ASEPTIC GERMINATION AND MICROPROPAGATION OF STEMMACANTHA SERRATULOIDES (GEORGI) M. DITTRICH

I.F. Rakhmatullina, Ya.P. Mineev, B.R. Kuluev
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Abstract

Stemmacantha serratuloides (Georgi) M. Dittrich is a perennial herbaceous medicinal plant, a source of a number of phytoecdysteroids with adaptogenic, anabolic and tonic effects. Due to the rarity of this plant species and the strong dependence of its seed productivity on weather conditions, the relevance of research aimed at its biotechnological cultivation and reproduction is high. The aim of this study was to introduce S. serratuloides plants from the Cis-Ural population of the Republic of Bashkortostan into in vitro culture and to develop an effective protocol for micropropagation of this species. It was shown that an effective method of preparing seeds for in vitro culture is their successive sterilization with 96% ethanol (1 min) and 20% bleach (20 min), as well as me- chanical scarification, without a preliminary stratification step. When using 1 mg/l of 2,4-dichlorophenoxyacetic acid and 1.5 mg/l of 6-benzylaminopurine on Murashige-Skoog medium, no regeneration of shoots on explants of cotyledons and hypocotyls occurred. Shoot regeneration was induced from root explants using Murashige-Skoog medium supplemented with 6-benzylaminopurine and indoleacetic acid at concentrations of 1 mg/l and 1.5 mg/l, respectively. Rooting of shoots was carried out on MS medium containing 0.25 mg/L IAA. This micropropagation technology can be used for rapid propagation of plants for various biotechnological purposes, for example, for further transformation by Agrobacterium rhizogenes and creating of hairy root cultures.
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无菌发芽和微繁殖茎苋serratuloides (georgi) m. dittrich
Stemmacantha serratuloides (Georgi) M. Dittrich 是一种多年生草本药用植物,是多种具有适应、合成代谢和滋补作用的植物蜕皮激素的来源。由于该植物物种的稀有性及其种子产量对天气条件的依赖性很强,对其进行生物技术栽培和繁殖的研究具有很高的现实意义。本研究的目的是将巴什科尔托斯坦共和国西乌拉尔种群中的 S. serratuloides 植物引入离体培养,并制定该物种微繁殖的有效方案。研究表明,准备离体培养种子的有效方法是用 96% 的乙醇(1 分钟)和 20% 的漂白剂(20 分钟)连续灭菌,并进行机械除痕,而不进行初步分层。在 Murashige-Skoog 培养基上使用 1 毫克/升的 2,4-二氯苯氧乙酸和 1.5 毫克/升的 6-苄基氨基嘌呤时,子叶和下胚轴的外植体上没有芽再生。使用添加了 6-苄基氨基嘌呤和吲哚乙酸(浓度分别为 1 毫克/升和 1.5 毫克/升)的 Murashige-Skoog 培养基,从根部外植体诱导芽再生。芽的生根在含有 0.25 毫克/升 IAA 的 MS 培养基上进行。这种微繁殖技术可用于植物的快速繁殖,以达到各种生物技术目的,例如通过根瘤农杆菌进行进一步转化和创建毛细根培养物。
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