Articles
SWEETPOTATO NODAL CULTURE, PLANTLET GROWTH UNDER PHOTOMIXOTROPHIC CONDITIONS AND CONFIRMATION OF CYTOGENETIC STABILITY
Article number
703_25
Pages
205 – 210
Language
English
Abstract
In order to overcome the limitations of growth imposed by conventional tissue culture vessels, the newly developed gas-permeable Vitron film vessel was applied in the photomixotrophic micropropagation of sweetpotato using nodes 4 and 5 (confirmed to have the highest regeneration capacity and to be cytogenetically stable). Photoautotrophic cultures (CO2-enrichment, sugar-free) of leafless single nodes induce shoots poorly.
Moreover, the photoheterotrophic (sucrose-enriched medium) culture of nodes of sweetpotato plants on agar-based medium in conventional, closed vessels (polycarbonate) have been shown to be inferior to that of plantlets grown on the same medium in the Vitron under photomixotrophic conditions.
Consequently, to further characterize the importance of sucrose and CO2 level on the effectiveness of photomixotrophic culture, the present study was conducted.
Despite differences in RAPD banding, acclimatized plants did not exhibit any marked phenotypic differences.
Cytological (flow cytometry) analyses demonstrated that in vitro and ex vitro cultures were very stable, exhibiting no (endo)polyploidy.
Moreover, the photoheterotrophic (sucrose-enriched medium) culture of nodes of sweetpotato plants on agar-based medium in conventional, closed vessels (polycarbonate) have been shown to be inferior to that of plantlets grown on the same medium in the Vitron under photomixotrophic conditions.
Consequently, to further characterize the importance of sucrose and CO2 level on the effectiveness of photomixotrophic culture, the present study was conducted.
Despite differences in RAPD banding, acclimatized plants did not exhibit any marked phenotypic differences.
Cytological (flow cytometry) analyses demonstrated that in vitro and ex vitro cultures were very stable, exhibiting no (endo)polyploidy.
Publication
Authors
D.T.T. Giang, M. Tanaka, J.A. Teixeira da Silva
Keywords
flow cytometry, photoautotrophy, RAPDs, somaclonal variation
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