Literature DB >> 4722033

Shapes of curves of pH-dependence of reactions.

H B Dixon.   

Abstract

A simple case is considered in which the rate of a two-step reaction depends on pH because the intermediate formed in the first step has to gain (or lose) a proton before it can react in the second step, and in which the rate-determining step therefore changes with pH. The curves of reaction rate against pH are shown to be symmetrical, and the sharpest peak possible has a width at half its height of 1.53pH units, i.e. of 2log(3+2 radical2). Any particular curve for this situation proves to be identical with a curve that could be generated for the pH-dependence of a single-step reaction in which the rate is proportional to the concentration of a particular ionic form of a reactant. Curves for the latter situation, however, can have forms impossible for the former case in which the rate-determining step changes, but only if the protonations that activate and deactivate the reactant are co-operative. The peak can then become even sharper, and its width at half its height can fall to 1.14pH units, i.e. to 2log(2+ radical3).

Mesh:

Year:  1973        PMID: 4722033      PMCID: PMC1177448          DOI: 10.1042/bj1310149

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  3 in total

1.  On the interpretation of the pH variation of the maximum initial velocity of an enzyme-catalyzed reaction.

Authors:  R A ALBERTY; V MASSEY
Journal:  Biochim Biophys Acta       Date:  1954-03

2.  A Note on the Kinetics of Enzyme Action.

Authors:  G E Briggs; J B Haldane
Journal:  Biochem J       Date:  1925       Impact factor: 3.857

3.  PK of the lysine amino group at the active site of acetoacetate decarboxylase.

Authors:  D E Schmidt; F H Westheimer
Journal:  Biochemistry       Date:  1971-03-30       Impact factor: 3.162

  3 in total
  18 in total

1.  Biochemical and X-ray crystallographic studies on shikimate kinase: the important structural role of the P-loop lysine.

Authors:  T Krell; J Maclean; D J Boam; A Cooper; M Resmini; K Brocklehurst; S M Kelly; N C Price; A J Lapthorn; J R Coggins
Journal:  Protein Sci       Date:  2001-06       Impact factor: 6.725

2.  PH-dependence of the steady-state rate of a two-step enzymic reaction.

Authors:  K Brocklehurst; H B Dixon
Journal:  Biochem J       Date:  1976-04-01       Impact factor: 3.857

3.  Changes in the kinetic behaviour of threonine transport into Trypanosoma brucei elicited by variation in hydrogen ion concentration.

Authors:  H P Voorheis
Journal:  Biochem J       Date:  1977-04-15       Impact factor: 3.857

4.  Factorization of the Michaelis functions.

Authors:  H B Dixon
Journal:  Biochem J       Date:  1975-11       Impact factor: 3.857

5.  pH-activity curves for enzyme-catalysed reactions in which the hydron is a product or reactant.

Authors:  H B Dixon; K Brocklehurst; K F Tipton
Journal:  Biochem J       Date:  1987-12-01       Impact factor: 3.857

6.  Derivation of molecular pK values from pH-dependences.

Authors:  H B Dixon
Journal:  Biochem J       Date:  1979-01-01       Impact factor: 3.857

7.  Estimation of the dissociation constants of enzyme-substrate complexes from steady-state measurements. Interpretation of pH-independence of Km.

Authors:  A Cornish-Bowden
Journal:  Biochem J       Date:  1976-02-01       Impact factor: 3.857

8.  Characterization of the papain active centre by using two-protonic-state electrophiles as reactivity probes. Evidence for nucleophilic reactivity in the un-interrupted cysteine-25-histidine-159 interactive system.

Authors:  M Shipton; K Brochlehurst
Journal:  Biochem J       Date:  1978-05-01       Impact factor: 3.857

9.  Mechanism of the reaction of papain with substrate-derived diazomethyl ketones. Implications for the difference in site specificity of halomethyl ketones for serine proteinases and cysteine proteinases and for stereoelectronic requirements in the papain catalytic mechanism.

Authors:  K Brocklehurst; J P Malthouse
Journal:  Biochem J       Date:  1978-11-01       Impact factor: 3.857

10.  Proton transfer in the mechanism of polyadenylate polymerase.

Authors:  Paul B Balbo; Andrew Bohm
Journal:  Biochem J       Date:  2009-05-13       Impact factor: 3.857

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