Joseph T, Yeoh H-H, Loh C-S
Department of Biological Sciences, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260 e-mail:
Plant Cell Rep. 2000 Apr;19(5):535-538. doi: 10.1007/s002990050769.
The report describes a system for somatic embryogenesis and direct plant regeneration from the embryos of Manihot glaziovii. Somatic embryos were obtained by culturing young leaf lobes (3-6 mm long) adjacent to the apex in Murashige and Skoog medium containing 18 μM 2,4-dichlorophenoxy acetic acid for 20 days and then transferring them to a maturation medium with 0.5 μM 6-benzylaminopurine. Secondary embryogenesis was induced from cotyledonary segments of somatic embryos by using the same protocol as that for primary embryogenesis. For regeneration, somatic embryos were cultured in medium supplemented with 10 M kinetin and 53.4% of them developed into plantlets. Linamarin and linamarase were not detected in calli or in somatic embryos. Linamarin content was found to be highest in leaves of regenerated plantlets, followed by stem and root tissues. Levels of linamarase activity were almost the same in leaves and stem tissues and very low in roots.
该报告描述了一种用于木薯体细胞胚胎发生和从其胚胎直接再生植株的系统。通过在含有18μM 2,4 - 二氯苯氧乙酸的Murashige和Skoog培养基中培养靠近顶端的幼叶裂片(3 - 6毫米长)20天,然后将其转移到含有0.5μM 6 - 苄基腺嘌呤的成熟培养基中,获得体细胞胚。通过使用与初级胚胎发生相同的方案,从体细胞胚的子叶节段诱导二次胚胎发生。为了再生,将体细胞胚在添加了10M激动素 的培养基中培养,其中53.4%发育成了小植株。在愈伤组织或体细胞胚中未检测到亚麻苦苷和亚麻苦苷酶。发现再生小植株的叶片中亚麻苦苷含量最高,其次是茎和根组织。亚麻苦苷酶活性水平在叶片和茎组织中几乎相同,在根中非常低。