Biotechnological applications of peroxidases (original) (raw)
2000, Phytochemistry Reviews
Peroxidases are widely distributed in nature. Reduction of peroxides at the expense of electron donating substrates, make peroxidases useful in a number of biotechnological applications. Enzymes such as lignin peroxidase and manganese peroxidase, both associated with lignin degradation, may be successfully used for biopulping and biobleaching in the paper industry, and can produce oxidative breakdown of synthetic azo dyes. Oxidative polymerization of phenols and aromatic amines conducted by horseradish peroxidase (HRP) in water and watermiscible organic solvents, may lead to new types of aromatic polymers. Site directed mutagenesis of HRP has been used to improve the enantioselectivity of arylmethylsulfide oxidations. Peroxidase has a potential for soil detoxification, while HRP as well as soybean and turnip peroxidases have been applied for the bioremediation of wastewater contaminated with phenols, cresols, and chlorinated phenols. Peroxidase based biosensors have found use in analytical systems for determination of hydrogen peroxide and organic hydroperoxides, while coimmobilized with a hydrogen peroxide producing enzyme, they can be used for determination of glucose, alcohols, glutamate and choline. Peroxidase has also been used for practical analytical applications in diagnostic kits, such as quantitation of uric acid, glucose, cholesterol, lactose, and so on. Enzyme linked immunorbent assay (ELISA) tests on which peroxidase is probably the most common enzyme used for labeling an antibody, are a simple and reliable way of detecting toxins, pathogens, cancer risk in bladder and prostate, and many other analytes. Directed evolution methods, appear to be a valuable alternative to engineer new catalyst forms of plant peroxidases from different sources to overcome problems of stability and to increase thermal resistance. Abbreviations: A-electron donor; A •-oxidized donor; AH-reduced electron donor; CDH-cellobiose dehydrogenase; CoI-compound I; CoII-compound II; EIA-enzyme immunoassay; ELISA-enzyme linked immunosorbent assay; EPR-electron paramagnetic resonance; ESR-electron spin resonance; ET-electron transfer; GC-MS-gas chromatography-Mass spectrometry; HPLC-high performance liquid chromatography; HRP-horseradish peroxidase; hTNF-alpha-Human tumor necrosis factor-alpha; IAA-indole-3-acetic acid; LiP-lignin peroxidase; MnP-manganese peroxidase; PEG-polyethylene glycol; TLC-thin layer chromatography; UKP-hard wood kraft pulp.