IN VITRO MICROPROPAGATION STUDIES ON SHOOT TIP EXPLANTS OF SOLANUM TORVUM (SWARTZ) – AN IMPORTANT MEDICINAL PLANT
T Ugandhar
Abstract
T Ugandhar
Abstract
In vitro micropropagation protocol was developed for the annual medicinal herb Solanum torvum (Solanaceae) by the in vitro culture of shoot tip explants of mature plant. Shoot tips of 30-35 days old field grown eggplants were used for shoot tip explants culture of in vitro micropropagation. Surface sterilization of shoot tips was found to be the best in 0.1% HgCl2 solution for Three minutes. For primary establishment of isolated shoot tip on MS medium fortified with (BAP/Kn/TDZ) (0.5-5.0 mg/L), IAA (0.5 mg/L)+ (BAP/KN/TDZ) (1.0-3.0 mg/L) for multiple shoot induction. Multiple shoots proliferation was best observed at IAA (0.5 mg/L) + (3.0 mg/L) TDZ from the shoot explants within four weeks of culture. Shoot number per explants ranged between 2 and 6 Individual shoots were aseptically excised and sub cultured in the same media for shoot elongation. The elongated shoots were transferred to IBA (1.0mg/L–3.0mg/L) for root induction. Rooting was observed within two weeks of culture. Rooted plantlets were successfully hardened under culture conditions and subsequently established in the field conditions. The recorded survival rate of the plants was 86%. Plants looked healthy with no visually detectable phenotypic variations. The plantlets (12–16- week-old) were successfully acclimatized in soil with 87% survival frequency
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
In vitro micropropagation protocol was developed for the annual medicinal herb Solanum torvum (Solanaceae) by the in vitro culture of shoot tip explants of mature plant. Shoot tips of 30-35 days old field grown eggplants were used for shoot tip explants culture of in vitro micropropagation. Surface sterilization of shoot tips was found to be the best in 0.1% HgCl2 solution for Three minutes. For primary establishment of isolated shoot tip on MS medium fortified with (BAP/Kn/TDZ) (0.5-5.0 mg/L), IAA (0.5 mg/L)+ (BAP/KN/TDZ) (1.0-3.0 mg/L) for multiple shoot induction. Multiple shoots proliferation was best observed at IAA (0.5 mg/L) + (3.0 mg/L) TDZ from the shoot explants within four weeks of culture. Shoot number per explants ranged between 2 and 6 Individual shoots were aseptically excised and sub cultured in the same media for shoot elongation. The elongated shoots were transferred to IBA (1.0mg/L–3.0mg/L) for root induction. Rooting was observed within two weeks of culture. Rooted plantlets were successfully hardened under culture conditions and subsequently established in the field conditions. The recorded survival rate of the plants was 86%. Plants looked healthy with no visually detectable phenotypic variations. The plantlets (12–16- week-old) were successfully acclimatized in soil with 87% survival frequency
Key concepts: Shoot, Explant culture, Micropropagation, Biology, Botany, Murashige and Skoog medium, Sterilization (economics), Horticulture