A simple and sensitive method for the assay of trans-cinnamic acid 4-hydroxylase by use of tritiated substrate is described. This method is based on the migration of tritium during the enzyme-catalyzed hydroxylation. The hydroxylase activity is detected in microsomes from Phaseohs mungo. The tritiu
A spectrophotometric assay for trans-cinnamic acid 4-hydroxylase activity
โ Scribed by C.J. Lamb; P.H. Rubery
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- English
- Weight
- 417 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0003-2697
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โฆ Synopsis
trans-Cinnamic acid 4-hydroxylase (trans-cinnamic acid, NAD'PH: oxygen oxidoreductase [4-hydroxylating]) can be rapidly and precisely assayed by the spectrophotometric measurement of the production of 4-hydroxy-trans-cinnamic acid at 340 nm after acidification of the reaction mixture and subsequent readjustment to pH 11. For the assay of crude extracts and other preparations with high intrinsic absorption at 340 nm, the assay can be modified by extraction of the 4hydroxy-trans-cinnamic acid from the acidified assay mixture through diethyl ether into alkali before spectrophotometric estimation. trans-Cinnamic acid 2hydroxylase can be routinely detected and assayed in the same extract. 554
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