首页> 外文期刊>Journal of Plant Biochemistry and Biotechnology >In vitro micropropagation of Silybum marianum L from various explants and silybin content
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In vitro micropropagation of Silybum marianum L from various explants and silybin content

机译:不同植株和水飞蓟宾含量对水飞蓟素的体外微繁殖

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摘要

Regeneration from leaf, shoot apex and nodal segments of in vivo and in vitro seedlings, and enhancement in silybin content have been achieved in Silybum marianum. The explants callused within four weeks on Murashige and Skoog's medium (MS) (1) supplemented with #alpha#-naphthaleneacetic acid (NAA, 0.1 mg l~-1), + 6-benzylaminopurine (BAP, 0.3 mg l~-1) + Zeatin (Zt, 0.3 mg l~-1). Upon transfer to MS + NAA (0.1 mg l~-1) + Zt (0.5 mg l~-1), the callus differentiated multiple shoots followed by rooting in 100% cultures of all the explants within ten weeks. Direct shoot regeneration could be obtained only from nodal segments after 4 weeks on MS + Indole-3-acetic acid (IAA, 0.1 mg l~-1) + Kinetin (Kn, 0.5 mg l~-1) in 100% cultures. Rooting of these shoots was achieved after 2 weeks on MS + NAA (0.1 mg l~-1) + Zt (0.5 mg l~-1). Plantlets could be successfully transplanted to soil. Yield of silybin content in the cultured tissues varied with age and composition of the medium. Maximum yield resulted after eight weeks on media supplemented with zeatin.
机译:体内和体外幼苗从叶,茎尖和节节的再生,以及水飞蓟素中水飞蓟宾含量的提高均已实现。外植体在Murashige和Skoog培养基(MS)(1)上补充了#alpha#-萘乙酸(NAA,0.1 mg l〜-1)+ 6-苄基氨基嘌呤(BAP,0.3 mg l〜-1)在四个星期内within愈+玉米蛋白(Zt,0.3 mg l〜-1)。转移至MS + NAA(0.1 mg l-1)+ Zt(0.5 mg l-1)后,愈伤组织分化出多个芽,然后在十周内生根于所有外植体的100%培养物中。在100%培养液中,在MS +吲哚-3-乙酸(IAA,0.1 mg l〜-1)+激动素(Kn,0.5 mg l〜-1)上培养4周后,仅从节段获得直接芽再生。这些芽在MS + NAA(0.1 mg l〜-1)+ Zt(0.5 mg l-1)上2周后生根。幼苗可以成功移植到土壤中。培养组织中水飞蓟宾含量的产量随培养基的年龄和组成而变化。在补充玉米素的培养基上八周后,产量最高。

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