词条 | Glycine betaine aldehyde |
释义 |
| Reference = | Name = Glycine betaine aldehyde | ImageFile = Betaine aldehyde.svg | ImageSize = 200px | IUPACName = N,N,N-trimethyl-2-oxoethanaminium | OtherNames = Betaine aldehyde |Section1={{Chembox Identifiers | CASNo = 7418-61-3 | CASNo1 = 7758-31-8 | CASNo1_Comment = (chloride salt) | ChemSpiderID = 244 | InChI = 1/C5H12NO/c1-6(2,3)4-5-7/h5H,4H2,1-3H3/q+1 | InChIKey = SXKNCCSPZDCRFD-UHFFFAOYAL | PubChem = 249 | SMILES = O=CC[N+](C)(C)C | ChEBI = 15710 | KEGG = C00576 }} |Section2={{Chembox Properties | C=5 | H=12 | N=1 | O=1 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}Glycine betaine aldehyde, often simply called betaine aldehyde,[1] is an intermediate in the metabolism of glycine, serine and threonine. The human aldehyde dehydrogenase ({{EC number|1.2.1.3}}) stimulates the transformation of betaine aldehyde to glycine betaine. Betaine aldehyde is a substrate for choline dehydrogenase (mitochondrial).[2] Chemical structureGlycine betaine aldehyde is a short chain aldehyde and quaternary ammonium compound. It can be considered a derivative of the amino acid glycine. Its chemical formula is C5H12NO+. Biological functionGlycine betaine aldehyde is a component of glycine, serine and threonine metabolism. It also serves as an osmolyte. It can be found in cytoplasm and mitochondria within the kidney, neurons, and stratum corneum.[3] References1. ^Betaine aldehyde, Biological Magnetic Resonance Data Bank 2. ^{{cite journal |author=Yilmaz JL, Bülow L. |title= Enhanced stress tolerance in Escherichia coli and Nicotiana tabacum expressing a betaine aldehyde dehydrogenase/choline dehydrogenase fusion protein.|journal=Biotechnol Prog. |volume=18|issue=6 |pages=1176–82|date=December 2002 |pmid=12467448|url= |doi=10.1021/bp020057k}} 3. ^Metabocard for Dimethylglycine, Human Metabolome Database 2 : Aldehydes|Quaternary ammonium compounds |
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