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使用赋予条件表型的lacIq/Ptrp-lac质粒和转座子对假单胞菌基因产物进行分析。

Analysis of Pseudomonas gene products using lacIq/Ptrp-lac plasmids and transposons that confer conditional phenotypes.

作者信息

de Lorenzo V, Eltis L, Kessler B, Timmis K N

机构信息

Centro de Investigaciones Biológicas CSIC, Madrid, Spain.

出版信息

Gene. 1993 Jan 15;123(1):17-24. doi: 10.1016/0378-1119(93)90533-9.

Abstract

Novel transposon and plasmid-based broad-host-range expression systems have been developed to facilitate the genetic analysis of gene products of Pseudomonas and related Gram- bacteria. The properties of lacIq/Ptrp-lac were used to construct mini-Tn5 expression vector transposons and RSF1010-derived plasmids for controlled expression and generation of conditional phenotypes. These plasmids were used to hyper-express the XylS regulator of the meta operon of the TOL plasmid of P. putida or the bphB and bphC genes of the polychlorobiphenyl-degrading pathway of Pseudomonas sp. LB400 in different strains of Pseudomonas instead of in Escherichia coli. Specific activity of 2.3 dihydroxybiphenyl dioxygenase (bphC gene product) was increased tenfold when hyperproduced in its native host as compared to E. coli, but under the same in vivo conditions, the XylS regulator formed protein aggregates. The other lacIq/Ptrp-lac-based expression vector presented here, transposon mini-Tn5 lacIq/Ptrc, facilitates the insertion of genetic cassettes containing heterologous genes under the control of lac inducers in the chromosome of target bacteria, as shown by monitoring expression of a lacZ reporter cloned in mini-Tn5 lacIq/Ptrc and inserted in the chromosome of P. putida.

摘要

已经开发出新型转座子和基于质粒的广宿主范围表达系统,以促进对假单胞菌及相关革兰氏阴性菌基因产物的遗传分析。利用lacIq/Ptrp-lac的特性构建了微型Tn5表达载体转座子和源自RSF1010的质粒,用于控制表达和产生条件表型。这些质粒用于在不同的假单胞菌菌株中过量表达恶臭假单胞菌TOL质粒间位操纵子的XylS调节子或假单胞菌属LB400多氯联苯降解途径的bphB和bphC基因,而不是在大肠杆菌中。与在大肠杆菌中相比,2,3-二羟基联苯双加氧酶(bphC基因产物)在其天然宿主中过量产生时,比活性提高了10倍,但在相同的体内条件下,XylS调节子形成了蛋白质聚集体。本文介绍的另一种基于lacIq/Ptrp-lac的表达载体,转座子微型Tn5 lacIq/Ptrc,有助于将含有在lac诱导物控制下的异源基因的遗传盒插入靶细菌的染色体中,通过监测克隆在微型Tn5 lacIq/Ptrc中并插入恶臭假单胞菌染色体中的lacZ报告基因的表达可以证明这一点。

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