Lee T Y, Makino K, Shinagawa H, Nakata A
Department of Experimental Chemotherapy, Osaka University, Japan.
J Bacteriol. 1990 May;172(5):2245-9. doi: 10.1128/jb.172.5.2245-2249.1990.
A DNA fragment of Escherichia coli cloned on pBR322 elevated the production of alkaline phosphatase and phosphate-binding protein in a phoR phoM strain. Nucleotide sequence analysis and enzyme assays revealed that the DNA fragment contained the ackA gene, which codes for acetate kinase. A high gene dosage of ackA was needed to induce the production of alkaline phosphatase and phosphate-binding protein in this strain. Overexpression of ackA elevated the intracellular ATP concentration, an effect that might be related to activation of the phosphate regulon in the phoR phoM strain.