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首页> 外文期刊>Journal of Applied Phycology >Tools for microalgal biotechnology: development of an optimized transformation method for an industrially promising microalga—Tetraselmis chuii
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Tools for microalgal biotechnology: development of an optimized transformation method for an industrially promising microalga—Tetraselmis chuii

机译:微藻生物技术工具:为工业上​​有前景的微藻Tetraselmis chuii开发优化的转化方法

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摘要

Tetraselmis chuii is a biotechnologically promising green microalga that is commonly used in aquaculture. Development of reliable and easy genetic transformation procedures is essential for the improvement of this microalga. Here, we report the development of a suitable method for the stable genetic transformation of T. chuii via Agrobacterium tumefaciens. Following a statistical experimental design, seven factors were tested for their effect on the transformation efficiency. The effects of temperature, pH, and the interaction between acetosyringone concentration and co-culturing period were statistically significant. These main factors were subsequently optimized to the following values: 27 °C co-culturing temperature, pH 5.0, and 150 μM acetosyringone concentration. Transformation was verified by PCR on different target genes present in the T-DNA as well as by the determination of GUS activity from the reporter gene. Genetic stability of the transformed clones was examined by culturing under non-selective conditions in phleomycin-free medium for 6 months. Transformed clones were stable as indicated by the maintenance of the resistance to phleomycin (PhlR). In summary, an easy and reliable genetic transformation method for T. chuii was developed. The use of A. tumefaciens provides a useful method for the genetic engineering of this biotechnologically promising microalga.
机译:Tetraselmis chuii是一种在生物技术上很有前途的绿色微藻,常用于水产养殖。开发可靠且容易的遗传转化程序对于改善这种微藻至关重要。在这里,我们报告了通过根癌土壤杆菌稳定转化T. chuii的合适方法的发展。根据统计实验设计,测试了七个因素对转化效率的影响。温度,pH值以及乙酰丁香酮浓度与共培养时间之间的相互作用均具有统计学意义。随后将这些主要因素优化为以下值:27°C共培养温度,pH 5.0和150μM乙酰丁香酮浓度。通过PCR对T-DNA中存在的不同靶基因以及通过确定报告基因的GUS活性来验证转化。通过在非选择性条件下在不含phleomycin的培养基中培养6个月来检查转化克隆的遗传稳定性。如对phleomycin(PhlR)的抗性维持所表明的,转化的克隆是稳定的。综上所述,开发了一种简便,可靠的遗传学方法。根癌农杆菌的使用为该生物技术前景广阔的微藻的基因工程提供了有用的方法。

著录项

  • 来源
    《Journal of Applied Phycology》 |2015年第1期|223-232|共10页
  • 作者单位

    Grupo de investigación “Biotecnología de Productos Naturales” (BIO-279) Centro de Investigación en Biotecnología Agroalimentaria (BITAL) Campus Internacional de Excelencia Agroalimentario (CeiA3) Universidad de Almería">(1);

    Grupo de investigación “Biotecnología de Productos Naturales” (BIO-279) Centro de Investigación en Biotecnología Agroalimentaria (BITAL) Campus Internacional de Excelencia Agroalimentario (CeiA3) Universidad de Almería">(1);

    Grupo de investigación “Biotecnología de Productos Naturales” (BIO-279) Centro de Investigación en Biotecnología Agroalimentaria (BITAL) Campus Internacional de Excelencia Agroalimentario (CeiA3) Universidad de Almería">(1);

    Grupo de investigación “Biotecnología de Productos Naturales” (BIO-279) Centro de Investigación en Biotecnología Agroalimentaria (BITAL) Campus Internacional de Excelencia Agroalimentario (CeiA3) Universidad de Almería">(1);

    Grupo de investigación “Biotecnología de Productos Naturales” (BIO-279) Centro de Investigación en Biotecnología Agroalimentaria (BITAL) Campus Internacional de Excelencia Agroalimentario (CeiA3) Universidad de Almería">(1);

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Microalgae; Genetic transformation; Tetraselmis chuii; Transformant stability; Agrobacterium tumefaciens;

    机译:微藻;基因转化;Tetraselmis chuii;变压器稳定性;根癌农杆菌;

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