An aldolase gene has been cloned from Methanococcus jannaschii. The coding region of the gene has been expressed in E. coli using a pET system to a level of 30% of total cellular proteins. The protein was purified to more than 95% homogeneity by heat treatment and ion exchange chromatography. The protein performed an aldol condensation reaction with glyceraldehyde as substrate and dihydroxyacetone phosphate as a carboxyl donor. The protein was determined to be a type II aldolase which requires the Zn 2+ ion as a metal cofactor. This enzyme has a broad range of optimum pH (7-9) and temperature (50-80°C). It shows strong stability against heat, chemical denaturants, as well as a high percentage of organic solvents. The half-life of this enzyme at 85°C is more than 24 h and it maintains more than 90% of aldolase activity in the presence of 6 M urea, 50% acetonitrile, or 15% isopropyl alcohol.
|Number of pages||5|
|Journal||Journal of Biochemistry and Molecular Biology|
|Publication status||Published - 1998 Mar 31|
- Methanococcus jannaschii
ASJC Scopus subject areas
- Molecular Biology