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Título : Enhanced induction of microspore embryogenesis after n-butanol treatment in wheat (Triticum aestivum L.) anther culture
Autor : Soriano Castán, Mercedes ; Cistué Sola, Luis ; Castillo Alonso, Ana María
Palabras clave : Doubled haploid
Androgenesis
Bread wheat
n-butanol
Fecha de publicación : may-2008
Editor: Springer
Citación : Plant Cell Report, Vol 27:805-811
Resumen: The aim of this study was the improvement of embryo production in wheat anther culture. Three butanol alcohols, n-butanol, sec-butanol and tert-butanol, were evaluated for their effect on microspore embryogenesis in two spring cultivars of wheat, Pavon and Caramba. Application of n-butanol, at 0.1 and 0.2% (v/v) in the induction media for five hours, highly improved embryo production in both cultivars. Sec- and tert-butanol performed similarly to control plates. Regeneration ability was unaffected by any butyl-alcohol treatment. As a consequence of the higher embryo production after n-butanol treatment, the number of green regenerated plants increased up to 5 times in cultivar Pavon and up to 3 times in cultivar Caramba. The percentage of green plants was improved or unaffected by the treatment. Doubled haploid plant production was between 2 and 4 times higher after n-butanol treatment than in control plates. Therefore, n-butanol was successfully applied in the production of wheat doubled haploids. This primary alcohol is known as an activator of phospholipase D and has been previously reported to disrupt cortical microtubules and detach them from the plasma membrane in plants. Its effects on androgenetic induction could confirm the importance of microtubule regulation in plant cell fate, specifically in microspore development. A possible implication of phospholipase D is discussed.
Descripción : The original version is available at http://www.springerlink.com/content/100383/
Versión del editor: http://www.springerlink.com/content/v302947634352057/fulltext.pdf
URI : http://hdl.handle.net/10261/7983
DOI: 10.1007/s00299-007-0500-y
ISSN: 0721-7714 (Print)
1432-203X (Online)
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