The Reduction of Azo Dyes by the Intestinal Microflora
- 1 January 1992
- journal article
- research article
- Published by Taylor & Francis in Critical Reviews in Microbiology
- Vol. 18 (3) , 175-190
- https://doi.org/10.3109/10408419209114557
Abstract
Azo dyes are widely used in the textile, printing, paper manufacturing, pharmaceutical, and food industries and also in research laboratories. When these compounds either inadvertently or by design enter the body through ingestion, they are metabolized to aromatic amines by intestinal microorganisms. Reductive enzymes in the liver can also catalyze the reductive cleavage of the azo linkage to produce aromatic amines. However, evidence indicates that the intestinal microbial azoreductase may be more important than the liver enzymes in azo reduction. The azoreductase activity in a variety of intestinal preparations was affected by various dietary factors such as cellulose, proteins, fibers, antibiotics, or supplementation with live cultures of lactobacilli. In this article, we examine the significance of the capacity of intestinal bacteria to reduce azo dyes and the conditions of azo reduction. Many azo dyes, such as Acid Yellow, Amaranth, Azodisalicylate, Chicago Sky Blue, Congo Red, Direct Black 38, Direct Blue 6, Direct Blue 15, Direct Brown 95, Fast Yellow, Lithol Red, Methyl Orange, Methyl Red, Methyl Yellow, Naphthalene Fast Orange 2G, Neoprontosil, New Coccine, Orange II, Phenylazo-2-naphthol, Ponceau 3R, Ponceau SX, Red 2G, Red 10B, Salicylazosulphapyridine, Sunset Yellow, Tartrazine, and Trypan Blue, are included in this article. A wide variety of anaerobic bacteria isolated from caecal or fecal contents from experimental animals and humans have the ability to cleave the azo linkage(s) to produce aromatic amines. Azoreductase(s) catalyze these reactions and have been found to be oxygen sensitive and to require flavins for optimal activity.Keywords
This publication has 103 references indexed in Scilit:
- A case‐sar study of mammalian hepatic azoreductionJournal of Toxicology and Environmental Health, 1988
- Metabolism of 1‐, 3‐, and 6‐nitrobenzo[a]pyrene by intestinal microfloraJournal of Toxicology and Environmental Health, 1988
- Use of a semicontinuous culture system as a model for determining the role of human intestinal microflora in the metabolism of xenobioticsJournal of Microbiological Methods, 1987
- Comparative mutagenicity studies of AZO dyes and their reduction products insalmonella typhimuriumJournal of Toxicology and Environmental Health, 1986
- A comparison of the activity of five microbial enzymes in cecal content from rats, mice, and hamsters, and response to dietary pectinnToxicology and Applied Pharmacology, 1983
- Trypan blue: Identification and teratogenic and oncogenic activities of its coloured constituentsChemico-Biological Interactions, 1976
- A deficiency of dietary fiber may be one cause of certain colonic and venous disordersDigestive Diseases and Sciences, 1976
- Metabolism of Xenobiotics by Strains of Intestinal BacteriaActa Pharmacologica et Toxicologica, 1972
- Metabolism of 4-Dimethylaminoazobenzene and Related Compounds. III. Metabolites of 4-Dimethylaminoazobenzene in Rat Bile and Influence of DAB Feeding on their AmountsCHEMICAL & PHARMACEUTICAL BULLETIN, 1963
- THE CARCINOGENICITY OF CERTAIN DERIVATIVES OF p-DIMETHYLAMINOAZOBENZENE IN THE RATThe Journal of Experimental Medicine, 1948