首页> 外文期刊>Plant Science: An International Journal of Experimental Plant Biology >Production of Taxol registered trade mark sign and baccatin III by a selected Taxus baccata callus line and its derived cell suspension culture
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Production of Taxol registered trade mark sign and baccatin III by a selected Taxus baccata callus line and its derived cell suspension culture

机译:选定的红豆杉愈伤组织系产生紫杉醇注册商标符号和浆果赤霉素Ⅲ及其衍生的细胞悬浮培养物

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Small callus pieces excised from a selected 1-year-old stable callus line of Taxus baccata were grown on B5 solid medium supplemented with either phenylalanine (1 mM) or the elicitor compound VSO inferior 4 (0.05 or 0.1 mM). Under these conditions, callus growth and the production of Taxol registered trade mark sign and baccatin III were tested during 8 weeks of culture. Growth was enhanced by the presence of both phenylalanine and VSO inferior 4. The elicitor compound VSO inferior 4 (0.05 and 0.1 mM) moreover clearly increased Taxol registered trade mark sign and baccatin III production, especially at the end of the culture. The specific activity of PAL in callus pieces cultured under the different conditions studied, is also considered. In addition, liquid cultures were prepared from the selected callus line in order to study the effect of the VSO inferior 4 addition to the culture medium on Taxol registered trade mark sign and baccatin III production. The presence of this elicitor (VSO inferior 4; 0.05 mM), increased Taxol registered trade mark sign and baccatin III production (by a factor of 2.5 and 3.6, respectively) from 5.2 mu g g superior - superior 1 DW to 13.1 mu g g superior - superior 1 DW for Taxol registered trade mark sign and from 4.4 mu g g superior - superior 1 DW to 16.0 mu g g superior - superior 1 DW for baccatin III in the T. baccata cell suspension cultures. It also increased their release into the medium by a factor of 3.2 and 2.2, respectively.
机译:从选定的一年生红豆杉稳定愈伤组织系中切下的小愈伤组织块在补充了苯丙氨酸(1 mM)或激发子化合物VSO下4(0.05或0.1 mM)的B5固体培养基上生长。在这些条件下,在培养的8周内测试了愈伤组织的生长以及紫杉醇注册商标符号和浆果赤霉素III的产生。苯丙氨酸和VSO劣4的存在促进了生长。此外,引发剂化合物VSO劣4(0.05和0.1 mM)明显增加了紫杉醇注册商标和浆果赤霉素III的产生,尤其是在培养结束时。还考虑了在研究的不同条件下培养的愈伤组织碎片中PAL的比活性。另外,从选定的愈伤组织系制备液体培养物,以研究向培养基中添加VSO劣等4对紫杉醇注册商标符号和浆果赤霉素III产生的影响。该激发子的存在(VSO劣于4; 0.05 mM)使紫杉醇注册商标符号和浆果赤霉素III的产量(分别为5.2毫克/千克和1毫克/千克)提高了(分别为2.5和3.6倍)-紫杉醇注册商标标志的优1 DW和优百克-III优1 DW至16.0微克gg-浆果赤霉素III在T.baccata细胞悬浮培养物中优1 DW。它还使它们向培养基中的释放分别增加了3.2和2.2倍。

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