Artículos de revistas
BIOSYNTHESIS OF A TRYPANOCIDE BY CHROMOBACTERIUM-VIOLACEUM
Registro en:
World Journal Of Microbiology & Biotechnology. Rapid Science Publishers, v. 10, n. 6, n. 686, n. 690, 1994.
0959-3993
WOS:A1994PT15800016
10.1007/BF00327960
Autor
DURAN, N
ANTONIO, RV
HAUN, M
PILLI, RA
Institución
Resumen
Radio-isotope studies indicated not only that L-tryptophan can serve as carbon source for synthesis of the trypanocide, violacein by Chromobacterium violaceum (BB-78 strain) but also that isatin and indole 3-acetic acid are both important metabolic intermediates. Using 3-indolyl [2-C-14] and [1-C-14] acetic acid, it was found that the carboxylic carbon was not eliminated and that indole-3-acetic acid was incorporated intact into the pigment structure. N-Ethyl(5-hydroxy-indol-3-yl)-2-indolylethylamide is also an important metabolic intermediate in the violacein biosynthesis. This is the first report of a metabolic scheme for violacein synthesis which includes an intermediate other than L-tryptophan. 10 6 686 690