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Exploring the production of high-value compounds in plant Catharanthus roseus hairy roots and yeast Yarrowia lipolytica

机译:探索植物长春花毛状根和酵母解脂耶氏酵母中高价值化合物的生产

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This dissertation focuses on studying the production of two categories of high-value compounds in bio organisms. The first group is terpenoid indole alkaloids (TIAs) in plant Catharanthus roseus, and the second group is wax esters, one of fatty acid derivatives.;TIAs belong to secondary metabolites in C. roseus and some of them have wide pharmaceutical applications. In particular, vinblastine and vincristine are two TIAs with anticancer properties and have been marked and used in chemotherapeutic reagents. The biggest issue for TIA production is that the content of those secondary metabolites in plant is extremely low. To improve the TIA production, we studied the regulation mechanism of the TIA pathway and explored the feasibility of valuable TIA production in hairy root culture.;Compared with the whole plant, plant tissue culture, such as hairy root culture, has many advantages, like fast growth, large-scale cultivation, and ease of genetic engineering. But the biggest issue for hairy root is that the vinblastine and vincristine synthetic pathway is blocked, mainly one of their precursors, vindoline, can not be synthesized in hairy root. To explore whether C. roseus hairy root could produce the intermediates in the vindoline pathway by overexpressing the pathway enzymes, we co-expressed the first two genes, tabersonine 16-hydrolase (T16H) and 16-O-methyltransferase (16OMT) in the vindoline pathway into hairy root. Transcriptional analysis and metabolic profiling were done to compare the difference between the parent hairy root lines and the engineered hairy root lines.;For the metabolic profiling, since the standards for those intermediates were not available, we prepared in-house standards by expressing the plant genes in Saccharomyces cerevisiae, fed substrate, and purified TIA compounds from yeast cell culture. Liquid chromatography (LC) coupled with either photodiode array detector (PDA) or mass spectrometry (MS) were applied to isolate and analyze the TIA compounds by their UV-Visible absorption spectra and molecular weights.;In addition, fundamental research was done in C. roseus hairy root to study the effects of transcription regulators on the transcript levels and metabolite levels of the TIA pathway. Two of the seven reported transcription activators of the TIA pathway, octadecanoid-responsive Catharanthus AP2-domain 2(ORCA3) and MYB-like DNA-binding protein (BPF1), were overexpessed in hairy root separately, Two of the transcription repressors, G-box binding factors (GBF1 and GBF2), were knocked down by RNA interface in hairy root. And the transcription analysis and metabolic profiling of the transcription regulator-engineered hairy root lines were done to see what were the effects caused by those regulators.;Wax esters have a lot of applications in lubricant, skin care products, cosmetics, inking, and coating industries. Currently the main bio source for high-performed wax ester is from the seeds of jojoba. The tight supply makes wax esters high-value compounds. To reduce the production cost, we introduced the wax ester biosynthetic pathway into an oleaginous yeast, Yarrowia lipolytica. The free fatty alcohol, and wax ester were quantified in the engineered Y. lipolytica.;To provide more substrate for wax ester synthesis, we knocked out some genes in the substrate competitive pathways, and constructed four strains with different combination of knockout genes. To utilize the most abundant fatty acid types in Y. lipolytica, we compared three fatty acyl-CoA reductases (FAR), the first enzyme in the wax ester pathway, from different species. It was found that those three FARs had different substrate specificity and the wax ester production varied a lot in those strains.;To solve the plasmid instability issue, we randomly integrated FAR gene and WS gene into Y. lipolytica genome, and studied the effect of nitrogen limited fermentation on the wax ester production in one of our best strains.
机译:本文主要研究生物有机体中两类高价值化合物的生产。第一组是植物长春花中的萜类吲哚生物碱(TIA),第二组是脂肪酸衍生物之一的蜡酯。TIA属于玫瑰状念珠菌中的次生代谢产物,其中一些具有广泛的药学应用。特别是长春碱和长春新碱是两种具有抗癌特性的TIA,已被标记并用于化学治疗剂中。 TIA生产的最大问题是植物中这些次生代谢产物的含量极低。为了提高TIA的产量,我们研究了TIA途径的调控机制,并探讨了在有毛根培养中有价值的TIA产生的可行性。与整株植物相比,有毛根培养等植物组织培养具有很多优势,例如快速增长,大规模种植和易于基因工程。但是长毛根的最大问题是长春碱和长春新碱的合成途径受阻,主要是它们的前体之一长春花碱不能在长毛根中合成。为了探讨玫瑰色毛状根是否可以通过过表达途径酶而在长春花碱途径中产生中间体,我们在长春花碱中共同表达了前两个基因:烟粉碱16-水解酶(T16H)和16-O-甲基转移酶(16OMT)进入毛状根的途径。进行了转录分析和代谢谱分析,以比较亲本毛状根系和工程毛状根系之间的差异。对于代谢谱,由于没有这些中间体的标准,我们通过表达植物来制备内部标准酿酒酵母基因,进料底物和酵母细胞培养物中提纯的TIA化合物。采用液相色谱(LC)结合光电二极管阵列检测器(PDA)或质谱(MS)来分离和分析TIA化合物的紫外可见吸收光谱和分子量。此外,在C中进行了基础研究玫瑰毛状根,以研究转录调节剂对TIA途径的转录水平和代谢产物水平的影响。 TIA途径的七个报道的转录激活因子中,两个在毛状根中过度过量,即十八烷类响应长春花AP2-结构域2(ORCA3)和MYB样DNA结合蛋白(BPF1)过分过量,两个转录抑制因子G-盒结合因子(GBF1和GBF2)被毛状根的RNA界面击倒。然后对转录调节剂工程化的毛状根系进行了转录分析和代谢谱分析,以了解这些调节剂引起的作用。蜡酯在润滑剂,皮肤护理产品,化妆品,着墨和涂料中有许多应用行业。目前,高性能蜡酯的主要生物来源是霍霍巴种子。紧张的供应使蜡酯成为高价值的化合物。为了降低生产成本,我们将蜡酯的生物合成途径引入了油性酵母解脂耶氏酵母。在工程解脂耶氏酵母中定量了游离脂肪醇和蜡酯。为了为蜡酯合成提供更多底物,我们在底物竞争途径中敲除了一些基因,并构建了具有不同敲除基因组合的四个菌株。为了利用解脂耶氏酵母中最丰富的脂肪酸类型,我们比较了三种脂肪酰基辅酶A还原酶(FAR),这是蜡酯途径中的第一种酶,来自不同物种。发现这三个FARs具有不同的底物特异性,并且在这些菌株中蜡酯的产生变化很大。为解决质粒不稳定性问题,我们将FAR基因和WS基因随机整合到解脂耶氏酵母基因组中,并研究了其作用。氮限制了我们最好菌株之一中蜡酯生产的发酵。

著录项

  • 作者

    Zhao, Le.;

  • 作者单位

    Iowa State University.;

  • 授予单位 Iowa State University.;
  • 学科 Chemical engineering.;Biochemistry.
  • 学位 Ph.D.
  • 年度 2017
  • 页码 118 p.
  • 总页数 118
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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