FIELD: biotechnology, genetic engineering. SUBSTANCE: invention relates to methods for detection of human virus T-cellular leukosis of the first type (HTLV-1). Invention involves preparing recombinant plasmid DNA providing high level of hybrid env-protein HTLV-1 production showing antigenic properties and preparing the strain-producer of the protein indicated. Plasmid pESG is obtained by fusion of plasmid pVR-291 fragment encoding E. coli β-galacosidase, two polylinkers, start replication region and gene determining resistance to ampicillin with plasmid pBEI fragment containing the sequence for env-protein HTLV-1. E. coli cells were transformed with the obtained plasmid and the strain GKV/pESG producing hybrid protein and containing specific virus-specific sequences of the gene env HTLV-1 is selected. Yield of protein showing antigenic properties of HTLV-1 at culturing the strain GKV/pESG is 200-350 mg/1 l cell suspension. EFFECT: improved method of plasmid preparing, increased yield of protein. 3 cl, 3 dwg
Authors
Dates
1997-06-10—Published
1994-08-16—Filed