元多肽诱导番茄(Solanum lycopersicum L.)不同外植体的嫩枝器官发生和植株再生

Vasudha Marapaka, Kranthikumar Gande, Vaishnavi Anumula, Venkataiah Peddaboina
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摘要

番茄(Solanum lycopersicum L.)是茄科植物中最重要的蔬菜作物。与其他嘌呤类细胞分裂素(如 6-苄基氨基嘌呤(BAP)和 Kinetin(KIN))相比,2.0 毫克/升的不同浓度的偏东莨菪碱(mT)能从番茄的不同外植体中产生最多的芽。添加 0.1 毫克/升的吲哚-3-乙酸(IAA)和 2.0 毫克/升的 mT 后,从两个番茄栽培品种基因型中获得的子叶(18.6)比下胚轴(13.8)和叶片(11.9)外植体产生的芽数量最多。与 ArkaRakshak(AR)番茄栽培品种相比,ArkaSamrat(AS)栽培品种的诱导反应更好,芽的产量最高。从芽簇中分离出芽,然后将其培养到含 1.0 毫克/升 IAA 的生根培养基中,结果发现该浓度是两种番茄栽培品种诱导生根的最合适浓度。完整植株移至温室后,AS 和 AR 栽培品种的成活率分别为 93% 和 89%。再生植株的形态与母株没有任何差异。通过农杆菌介导的转化和使用基因组编辑工具生成基因组靶向突变体,这种植物再生系统在遗传改良方面是可行的。
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Meta-Topolin Induced Shoot Organogenesis and Plant Regeneration from Different Explants of Tomato (Solanum lycopersicum L.)
Tomato (Solanum lycopersicum L.) is the most prominent vegetable crop in the Solanaceae family. The varying concentrations of meta-Topolin (mT) evaluated at 2.0 mg/l generated the highest number of shoots than other purine-type cytokinins, like 6-Benzylaminopurine (BAP) and Kinetin (KIN) from diverse explants of tomato. The addition of Indole 3-acetic acid (IAA) at 0.1 mg/l with 2.0 mg/l mT triggered the production of the optimum number of shoots (18.6) from cotyledon than hypocotyl (13.8) and leaf (11.9) explants obtained from two genotypes of tomato cultivars. The ArkaSamrat (AS) cultivar was observed to be better responsive for induction and maximum production of shoots than the ArkaRakshak (AR) cultivar of tomato. The shoots were separated from the clusters of shoots and then cultured to the rooting medium containing IAA at 1.0 mg/l, which was found to be the most suitable concentration for induction rooting in both tomato cultivars. The complete plants were shifted to the greenhouse and recorded 93% and 89% survival rates in AS and AR cultivars, respectively. The regenerated plants did not show any variation in morphology with their mother plants. This plant regeneration system can be feasible for genetic improvement through the Agrobacterium-mediated transformation and generation of genome-targeted mutants using genome editing tools.
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