Honokiol and Magnolol Production by in vitro Micropropagated Plants of Magnolia dealbata, an Endangered Endemic Mexican Species

Author:

Domínguez Fabiola12,Chávez Marco3,Garduño-Ramírez María Luisa4,Chávez-Avila Víctor M.5,Mata Martín6,Cruz-Sosa Francisco2

Affiliation:

1. Laboratorio de Biotecnología, Centro de Investigación Biomédica de Oriente (CIBIOR), Instituto Mexicano del Seguro Social (IMSS), Km. 4.5, Carretera Federal Atlixco-Metepec, 74360 Metepec, Puebla, México

2. Departamento de Biotecnología, Universidad Autónoma Metropolitana-Iztapalapa (UAM-Iztapalapa), Av. San Rafael Atlixco no. 186, Col. Vicentina, 09340 México, D.F., México

3. Laboratorio de Fitofármacos, Unidad de Investigación en Enfermedades Neurológicas (UIEN), Centro Médico Nacional Siglo XXI (CMN-SXXI), Instituto Mexicano del Seguro Social (IMSS), Av. Cuauhtémoc 330, Col. Doctores, 06720 México, D.F., México

4. Centro de Investigaciones Químicas, Universidad Autónoma del Estado de Morelos (UAEM), Av. Universidad 1001, Col. Chamilpa, 62210 Cuernavaca, Morelos, México

5. Jardín Botánico, Instituto de Biología, Universidad Nacional Autónoma de México (UNAM), Ciudad Universitaria (CU), 04510 México, D.F., México

6. Laboratorio de Cultivo de Tejidos Vegetales, Instituto de Ecología, A.C., UNAM, Km. 2.5, Antigua Carretera a Coatepec 351, Congregación El Haya, 91070 Xalapa, Veracruz, México

Abstract

An efficient protocol for the in vitro propagation of Magnolia dealbata Zucc., an important medicinal plant that is the source of the anxiolytic and anticancer compounds honokiol and magnolol, was established. This plant is wild-crafted, and conservationists have expressed concerns with regard to the sustainability of production. In the present work, two factors were found to be of importance for the regeneration of M. dealbata and the production of honokiol and magnolol. These factors were the type of explants and the combination and concentration of plant-growth regulators. Green, compact, nodular organogenic callus was obtained from leaf explants in a medium fortified with Murashige and Skoog salts and supplemented with 1.5 mg/L 2,4-dicholorophenoxyacetic acid and 1.5 mg/L kinetin. Shoot multiplication from callus cultures was achieved in the Murashige and Skoog (MS) medium with 1.5 mg/L thidiazuron (TDZ). Phenol secretion was controlled by the addition of 250 mg/L of activated charcoal. For rooting, shoots were transferred to MS medium supplemented with several auxins. After root induction, the plants were hardened in earthen pots containing sand, soil, and vermiculite. The contents of honokiol (HK) and magnolol (MG) were determined in different plant materials by high-performance liquid chromatography-diode-array detection techniques. This analysis revealed that the honokiol and magnolol content in aerial and underground parts of micropropagated M. dealbata were higher than that observed in wild plants (both 6 months old). Our results suggest that conservation of M. dealbata is possible by means of in vitro multiplication of leaf-derived callus. The usefulness of M. dealbata regeneration and production of HK and MG may be attributed to the proper selection of explant sourcing and identification of the correct growth medium to support adequate growth. This careful selection of explants and growth medium leads to a very useful source of plant material for pharmacological and phytomedicinal screening applications and, above all, would safeguard this plant species from the threat of extinction.

Publisher

SAGE Publications

Subject

Complementary and alternative medicine,Plant Science,Drug Discovery,Pharmacology,General Medicine

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