Title | Molecular cloning and amplification of the adenylate cyclase gene |
Publication Type | Journal Article |
Year of Publication | 1981 |
Authors | Wang JY, Clegg DO, Koshland DE |
Journal | Proceedings of the National Academy of Sciences |
Volume | 78 |
Issue | 8 |
Pagination | 4684-8 |
Date Published | 1981 Aug |
ISSN | 0027-8424 |
Keywords | Adenylyl Cyclases, Bacteriophage lambda, Chromosome Mapping, Cloning, Molecular, Cyclic AMP, Gene Amplification, Gene Expression Regulation, Genes, Molecular Weight, Operon, Plasmids, Salmonella typhimurium |
Abstract | A segment of DNA containing cya, the gene for adenylate cyclase [ATP pyrophosphate-lyase (cyclizing), EC 4.6.1.1], has been isolated from Salmonella typhimurium. The phage lambda gt4 was used as a cloning vector and adenylate cyclase-positive hybrid phages were isolated that complemented adenylate cyclase-negative bacteria. The cloned DNA fragment encodes a polypeptide of molecular weight 81,000 that gives rise to adenylate cyclase activity. This protein represents a functional mutant of the bacterial adenylate cyclase. When the cya gene was amplified by inserting into a multicopy plasmid, the enzyme activity was overproduced 20-fold, but the cyclic AMP level increased only 60%, suggesting several probable regulatory mechanisms. Overproduction of enzymes by recombinant DNA techniques can be a useful probe of relationships in the metabolizing organism in vivo. |
Alternate Journal | Proc. Natl. Acad. Sci. U.S.A. |
PubMed ID | 6272270 |
PubMed Central ID | PMC320227 |