Glucose Binding Isotope Effects in the Ternary Complex of Brain Hexokinase Demonstrate Partial Relief of Ground-State Destabilization

2003 ◽  
Vol 125 (16) ◽  
pp. 4672-4673 ◽  
Author(s):  
Brett E. Lewis ◽  
Vern L. Schramm

1986 ◽  
Vol 64 (6) ◽  
pp. 1206-1214 ◽  
Author(s):  
Helen Alma Joly ◽  
Kenneth Charles Westaway

Secondary α and β hydrogen–deuterium kinetic isotope effects have been used together to show that the SN reaction between 1-phenylethyldimethylphenylammonium ion and bromide or iodide ion in chloroform occurs by way of an SN2 mechanism within a triple ion in spite of the fact that it reacts faster than the primary substrate, benzyldimethylphenylammonium bromide. The very loose transition state and steric effects in the ground state appear to be responsible for the unusually fast SN2 reactions between 1-phenylethyldimethylphenylammonium ion and halide ions in chloroform.



2005 ◽  
Vol 103 (13) ◽  
pp. 1757-1763 ◽  
Author(s):  
J. Zhou ◽  
B. Zhang ◽  
J. J. Lin ◽  
K. Liu
Keyword(s):  


2000 ◽  
Vol 104 (7) ◽  
pp. 1524-1531 ◽  
Author(s):  
Meredith Porembski ◽  
James C. Weisshaar


1986 ◽  
Vol 233 (2) ◽  
pp. 347-350 ◽  
Author(s):  
G Pettersson

Model studies are presented which demonstrate that reactions proceeding by a random ternary-complex mechanism may exhibit most pronounced deviations from Michaelis-Menten kinetics even if the reaction is effectively ordered with respect to net reaction flow. In particular, the kinetic properties and reaction flow characteristics of glucokinase can be accounted for in such terms. It is concluded that insufficient evidence has been presented to support the idea that glucokinase operates by a ‘mnemonical’ type of mechanism involving glucose binding to distinct conformational states of free enzyme. The sigmoidal rate behaviour of glucokinase can presently be more simply explained in terms of glucose binding to differently ligated states of the enzyme.



1979 ◽  
Vol 10 (1) ◽  
Author(s):  
H. KWART ◽  
D. A. BENKO ◽  
J. STREITH ◽  
J. L. SCHUPPISER


1999 ◽  
Vol 54 (3-4) ◽  
pp. 191-194 ◽  
Author(s):  
B. Pranszke ◽  
P. Kierzkowski ◽  
A. Kowalski

Chemiluminescent reactions of calcium atoms in the metastable 3Pj and 1D2 states with CH3I and CD3I were studied in a beam-gas arrangement. Calcium monoiodide spectra associated with transitions from the electronic A 2Π, B 2Σ+ and C 2Π states to the X 2Σ+ ground state were recorded. Total collision and chemiluminescence cross sections were measured. It was found that isotopic substitution in the methyl group does not change the reaction cross sections and the chemiluminescence spectra.



1978 ◽  
Vol 100 (20) ◽  
pp. 6502-6504 ◽  
Author(s):  
H. Kwart ◽  
D. A. Benko ◽  
J. Streith ◽  
J. L. Schuppiser


Sign in / Sign up

Export Citation Format

Share Document