1.1.1.119: glucose 1-dehydrogenase (NADP+)
This is an abbreviated version!
For detailed information about glucose 1-dehydrogenase (NADP+), go to the full flat file.
Word Map on EC 1.1.1.119
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1.1.1.119
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photorespiration
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megaterium
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synthesis
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photorespiratory
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2-ketogluconate
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biocatalysis
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analysis
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industry
- 1.1.1.119
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photorespiration
- megaterium
- synthesis
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photorespiratory
- 2-ketogluconate
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biocatalysis
- analysis
- industry
Reaction
Synonyms
beta-D-glucose: NAD(P) 1-oxidoreductase, dehydrogenase, glucose (nicotinamide adenine dinucleotide phosphate), GDH, GlcDH, GlcDH 2, glucose dehydrogenase, glucose-1-dehydrogenase, glucose-1-DH, halophilic glucose dehydrogenase, Hm GDH, NAD(P)+ glucose dehydrogenase, NAD(P)-dependent GDH, NADP-dependent glucose dehydrogenase, NADP-glucose-1-dehydrogenase, NADP-linked aldohexose dehydrogenase, nicotinamide adenine dinucleotide (phosphate)-dependent glucose-1-dehydrogenase, nicotinamide adenine dinucleotide phosphate-linked aldohexose dehydrogenase, STK_17040
ECTree
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Application
Application on EC 1.1.1.119 - glucose 1-dehydrogenase (NADP+)
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analysis
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method for determination of D-glucose- and D-galactose levels in glycoconjugates. The NAD(P)H produced from the enzymatic oxidation of the monosaccharides reacts with a CuSO4-bathocuproinedisulfonic acid reagent to produce a color complex absorbing maximally at 486 nm. With galactose dehydrogenase and glucose dehydrogenase serving as the model enzymes, reaction analysis gives a linear plot from 2.5 to 250 nmol of sugar. Method has been applicated to sugar released by acid hydrolysis from lactose, porcine submaxillary mucin and raffinose was quantified
industry
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Optimizing whole-cell biocatalysts by integrating a recombinant intracellular NADPH regeneration system through co-expression of a glucose facilitator from Zymomonas mobilis for uptake of unphosphorylated glucose and a NADP+-dependent glucose dehydrogenase from Bacillus megaterium that oxidizes glucose to gluconolactone.
synthesis
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use of enzyme in enzyme-catalyzed synthesis system for poly(3-hydroxybutyrate), enzyme catalyzes regeneration of NADPH, system yields 5.6 mg of poly(3-hydroxybutyrate), in a 5 ml-reaction mixture
synthesis
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Escherichia coli strain expressing both recombinant glucose 1-dehydrogenase and a glucose facilitator for uptake of unphosphorylated glucose shows a nine times higher initial alpha-pinene oxide formation rate corresponding to a sixfold higher yield of 20 mg per g cell dry weight after 1.5 h and to a sevenfold increased alpha-pinene oxide yield in the presence of glucose compared to glucose-free conditions
synthesis
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glucose dehydrogenase is generally used to regenerate the expensive cofactor NADPH by oxidation of D-glucose to gluconolactone