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A food-grade cloning vector for lactic acid bacteria based on the nisin immunity gene nisI

机译:基于乳链菌肽免疫基因nisI的乳酸菌食品级克隆载体

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摘要

A new food-grade cloning vector for lactic acid bacteria was constructed using the nisin immunity gene nisI as a selection marker. The food-grade plasmid, pLEB590, was constructed entirely of lactococcal DNA: the pSH71 replicon, the nisI gene, and the constitutive promoter P45 for nisI expression. Electroporation into Lactococcus lactis MG1614 with 60 international units (IU) nisin/ml selection yielded approximately 105 transformants/µg DNA. MG1614 carrying pLEB590 was shown to be able to grow in medium containing a maximum of 250 IU nisin/ml. Plasmid pLEB590 was succesfully transformed into an industrial L. lactis cheese starter carrying multiple cryptic plasmids. Suitability for molecular cloning was confirmed by cloning and expressing the proline iminopeptidase gene pepI from Lactobacillus helveticus in L. lactis and Lb. plantarum. These results show that the food-grade expression system reported in this paper has potential for expression of foreign genes in lactic acid bacteria in order to construct improved starter bacteria for food applications.
机译:使用乳链菌肽免疫基因nisI作为选择标记,构建了一种新的食品级乳酸菌克隆载体。食品级质粒pLEB590完全由乳球菌DNA构建:pSH71复制子,nisI基因和nisI表达的组成型启动子P45。用60个国际单位(IU)乳酸链球菌素/ ml选择物对乳酸乳球菌MG1614进行电穿孔可产生约105 转化子/μgDNA。携带pLEB590的MG1614被证明能够在最高250 IU乳链菌肽/ ml的培养基中生长。将质粒pLEB590成功转化到带有多个隐性质粒的工业乳酸乳干酪发酵剂中。通过在乳酸乳杆菌和Lb中克隆和表达来自瑞士乳杆菌的脯氨酸亚肽肽酶基因pepI来证实分子克隆的适用性。车前草。这些结果表明,本文报道的食品级表达系统具有在乳酸菌中表达外源基因的潜力,以便构建用于食品应用的改良的发酵菌。

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  • 来源
    《Applied Microbiology and Biotechnology》 |2002年第5期|467-471|共5页
  • 作者

    T. Takala; P. Saris;

  • 作者单位

    Department of Applied Chemistry and Microbiology Division of Microbiology Viikinkaari 9 P.O. Box 56 00014 University of Helsinki Finland;

    Department of Applied Chemistry and Microbiology Division of Microbiology Viikinkaari 9 P.O. Box 56 00014 University of Helsinki Finland;

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