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[[Apiose 1-reductase]] uses [[D-apiitol]] and [[nicotinamide adenine dinucleotide|NAD<sup>+</sup>]] to produce D-apiose, [[nicotinamide adenine dinucleotide|NADH]], and [[hydrogen ion|H<sup>+</sup>]]. |
[[Apiose 1-reductase]] uses [[D-apiitol]] and [[nicotinamide adenine dinucleotide|NAD<sup>+</sup>]] to produce D-apiose, [[nicotinamide adenine dinucleotide|NADH]], and [[hydrogen ion|H<sup>+</sup>]]. |
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[[Flavone apiosyltransferase]] uses [[UDP-apiose]] and [[5,7,4'-trihydroxyflavone 7-O-beta-D-glucoside]] to produce [[uridine diphosphate|UDP]], [[5,7,4'-trihydroxyflavone]] (apigenin), and |
[[Flavone apiosyltransferase]] uses [[UDP-apiose]] and [[5,7,4'-trihydroxyflavone 7-O-beta-D-glucoside]] to produce [[uridine diphosphate|UDP]], [[5,7,4'-trihydroxyflavone]] (apigenin), and 7-O-[beta-D-apiosyl-(1->2)-beta-D-glucoside. |
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==External links== |
==External links== |
Revision as of 03:25, 27 March 2012
Names | |
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IUPAC name
2,3,4-trihydroxy-3-(hydroxymethyl)butanal
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Other names
D-apiose
3-C-(hydroxymethyl)-D-glycerotetrose apio-β-D-furanosyl | |
Identifiers | |
3D model (JSmol)
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ChemSpider | |
PubChem CID
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Properties | |
C5H10O5 | |
Molar mass | 150.13 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Apiose is a branched-chain sugar found as residues in galacturonans-type pectins; that occurs in parsley and many other plants.
Apiose 1-reductase uses D-apiitol and NAD+ to produce D-apiose, NADH, and H+.
Flavone apiosyltransferase uses UDP-apiose and 5,7,4'-trihydroxyflavone 7-O-beta-D-glucoside to produce UDP, 5,7,4'-trihydroxyflavone (apigenin), and 7-O-[beta-D-apiosyl-(1->2)-beta-D-glucoside.
External links