Protocol for the micropropagation of grape variety “Cabernet Franc”: Preliminary results

Authors

  • M. Magaña González Facultad de Ciencias Agrícolas y Forestales; Universidad Autónoma de Chihuahua; C.P. 33000, Cd. Delicias Chihuahua, México. Author
  • S. Pérez Álvarez Facultad de Ciencias Agrícolas y Forestales; Universidad Autónoma de Chihuahua; C.P. 33000, Cd. Delicias Chihuahua, México. Author https://orcid.org/0000-0002-9211-0797 (unauthenticated)
  • C. M. Escobedo Bonilla Instituto Politécnico Nacional; CIIDIR Unidad Sinaloa; C.P. 81101, Guasave, Sinaloa, México. Author
  • E. Sánchez Chávez Centro de Investigación en Alimentación y Desarrollo A.C. Unidad Delicias; C.P. 33089, Delicias, Chihuahua, México. Author
  • J. Rascón Solano Facultad de Ciencias Agrícolas y Forestales; Universidad Autónoma de Chihuahua; C.P. 33000, Cd. Delicias Chihuahua, México. Author
  • R. Hernández Campos Universidad Autónoma Metropolitana; Departamento de Biotecnología; Unidad Iztapalapa; C.P. 09340, Ciudad de México, México. Author
  • M. A. Magallanes Tapia Instituto Politécnico Nacional; CIIDIR Unidad Sinaloa; C.P. 81101, Guasave, Sinaloa, México. Author

Keywords:

Disinfection, In vitro multiplication, Plant growth regulators, Vitis vinifera L.

Abstract

Micropropagation is a technique that allows producing disease-free plants, in large quantities and in a short time. The aim of this study was to establish the protocol for disinfection and in vitro multiplication of the grape (Vitis vinifera L.) of the Cabernet Franc variety using axillary buds as a source of explant. The buds received the following three disinfection treatments: (T1) Captan and Triadimefon for 10 min and 9% sodium hypochlorite (NaClO) for 10 min, (T2) 75% ethyl alcohol for 5 min and 2% NaClO for 20 min and (T3) 75% ethyl alcohol for 10 min and 2% NaClO for 20 min. Then they were established in Murashige and Skoog (MS) culture medium with four treatments for multiplication: (T1) 6-benzylaminopurine (6BAP) 1.0 mg L-1 + Kinetin 0.5 mg L-1; (T2) Kinetin 3.0 mg L-1 + gibberellic acid (AG3) 1.0 mg L-1; (T3) 6BAP 1.0 mg L-1 + Kinetin 0.5 mg L-1 + indole acetic acid (IAA) 0.2 mg L-1; and (T4) Kinetin 1.5 mg L-1 + naphthalene acetic acid (ANA) 0.5 mg L-1. The disinfection percentage, bud development (multiplication) and multiplication coefficient were evaluated in five subcultures. The best response obtained in the disinfection treatments was with T2 and T3, obtaining 100% of the buds free of pathogens. In the multiplication phase, T4, obtained a vine bud multiplication frequency of 8.57 was obtained and T1 a multiplication coefficient of 3.8. Finally, with this research, a protocol for the disinfection and in vitro multiplication of vine buds of the “Cabernet Franc” variety was established.

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Published

2024-05-01

How to Cite

Magaña González, M., Pérez Álvarez, S., Escobedo Bonilla, C. M., Sánchez Chávez, E., Rascón Solano, J., Hernández Campos, R., & Magallanes Tapia, M. A. (2024). Protocol for the micropropagation of grape variety “Cabernet Franc”: Preliminary results. RIIIT Revista Internacional de Investigación E Innovación Tecnológica, 12(68), 1-14. https://revistas.uadec.mx/RIIIT/article/view/984