysis of a Glycoside Hydrolase Family 97 Enzyme from Bacteroides thetaiotaomicron. J. Biol. Chem. 283: 36328-36337 [Abstract] [Full Text]  
  • Wexler, H. M. (2007). Bacteroides: the Good, the Bad, and the Nitty-Gritty. Clin. Microbiol. Rev. 20: 593-621 [Abstract] [Full Text]  
  • Bjursell, M. K., Martens, E. C., Gordon, J. I. (2006). Functional Genomic and Metabolic Studies of the Adaptations of a Prominent Adult Human Gut Symbiont, Bacteroides thetaiotaomicron, to the Suckling Period. J. Biol. Chem. 281: 36269-36279 [Abstract] [Full Text]  
  • Ramsay, A. G., Scott, K. P., Martin, J. C., Rincon, M. T., Flint, H. J. (2006). Cell-associated {alpha}-amylases of butyrate-producing Firmicute bacteria from the human colon.. Microbiology 152: 3281-3290 [Abstract] [Full Text]  
  • Spence, C., Wells, W. G., Smith, C. J. (2006). Characterization of the Primary Starch Utilization Operon in the Obligate Anaerobe Bacteroides fragilis: Regulation by Carbon Source and Oxygen. J. Bacteriol. 188: 4663-4672 [Abstract] [Full Text]  
  • Moon, K., Shoemaker, N. B., Gardner, J. F., Salyers, A. A. (2005). Regulation of Excision Genes of the Bacteroides Conjugative Transposon CTnDOT. J. Bacteriol. 187: 5732-5741 [Abstract] [Full Text]  
  • Sonnenburg, J. L., Xu, J., Leip, D. D., Chen, C.-H., Westover, B. P., Weatherford, J., Buhler, J. D., Gordon, J. I. (2005). Glycan Foraging in Vivo by an Intestine-Adapted Bacterial Symbiont. Science 307: 1955-1959 [Abstract] [Full Text]  
  • Stappenbeck, T. S., Hooper, L. V., Gordon, J. I. (2002). Developmental regulation of intestinal angiogenesis by indigenous microbes via Paneth cells. Proc. Natl. Acad. Sci. USA 99: 15451-15455 [Abstract] [Full Text]