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Chimera of alcohol dehydrogenase by exchange of the cofactor binding domain res 153-295 of C. beijerinckii ADH by T. brockii ADH

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=Chimera Χ22<sub>(CTC)</sub> ([[3fpl]])=
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The NADP<sup>+</sup>-dependent [http://en.wikipedia.org/wiki/Alcohol_dehydrogenase alcohol dehydrogenases] ([http://www.expasy.org/enzyme/1.1.1.2 EC 1.1.1.2]) from the [http://en.wikipedia.org/wiki/Thermophile thermophile] ''Thermoanaerobacter brockii'' (TbADH), the [http://en.wikipedia.org/wiki/Mesophile mesophilic] [http://en.wikipedia.org/wiki/Bacteria bacterium] [http://en.wikipedia.org/wiki/Clostridium_beijerinckii ''Clostridium beijerinckii''] (CbADH), and the [http://en.wikipedia.org/wiki/Protozoa protozoan] [http://en.wikipedia.org/wiki/Parasitism parasite] [http://en.wikipedia.org/wiki/Entamoeba_histolytica ''Entamoeba histolytica''] (EhADH1) are <scene name='3fsr/Cv/3'>homotetrameric</scene> [http://en.wikipedia.org/wiki/Tetrameric_protein] ([http://en.wikipedia.org/wiki/Protein_subunit monomers] are colored in different colors) secondary alcohol dehydrogenases. Each <scene name='3fsr/Cv/4'>monomer</scene> of these alcohol dehydrogenases consists of two domains: the <scene name='3fsr/Cv/5'>cofactor-binding domain</scene> <font color='blueviolet'><b> (residues 154−294 for TbADH)</b></font> and the <scene name='3fsr/Cv/6'>catalytic domain</scene> (<font color='red'><b>residues 1−153 and 295−351 for TbADH</b></font>; contains [http://en.wikipedia.org/wiki/Zinc Zn<sup>2+</sup>] at the [http://en.wikipedia.org/wiki/Active_site active site]) separated by a deep cleft. Although, all these three ADHs revealed a high degree of [http://en.wikipedia.org/wiki/Conserved_sequence sequence conservation] (62-75% identity), them significantly differ in [http://en.wikipedia.org/wiki/Thermostability thermostability]. The [http://en.wikipedia.org/wiki/Cofactor_(biochemistry) cofactor]-binding domains (residues 153−295) of TbADH, CbADH, and EhADH1 were mutually <scene name='3fsr/Cv/7'>exchanged</scene> and 3 corresponding chimeras were constructed.
The NADP<sup>+</sup>-dependent [http://en.wikipedia.org/wiki/Alcohol_dehydrogenase alcohol dehydrogenases] ([http://www.expasy.org/enzyme/1.1.1.2 EC 1.1.1.2]) from the [http://en.wikipedia.org/wiki/Thermophile thermophile] ''Thermoanaerobacter brockii'' (TbADH), the [http://en.wikipedia.org/wiki/Mesophile mesophilic] [http://en.wikipedia.org/wiki/Bacteria bacterium] [http://en.wikipedia.org/wiki/Clostridium_beijerinckii ''Clostridium beijerinckii''] (CbADH), and the [http://en.wikipedia.org/wiki/Protozoa protozoan] [http://en.wikipedia.org/wiki/Parasitism parasite] [http://en.wikipedia.org/wiki/Entamoeba_histolytica ''Entamoeba histolytica''] (EhADH1) are <scene name='3fsr/Cv/3'>homotetrameric</scene> [http://en.wikipedia.org/wiki/Tetrameric_protein] ([http://en.wikipedia.org/wiki/Protein_subunit monomers] are colored in different colors) secondary alcohol dehydrogenases. Each <scene name='3fsr/Cv/4'>monomer</scene> of these alcohol dehydrogenases consists of two domains: the <scene name='3fsr/Cv/5'>cofactor-binding domain</scene> <font color='blueviolet'><b> (residues 154−294 for TbADH)</b></font> and the <scene name='3fsr/Cv/6'>catalytic domain</scene> (<font color='red'><b>residues 1−153 and 295−351 for TbADH</b></font>; contains [http://en.wikipedia.org/wiki/Zinc Zn<sup>2+</sup>] at the [http://en.wikipedia.org/wiki/Active_site active site]) separated by a deep cleft. Although, all these three ADHs revealed a high degree of [http://en.wikipedia.org/wiki/Conserved_sequence sequence conservation] (62-75% identity), them significantly differ in [http://en.wikipedia.org/wiki/Thermostability thermostability]. The [http://en.wikipedia.org/wiki/Cofactor_(biochemistry) cofactor]-binding domains (residues 153−295) of TbADH, CbADH, and EhADH1 were mutually <scene name='3fsr/Cv/7'>exchanged</scene> and 3 corresponding chimeras were constructed.
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The cofactor-binding domain of thermophilic TbADH was replaced with the cofactor-binding domain of its mesophilic counterpart CbADH (chimera Χ21<sub>(TCT)</sub>, [[3fsr]]). This domain replacement significantly destabilized the parent thermophilic enzyme (ΔT<sub>1/2</sub> = −18 °C). But the reverse exchange in CbADH (chimera Χ22<sub>(CTC)</sub>, [[3fpl]]), had little effect on the thermal stability of the parent mesophilic protein. The exchange of the cofactor-binding domain of TbADH with the [http://en.wikipedia.org/wiki/Homology_(biology) homologous] domain of EhADH1 (chimera Χ23<sub>(TET)</sub>, [[3fpc]]) substantially reduced the thermal stability of the thermophilic ADH (ΔT<sub>1/2</sub> = −51 °C) and interfered the oligomerization of the enzyme.
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The cofactor-binding domain of thermophilic TbADH was replaced with the cofactor-binding domain of its mesophilic counterpart CbADH (chimera Χ21<sub>(TCT)</sub>, [[3fsr]]). This domain replacement significantly destabilized the parent thermophilic enzyme (ΔT<sub>1/2</sub> = −18 °C). But the reverse exchange in CbADH (chimera Χ22<sub>(CTC)</sub>, [[3fpl]]), had little effect on the thermal stability of the parent mesophilic protein.
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The double [http://en.wikipedia.org/wiki/Mutation mutant] of the chimera Χ21<sub>(TCT)</sub> (cofactor-binding domain of thermophilic TbADH replaced by that of mesophilic CbADH) Q165E/S254K-X21<sub>(TCT)</sub> ([[3ftn]]) was constructed by [http://en.wikipedia.org/wiki/Site-directed_mutagenesis site-directed mutagenesis]. In both TbADH and CbADH, Lys257 and Asp237 form an intrasubunit ion pair, in TbADH, Asp237 is also involved in an ion pair bridge with Arg304 of the adjacent monomer. In addition, Arg304 forms intersubunit salt bridge with Glu165 of the first monomer. Therefore, a <scene name='3fsr/Al/2'>four-member ion pair network</scene> involving Lys257, Asp237, and Glu165 of one monomer and Arg304 of the adjacent one is present in TbADH (the names of monomers are in brackets). However in mesophilic CbADH (and, therefore, in the chimera Χ21<sub>(TCT)</sub>, [[3fsr]]) the Gln is situated in position 165 (instead Glu of TbADH) and Met in position 304 (instead Arg of TbADH), so, such an ion pair network does not exist. In the double mutant Q165E/S254K-X21<sub>(TCT)</sub> reverse mutation Q165E reconstructs this network (as in parent thermophilic TbADH) that led to significant enhancement of the thermal stability of CbADH (ΔT<sub>1/2</sub><sup>60 min</sup> = 5.4 °C). <font color='magenta'><b>Chimera X21<sub>(TCT)</sub> ([[3fsr]]) is colored magenta</b></font> and <font color='cyan'><b>the double mutant Q165E/S254K-X21<sub>(TCT)</sub> cyan</b></font> ([[3ftn]]). In chimera X21<sub>(TCT)</sub>, position 254 is occupied by Ser (due to sequence of exchanged domain). The replacement of Ser254 of CbADH with Lys significantly enhances the stability of the enzyme, due to the formation of <scene name='3fsr/Al/3'>intrasubunit Lys254 and Glu280 ion pair</scene>. However, this replacing of Ser254 by Lys had a negligible effect on the thermal stability, in contrast to mutation Q165E mentioned above.
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The <scene name='3fsr/Al1/2'>comparison</scene> of overall Cα backbone of all these chimeras (rmsd 0.45-0.65 Å) with those of the parent enzymes, did not reveal significant structural changes. So, the differences in the thermal stability of the chimeras and the parent enzymes could be caused by relatively small specific changes located at the important points of the NADP<sup>+</sup>-dependent alcohol dehydrogenases. For example see Cα superposition for the <font color='red'><b>X23<sub>(TET)</sub> chimera (red)</b></font> ([[3fpc]]) and its parent ADHs (<font color='blue'><b>TbADH, colored blue</b></font> ([[1ped]]), and <font color='lime'><b>EhADH1, colored lime</b></font> ([[1y9a]]). The [http://en.wikipedia.org/wiki/Root_mean_square_deviation RMSDs] of the TbADH−EhADH1, TbADH−Χ23<sub>(TET)</sub>, and EhADH1−Χ23<sub>(TET)</sub> were 0.68, 0.56, and 0.48 Å, respectively.
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Revision as of 10:54, 12 June 2012

PDB ID 3fpl

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Reference

Biochemical and structural properties of chimeras constructed by exchange of cofactor binding domains in alcohol dehydrogenases from thermophilic and mesophilic microorganisms., Goihberg E, Peretz M, Tel-Or S, Dym O, Shimon LJ, Frolow F, Burstein Y.Biochemistry. 2010 Jan 26. Epub ahead of print

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