|Home | About | Journals | Submit | Contact Us | Français|
Recently, we have demonstrated that the 26-47 segment of Salmonella enterica serovar Typhimurium flagellin is capable of mediating flagellar export. In order to reveal whether other parts of the N-terminal region have any significant influence on secretion, a series of plasmids were constructed containing the lac promoter followed by the 26-47, 2-65, or 2-192 portion of Salmonella flagellin, to which various heterologous proteins of different size were fused (18 constructs overall). Essentially, all three segments could drive protein export; however, the nature of the attached polypeptide also had a significant effect on secretion efficiency. When low export efficiency was observed, it was mainly caused by inclusion body formation. Our data provide strong support for the idea that a short segment within the disordered N-terminal region of axial proteins is recognized by the flagellar type III export machinery. The 26-47 segment of flagellin contains all of the necessary information to direct translocation of attached polypeptide chains. This short (positions 26 to 47) flagellin segment attached to recombinant proteins can be used for secreted protein expression. Certain fusion proteins that are easily degraded within the cells were found to be intact in the medium, implying a potential application of this expression system for proteins with high proteolytic susceptibility.
The bacterial flagellum is a biological nanomachine for locomotion. A membrane embedded molecular motor rotates a long helical filament that works as a propeller driving the bacterium through the liquid environment. The filamentous portion of flagellum extends from the cytoplasm to the cell exterior and involves several substructures: the rod, the hook, the hook-filament junction, the long helical filament, and a cap at the filament tip.
The flagellar proteins forming the structures lying beyond the cytoplasmic membrane are synthesized in the cell and exported sequentially by the flagellum-specific protein export apparatus from the cytoplasm to the site of assembly at the distal end of the growing filament (23). Thousands of subunits must be translocated through the narrow (20 to 25 Å wide) central channel of the flagellum (42) in a mostly unfolded conformation. It is puzzling how subunits can be efficiently transported through the hollow core of filaments over large (10- to 15-μm) distances. The hydrophilic inner surface of the channel is supposed to be essential for rapid and efficient transport. It is an interesting question whether the export channel is specialized for the delivery of flagellar proteins, or whether it is capable of passing a wide variety of polypeptide chains.
The flagellar protein export system is thought to exist at the cytoplasmic face of the basal body to distinguish flagellar proteins from other cytoplasmic proteins and to facilitate their transportation (28). Since the identification and enzymatic characterization of FliI ATPase as a component of the flagellar protein export system, it had been thought that the flagellar protein export is driven by the energy of ATP hydrolysis (37). Recent studies, however, have clearly shown that the proton motive force across the cytoplasmic membrane is responsible for driving the export process that involves unfolding of export substrate proteins and translocation of the unfolded chains with the help of the FliI hexamer ring complex (27, 31).
The flagellar protein export system belongs to the family of the type III secretion systems (T3SSs) (4), which also include those for secretion of virulence factors by a wide variety of pathogenic bacteria (15). The nature of the signal directing flagellar protein secretion is still debated because the protein substrates have no cleavable signal sequences or do not share any obvious consensus sequence (12). It has been suggested that the recognition of flagellar export substrates may involve mRNA signals (25), but a growing amount of evidence indicates that the signal is located in the disordered N-terminal region of the secreted proteins (6, 11, 12, 19, 33, 36, 40). For example, residues 38 to 58 of Caulobacter crescentus flagellar hook protein were found to be essential for secretion (19). Similarly, it has been demonstrated that the export signal of the hook scaffolding protein FlgD of Escherichia coli is located exclusively within the N-terminal 71 amino acids (40). Single amino acid substitutions within the N-terminal region of the anti-sigma factor FlgM (6), which is also exported by the flagellum-specific export apparatus, severely impair its export.
Our previous experiments have suggested that the 26-47 disordered segment of Salmonella flagellin contains the recognition signal for the flagellar export machinery (36). When this segment was attached to the small CCP2 domain of the human C1r complement protein, the fusion construct was secreted into the culture medium. The objective of the present study was to explore whether other N-terminal portions of flagellin have any significant influence on secretion. We also aimed to reveal whether the recognition signal can facilitate translocation of a wide variety attached foreign proteins through the flagellum-specific export pathway, which may open up the possibility to use the flagellar export system to secrete heterologous proteins overexpressed in bacteria.
The Salmonella enterica serovar Typhimurium ΔfliC strain, SJW2536 (30), was kindly provided by Kenji Oosawa (Nagoya University, Nagoya, Japan). The pGFP plasmid was purchased from Clontech, and the pTWIN-MBP1 plasmid was from New England Biolabs. Genes for human C1r (9), human IFN-α2b (unpublished data), and Thermotoga maritima xylanase A (16) have been available in our laboratory. The gene cassette containing a polyhistidine tag, the 26-47 serovar Typhimurium flagellin segment, and the enterokinase (EK) site was made by gene synthesis (GeneScript). The cassette was placed between the HindIII and KpnI sites of pGFP, resulting in the pVJGFPa plasmid (Fig. (Fig.1A).1A). Synthetic genes of similar cassettes (GeneScript) containing the 2-65 and the 2-192 segments were placed between the HindIII and NheI sites into pVJGFPa, replacing the short segment, and resulting in plasmids pVJGFPb and pVJGFPc. Five genes, CCP2, CCP1-CCP2, alpha interferon (IFN-α), XAcat, and maltose-binding protein (MBP), were amplified by PCR using primers listed in Table Table1.1. The PCR products were digested with NheI and BamHI enzymes, except for MBP, which was digested with NheI and XhoI. The products then were cloned into each of the pVJGFPa, pVJGFPb, and pVJGFPc vectors resulting in the plasmids listed in Table Table22 . E. coli Top10 (from Invitrogen) was used for general cloning and plasmid production.
To make electrocompetent serovar Typhimurium SJW2536, cells were grown in LB until the optical density at 600 nm (OD600) reached about 0.6, and then they were washed twice with ice-cold sterile water and suspended in the same containing 10% glycerol. For electroporation, 50 to 200 ng of plasmid DNA was used, and a 2.5-kV voltage was applied with a 5-ms time constant. Transformed cells were plated onto LB agar containing 100 μg of ampicillin/ml.
For protein expression, a 1% (vol/vol) overnight Salmonella culture was inoculated into LB medium containing 100 μg of ampicillin/ml, and the cells were grown for 3 to 4 h (OD600 ≈ 0.6) when 0.4 mM IPTG (isopropyl-β-d-thiogalactopyranoside) was added. Samples were taken after an additional 3 to 4 h of incubation, when the OD600 reached about 1.
The cells were harvested by centrifugation, resuspended in 1/10 volume of water, and then lysed in an equal volume of standard SDS-PAGE sample buffer by heating and vortexing. The cell culture medium was concentrated 50-fold in spin concentrators (Millipore) before an equal volume of standard SDS-PAGE reducing sample buffer was added. The samples were analyzed on 12% gels by using the standard Tris-glycine buffer system. Then, 20-μl portions of the samples above were used for Coomassie blue-stained gels, and 10-μl portions were used for the Western blots. For the Western blots, after transfer to nitrocellulose membranes, the fusion proteins were detected by using a monoclonal anti-polyhistidine-alkaline phosphatase conjugate antibody (catalog no. A-5588; Sigma). For the analysis of inclusion bodies and soluble intracellular proteins, the cells were disrupted by ultrasonic treatment. Cells were harvested by centrifugation and resuspended in a 1/5 volume of sonication buffer (50 mM NaCl, 50 mM Tris-HCl [pH 8.0], 1 mM EDTA, 1% Triton X-100), and then 10% (wt/vol) of glass beads (catalog no. G8893; Sigma) were added, and the cells were sonicated extensively (six times for 15 s at maximum power on ice in a final volume of 1 ml). The soluble and insoluble fractions were separated by centrifugation, the pellet was washed once with sonication buffer, and finally the pellet was resuspended in the same volume as the soluble fraction. To portions of the lysates and the inclusion body suspensions, equal volumes of standard SDS-PAGE reducing sample buffer were added; the samples were then heated, and 20-μl aliquots were analyzed by SDS-PAGE and Western blotting.
In order to determine the spontaneous lysis of the host cells, the relative levels of Salmonella's own MBPs were determined from the cells and from the medium. The endogenous intracellular MBP of Salmonella lacks any secretion signal; therefore, it can leak into the medium only by cell lysis. Cells and medium of 400 ml of SJW2536 culture in LB (OD600 ≈ 1) were separated by centrifugation. The cells were lysed by extensive ultrasonic treatment, and the clarified lysate was made up to a 400-ml final volume with 200 mM NaCl, 20 mM Tris-HCl (pH 7.4), and 1 mM EDTA (column buffer). The medium (400 ml) was composed of NaCl, Tris-HCl (pH 7.4), and EDTA to the same concentrations as in the column buffer. Both were loaded to 1-ml amylose resin columns (New England Biolabs catalog no. E8022), washed with column buffer, and eluted in 3 ml of the same buffer containing 10 mM maltose. Purified MBP from the cells (15 μl plus sample buffer per lane) was analyzed by SDS-PAGE and Western blotting. To obtain a detectable amount of protein, a 750-μl aliquot of MBP purified from the medium was precipitated with 20% trichloroacetic acid before SDS-PAGE and Western blot analysis. MBP was detected by using mouse monoclonal anti-MBP (Sigma catalog no. M1321) and anti-mouse-IgG alkaline phosphatase conjugate (Sigma catalog no. A2429) antibodies. Based on the observed band intensities and the amounts loaded onto the gels, the spontaneous cell lysis was estimated to be ca. 0.4%.
Secretion of the various fusion proteins by serovar Typhimurium, which varied in size from 9 to 40 kDa, was examined by estimating the concentration of the fusion proteins within the cells and in the cell culture supernatant applying densitometric analysis of the Coomassie blue-stained SDS-polyacrylamide gels. The band intensities were corrected with the intensity of the host protein band with the same apparent molecular weight in the neighboring lane. The bands of the molecular weight marker, which contain known amounts of the respective proteins, were used as a reference to determine the amount of the fusion protein in each lane. The concentrations were calculated from the loaded volume and the determined amount. Since the amount of the Coomassie blue stain bound to the same amount of different proteins might be somewhat different, this method does not provide an accurate measure of the levels of the expressed fusion proteins; nevertheless, it allows determination of the relative levels of the same fusion protein in the cells and in the medium. In some cases the fusion products could only be detected by Western blotting that was used to identify the His-tagged polypeptide chains. In these cases (e.g., 2-65-IFN-α and 2-192-MBP) the export efficiencies and at least one of the concentration values were estimated based on the Western blot intensities, because the corresponding band on the Coomassie blue-stained gel could not be identified. At least 1 mg of fusion protein/liter in the cells and 0.2 mg/liter in the medium is required for a clear detection on Coomassie blue-stained gels because of the host protein background. These upper limits were taken into account when the concentration values were estimated, since bands detected only by Western blot are probably equal or lower than these values. Export percent efficiencies were calculated from the levels of the fusion proteins in the cells and in the medium as follows: [(amount of intact protein in the medium)/(amount of intact protein in the medium + amount of intact protein in the cells)] × 100. This simple equation does not include degradation products; hence, it may underestimate the “true” export efficiency if the protein is degraded in the medium after secretion. Also, degradation in the cells may result in the loss of the export signal; therefore, the protein may get trapped inside the cells.
Serovar Typhimurium SJW2536 harboring pVJMBPa was grown as described above. The cells were pelleted at 5,000 × g for 15 min at 4°C, and the supernatant was used for the subsequent steps. A total of 500 ml of the medium containing 26-47-MBP was buffer exchanged by diafiltration (using a 10-kDa cutoff Sartorius Sartocon slice cassette) to 400 mM NaCl, 10 mM imidazole, 50 mM sodium phosphate [pH 7.5], 0.01% NaN3). At the same time, the volume was reduced to about 200 ml. The sample was loaded onto a 5-ml Ni-NTA Superflow column (Qiagen), washed, and then eluted with the same buffer but containing 400 mM imidazole. The two 5-ml fractions containing 26-47-MBP were combined, and the buffer was exchanged by dialysis with 50 mM Tris-HCl, 0.2 mM CaCl2 [pH 7.5], and 0.1% Tween 20. Recombinant EK (Sigma catalog no. E-4906) was added at a 26-47-MBP/EK ratio of ca. 20:1 (wt/wt) to a solution of 0.1 to 0.15 mg of 26-47-MBP/ml, followed by incubation for 30 h at room temperature. Then, 5 ml of the digested protein was loaded onto a 1-ml amylose resin column (New England Biolabs catalog no. E8022), washed with 200 mM NaCl-20 mM Tris-HCl [pH 7.4]-1 mM EDTA, and eluted with the same buffer containing 10 mM maltose. The majority of the eluted MBP was found in three of the 1-ml fractions.
DNA fragments encoding the 26-47, 2-65, or 2-192 segment of serovar Typhimurium flagellin were prepared by gene synthesis. The synthetic constructs contained portions encoding a His6 tag before, and an EK cleavage site after the flagellar segment. The His6 tag facilitates easy purification and aids detection by Western blotting, whereas the EK cleavage site allows removal of the tag if necessary. The synthetic genes were placed into the lac promoter based pGFP plasmid in frame with the green fluorescent protein (GFP) gene. The resulting plasmids were named pVJGFPa, pVJGFPb, and pVJGFPc, respectively (Fig. (Fig.1A).1A). These initial plasmids are already capable of expressing fusion proteins made of the flagellar signals and jellyfish (Aequorea victoria) GFP. Genes of various heterologous proteins, all ending with a stop codon, were placed into each of the pVJGFP plasmids in frame with the coding sequence the flagellin segment right after the EK cleavage site. The inserted genes encoded the following proteins or protein domains: human C1r CCP2 domain (CCP2), human C1r CCP1-CCP2 domain pair (CCP1-CCP2), human alpha2b interferon (IFN-α), T. maritima xylanase A catalytic domain (XAcat), and E. coli MBP. Proteins 9 to 40 kDa in size (14 to 63 kDa with the attached segments) were selected in order to test the size limit for the flagellar export apparatus to unfold and export proteins. Of the chosen proteins, four were eukaryotic, three contained disulfide bridges, two were comparable in size with flagellin (51 kDa), and none of them was export substrate of a T3SS or contained any secretion elements besides the attached segment. Overall, 18 constructs were made, including the initial plasmids (Fig. (Fig.1B).1B). The names of the different plasmids are listed in the first column of Table Table2.2. From here on fusion proteins are referred to by the signal and the short name of the attached protein, e.g., 2-192-CCP2 refers to the human C1r CCP2 domain attached to the 2-192 flagellin segment supplemented with the extra tags. It is important to note that except for gene segments encoding the 26-47, 2-62, or 2-192 portions of flagellin, none of the constructs contained any other flagellar nucleotide sequences from the coding or noncoding regions.
The secretion yield of the fusion proteins was determined by comparing the relative levels of a given protein in the medium and in the cells obtained from the densitometric analysis of Coomassie stained gels (Fig. (Fig.2A2A and Table Table2).2). The appropriate bands were identified by Western blotting detecting the His tag present on all fusion products (Fig. (Fig.2B).2B). In eight cases the export yield of the total intact protein was rather low (below 5%) or nothing at all, and in eleven cases the concentration of the exported fusion proteins was <1 mg/liter or 0. In contrast, the flagellar system exports flagellin very efficiently: 6 to 10 mg of monomeric flagellin/liter was secreted at a similar cell density in mutant strains (13, 14, 18), and flagellin was the major protein in the medium. In our experiments, we observed comparable levels in four cases (26-47-CCP2, 2-65-CCP2, 2-192-CCP2, and 26-47-MBP), where the produced fusion protein was the major protein in the medium, while in two other cases (2-65-MBP and 2-192-XAcat) a degradation product of the produced fusion protein appeared to be the most abundant component. Low export and high intracellular expression is best exemplified with GFP. It is expressed at a high level (33 to 44 mg/liter) with all three flagellar segments intracellularly, whereas only 0.6 to 1 mg/liter is exported to the medium. GFP is known to form intracellular aggregates (35); therefore, we separated the cell lysates to soluble and insoluble fractions and analyzed them by SDS-PAGE. GFP was found to be expressed >85% in the form of inclusion bodies. Taking this into account, soluble GFP is exported with >17% efficiency to the medium by any of the signals used as opposed to approximately a mere 2% of the total expressed protein. The analysis was extended to all constructs, and the results were added to Table Table2.2. As an example, Fig. Fig.33 shows the results of SDS-PAGE and Western blot analyses of the soluble and insoluble cellular fractions obtained with constructs containing the 26-47 signal.
The basal lysis of Salmonella SJW2536 host cells was estimated from the relative levels of Salmonella's endogenous MBP within the cells and in the medium. The endogenous intracellular MBP of Salmonella lacks any secretion signal; therefore, it can leak into the medium only by cell lysis. The highly soluble MBP was purified from the cells and from the medium on amylose resin in an identical setup for both the medium and the cells; therefore, the loss during purification is similar in both cases. The purified and at the same time concentrated MBP was analyzed by SDS-PAGE and Western blotting (Fig. (Fig.4).4). Based on the observed band intensities and the amounts loaded onto the gels, spontaneous cell lysis is estimated to be ca. 0.4%. Based on this observation, export yields of greater than ca. 1% can be considered significant. Of the 18 fusion proteins examined, 14 fell into this category. In the remaining four cases, degradation or inclusion body formation prevented significant export of the intact protein.
It is important to note that protein degradation, inclusion body formation, and various expression levels complicate interpretation of the data. Nevertheless, the general trend seems to be that the short (26-47 and 2-65) segments resulted in somewhat better export yield, and the shortest (26-47) signal gave the highest protein levels in the medium. Overall, 14 of 18 fusion proteins were exported into the medium of serovar Typhimurium with significant efficiency. In one case (26-47-IFN-α) all of the expressed recombinant protein was found in the form of inclusion bodies, and no export was observed, whereas in the cases of 2-65-XAcat and 2-192-XAcat only degradation products were detected mainly in the medium. In the case of 2-192-MBP, intact protein export is detectable but is not significant, probably due to degradation. In our study we focused on the secretion of intact fusion proteins, since degradation products may be exported with quite different efficiencies or not at all if the flagellar segment is removed. In most cases, the intact fusion proteins could be detected in the medium, indicating that each attached signal, regardless of the length, can mediate protein export, provided that at least a fraction of the protein in question is soluble. In four cases the export was so efficient that 100% of the soluble fusion protein was found in the medium. In all four of these cases the short (26-47 or 2-65) signals were used. On the other hand, the longest signal (the 2-192 signal) gave somewhat higher protein levels in the medium than the 2-65 one, and for IFN-α only the longest signal produced significant levels of the fusion protein in the medium. The results are summarized on Fig. Fig.55 comparing the export efficiencies of the total expressed and the soluble fusion proteins.
The structure of the bacterial flagellum and the components of the export system are fairly well characterized (5, 24, 26); however, the signal governing the export of flagellar proteins is still somewhat mysterious. The flagellar secretion system (flagellar T3SS) is closely related to the T3SSs of virulence factors of pathogenic bacteria. Salmonella has two such systems encoded by the salmonella pathogenicity islands 1 and 2 (SPI-1 T3SS and SPI-2 T3SS). Likely, the mechanisms governing export by the different pathways shares some common characteristics. Proteins secreted by any of the type III secretion pathways do not possess a classical signal sequence. Certain studies suggested that the signal sequence is found at the mRNA level (1, 25) or that the combination of an N-terminal signal and a structural element in the mRNA is required (3). On the other hand, a growing number of data support that the signal is contained at the protein level, and it is located at or near the N terminus (6, 12, 17, 19, 22, 36, 39, 40). The identified signal sequences of different flagellar proteins, however, do not show any significant sequence similarity, which indicates that determinants should be at higher than the primary structural level.
Interestingly, monomeric flagellin has been shown to be secreted by the SPI-1 T3SS and even translocated into the host cell cytosol (32, 34). Normally, flagellin is exported primarily by the flagellar T3SS; it polymerizes to form the filament, and only a small fraction of monomeric flagellin is leaked into the medium. Further research is required to clarify to what extent is the SPI-1 T3SS is involved in the secretion of the fusion proteins presented here. Involvement of the SPI-2 T3SS is unlikely because it is not active in Salmonella cultured in LB medium (7). Flagellin is not the only protein that can be exported by more than just one pathway. For example, SopE, which is secreted specifically by the SPI-1 T3SS, can be exported by the flagellar T3SS as well when its interaction with its cognate chaperone is abolished by mutations (10). It seems likely that the basic mechanism by which the different type III systems recognize their substrates is closely related, and the signal recognized by one system can be recognized by the other under certain circumstances (21). Determinants other than the N-terminal polypeptide signal may be required for targeting the specific protein to the appropriate export system (10).
We have previously identified a short segment spanning from the 26 to 47 amino acids of S. enterica serovar Typhimurium flagellin as a minimal export signal (36). Other partially or fully overlapping segments (1 to 35 and 1 to 48) have also been shown to facilitate export of an attached reporter protein (34). The objective of the present study was to explore whether there is any benefit, in terms of secretion efficiency, to using larger N-terminal portions of flagellin than the identified minimal signal. One reporter gene is, however, not sufficient to characterize the effect of signal length on protein export, since every construct is different in terms of expression level, inclusion body formation, and degradation. To average out the influence of these factors on the export yield, we used six different proteins to adequately answer this question. Three different segments of flagellin (26 to 47, 2 to 65, and 2 to 192) were tested, fused to the N terminus of each selected protein (18 constructs overall). The first ~65 residues of flagellin, which represent the entire N-terminal unstructured region, were chosen because terminal disorder is thought to be the common characteristics of export substrates (29, 38), whereas approximately the first 190 residues encompass the highly conserved N-terminal part of the molecule (2), and the first report used about the same fragment that demonstrated that the N-terminal part of flagellin contains the signal (20). It was found that any of the attached segments resulted in export of nearly all proteins with various yields. The major reason hindering secretion was inclusion body formation of certain fusion proteins. When only the soluble fraction of the expressed proteins was considered, the export efficiency was fairly high with all signals. The average efficiency was 44% overall, and 46, 52, and 35% with the 26-47, 2-65, and 2-192 segments, respectively (Fig. (Fig.5).5). A quantitative comparison (Table (Table2)2) suggested that the specific characteristics of a given fusion protein rather than the attached signal caused differences in export efficiency. An important feature of the DNA constructs is that they do not contain any flagellar nucleotide sequences from the untranslated or coding region other than the ones encoding the 26-47, 2-62, or 2-192 segment. Our data provide strong support for the idea that a short segment within the N-terminal region of axial proteins is recognized by the flagellar type III export machinery and no mRNA signal is required.
Flagellar axial proteins have to be delivered to their assembly destination at the tip of the growing structure. Since the diameter of the central channel of the flagellum is only ~2 nm, proteins to be exported must be largely unfolded for entry into and translocation through the channel. The successive process of unfolding and translocation of export substrates is driven by the proton motive force across the cell membrane (27, 31), i.e., the flagellar secretion apparatus functions as a proton-driven protein exporter. Our experiments show that the 22-residue long export signal contains all of the necessary information to direct translocation of export substrates or attached heterologous polypeptide chains. It is interesting that an additional sequence element such as the His6 tag present in all constructs is tolerated N-terminal to the signal sequence.
Secretion of recombinant proteins overexpressed in bacteria is still not solved satisfactorily. T3SSs have the potential to be used as effective tools for the secretion of recombinant proteins (8, 11, 25, 36, 41). A major advantage of secreted protein expression is that cell disruption is no longer required before purification, and the starting material is less contaminated with host proteins, lipopolysaccharides, and nucleic acids. It gives a chance that certain proteins which are degraded or form intracellular aggregates can be expressed in intact and soluble form. Solubility, however, does not necessarily mean that the protein of interest is correctly folded. Axial flagellar proteins are translocated in a largely unfolded state through the narrow export channel by the flagellar T3SS. It is plausible to assume that fusion proteins containing the export signal are also transported to the medium in an unfolded form, where they may or may not adopt their native conformation. Anyway, the lack of competing aggregation facilitates the folding process. The flagellin-deficient serovar Typhimurium strain SJW2536 was used in our experiments (30). As a result, the export apparatus was not overloaded with the most abundant flagellar protein, flagellin. Since SJW2536 can assemble only the basal body and the hook part of the flagellum, the expressed fusion proteins do not need to travel through a very long filament.
Our constructs were designed to contain a His6 tag at the N terminus. This modification enables easy detection and purification in one step on a Ni2+ affinity matrix. Another feature of the constructs is that they contain an EK cleavage site right after the flagellin segment. The EK site enables selective removal of the preceding flagellar and other sequence elements from the expressed protein. As an example, purification of 26-47-MBP was characterized in detail mainly because it was secreted to the medium at the highest concentration (although not with the highest efficiency), and its binding to amylose resin, followed by elution with maltose, makes it easy to check whether it is correctly folded. 26-47-MBP was purified with an ~60% yield on a Ni-NTA Superflow column from the medium of SJW2536 harboring pVJMBPa (Fig. (Fig.6).6). After purification, the secretion tag was removed by digestion with EK. The EK-treated protein was loaded onto an amylose-agarose resin. Approximately 60% of MBP was bound and could be eluted from the column (Fig. (Fig.6),6), indicating that at least this portion was correctly folded. Another examined protein, 26-47-CCP2, however, remained unfolded or at least did not adopt a native-like fold after secretion (data not shown). This protein is curiously hardly detectable within the cells but found at a high concentration in the medium. A plausible explanation for this observation is that the unfolded 26-47-CCP2 that was not exported is rapidly degraded in the cells.
These preliminary experiments indicate that fusion proteins carrying N-terminal flagellin segments can be efficiently secreted into the medium of serovar Typhimurium SJW2536 and purified with ease. As demonstrated by 26-47-MBP, they may acquire the correct fold after secretion. This expression system also has a potential for unfolded or unstructured proteins that are easily degraded intracellularly but may escape proteolysis if secreted efficiently into the medium.
In summary, all of the examined N-terminal flagellin segments were recognized by the export apparatus and could mediate protein export. Our data reinforce the hypothesis that the export signal for the flagellar T3SS is located at the protein level near the N terminus of export substrates. The identified minimal, 22-residue-long signal in flagellin contains all of the essential information to direct export of attached heterologous proteins by the flagellar export system. Our results demonstrate that the export channel is not specialized for the delivery of flagellar proteins but capable of passing a wide variety of polypeptide chains. N-terminal flagellin segments containing the export signal combined with a His6 tag can be attached to heterologous proteins, facilitating their secreted expression and easy purification from the medium.
We thank Kenji Oosawa for the SJW2536 strain, Márton Megyeri for help with cloning of the IFN-α2b gene, Katalin Szilágyi for the refolded C1r CCP2, Balázs Major for technical help, and Szilárd Kamondi for the cloned XAcat gene.
The support of Hungarian Scientific Research Fund (OTKA) grants NI61915 and NK77978, National Development Agency grant KMOP-1.1.2-07/1-2008-0003, and Hungarian National Office for Research and Technology (NKTH-KPI) grant GVOP-3.1.1-0386/3.0 is acknowledged.
Published ahead of print on 11 December 2009.