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Increased taxol production in Taxus x media through metabolic engineering approaches.

机译:通过代谢工程方法提高了Taxus x培养基中紫杉醇的产量。

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摘要

Scope and method of study. Taxol, originally isolated form the bark of Taxus brevifolia, is regarded as one of the best anti-cancer medicines developed from plant sources. However, its supply has been problematic since its discovery and has not been completely solved yet. The purpose of this study was to improve the production of Taxol by biotechnological approaches. As the first step, high performance liquid chromatography (HPLC) was employed to screen high-taxoid-yielding Taxus x media plants from 17 cultivars with different growth characteristics. Agrobacterium tumefaciens-mediated genetic transformation was then performed to transfer the high-efficiency-promoter-driven gene of taxadiene synthase, which is assumed to catalyze the first committed and rate-limiting step in the Taxol biosynthesis pathway, into tobacco leaf disks, in vitro Taxus suspension cells and in planta Taxus x media somatic cells. Lastly, gene expression profiling by cDNA-AFLP was conducted to detect alterations of gene expression in yew suspension cells upon methyl jasmonate (MeJA) and salicylic acid (SA) elicitation.; Findings and conclusions. For the T. x media cultivars screening, three cultivars with fast growth rate and upright growing form were found to contain the highest Taxol content ('Coleana', 378 mug/g; 'Hicksii', 322 mug/g; and 'Stovekenii', 309 mug/g). The in planta genetic transformation of 'Hicksii' plant with taxadiene synthase over-expression significantly increased Taxol production in the A. tumefaciens-induced gall tissues. The expression of the integrated green fluorescent protein (GFP) gene was visualized in the transformed 'Hicksii' suspension culture cells; and the integration and transcription of the taxadiene synthase gene was also detected in the tissues developed from the tobacco leaf disk transformation. For the cDNA-AFLP gene expression profiling, a total of 157 differentially expressed gene fragments were isolated, some of which were found to represent pathogenesis or stress-related genes based on BLAST search.
机译:研究范围和方法。紫杉醇最初是从短叶红豆杉的树皮中分离出来的,被认为是从植物来源开发的最好的抗癌药物之一。然而,自发现以来,其供应一直存在问题,并且尚未完全解决。这项研究的目的是通过生物技术方法提高紫杉醇的产量。第一步,采用高效液相色谱(HPLC)从具有不同生长特性的17个品种中筛选出高产紫杉类的Taxus x培养基植物。然后进行了根癌农杆菌介导的遗传转化,以将高效启动子驱动的紫杉二烯合酶基因转移到烟草叶盘中,该基因被认为可催化紫杉酚生物合成途径中的第一个承诺的限速步骤。红豆杉悬浮细胞和植物中的红豆杉x培养基体细胞。最后,通过茉莉酸甲酯(MeJA)和水杨酸(SA)诱导,利用cDNA-AFLP进行了基因表达谱分析,以检测紫杉悬浮细胞中基因表达的变化。结论和结论。对于T.x培养基品种筛选,发现三个生长速度快且直立生长的品种的紫杉酚含量最高('Coleana',378杯/克;'Hicksii',322杯/克;'Stovekenii' 309杯/克)。紫杉二烯合酶过量表达的'Hicksii'植物在植物体内的遗传转化显着增加了根癌农杆菌诱导的胆组织中紫杉醇的产量。整合的绿色荧光蛋白(GFP)基因的表达在转化的'Hicksii'悬浮培养细胞中可见。烟叶圆盘转化产生的组织中也检测到紫杉二烯合酶基因的整合和转录。对于cDNA-AFLP基因表达谱,总共分离了157个差异表达的基因片段,其中一些基于BLAST搜索被发现代表发病机理或与压力相关的基因。

著录项

  • 作者

    Wang, Xinkun.;

  • 作者单位

    Oklahoma State University.;

  • 授予单位 Oklahoma State University.;
  • 学科 Biology Molecular.; Biology Cell.
  • 学位 Ph.D.
  • 年度 2003
  • 页码 100 p.
  • 总页数 100
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子遗传学;细胞生物学;
  • 关键词

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