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- W4240765805 abstract "This chapter discusses the determination of transaldolase. Glyceraldehyde 3-phosphate produced in the reaction is converted to dihydroxyacetone phosphate by triosephosphate isomerase. This product is measured with reduced diphosphopyridine nucleotide (DPNH) and α-glycerophosphate dehydrogenase. Under appropriate conditions the rate of oxidation of DPNH is proportional to the quantity of transaldolase present. The reaction is measured spectrophotometrically by the change in absorbanee at 340mμ. One unit is defined as the quantity of enzyme necessary to cleave 1 micromole of fructose 6-phosphate per minute under the conditions of the assay. Specific activity is expressed as units per milligram of protein. Determine protein by the turbidimetrie method of Bücher. The purified proteins are homogeneous by sedimentation velocity analysis. The molecular weights, estimated from sedimentation equilibrium experiments, are 76,100 for type 1 and 65,900 for type 3. Both enzyme types are stable in the neutral pH range between 0° and 25°." @default.
- W4240765805 created "2022-05-12" @default.
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- W4240765805 date "1966-01-01" @default.
- W4240765805 modified "2023-09-26" @default.
- W4240765805 title "[88] Transaldolase" @default.
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- W4240765805 doi "https://doi.org/10.1016/0076-6879(66)09100-6" @default.
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