Planta Med 2010; 76(4): 386-392
DOI: 10.1055/s-0029-1186166
Biochemistry, Molecular Biology and Biotechnology
Original Papers
© Georg Thieme Verlag KG Stuttgart · New York

Transformed Cell Suspension Culture of Galphimia glauca Producing Sedative Nor-friedelanes

Anabel Ortíz1 , Alexandre Cardoso-Taketa2 , Mario Rodríguez Monroy3 , Jesús Arellano3 , Georgina Hernández3 , María Luisa Villarreal1
  • 1Centro de Investigación en Biotecnología, Universidad Autónoma del Estado de Morelos, Cuernavaca, Morelos, México
  • 2Centro de Investigación en Productos Bióticos, Instituto Politécnico Nacional, Yautepec, Morelos, México
  • 3Centro de Ciencias Genómicas, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, México
Further Information

Publication History

received May 23, 2009 revised July 28, 2009

accepted August 26, 2009

Publication Date:
06 October 2009 (online)

Abstract

The Mexican species Galphimia glauca (Cav.) Kuntze (Malphigiaceae) synthesises a family of sedative and anxiolytic nor-secofriedelanes, designated as galphimines. These active principles accumulate at low concentration in the aerial parts of plants from wild populations. Transformed calluses and cell suspension cultures of this species were established in order to induce a greater production of nor-friedelanes. The cell suspension line GgBa was selected and grown over a period of two years of continuous subculturing in MS nutrient medium in the absence of growth regulators. PCR and Southern blot analyses were employed in order to confirm that the rol A gene had been integrated into the plant genome. Batch cultures of the GgBa cell line were grown over a 32-day period and first-order growth kinetics was observed, reaching a specific growth rate (µ) of 0.13 d−1. The production of glaucacetalin A (10), a triterpenoid related to the known galphimines, was quantified in the nutrient medium by HPLC. The transformed cell suspension culture GgBa also synthesised a novel nor-friedelane, given the name glaucacetalin D (13). High-resolution spectroscopic and spectrometric techniques were employed to elucidate the structure of 13. This triterpene has never been observed in wild plant tissues or in other in vitro cultures. Maslinic acid (14) was identified in cell biomasses. The triterpene production of the cell line GgBa was as follows: glaucacetalin A, 2.7 mg/L; glaucacetalin D, 2.9 mg/L and maslinic acid, 2.4 mg/g dry weight. The sedative activity of compounds 10 and 13 was demonstrated in ICR mice by using the sodium pentobarbital-induced hypnosis model. No cytotoxicity of 10 and 13 was exhibited against KB, MCF-7 and HF6 human cancer cell lines.

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Dr. María Luisa Villarreal

Centro de Investigación en Biotecnología
Universidad Autónoma del Estado de Morelos
Av. Universidad 1001

Col. Chamilpa

Cuernavaca

62209 Morelos

Mexico

Phone: + 52 77 73 29 70 57

Fax: + 52 77 73 29 70 30

Email: luisav@cib.uaem.mx

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