An expeimental protocol is described for a biochemistry laboratory on enzyme kinetics using glucose oxidase coupled to a horseradish peroxidase/colored dye system to yield an easily visualized and quantitated product. The experiment is designed to illustrate the concepts of specific activity, substrate specificity and kinetic parameters. Optional extensions of the protocol could explore parameters of coupled enzyme systems, reversible inhibition and enzyme immobilization
Kinetic enzymatic methods for analysis of substrates can be made optimum for a sensitive photometric...
Cytochrome C Nitrate Reductase is an anerobic enzyme that shows promise for study to generate raw ma...
A custom capillary electrophoresis system with post-column chemiluminescence detection (CE-CL) was u...
In order to determine the kinetic parameters of glucose oxidation catalysed by the enzyme glucose ox...
The kinetic behavior of a system of multiple enzymes in solution was studied in a variable volume ba...
In order to determine the kinetic parameters of glucose oxidation catalysed by the enzyme glucose ox...
This paper describes two complementary bioanalytical experiments for analyzing the concentration of ...
ABSTRACT: The intracellular environment in which bio-logical reactions occur is crowded with macromo...
The peroxidase-NADH system is one of the few biochemical examples among known in vitro chemical osci...
Enzymes are ubiquitous in the fields of biology and microbiology, catalyzing critical reactions and ...
1. A theory is developed to account for the kinetics of coupled-enzyme reactions without assuming th...
AbstractThe kinetics of the glucose oxidase-catalyzed reaction of glucose with O2, which produces gl...
Most biochemical transformations involve more than one substrate. Bisubstrate enzymes catalyze multi...
Abstract The purpose of our project is to indirectly monitor the enzymatic activity of glucose oxida...
The roles of chemical kinetics and mass transfer in three types of bioreactors (packed-column reacto...
Kinetic enzymatic methods for analysis of substrates can be made optimum for a sensitive photometric...
Cytochrome C Nitrate Reductase is an anerobic enzyme that shows promise for study to generate raw ma...
A custom capillary electrophoresis system with post-column chemiluminescence detection (CE-CL) was u...
In order to determine the kinetic parameters of glucose oxidation catalysed by the enzyme glucose ox...
The kinetic behavior of a system of multiple enzymes in solution was studied in a variable volume ba...
In order to determine the kinetic parameters of glucose oxidation catalysed by the enzyme glucose ox...
This paper describes two complementary bioanalytical experiments for analyzing the concentration of ...
ABSTRACT: The intracellular environment in which bio-logical reactions occur is crowded with macromo...
The peroxidase-NADH system is one of the few biochemical examples among known in vitro chemical osci...
Enzymes are ubiquitous in the fields of biology and microbiology, catalyzing critical reactions and ...
1. A theory is developed to account for the kinetics of coupled-enzyme reactions without assuming th...
AbstractThe kinetics of the glucose oxidase-catalyzed reaction of glucose with O2, which produces gl...
Most biochemical transformations involve more than one substrate. Bisubstrate enzymes catalyze multi...
Abstract The purpose of our project is to indirectly monitor the enzymatic activity of glucose oxida...
The roles of chemical kinetics and mass transfer in three types of bioreactors (packed-column reacto...
Kinetic enzymatic methods for analysis of substrates can be made optimum for a sensitive photometric...
Cytochrome C Nitrate Reductase is an anerobic enzyme that shows promise for study to generate raw ma...
A custom capillary electrophoresis system with post-column chemiluminescence detection (CE-CL) was u...