植物生长调节剂对 Saposhnikovia divaricata (Turcz. ex Ledeb.) Schischk 体外再生的影响

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-09-13 DOI:10.1007/s11627-024-10462-9
Tatiana Zheleznichenko, Tatyana Elisafenko, Bayarma Zhigmittsyrenova, Maksim Kazakov, Vasilii Taraskin
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引用次数: 0

摘要

Saposhnikovia divaricata (Turcz. ex Ledeb.) Schischk 是一种药用植物,具有广泛的药理活性,这要归功于它含有各种生物活性化合物,包括色酮。对这种植物的无节制采伐导致其自然资源枯竭。我们对 S. divaricata 的体外再生能力进行了研究。通过对种子消毒和发芽,建立了有果皮和无果皮的无菌培养。在 Murashige 和 Skoog 培养基上,在不同细胞分裂素(苄氨基嘌呤、甲托品和噻嘧磺隆,浓度分别为 0.1 µM、0.5 µM 和 1.0 µM)的存在下,通过直接形态发生实现了不定芽的形成。经测定,最理想的外植体是无菌苗的子叶节,因为根据所用细胞分裂素的类型和浓度,每个外植体可快速产生 1.4 ± 0.5 至 10.2 ± 2.0 个微芽。离体幼苗的第一片真叶也能成功再生。微芽直接从外植体组织中形成,数量从 1.7 ± 0.7 到 4.4 ± 0.9 不等。噻虫隆诱导的小芽数量最多,但用元多菌灵培养后,再生植株的生根频率最高,从 66% 到 97% 不等。用 2,4-二氯苯氧乙酸(10.0 µM)培养第一片真叶时,可获得体细胞胚。形态发生是通过间接途径(通过胼胝体形成阶段)进行的,伴随着多达 24.2 ± 6.1 个体细胞胚的形成,生根率达到 96%。这些研究为制定 S. divaricata 的克隆微繁殖方案提供了初步依据。
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Influence of plant growth regulators on in vitro regeneration of Saposhnikovia divaricata (Turcz. ex Ledeb.) Schischk

Saposhnikovia divaricata (Turcz. ex Ledeb.) Schischk is a medicinal plant with a broad spectrum of pharmacological activities, which are attributed to the presence of various bioactive compounds, including chromones. The uncontrolled harvesting of this plant has resulted in the depletion of its natural resources. The ability of S. divaricata to regenerate in vitro was studied. Aseptic culture was established by sterilizing seeds and germinating them, both with and without the pericarp. Adventitious shoot formation through direct morphogenesis was achieved on Murashige and Skoog medium in the presence of different cytokinins: benzylaminopurine, meta-topolin, and thidiazuron, at concentrations of 0.1 µM, 0.5 µM, and 1.0 µM. It has been determined that the most preferable explants were the cotyledonary nodes of aseptic seedlings, as they enable the rapid production of 1.4 ± 0.5 to 10.2 ± 2.0 microshoots per explant, depending on the type and concentration of the cytokinin used. Successful regeneration also occurred from the first true leaves of seedlings in vitro. Microshoots were formed directly from the explant tissues, with their quantity ranging from 1.7 ± 0.7 to 4.4 ± 0.9. The highest number of microshoots was induced by thidiazuron, but after cultivation with meta-topolin, the regenerated plants showed the highest frequency of rooting, ranging from 66 to 97%. Somatic embryoids were obtained when the first true leaves were cultivated with 2,4-dichlorophenoxyacetic acid (10.0 µM). Morphogenesis occurred via the indirect pathway (through the callus formation stage), accompanied by the formation of up to 24.2 ± 6.1 somatic embryoids, with a rooting frequency reaching 96%. These studies provide a preliminary basis for developing a protocol for the clonal micropropagation of S. divaricata.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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