Estefany Alejandra Sánchez-Mendoza
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Estefany Alejandra Sánchez-Mendoza has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Alberto Margarito García Munguía
Universidad Autónoma de Aguascalientes
1 shared publication - Eugenio Pérez-Molphe-Balch
Unidad de Biotecnología Vegetal, Centro de Ciencias Básicas, Universidad Autónoma de Aguascalientes, Aguascalientes 20131, Mexico
1 shared publication - Graciela M. L. Ruiz Aguilar
Universidad de Guanajuato
1 shared publication - Héctor Gordon Núñez-Palenius
Universidad de Guanajuato, Campus Irapuato-Salamanca. Guanajuato, México
1 shared publication - Rafael Guzmán Mendoza
Departamento de agronomía, Universidad de Guanajuato
1 shared publication - Rogelio Costilla-Salazar
Departamento de Ciencias Ambientales, División de Ciencias de la Vida, Campus Irapuato-Salamanca, Universidad de Guanajuato, Irapuato 36500, Mexico
1 shared publication
Latest Publications
- Open Access
Plant Growth Regulators Use in the In Vitro Culture of Agave Species
Agave species possess substantial cultural, ecological, and economic significance, particularly in Mexico, where they are traditionally utilized for food, fiber, and beverages. Their industrial relevance has expanded to include bioenergy, nutraceuticals, and sustainable agriculture. However, conventional propagation methods are constrained by long life cycles, low seed germination rates, and susceptibility to phytopathogens. In vitro culture has emerged as a pivotal biotechnological strategy for clonal propagation, germplasm conservation, and physiological enhancement. This review presents a critical synthesis of plant growth regulators (PGRs) employed in agave micropropagation, emphasizing their roles in organogenesis, somatic embryogenesis, shoot proliferation, and rooting. Classical PGRs such as 6-benzylaminopurine (BAP), benzyladenine (BA), 2,4-dichlorophenoxyacetic acid (2,4-D), indole-3-acetic acid (IAA), and indole-3-butyric acid (IBA) are widely utilized, with BA + 2,4-D and BA + IAA combinations demonstrating high efficiency in embryogenic callus induction and shoot multiplication. Additionally, non-traditional regulators such as abscisic acid (ABA) and putrescine (Put) have been shown to affect embryo maturation. This review synthesizes recent studies on agave in vitro culture protocols, identifies trends in PGR use, and highlights key research gaps. These insights reveal opportunities for innovation and underscore the need for species-specific optimization and molecular validation to improve reproducibility and scalability.
Open AccessPlant Growth Regulators Use in the In Vitro Culture of Agave Species
Agave species possess substantial cultural, ecological, and economic significance, particularly in Mexico, where they are traditionally utilized for food, fiber, and beverages. Their industrial relevance has expanded to include bioenergy, nutraceuticals, and sustainable agriculture. However, conventional propagation methods are constrained by long life cycles, low seed germination rates, and susceptibility to phytopathogens. In vitro culture has emerged as a pivotal biotechnological strategy for clonal propagation, germplasm conservation, and physiological enhancement. This review presents a critical synthesis of plant growth regulators (PGRs) employed in agave micropropagation, emphasizing their roles in organogenesis, somatic embryogenesis, shoot proliferation, and rooting. Classical PGRs such as 6-benzylaminopurine (BAP), benzyladenine (BA), 2,4-dichlorophenoxyacetic acid (2,4-D), indole-3-acetic acid (IAA), and indole-3-butyric acid (IBA) are widely utilized, with BA + 2,4-D and BA + IAA combinations demonstrating high efficiency in embryogenic callus induction and shoot multiplication. Additionally, non-traditional regulators such as abscisic acid (ABA) and putrescine (Put) have been shown to affect embryo maturation. This review synthesizes recent studies on agave in vitro culture protocols, identifies trends in PGR use, and highlights key research gaps. These insights reveal opportunities for innovation and underscore the need for species-specific optimization and molecular validation to improve reproducibility and scalability.