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A simple procedure for the micropropagation of Cistus incanus L. from aseptic seedlings and ex vitro plants

机译:从无菌幼苗和离体植物中微繁殖Cistus incanus L.的简单程序

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摘要

In the framework of research into the association between C. incanus and its symbiont Tuber melanosporum, a procedure for micropropagating the host plant was required. For seed germination, the use of 10% NaOCl or concentrated sulfuric acid allowedhigh germinability on 0.6% water agar. Transfer to a Woody Plant Medium plus 0.5 mg/litre-1 indolebutyric acid [IBA] for two months resulted in uniform aseptic seedlings. For apical and nodal explants from outdoor plants, a mild disinfection procedure followed by application of antibiotics yielded cultures with bud growth. The best medium for multiplication of apical and nodal segments was MS+0.1 mg litre-1 benzyladenine, while a good medium for rooting was MS unsupplemented with plant growth regulators. To assure acclimatization, rooted plantlets should be allowed to develop canopy and roots for at least 8 weeks prior to potting. A high survival rate was recorded when plants were covered for 2 weeks. Acclimatized plants have been successfully colonized with T. melanosporum.
机译:在对印度隐孢子虫及其共生块茎黑色素菌之间的关联进行研究的框架中,需要一种微繁殖宿主植物的程序。对于种子发芽,使用10%NaOCl或浓硫酸可在0.6%的水琼脂上实现高发芽性。转移到加有0.5 mg / L-1吲哚丁酸[IBA]的木本植物培养基中两个月,得到均匀的无菌幼苗。对于来自室外植物的顶端和节点外植体,温和的消毒程序随后应用抗生素即可产生带有芽生长的培养物。根尖和节段繁殖的最佳培养基是MS + 0.1 mg litre-1苄腺嘌呤,而生根的最佳培养基是MS不添加植物生长调节剂的培养基。为确保适应环境,盆栽前至少8周应允许生根的小植株生长冠层和根。当植物覆盖2周时,记录到较高的成活率。驯化的植物已成功地用黑毛孢菌定殖。

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