Micropropagation Protocols for Three Elite Genotypes of Stevia rebaudiana Bertoni
2024
Luis Alfonso Rodriguéz-Páez | Yirlis Yadeth Pineda-Rodriguez | Marcelo F. Pompelli | Ana Melisa Jimenez-Ramirez | Osmin José Genes-Avilez | Juan de Dios Jaraba-Navas | Alfredo Jarma-Orozco | Enrique Combatt-Caballero | Luis Eliécer Oviedo Zumaqué | Isidro Elias Suarez-Padron | Maria Ileana Oloriz-Ortega | Novisel Veitía Rodríguez
The Stevia rebaudiana Germplasm Bank at the University of Cordoba, Colombia, plays a pivotal role in conserving and efficiently utilizing the genetic variability of this species. Despite safeguarding promising genotypes with valuable traits, such as late flowering or a significant diterpenoid glycoside content, there is a need for an efficient mass propagation protocol for elite genotypes. This study aims to develop efficient in vitro micropropagation protocols for three elite S. rebaudiana genotypes (L020, L102, and Morita II). The methods employed various combinations of cytokinins and auxins following organogenesis protocols. The results showed that optimal shoot multiplication (17.3 shoots per explant) for L020 was achieved when cultures were grown on a basal medium MS supplemented with 1 &mu:M 6-benzylaminopurine (BAP). For L102, optimal shoot multiplication (18.5 shoots per explant) was achieved in MS supplemented with 1 &mu:M BAP and 0.5 &mu:M naphthalene acetic acid (NAA), while for Morita II, the best treatment was an MS supplemented with 2 &mu:M BAP and 0.5 &mu:M NAA, producing 16.4 shoots per explant. This study successfully achieved micropropagation for promising S. rebaudiana genotypes, highlighting the significant impact of genotype on tissue culture, particularly in shoot multiplication. Developing a successful micropropagation system is crucial for the conservation and improvement of S. rebaudiana, with significant implications for its future use and performance.
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