Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2075748Erstellt: 26. Oktober 2026

DL-Arabinose → L-arabinono-1,4-lactone

https://huagongshe.com/reaction/2075748

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDL-ArabinoseHCID 854—
Eduktaldehydo-D-XyloseHCID 644160—
Eduktaldehydo-L-arabinoseHCID 5460291—
EduktD-xylonic acidHCID 6602431—
ProduktL-arabinono-1,4-lactoneHCID 191190—
ProduktL-Arabonic acidHCID 6602426—

Reaktionsschritte

Microbial synthesis begins with pentose oxidation using fermentor-controlled cultures (e.g., 1 L scale) of Pseudomonas fragi ATCC4973. (Buchert, J.; Viikari, L.; Linko, M.; Markkanen, P. Biotechnol. Lett. 1986, 8, 541. and Weimberg, R. J. Bio. Chem. 1961, 236, 629). D-xylose (100 g/L) is oxidized at 30° C. to D-xylonic acid and produces a 70% yield (77 g/L). L-arabinose is similarly oxidized and produces a 54% overall yield to a mixture of L-arabino-1,4-lactone (40 g/L) and L-arabinonic acid (15 g/L). The lactone is subsequently hydrolyzed to L-arabinonic acid. Escherichia coli constructs are then employed for the conversion of D-xylonic acid and L-arabinonic acid into the respective enantiomers of 1,2,4-butanetriol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07923226B2
Quelldatensatzuspto-grants-2011_04
ORD IDord-c72ab3d60a2141c6bbdf6803ff5d9f8a
Quellennotizuspto-grants-2011_04