| Literature DB >> 33873617 |
A Turrini1, C Sbrana2, L Pitto3, M Ruffini Castiglione2, L Giorgetti2, R Briganti2, T Bracci2, M Evangelista3, M P Nuti1,2, M Giovannetti1,2.
Abstract
• Transformed aubergine plants constitutively expressing the Dm-AMP1 antimicrobial defensin (from Dahlia merckii) were generated and characterized. • Transgenic plants were selected on kanamycin and screened by polymerase chain reaction analysis. The expression of Dm-AMP1 in plant tissues and its release in root exudates were detected by Western blot analyses. Dm-AMP1 localization was performed by immunohistochemical experiments. • Dm-AMP1 expression ranged from 0.2% to 0.48% of total soluble proteins in primary transformants and from 0.16% to 0.66% in F2 plants. Transformed clones showed resistance to the pathogenic fungus Botrytis cinerea, whose development on leaves was reduced by 36-100%, with respect to controls. The protein was released in root exudates of the transformed plants and was active in reducing the growth of the co-cultured pathogenic fungus Verticillium albo-atrum, whereas it did not interfere with recognition responses and symbiosis establishment by the arbuscular mycorrhizal fungus Glomus mosseae. • Dm-AMP1 transformants may represent a useful model to study the interactions between genetically modified plants and pathogenic fungi or beneficial nontarget microorganisms.Entities:
Keywords: Botrytis cinerea; Solanum melongena; Verticillium albo-atrum; arbuscular mycorrhizal fungi; defensin; transformed plants
Year: 2004 PMID: 33873617 DOI: 10.1111/j.1469-8137.2004.01107.x
Source DB: PubMed Journal: New Phytol ISSN: 0028-646X Impact factor: 10.151