Fatima Nigar, Ahmad Naseem, Ahmad Iqbal, Anis Mohammad
Department of Agricultural Microbiology, Aligarh Muslim University, Aligarh, 202 002, India,
Appl Biochem Biotechnol. 2015 Sep;177(1):118-36. doi: 10.1007/s12010-015-1732-x. Epub 2015 Jul 8.
An improved and methodical in vitro shoot morphogenic approach through axillary bud multiplication was established in a drug yielding plant, Withania somnifera L. Effects of plant growth regulators [6-benzyladenine (BA), kinetin (Kin), 2-isopentenyladenine (2iP), and thidiazuron (TDZ)] either singly or in combination with α-napthalene acetic acid (NAA), indole-3-butyric acid (IBA), and indole-3-acetic acid (IAA) in Murashige and Skoog (MS) medium were tested. The highest regeneration frequency (90 %) with optimum number of shoots (32 ± 0.00)/explant were obtained on MS medium fortified with 2.5 μM 6-benzyladenine (BA) and 0.5 μM NAA and 30 g/l sucrose at pH 5.8. Among the tried TDZ concentrations, 0.5 μM resulted in maximum number of shoots (20.4 ± 0.40)/explant after 4 weeks of exposure. The proliferating shoot cultures established by repeated subculturing of the mother explants on the hormone-free medium produced the highest shoot number (29.4 ± 0.40) with shoot length (6.80 ± 0.12 cm)/explant at fourth subculture passage, which a decline in shoot proliferation was recorded. Different concentrations of NAA were tested for ex vitro rooting of microshoots. The maximum percentage of rooting 100 % with maximum roots (18.3 ± 0.1) was achieved in soilrite when basal portion of the microshoots were treated with 200 μM (NAA) for 15 min per shoot. The plantlets went through hardening phase in a growth chamber, prior to ex vitro transfer. The PCR-based single primer amplification reaction (SPAR) methods which include random amplified polymorphic DNA (RAPD) and direct amplification of minisatellite DNA (DAMD) markers has been used for assessment of genetic stability of micropropagated plantlets. No variation was observed in DNA fingerprinting patterns among the micropropagated and the donor plants illustrating their genetic uniformity.
在一种产药植物印度人参(Withania somnifera L.)中,通过腋芽增殖建立了一种改进的、系统的离体芽形态发生方法。测试了植物生长调节剂[6-苄基腺嘌呤(BA)、激动素(Kin)、2-异戊烯基腺嘌呤(2iP)和噻二唑素(TDZ)]单独或与α-萘乙酸(NAA)、吲哚-3-丁酸(IBA)和吲哚-3-乙酸(IAA)组合添加到Murashige和Skoog(MS)培养基中的效果。在添加2.5μM 6-苄基腺嘌呤(BA)、0.5μM NAA和30g/l蔗糖且pH为5.8的MS培养基上,获得了最高的再生频率(90%)和最佳的芽数(32±0.00个/外植体)。在所测试的TDZ浓度中,0.5μM的TDZ在处理4周后每个外植体产生的芽数最多(20.4±0.40个)。通过将母外植体在无激素培养基上反复继代培养建立的增殖芽培养物,在第四次继代培养时每个外植体产生的芽数最多(29.4±0.40个),芽长为(6.80±0.12cm),此时记录到芽的增殖有所下降。测试了不同浓度的NAA对微芽进行离体生根的效果。当微芽基部用200μM(NAA)处理,每株处理15分钟时,在土壤基质中生根率最高可达100%,根的数量最多(18.3±0.1条)。在移栽到体外之前,试管苗在生长室中经历了炼苗阶段。基于PCR的单引物扩增反应(SPAR)方法,包括随机扩增多态性DNA(RAPD)和小卫星DNA直接扩增(DAMD)标记,已用于评估微繁殖试管苗的遗传稳定性。在微繁殖植株和供体植株之间未观察到DNA指纹图谱的差异,表明它们具有遗传一致性。