5'-Atp → Uridine-Diphosphate-N-Acetylglucosamine

HRID 928866

Reaktionsgleichung

Reaktionsgleichung von HRID 928866
[OH:1][CH:2]1[O:10][C@H:9]([CH2:11][OH:12])[C@@H:7]([OH:8])[C@H:5]([OH:6])[C@H:3]1[NH2:4].P([O:25][CH2:26][C@H:27]1O[C@@H](N2C3N=CN=C(N)C=3N=C2)[C@H](O)[C@@H]1O)(OP(OP(O)(O)=O)(O)=O)(=O)O.[CH:44]1[C:50](=[O:51])[NH:49][C:47](=[O:48])[N:46]([C@@H:52]2[O:56][C@H:55]([CH2:57][O:58][P:59]([O:62][P:63]([O:66]P(O)(O)=O)([OH:65])=O)([OH:61])=[O:60])[C@@H:54]([OH:71])[C@H:53]2[OH:72])[CH:45]=1.C(O)C(N)(CO)CO.Cl.[Mg+2].[Cl-].[Cl-]>O.CO.CCOC(C)=O>[CH3:27][C:26]([NH:4][C@H:3]1[C@@H:2]([O:1][P:63]([O:62][P:59]([O:58][CH2:57][C@H:55]2[O:56][C@@H:52]([N:46]3[C:47](=[O:48])[NH:49][C:50](=[O:51])[CH:44]=[CH:45]3)[C@H:53]([OH:72])[C@@H:54]2[OH:71])([OH:61])=[O:60])([OH:66])=[O:65])[O:10][C@H:9]([CH2:11][OH:12])[C@@H:7]([OH:8])[C@@H:5]1[OH:6])=[O:25]

Komponenten

9

Edukt 5

HCID 59575'-AtpHCID 6133Uridine 5'-triphosphateHCID 93573Tromethamine hydrochlorideHCID 439213D-GlucosamineHCID 5360315Magnesium Chloride

Produkt 1

HCID 445675Uridine-Diphosphate-N-Acetylglucosamine

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 887MethanolLösungsmittelHCID 962WaterLösungsmittel3×HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

One-Pot Three-Enzyme Synthesis of UDP-Sugars T5b-9-T5b-13. This was carried out as shown in FIG. 4. Glucosamine derivatives T5b-1-T5b-5 (50 to 300 mg, 1.0 eq.), ATP (1.2 eq.), and UTP (1.2 eq.) were dissolved in water in a 50 mL centrifuge tube containing Tris-HCl buffer (100 mM, pH 8.0) and MgCl2 (10 mM). After the addition of appropriate amount of NanK_ATCC55813 (3.2-4.8 mg), PmGlmU (5-7.5 mg), and PmPpA (2.5-5 mg), water was added to bring the volume of the reaction mixture to 20 mL. The reaction was carried out by incubating the solution in an isotherm incubator for 24 hr to 48 hr at 37° C. with gentle shaking. Product formation was monitored by TLC (EtOAc:MeOH:H2O=3:2:1 by volume) with p-anisaldehyde sugar staining. The reaction was stopped by adding the same volume of ice-cold ethanol and incubating at 4° C. for 30 min. The mixture was concentrated and passed through a BioGel P-2 gel filtration column to obtain the desired product. Silica gel column purification (EtOAc:MeOH:H2O=4:2:1) was applied when necessary to achieve further purification.

Aufarbeitung

  1. additionwas added
  2. customfor 24 hr to 48 hr
  3. customat 37° C.
  4. additionby adding the same volume of ice-cold ethanol
  5. concentrationThe mixture was concentrated
  6. filtrationpassed through a BioGel P-2 gel filtration column

Quellen und Nachweise

ORD-Eintrag
ord-c34f030f2f9648be9778132d2edf9cd6
Quelldatensatz
uspto-grants-2016_03
Patentnummer
US09290530B2

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