Sahoo Y, Chand P K
Plant Tissue and Cell Culture Facility, Post-Graduate Department of Botany, Utkal University, Bhubaneswar-751004, Orissa, India, , , , , , IN.
Plant Cell Rep. 1998 Dec;18(3-4):301-307. doi: 10.1007/s002990050576.
A protocol is described for rapid and large-scale propagation of the woody aromatic and medicinal shrub Vitex negundo by in vitro culture of nodal segments from mature plants. Of the three different cytokinins - N-benzyladenine (BA), kinetin, and thidiazuron - evaluated as supplements to Murashige and Skoog (MS) medium, BA at an optimal concentration of 2.0 mg/l was most effective in inducing bud break. Although callus-free multiple-shoot formation was a function of cytokinin activity alone, faster bud break coupled with an enhanced frequency of shoot development (92%) and internode elongation were dependent on the synergistic influence of gibberellic acid (GA) when used at an optimal concentration (0.4 mg/l) along with BA (2.0 mg/l). The frequency of shoot proliferation was markedly influenced by the explanting season. By repeated subculturing of nodal segments harvested from the in vitro-formed axenic shoots on MS containing 1.0 mg/l BA and 0.4 mg/l GA, prolific shoot cultures free from proximal callusing and showing a high-frequency multiplication rate were established. The percentage shoot multiplication (98-100%) as well as the number of shoots per node (six to eight) were highest during the first three culture passages, after which there was a gradual decline in shoot development. Rooting was best induced (94%) in shoots excised from proliferated shoot cultures on half-strength MS medium augmented with an optimal combination of indole-3-acetic acid and indole-3-butyric acid each at 1.0 mg/l. Vermi-compost was the most suitable planting substrate for hardening inside a plant growth chamber and its use ensured high-frequency survival (93%) of regenerated plants prior to outdoor transfer. Micropropagated plants established in garden soil were uniform and identical to the donor plant with respect to growth characteristics as well as vegetative and floral morphology.
本文描述了一种通过对成熟植株的节段进行离体培养,快速大规模繁殖木本芳香药用灌木黄荆的方法。在作为Murashige和Skoog(MS)培养基补充剂评估的三种不同细胞分裂素——N-苄基腺嘌呤(BA)、激动素和噻苯隆中,最佳浓度为2.0 mg/l的BA在诱导芽萌发方面最有效。虽然无愈伤组织的多芽形成仅取决于细胞分裂素的活性,但当与BA(2.0 mg/l)一起以最佳浓度(0.4 mg/l)使用赤霉素(GA)时,更快的芽萌发以及芽发育频率的提高(92%)和节间伸长取决于GA的协同作用。芽增殖频率受外植体季节的显著影响。通过在含有1.0 mg/l BA和0.4 mg/l GA的MS培养基上对离体形成的无菌芽收获的节段进行反复继代培养,建立了无近端愈伤组织且具有高频增殖率的多芽培养物。在前三次培养传代期间,芽增殖百分比(98 - 100%)以及每个节点的芽数(六到八个)最高,此后芽发育逐渐下降。在添加了各自浓度为1.0 mg/l的吲哚-3-乙酸和吲哚-3-丁酸最佳组合的半强度MS培养基上,从增殖芽培养物中切下的芽诱导生根效果最佳(94%)。蚯蚓堆肥是植物生长室内驯化最合适的种植基质,使用它可确保再生植株在室外移栽前具有高频成活率(93%)。在花园土壤中定植的微繁殖植株在生长特性以及营养和花形态方面与供体植株一致且相同。