首页> 外国专利> Gene cassette of anchorage of the mer - R, tape expressu00e7o - anchor of mer - R, plasmideo recombinant bacterial lineage transgu00canica, use of said gene, use of this lineage in processes of environmental biorremediau00c7u00e7o

Gene cassette of anchorage of the mer - R, tape expressu00e7o - anchor of mer - R, plasmideo recombinant bacterial lineage transgu00canica, use of said gene, use of this lineage in processes of environmental biorremediau00c7u00e7o

机译:mer-R的基因盒,磁带表达-mer-R的锚,质粒重组细菌谱系转染 u00canica,所述基因的用途,该谱系在环境生物修复的过程中的用途 u00c7 u00e7o

摘要

Invention patent "gene cassette of anchorage of the mer - R, tape expressu00e7o - anchor of mer - R, plasmideo recombinant bacterial lineage transgu00canica, use of said gene, use of this lineage in processes of environmental biorremediau00c7u00e7o".The present invention relates to the construction and insertion of a vector of broad spectrum for gram negative bacteria, containing a gene sequence that can be expressed, allows anchoring of a protein chelating ions of mercury on the cell surface of gram negative bacteria.For this, the regulatory gene was isolated from plasmid pmol30 Merr of cupriavidus metallidurans, line ch34 (SEQ. ID No. 1) and inserted into cloning vector pgemt, resulting in the plasmid pgemt Hg (SEQ. ID No. 2).The expression vector containing the sequence corresponding to the tape to the expression and anchoring of heterologous proteins in gram negative bacteria under the control of the Da pan (SEQ. ID No. 3), derived from the plasmid pcm2, was obtained by polymerase chain reaction (PCR). The Merr gene was fused expression vector, amplified, resulting in the construction of the plasmid pcmhg (SEQ.ID No. 4). In addition, the present application provides mutant strains of gram negative bacteria containing said recombinant plasmid, method of production, beyond reporting the possible use of transgenic strains for the absorption of ions of mercury in environmental bioremediation processes.
机译:发明专利“ mer-R的基因盒,Rap胶带表达”-mer-R的锚,质粒重组细菌谱系transg u00canica,所述基因的用途,该谱系在环境生物修复过程中的用途本发明涉及用于革兰氏阴性细菌的广谱载体的构建和插入,该载体含有可以表达的基因序列,该载体允许将汞的蛋白质螯合离子锚定在革兰氏阴性细菌的细胞表面上。为此,将调控基因从金属鸟粪铜绿体的质粒pmol30 Merr ch34(SEQ.ID No.1)中分离出来,并插入克隆载体pgemt中,得到质粒pgemt Hg(SEQ.ID No.2)。通过polym获得了一种表达载体,该表达载体包含与质粒对应的序列,该序列对应于在Da pan控制下在革兰氏阴性细菌中表达和锚定异源蛋白的序列(SEQ。ID No. 3)。擦除链反应(PCR)。将Merr基因融合表达载体,扩增,从而构建质粒pcmhg(SEQ.ID No.4)。另外,本申请提供了含有所述重组质粒的革兰氏阴性细菌的突变株,生产方法,而不是报道了在环境生物修复过程中可能使用转基因株吸收汞离子。

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