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A family of promoter probe vectors incorporating autofluorescent and chromogenic reporter proteins for studying gene expression in gram-negative bacteria

机译:结合了自身荧光和生色报道蛋白的启动子探针载体家族,用于研究革兰氏阴性细菌中的基因表达

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摘要

A series of promoter probe vectors for use in Gram-negative bacteria has been made in two broad-host-range vectors, pOT (pBBR replicon) and pJP2 (incP replicon). Reporter fusions can be made to gfpUV, gfpmut3.1, unstable gfpmut3.1 variants (LAA, LVA, AAV and ASV), gfp+, dsRed2, dsRedT.3, dsRedT.4, mRFP1, gusA or lacZ. The two vector families, pOT and pJP2, are compatible with one another and share the same polylinker for facile interchange of promoter regions. Vectors based on pJP2 have the advantage of being ultra-stable in the environment due to the presence of the parABCDE genes. As a confirmation of their usefulness, the dicarboxylic acid transport system promoter (dctAp) was cloned into a pOT (pRU1097)- and a pJP2 (pRU1156)-based vector and shown to be expressed by Rhizobium leguminosarum in infection threads of vetch. This indicates the presence of dicarboxylates at the earliest stages of nodule formation.
机译:已在两个广泛宿主范围的载体pOT(pBBR复制子)和pJP2(incP复制子)中制备了一系列用于革兰氏阴性细菌的启动子探针载体。可以对gfpUV,gfpmut3.1,不稳定的gfpmut3.1变体(LAA,LVA,AAV和ASV),gfp +,dsRed2,dsRedT.3,dsRedT.4,mRFP1,gusA或lacZ进行Reporter融合。 pOT和pJP2这两个载体家族彼此兼容,并共享相同的多连接子,可方便地交换启动子区域。由于存在parABCDE基因,基于pJP2的载体具有在环境中超稳定的优势。为了证实其有用性,将二羧酸转运系统启动子(dctAp)克隆到基于pOT(pRU1097)和基于pJP2(pRU1156)的载体中,并证明由豆科根瘤菌在紫etch的感染线上表达。这表明在结节形成的最早阶段存在二羧酸盐。

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