The guanine nucleotide exchange factor EF-1 beta gene from the thermoacidophilic archaeon Sulfolobus solfataricus (SsEF-1 beta) was amplified by PCR and cloned into the pT7-7 expression vector, One of four selected clones harbored the T160C nucleotide substitution leading to the Y54H amino acid change in a hydrophobic region of SsEF-1 beta, caused by a nucleotide misincorporation of the Tag DNA polymerase during PCR. The resulting plasmids were used to transform the Escherichia coli BL21(DE3)pLysE strain. Upon induction with isopropyl beta-D-thiogalactopyranoside about 1.4 mg of the recombinant SsEF-1 beta (recSsEF-1 beta) and Y54HSsEF-1 beta were obtained from 1 liter of cell culture, recSsEF-1 beta and Y54HSsEF-1 beta were both able to catalyze the GDP/GTP exchange on SsEF-1 alpha as observed with the wild-type SsEF-1 beta, In addition, the heat inactivation profiles of recSsEF-1 beta and Y54HSsEF-1 beta were identical, being both half inactivated after 30 min treatment at 105 degrees C. These results suggest that Tyr 54 is not essential for the nucleotide exchange activity and is not involved in the thermostability of SsEF-1 beta.

Expression in Escherichia coli of the elongation factor 1 beta gene and its nucleotide T160C mutant from the archaeon Sulfolobus solfataricus

MASULLO, Mariorosario;
1998-01-01

Abstract

The guanine nucleotide exchange factor EF-1 beta gene from the thermoacidophilic archaeon Sulfolobus solfataricus (SsEF-1 beta) was amplified by PCR and cloned into the pT7-7 expression vector, One of four selected clones harbored the T160C nucleotide substitution leading to the Y54H amino acid change in a hydrophobic region of SsEF-1 beta, caused by a nucleotide misincorporation of the Tag DNA polymerase during PCR. The resulting plasmids were used to transform the Escherichia coli BL21(DE3)pLysE strain. Upon induction with isopropyl beta-D-thiogalactopyranoside about 1.4 mg of the recombinant SsEF-1 beta (recSsEF-1 beta) and Y54HSsEF-1 beta were obtained from 1 liter of cell culture, recSsEF-1 beta and Y54HSsEF-1 beta were both able to catalyze the GDP/GTP exchange on SsEF-1 alpha as observed with the wild-type SsEF-1 beta, In addition, the heat inactivation profiles of recSsEF-1 beta and Y54HSsEF-1 beta were identical, being both half inactivated after 30 min treatment at 105 degrees C. These results suggest that Tyr 54 is not essential for the nucleotide exchange activity and is not involved in the thermostability of SsEF-1 beta.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11367/21854
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