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Arginine catabolism by Treponema denticola
Journal of Bacteriology
|November 1, 1976
Summary
Treponema denticola utilizes arginine for energy through the arginine deiminase pathway. This oral bacterium converts arginine-derived ornithine into proline, a unique metabolic adaptation.
Area of Science:
- Microbiology
- Bacterial Metabolism
- Oral Microbiome
Background:
- Treponema denticola is an anaerobic bacterium found in the human mouth.
- It is known to ferment various substrates, including amino acids and glucose.
- Understanding its metabolic pathways is crucial for comprehending its role in the oral environment.
Purpose of the Study:
- To investigate the metabolic fate of L-arginine in Treponema denticola.
- To elucidate the specific enzymes and pathways involved in arginine utilization.
- To identify any unique metabolic characteristics of T. denticola compared to other bacteria using similar pathways.
Main Methods:
- Analysis of amino acid utilization and product formation by T. denticola cell suspensions.
- Radiotracer studies using L-[U-14C]ornithine to track metabolic conversions.
- Enzyme assays to detect arginine deiminase and ornithine carbamoyltransferase activities in cell extracts.
Main Results:
- Treponema denticola metabolized L-arginine to citrulline, ammonia (NH3), carbon dioxide (CO2), proline, and ornithine.
- L-citrulline was further metabolized to CO2, NH3, ornithine, and proline.
- Radioactive labeling confirmed the conversion of L-ornithine to proline, which was also excreted by growing cells.
- Enzyme assays detected arginine deiminase and ornithine carbamoyltransferase activities.
- Carbamoylphosphate dissimilation by cell extracts produced adenosine triphosphate (ATP).
Conclusions:
- Treponema denticola derives energy from L-arginine via the arginine deiminase pathway.
- A significant portion of the ornithine generated from L-arginine is converted to proline by T. denticola.
- This proline production represents a distinct metabolic feature of T. denticola within the context of arginine deiminase pathway utilization.