Non-classical azoreductase secretion in Clostridium perfringens in response to sulfonated azo dye exposure
| Autor: | Jessica M. Morrison, Gilbert H. John |
|---|---|
| Rok vydání: | 2015 |
| Předmět: |
chemistry.chemical_classification
Clostridium perfringens Mutant Periplasmic space Flavin group Biology Nitroreductases medicine.disease_cause Microbiology Gene Knockout Techniques Infectious Diseases Enzyme Secretory protein chemistry Biochemistry Oxidoreductase medicine Secretion NADH NADPH Oxidoreductases Anaerobiosis Sulfones Periplasmic Proteins Azo Compounds |
| Zdroj: | Anaerobe. 34 |
| ISSN: | 1095-8274 |
| Popis: | Clostridium perfringens, a strictly anaerobic microorganism and inhabitant of the human intestine, has been shown to produce an azoreductase enzyme (AzoC), an NADH-dependent flavin oxidoreductase. This enzyme reduces azo dyes into aromatic amines, which can be carcinogenic. A significant amount of work has been completed on the activity of AzoC. Despite this, much is still unknown, including whether azoreduction of these dyes occurs intracellularly or extracellulary. A physiological study of C. perfringens involving the effect of azo dye exposure was completed to answer this question. Through exposure studies, azo dyes were found to cause cytoplasmic protein release, including AzoC, from C. perfringens in dividing and non-dividing cells. Sulfonation (negative charge) of azo dyes proved to be the key to facilitating protein release of AzoC and was found to be azo-dye-concentration-dependent. Additionally, AzoC was found to localize to the Gram-positive periplasmic region. Using a ΔazoC knockout mutant, the presence of additional azoreductases in C. perfringens was suggested. These results support the notion that the azoreduction of these dyes may occur extracellularly for the commensal C. perfringens in the intestine. |
| Databáze: | OpenAIRE |
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