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首页> 外文期刊>African Journal of Biotechnology >Evaluation of somatic embryogenesis and plant regeneration in tissue culture of ten sorghum (Sorghum bicolor L.) genotypes
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Evaluation of somatic embryogenesis and plant regeneration in tissue culture of ten sorghum (Sorghum bicolor L.) genotypes

机译:十个高粱(Sorghum bicolor L.)基因型组织培养中体细胞胚发生和植物再生的评估

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摘要

Optimization of tissue culture conditions for Sorghum bicolor L. through somatic embryogenesis from immature embryos is important for the genetic manipulation and improvement of this agronomically valuable crop. In an attempt to develop a successfully reproducible in vitro regeneration protocol for a group of diverse sorghum genotypes, 10 sorghum lines including locally adapted and commercially important elite genotypes were assessed for their regeneration potential on different culture media–containing adequate growth regulators combinations. The maximum response of embryogenic callus induction was obtained from explants cultured on Murashige and Skoog (MS) medium supplemented with 1.5 mgL-1 of 2,4-dichlorophenoxyacetic acid (2,4-D) and 0.7 mgL-1 L-proline. The addition of kinetin to the MS-based culture media had a negative effect on the formation of embryogenic calli. The results reveal that embryogenic callus formation and regeneration were highly genotype dependent. The line LG3 revealed the highest mean number of embryogenic callus (47.5 ± 6.0%) across the media tested. On the other hand, SPP462 was the least responsive (13.4 ± 3.3%) to embryogenic callus induction. The regeneration percentage of the different genotypes ranged from zero to 22.1%. The lines LG3, LG4, Dorado, SPGM94021 and SPMD94001 succeeded to form shoots on the three tested regeneration media. Nevertheless, the genotypes LG8 and TX2794 produced shoots on only two out of the three media. Three lines failed to regenerate on any of the tested media. Adding 0.5 mgL-1 naphthalene acetic acid and 0.5 mgL-1 of indole-3-butyric acid (IBA) did not enhance the root induction. Regenerated shoots developed into normal mature plants. Regeneration of sorghum genotypes could be improved through the use of different auxins and cytokinins in callus induction and shoot formation media. The auxin, 2,4-D was critical for the induction of embryogenic calli. However, the addition of the cytokinin (kinetin) adversely affected the formation of embryogenic callus. On the other hand, the shoot induction was more influenced by the addition of indole-3-acetic acid (IAA), 6-benzylaminopurine (BA) and thidiazuron (TDZ).
机译:通过从未成熟胚的体细胞胚发生优化高粱双色组织培养条件对于遗传操纵和改良这种具有农业价值的农作物非常重要。为了为一组不同的高粱基因型开发成功的可再生体外再生方案,对包括本地适应的和商业上重要的精英基因型在内的10个高粱品系在不同培养基上的再生潜力进行了评估,这些培养基含有足够的生长调节剂组合。从在补充有1.5 mgL-1的2,4-二氯苯氧基乙酸(2,4-D)和0.7 mgL-1 L-脯氨酸的Murashige和Skoog(MS)培养基上培养的外植体获得胚发生愈伤组织诱导的最大响应。将激动素添加到基于MS的培养基中对胚性愈伤组织的形成具有负面影响。结果表明,胚性愈伤组织的形成和再生高度依赖基因型。 LG3品系显示在所有测试培养基中,最高的胚性愈伤组织平均数(47.5±6.0%)。另一方面,SPP462对胚性愈伤组织的诱导反应最少(13.4±3.3%)。不同基因型的再生百分比范围从零到22.1%。 LG3,LG4,Dorado,SPGM94021和SPMD94001等品系成功在三种经过测试的再生培养基上形成芽。然而,基因型LG8和TX2794仅在三种培养基中的两种上产生芽。三行无法在任何经过​​测试的介质上再生。加入0.5 mgL-1萘乙酸和0.5 mgL-1吲哚-3-丁酸(IBA)不会增强根诱导。再生的嫩芽发育成正常的成熟植物。通过在愈伤组织诱导和芽形成培养基中使用不同的生长素和细胞分裂素,可以提高高粱基因型的再生。 2,4-D生长素对于诱导胚性愈伤组织起关键作用。但是,添加细胞分裂素(激肽)会不利地影响胚性愈伤组织的形成。另一方面,加入吲哚-3-乙酸(IAA),6-苄基氨基嘌呤(BA)和噻二唑酮(TDZ)对芽诱导的影响更大。

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