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1.
J Am Chem Soc ; 135(7): 2509-11, 2013 Feb 20.
Article in English | MEDLINE | ID: mdl-23373756

ABSTRACT

The catalytic effects of perdeuterating the pyridoxal phosphate-dependent enzyme alanine racemase from Geobacillus stearothermophilus are reported. The mass of the heavy perdeuterated form is ~5.5% greater than that of the protiated form, causing kinetic isotope effects (KIEs) of ~1.3 on k(cat) and k(cat)/K(M) for both L- and D-alanine. These values increase when Cα-deuterated alanine is used as the substrate. The heavy-enzyme KIEs of ~3 on k(cat)/K(M) with deuterated substrates are greater than the product of the individual heavy-enzyme and primary substrate KIEs. This breakdown of the rule of the geometric mean is likely due to coupled motion between the protein and the proton-transfer reaction coordinate in the rate-limiting step. These data implicate a direct role for protein vibrational motions in barrier crossing for proton-transfer steps in alanine racemase.


Subject(s)
Alanine Racemase/chemistry , Deuterium , Geobacillus stearothermophilus/enzymology , Protons , Deuterium/chemistry , Kinetics , Molecular Structure
2.
J Mol Biol ; 425(8): 1378-89, 2013 Apr 26.
Article in English | MEDLINE | ID: mdl-23396064

ABSTRACT

Identification of residues responsible for functional specificity in enzymes is a challenging and important problem in protein chemistry. Active-site residues are generally easy to identify, but residues outside the active site are also important to catalysis and their identities and roles are more difficult to determine. We report a method based on analysis of multiple sequence alignments, embodied in our program Janus, for predicting mutations required to interconvert structurally related but functionally distinct enzymes. Conversion of aspartate aminotransferase into tyrosine aminotransferase is demonstrated and compared to previous efforts. Incorporation of 35 predicted mutations resulted in an enzyme with the desired substrate specificity but low catalytic activity. A single round of DNA back-shuffling with wild-type aspartate aminotransferase on this variant generated mutants with tyrosine aminotransferase activities better than those previously realized from rational design or directed evolution. Methods such as this, coupled with computational modeling, may prove invaluable in furthering our understanding of enzyme catalysis and engineering.


Subject(s)
Computational Biology/methods , DNA Mutational Analysis , Escherichia coli/enzymology , Mutation, Missense , Protein Engineering/methods , Amino Acid Sequence , Aspartate Aminotransferases/genetics , Aspartate Aminotransferases/metabolism , Escherichia coli/genetics , Models, Molecular , Molecular Sequence Data , Protein Conformation , Sequence Alignment , Substrate Specificity , Tyrosine Transaminase/genetics , Tyrosine Transaminase/metabolism
3.
J Am Chem Soc ; 132(47): 16953-61, 2010 Dec 01.
Article in English | MEDLINE | ID: mdl-21058708

ABSTRACT

The mechanisms of pyridoxal 5'-phosphate (PLP)-dependent enzymes require substrates to form covalent "external aldimine" intermediates, which absorb light strongly between 410 and 430 nm. Aspartate aminotransferase (AAT) is a prototypical PLP-dependent enzyme that catalyzes the reversible interconversion of aspartate and α-ketoglutarate with oxalacetate and glutamate. From kinetic isotope effects studies, it is known that deprotonation of the aspartate external aldimine C(α)-H bond to give a carbanionic quinonoid intermediate is partially rate limiting in the thermal AAT reaction. We show that excitation of the 430-nm external aldimine absorption band increases the steady-state catalytic activity of AAT, which is attributed to the photoenhancement of C(α)-H deprotonation on the basis of studies with Schiff bases in solution. Blue light (250 mW) illumination gives an observed 2.3-fold rate enhancement for WT AAT activity, a 530-fold enhancement for the inactive K258A mutant, and a 58600-fold enhancement for the PLP-Asp Schiff base in water. These different levels of enhancement correlate with the intrinsic reactivities of the C(α)-H bond in the different environments, with the less reactive Schiff bases exhibiting greater enhancement. Time-resolved spectroscopy, ranging from femtoseconds to minutes, was used to investigate the nature of the photoactivation of C(α)-H bond cleavage in PLP-amino acid Schiff bases both in water and bound to AAT. Unlike the thermal pathway, the photoactivation pathway involves a triplet state with a C(α)-H pK(a) that is estimated to be between 11 and 19 units lower than the ground state for the PLP-Val Schiff base in water.


Subject(s)
Aspartate Aminotransferases/metabolism , Biocatalysis/radiation effects , Light , Pyridoxal Phosphate/metabolism , Aspartate Aminotransferases/chemistry , Aspartate Aminotransferases/genetics , Kinetics , Mutation , Photochemical Processes , Protons , Pyridoxal Phosphate/chemistry , Schiff Bases/chemistry , Solutions , Temperature
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