Ectomicorriza in vitro entre Hydnangium sp. e Eucalyptus grandis e análises de seqüências de genes de Hydnangium sp.

• Ano de defesa: 2009
• Autor(a) principal: Walter, Juline Marta
• Orientador(a): Araujo, Elza Fernandes de
• Banca de defesa: Tótola, Marcos Rogério , Ribon, Andréa de Oliveira Barros
• Tipo de documento: Dissertação
• Tipo de acesso: Acesso aberto
• Idioma: por
• Instituição de defesa: Universidade Federal de Viçosa
• Programa de Pós-Graduação: Mestrado em Microbiologia Agrícola
• Departamento: Associações micorrízicas; Bactérias láticas e probióticos; Biologia molecular de fungos de interesse
• País: BR
• Palavras-chave em Português: Ectomicorriza; Micorrização in vitro; Hydnangium sp.; ATP sintaxe; Acetil-CoA acetiltransferase
• Palavras-chave em Inglês: Ectomycorrhiza; In vitro mycorrhization; Hydnangium sp.; ATP sintase; Acetyl-CoA acetyltransferase
• Área do conhecimento CNPq: CNPQ::CIENCIAS AGRARIAS::AGRONOMIA::FITOSSANIDADE::MICROBIOLOGIA AGRICOLA
• Link de acesso: http://locus.ufv.br/handle/123456789/5302

Hydnangium sp. is a basidiomycetous fungus that is capable of forming ectomycorrhiza with Eucalyptus species. The in vitro mycorrhization system is widely used for mycorrhizal interactions studies, becoming a simple and reproducible system for the symbiosis-regulated genes expression analysis. In this work, the in vitro mycorrhization system for the Hydnangium sp. and Eucalyptus grandis interaction was performed for the colonization, differentiation and functioning phases for the ectomicorriza formation. The colonization phase were verified after five days of inoculation with the Hydnangium sp., the differentiation phase after ten days and the functioning phase after 20 days of inoculation. The extern morphology was analyzed by stereomicroscopy and the section microscopy was performed for the mantle and Hartig net detection. The total RNA extraction was performed for each phase, with the objective of to analyze genes expression. However, the material quantity from roots of 130 seedlings for each phase was insufficient for the transcripts detection through RTPCR. The intron analysis of the partial sequences of the genes that encode ATP sintase (atp) and acetyl-CoA acetyltransferase (aat) of Hydnangium sp. enabled two introns identification in partial sequence of atp gene (53 and 65 bp), while in partial sequence of aat gene were identified three introns (52, 52 e 46 bp). All introns analyzed have the canonical sequence 5 GT 3 AG on splicing sites, ranging the adjacent nucleotides. The phylogenetic analysis, using the partial sequences of amino acids of atp and aat genes, enabled the correct group separation, corroborating the Hydnangium sp. classification as belonging the same family of Laccaria bicolor.