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四倍体刺槐腋芽培养及克隆植株RAPD分析的有效方法

An effective method for axillary bud culture and RAPD analysis of cloned plants in tetraploid black locust.

作者信息

Shu Q Y, Liu G S, Qi D M, Chu C C, Liu J, Li H J

机构信息

Key Laboratory of Photosynthesis and Environmental Molecular Physiology, Institute of Botany, Chinese Academy of Sciences, 100093 Beijing, China.

出版信息

Plant Cell Rep. 2003 Oct;22(3):175-80. doi: 10.1007/s00299-003-0661-2. Epub 2003 Aug 7.

Abstract

An efficient micropropagation technique by axillary bud multiplication was established for cloning tetraploid black locust tree (Robinia pseudoacacia L.). The result showed that the optimal medium for shoot multiplication and elongation was Murashige and Skoog (MS) medium supplemented with 0.5 mg/l 6-benzylaminopurine in combination with 0.5 mg/l kinetin and 0.1 mg/l 1-naphthaleneacetic acid. The best medium for rooting was half-strength MS medium with 0.25 mg/l indole-3-butyric acid. In the present report, we examined the genetic fidelity of the micropropagated plants by the randomly amplified polymorphic DNA (RAPD) method with 25 primers. The cloned plants of tetraploid black locust showed complete stability.

摘要

通过腋芽增殖建立了一种高效的四倍体刺槐(Robinia pseudoacacia L.)克隆微繁殖技术。结果表明,用于芽增殖和伸长的最佳培养基是添加了0.5 mg/l 6-苄基腺嘌呤、0.5 mg/l激动素和0.1 mg/l 1-萘乙酸的Murashige和Skoog(MS)培养基。生根的最佳培养基是含有0.25 mg/l吲哚-3-丁酸的1/2强度MS培养基。在本报告中,我们用25种引物通过随机扩增多态性DNA(RAPD)方法检测了微繁殖植株的遗传稳定性。四倍体刺槐的克隆植株表现出完全的稳定性。

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