Reaktion #2045072

ord-24980521f3fa45ffb64028fdc96878d1

Reaktionsgleichung

O=C[C@H](O)[C@@H](O)[C@H](O)CO
xylose
O=Cc1ccco1
furfural
O=C[C@H](O)[C@@H](O)[C@H](O)CO
xylose
O=Cc1ccco1
furfural
O=Cc1ccco1
furfural
→
OC[C@@H](O)[C@H](O)[C@@H](O)CO
xylitol

Edukte

O=C[C@H](O)[C@@H](O)[C@H](O)CO
xylose
O=Cc1ccco1
furfural
O=C[C@H](O)[C@@H](O)[C@H](O)CO
xylose
O=Cc1ccco1
furfural
O=Cc1ccco1
furfural

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

In addition, the strain of the present invention has high tolerance to the toxic inhibitor furfural, which is often existed in the pretreated lignocellulosic hydrolysate. The fermentation experiments with a synthetic xylose solution supplemented with furfural show that the strain can grow in the xylose solution containing 3 g/L of furfural and produce xylitol, and the yield is very similar to that of the xylose fermentation without furfural.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08409835B2uspto-grants-2013_04