New Regulatory Gene That Contributes to Control of Bacteroides thetaiotaomicron Starch Utilization Genes
Open Access
- 15 December 2001
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 183 (24) , 7198-7205
- https://doi.org/10.1128/jb.183.24.7198-7205.2001
Abstract
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 α-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 α-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.Keywords
This publication has 14 references indexed in Scilit:
- Studies on transformation of Escherichia coli with plasmidsPublished by Elsevier ,2006
- Production of Two Proteins Encoded by the Bacteroides Mobilizable Transposon NBU1 Correlates with Time-Dependent Accumulation of the Excised NBU1 Circular FormJournal of Bacteriology, 2001
- Multiple Gene Products and Sequences Required for Excision of the Mobilizable Integrated Bacteroides Element NBU1Journal of Bacteriology, 2000
- Insights into erythromycin action from studies of its activity as inducer of resistanceAntimicrobial Agents and Chemotherapy, 1995
- Location and characterization of genes involved in binding of starch to the surface of Bacteroides thetaiotaomicronJournal of Bacteriology, 1992
- Use of an Escherichia coli beta-glucuronidase gene as a reporter gene for investigation of Bacteroides promotersJournal of Bacteriology, 1991
- Characterization of a neopullulanase and an alpha-glucosidase from Bacteroides thetaiotaomicron 95-1Journal of Bacteriology, 1991
- Genetic evidence that outer membrane binding of starch is required for starch utilization by Bacteroides thetaiotaomicronJournal of Bacteriology, 1989
- Regions in Bacteroides plasmids pBFTM10 and pB8-51 that allow Escherichia coli-Bacteroides shuttle vectors to be mobilized by IncP plasmids and by a conjugative Bacteroides tetracycline resistance elementJournal of Bacteriology, 1986
- A Broad Host Range Mobilization System for In Vivo Genetic Engineering: Transposon Mutagenesis in Gram Negative BacteriaBio/Technology, 1983