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首页> 外文期刊>Plant Growth Regulation: An International Journal on Natural and Synthetic Regulators >In vitro morphogenetic responses and comparative analysis of phthalides in the highly valued medicinal plant Ligusticum porteri Coulter & Rose
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In vitro morphogenetic responses and comparative analysis of phthalides in the highly valued medicinal plant Ligusticum porteri Coulter & Rose

机译:珍贵药用植物女贞(Ligusticum porteri Coulter&Rose)中邻苯二甲酸酯的体外形态发生反应和比较分析

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摘要

The morphogenetic response of Ligusticum porteri, a medicinal and ceremonial plant, was investigated as part of the conservation strategy of this wild species and was compared to that of a cultivated species, Petroselinum crispum. Seeds were germinated in half strength Murashige and Skoog medium. Plantlets were excised into root, cotyledon, petiole, stem and leaf explants and cultured in an induction medium supplemented with the range of 0-18.09 μM 2,4-dichlorophenoxyacetic acid (2,4-D) or 0-21.48 μM α-naphthaleneacetic acid in combination with 0-13.31 μM 6-benzylaminopurine. Calli derived from leaf, seeds, petiole, stem and roots, mature aerial parts and roots extracts of L. porteri and P. crispum were analyzed by thin layer chromatography and gas chromatography coupled to mass spectrometry. 3-Butylidenephthalide (6.3%) was identified along with other 23 compounds from mature aerial parts extract of L. porteri and also in its roots (20.8%). 3-n-Butylphthalide (0.7%) and 3,6,7,-trimethoxy-isobenzofuran-13(H)-one (4.9%) were identified from the roots of P. crispum. 3-Butylidenephthalide was identified from two petiole (0.9%; 0.26%) and one stem (0.8%) callus extracts of L. porteri. This is the first report on phthalides production from in vitro cultures of L. porteri. The results indicated that in vitro cultures of this plant possess the biosynthetic machinery for the biosynthesis of these highly valuable compounds.
机译:作为该野生物种保护策略的一部分,对药用和观赏植物女贞属的形态发生反应进行了研究,并将其与栽培物种Petroselinum crispum进行了比较。种子在半强度的Murashige和Skoog培养基中发芽。将小苗切成根,子叶,叶柄,茎和叶外植体,并在补充了0-18.09μM2,4-二氯苯氧乙酸(2,4-D)或0-21.48μMα-萘乙酸的范围的诱导培养基中进行培养。酸与0-13.31μM的6-苄基氨基嘌呤结合使用。用薄层色谱法和气相色谱-质谱联用技术分析了来自L. porteri和P. crispum的叶,种子,叶柄,茎和根,成熟的地上部分和根提取物的愈伤组织。从门氏乳杆菌成熟的地上部分提取物中和其根部(20.8%)中鉴定出3-丁烯酞(6.3%)以及其他23种化合物。从crispum的根中鉴定出3-正丁基邻苯二甲酸酯(0.7%)和3,6,7,-三甲氧基-异苯并呋喃-13(H)-one(4.9%)。从Port L. porteri的两个叶柄(0.9%; 0.26%)和一个茎(0.8%)的愈伤组织提取物中鉴定出3-丁二烯。这是关于从门氏乳杆菌体外培养物中生产邻苯二甲酸盐的首次报道。结果表明,该植物的体外培养物具有用于生物合成这些高价值化合物的生物合成机制。

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