Abstract

Suspension cell cultures allow to save plant material when obtaining biologically active compounds of natural origin. As a result of the studies, optimal parameters were selected to increase the formation of biologically active metabolites in suspension cell cultures of such medicinal plants as Maackia amurensis Rupr., Hyssopus officinalis L. and Saposhnikovia divaricata (Turcz.) Schischk. Medicinal plants are a large group of plants used as raw materials for the production of medicinal and preventive drugs for medical and animal use. The assortment of phytopreparations is constantly expanding due to the increased demand for natural remedies, due to their less aggressive and toxic nature compared to synthetic ones [1]. Cultivation of medicinal plants in the form of isolated cells in vitro is one of the most modern technologies for rapidly obtaining a large biomass of plant material with stable growth features year-round under controlled conditions [2]. It is known that cells in vitro grow faster and have peculiarities of synthesis and accumulation of biologically active substances compared to intact plants [3]. Isolated cells, unlike tissue cells, also have an advantage for their use as a source of active metabolites, since they have the ability to release these compounds into the intercellular space [4]. The goal of this paper was to select parameters for increasing the biosynthetic activity of cultured suspension cultures of medicinal plant cells in vitro by optimizing cultivation conditions and introducing precursors of secondary metabolite biosynthesis into the nutrient media.

Highlights

  • Suspension cell cultures allow to save plant material when obtaining biologically active compounds of natural origin

  • Suspension cultures of cells of medicinal plants of Maakia amurskaya, Saphnikova prostrate and Hyssopus medicinalis were grown on nutrient media containing per 1,000 ml: base medium – MS, sucrose – 30 g; myo-inositol – 100 mg; 6-benzylaminopurine (BAP) – 0.5 mg; s-naphthylacetic acid (NAA) – 2 mg; casein hydrolysate – 50 mg and thiamine – 0.1 mg with addition:

  • − for Maackia amurensis: methyl jasmonate – 0.5 mg; − for Saposhnikovia divaricata: Triton X-100 –2 mg; − for Hyssopus officinalis: gibberellic acid (HA3) –2 mg. 7-O-gentiobioside formonononetin (GBF), daisin, genistein, and 10-3-Ogentiobiosylmaacchia were identified as active biochemical compounds in Maakia amur cell culture

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Summary

Introduction

Suspension cell cultures allow to save plant material when obtaining biologically active compounds of natural origin. The growth index (I), specific growth rate in the exponential phase (μ), economic coefficient (Y), and doubling time (τ) were calculated according to standard methods [6].

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