植物生长调节剂对苦楝悬浮培养细胞抗氧化酶活性和次生代谢产物产生的影响。

F. Ahmadpoor, N. Zare, Rasool Asghari, Parisa Sheikhzadeh-Mosadeg
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引用次数: 0

摘要

摘要本研究研究了植物生长调节剂和外植体类型对苦楝愈伤组织诱导、悬浮培养细胞生长、抗氧化酶活性以及芦丁、槲皮素和山奈酚积累的影响。我们的研究表明,与叶片外植体相比,花序和叶柄外植体的愈伤组织诱导率较高,而叶片外植体在含有5 mg l - 1 NAA和5 mg l - 1 BAP以及5 mg l - 1 NAA和3 mg l - 1 kinetin Kin的MS培养基上的愈伤组织生长最高。此外,将叶片和花序愈伤组织转移到添加1 mg l−1 2,4-二氯苯氧乙酸(2,4- d)+1 mg l−1 Kin/BAP的MS液体培养基中,细胞生长最快。在含有3 mg l - 1 NAA和3 mg l - 1 BAP的MS液体培养基中,叶细胞悬浮培养的抗氧化酶活性最高,蛋白质含量最低。在含有3 mg l−1 NAA+1 mg l−1 BAP的MS培养基中,花序细胞的芦丁积累量最高(47.536 mg g−1 FW)。然而,叶柄细胞悬浮培养中槲皮素(8.570 mg g−1 FW)和山奈酚(5.420 mg g−1 FW)积累量最高的是MS培养基(1 mg l−1 2,4- d +1 mg l−1 Kin)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of plant growth regulators on the antioxidant enzyme activity and secondary metabolite production in the cell suspension cultures of Melia azedarach L.
ABSTRACT In the present study, we investigated the effect of plant growth regulators and explant type on callus induction, cell suspension culture growth, antioxidant enzyme activity, and accumulation of rutin, quercetin, and kaempferol in M. azedarach L. cell cultures. Our studies showed that the inflorescence and petiole explants had a high percentage of callus induction compared to the leaf explants, whereas the highest callus growth was obtained from the leaf explants cultured on the MS medium containing 5 mg l−1 NAA and 5 mg l−1 BAP and 5 mg l−1 NAA and 3 mg l−1 kinetin Kin. Furthermore, the highest cell growth was obtained from the leaf and inflorescence calli transferred to liquid MS medium supplemented with 1 mg l−1 2,4-dichlorophenoxyacetic acid (2,4-D)+1 mg l−1 Kin/BAP. The highest activity of antioxidant enzymes and the lowest protein content was related to the leaf cell suspension cultures in liquid MS medium containing 3 mg l−1 NAA and 3 mg l−1 BAP. The inflorescence cell suspension cultures in the MS medium containing 3 mg l−1 NAA+1 mg l−1 BAP exhibited the highest rutin accumulation (47.536 mg g−1 FW). However, the highest amount of quercetin (8.570 mg g−1 FW) and kaempferol (5.420 mg g−1 FW) accumulation were obtained from the petiole cell suspension cultures in the MS medium with 1 mg l−1 2,4-D +1 mg l−1 Kin.
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