首页> 外文期刊>Applied Microbiology and Biotechnology >Characterization of pNI10 plasmid in Pseudomonas, and the construction of an improved Escherichia and Pseudomonas shuttle vector, pNUK73
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Characterization of pNI10 plasmid in Pseudomonas, and the construction of an improved Escherichia and Pseudomonas shuttle vector, pNUK73

机译:假单胞菌中pNI10质粒的鉴定以及改良的大肠杆菌和假单胞菌穿梭载体pNUK73的构建

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摘要

The complete nucleotide sequence of pNI10 (3.75 kb), from which pNI105 and pNI107 were constructed as medium-host-range vectors for Gram-negative bacteria, was determined. A fragment of about 2.1 kb of pNI10 was essential for replication in Escherichia coli and Pseudomonas fluorescens. This fragment encodes a putative origin of replication (ori) and one putative replication-controlling protein (Rep). An improved version of the medium-host-range plasmid vector pNUK73 (5.13 kb) was constructed with the basic-replicon of pNI10 and pHSG298 (2.68 kb). We show that expression in pseudomonads of the bromoperoxidase gene (bpo) of Pseudomonas putida, inserted downstream of the lac promoter in pNUK73, resulted in about 30% (13.6 U/l culture) of the enzyme level obtained in E. coli.
机译:确定了pNI10的完整核苷酸序列(3.75 kb),从中构建了pNI105和pNI107作为革兰氏阴性细菌的中等宿主范围载体。 pNI10约2.1 kb的片段对于在大肠杆菌和荧光假单胞菌中复制至关重要。该片段编码一个假定的复制起点(ori)和一个假定的复制控制蛋白(Rep)。用pNI10和pHSG298(2.68 kb)的碱性复制子构建了中等宿主范围质粒载体pNUK73(5.13 kb)的改进版。我们显示在假单胞菌恶臭假单胞菌的溴过氧化物酶基因(bpo)中的表达,插入到pNUK73 lac启动子的下游,导致在大肠杆菌中获得的酶水平约为30%(13.6 U / l培养物)。

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  • 来源
    《Applied Microbiology and Biotechnology》 |2003年第3期|240-246|共7页
  • 作者单位

    Biotechnology Research Center Toyama Prefectural University;

    Biotechnology Research Center Toyama Prefectural University;

    Department of Applied Chemistry and Biotechnology Faculty of Engineering Fukui University;

    Department of Applied Chemistry and Biotechnology Faculty of Engineering Fukui University;

    Department of Applied Chemistry and Biotechnology Faculty of Engineering Fukui University;

    Department of Applied Chemistry and Biotechnology Faculty of Engineering Fukui University;

    Gifu Research and Development Center Amano Enzyme;

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