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首页> 外文期刊>African Journal of Biotechnology >Establishment of an efficient callus induction and plant regeneration system in some wheat (Triticum aestivum L.) cultivars grown in Sudan
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Establishment of an efficient callus induction and plant regeneration system in some wheat (Triticum aestivum L.) cultivars grown in Sudan

机译:在苏丹种植的一些小麦(Triticum aestivum L.)品种中建立有效的愈伤组织诱导和植物再生系统

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A procedure for callus induction and plant regeneration was developed for wheat (Triticum aestivum)?cultivars grown in Sudan. Mature embryos of cultivar Khaleefa removed from surface sterilized seeds were used as explants. For callus induction, explants were cultured on Murashige and Skoog medium (MS) supplemented with different levels (1.5 to 4.0 mg/l) of 2,4-dichlorophenoxy acetic acid (2,4-D), indole-3- butyric acid (IBA) and indole-3- acetic acid (IAA). After 4 weeks of culture, the highest callus fresh weight (0.05 ± 0.01 g) was obtained on MS medium supplemented with 2.0 mg/L of 2,4-D. For shoot regeneration, the developed calli were transferred to MS medium without growth regulators or with different levels (0.1 to 3.0 mg/l) of 5-phenylcarbamoylamino-1,2,3-thiadiazole (thidiazuron) (TDZ), benzyladenine (BA) and kinetin (KN) alone or in combination with 2.0 mg/L of 2,4-D. After 6 weeks of culture, the best result for regeneration percentage (40%) was obtained on MS medium without growth regulators. Callus derived shoots were rooted most effectively in half-strength MS medium without or with different levels of IBA. To determine the genotypic effect, the developed procedure was used to evaluate the regeneration ability of other 5 Sudanese wheat cultivars. Significant differences were observed between genotypes for plant regeneration ability, indicating that these criteria are genotype dependent. The acclimatized regenerated plants were morphologically uniform with normal leaf shape and growth pattern under greenhouse conditions.
机译:针对苏丹种植的小麦(Triticum aestivum)品种开发了诱导愈伤组织和植物再生的方法。从表面消毒种子中取出的品种Khaleefa的成熟胚用作外植体。为了诱导愈伤组织,将外植体在补充了不同水平(1.5至4.0 mg / l)的2,4-二氯苯氧基乙酸(2,4-D),吲哚-3-丁酸(1.5-4.0 mg / l)的Murashige和Skoog培养基(MS)上进行培养。 IBA)和吲哚-3-乙酸(IAA)。培养4周后,在补充有2.0 mg / L的2,4-D的MS培养基上获得最高的愈伤组织鲜重(0.05±0.01 g)。为了进行芽再生,将发育的愈伤组织转移至没有生长调节剂或具有不同水平(0.1至3.0 mg / l)的5-苯基氨基甲酰基氨基-1,2,3-噻二唑(噻二唑)(TDZ),苄基腺嘌呤(BA)的MS培养基中和激动素(KN)单独或与2.0 mg / L的2,4-D组合使用。培养6周后,在没有生长调节剂的MS培养基上获得了最佳的再生百分率结果(40%)。愈伤组织衍生的芽最有效地扎根于半强度MS培养基中,该培养基不含或不含不同的IBA。为了确定基因型效应,使用开发的程序评估了其他5个苏丹小麦品种的再生能力。观察到植物再生能力的基因型之间存在显着差异,表明这些标准是基因型依赖性的。在温室条件下,适应的再生植物在形态上是均匀的,具有正常的叶片形状和生长方式。

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