1975
DOI: 10.1016/s0021-9258(19)41023-5
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Experiments in marine biochemistry. Homarine metabolism in Penaeus duorarum.

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Cited by 12 publications
(2 citation statements)
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“…Homarine and trigonelline are structural isomers made by different biosynthetic pathways that both involve SAM‐dependent methyltransferases (Hall and Gurin, 1975; Ashihara, 2008). The 13 C 1 isotopologue of trigonelline increased in both experiments, with a greater increase in the south than in the north (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…Homarine and trigonelline are structural isomers made by different biosynthetic pathways that both involve SAM‐dependent methyltransferases (Hall and Gurin, 1975; Ashihara, 2008). The 13 C 1 isotopologue of trigonelline increased in both experiments, with a greater increase in the south than in the north (Fig.…”
Section: Resultsmentioning
confidence: 99%
“…Biochemically, the sources and sinks for homarine and trigonelline are likely distinct. Trigonelline is produced from nicotinic acid ( 47 ), while homarine is decarboxylated from quinolinic acid, which is produced from tryptophan ( 48 ), though the exact enzyme that performs the decarboxylation has not been characterized. The first step of bacterial trigonelline degradation is the opening of the aromatic ring by the TgnA/TgnB oxygenase system ( 40 ).…”
Section: Resultsmentioning
confidence: 99%