1942
DOI: 10.1515/bchm2.1942.273.4-5.163
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Zur Kenntnis des intermediären Stoffwechsels des Histidins. 5. Mitteilung

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Cited by 13 publications
(7 citation statements)
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“…As in most earlier studies, no urocanic acid was excreted after histidine was fed to dogs or injected in large doses into rabbits (143) or guinea pigs (145). Contrary to the report (146) that uro canic acid is formed as an intermediate by histidase none could be detected upon incubating histidine with liver tissue (143). However, aqueous liver extracts converted urocanic acid to a substance from which one equivalent of ammonia was liberated by strong alkali, but only a trace by sodium carbonate (143).…”
supporting
confidence: 66%
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“…As in most earlier studies, no urocanic acid was excreted after histidine was fed to dogs or injected in large doses into rabbits (143) or guinea pigs (145). Contrary to the report (146) that uro canic acid is formed as an intermediate by histidase none could be detected upon incubating histidine with liver tissue (143). However, aqueous liver extracts converted urocanic acid to a substance from which one equivalent of ammonia was liberated by strong alkali, but only a trace by sodium carbonate (143).…”
supporting
confidence: 66%
“…Contrary to the report (146) that uro canic acid is formed as an intermediate by histidase none could be detected upon incubating histidine with liver tissue (143). However, aqueous liver extracts converted urocanic acid to a substance from which one equivalent of ammonia was liberated by strong alkali, but only a trace by sodium carbonate (143). The responsible enzyme (urocanicase) and histidase were each nearly completely separable from the other.…”
contrasting
confidence: 61%
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