Alternative Oxidase (AtAox) c78s Mutant Expression at Escherichia coli (SASX41DB)
2007
Ira Djajanegara
Alternative oxidase (AOX) is the terminal oxidase operating in the mitochondrial electron transport chain. The enzyme is activated by organic acid such as pyruvate and by reduction process. Based on sequences alignment of alternative oxidase gene (Aox) found in several organisms, there are 2 conserved cysteine residues. In order to investigate the importance of those cysteine residues on the activity of AOX, mutation at cysteine residue number 78 of Aox gene isolated from Arabidopsis thaliana (AtAox) was conducted. Cysteine at position number 78 was changed into serine and the c78s mutant was expressed in Escherichia coli strain SASX41DB. This particular E. coli strain is unable to grow aerobically unless transformed with Arabidopsis Aox gene (AtAox). Expression studies on c78s mutant showed that this mutant cannot be oxididized and can not be activated by pyruvic acid. This mutant is acivated by succinate instead of pyruvate. Mutation at cysteine closer to the N residue is affecting both organic acid and redox activation. Therefore, it is concluded that cysteine residue closer to the N residue is the site for both activation by pyruvate as well as activation by reduction process. Keywords : Alternative oxidase, site-directed mutation, SASx41DB, cysteine residues
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