The brown rust susceptible sugarcane genotype B4362 was subjected to in vitro tissue culture and physical and chemical mutation induction procedures. Five brown rust resistant mutants with hypersensitive response to Puccinia melanocephala were selected out of a total population of 11 167 regenerated plants. High selection frequency was obtained with both mutagenic treatments, although chemical mutagenesis (NaN3) resulted in higher selection frequencies for brown rust resistance than gamma irradiation (60Co). The brown rust resistant mutants showed variations in molecular, morphological, and agronomic traits. Traits such as internode shape, bud shape, leaf sheath hairiness, outer auricule shape, intensity of flowering, stool growth habit, number of stalks per stool, and smut susceptibility were modified in brown rust resistant mutants. In addition, sugar yield was improved in two mutants with increments in stalk length, stalk number, and stalk diameter. Mutation induction proved to be suitable for the generation of new sources of brown rust resistance in sugarcane.

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 μM 6-benzylaminopurine (BAP). For L102, optimal shoot multiplication (18.5 shoots per explant) was achieved in MS supplemented with 1 μM BAP and 0.5 μM naphthalene acetic acid (NAA), while for Morita II, the best treatment was an MS supplemented with 2 μM BAP and 0.5 μM 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.

The Germplasm Bank of Stevia rebaudiana segregants of the University of Córdoba is a strategy for the use of genetic variability and efficient crop yield. There are genotypes with important characteristics such as: high tolerance to salt stress and climatic change (high CO₂ in the Earth surface), late flowering, erect architecture, and high contents of steviol glycosides. However, there is a lack of in-depth studies of morphophysiological and biochemical indicators such as gas exchange, chlorophyll a fluorescence, chloroplast pigments, and antioxidant systems, which allow us to develop early selection tools for elite genotypes. The genotypes (L020, Morita II, and L102) were found to have elite characteristics such as high efficiency in water use, excellent biomass production, and a more robust antioxidant system than the genotypes (L057 and L082). The L020 genotype presented the highest content of stevioside and rebaudioside A, followed by the Morita II genotype. We found a close correlation between the electron transport rate and the mechanisms that increase photosystem complexes. In this sense, non-photochemical cooling modulated by the release of heat by the leaves is a fact that is confirmed by the greater activity of the xanthine pool to protect the photochemical complexes in S. rebaudiana.

Stevia rebaudiana Bertoni is a strategically important perennial crop because it is the main botanical source of steviol glycosides, a group of high-intensity, non-caloric sweeteners increasingly demanded by the global food and beverage industry. Despite the rapid expansion of stevia cultivation, commercial production remains strongly dependent on a narrow genetic base, particularly on clonally propagated cultivars such as ‘Morita II’, which has long served as the industrial benchmark because of its favourable rebaudioside A profile and processing consistency. This dependence has raised concerns about limited adaptive capacity, genetic erosion and restricted long-term breeding progress. In this review, we provide an integrated and critical synthesis of current knowledge on the genetic diversity of S. rebaudiana, the biosynthetic and regulatory architecture of steviol glycosides, and the conventional and emerging strategies available for crop improvement. Unlike previous reviews, this article explicitly connects domestication-driven genetic bottlenecks, wild germplasm mobilisation, metabolic pathway regulation, advanced analytical phenotyping and precision breeding into a single systems-oriented framework. We examine the roles of wild germplasm, somaclonal variation, polyploidy, molecular markers, omics-assisted approaches and transgene-free genome editing as complementary tools to broaden the stevia breeding base while preserving industrial quality standards. We finally propose an integrative roadmap for the sustainable genetic improvement of stevia, positioning ‘Morita II’ not as an endpoint, but as a benchmark within a broader diversification strategy.