Wolfenden_2011_J.Am.Chem.Soc_133_13821

Reference

Title : The neutral hydrolysis of simple carboxylic esters in water and the rate enhancements produced by acetylcholinesterase and other carboxylic acid esterases - Wolfenden_2011_J.Am.Chem.Soc_133_13821
Author(s) : Wolfenden R , Yuan Y
Ref : Journal of the American Chemical Society , 133 :13821 , 2011
Abstract :

Experiments at elevated temperatures permit the determination of rate constant and thermodynamic activation parameters for the neutral hydrolysis of the neurotransmitter acetylcholine in water. At 25 degrees C, the extrapolated rate constant for the uncatalyzed (or neutral) hydrolysis of acetylcholine is 3.9 x 10(-7) s(-1) at 25 degrees C (DeltaH(double dagger) = 20.0 kcal/mol; TDeltaS(double dagger) = -6.1 kcal/mol). Acetylcholine is more susceptible to neutral and base-catalyzed hydrolysis than ethyl acetate but less susceptible to acid-catalyzed hydrolysis. For acetylcholinesterase from the electric eel, the catalytic proficiency [(k(cat)/K(m))/k(neutral)] is 2 x 10(16) M(-1), comparable in magnitude with the catalytic proficiencies of aminohydrolases that act on peptides and nucleosides.

PubMedSearch : Wolfenden_2011_J.Am.Chem.Soc_133_13821
PubMedID: 21793525

Related information

Citations formats

Wolfenden R, Yuan Y (2011)
The neutral hydrolysis of simple carboxylic esters in water and the rate enhancements produced by acetylcholinesterase and other carboxylic acid esterases
Journal of the American Chemical Society 133 :13821

Wolfenden R, Yuan Y (2011)
Journal of the American Chemical Society 133 :13821