Estabrooks Tammy, Browne Robin, Dong Zhongmin
Department of Biology, Saint Mary's University, Halifax, Nova Scotia, Canada.
Plant Cell Rep. 2007 Feb;26(2):153-60. doi: 10.1007/s00299-006-0231-5. Epub 2006 Sep 14.
Somatic embryogenesis (SE) offers vast potential for the clonal propagation of high-value roses. However, some recalcitrant cultivars unresponsive to commonly employed SE-inducing agents and low induction rates currently hinder the commercialization of SE technology in rose. Rose SE technology requires improvement before it can be implemented as a production system on a commercial scale. In the present work, we assessed 2,4,5-trichlorophenoxyacetic acid (2,4,5-T), a synthetic auxin not previously tested in rose, for its effectiveness to induce SE in the rose cultivar "Livin' Easy" (Rosa sp.). We ran a parallel comparison to the commonly used 2,4-dichlorophenoxyacetic acid (2,4-D). We tested each auxin with two different basal media: Murashige and Skoog (MS) basal medium and woody plant medium (WPM). MS medium resulted in somatic embryo production, whereas WPM did not. 2,4,5-T induced SE over a greater concentration range than 2,4-D's and resulted in significantly greater embryo yields. 2,4,5-T at a concentration of 10 or 25 microM was better for embrygenic tissue initiation than 2,4,5-T at 5 microM. Further embryo development occurred when the tissue was transferred to plant growth regulator (PGR) free medium or media with 40% the original auxin concentration. However, the PGR-free medium resulted in a high percentage of abnormal embryos (32.31%) compared to the media containing auxins. Upon transfer to germination medium, somatic embryos successfully converted into plantlets at rates ranging from 33.3 to 95.2%, depending on treatment. Survival rates 3 months ex vitro averaged 14.0 and 55.6% for 2,4-D- and 2,4,5-T-derived plantlets, respectively. Recurrent SE was observed in 60.2% of the plantlets growing on germination medium. This study is the first report of SE in the commercially valuable rose cultivar 'Livin' Easy' (Rosa sp.) and a suitable methodology was developed for SE of this rose cultivar.
体细胞胚胎发生(SE)为高价值玫瑰的克隆繁殖提供了巨大潜力。然而,一些对常用SE诱导剂无反应的顽固品种以及目前较低的诱导率阻碍了SE技术在玫瑰中的商业化。玫瑰SE技术在能够作为商业规模的生产系统实施之前需要改进。在本研究中,我们评估了2,4,5-三氯苯氧乙酸(2,4,5-T),一种之前未在玫瑰中测试过的合成生长素,对玫瑰品种“Livin' Easy”(Rosa sp.)诱导SE的有效性。我们与常用的2,4-二氯苯氧乙酸(2,4-D)进行了平行比较。我们用两种不同的基础培养基测试了每种生长素:Murashige和Skoog(MS)基础培养基以及木本植物培养基(WPM)。MS培养基产生了体细胞胚胎,而WPM没有。2,4,5-T在比2,4-D更大的浓度范围内诱导SE,并且产生了显著更高的胚胎产量。浓度为10或25微摩尔的2,4,5-T比5微摩尔的2,4,5-T更有利于胚性组织的起始。当组织转移到不含植物生长调节剂(PGR)的培养基或含有原始生长素浓度40%的培养基中时,会发生进一步的胚胎发育。然而,与含有生长素的培养基相比,不含PGR的培养基产生了高比例的异常胚胎(32.31%)。转移到萌发培养基后,体细胞胚胎根据处理不同以33.3%至95.2%的速率成功转化为植株。2,4-D和2,4,5-T来源的植株在离体3个月后的存活率分别平均为14.0%和55.6%。在生长于萌发培养基上的60.2%的植株中观察到了反复的SE。本研究是关于具有商业价值的玫瑰品种“Livin' Easy”(Rosa sp.)中SE的首次报道,并为该玫瑰品种的SE开发了合适的方法。