低成本农化剂噻唑脲对抗旱树种白杨高频再生的影响。

Eliud Sagwa Mulanda, Mark Ochieng Adero, Nelson Onzere Amugune, Elijah Akunda, Jenesio I Kinyamario
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引用次数: 12

摘要

Melia volkensii Gurke是一种耐旱树种,原产于东非干旱和半干旱地区(ASALs),在农林业和可持续生计方面具有巨大但未充分利用的潜力。它的栽培受到传统繁殖方法困难的限制。作为唯一的植物生长调节剂(PGR), thidiazuron (TDZ)在植物组织培养中诱导再生的能力的充分利用受到高成本的阻碍。本研究测试了一种低成本农用化学品TDZ对沃肯氏芽孢杆菌体外繁殖的有效性。将成熟种子的合子胚培养在含有金泰化工有限公司农化TDZ 0 ~ 4mg /L的Gamborg’s B5培养基上。,中国。愈伤组织诱导率为96.67 ~ 100%。TDZ浓度为0.05 mg/L时愈伤组织鲜质量显著增大(方差分析,P < 0.001)。TDZ对胚胎发生性的影响在一定浓度范围内是显著的(方差分析,P < 0.001)。在无激素的B5培养基上继代培养14天后可形成多个体胚。将体细胞胚转移到1/2 MS添加0.1 mg/L 6-苄基氨基嘌呤和10%椰子水的培养基中,形成微芽,微芽伸长。kingtaitdz在volkensii组织培养中表现出较高的效力和适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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High-Frequency Regeneration of the Drought-Tolerant Tree Melia volkensii Gurke Using Low-Cost Agrochemical Thidiazuron.

Melia volkensii Gurke is a drought-tolerant tree native to East Africa's arid and semiarid lands (ASALs), with vast but underutilized potential for agroforestry and sustainable livelihoods in the ASALs. Its cultivation is limited by difficulties in propagation via conventional means. Full exploitation of the ability of thidiazuron (TDZ) to elicit regeneration in plant tissue cultures, as sole plant growth regulator (PGR), is hampered by high costs. This study tested the effectiveness of a low-cost agrochemical TDZ for in vitro propagation of M. volkensii. Zygotic embryos from mature seeds were cultured on Gamborg's B5 medium containing 0 to 4 mg/L of agrochemical TDZ from Kingtai Chemicals Co.,Ltd., China. Callus induction frequency was 96.67 to 100%. Significantly large callus fresh mass was produced at 0.05 mg/L TDZ concentration (ANOVA, P < 0.001). The effect of TDZ on embryogenicity was significant over certain ranges of concentrations (Anova, P < 0.001). Multiple somatic embryos developed within 14 days of subculture to hormone-free B5 medium. Somatic embryos developed into microshoots which elongated when transferred to 1/2 MS medium supplemented with 0.1 mg/L 6-benzylaminopurine plus 10% coconut water. The Kingtai-TDZ showed a high potency and suitability for use in M. volkensii tissue culture.

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