Trimethylamine oxide
Trimethylamine oxide has a thermo-protective role in dogfish RBCs. It can stimulate both the anaerobic growth rate and the growth yield of Proteus NTHC 153 by serving as a terminal electron acceptor in an oxidative phosphorylation process.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to
24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
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The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Food Chem. 2013 Dec 15;141(4):3881-8.
ESR studies on the thermal decomposition of trimethylamine oxide to formaldehyde and dimethylamine in jumbo squid (Dosidicus gigas) extract.[Pubmed:
23993561]
METHODS AND RESULTS:
The effects of ferrous iron, heating temperature and different additives on the decomposition of Trimethylamine oxide (TMAO) to formaldehyde (FA) and dimethylamine (DMA) and generation of free radicals in jumbo squid (Dosidicus gigas) extract during heating were evaluated by electron spin resonance (ESR). The thermal decomposition of Trimethylamine oxide to TMA, DMA and FA and free radical signals was observed in squid extract, whereas no DMA, FA and free radical signals were detected in cod extract or in aqueous Trimethylamine oxide solution in vitro at high temperatures. Significant increase in levels of DMA, FA and radicals intensity were observed in squid extract and Trimethylamine oxide solution in the presence of ferrous iron with increasing temperature. Hydrogen peroxide stimulated the production of DMA, FA and ESR signals in squid extract, while citric acid, trisodium citrate, calcium chloride, tea polyphenols and resveratrol had the opposite effect.
CONCLUSIONS:
Similar ESR spectra of six peaks regarded as amminium radical were detected in the squid extract and Trimethylamine oxide-iron(II) solution, suggesting that the amminium radical was involved in the decomposition of Trimethylamine oxide.
Physiol Biochem Zool. 2014 Sep-Oct;87(5):652-62.
Coordination of chemical (trimethylamine oxide) and molecular (heat shock protein 70) chaperone responses to heat stress in elasmobranch red blood cells.[Pubmed:
25244377]
METHODS AND RESULTS:
Using the dogfish (Squalus acanthias) red blood cell (RBC) as a model, we examined whether elasmobranch cells with naturally high concentrations of the chemical chaperone Trimethylamine oxide (TMAO) would induce the molecular chaperone heat shock protein 70 (HSP70) when exposed to an acute thermal stress.
Our hypothesis was that Trimethylamine oxide is itself capable of preventing damage and preserving cellular function during thermal stress and thus that the heat shock response would be inhibited/diminished. We incubated RBCs in vitro with and without physiologically relevant concentrations of Trimethylamine oxide at 13°C and then exposed cells to a 1-h acute heat shock at 24°C. HSP70 protein expression was elevated in dogfish RBCs after the acute heat stress, but this induction was inhibited by extracellular Trimethylamine oxide. Regardless of the presence of Trimethylamine oxide and/or HSP70, we did not observe any cell damage, as indicated by changes in caspase 3/7 activity, protein carbonyls, membrane viability, or levels of ubiquitin. We also saw no change in RBC cell function, as determined by hemoglobin oxygen affinity or carrying capacity, in cells lacking the heat shock response but protected by Trimethylamine oxide.
CONCLUSIONS:
This study demonstrates that there is cellular coordination between chemical and molecular chaperones in response to an acute thermal stress in dogfish RBCs and suggests that Trimethylamine oxide has a thermoprotective role in these cells, thus eliminating the need for a heat shock response.
J Gen Microbiol. 1979 Jun;112(2):315-20.
Trimethylamine oxide: a terminal electron acceptor in anaerobic respiration of bacteria.[Pubmed:
479836 ]
METHODS AND RESULTS:
Trimethylamine oxide (TMAO) stimulated both the anaerobic growth rate and the growth yield of Proteus NTHC 153. The molar growth yield from glucose and pyruvate in tryptone/yeast extract medium doubled in the presence of TMAO, and the organism grew anaerobically on the non-fermentable substrates L-lactate and formate when TMAO was added to the medium.
CONCLUSIONS:
We conclude that TMAO stimulated growth by serving as a terminal electron acceptor in an oxidative phosphorylation process.
Journal of Agricultural & Food Chemistry,1998 ,46 (12):5232-7.
Analysis of volatile compounds formed from fish oil heated with cysteine and trimethylamine oxide.[Reference:
WebLink]
METHODS AND RESULTS:
Volatile compounds formed in the headspace of menhaden fish oil heated with cysteine or cysteine and Trimethylamine oxide (TMAO) were analyzed by gas chromatography and gas chromatography/mass spectrometry. Among >150 gas chromatographic peaks, 105 compounds were positively identified. Among the 45 compounds identified in the headspace of heated fish oil without TMAO or cysteine, the major compounds identified were aldehydes. When fish oil was heated with cysteine, the number of volatiles formed increased (77 compounds identified), and the addition of TMAO further increased the number of volatiles formed (87 compounds identified). The major compounds identified were 26 heterocyclic compounds: 8 furans, 8 pyridines, 1 pyrrole, 4 thiazoles, 3 thiazolines, and 2 thiophenes.
CONCLUSIONS:
TMAO acted as a promoter of the oxidative degradation of fish oil and cysteine rather than as a reactant for the nitrogen sources. The heterocyclic compounds identified are believed to contribute to the flavor of cooked fish.