Characteristics of detergent-resistant phospholipase A overproduced in E. coli cells bearing its cloned structural gene.
Article Details
- CitationCopy to clipboard
Homma H, Chiba N, Kobayashi T, Kudo I, Inoue K, Ikeda H, Sekiguchi M, Nojima S
Characteristics of detergent-resistant phospholipase A overproduced in E. coli cells bearing its cloned structural gene.
J Biochem. 1984 Dec;96(6):1645-53.
- PubMed ID
- 6397463 [ View in PubMed]
- Abstract
Detergent-resistant phospholipase A (DR-phospholipase A) of E. coli is a 28K-dalton protein and is exclusively located in the outer membrane. We cloned the pldA gene of E. coli, which is responsible for the activity of DR-phospholipase A. Strains bearing the plasmid which contained the pldA gene yielded a large amount of the outer membrane protein with a molecular weight of about 28K daltons and overproduced 20 to 65 times as much DR-phospholipase A activity as the wild type strain. Experiments with minicells and maxicells revealed that the pldA-containing plasmid was coding for a 28K protein. These results strongly indicated that pldA is the structural gene for DR-phospholipase A. There was apparently no difference with respect to the association of the enzyme with the envelope fraction between the overproducer and the wild type strain. The overproduced enzyme was properly transported to the outer membrane. Neither the growth rate nor the phospholipid composition of the overproducer was remarkably different from in the wild type strain. Thus, the overproduction of DR-phospholipase A apparently caused no phenotypic variations. E. coli has very excessive ability to transport and integrate the outer membrane protein.