Development of a highly efficient system for assessing recombinant gene expression in plant cell suspensions via Agrobacterium tumefaciens transformation.

Authors:
Alejandro Fuentes
Alejandro Fuentes
Center for Genetic Engineering and Biotechnology
Meilyn Rodriguez
Meilyn Rodriguez
Center for Genetic Engineering and Biotechnology
Nadia Ramirez
Nadia Ramirez
Center for Genetic Engineering and Biotechnology
Merardo Pujol
Merardo Pujol
Center for Genetic Engineering an d Biotechnology
Corporate Executive Officer
Havana | Cuba

Biotechnol Appl Biochem 2004 Jun;39(Pt 3):355-61

Plant Department, Center for Genetic Engineering and Biotechnology, Ave. 31 e/158 y 190, Cubanacán, Playa POB 6162, Havana 10600, Cuba.

A transient gene-expression system was developed and used to characterize promoter strength, to verify suitability of bacterial gene modifications for expression in plant cells, and to express active antibody molecules. The system is based on suspension tobacco cells transformed by Agrobacterium in a transient way. Conditions such as pre-culture of tobacco cells and the co-cultivation period were identified as determinants to achieve high expression levels. Under established conditions the activity strength of CaMV (cauliflower mosaic virus) 35 S and ToMoTV (tomato mottle taino virus) AL1 promoters were compared. A modified cry gene sequence from Bacillus thuringiensis was expressed and detected by Western-blot analysis. A monoclonal antibody against anti-(hepatitis B virus surface antigen) was produced in such quantities as to allow testing of biological activity and preliminary characterization.

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Source
http://dx.doi.org/10.1042/BA20030192DOI Listing
June 2004
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