首页> 外文学位 >Genetic Engineering of Lactobacillus casei for Surface Displaying the Green Fluorescent Protein: an Effort towards Monitoring the Survival and Fate of Probiotic Bacteria in the Gastrointestinal Tract Environment.
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Genetic Engineering of Lactobacillus casei for Surface Displaying the Green Fluorescent Protein: an Effort towards Monitoring the Survival and Fate of Probiotic Bacteria in the Gastrointestinal Tract Environment.

机译:干酪乳杆菌的基因工程,用于表面展示绿色荧光蛋白:努力监测胃肠道环境中益生菌的生存和命运。

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摘要

With the introduction of antibiotics in animal feed becoming less popular, the agricultural industry has begun a shift towards the use of probiotics in animal feed. Since there is no current method to evaluate the risks of using genetically modified probiotics in animal feed. The goal of this project was to create a genetically modified model organism for risk assessment. The genetic marker for that was chosen was GFP that was to be expressed on the surface of the cell. The fluorescent properties allow for visualisation of the genetically modified bacteria and the surface expression would allow for the easy capture and recovery of the bacteria for culturing and cell counts. Genome wide screens were performed using the CW PRED algorithm to locate proteins with LPXTG motif for cell wall anchoring. 16 hypothetical proteins were detected and 6 were selected as candidates for possible surface display of GFP. Of these candidates, the novel L. casei protein LSEI_2320 was found to be expressed at the mRNA during early growth by RT PCR and at then protein level during stationary phase with western blot. This LPXTG protein was found at the surface of L. casei ATCC334 during stationary phase and late stationary phase with immunofluorescence microscopy. A genetically modified L. casei ATCC334 was constructed using the surface protein LSEI_2320 locus as a region for recombination with the pRV300 suicide plasmid. Genetic modification of the locus by the insertion of a GFP reporter region just before the predicted signal peptide site resulted in the abrogation of the expression of LSEI_2320 from the cell surface at the late stationary phase. It appears that this particular gene is not necessary to cell survival even though it is abundantly expressed on the cell surface and can be used as a location for genetic modification in L. casei ATCC334.
机译:随着在动物饲料中引入抗生素的不那么流行,农业开始向在动物饲料中使用益生菌的转变。由于目前没有方法来评估在动物饲料中使用转基因益生菌的风险。该项目的目标是创建一种用于风险评估的转基因模型生物。为此选择的遗传标记是要在细胞表面表达的GFP。荧光性质允许对转基因细菌进行可视化,并且表面表达将便于细菌的捕获和回收以进行培养和细胞计数。使用CW PRED算法进行了全基因组筛选,以定位具有LPXTG基序的蛋白,用于细胞壁锚定。检测了16种假设的蛋白,并选择了6种作为可能的GFP表面展示的候选蛋白。在这些候选物中,发现新型干酪乳杆菌蛋白LSEI_2320在早期生长期间通过RT PCR在mRNA上表达,然后在蛋白质固定阶段通过western blot在蛋白质水平上表达。用免疫荧光显微镜在固定期和固定期后期在干酪乳杆菌ATCC334的表面发现该LPXTG蛋白。使用表面蛋白LSEI_2320基因座作为与pRV300自杀质粒重组的区域,构建了基因修饰的干酪乳杆菌ATCC334。通过在预期的信号肽位点之前插入GFP报告基因区域来对基因座进行遗传修饰,导致在静止后期从细胞表面消除LSEI_2320的表达。尽管该特定基因在细胞表面大量表达,但似乎可以作为细胞存活所必需的基因,并且可以用作干酪乳杆菌ATCC334中遗传修饰的位置。

著录项

  • 作者

    Chan, Colin.;

  • 作者单位

    University of Ottawa (Canada).;

  • 授予单位 University of Ottawa (Canada).;
  • 学科 Chemistry Biochemistry.;Biology Microbiology.;Biology Genetics.
  • 学位 M.Sc.
  • 年度 2014
  • 页码 110 p.
  • 总页数 110
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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