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The complex metabolism of trimethylamine in humans: endogenous and exogenous sources–CORRIGENDUM

Published online by Cambridge University Press:  23 November 2016

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Abstract

Information

Type
Corrigendum
Copyright
Copyright © Cambridge University Press 2016 
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Figure 2. TMA precursors and synthesis in the human digestive tract. (a) Chemical formulae of TMA, its precursors trimethylamine-N-oxide, choline, phosphatidylcholine, carnitine, betaine, and its degradation products DMA and methylamine. (b) Schematic representation of the origin and fate of human gut TMA, which is synthesised using dietary precursors such as choline, carnitine by gut microbial enzymes. Choline TMA lyase acts upon choline leading to the synthesis of TMA (Ref. 116). TMA is then oxidised to TMAO by either mammalian hepatic FMO3 or by the action of microbial TMM (Ref. 33). TMAO can further be degraded to DMA and formaldehyde by the action of TDM (Ref. 40), whereas TMA is metabolised to methane and ammonia by the action of TMADH (Ref. 39).

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Figure 5.