| Literature DB >> 25674610 |
Chigurupati Phaneendra1, K R S Sambasiva Rao2, Reetika Kapoor3, R K Jain3, Bikash Mandal3.
Abstract
Availability of adequate quantity of purified virus preparation from plant tissue is the major limitation in producing polyclonal antibodies (PAb) to begomovirus. Very few examples show successful utilization of E. coli expressed recombinant coat protein (CP) for immuno diagnosis of begomoviruses. In the present study, ~771 bp CP gene (~29.0 kDa) of Pumpkin yellow vein mosaic virus (PYVMV) was expressed as a ~71.0 kDa fusion protein with maltose binding protein (MBP) (~42.0 kDa) in E. coli. The MBP-CP was obtained in soluble state. The PAb to the purified fusion protein successfully detected PYVMV and other bipartite and monopartite begomoviruses in the field samples at 1:250 dilution in enzyme linked immunosorbent assay. Our study for the first time showed that MBP-tag fusion CP was suitable to produce diagnostic antibody to begomoviruses.Entities:
Keywords: Coat protein gene; ELISA; Pumpkin yellow vein mosaic virus; Recombinant protein; Western blot
Year: 2014 PMID: 25674610 PMCID: PMC4188205 DOI: 10.1007/s13337-013-0189-1
Source DB: PubMed Journal: Virusdisease ISSN: 2347-3584