Reference : Directed evolution on the cold adapted properties of TAB5 alkaline phosphatase
Scientific journals : Article
Life sciences : Biochemistry, biophysics & molecular biology
http://hdl.handle.net/2268/16631
Directed evolution on the cold adapted properties of TAB5 alkaline phosphatase
English
Koutsioulis, D. [> > > >]
Wang, E. [> > > >]
Tzanodaskalaki, M. [> > > >]
Nikiforaki, D. [> > > >]
Deli, A. [> > > >]
Feller, Georges mailto [Université de Liège - ULg > Département des sciences de la vie > Labo de biochimie >]
Heikinheimo, P. [> > > >]
Bouriotis, V. [> > > >]
2008
Protein Engineering, Design & Selection
Oxford University Press
21
5
319-27
Yes (verified by ORBi)
International
1741-0126
1741-0134
[en] Alkaline Phosphatase/*chemistry/genetics ; Binding Sites ; Calorimetry, Differential Scanning ; Dimerization ; Directed Molecular Evolution ; Kinetics ; Mutagenesis, Site-Directed ; Mutation ; Protein Conformation ; Protein Denaturation ; Protein Engineering/*methods ; Protein Folding ; Recombination, Genetic ; Temperature ; Thermodynamics
[en] Psychrophilic alkaline phosphatase (AP) from the Antarctic strain TAB5 was subjected to directed evolution in order to identify the key residues steering the enzyme's cold-adapted activity and stability. A round of random mutagenesis and further recombination yielded three thermostable and six thermolabile variants of the TAB5 AP. All of the isolated variants were characterised by their residual activity after heat treatment, Michaelis-Menten kinetics, activation energy and microcalorimetric parameters of unfolding. In addition, they were modelled into the structure of the TAB5 AP. Mutations which affected the cold-adapted properties of the enzyme were all located close to the active site. The destabilised variants H135E and H135E/G149D had 2- and 3-fold higher kcat, respectively, than the wild-type enzyme. Wild-type AP has a complex heat-induced unfolding pattern while the mutated enzymes loose local unfolding transitions and have large shifts of the Tm values. Comparison of the wild-type and mutated TAB5 APs demonstrates that there is a delicate balance between the enzyme activity and stability and that it is possible to improve the activity and thermostability simultaneously as demonstrated in the case of the H135E/G149D variant compared to H135E.
http://hdl.handle.net/2268/16631
2008/04/16

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