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Optimization of root proliferation medium for Hyoscyamus niger L.

机译:黑hyoscyamus niger L.根增殖培养基的优化。

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Untransformed root culture ofHyoscyamus nigercould be induced from petiole explants on solid MS medium supplemented with 2.0 mg l–1IBA after four weeks of incubation under continuous light of 32.5 µmol m-2s-1. However, liquid MS medium supplemented with 0.5 mg l–1IBA was found to be better for root proliferation. Cultures at the third subculture cycle during root proliferation showed maximum root biomass production either under continuous light (3.69±1.00 g) or in total darkness (4.02±0.94 g). Step-wise optimization of culture medium components was carried out by manipulating the MS macronutrients, myo-inositol, Fe-EDTA and sucrose. The optimum root biomass producing medium was established as modified MS medium containing altered concentrations of macronutrients (15.0 mM NH4NO3, 33.1 mM KNO3, 3.19 mM CaCl.2H2O, 1.9 mM MgSO4.7H2O and 1.4 mM KH2PO4), 9.6 mM myo-inositol, 0.1 mM Fe-EDTA and 3% sucrose supplemented with 0.5 l–1mg IBA.
机译:在32.5μmolm-2s-1的连续光照下孵育四周后,可以从叶柄外植体在添加了2.0 mg l-1IBA的固体MS培养基上,从叶柄外植体诱导出未转化的黑质丝酵母的根培养物。然而,发现补充有0.5mg I-1IBA的液体MS培养基对于根增殖更好。在根系增殖的第三个继代培养周期中,在连续光照(3.69±1.00 g)或完全黑暗(4.02±0.94 g)的条件下,根系生物量最大。通过控制MS大量营养素,肌醇,Fe-EDTA和蔗糖进行培养基成分的逐步优化。确定了最佳的根系生物量生产培养基为改良的MS培养基,其中包含改变的常量营养素浓度(15.0 mM NH4NO3、33.1 mM KNO3、3.19 mM CaCl.2H2O,1.9 mM MgSO4.7H2O和1.4 mM KH2PO4),9.6 mM肌醇,0.1 mM Fe-EDTA和3%蔗糖补充0.5 l-1mg IBA。

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