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The periodontal pathogen Porphyromonas gingivalis is an obligate anaerobe that requires heme for growth. To understand its heme acquisition mechanism, we focused on a hemin-binding protein (HBP35 protein), possessing one thioredoxin-like motif and a conserved C-terminal domain, which are proposed to be involved in redox regulation and cell surface attachment, respectively.
We observed that the hbp35 gene was transcribed as a 1.1-kb mRNA with subsequent translation resulting in three proteins with molecular masses of 40, 29 and 27 kDa in the cytoplasm, and one modified form of the 40-kDa protein on the cell surface. A recombinant 40-kDa HBP35 exhibited thioredoxin activity in vitro and mutation of the two putative active site cysteine residues abolished this activity. Both recombinant 40- and 27-kDa proteins had the ability to bind hemin, and growth of an hbp35 deletion mutant was substantially retarded under hemin-depleted conditions compared with growth of the wild type under the same conditions.
P. gingivalis HBP35 exhibits thioredoxin and hemin-binding activities and is essential for growth in hemin-depleted conditions suggesting that the protein plays a significant role in hemin acquisition.
Porphyromonas gingivalis has been implicated as a major pathogen associated with chronic periodontitis. The establishment of P. gingivalis at a periodontal site and progression of disease is dependent on the ability of the bacterium to utilize essential nutrients, of which iron (preferably in the form of heme) plays a crucial role. P. gingivalis lacks the majority of enzymes in the biosynthetic pathway for the porphyrin ring, hence it is unable to synthesize protoporphyrin IX, the precursor of heme [1-3]; and unlike other Gram-negative bacteria, P. gingivalis does not produce siderophores . Although several studies have shown that P. gingivalis acquires heme from the host environment using gingipains, lipoproteins and specific outer-membrane receptors [3-5], the precise mechanisms by which P. gingivalis acquires heme are still unknown.
The gene encoding the P. gingivalis outer membrane 40-kDa protein (OMP40) was first cloned by Abiko et al. . As the recombinant OMP40 protein was demonstrated to exhibit hemin binding ability, and the molecular mass of the mature polypeptide determined by mass spectrometric analysis was 35.3 kDa, the protein was designated as HBP35 . However, characterization of the hbp35 gene at the transcriptional and translational levels in P. gingivalis and contribution of HBP35 protein to hemin utilization have not been elucidated.
HBP35 protein has unique characteristics including the presence of one thioredoxin-like motif and a conserved C-terminal domain. Recently, it has been reported that the C-terminal domain of a group of P. gingivalis outer membrane proteins plays a crucial role in the coordinated process of exportation and attachment of those proteins onto the cell surface  and that some of the C-terminal domain containing proteins, including RgpB, are glycosylated [9,10]. The last five residues of the C-terminal domain are well conserved not only in P. gingivalis but also in other oral pathogens, and that the last two C-terminal residues (VK) of RgpB have been shown to be essential for correct transport and posttranslational modification . However, the transportation and posttranslational modification mechanisms of C-terminal domain containing proteins other than RgpB remain poorly understood.
In this study, we presented the first evidence that the hbp35 gene produces three translational products in P. gingivalis. One was a 40-kDa protein that was transported to the outer membrane and glycosylated on the cell surface, resulting in diffuse proteins with molecular masses of 50-90 kDa. The others were smaller truncated 29- and 27-kDa proteins. We constructed HBP35-deficient mutants to elucidate the role of the gene products in this microorganism and found that the HBP35 protein (40-kDa) exhibited thioredoxin activity and bound hemin and that its C-terminal domain was involved in its transport to the outer membrane. The protein was also essential for growth of the bacterium in a hemin-depleted environment.
To gain insights into the biological significance of HBP35 in P. gingivalis, HBP35-deficient mutants, which had full length deletion of, or insertion in, the hbp35 gene, were constructed from the wild-type strain 33277. Immunoblot analysis with an anti-HBP35 antibody revealed that whole cell extracts of P. gingivalis 33277 showed three protein bands with apparent molecular masses of 40, 29, and 27 kDa and diffuse bands of 50-90 kDa (Figure (Figure1).1). No protein bands other than those of 70 and 65 kDa indicated by asterisks, which might be non-specific, were detected in the hbp35 full length deletion mutant (KDP166), whereas the hbp35 insertion mutant (KDP164), which had an insertion of the ermF-ermAM DNA cassette just upstream of the F110 residue within the HBP35 protein, showed 29-and 27-kDa proteins (Figure (Figure1).1). We checked independent 18 isolates of KDP164 and 5 isolates of KDP166. All of the isolates showed the same results as shown in Figure Figure1.1. The 40-kDa protein appeared as the full length gene product of hbp35, which coincided with results of previous studies [6,7].
Both full length deletion and insertion P. gingivalis hbp35 mutants formed black pigmented colonies on blood agar plates. No difference was observed in Rgp, Kgp and hemagglutinating activities between the hbp35 mutants and the wild type (data not shown). These results suggest that HBP35 does not influence expression of gingipain-encoding genes.
To determine whether the hbp35 gene produces multiple transcripts, total RNAs were prepared from the wild type and hbp35 mutants. Northern blot analysis was then carried out with an hbp35 DNA probe that hybridized to the hbp35 region coding for Q22-P344. The wild type showed a 1.1-kb transcript hybridizing to the hbp35 probe (Additional file 1). In the hbp35 insertion and full length deletion mutants, there was no 1.1-kb transcript, indicating that the 1.1-kb mRNA was produced from the hbp35 gene. The hbp35 insertion mutant produced transcripts with 1.3-2.2 kb that hybridized to the probe. The ermF probe hybridized to transcripts with similar length in the hbp35 insertion mutant (Additional file 1).
In an approach to understand the potential roles of HBP35 proteins with different molecular masses, we fractionated cells of the wild type and the hbp35 insertion mutant into cytoplasm/periplasm, total membrane, and inner and outer membrane fractions. These fractions were subjected to SDS-PAGE and immunoblot analysis with the anti-HBP35 antibody. The diffuse bands of 50-90 kDa proteins were mainly detected in the outer membrane fraction, whereas the 40-kDa protein was detected in every fraction of the wild type but mainly in the inner membrane fraction. The 29-and 27-kDa proteins were mainly detected in the cytoplasm/periplasm fraction of the wild type and hbp35 insertion mutant (Figure (Figure22).
To determine whether the 27-kDa protein is a truncated form of the HBP35 protein, an immunoprecipitation experiment using the hbp35 insertion mutant (KDP164) cell lysate was carried out with the anti-HBP35 antibody. The resulting immunoprecipitate contained a 27-kDa protein band (Additional file 2), which was digested with trypsin followed by MALDI-TOF mass spectrometric analysis. The 27-kDa protein was found to be derived from a 3'-portion of hbp35, with PMF sequence coverage of 37% of full length protein (Figure (Figure3A).3A). The maximum mass error among the identified 10 tryptic peptides was 14 ppm. Since the detected tryptic peptide located at the most N-terminal region of HBP35 starts from G137 and since the insertion site of the ermF-ermAM DNA cassette in the insertion mutant is just upstream of F110, it is feasible that the 27-kDa protein uses M115 or M135 as the alternative translation initiation site.
To clarify the N-terminal amino acid residue of the truncated HBP35 proteins, we introduced amino acid substitution mutations of [M115A] or/and [M135A] to the hbp35 insertion mutant (KDP164) producing the 29-and 27-kDa HBP35 proteins (Additional file 3). As shown in Figure Figure3B,3B, the 27-kDa protein was not observed in the hbp35 [M135A] insertion mutant (KDP169), while the 29-kDa protein was not observed in the hbp35 [M115A] insertion mutant (KDP168), suggesting that M115 and M135 are the N-terminal amino acid residues of the 29-and 27-kDa proteins, respectively. The use of M115 and M135 as alternative translation initiation sites was supported by the finding that no HBP35 translational product was detected in the hbp35 [M115A and M135A] insertion mutant (KDP170). Moreover, recombinant HBP35 proteins with a C-terminal histidine-tag were produced in an E. coli strain expressing the hbp35 gene and purified by a histidine-tag purification system. Immunoblot analysis revealed that the purified products contained 40-, 29-, and 27-kDa proteins immunoreactive to the anti-HBP35 anitibody. Edman sequencing revealed that the N-terminal amino acid residue of the recombinant 27-kDa protein was M135 (Additional file 4).
Shibata et al.  found that a purified rHBP35 protein (Q22-P344) could bind hemin and that HBP35 was suggested to possess a putative heme binding sequence (Y50CPGGK55). To determine the hemin binding region of HBP35, we constructed and purified rHBP35 (Q22-P344), rHBP35 (Q22-P344 with C48S and C51S) and truncated rHBP35 (M135-P344) proteins with N-terminal histidine-tags using a histidine-tag purification system and carried out hemin binding assays using a hemoprotein peroxidase assay. As shown in Figure Figure4B,4B, all of the rHBP35 (Q22-P344), rHBP35 (Q22-P344 with C48S and C51S) and truncated rHBP35 (M135-P344) proteins were found to have hemin binding ability, implying that the hemin binding site is located in M135-P344 of HBP35 protein.
Since HBP35 protein is a hemin-binding protein, we determined the contribution of HBP35 proteins to acquisition or intracellular storage of heme. The hbp35 insertion mutant, the full length deletion mutant, the complemented strain which was constructed by replacing the intact hbp35 gene into the hbp35 full length deletion mutant, and the wild-type strain were hemin-starved after being grown in enriched BHI broth containing hemin (Figure (Figure5).5). Hemin starvation resulted in retardation of the growth of the hbp35 mutants compared to that of the wild type, whereas the complemented strain partially recovered the growth retardation of the hbp35 deletion mutant under the hemin-depleted condition. Even under the hemin replete condition, the hbp35 mutants grew more slowly than the wild type, suggesting that HBP35 plays a role in hemin utilization in a sufficient hemin concentration (5 μg/ml).
Shiroza et al.  have shown that an hbp35 gene-containing plasmid complemented the defects in motility and alkaline phosphatase activity of an E. coli dsbA mutant. This finding indicates that HBP35 is exported to the periplasm in a dsbA mutant and plays a role in the disulfide bond formation . The HBP35 protein has a thioredoxin motif in the N-terminal region. We performed an insulin reduction assay to determine whether HBP35 has thioredoxin activity. Reduction of disulfide bonds of insulin by thioredoxin activity generates free A and B chains of insulin, and the resulting B chain is precipitated, which can be measured by the increase in turbidity . The reducing activity of rHBP35 (Q22-P344) was higher than that of E. coli thioredoxin, whereas no activity was detected in rHBP35 (Q22-P344 with C48S and C51S), indicating that HBP35 protein exhibits thioredoxin activity and that the two cysteine residues (C48 and C51) are crucial for this activity (Figure (Figure66).
Nguyen et al.  revealed glycosylation of RgpB by immunoblot analysis with a monoclonal antibody (MAb 1B5) that recognizes the anionic polysaccharide of A-LPS [10,15]. To determine whether HBP35 is glycosylated, we carried out an immunoprecipitation experiment. Immunoprecipitates from the protein extracts of KDP136 (gingipain-null mutant) with an anti-HBP35 rabbit polyclonal antibody contained the 40-kDa protein and diffuse proteins of 50-90 kDa, which were revealed by immunoblot analysis with an anti-HBP35 mouse monoclonal antibody (MAb Pg-ompA2) . The diffuse proteins of 50-90 kDa immunoreacted with MAb 1B5, indicating that HBP35 is associated with anionic polysaccharide on the cell surface (Figure (Figure7).7). It is likely that the diffuse bands are HBP35 proteins binding to anionic polysaccharides with different numbers of repeating units.
As HBP35 contains the C-terminal domain motif that may play a role in export and cell surface attachment, and that the presence of diffuse bands of 50-90 kDa proteins is similar to that of RgpB [8-11], it is possible that HBP35 is transported to the outer membrane and anchored to the cell surface by the same transport system as RgpB. Nguyen et al.  reported that the last five C-terminal residues (KVIVK) of RgpB play a significant role in the post-translational modification/proteolytic processing and exportation of proteins to the outer membrane. To determine whether the last five C-terminal residues (K340VLVP344) of HBP35 play a role similar to that of RgpB, we constructed an hbp35 deletion of K340-P344 mutant and found that the mutant showed no diffuse bands but only 33-and 31-kDa proteins, which may have been generated by degradation of HBP35 protein accumulating in the cell (Figure (Figure8).8). The result suggests that the last five C-terminal residues have an important role in the transport of HBP35 protein to the cell surface.
As P. gingivalis requires heme as the source of iron and protoporphyrin IX, a heme binding and transport system is essential for the microorganism to survive. Recently, several TonB-linked outer membrane receptors for heme utilization, including HmuR, Tlr, IhtA and HemR, have been reported . The ability to store heme in bacterial cells appears to provide a nutritional advantage for survival of the bacterium in the iron-limited environment of a healthy gingival crevice . In fact, heme can bind the P. gingivalis cell surface and may then be transported into the cell by an energy-dependent process . Shibata et al.  found that purified rHBP35 protein (Q22-P344) could bind hemin but not hemoglobin or lactoferrin. HBP35 was suggested to possess a putative heme binding sequence (Y50CPGGK55), however, we found in this study that hemin could bind the mutant rHBP35 (Q22-P344 with C48S and C51S) and the truncated rHBP35 (M135-P344) (Figure (Figure4B),4B), indicating that the hemin binding site is located between M135 and P344. The hbp35 mutants grew more slowly than the wild type in hemin-depleted conditions and even in the condition with a sufficient hemin concentration (5 μg/ml), indicating that HBP35 protein plays a role in hemin utilization in various hemin levels.
The truncated HBP35 proteins of 27-and 29-kDa, which were derived from a 3'-portion of the hbp35 gene, were mainly located in the cytoplasm/periplasm fraction. This finding together with the fact that there is no signal peptide region in the two proteins suggests that these proteins are located in the cytoplasm and contribute to the intracellular storage of heme as does bacterioferritin (Figure (Figure6).6). Similar protein expression has been found in Neisseria meningitidis: two forms of PilB protein are produced from the pilB gene. One is secreted to the outer membrane as a whole polypeptide with methionine sulfoxide reductase (Msr) A and B activities, and the other is a truncated form lacking an N-terminal thioredoxin domain, which is generated from an internal AUG initiation codon and is located in the cytoplasm .
Hiratsuka et al.  have previously reported that HBP35 shows no significant similarity with any other known proteins. As the truncated rHBP35 (M135-P344) protein has hemin binding activity, H204-H206, H252-H253, and H261 within the truncated protein may interact with heme, in a similar fashion to the myoglobin and hemoglobin heme pockets in which two histidines hold heme through interaction with the central iron atom .
Recently, Dashper et al.  reported that expression of the hbp35 gene in strain W50 was not induced under a hemin-limited condition. We also observed that expression of the hbp35 gene in 33277 was not induced under hemin-depleted conditions (data not shown). Although HmuR, which is one of the hemin receptors, has been found to be regulated by one transcriptional activator , it seems unlikely that expression of the hbp35 gene is regulated by a specific transcriptional activator under hemin-depleted conditions.
Physiological roles of thioredoxins (Trxs) in P. gingivalis have not been established. In general, the intracellular environment is maintained in a reduced condition because of the presence of small proteins with redox-active cysteine residues, including Trxs, glutaredoxins (Grxs), monocysteine tripeptide glutathione (GSH) and other low-molecular-weight thiols [24,25]. In this regard, analysis of the P. gingivalis 33277 and W83 genome sequences revealed the presence of thioredoxin reductase (TrxB; PGN1232 in 33277, PG1134 in W83), thioredoxin homologue (PGN0033 in 33277, PG0034 in W83), and 5 thioredoxin family proteins (PGN0373, PGN0488, PGN0659 (HBP35), PGN1181, and PGN1988 in 33277, PG0275, PG0616 (HBP35), PG1084, PG1638, and PG2042 in W83), and the absence of Grx, γ-glutamyl-L-cysteine-synthase and GSH synthetase. Recently, it has been shown that Bacteroides fragilis, which is phylogenetically close to P. gingivalis, possesses the TrxB/Trx system as the only reductive system for oxidative stress . We previously showed that the thioredoxin protein (PGN0033) was increased when cells were exposed to atmospheric oxygen . Although physiological roles of the thioredoxin domain of HBP35 protein are unknown at present, the diffuse bands of 50-90 kDa proteins, which contain the thioredoxin domain and are located on the outer membrane, may contribute to the maintenance of the redox status of the cell surface. However, we have not obtained a positive result indicating that HBP35 protein plays a role in protection against oxidative stresses so far.
Amino acid sequences in the RgpB that are necessary for transport of the protein to the outer membrane have been reported [8,11]. When recombinant truncated RgpB lacking its C-terminal 72 residues was produced in P. gingivalis, there was an altered distribution of the protein in the culture supernatant and periplasm. Seers et al.  reported the importance of the C-terminal domain of RgpB for attachment to the outer membrane and suggested that the domain is involved in a coordinated process of export and attachment to the cell surface. Nguyen et al.  found that the last five C-terminal residues of RgpB are conserved in a number of proteins of not only P. gingivalis but also other periodontal pathogens such as Prevotella intermedia and Tannerella forsythia and that they have an important role in mediating correct folding of the nascent protein, which is then transported across the periplasm to be fully glycosylated during its translocation across or on the outer membrane for anchorage to the outer leaflet of the outer membrane. The last five C-terminal residues of HBP35 (KVLVP) contain a stretch of polar-hydrophobic residues as well as those of RgpB (KVIVK). We found in this study that the diffuse bands of 50-90 kDa proteins, which were the main products of the hbp35 gene in the wild type, disappeared in the mutant strain lacking the last five C-terminal residues of HBP35, suggesting that, like RgpB, the C-terminal region of HBP35 plays an important role in transport of HBP35 to the outer membrane and anchorage to the membrane. Very recently, we found a novel protein secretion system (Por secretion system) in bacteria such as P. gingivalis belonging to phylum Bacteroidetes and suggested that the secretion system uses the C-terminal domain as a transportation signal . HBP35 may therefore be transported to the cell surface via this secretion system.
The diffuse HBP35 protein bands of 50-90 kDa were immunoreactive with APS-recognizing MAb 1B5, indicating that a part of HBP35 protein is glycosylated, which is coordinated with the process of export. Rangarajan et al.  have recently shown that the anionic polysaccharide is associated with lipid A and they therefore renamed it LPS with APS repeating unit (A-LPS). HBP35 therefore as well as RgpB may be glycosylated on the cell surface by attachment to A-LPS.
We found that the hbp35 gene produced a 1.1-kb transcript and several translational products; (i) a 40-kDa HBP35, which was derived from the whole hbp35 gene, was mainly located in the inner membrane, (ii) 29-and 27-kDa HBP35 proteins were N-terminal-truncated products lacking the signal peptide sequence and the thioredoxin domain and were mainly located in the cytoplasm, and (iii) diffuse HBP35 bands of 50-90 kDa proteins were glycosylated and located on the outer membrane. Analysis of these HBP35 proteins revealed that they played a significant role in heme acquisition. The last five C-terminal residues of HBP35 were crucial for the secretion to the outer membrane.
All bacterial strains and plasmids used in this study are listed in Additional file 5.
P. gingivalis strains were grown anaerobically (80% N2, 10% CO2, 10% H2) in enriched brain-heart infusion (BHI) broth (Becton Dickinson) or on enriched Trypto-soya (TS) agar plates (Nissui) supplemented with 5 μg/ml hemin (Sigma) and 0.5 μg/ml menadione (Sigma). Luria-Bertani (LB) broth and LB agar plates were used for growth of E. coli strains. Antibiotics were used at the following concentrations: ampicillin (Ap; 100 μg/ml for E. coli, 10 μg/ml for P. gingivalis), erythromycin (Em; 10 μg/ml for P. gingivalis), tetracycline (Tet; 0.7 μg/ml for P. gingivalis), kanamycin (Km; 50 μg/ml for E. coli).
Proteinase inhibitors Nα-p-tosyl-L-lysine chloromethyl ketone (TLCK) and iodoacetamide were purchased from Wako, and leupeptin was obtained from Peptide Institute.
P. gingivalis W83 and 33277 genome sequence data were obtained from [GenBank: AE015924] and [GenBank: AP009380], respectively. The DNA primers used in this study are shown in Additional file 6. P. gingivalis hbp35 insertion mutant was constructed as follows. A DNA fragment corresponding to a region (0.80 kb) containing the C-terminal lower portion of PG0615 and the N-terminal upper portion of the PG0616 gene was generated by PCR using P. gingivalis W83 chromosomal DNA as the template with a forward primer, MS1, containing a KpnI site (underlined) and a backward primer, MS2, containing an EcoRI site (underlined). The resulting fragment was cloned into the pGEM-T Easy vector (Promega) to yield pKD732. A DNA fragment corresponding to a region (0.70 kb) containing the C-terminal portion of the PG0616 gene was generated by PCR using P. gingivalis W83 chromosomal DNA as the template with a forward primer, MS3, containing a BglII site (underlined) and a backward primer, MS4, containing a NotI site (underlined). The resulting fragment was cloned into the pGEM-T Easy vector to yield pKD733. The BglII-NotI region of pKD733 containing the 0.70-kb fragment was swapped with both equivalent sites of pKD704 , resulting in pKD734. The KpnI-EcoRI region of pKD732 containing the 0.80-kb fragment was swapped with both equivalent sites of pKD734, resulting in pKD735. Proper orientation of the pKD735 gene was confirmed by DNA sequence analysis. The pKD735 plasmid DNA was linearlized by NotI and introduced into P. gingivalis 33277 by electroporation . The cells were spread on TS agar containing 10 μg/ml Em and incubated anaerobically for 7 days. Proper sequence replacement of the Em-resistant transformants (KDP164 [insertion mutant]) was verified by Southern and Western blot analyses. P. gingivalis hbp35 whole gene deletion mutant from 33277 was constructed as follows. A DNA fragment corresponding to a region (0.49 kb) within the PG0615 gene and upstream region of PG0616 gene was generated by PCR using pMD125  as the template with a forward primer, MS5, containing an SphI site (underlined) and a backward primer, MS6, containing a BamHI site (underlined). The resulting fragment was cloned into the pGEM-T Easy Vector to yield pKD737. A DNA fragment corresponding to a region (0.47 kb) located between the PG0617 gene and PG0618 gene upper region was obtained by PCR with a forward primer, MS7, containing a PstI site (underlined) and a backward primer, MS8, containing an SacI site (underlined). The resulting fragment was cloned into pCR4 (Invitrogen) to yield pKD738. The SphI-BamHI region of pKD737 containing the 0.49-kb fragment was inserted into the same sites of pAL30  which contains the ermF gene in the pGEM-T Easy Vector and was located at the upper region of the ermF DNA block (1.2 kb), resulting in pKD739. The PstI-SacI site of pKD738 was inserted into the same sites of pKD739 that was located at the lower region of the ermF DNA block, resulting in pKD740. The pKD740 plasmid was linearlized by SacI and introduced into P. gingivalis 33277 by electroporation. Proper sequence replacement of the resulting Em-resistant transformant (KDP166 [deletion mutant]) was verified by PCR analysis.
To create an hbp35 mutant lacking the last five amino acid residues (K340-P344), a DNA fragment corresponding to a region (1.5 kb) containing the C-terminal lower portion of PG0615 and PG0616 lacking K340-P344 was generated by PCR using pMD125 as the template with a forward primer, MS9, containing a KpnI site (underlined) and a backward primer, MS10, containing a BamHI site (underlined). The resulting fragment was cloned into the pCR4 vector to yield pKD741. A DNA fragment corresponding to a region (0.47 kb) containing the PG0617 gene and PG0618 gene upper region was generated by PCR using pMD125 as the template with a forward primer, MS11, containing a BamHI site (underlined) and a backward primer, MS12, containing a NotI site (underlined). The resulting fragment was cloned into the pGEM-T Easy Vector to yield pKD742. The BamHI-NotI site of pKD742 was inserted into the same sites of pKD741 to yield pKD743. To create a BglII site located 8 bp upstream of PG0617 in pKD743, the two-stage PCR-based overlap extension method  was applied. MS9 and MS12, containing a NotI site (underlined), were used as external primers, and MS13, containing a BglII site (underlined), and MS14, containing a BglII site (underlined), were used as internal primers. Briefly, the amplified PCR fragments with MS9 and MS14 or with MS13 and MS12 were purified and further amplified with MS9 and MS12 primers by using both fragments as the template and was cloned into the pBluescript SK-, yielding pKD744. The ermF-ermAM DNA block (2.1 kb) from pKD399  was inserted into the BglII site of pKD744 that was located at the junction of the 1.5-kb hbp35 gene-containing fragment and the 0.47-kb hbp35 downstream fragment to yield pKD745. The pKD745 plasmid was linearlized by NotI and introduced into P. gingivalis 33277 by electroporation. Proper sequence replacement of the resulting Em-resistant transformant (KDP167) was verified by PCR analysis.
To construct a strain where the hbp35 would be restored, the KpnI-BglII site of pKD744 was swapped with the PCR fragment which was amplified by MS9 and a backward primer, MS14, containing a BglII site (underlined) using pMD125 as the template to yield pKD754, and then the BamHI-BamHI fragment containing the cepA DNA block by using CEPFOR and CEPREV primers from pCS22 was inserted into the BglII site of pKD754 to yield pKD755. The pKD755 plasmid was linearlized by NotI and introduced into KDP166 by electroporation. Proper sequence replacement of the resulting Ap-resistant transformant (KDP171) was verified by PCR and immunoblot analyses.
To create hbp35 insertion mutants with M115A and/or M135A, site-directed mutagenesis was performed using a QuickChange II Site-Directed Mutagenesis kit (Stratagene, La Jolla, CA, USA). The hbp35 insertion mutant targeting vector containing M115A substitution (pKD746) was constructed with the oligonucleotide sense primer MS15, containing an M115A substitution (underlined), and antisense primer MS16, containing an M115A substitution (underlined), and the recombinant plasmid pKD735 as the template. The hbp35 insertion mutant targeting vectors containing M135A (pKD747) or M115A M135A substitutions (pKD748) were constructed with the oligonucleotide sense primer MS17, containing an M135A substitution (underlined), and antisense primer MS18, containing an M135A substitution (underlined), and the recombinant plasmid pKD735 and pKD746 as the template. To create hbp35[M115A], hbp35[M135A] or hbp35[M115A M135A] insertion mutants which had an insertion with the ermF-ermAM DNA cassette that was located just upstream of F110, pKD746, pKD747 and pKD748 were linearlized with NotI and introduced into P. gingivalis 33277, giving KDP168, KDP169 and KDP170, respectively.
To create a recombinant HBP35 protein (A1-P344) with a C-terminal histidine-tag overexpression system, a 1.0-kb PCR fragment was amplified using forward primer MS19, containing an NcoI site (underlined) and backward primer MS20, containing an XhoI site (underlined), and then cloned into the pCR4 to yield pKD749. The EcoRI-XhoI sites of pKD749 were inserted into the same sites of pET21d(+), resulting in pKD750. To create a recombinant HBP35 protein (Q22-P344) with an N-terminal histidine-tag overexpression system, a 0.97-kb PCR fragments were amplified using forward primer MS21 and backward primer MS22 and then cloned into the pET30 Ek/LIC vector (Novagen), resulting in pKD751. Site-directed mutagenesis of the thioredoxin active site in HBP35 was performed using a QuickChange II Site-Directed Mutagenesis kit. A double amino acid substitution mutant (rHBP35 Q22-P344 with C48S C51S) was created with the oligonucleotide sense primer MS23, containing C48S and C51S substitutions (underlined), and antisense primer MS24, containing C48S and C51S substitutions (underlined), using the recombinant plasmid pKD751 as the template to yield pKD752. Proper mutation was confirmed by DNA sequencing. To create a recombinant truncated HBP35 protein (M135-P344) with an N-terminal histidine-tag overexpression system, a 0.66-kb PCR fragments were amplified using forward primer MS25 and backward primer MS22, and then cloned into pET30Ek/LIC vector, resulting in pKD753.
E. coli BL21(DE3)pLysS harboring pKD750, pKD751, pKD752 or pKD753 was cultured in LB medium containing 100 μg/ml of Ap at 37°C to OD600 of 0.4-0.6, and then IPTG was added to the culture at 1 mM, followed by an additional 3-h incubation. The cells were harvested, suspended in buffer A (50 mM NaH2PO4 [pH 8.0], 500 mM NaCl, 10 mM imidazole) and then disrupted with a French Press. The mixture was centrifuged at 3,000 × g for 15 min to separate the inclusion body fraction (pellet) from the soluble fraction (supernatant). The supernatant was loaded onto a pre-equilibrated Ni2+-NTA agarose column (Invitrogen) of 2 ml in bed volume and incubated at 4°C for 30 min. The column was washed three times with buffer B (50 mM NaH2PO4 [pH 8.0], 500 mM NaCl, 20 mM imidazole) and the bound protein was eluted with 10 ml of elution buffer (50 mM NaH2PO4 [pH 8.0], 500 mM NaCl, 250 mM imidazole) as 1-ml fractions. The fractions were analyzed by SDS-PAGE. The pure fractions were pooled and then dialyzed against milliQ water and stored at -20°C until further use. N-terminal amino acid sequencing (Edman sequencing) of the purified rHBP35 protein with the C-terminal histidine-tag was carried out using the service facility in CSIRO (Melbourne, Australia).
SDS-PAGE was performed according to the method of Laemmli . Protease inhibitors (leupeptin and TLCK) were added to Laemmli solubilizing buffer to avoid proteolysis by endogenous proteases. The gels were stained with 0.1% Coomassie Brilliant Blue R-250 (CBB). For immunoblotting, proteins on SDS-PAGE gels were electrophoretically transferred onto polyvinylidene fluoride (PVDF) membranes (Immobilon P; Millipore) as described previously . The blotted membranes were detected with an anti-HBP35 polyclonal antibody .
P. gingivalis cells were harvested from 400 ml of fully-grown culture by centrifugation at 10,000 × g for 30 min at 4°C, washed twice with 10 mM HEPES-NaOH (pH 7.4) containing 0.15 M NaCl, and resuspended in 20 ml of HEPES containing 0.1 mM TLCK, 0.1 mM leupeptin and 0.2 mM PMSF. The cells were disrupted with a French Press by three passes at 100 MPa in the presence of 25 μg/ml each of RNase and DNase. Unbroken cells were removed by centrifugation at 1,000 × g for 10 min and the supernatant was subjected to ultracentrifugation at 100,000 × g for 60 min. The precipitates were treated with 1% Triton-X100 in HEPES containing 20 mM MgCl2 for 30 min at 20°C. The inner and outer membrane fractions were recovered as a supernatant and a pellet, respectively, by ultracentrifugation at 100,000 × g for 60 min at 4°C .
To identify the 27-kDa protein, P. gingivalis KDP161 cells were harvested, and the cell pellets were dissolved with RIPA buffer (150 mM NaCl, 1% Nonidet P-40, 0.5% deoxycholate, 0.1% SDS and 50 mM Tris-HCl, pH 8.0) and then immunoprecipitated by EZview red protein A affinity gel (Sigma) with anti-HBP35 polyclonal antibody, followed by SDS-PAGE analysis with CBB staining and immunoblot analysis. Protein bands from the SDS-PAGE gel were excised and subjected to in-gel tryptic digestion as described previously [8,9]. Gel pieces were washed in 50 mM NH4HCO3-ethanol (1:1, vol/vol), reduced, alkylated with dithiothreitol and iodoacetamide, respectively, and digested with sequencing-grade modified trypsin (10 ng/μl) (Promega) overnight at 37°C. Each digest (0.5 μl) was then analyzed by mass spectrometry using an Ultraflex TOF/TOF instrument (Bruker Daltonics, Bremen, Germany) in positive-ion and reflectron mode. A saturated solution of α-cyano-4-hydroxycinnamic acid was prepared in 97:3 (vol/vol) acetone-0.1% aqueous trifluoroacetic acid (TFA). A thin layer of matrix was prepared by pipetting and immediately transferring 2 μl of this solution onto 600-μm anchors of an AnchorChip target plate (Bruker Daltonics). The tryptic digest sample (0.5 μl) was then deposited onto the thin layers with 2.5 μl of 0.1% (vol/vol) TFA for 1 min. Mass spectra were calibrated by external calibration using a standard peptide mix (Bruker Daltonics). Proteins were identified by PMF against the P. gingivalis database (available at The Institute for Genomic Research [TIGR] website [http://www.tigr.org]) using an in-house Mascot search engine (Matrix Science Ltd., London, United Kingdom) and BioTools 2.2 software (Bruker Daltonics) and by comparison with tryptic peptide mass lists generated by using General Protein Mass Analysis for Windows software (Lighthouse Data, Odense, Denmark).
Total RNA extraction and Northern blot analysis of mRNA were carried out as described previously  with some modifications. The 0.96-kb DNA fragment coding for Q22 to P344 of HBP35 and the 0.80-kb DNA fragment coding for M1 to S266 of ErmF were obtained by PCR that were used as the radiolabelled hbp35 and ermF probes, respectively. To label the DNA probes, [α-32P]dCTP and the ready-to-go DNA labeling beads kit (GE Healthcare) was used. The radiolabelled products were analyzed with a fluoro-image analyzer FLA-5100 (Fujifilm).
Hemin binding to rHBP35 proteins was assayed using the catalytic property of hemoprotein, which has peroxidase activity in the presence of H2O2, by the method of Shibata et al.  with some modifications. Ten microliters of protein solution (2 μg) was treated with 1.5 μl of 1.25 mM hemin for 2 h at room temperature. After SDS-PAGE, the gel was washed twice for 30 min in TBS buffer (10 mM Tris-HCl, pH 7.5, 0.9% NaCl) and then exposed to a reaction buffer (1 mg of 4-methoxy-1-naphthol, 20 μl H2O2 in 50 ml TBS buffer) for 30 min at room temperature.
To determine the ability for growth under hemin starvation conditions, bacterial strains to be tested were first grown in the presence of hemin for 48 h and then deprived of hemin. The overnight cultures were prepared by growing the strains in hemin-containing enriched BHI broth overnight. In the case of first grown in hemin-containing BHI broth for 48 h, the overnight cultures were diluted 50-fold with hemin-containing BHI broth. Then the first grown bacterial cultures to be tested were diluted 50-fold with hemin-free BHI broth. The cell density of the culture was measured at OD595.
A fresh solution of 1 mg/ml insulin was prepared in 100 mM potassium phosphate, 2 mM EDTA, pH 7.0. The assay mixture contained a total volume of 800 μl of 100 mM potassium phosphate, 2 mM EDTA, pH 7.0, 0.13 mM insulin, 1 mM DTT, and 1 μM of freshly purified recombinant histidine-tagged HBP35 protein in the standard insulin disulfide reduction assay . The increase in turbidity due to formation of the insoluble insulin B chain was measured at OD650 and 30°C. One micromolar fresh E. coli thioredoxin 1 (Sigma) was used as a positive control.
The harvested P. gingivalis KDP136 (gingipain-null mutant) cells  were dissolved with RIPA buffer (150 mM NaCl, 1% Nonidet P-40, 0.5% deoxycholate, 0.1% SDS and 50 mM Tris-HCl, pH 8.0) under absence of protease inhibitors and immunoprecipitated by protein G agarose beads (GE Healthcare) with 5 μg of anti-HBP35 polyclonal antibody or 5 μg of anti-Dps polyclonal antibody, or without an antibody. Each resulting precipitate was dissolved with the same volume of the sample buffer and loaded on an SDS-10% polyacrylamide gel. Immunoblot analysis was performed with MAb 1B5 , MAb Pg-ompA2  and anti-Dps antibody .
MS, YA, ECR and KN designed the study. MS wrote the manuscript with BP, ECR and KN. MS, YS, TS, HY, BP, YYC, KS and MN performed the experiments in this study. Especially, MS participated in almost all of the study, HY measured gingipain activity, YYC performed MALDI-TOF mass spectrometric analysis, and MN performed hemagglutinating assay. All authors read and approved the final manuscript.
Northern blot analysis of hbp35 mRNA. Total RNAs were electrophoresed, blotted, hybridized with the hbp35 DNA probe (left) or the ermF DNA probe (right), and subjected to autoradiography (see Methods). Lane 1, 33277; lane 2, KDP164 (hbp35 insertion mutant); lane 3, KDP166 (hbp35 deletion mutant).
Preparation of the anti-HBP35-immunoreactive 27-kDa protein for PMF analysis. Immunoprecipitates of lysates of KDP164 (hbp35 insertion mutant) with anti-HBP35 antibody was analyzed by SDS-PAGE followed by staining with CBB (left) or immunoblot analysis with anti-HBP35 antibody (right). A 27-kDa protein band on the gel indicated was subjected to PMF analysis.
Structures of the HBP35 protein and the hbp35 gene. A. Domain organization of HBP35 protein. HBP35 contains a signal peptide region, a thioredoxin domain and a C-terminal domain. B. The hbp35 gene loci in various mutant strains. Mutated hbp35 genes of KDP164 (hbp35 insertion mutant), KDP168 (hbp35 [M115A] insertion mutant), KDP169 (hbp35 [M135A] insertion mutant) and KDP170 (hbp35 [M115A M135A] insertion mutant) were depicted.
N-terminal amino acid sequencing of the recombinant 27-kDa protein produced in an E. coli expressing the hbp35 gene. rHBP35 products, which were partially purified using a C-terminal histidine-tag, were analyzed by SDS-PAGE followed by staining with CBB (left) or immunoblot analysis with anti-HBP35 antibody (right). The N-terminal amino acid sequence of the recombinant 27-kDa protein was determined by Edman sequencing, resulting in M135 as an N-terminal residue.
Bacterial strains and plasmids used in this study.
Oligonucleotides used in this study.
We thank Kaiting Ng for advice on some aspects of molecular work. We also thank members of the Division of Microbiology and Oral Infection, Nagasaki University Graduate School of Biomedical Sciences, and Cooperative Research Centre for Oral Health Science, Melbourne Dental School, University of Melbourne for helpful discussion. This work was supported by Grants-in-Aid (20249073 and 20791341) for scientific research from the Ministry of Education, Science, Sports, Culture, and Technology, Japan to KN and MS, respectively, by the Global COE Program at Nagasaki University to KN and in part by the president's discretionary fund of Nagasaki University, Japan to MS.