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G4134

Sigma-Aldrich

Glucose-6-phosphat-Dehydrogenase aus Backhefe (S. cerevisiae)

Type IX, lyophilized powder, 200-400 units/mg protein (modified Warburg-Christian)

Synonym(e):

G-6-P-DH, Zwischenferment

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CHF 118.00
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CHF 410.00
1000 UNITS
CHF 639.00

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100 UNITS
CHF 118.00
250 UNITS
CHF 237.00
500 UNITS
CHF 410.00
1000 UNITS
CHF 639.00

About This Item

CAS-Nummer:
EC-Nummer:
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352204
NACRES:
NA.54

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Typ

Type IX

Qualitätsniveau

Form

lyophilized powder

Spezifische Aktivität

200-400 units/mg protein (modified Warburg-Christian)

Mol-Gew.

128 kDa

β-NADP- und β-NADPH-Gehalt

≤10 mmol/mol

Anwendung(en)

agriculture

Versandbedingung

dry ice

Lagertemp.

−20°C

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Allgemeine Beschreibung

Research area: Cell Signaling

Glucose-6-phosphate dehydrogenase (G6PD) is a key metabolic enzyme of the pentose phosphate pathway. In S. cerevisiae, it is encoded by the ZWF1 gene. G6PD exists as a tetramer in its active form.[1]

Anwendung

Glucose-6-phosphate dehydrogenase is used:
  • To test ketose reductase activity in developing maize endosperm.[2]
  • For recycling microassay of β-NADP and β-NADPH.[3][4]
  • To measure the intracellular levels of NADPH and total NADP.[5]
  • To measure the nicotinamide adenine dinucleotide (NAD) kinase kinetic assay activity.[6]

Biochem./physiol. Wirkung

Glucose-6-Phosphat-Dehydrogenase katalysiert die Umwandlung von Glucose-6-Phosphat in 6-Phosphogluconolaceton und damit den ersten Schritt des Pentose-Phosphat-Wirkungsweges.
Glucose-6-phosphate dehydrogenase catalyzes the rate-limiting step in the pentose phosphate pathway. Its function involves the conversion of glucose-6-phosphate to 6-phosphogluconolacetone while generating NADPH, which is essential for the regeneration of glutathione The glutathione system utilizes nicotinamide adenine dinucleotide phosphate hydrogen (NADPH) to effectively eliminate excess hydrogen peroxide.[7] Glucose-6-phosphate dehydrogenase (G6PD) plays an important role in regulating cell growth and survival. Their levels are higher in cells undergoing normal and neoplastic growth. Increased glucose-6-phosphate dehydrogenase activity plays a pivotal role in preventing reactive oxygen species mediated cell death.[8] Glucose-6-phosphate dehydrogenase is over expressed in several cancers whereas its activity is reduced in hyperglycemia. A deficiency in glucose-6-phosphate dehydrogenase causes hemolysis.[9]

Einheitendefinition

One unit will oxidize 1.0 μmole of D-glucose 6-phosphate to 6-phospho-D-gluconate per min in the presence of NADP at pH 7.4 at 25 °C.

Physikalische Form

Lyophilized powder essentially sulfate-free, containing approx. 20% sodium citrate

Piktogramme

Health hazard

Signalwort

Danger

H-Sätze

Gefahreneinstufungen

Resp. Sens. 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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Die Dokumentenbibliothek aufrufen

The Pentose Phosphate Pathway in Yeasts-More Than a Poor Cousin of Glycolysis
Bertels LK, et al.
Biomolecules, 11(5), 725-725 (2021)
Glucose-6-phosphate dehydrogenase, NADPH, and cell survival
Stanton R C
IUBMB Life, 64(5), 362-369 (2012)
The global prevalence of glucose-6-phosphate dehydrogenase deficiency: A systematic review and meta-analysis
Nkhoma ET and Poole C
Blood Cells, Molecules and Diseases, 42, 267?278-267?278 (2009)
Impact of glucose-6-phosphate dehydrogenase deficiency on the pathophysiology of cardiovascular disease
Hecker PA, et al.
American Journal of Physiology. Heart and Circulatory Physiology, 304(4), H491-H500 (2013)
D Oh et al.
Molecular and cellular biology, 10(4), 1415-1422 (1990-04-01)
The Saccharomyces cerevisiae GAL5 (PGM2) gene was isolated and shown to encode the major isozyme of phosphoglucomutase. Northern (RNA) blot hybridization revealed that the GAL5 transcript level increased three- to fourfold in response to galactose and was severely repressed in

Protokolle

Measure hexokinase activity using a continuous spectrophotometric rate-determination assay at 340 nm, catalyzing D-hexose sugar phosphorylation using ATP.

To measure glucose-6-phosphate dehydrogenase activity, beta-nicotinamide adenine dinucleotide phosphate is used in a spectrophotometric rate determination assay at 340 nm.

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