Abstract
The development of plasmid-mediated gene expression control in bacteria revolutionized the field of bacteriology. Many of these expression control systems rely on the addition of small molecules, generally metabolites or non-metabolized analogs thereof, to the growth medium to induce expression of the genes of interest. The paradigmatic example of an expression control system is the lac system from Escherichia coli, which typically relies on the Ptac promoter and the Lac repressor, LacI. In many cases, however, constitutive gene expression is desired, and other experimental approaches require the coordinated control of multiple genes. While multiple systems have been developed for use in E. coli and its close relatives, the utility and/or functionality of these tools does not always translate to other species. For example, for the Gram-negative pathogen, Legionella pneumophila, a causative agent of Legionnaires’ Disease, the aforementioned Ptac system represents the only well-established expression control system. In order to enhance the tools available to study bacterial gene expression in L. pneumophila, we developed a plasmid, pON.mCherry, which confers constitutive gene expression from a mutagenized LacI binding site. We demonstrate that pON.mCherry neither interferes with other plasmids harboring an intact LacI-Ptac expression system nor alters the growth of Legionella species during intracellular growth. Furthermore, the broad-host range plasmid backbone of pON.mCherry allows constitutive gene expression in a wide variety of Gram-negative bacterial species, making pON.mCherry a useful tool for the greater research community.
Highlights
The lac operon promoter has been widely employed as a means for gene induction in a wide array of bacteria, ranging from Gram-negative to Gram-positive organisms
There have been a variety of additional induction systems developed to help solve this problem, including plasmid systems that are controlled by small molecules such as arabinose, tetracycline and xylose [1,2,3]
It is desirable to achieve constitutive gene expression in the absence of an inducing substance, if, for example the inducer is known to induce off target effects—such as inducing the expression of genes within the host bacterium, as could be the case for both IPTG and arabinose [1, 4]
Summary
The lac operon promoter has been widely employed as a means for gene induction in a wide array of bacteria, ranging from Gram-negative to Gram-positive organisms. The ability to control the expression of multiple genes within a given bacterial culture simultaneously is desired. Examples of such experiments include fluorescent microscopy imaging techniques or assessing how two proteins function together and/or independently. PON.mCherry, a constitutive expression plasmid for gram negative bacteria within a given bacterial cell. In these experiments, the ability to concurrently control the expression of multiple genes can greatly assist the researcher in studying a particular phenomenon. It is desirable to achieve constitutive gene expression in the absence of an inducing substance, if, for example the inducer is known to induce off target effects—such as inducing the expression of genes within the host bacterium, as could be the case for both IPTG and arabinose [1, 4]
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