Lualon Wanwimon, De-Eknamkul Wanchai, Tanaka Hiroyuki, Shoyama Yukihiro, Putalun Waraporn
Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen, 40002, Thailand.
Z Naturforsch C J Biosci. 2008 Jan-Feb;63(1-2):96-100. doi: 10.1515/znc-2008-1-218.
An efficient in vitro method for multiple shoot bud induction and regeneration has been developed in Artemisia annua L. using leaf and stem explants in various concentrations and combinations of plant growth regulators to evaluate the frequency of regeneration. The sources of explants as well as plant growth regulators in the medium were found to influence the multiple shoot induction. The result shows that the stem segment cultured on Murashige and Skoog (MS) medium supplemented with 0.1 mg/l thidiazuron (TDZ) gave a perfect shoot formation (100%) and good shoot multiplication (57 shoots/explant) after 2 weeks of culture. Healthy regenerated shoots were elongated and rooted in MS medium without hormones. The artemisinin content in plants regenerated from stem explants using 0.1 mg/l TDZ was (3.36 +/- 0.36) microg/mg dry weight and two-fold higher than that of in vitro grown plants of the same age [(1.73 -/+ 0.23) microg/mg DW]. This system exhibited a potential for a rapid propagation of shoots from the stem explant and makes it possible to develop a clonal propagation of A. annua.
利用青蒿的叶片和茎段外植体,在不同浓度和组合的植物生长调节剂条件下,已开发出一种高效的体外多芽诱导和再生方法,以评估再生频率。研究发现,外植体来源以及培养基中的植物生长调节剂会影响多芽诱导。结果表明,在添加了0.1毫克/升噻苯隆(TDZ)的Murashige和Skoog(MS)培养基上培养的茎段,培养2周后形成了完美的芽(100%),且芽增殖良好(每个外植体57个芽)。健康的再生芽在无激素的MS培养基中伸长并生根。使用0.1毫克/升TDZ从茎外植体再生的植株中,青蒿素含量为(3.36±0.36)微克/毫克干重,比同龄体外生长植株的青蒿素含量[(1.73±0.23)微克/毫克干重]高出两倍。该系统显示出从茎外植体快速繁殖芽的潜力,并使得青蒿的克隆繁殖成为可能。