Light-emitting diodes and their potential in callus growth, plantlet development and saponin accumulation during somatic embryogenesis of Panax vietnamensis Ha et Grushv.

In recent years, LED (light-emitting diode) has been the subject of research within the field of plant growth and development. However, there has been little discussion about using LED in vitro cultures of Panax vietnamensis, one of the important medicinal plants belonging to the Panax genus. This study examines the influence of various LED lamps on callus growth and plant formation of P. vietnamensis. Results show significant differences in growth and development, as various light conditions were suitable for different stages. Callus of 70 mg in fresh weight cultured under yellow LEDs resulted in growth of 1197 mg in fresh weight and 91.7 mg of dry weight, within a period of three months. The most effective plant formation was obtained when embryogenic calli were cultured under the combination of 60% red LED and 40% blue LED with an average of 11.21 plantlets per explant; the shoot clump fresh weight and dry weight were of 1147 and 127 mg, respectively, and the average plant height was 3.1 cm. It was also shown that this light condition was the most efficient for P. vietnamensis in vitro plant growth and development. This study provided additional evidence regarding the influence of different LEDs on ginsenoside production applying high-performance liquid chromatography (HPLC) analysis with photo-diode array (PDA) detection at ultraviolet (UV) wavelength 203 nm. The highest MR2 content was recorded when plants maintained under 20% red LED combined with 80% blue LED. However, the highest Rg1 and Rb1 content was found under fluorescent light. The results presented might provide new strategies using LEDs for adequate micropropagation protocols of P. vietnamensis.

Protocol for inducing flower color somaclonal variation in Torenia (Torenia fournieri Lind.).

White or light purple flower color Torenia (Torenia fournieri Lind.) varieties were successfully developed from the parental variety having violet flowers. This was accomplished by reducing Fe micronutrient in the culture media for the induction of in vitro flowering. The flower induction was highest in modified Murashige and Skoog (MS) medium containing ½ strength of macroelements, microelements, organic additives, and full Fe (M1) when compared to MS medium containing ½ strength of macronutrients, micronutrients, full Fe, and full organic additives (M2). The flower color was stable in two new Torenia varieties through three generations ex vitro. The results showed a wide range of somaclonal variation in flower colors; early flowering occurred in MS medium containing ½ strength of macroelements, microelements, Fe, and full strength of organic additives (M3). The selection of desirable somaclones and their micropropagation in subsequent generations led to the development of new and stable Torenia lines.