The tyrosinase-tyrosine reaction
- 1 January 1930
- journal article
- research article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 24 (2) , 239-249
- https://doi.org/10.1042/bj0240239
Abstract
Tyramine and 34-dihydroxyphenylethylamine yielded 5:6-dihy-droxyindole; 3:4-dihydroxyphenylethylamine yielded 5: 6-dihydroxy-N-methylindole; and N-methyltyrosine also yielded a pressor substance with tyrosinase. Silver oxide oxidized 3:4-dihydroxyphenylalanine and 3:4-dihydroxyphenylethylmethylamine to 5:6-dihydroxyin-dole-2-carboxylic acid and 5:6-dihydroxy-N-methylindole respectively. Tyrosinase gave the same results as silver oxide. Results of a study of the O uptake in the production of melanin are given.This publication has 3 references indexed in Scilit:
- The Action of Tyrosinase on PhenolsBiochemical Journal, 1927
- The Tyrosinase-tyrosine ReactionBiochemical Journal, 1927
- The Tyrosinase-Tyrosine ReactionBiochemical Journal, 1926