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In vitro biosynthesis and quantification of plumbagin in cell suspension culture of Plumbago zeylanica

机译:羽衣甘蓝细胞悬浮培养中羽囊白蛋白的体外生物合成与定量

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摘要

Plumbagin is the major alkaloid responsible for medicinal activities of Plumbago zeylanica. Experiments were conducted to quantify secondary metabolite (plumbagin) production in calli / cell clumps/embryoid acquired from cell suspension culture of P.zeylanica. Higher plumbagin amount was detected in one-month-old calli / cell clumps/embryoid fraction (0.428mg/100gm), liquid culture medium fraction free of calli / cell clumps/embryoid (0.357 mgL~(-1)) acquired from cell suspension culture as well asin two-months-old rhizogenic calli (1.257 mg per gm) on culture medium MS3D.5IB ((MS+3.0 mgL~(-1) 2,4-D + 0.5 mgL~(-1) IBA). Linearly increased plumbagin concentration in both fractions of cell suspension culture was recorded with increased concentrationof 2,4-D. MS2D.5IB (MS+2.0 mgL~(-1) 2,4-D + 0.5 mgL~(-1) IBA) was found the best culture medium in increasing growth and rhizogenic calli response in liquid medium.
机译:Plumbagin是负责西兰花(Plumbago zeylanica)药用活动的主要生物碱。进行了实验,以量化在从P.zeylanica的细胞悬浮培养物中获得的愈伤组织/细胞团/胚状体中次生代谢产物(羽扇豆蛋白)的产生。从细胞悬液中获得的一个月大的愈伤组织/细胞团/胚状体部分(0.428mg / 100gm),无愈伤组织/细胞团/胚状体的液体培养基部分(0.357mgL〜(-1))中检测到更高的铅素含量以及在培养基MS3D.5IB((MS + 3.0 mgL〜(-1)2,4-D + 0.5 mgL〜(-1)IBA)上培养两个月大的发根愈伤组织(1.257 mg / gm)。记录到细胞悬浮培养的两个部分中的铅蛋白浓度线性增加,而2,4-D. MS2D.5IB的浓度增加(MS + 2.0 mgL〜(-1)2,4-D + 0.5 mgL〜(-1)IBA)被发现是在液体培养基中增加生长和发根愈伤组织反应的最佳培养基。

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