首页> 外文期刊>The Journal of Horticultural Science & Biotechnology >In vitro leaf-shoot regeneration and somaclone selection for sodium chloride tolerance in quince and pear.
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In vitro leaf-shoot regeneration and somaclone selection for sodium chloride tolerance in quince and pear.

机译:木瓜和梨的离体叶片再生和索莫克隆选择耐氯化钠。

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摘要

The aims of this research were to set up in vitro procedures to obtain NaCl-tolerant somaclones of the quince rootstock 'BA 29' and pear cvs. 'Conference' and 'Abbe Fetel', and to evaluate the selection-pressure effect of NaCl in the regeneration medium. Shoot regeneration was induced in leaf-explants on media enriched with 5.4 micro M alpha -naphthalene acetic acid (NAA), 4.5 micro M thidiazuron (TDZ) and variable concentrations of NaCl (0, 3 or 5 g l-1 for pear; 0, 5 or 10 g l-1 for quince). Regeneration was strongly negatively affected by the presence of salt in the culture media. It was inhibited by 5 g l-1 NaCl, and completely prevented by 10 g l-1 NaCl in 'BA 29'. No regeneration was obtained from 'Abbe Fetel' leaf explants, even at 5 g l-1 NaCl. Moreover, the few 'Abbe Fetel' and 'Conference' shoots regenerated at 3 and 5 g l-1 NaCl, respectively, could not survive transplantation. All shoots derived from each adventitious shoot were referred to as a somaclone and labelled with two numbers, the first referring to the NaCl concentration and the second being a progressive number. All were sub-cultured repeatedly on a standard medium before testing their salt tolerance in vitro. Somaclones and controls (shoots obtained by conventional micropropagation) were compared for proliferation, growth and rooting on standard and NaCl-enriched media (5 and 10 g l-1 NaCl for proliferation; 5 and 7.5 g l-1 NaCl for rooting). Shoot proliferation rate (PR), shoot relative growth rate [RGR=(final weight - initial weight)/initial weight], and proportion (%) of rooting of somaclones and controls were significantly reduced by salt in 'BA 29' and in the two pear cultivars, although great variability was found between somaclones regenerated at each NaCl concentration. No shoot proliferation occurred at the highest NaCl concentration. Most somaclones of 'BA 29' had higher shoot PR and RGR than controls on standard medium, and the presence of 5 g l-1 NaCl in the regeneration (induction, expression) media increased proliferation and growth across all NaCl concentrations. Moreover, a few somaclones regenerated at 5 g l-1 NaCl showed better root development on salt-enriched media. The most promising 'BA 29' somaclone seemed to be 5-3, whose RGR remained high in up to 10 g l-1 NaCl, and which showed a high proportion of rooting (75%) and root development at 5 g l-1 NaCl. Also notable for its slightly higher shoot PR, RGR and better rooting on 5 g l-1 NaCl-enriched media, was somaclone 5-4. Among the pears, most 'Abbe Fetel' somaclones (all from regeneration media lacking NaCl) grew and proliferated more than the controls across all NaCl concentrations. These differences were significant for somaclone 0-8. Some somaclones produced more and longer roots than controls on standard medium, while only a few very short roots were found in a few somaclones and none in the controls on NaCl-enriched media. Many 'Conference' somaclones had lower shoot PR than the controls up to 5 g l-1 NaCl, especially those regenerated in the absence of salt. Greater proliferation and growth were observed for somaclone 3-5, and better growth for somaclone 3-10 in the presence of salt. Moreover, some other somaclones regenerated in the presence of salt (i.e., 3-3, 3-5, 3-6 and, especially, 3-8) showed interesting rooting behaviour on NaCl-enriched media. Across all combinations, 'Conference' somaclone 3-5 seemed the most tolerant, with good proliferation, growth and rooting on NaCl-enriched media. Thus, the present results suggest that the regeneration-selection protocols described here can be useful for inducing somaclonal variation and NaCl tolerance in pear and quince, and indicate a positive NaCl selection-pressure effect in obtaining in vitro NaCl-tolerant variants of 'BA 29' and of 'Conference' pear..
机译:这项研究的目的是建立体外程序,以获得木瓜砧木“ BA 29”和梨cvs的耐NaCl的体细胞克隆。 “会议”和“阿贝·费特尔”,并评估再生介质中氯化钠的选择压力效应。在富含5.4 micro Mα-萘乙酸(NAA),4.5 micro M噻唑隆(TDZ)和可变浓度的NaCl(梨为0、3或5 g l-1)的培养基上,在叶片外植体中诱导嫩芽再生。 ,木瓜5或10 g l-1)。培养基中盐的存在对再生产生了极大的负面影响。在'BA 29'中,它被5 g l-1 NaCl抑制,并被10 g l-1 NaCl完全阻止。即使从5 g l-1 NaCl中也无法从“ Abbe Fetel”叶片外植体获得再生。此外,分别在3 g和5 g l-1 NaCl再生的少数'Abbe Fetel'和'Conference'芽不能存活。来自每个不定芽的所有芽均被称为索马克克隆,并用两个数字标记,第一个是指NaCl浓度,第二个是递进数字。在体外测试其耐盐性之前,将所有这些在标准培养基上重复传代培养。比较生长激素和对照(通过常规微繁殖获得的芽)的增殖,生长和在标准和富含NaCl的培养基上的生根(5和10 g -1 NaCl的增殖; 5和7.5 g -1 NaCl的生根)。在'BA 29'和'BA 29'中,盐分显着降低了芽的增殖率(PR),芽的相对生长率[RGR =(最终重量-初始重量)/初始重量],以及对照的生根菌和对照生根的比例(%)。两个梨品种,尽管在每个NaCl浓度下再生的somaclone之间存在很大的差异。在最高的NaCl浓度下,没有芽增殖。在标准培养基上,大多数'BA 29'的体细胞克隆的芽PR和RGR高于对照,并且在再生(诱导,表达)培养基中存在5 g l-1 NaCl可以在所有NaCl浓度下增加增殖和生长。此外,在5 g l-1 NaCl处再生的一些松果克隆在富含盐的培养基上显示出更好的根系发育。最有前途的'BA 29'somaclone似乎是5-3,在10 g l-1 NaCl中其RGR仍然很高,并且在5 g l-1时显示出高比例的生根(75%)和根系发育氯化钠Somaclone 5-4还因其较高的芽PR,RGR和在5 g l-1 NaCl富集的培养基上更好的生根而著名。在梨中,大多数“ Abbe Fetel”体细胞无性繁殖体(均来自缺乏NaCl的再生培养基)在所有NaCl浓度下均比对照生长和增殖更多。这些差异对于索马克隆0-8而言是显着的。与标准培养基上的对照相比,某些茄基克隆产生的根更多且更长,而在少数茄基克隆中,仅发现了极短的根,而在富含NaCl的培养基上的对照中未发现根。许多“会议型”松果体的芽PR均低于对照,最高至5 g l-1 NaCl,尤其是那些在无盐条件下再生的芽。在盐存在下,索马克隆3-5观察到更大的增殖和生长,索马克隆3-10观察到更好的生长。此外,在盐的存在下(即3-3、3-5、3-6,尤其是3-8)再生的一些其他松果克隆在富含NaCl的培养基上表现出有趣的生根行为。在所有组合中,“会议”索马克隆3-5似乎是最耐受的,具有良好的增殖,生长和在富含NaCl的培养基上生根的能力。因此,目前的结果表明,本文所述的再生选择方案可用于诱导梨和木瓜的体细胞克隆变异和NaCl耐性,并且在获得'BA 29的体外NaCl耐性变体中表明具有积极的NaCl选择压力作用。 ”和“会议”梨。

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