Author:
Pereira Flávia D.,B.P. Pinto José Eduardo,Rosado Luciana D.S.,Rodrigues Helen C.A.,Bertolucci Suzan K.V.,Lameira Osmar A.
Abstract
The aim of the study was to develop a method for the in vitro propagation of Ananas erectifolius (Bromeliaceae), a fiber-rich Amazonian species. In vitro cultures were established from axillary buds of field-grown plants cultured on medium without plant growth regulators (PGRs). Stumps were excised from in vitro plantlets and incubated under dark conditions on medium supplemented with different combinations of 1-naphthaleneacetic acid (NAA), kinetin, and gibberellic acid (GA3). The most efficient induction of etiolated shoots occurred on explants cultured in the presence of NAA at 10.74 μm (T1 medium) or NAA at 5.37 μm + GA3 at 3 μm (T2 medium). Apical tips and nodal segments of the etiolated shoots were recultured under a 16-h photoperiod in medium without PGRs, and the effects of residual PGRs were evaluated by determining the numbers and lengths of plantlets that regenerated within 30 days. Residual PGRs exhibited no effect on the length of the regenerated plantlets but significantly affected the number of plantlets regenerated from nodal segments but not from apical tips. Nodal segments and apical tips derived from etiolated shoots produced, respectively, on T2 and T1 medium were most appropriate for plantlet regeneration. Nearly all (98%) regenerated plantlets formed roots when cultured in liquid medium without PGRs, and all plantlets survived acclimatization under greenhouse conditions. The stumps originating from etiolated shoots regenerated new etiolated shoots when recultured in the dark on medium without PGRs, thus providing a supply of new explants for plant regeneration.
Publisher
American Society for Horticultural Science
Cited by
2 articles.
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