Kikowska Małgorzata, Sliwinska Elwira, Thiem Barbara
Department of Pharmaceutical Botany and Plant Biotechnology, University of Medical Sciences in Poznan, 14 Św. Marii Magdaleny St., 61-861 Poznań, Poland.
Laboratory of Molecular Biology and Cytometry, Department of Agricultural Biotechnology, UTP University of Science and Technology, Prof. S. Kaliskiego Ave. 7, 85-789, Bydgoszcz, Poland.
Plants (Basel). 2020 Apr 13;9(4):498. doi: 10.3390/plants9040498.
L. is a high-value herb and a source of important compounds that include phenolics, triterpenoid saponins, and essential oils. The present report indicates successful micropropagation of this species. In our study, medium supplemented with BAP 2.0 mg/L, IAA 1.0 mg/L, and GA 1.0 mg/L was found to be the most suitable for long-term culture and for effective proliferation, irrespective of the passage number. Roots induction, without basal callus formation, was observed when individual microshoots were placed on Murashige & Skoog medium augmented with auxin, and formation was the most advantageous in the presence of NAA alone or when combined with IAA or IBA. The encapsulated propagules were tested for their capability to endure different storage periods under low temperature. Therefore, we developed an efficient method for synseeds production by encapsulation of axillary buds in the sodium alginate matrix, storage for 2, 4, and 6 months, as well as the regeneration process. The maximum regeneration rate of 74% ± 2.72% was observed for axillary buds encapsulated in 4% sodium-alginate complexed with 300 mM calcium chloride after 2 months of storage at low temperature. This is the first report on micropropagation and somatic seeds production.
L.是一种高价值草药,也是包括酚类、三萜皂苷和精油在内的重要化合物的来源。本报告表明该物种的微繁殖取得成功。在我们的研究中,发现添加2.0 mg/L BAP、1.0 mg/L IAA和1.0 mg/L GA的培养基最适合长期培养和有效增殖,与传代次数无关。当将单个微芽置于添加了生长素的Murashige & Skoog培养基上时,观察到无根状愈伤组织形成的生根诱导,且单独存在NAA或与IAA或IBA组合时生根最为有利。对包囊繁殖体在低温下耐受不同储存期的能力进行了测试。因此,我们开发了一种通过将腋芽包囊在海藻酸钠基质中、储存2、4和6个月以及再生过程来生产人工种子的有效方法。在低温储存2个月后,观察到包囊在与300 mM氯化钙络合的4%海藻酸钠中的腋芽的最大再生率为74%±2.72%。这是关于微繁殖和体细胞种子生产的第一份报告。