- Short Report
- Open Access
Constitutive and regulated expression vectors to construct polyphosphate deficient bacteria
© Chávez et al; licensee BioMed Central Ltd. 2009
- Received: 27 January 2009
- Accepted: 26 March 2009
- Published: 26 March 2009
Inorganic polyphosphate (polyP), a polymer of tens or hundreds of phosphate residues linked by ATP-like bonds, is found in all organisms and performs a wide variety of functions. PolyP is synthesized in bacterial cells by the actions of polyphosphate kinases (PPK1 and PPK2) and degraded by an exopolyphosphatase (PPX). Bacterial cells with polyP deficiencies are impaired in many structural and important cellular functions such as motility, quorum sensing, biofilm formation and virulence. Knockout mutants of the ppk1 gene have been the most frequent strategy employed to generate polyP deficient cells.
As an alternative method to construct polyP-deficient bacteria we developed constitutive and regulated broad-host-range vectors for depleting the cellular polyP content. This was achieved by the overexpression of yeast exopolyphosphatase (PPX1). Using this approach in a polyphosphate accumulating bacteria (Pseudomonas sp. B4), we were able to eliminate most of the cellular polyP (>95%). Furthermore, the effect of overexpression of PPX1 resembled the functional defects found in motility and biofilm formation in a ppk1 mutant from Pseudomonas aeruginosa PAO1. The plasmids constructed were also successfully replicated in other bacteria such as Escherichia coli, Burkholderia and Salmonella.
To deplete polyP contents in bacteria broad-host-range expression vectors can be used as an alternative and more efficient method compared with the deletion of ppk genes. It is of great importance to understand why polyP deficiency affects vital cellular processes in bacteria. The construction reported in this work will be of great relevance to study the role of polyP in microorganisms with non-sequenced genomes or those in which orthologs to ppk genes have not been identified.
- Knockout Mutant
- Electron Dense Granule
- High Copy Number Plasmid
- Polyphosphate Kinase
Polyphosphate (polyP) is a ubiquitous linear polymer of hundreds of orthophosphate residues (Pi) linked by "high-energy" phosphoanhydride bonds. The best-known enzymes involved in the metabolism of polyP in bacteria are the polyphosphate kinases (PPKs) that catalyze the reversible conversion of the terminal phosphate of ATP (or GTP) into polyP and the exopolyphosphatase (PPX) that processively hydrolyzes the terminal residues of polyP to liberate Pi [1, 2].
The involvement of polyP in the regulation of both, enzyme activities and the expression of large groups of genes is the basis for the survival of different bacteria, including pathogens, to stressing conditions and during adaptation to the stationary phase of growth [2, 3]. PPK1 knockout mutant cells lacking polyP survive poorly during growth in the stationary phase and are less resistant to heat, oxidants, osmotic challenge, antibiotics and UV [4–8]. Important cellular process such as motility, quorum sensing, biofilm development and virulence are also affected [9–11]. In addition to homologues of PPK1, another widely conserved polyP enzyme is PPK2 [12, 13]. In contrast to the ATP-dependent polyP synthetic activity of PPK1, PPK2 preferentially catalyses the opposite reaction, i.e. poly P-driven synthesis of GTP from GDP. Orthologs to both proteins have been found in many bacterial genomes. Some bacteria possess orthologs of either PPK1 or PPK2, or both, or neither. For example, E. coli has only PPK1 and Pseudomonas aeruginosa PAO1 contains both. Interestingly, the enzyme in charge of polyP synthesis still remains unknown in several bacteria containing the biopolymer .
As a tool to remove cellular polyP content, we report here the construction of expression vectors with constitutive and regulated promoters that overexpress in bacteria the yeast PPX1 fused to a hexa histidine-tag (6 Ht). Both, constitutive and inducible expression of PPX1 removed almost all cellular polyP (>96%) in polyP-accumulating Pseudomonas sp. B4. The absence of the biopolymer was confirmed by transmission electron microscopy (TEM) and by quantification using a two-step method . Recombinant polyP-deficient cells resembled ppk1 mutants of many bacteria in their functional defects found in motility and biofilm formation. However, these vectors have a greater advantage compared with previously described methods since they could be used in bacteria with unknown genome sequences or in those for which ppk orthologs have not been found. Furthermore, the regulated expression of PPX1 allowed us to induce polyP deficiency when required. Importantly, the vectors used in this work have been successfully replicated in other bacteria from the Escherichia, Salmonella, Pseudomonas and Burkholderia genus demonstrating the wide utility of this approach.
Polyphosphate content in recombinant Pseudomonas sp. B4 cells
PolyP in the form of electron dense granules can be seen when Pseudomonas sp. B4 is grown in the presence of biphenyl in minimal medium (M9) [15, 16] (Figure 3B, control). Nevertheless, these granules were not present in constitutive polyP(-) (pS7PPX1) cells (Figure 3B). Quantification of polyP in these samples confirmed the removal of almost all cellular polyP (data not shown). These findings clearly show that overexpression of PPX1 is an excellent method to remove cellular polyP.
Functional analysis of constitutive and inducible polyP deficient Pseudomonas sp. B4 cells
The results from this study demonstrate the usefulness of expression vectors for producing polyphosphate deficient bacteria. As far as we know, this strategy was employed only once in E. coli by using a very high copy number plasmid with a potent promoter . Overexpression of recombinant proteins from multiple-copy plasmids can result in expression levels of up to 40% of the total cell protein. However, in most cases, this results in the formation of insoluble protein aggregates known as inclusion bodies, which may affect the activity of the expressed proteins [19, 20]. In our case, plasmids pMLS7 and pMLBAD are derivatives of the pBBR1 plasmid , originally isolated from Bordetella bronchiseptica, which is maintained at around 20 to 30 copies per cell. This feature allowed us both, to actively express yeast PPX1 and to avoid affecting the general translation process in the host cell.
To our knowledge this is the first report of polyP-deficient bacteria being generated by constitutive and regulated low copy number vectors. The use of this approach allows the researcher to avoid using knockout mutants, which is currently the most commonly used procedure to diminish polyP content in bacteria. This is important for several reasons. First, the generation of knockout mutants requires the knowledge of the PPK sequence to be deleted and in the cases of bacteria with unknown genome sequences, this requires the isolation, cloning and sequencing of the corresponding gene. Second, in many bacteria there is more that one ppk gene responsible for polyP synthesis in the cell [12, 17]. As a consequence, to abolish most of the polyP in these bacteria, more than one deletion would be necessary. Finally, despite the presence of polyP, in many bacteria no ppk orthologs have been found in their genomes. For this kind of bacteria our approach is the only reliable method to generate polyP deficiency. Even more, considering that the enzymes in charge of polyP synthesis are still unknown in Archaea and Eukarya, overexpression of PPX1 can be an effective method to produce polyP scarcity in these domains of life. We have demonstrated in this study that, regardless of the number of ppk genes or their equivalents present in a genome, the overexpression of yeast PPX1 eliminates almost all cellular polyP contents.
Knockout mutants are very sable throughout generations and one possible disadvantage of our method compared to the deletion strategy could be the plasmid stability in the transformants. Nevertheless, despite strain variations, these plasmids remain relatively stable for a number of generations in the absence of selection (88% in Burkholderia cepacia and 92% in Escherichia coli) . In the case of Pseudomonas sp. B4 plasmid stability was around 90% (data not shown) but lower levels of stability might be found in other strains depending on their expression levels of Rep protein, some host-specific effects on plasmid partition or due to incompatibility with indigenous plasmids.
Another important aspect of the present construction is the use of a tag (His6t) that allows to follow up easily the expression of PPX1 during the experiments.
We have also established that the arabinose-inducible/glucose-repressible promoter permits to design experiments where polyP can be depleted when required. This approach will help to clarify the role of polyP in bacterial pathogenesis and other important microbial functions.
Altogether, these results demonstrate that overexpression of PPX1 generates functional defects similar to those previously described in ppk1 mutants. However, the use of the new constructions reported here constitutes an advantageous alternative method to study polyP deficiency in bacteria possessing more than one ppk gene or in those in which the enzymatic activity synthesizing polyP is unknown.
PolyP has numerous and varied biological functions that have been discovered mainly by studying its deficiency in bacteria. To better understand the function of polyP is necessary then to have simple approaches to eliminate this biopolymer in the cell. In this study we developed broad-host-range constitutive and regulated vectors that deplete cellular polyP. We conclude that these vectors will function as suitable and efficient genetic systems for characterizing polyP deficiency in bacteria, especially in those microorganisms with unknown genome sequences.
Bacterial strains, genomic DNA, plasmids and growth conditions
Strains and plasmids used in this study
Pseudomonas sp. B4 constitutive polyP(-)
Pseudomonas sp. B4 transfomant with pS7PPX1 plasmid
Pseudomonas sp. B4 constitutive control
Pseudomonas sp. B4 transfomant with
Pseudomonas sp. B4 regulated polyP(-)
Pseudomonas sp. B4 transfomant with pBADPPX1 plasmid
Pseudomonas sp. B4 regulated control
Pseudomonas sp. B4 transfomant with pMLBAD plasmid
Escherichia coli NR100
M15 (pREP) derivative with pQE30PPK plasmid
T-vector cloning system
Broad-host range regulated expression vector
Broad-host range constitutive expression vector
pGEM®-T-easy with PPX1 gene from S. cerevisiae. (His6 tag)
pMLS7 with PPX1 gene from S. cerevisiae. (His6 tag)
pMLBAD with PPX1 gene from S. cerevisiae. (His6 tag)
PolyP quantification. Purified recombinant His6-PPK was prepared by using E. coli strain NR 100 as described previously [23, 24] and this preparation was used in the polyP assay described below. The protein concentration was determined by the method of Bradford (Coomassie Plus protein Assay, Pierce). PolyP was quantified by using a two-step conversion of polyP into ATP by PPK and quantification of ATP by using luciferase to generate light [14, 25]. PolyP was extracted from small pellet cells by using Glassmilk. The resulting PolyP was assayed by using the reverse reaction of E. coli PPK in ADP excess. Finally, the ATP generated was determined by using the luciferase (Boehringer Mannheim) reaction, and the luminescence was measured with a luminometer (BioScan Lumi/96). Concentration of polyP was expressed in terms of Pi residues.
Assay for PPX activity and TLC analysis of the reaction products. First, radioactively labelled polyP with a chain length of 750 residues was prepared as previously described . The identity and purity were determined by its susceptibility to hydrolysis by PPX1.
PPX activity was determined as previously described , with the following modifications. A 50 μl reaction mixture contained 50 mM Tris/acetate (pH 7.0), 1 mM MnCl2, 100 mM KCl, 50 μg extract protein and 250 μM [33P] polyP750. Reactions were stopped after incubation of the mixtures for 60 min at 65°C. After this, 4 μl was taken from each reaction mixture and loaded on polyethyleneimine-cellulose plates (Merck). For TLC, samples of 4 μl were separated in 0.75 M KH2PO4 (pH 3.5). Radioactive spots were visualized and quantified by using a Phosphorimager (Molecular Imager FX Systems, Bio-Rad). One unit of enzyme was defined as the amount releasing 1 pmol of phosphate from polyP min-1.
More details about the Methods employed in this work were included in the Additional File 1.
This research was supported by Grants 1070986 and 11070180 from Fondecyt and ICM P05-001-F from Mideplan.
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