Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Nitrophenylgalactosides | HCID 96647 | — |
| Edukt | aldehydo-D-Xylose | HCID 644160 | — |
| Edukt | Gaxilose | HCID 3082054 | — |
| Edukt | Mercapto-ethanol | HCID 4713212 | — |
| Edukt | Magnesium Chloride | HCID 5360315 | — |
| Edukt | Monopotassium phosphate dipotassium phosphate | HCID 21889592 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-Nitrophenol | HCID 6947 | — |
Reaktionsschritte
In order to synthesize 4-O-β-D-galactopyranosyl-D-xylose, 5 g of o-nitrophenyl β-D-galactopyranoside (Gal-ONP) and 25 g of D-xylose were dissolved in 330 ml of water buffered to a pH of 7 (0.05 M KH2PO4/K2HPO4, 1 mM MgCl2, 5 mM mercaptoethanol), 2 mg (640 u) of E. coli β-galactosidase enzyme were added and the solution thus obtained was subjected to incubation at 37° C. in an orbital stirrer until the Gal-ONP was practically consumed (approximately 2 hours). Following the methodology put forth in example 3, the reaction was stopped by heating at 100° C. for 10 minutes and the ortho-nitrophenol formed was extracted with ethyl acetate. The aqueous solution was concentrated up to an approximate volume of 50 ml, filtered through glass wool and passed through the active carbon/celite column.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07537909B2 |
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| Quelldatensatz | uspto-grants-2009_05 |
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| ORD ID | ord-7dc500de84b94e2e965eac6679d7d64a |
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| Quellennotiz | uspto-grants-2009_05 |
|---|