Effect of aluminum on the in vitro activity of acid phosphatases of four potato clones grown in three growth systems

The aim of this study was to assess the effect of aluminum on the in vitro activity of acid phosphatases (APases) of four potato clones, Macaca and Dakota Rose (Al-sensitive), and SMIC148-A and Solanum microdontum (Al-tolerant), grown in vitro, in hydroponics or in a greenhouse. The enzyme was assay...

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Published inBiologia plantarum Vol. 55; no. 1; pp. 178 - 182
Main Authors Tabaldi, L.A.,Universidade Federal de Santa Maria (Brasil). Dept. de Biologia, Cargnelutti, D.,Universidade Federal de Santa Maria (Brasil). Dept. de Quimica, Castro, G.Y.,Universidade Federal de Santa Maria (Brasil). Dept. de Biologia, Goncalves, J.F.,Universidade Federal de Santa Maria (Brasil). Dept. de Biologia, Rauber, R.,Universidade Federal de Santa Maria (Brasil). Dept. de Biologia, Bisognin, D.A.,Universidade Federal de Santa Maria (Brasil). Dept. de Fitotecnia, Schetinger, M.R.C.,Universidade Federal de Santa Maria (Brasil). Dept. de Quimica, Nicoloso, F.T.,Universidade Federal de Santa Maria (Brasil). Dept. de Biologia
Format Journal Article
LanguageEnglish
Published Dordrecht Springer Netherlands 01.03.2011
Institute of Experimental Botany of the Czech Academy of Sciences
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Summary:The aim of this study was to assess the effect of aluminum on the in vitro activity of acid phosphatases (APases) of four potato clones, Macaca and Dakota Rose (Al-sensitive), and SMIC148-A and Solanum microdontum (Al-tolerant), grown in vitro, in hydroponics or in a greenhouse. The enzyme was assayed in vitro in the presence of 0, 1.85, 3.70, 5.55 and 7.40 mM Al. In plantlets grown in vitro, root APases were inhibited by Al in all clones, while shoot APases were inhibited by Al in S. microdontum and Dakota Rose and increased in Macaca at all Al concentrations. In plantlets grown in hydroponics, root APases increased in Macaca at 1.85 mM Al, whereas decreased at all Al levels in S. microdontum. In greenhouse plantlets, root APases decreased at 7.40 mM Al in S. microdontum and SMIC148-A, and at 3.70, 5.55 and 7.40 mM Al in Dakota Rose. Shoot APases decreased in Macaca and SMIC148-A. Conversely, in Dakota Rose, APases increased at 1.85 and 3.70 mM Al. These results show that the effect of Al toxicity on in vitro APase activity depends not only on Al availability but also on the plant organ, genetic background, and the growth conditions. Therefore, it suggests that acid phosphatases activity assessed in vitro might not be a good parameter to validate the screening for adaptation of potato clones to Al toxicity.
Bibliography:F61
2011000506
H50
http://wwwueb.asuch.cas.cz/bp/bp.htm
ISSN:0006-3134
1573-8264
DOI:10.1007/s10535-011-0026-6