Citrate synthases from both thermophilic and halophilic Archaea have been purified to homogeneity using affinity chromatography on Matrex Gel Red A and elution with a combination of substrate (oxaloacetate) and product (coenzyme A). In a number of cases, purification from cell-extract to protein suitable for N-terminal sequencing can be achieved by this single-step procedure. The method is particularly useful in the rapid purification of a thermophilic archaeal citrate synthase from a cloned gene expressed in a mesophilic host.
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UNIV MARIA CURIE SKLODOWSKA,DEPT BIOCHEM,PL MC SKLODOWSKIEJ 3,PL-20031 LUBLIN,POLANDUNIV MARIA CURIE SKLODOWSKA,DEPT BIOCHEM,PL MC SKLODOWSKIEJ 3,PL-20031 LUBLIN,POLAND
GRZYWNOWICZ, K
LOBARZEWSKI, J
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UNIV MARIA CURIE SKLODOWSKA,DEPT BIOCHEM,PL MC SKLODOWSKIEJ 3,PL-20031 LUBLIN,POLANDUNIV MARIA CURIE SKLODOWSKA,DEPT BIOCHEM,PL MC SKLODOWSKIEJ 3,PL-20031 LUBLIN,POLAND