Luo J-P, Jia J-F
Department of Biology, Lanzhou University, Lanzhou 730000, People's Republic of China, , , , , , CN.
Plant Cell Rep. 1998 Apr;17(6-7):567-570. doi: 10.1007/s002990050443.
An efficient procedure was developed for inducing callus and plant regeneration using hypocotyl segments of Astragalus adsurgens. The combinations and concentrations of different growth regulators were shown to be critical factors for both the frequency and the type of callus formation as well as for the potential of callus differentiation. Of the four morphologically distinct types of calli that were induced, a friable, yellow callus, i.e. type I, induced on MS medium supplemented with 9.0 µM 2,4-dichlorophenoxyacetic acid and 2.2 µM N-benzylaminopurine (BA), and then transferred to MS medium containing 0.5 µM α-naphthaleneacetic acid and 8.9 µM BA, exhibited the maximum frequency of shoot regeneration (75%). After regenerated shoots were transferred onto half-strength MS medium without growth regulators, they rooted and complete plants were obtained. Plantlet regeneration from callus cultures required 7-8 weeks.
利用斜茎黄芪的下胚轴切段,开发了一种高效的愈伤组织诱导和植株再生程序。不同生长调节剂的组合和浓度被证明是愈伤组织形成的频率和类型以及愈伤组织分化潜力的关键因素。在诱导出的四种形态不同的愈伤组织类型中,在添加了9.0 μM 2,4-二氯苯氧乙酸和2.2 μM N-苄基腺嘌呤(BA)的MS培养基上诱导出的一种易碎的黄色愈伤组织,即I型愈伤组织,然后转移到含有0.5 μM α-萘乙酸和8.9 μM BA的MS培养基上,其芽再生频率最高(75%)。将再生芽转移到不含生长调节剂的半强度MS培养基上后,它们生根并获得了完整植株。从愈伤组织培养物中再生小植株需要7-8周。