刺草愈伤组织的培养(1)GRISEB。:获取和植物化学分析

A. Pungin, L. Larceva, Maksim V. Kulakov, E. Popova
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摘要

近几十年来,由于盐生植物富含抗氧化、抗菌、抗炎和抗肿瘤等生物活性物质,对预防多种疾病具有重要意义,人们对盐生植物的兴趣日益增加。加里宁格勒地区生长着几种盐生植物,其中稀有种Spergularia marina (L.)。Griseb。特别令人感兴趣的是,其次生代谢产物的生物活性和含量尚未得到充分研究。本研究的目的是获得愈伤组织培养物,研究其提取物中酚类化合物的含量及其抗氧化活性。对诱导愈伤组织形成的生长调节剂和浓度进行了筛选。选择19种营养培养基进行愈伤组织的诱导。植物化学分析表明,愈伤组织提取物中酚类化合物和羟基肉桂酸含量显著,且具有较高的抗氧化活性。在19个愈伤组织培养中,在含有以下生长调节剂组合的Murashige和Skoog营养培养基上获得的培养物有望获得目标次生代谢物:0.25 mg/l TDZ和1 mg/l 2,4- d;TDZ 0.1 mg/l、2,4- d 1.5 mg/l;TDZ 0.25 mg/l、IBA 0.25 mg/l;TDZ 0.5 mg/l、IBA 0.25 mg/l;0.25 mg/l KinN和0.5 mg/l 2,4- d。
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CALLUS CULTURES OF SPERGULARIA MARINA (L.) GRISEB.: OBTAINING AND PHYTOCHEMICAL ANALYSIS
In recent decades, interest in halophyte plants has increased due to their high content of biologically active substances with powerful antioxidant, antimicrobial, anti-inflammatory and antitumor properties and promising for the prevention of various diseases. Several species of halophytes grow on the territory of the Kaliningrad region, among which the rare species Spergularia marina (L.) Griseb. is of particular interest, the biological activity and content of secondary metabolites of which have not been studied sufficiently. The purpose of this study was to obtain callus cultures, to study the content of some groups of phenolic compounds and the antioxidant activity of extracts. The study carried out the selection of growth regulators and concentrations that induce callus formation. 19 nutrient media were selected for the induction of S. marina callus cultures. The conducted phytochemical analysis showed a significant content of phenolic compounds and hydroxycinnamic acids, as well as a high level of antioxidant activity of extracts of callus cultures. Out of 19 callus cultures, cultures obtained on Murashige and Skoog nutrient media containing the following combinations of growth regulators are promising for obtaining target secondary metabolites: 0.25 mg/l TDZ and 1 mg/l 2,4-D; 0.1 mg/l TDZ and 1.5 mg/l 2,4-D; 0.25 mg/l TDZ and 0.25 mg/l IBA; 0.5 mg/l TDZ and 0.25 mg/l IBA; 0.25 mg/l KinN and 0.5 mg/l 2,4-D.
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