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Shoot Apex Culture of Dormant Buds in Chestnut

机译:射击栗子休眠芽的顶点文化

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Chestnuts (Castanea spp.) can be propagated by tissue culture methods such as meristem tip culture, shoot tip culture and bud culture. However, some limiting factors prevent using these methods extensively. For example, the explant collection periods of these methods are short, and the collection time is critical. In addition, shoot formation ratios of explants on the initial media and survival of these shootlets thereafter are generally low due to factors such as infection, browning, and vitrification. In this study the shoot apex of the dormant buds were used as the explants source for the first time. By use of this method the explant collection period was much longer and the mass multiplication probability increased. Three chestnut cultivars native to Turkey -'Sarraslama', 'Osmanoglu' and 'Haclomer' Castanea sativa Mill. -were used in the study in two years of experiments 2007 and 2008. Two main media were used as initial to obtain shootlets: MS (I/2×NH4NO3 and KNO3) and DKW (Driver-Kuniyuki walnut medium). In multiplication step MS (1/2×NH4NO3 medium was used with 0.5, 1.0, 1.5 mg/L BAP concentrations and in rooting MS (I/2×NH4NO3 with 1.0 and 2.0 mg/L IBA concentrations were used. Shootlet formation from the explants in 2008 was higher (66.6695.45%) than in 2007 (42.00-75.00%). MS (1/2×NH4NO3 and KNO3)medium has given successful results in this respect. Therefore it can be recommended as a growing medium. The multiplication coefficient varied between 3.12 to 3.57 in 2007 and 3.95 to 4.76 in 2008 according to the cuitivars. Rooting of the shootlets was difficult, and no rooted shootlet was obtained. However the experiment is now being continued, and new rooting media will be tested. The results obtained from this study showed that this method can be efficiently used in the mass multiplication of chestnuts.
机译:栗子(Castanea SPP)可以通过组织培养方法繁殖,例如营销尖端培养,芽尖培养和芽培养。然而,一些限制因素可以广泛使用这些方法。例如,这些方法的探测突然的收集周期短,并且收集时间至关重要。此外,由于感染,褐变和玻璃化等因素,初始介质和这些射击物的存活植物的芽形成比例通常是低的。在这项研究中,首次使用休眠芽的射击顶点作为外植体来源。通过使用这种方法,外植体的收集期更久,质量乘法概率增加。三个栗色品种原产于土耳其-'sarraslama','osmanoglu'和'haclomer'castanea sativa mill。 - 在2007和2008年两年的实验中使用的研究。两个主要媒体被用作初始才能获得霰弹球:MS(I / 2×NH4NO3和KNO3)和DKW(驱动程序 - kuniyuki核桃介质)。在倍增步骤中,使用0.5,1 / 2×NH 4 NO 3培养基,使用0.5,1.0,1.5mg / L培训浓度和生根MS(具有1.0和2.0mg / L IBA浓度的I / 2×NH 4 NO 3。从中拍摄2008年的外植体比2007年更高(66.6695.45%(42.00-75.00%)。MS(1/2×NH4NO3和KNO3)培养基在这方面已经成功地获得了成功的结果。因此,可以推荐作为不断增长的媒体。根据网卡赛,2007年和2008年的3.12至3.57之间的倍增系数在2008年的3.95至4.76之间。拍摄的根本难以获得,并且没有获得根的射击。然而,现在继续进行实验,并测试新的生根培养基。从该研究中获得的结果表明,该方法可以有效地用于栗子的质量倍增。

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