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Merck

G1881

α-Glycerophosphate Dehydrogenase-Triosephosphate Isomerase from rabbit muscle

Type III, ammonium sulfate suspension

Synonym(s):

GDH/TIM, α-GDH-TPI

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About This Item

UNSPSC Code:
12352204
NACRES:
NA.54
EC Number:
MDL number:

Product Name

α-Glycerophosphate Dehydrogenase-Triosephosphate Isomerase from rabbit muscle, Type III, ammonium sulfate suspension

biological source

rabbit muscle

type

Type III

form

ammonium sulfate suspension

GDH activity

75-200 units/mg protein (biuret)

TPI activity

750-2000 units/mg protein

storage temp.

2-8°C

Quality Level

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Application

α-Glycerophosphate Dehydrogenase-Triosephosphate Isomerase from rabbit muscle has been used in spectrophotometric aldolase assay and fructose 2,6 bisphosphate assay. It has also been used in erythrocyte transketolase (ETK) activity to study the prevalence of and factors associated with thiamin deficiency in obese.
α-glycerophosphate dehydrogenase was used in 2-deoxy-ribose 5-phosphate aldolase (DERA) cleavage (retroaldol) assay.

Biochem/physiol Actions

α-Glycerophosphate dehydrogenase (α-GPDH) has the ability to produce reactive oxygen species (ROS), that is induced by Ca2+.
α-glycerophosphate dehydrogenase catalyzes the conversion of dihydroxyacetone to glycerol phosphate. α-Glycerophosphate dehydrogenase (α-GPDH) has the ability to produce reactive oxygen species (ROS), that is induced by Ca2+. Triosephosphate isomerase (TPI) is an essential enzyme in the glycolytic pathway, responsible for converting dihydroxyacetone phosphate (DHAP) into glyceraldehyde-3 phosphate (GAP). TPI′s role is crucial in enhancing the efficiency of the catabolic process within glycolysis. However, a deficiency in TPI can lead to glycolytic enzymopathies, rare genetic disorders characterized by neurologic dysfunction and hemolytic anemia.

General description

Research area: Neuroscience

α-Glycerophosphate Dehydrogenase-Triosephosphate isomerase (α-GDH-TPI or GDH/TIM) is an enzyme mixture of α-glycerophosphate dehydrogenase (GDH) and triosephosphate isomerase (TPI).

Other Notes

(α-GDH) One unit will convert 1.0 μmole of dihydroxyacetone phosphate to α-glycerophosphate per min at pH 7.4 at 25 °C.
(TPI) One unit will convert 1.0 μmole of D-glyceraldehyde 3-phosphate to dihydroxyacetone phosphate per min at pH 7.6 at 25 °C.

Packaging

(Sold on the basis of α-GDH units.)

Physical form

Mixed crystalline suspension in 3.2 M (NH4)2SO4, with 0.05 g/L EDTA, pH 6.0

Storage Class

12 - Non Combustible Liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


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D Roberts et al.
The Biochemical journal, 183(2), 349-360 (1979-11-01)
1. The fluorescent ATP analogue 1,N6-etheno-ATP is a good substrate and an efficient allosteric inhibitor of rabbit skeletal-muscle phosphofructokinase. 2. Fluorescence energy transfer occurs between bound 1,N6-etheno-ATP and phosphofructokinase. 1,N6-Etheno-ATP fluorescence is enhanced, intrinsic protein fluorescence is quenched, and the
Prevalence of and factors associated with thiamin deficiency in obese Thai children
Densupsoontorn N, et al.
Asia Pacific Journal of Clinical Nutrition (2019)
The role of mitochondrial dehydrogenases in the generation of oxidative stress
Adam-Vizi V and Tretter L
Neurochemistry International, 62(5), 757-763 (2013)
Structural and Genetic Studies Demonstrate Neurologic Dysfunction in Triosephosphate Isomerase Deficiency Is Associated with Impaired Synaptic Vesicle Dynamics
Roland BP, et al.
PLoS Genetics, 12(3) (2016)
C R Hussey et al.
European journal of biochemistry, 80(2), 497-506 (1977-11-01)
A preparation of phosphofructokinase from rabbit skeletal muscle is described which exploits the association-dissociation properties of the enzyme. Phosphofructokinase to prepared is partially phosphorylated and may be fractioned into three distinct species with sedimentation coefficients of 30 S, 18 S

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