In vitro regeneration of Begonia homonyma — A threatened plant

Abstract

An efficient simple in vitro plant regeneration system was established for Begonia homonyma, a threatened ornamental and medicinal plant. Shoot multiplication was improved significantly with a concomitant decrease in shoot length from leaf explants cultured on Murashige and Skoog (MS) medium containing 15μM benzyladenine (BA) and 5μM naphthaleneacetic acid (NAA). Shoots were established further in MS medium with reduced concentrations of BA and NAA. Shoots exhibited an high frequency of necrosis. The highest numbers of shoots (37.2 per explant, 44.0mm) were obtained from shoot explants cultured on MS medium supplemented with 5μM gibberellic acid (GA3) and 0.5μM BA. Necrosis of shoots (10%) was controlled by using half-strength MS medium containing 2μM GA3 and 0.5μM BA for shoot explants derived from culture medium supplemented with 2μM meta-topolin riboside (mTR) and 0.5μM NAA. Rooting of shoots was effective in MS medium supplemented with 15gL−1 sucrose, 2μM indole-3-butyric acid (IBA) and 0.5μM NAA, while root elongation was best with a combination of 2μM IBA and 0.5μM phloroglucinol. All plantlets were successfully acclimatized in the greenhouse. The reported organogenesis systems reinforced the importance of hormonal, sucrose and phloroglucinol effects on in vitro plant regeneration. Organogenesis protocols described here provide systems for a conservation strategy, ex vitro gene bank and commercial planting, and for genetic transformation studies.