Growth of Alcaligenes sp. strain O-1 with 2-aminobenzenesulfonate (ABS; orthanilate) as sole source of carbon and energy requires expression of the soluble, multicomponent 2-aminobenzenesulfonate 2,3-dioxygenase system (deaminating) (ABSDOS) which is plasmid-encoded. ABSDOS was separated by anion-exchange chromatography to yield a
Inotropic activity of orthanilic and L-cysteic acid on isolated guinea-pig ventricular strips.
F Franconi et al.
Advances in experimental medicine and biology, 217, 159-165 (1987-01-01)
Journal of combinatorial chemistry, 8(2), 174-183 (2006-03-15)
A unique strategy for synthesis of narrowly distributed and inherently self-stabilized copolymer nanoparticles by a simple emulsifier-free polymerization from orthanilic acid and aniline was developed. The polymerization yield, electrical conductivity, size, and its distribution of the nanoparticles could be simultaneously
The Biochemical journal, 300 ( Pt 2), 429-436 (1994-06-01)
2-Aminobenzenesulphonic acid (2AS) is degraded by Alcaligenes sp. strain O-1 via a previously detected but unidentified intermediate. A mutant of strain O-1 was found to excrete this intermediate, which was isolated and identified by m.s., 1H- and 13C-n.m.r. as 3-sulphocatechol
Alcaligenes sp. strain O-1 grew with benzene sulfonate (BS) as sole carbon source for growth with either NH4+ or NH4+ plus orthanilate (2-aminobenzene sulfonate, OS) as the source(s) of nitrogen. The intracellular desulfonative enzyme did not degrade 3- or 4-aminobenzene
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