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首页> 外文期刊>Annals of Biological Research >Plant regeneration and cold preservation of Eureka lemon (Citrus limon [L.]Burm. f. [a??Eurekaa??]) by using sodium alginate-encapsulated shoot tips
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Plant regeneration and cold preservation of Eureka lemon (Citrus limon [L.]Burm. f. [a??Eurekaa??]) by using sodium alginate-encapsulated shoot tips

机译:使用海藻酸钠包裹的芽尖进行尤里卡柠檬(柑桔柠檬[L.] Burm。f。[a ?? Eurekaa ??])的植物再生和冷藏

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In this study, in vitro-derived shoot tips of Eureka lemon (Citrus limon [L.] Burm. f. [‘Eureka’]) were encapsulated in various concentrations of sodium alginate (Na-alginate) (3%, 4%, and 5%) dissolved in liquid MS medium supplemented with 50 g l−1 sucrose + 10 mg l−1 BAP + 1 mg l−1 NAA (SA1); liquid MS medium supplemented with 50 g l−1 sucrose (SA2) and distilled water with 50 g l−1 sucrose (SA3). Encapsulated and non-encapsulated shoot tips were stored at 4°C for different storage periods (1-8 weeks). Alginate matrix of 4% Na-alginate and 100 mM CaCl2·2H2O was found to be suitable for the production of alginate beads. Shoots obtained by root induction were transferred to MS medium containing 5 mg l−1 IBA. Encapsulated shoot tips on SA1 treatment were viable (50%) after 3 weeks of cold storage while non-encapsulated shoot tips lost their viability completely after 3 weeks. Addition of MS nutrient and hormones to the alginate matrix significantly affected the regeneration of shoot tips. The survival rate of shoot tips encapsulated in SA1 after 4 weeks was 30% while that of encapsulated in SA2 was 20%. However, shoot tips encapsulated in SA3 lost their viability. Conversion frequencies of shoot tips encapsulated with SA1 in MS medium with hormones and without hormones were 60% and 30%, respectively, after 1 week. Thus, the current synthetic seed technology could be useful in large-scale propagation and short-term conservation of citrus.
机译:在这项研究中,以各种浓度的海藻酸钠(海藻酸钠)(3%,4%, 5%)溶解在补充有50 gl-1蔗糖+ 10 mg -1 BAP + 1 mg -1 NAA(SA1)的液态MS培养基中;补充有50 g -1蔗糖(SA2)和50 g 1-1蔗糖(SA3)的蒸馏水的液态MS培养基。封装和未封装的芽尖在4°C下保存不同的保存时间(1-8周)。发现4%藻酸钠和100mM CaCl 2·2H 2 O的藻酸盐基质适合于藻酸盐珠的生产。将通过根诱导获得的芽转移到含有5 mg 1-1 IBA的MS培养基中。冷藏3周后,经SA1处理的胶囊化芽尖可以存活(50%),而未胶囊化的芽尖在3周后完全丧失了活力。在藻酸盐基质中添加MS营养素和激素会显着影响芽尖的再生。包埋于SA1中的芽梢的存活率在4周后为30%,而包埋于SA2中的则为20%。但是,封装在SA3中的芽尖失去了生存能力。 1周后,在含有激素和不含激素的MS培养基中,用SA1封装的梢的转换频率分别为60%和30%。因此,当前的合成种子技术可用于柑橘的大规模繁殖和短期保存。

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