Insoluble dye-protein complexes offer many advantages when used as substrates for proteolytie enzymes. The proteolytic split products can be separated from the starting substrat.e conveniently by filtration, and the concentration of the soluble colored products of hydrolysis can easily be measured a
A rapid assay for the glyoxalase enzyme system
β Scribed by Nicholas M. Alexander; James L. Boyer
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- English
- Weight
- 541 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0003-2697
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β¦ Synopsis
The glyoxalase enzyme system was first detected in animal tissues in 1913 (1,2). It is widely distributed in nature (3-6) and consists of two enzymes, glyoxalase I (S-lactoyl-glutathione methylglyoxal-lyase (isomerizing) , EC 4.4.1.5) and glyoxalase II (S-2-hydroxyacrylglutathione hydrolase, EC 3.1.2.6), plus the cofactor reduced gluthathione (GSH). This enzyme system catalyzes the conversion of some ketoaldehydes to hydroxy acids. For example, methylglyoxal is converted to lactic acid in a two-step reaction in the following manner:
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A stainless-steel cylindrical vessel is described with optical ports which can be pressurized to 1000 atm (hydrostatic). Constituents for enzymic reactions are injected directly into the vessel, sealed without use of tools, and pressurized. All these operations can be completed in about 10 sec. The
A simple, convenient, and quantitative method for the preparation of methylglyoxal (pyruvaldehyde) solutions is described. The method involved acid hydrolysis (5% HZS04) of pyruvaldehyde dimethyl acetal at 100Β°C for 25 min. The hydrolysis method is quite reproducible and does not require standardiza
## Abstract An enzymeβlinked immunosorbent assay (ELISA) was developed for detecting IgG antibodies to the Pitman Moore strain of rabies virus in sera from subjects immunised with HDCS vaccine. Endβpoint titres of antibody were determined using a pocket calculator preprogrammed to analyse absorbenc