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Food-Grade Delivery System for Controlled Gene Expression in Lactococcus lactis

机译:食品级传递系统,控制乳酸乳球菌中的基因表达

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A food-grade system for the delivery of desired genes to Lactococcus lactis, their inducible expression, and their transfer to related strains was established. Based on the thermosensitive pG+host replicon, two types of plasmid vectors were constructed which contained sections of either the chromosomal leu operon of L. lactis or the tel operon from the lactococcal sex factor. Genes cloned into the leu or tel sequences of these vectors were delivered to the homologous regions of the chromosome or the sex factor through two single crossovers, leading to integration of the recombinant plasmids and subsequent excision of the vector portions. Inducible transcription of integrated genes was achieved by using the nisin-controlled expression (NICE) system. To establish the signal transduction genes nisRK in L. lactis, the vectors pLNG1363 (targeted to the chromosome) and pUK500 (targeted to the sex factor) were constructed. Fusions of six different peptidase genes (pep) from Lactobacillus delbrueckii with the nisin-inducible promoter PnisA were delivered to the sex factor with derivatives of the vector pUK300. Food-grade recombinants of L. lactis were constructed which had the nisRK genes and individual PnisA::pep fusions integrated either separately into the chromosome and the sex factor or simultaneously into the sex factor. With both types of recombinants, expression of PnisA::pep fusions after induction with nisin was demonstrated. Depending on the loci used for integration of nisRK, variable induction rates were observed. Furthermore, an engineered sex factor carrying a PnisA::pepI fusion was transfered by conjugation between two strains of L. lactis at a frequency of 4 × 10?4.
机译:建立了食品级系统,用于将所需基因传递给乳酸乳球菌,它们的诱导型表达以及它们向相关菌株的转移。基于热敏pG + 宿主复制子,构建了两种类型的质粒载体,它们分别含有 L的染色体 leu 操纵子的片段。乳球菌性因子中的lactis tel 操纵子。克隆到这些载体的 leu tel 序列中的基因通过两次单交换传递至染色体或性别因子的同源区域,从而导致重组质粒整合然后切除载体部分。通过使用乳链菌肽控制的表达(NICE)系统实现了整合基因的诱导转录。在 L中建立信号转导基因 nisRK 。乳酸,构建了载体pLNG1363(针对染色体)和pUK500(针对性别因子)。交付了六个来自德氏乳杆菌的不同肽酶基因( pep )与乳链菌肽诱导型启动子 P nisA 的融合体与载体pUK300的衍生物的性因子有关。 Lem的食品级重组体。构建具有 nisRK 基因和单个 P nisA :: pep 融合体的乳酸菌分别进入染色体和性别因子或同时进入性别因子。用这两种重组体,都证明了用乳链菌肽诱导后 P nisA :: pep 融合体的表达。根据用于整合 nisRK 的基因座,观察到了不同的诱导率。此外,携带 P nisA :: pepI 融合蛋白的工程性别因子通过在两个 L菌株之间的缀合转移。乳酸的频率为4×10 ?4

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