Original Research ARTICLE
Recovery of the Peptidoglycan Turnover Product Released by the Autolysin Atl in Staphylococcus aureus Involves the Phosphotransferase System Transporter MurP and the Novel 6-phospho-N-acetylmuramidase MupG
- 1Microbiology/Biotechnology, Department of Biology, Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany
- 2Microbial Genetics, Department of Biology, Interfaculty Institute of Microbiology and Infection Medicine, University of Tübingen, Tübingen, Germany
The peptidoglycan of the bacterial cell wall undergoes a permanent turnover during cell growth and differentiation. In the Gram-positive pathogen Staphylococcus aureus, the major peptidoglycan hydrolase Atl is required for accurate cell division, daughter cell separation and autolysis. Atl is a bifunctional N-acetylmuramoyl-L-alanine amidase/endo-β-N-acetylglucosaminidase that releases peptides and the disaccharide N-acetylmuramic acid-β-1,4-N-acetylglucosamine (MurNAc-GlcNAc) from the peptido-glycan. Here we revealed the recycling pathway of the cell wall turnover product MurNAc-GlcNAc in S. aureus. The latter disaccharide is internalized and concomitantly phosphorylated by the phosphotransferase system (PTS) transporter MurP, which had been implicated previously in the uptake and phosphorylation of MurNAc. Since MurP mutant cells accumulate MurNAc-GlcNAc and not MurNAc in the culture medium during growth, the disaccharide represents the physiological substrate of the PTS transporter. We further identified and characterized a novel 6-phospho-N-acetylmuramidase, named MupG, which intracellularly hydrolyses MurNAc 6-phosphate-GlcNAc, the product of MurP-uptake and phosphorylation, yielding MurNAc 6-phosphate and GlcNAc. MupG is the first characterized representative of a novel family of glycosidases containing domain of unknown function 871 (DUF871). The corresponding gene mupG (SAUSA300_0192) of S. aureus strain USA300 is the first gene within a putative operon that also includes genes encoding the MurNAc 6-phosphate etherase MurQ, MurP, and the putative transcriptional regulator MurR. Using mass spectrometry, we observed cytoplasmic accumulation of MurNAc 6-phosphate-GlcNAc in ΔmupG and ΔmupGmurQ markerless non-polar deletion mutants, but not in the wild type or in the complemented ΔmupG strain. MurNAc 6-phosphate-GlcNAc levels in the mutants increased during stationary phase, in accordance with previous observations regarding peptidoglycan recycling in S. aureus.
Staphylococcus aureus is a small, spherical bacterium (∼1 μm diameter) belonging to the phylum firmicutes that can cause life-threatening infections due to the emergence of multi-drug resistance (Hiramatsu et al., 2014). As a Gram-positive bacterium, S. aureus is encased in a thick layer of peptidoglycan (PGN), which maintains cell shape and protects the cells from rupture due to high turgor pressure (Cabeen and Jacobs-Wagner, 2005). The general structure of the PGN is conserved in all eubacteria, consisting of a glycan backbone of two alternating β-1,4-glycosidically linked sugars N-acetylmuramic acid (MurNAc) and N-acetylglucosamine (GlcNAc) and polypeptides, connected to the D-lactyl moiety of MurNAc, that are partially crosslinked (Vollmer et al., 2008). The PGN polymer is synthesized by glycosyltransferases and transpeptidases [involving shape, elongation, division and sporulation (SEDS) family peptidoglycan synthases and penicillin binding proteins (PBPs)] through polymerization of GlcNAc-β-1,4-MurNAc-peptide building blocks, provided by lipid II precursors (Cho et al., 2016; Meeske et al., 2016). The overall peptidoglycan structure of S. aureus is different in some aspects compared to most other bacterial species. Firstly, pentaglycine (Gly5) bridges are attached to the ε-NH2 group of L-lysine (L-Lys) of the stem tetrapeptide L-alanine-D-isoglutamine-L-Lys-D-alanine (L-ala-D-isoGln-L-Lys-D-Ala) that are extensively cross-linked (degree of crosslinking of about 80%, dependent on the growth phase and growth conditions) with neighboring peptide stems via their carboxyl group of D-Ala (Gally and Archibald, 1993; Litzinger and Mayer, 2010). Secondly, the glycan chains are comparatively short. About 80% of the glycan chains of the mature cell wall have a predominant length of 3–10 disaccharides, the average degree of polymerization is 6 disaccharides, and only about 15% of the glycan chains have a degree of polymerization more than 25 (Boneca et al., 2000).
The coccus-shaped S. aureus divides sequentially in three orthogonal planes over three consecutive division cycles (Monteiro et al., 2015). Although elongation-specific cell wall synthesis machinery is absent, the cells elongate before initiation and after completion of the division septum (Monteiro et al., 2015). The final splitting of daughter cells is accompanied by fast reshaping of the flat septum to finally yield two coccoid offspring cells. Thus, the peptidoglycan is remarkably dynamic and it is constantly degraded during the cell cycle of S. aureus by peptidoglycan hydrolases (potential autolysins) (Foster, 1995; Ramadurai et al., 1999; Takahashi et al., 2002; Kajimura et al., 2005; Biswas et al., 2006; Frankel et al., 2011; Wheeler et al., 2015; Chan et al., 2016). The major autolysin of S. aureus, called Atl, is a multi-domain enzyme, composed of a secretion signal peptide, a propeptide of still unclear function, and two catalytic domains, an N-terminal N-acetylmuramoyl-L-alanine amidase as well as a C-terminal endo-β-N-acetylglucosaminidase domain, which are interrupted by cell wall binding repeats (Sugai et al., 1995). The enzyme undergoes proteolytic processing to generate two extracellular peptidoglycan hydrolases, a 62 kDa N-acetylmuramoyl-L-alanine amidase (AtlAM) and a 51 kDa endo-β-N-acetylglucosaminidase (AtlGL), which localize in a ring-like structure on the cell surface at the septal region, most likely binding to lipoteichoic acids, extending from the cell membrane (Yamada et al., 1996; Götz et al., 2014). Both Atl hydrolase entities can also be secreted and are found in the culture supernatants of some strains (Sugai et al., 1995). Atl functions during cell expansion and division, and it is required for proper daughter cell separation (Sugai et al., 1995; Biswas et al., 2006). Furthermore, Atl is associated with autolysis processes, e.g., during biofilm formation (Biswas et al., 2006; Bose et al., 2012). Besides AtlGL, S. aureus also possesses three other N-acetylglucosaminidases, SagA, SagB, and ScaH, which are important for proper septum formation at the final stage of cell division. SagB was also found to be responsible for shortening of newly synthesized glycan strands to their physiological length, thus ensuring flexibility during the cell elongation process (Wheeler et al., 2015; Chan et al., 2016). Interestingly, the S. aureus genome apparently does not encode any N-acetylmuramidases, with the exception of two putative lytic transglycosylases, IsaA and SceD (Stapleton et al., 2007), indicating that the processing of glycan strands in this organism involves endo-acting N-acetylglucosaminidases, besides peptidoglycan amidases and endopeptidases (Ramadurai et al., 1999; Kajimura et al., 2005; Frankel et al., 2011). The combined activities of these PGN hydrolases generate MurNAc-GlcNAc and peptides as final peptidoglycan turnover products.
It was calculated that during the process of PGN turnover in S. aureus, 15% (Wong et al., 1974) or up to 25% (Blümel et al., 1979) of cell wall material fragments are released per generation in the culture medium. However, the ability of Gram-positive bacteria in general to recycle these fragments was questioned for a long time. We recently elucidated that recycling occurs in different Gram-positive bacteria such as S. aureus, Bacillus subtilis, and Steptomyces coelicolor and revealed that the MurNAc 6-phosphate (MurNAc 6P) etherase MurQ (Borisova et al., 2016), responsible for the intracellular conversion of MurNAc 6P to GlcNAc 6-phosphate and D-lactate, is required for this process. In addition, we quantified the intracellular accumulation of MurNAc 6P in the markerless ΔmurQ mutant, showed that recycling of the MurNAc portion of peptidoglycan occurs predominantly during nutrient limitation within transition and stationary phase (Borisova et al., 2016). Furthermore we discovered that peptidoglycan recycling is essential for bacterial survival in the late stationary phase (Borisova et al., 2016). In S. aureus strain USA300, the murQ etherase gene (SAUSA300_0193) is encoded in an operon together with SAUSA300_0194, encoding the enzyme IIB and IIC domains of the MurNAc PTS-transporter MurP, SAUSA300_0195, encoding a MurR-like regulator, and SAUSA300_0192, encoding a protein with unknown function (Borisova et al., 2016).
We hypothesized that MurNAc-GlcNAc, the product of cell wall cleavage by Atl, rather than MurNAc, might be taken up and recycled in S. aureus and proposed a role of the gene SAUSA300_0192 of unknown function in this process. To prove this hypothesis, we generated markerless gene deletion mutants and investigated the intracellular and extracellular accumulation of specific recycling products in different growth phases by mass spectrometry. Our study showed that MurNAc 6P-GlcNAc accumulates in SAUSA300_0192 mutant, predominantly during stationary phase, and that this compound is generated by the uptake and phosphorylation of MurNAc-GlcNAc by the PTS transporter MurP. The SAUSA300_0192 gene was shown to encode a novel 6-phospho-N-acetylmuramidase, named MupG that hydrolyses MurNAc 6P-GlcNAc yielding MurNAc 6P and GlcNAc. MupG is the first characterized protein of a so far unexplored family of proteins containing the domain of unknown function 871 (DUF871). Altogether in this study we revealed the recycling pathway of the peptidoglycan sugar turnover product of the Atl autolysin in S. aureus.
Materials and Methods
Chemicals, Enzymes, and Oligonucleotides
Enzymes for DNA restriction and for cloning were purchased from New England Biolabs (Ipswich, USA) or Thermo Fischer Scientific (Waltham, MA, United States). The Gene JET plasmid miniprep kit, PCR purification kit, and Gene Ruler 1 kb marker were also purchased from Thermo Fisher Scientific and anhydrotetracycline was obtained from Biomol GmbH (Hamburg, Germany). Oligonucleotides were purchased from MWG Eurofins (Ebersberg, Germany) and are listed in Supplementary Table 1.
Bacterial Strains, Growth Conditions, and Plasmids
The bacterial strains and plasmids used in this study are listed in Supplementary Table 2. The construction of mutant strains and plasmids is also described in the Supplementary Material. Staphylococcus aureus USA300 JE2 strain was cultured aerobically in lysogeny broth (LB broth Lennox, Carl Roth) at 37°C and with continuous shaking at 160 rpm or on solid LB supplemented with 1.5% agar. S. aureus overnight cultures (∼16 h) were used to inoculate fresh LB medium to yield an initial optical density at 600 nm (OD600) of 0.05 for growth studies and for the determination of intracellular accumulation of N-acetylmuramic acid 6-phosphate-N-acetylglucosamine (MurNAc 6P-GlcNAc) at different growth phases. BM medium (10 g/l peptone, 5 g/l yeast extract, 1 g/l glucose, 5 g/l NaCl, 1 g/l K2HPO4) was used to prepare electrocompetent S. aureus JE2 cells and for the generation of the markerless ΔmupG and ΔmupGmurQ mutants (see Supplementary Data in the Supplementary Material). Antibiotics were used, when appropriate, at the following concentrations: 100 μg/ml ampicillin and 30 μg/ml kanamycin for E. coli and 10 μg/ml chloramphenicol for S. aureus.
Generation of Cytosolic Fractions and Reduction of Samples With NaBH4
Overnight cultures of S. aureus JE2 wild type, ΔmupG and ΔmupGmurQ mutants were used to inoculate LB medium to an initial OD600 of 0.05. Bacteria were grown at 37°C with constant shaking and harvested at mid-exponential growth phase (OD600 of 2.4, grown for ∼3–3.5 h), at transitional phase (OD600 of 7.2, grown for 9 h) and stationary phase (OD600 of 5.9, grown for 24 h). Afterward, 50 ml of the culture were transferred to Falcon tubes, bacteria were centrifuged at 4,000 × g for 10 min, washed with 20 ml deionized water, and pellets were frozen at -80°C. Bacterial samples were thawed at room temperature and suspended in different volumes of water to prepare cell suspensions with OD600 of 250 per ml in the different growth phases. Seven hundred microliters of the bacterial suspensions were transferred to new tubes containing ∼0.25 g glass beads (0.25–0.5 mm; Roth) and cells were disrupted in a cell homogenisor (Precellys Evolution, Bertin Technologies) at 6000 rpm for 30 s. This procedure was repeated 4 times, with cooling on ice for 1 min after the second cycle. Lysates were cooled briefly and subsequently centrifuged for 10 min at maximum speed in a microcentrifuge. Two hundred microliters of each supernatant was added to 800 μl of ice-cold acetone to precipitate remaining proteins. After centrifugation (12,000 × g for 10 min), the supernatant was transferred to a new tube, and samples were dried under vacuum for 2 h at 55°C and finally stored at 4°C prior to LC-MS measurements.
Reduction solution was freshly prepared for each experiment by adding 500 μl of 0.5 M borate buffer (pH 9) to 5 mg of sodium borohydride, as previously described (Schaub and Dillard, 2017). Thirty microliters of the cytosolic fractions or the culture supernatants were added to equal volumes of the reduction solution and samples were incubated for 20 min at room temperature. Reactions were adjusted to pH between 3 and 4 by adding 10 μl of 8.5% phosphoric acid. Samples were dried under vacuum at 45°C and pellets were solved in 30 μl of deionized water prior to LC-MS analysis.
Analysis of MurNAc 6P-GlcNAc Accumulation by LC-MS
Sample analysis of bacterial cytosolic fractions was conducted using an electrospray ionization-time of flight (ESI-TOF) mass spectrometer (MicrOTOF II; Bruker Daltonics), operated in negative or positive ion-mode that was connected to an UltiMate 3000 high performance liquid chromatography (HPLC) system (Dionex). For HPLC-MS analysis cytosolic samples were dissolved in 50 μl deionized water and 3 μl were injected into a Gemini C18 column (150 by 4.6 mm, 5 μm, 110 Å, Phenomenex). A 45 min program at a flow rate of 0.2 ml/min was used to separate compounds in the cytosolic fractions as previously described (Gisin et al., 2013). The mass spectra of the investigated samples were presented as base peak chromatograms (BPC), differential spectra (DS, obtained by subtraction of BPCmutant minus BPCwildtype) and extracted ion chromatograms (EIC) in DataAnalysis program and were presented in Prism 6 (GraphPad). The relative amounts of MurNAc 6P-GlcNAc in different growth phases and in mupG complementation experiments were determined by calculating the area under the curve (AUC) of the respective EIC spectra for MurNAc 6P-GlcNAc.
Construction of pET28a-mupG Plasmid and Heterologous Expression and Purification of MupG-His6
For heterologous overexpression in E. coli, the mupG gene was cloned in a pET28a(+) expression vector as a recombinant protein with a C-terminal His6-tag. Therefore, genomic DNA from S. aureus USA300 JE2 strain was used to amplify the mupG gene by PCR using primer pair MB-67 and MB-68. Both, the PCR product and vector were digested with NcoI and XhoI restriction enzymes, ligated by T4 DNA ligase and chemically competent E. coli DH5α cells were transformed with the ligation reaction mixture. The pET28a-mupG recombinant plasmid was isolated from kanamycin-resistant E. coli cells and DNA sequence was verified by sequencing. BL21(DE3) cells were then transformed with the pET28a-mupG plasmid and protein was expressed by addition of IPTG (isopropyl-β-D-thiogalactopyranoside), controlling the T7 inducible promoter.
For expression of MupG, an overnight culture of E. coli BL21(DE3) pET28a-mupG cells was diluted to an OD600 of 0.05 with LB medium supplemented with 30 μg/ml kanamycin (final volume of 1 l) and cells were grown at 37°C with shaking. MupG expression was induced by addition of 1 mM IPTG after the culture reached an OD600 of 0.75. Three hours after induction, bacteria were harvested by centrifugation (4,000 × g, 4°C, 20 min) and frozen at -20°C. Then, cells were solved in phosphate buffer A (20 mM Na2HPO4, 500 mM NaCl, pH 8), disrupted by sonication (Branson Sonifier 250, 3 times for 2 min, output 5, duty cycle of 50%) and cell debris were removed by centrifugation (38,000 × g, 4°C, 20 min). The soluble fraction was filtered (0.2 μm, Sarstedt) and the His-tagged protein was purified by Ni2+ affinity chromatograpy system Äkta Purifier on a 1 ml HisTrap HP column (GE Healthcare). A linear gradient over 30 min from 96% buffer A and 4% buffer B (20 mM Na2HPO4, 500 mM NaCl, 500 mM imidazole, pH 8) to 100% buffer B was used to elute the His-tagged enzyme from the column. The UV280nm active fractions were analyzed for MupG protein content on 13% SDS-PAGE gel. The MupG-His6 containing fractions were pooled and further purified by size-exclusion chromatography (HiLoad 16/600 Superdex 75 pg, GE Healthcare) with buffer A for elution. Protein purity was analyzed by SDS-PAGE and the extinction coefficient at 280 nm of 20,860 M-1 cm-1 was calculated based on amino acid composition with the ExPASy ProtParam tool. Protein was stored at -80°C in 10% glycerol solution.
The phylogenetic tree was based on the Pfam entry PF05913. A set of 519 amino acid sequences in this entry (for a complete list of proteins see Supplementary Table 3) were aligned using MAFFT (Katoh and Standley, 2013) under default settings and subsequently trimmed with trimAl in automated1 mode (Capella-Gutiérrez et al., 2009). Pfam PF05913 sequences with less than 200 amino acids were removed from the analysis. The maximum likelihood phylogenetic tree was constructed with RaxML using the Gamma Blosum62 Protein model and rapid bootstrapping algorithm (Stamatakis, 2014). The visualization and annotation was done with the program interactive Tree Of Life (iTOL) v3: an online tool for the display and annotation of phylogenetic and other trees (Letunic and Bork, 2016).
Accumulation of MurNAc 6-phosphate-GlcNAc in ΔmupG and ΔmupGmurQ Cells
The gene SAUSA300_0192, named mupG, encodes an uncharacterized, hypothetical protein that is classified as a member of a protein family of unknown function (DUF871). It is located upstream of murQ, murP and murR, encoded in an operon on the genome of S. aureus strain USA300_FPR3757 (according to the AureoWiki database1) (Fuchs et al., 1990). We recently showed that the PTS transporter MurP and the MurNAc 6-phosphate etherase MurQ are required for the recovery of the cell wall sugar N-acetylmuramic acid (MurNAc) in S. aureus and other Gram-positive bacteria (Borisova et al., 2016). Thus, we assumed that the enzyme MupG of S. aureus might also be involved in the recycling of peptidoglycan turnover products, possibly acting sequentially with MurQ within a joint catabolic pathway. To prove this hypothesis, we generated markerless S. aureus ΔmupG and ΔmupGmurQ deletion mutants (see Supplementary Data and Supplementary Figure 1) and we analyzed growth of these mutant strains in comparison with the parental (wild type) strain in nutrient-rich LB medium for 24 h (Figure 1). No significant differences in growth were detectable in all three strains during exponential growth phase, when monitoring the optical density at 600 nm (OD600). However, a slight reduction in OD600 was observed during late exponential and stationary phase for ΔmupG and ΔmupGmurQ, compared to the wild type cultures. A S. aureus USA300 JE2 ΔmurQ mutant, lacking the etherase enconding murQ, which is located in the same putative operon as mupG also showed a slight growth defect in these growth phases, as described previously in Borisova et al. (2016). Therefore, we also compared the growth of the ΔmupG mutant with the ΔmurQ mutant. Interestingly, ΔmupG cultures reached slightly lower optical density compared to the ΔmurQ cultures (see Supplementary Figure 2).
FIGURE 1. Growth kinetics of wild type and peptidoglycan recycling mutants in LB medium. S. aureus wild type (wt, black triangles), ΔmupG mutant (red triangle), and ΔmupGmurQ (green squares) cells were grown in LB medium under constant shaking and the optical density was monitored at 600 nm (OD600) up to 24 h. Experiment was performed in triplicates and data were presented in GraphPad Prism 6 as mean ± SD. Arrows indicate the time when samples were taken for the generation of cytosolic fractions in different growth phases.
Mass spectrometric analyses of cytosolic cell fractions of ΔmupG and ΔmupGmurQ cells revealed the accumulation of an intracellular recycling product in both mutant strains, which was absent in wild type cells. The accumulation product in both mutant strains occurred at the same retention time of 21.2 min and had an identical mass within the error of mass analysis of <5 ppm (ΔmupG cells, (M-H)- = 575.151 m/z and ΔmupGmurQ cells, (M-H)- = 575.148 m/z) (Figure 2). The accumulation of the same compound in both mutants and the absence of MurNAc 6P accumulation in the double mutant, which has been reported to accumulate in a ΔmurQ single mutant (Borisova et al., 2016), indicated that MupG and MurQ are indeed operating in the same peptidoglycan recovery pathway, with MupG presumably acting upstream of MurQ. The unknown accumulation product has a mass that is identical within the error of mass analysis with the theoretical mass of a phosphorylated disaccharide containing the sugars GlcNAc and MurNAc (calculated mass in negative ion mode (M-H)- = 575.1495 m/z and positive ion mode (M+H)+ = 577.164 m/z). To identify the chemical structure of the phosphorylated disaccharide, i.e., which sugar resides at the reducing end and which sugar is phosphorylated, we analyzed the fragmentation patterns obtained by in-source decay during mass analysis. We analyzed the intact cytosolic extracts of the ΔmupG cells containing the accumulation product, as well as the same samples after reduction with NaBH4 this time in positive ion-mode (Figure 3). As expected a mass shift of 2 Da occurred after treatment with NaBH4, in agreement with the expected reduction of a sugar hemiacetal at the reducing end yielding a sugar alcohol. The accumulation product in the ΔmupG extract with a mass of (M+H)+ = 577.166 m/z (non-reduced) was diminished [Figure 3A; calculated mass of a phosphorylated disaccharide containing GlcNAc and MurNAc in positive ion mode: (M+H)+ = 577.164 m/z)], and a new mass appeared with (M+H)+ = 579.178 m/z, corresponding to the same disaccharide reduced to sugar alcohol [calculated reduced form (M+H)+ = 579.1797 m/z] (Figure 3B). The fact that the phosphorylated disaccharide is reduced at the anomeric position indicated that the C1 position is not phosphorylated, but most likely the C6 position carries the phosphate group. Thus, four different chemical structures are imaginable, which were presented in Supplementary Figure 3A.
FIGURE 2. Analysis of cytosolic extracts from wild type, ΔmupG and ΔmupGmurQ cells by LC-MS. S. aureus JE2 wild type (wt) and mutant strains were grown in LB medium for 24 h. Macromolecules were removed from the cytosolic fractions by acetone precipitation and soluble extracts were analyzed by LC-MS in negative ion-mode. Representative mass spectra from at least three independent experiments are presented as base peak chromatograms (BPC) (×105 counts per s [cps]) in black and as differential spectra (DS, BPCmutant – BPCwt) (×105 [cps]) in red. DS of both mutants revealed the intracellular accumulation of a compound (absent in the wt cells) with an observed mass of (M-H)- = 575.151 m/z in ΔmupG cells and an observed mass of (M-H)- = 575.148 m/z) in ΔmupGmurQ cells.
FIGURE 3. Accumulation of MurNAc 6P-GlcNAc in ΔmupG cells. S. aureus ΔmupG was grown in LB medium to stationary phase (24 h). Acetone extracts of the cytosolic fractions were analyzed by LC-MS in positive ion-mode, before (A) and after (B) NaBH4 reduction. (A) Shown are the fragmentation patterns obtained by in-source decay of the compound that accumulates specifically in ΔmupG mutant cells and eluates at a retention time of 21.2–21.4 min, represented as extracted ion chromatogram with an observed mass of (M+H)+ = 577.166 m/z (EIC × 105 counts per s [cps], upper right corner). Representative mass spectra from three biological replicates are illustrated. (B) Shown are the fragmentation patterns after reduction of the sample with NaBH4, which results in the formation of a new compound that elutes at 21.0 min, represented by an EIC with an observed mass of (M+H)+ = 579.178 m/z (upper right corner). The mass spectra fragmentation patterns of both compounds were presented in Compass DataAnalysis program (Bruker) from 300 to 700 m/z. The obtained fragmentation pattern indicated that the substrate for MupG is MurNAc 6P-GlcNAc.
In the non-reduced sample (Figure 3A), the recycling product with the mass of (M+H)+ = 577.166 m/z was detected and also the Na+ and K+ adducts. Fragmentations included the neutral loss of GlcNAc (-221.092 Da; calculated exact mass loss of 221.089 Da), and a MurNAc 6P elimination product (see Supplementary Figure 3B) with a mass of (M+H)+ = 356.074 m/z (which is identical with the calculated m/z of this fragment). Besides, the loss of a phosphoryl group (-79.971 Da) and the loss of water (-18.013 Da), most likely at the anomeric site, was observed. The latter fragmentations caused the formation of a dephosphorylated recycling product [(M+H)+ = 497.195 m/z] and a dehydrated product [(M+H)+ = 559.152 m/z], respectively. From these MS result we could conclude that MurNAc, but not GlcNAc, is phosphorylated. After sample reduction, the mass of the accumulation product changed to (M+H)+ = 579.178 m/z (Figure 3B). Na+ and K+ adducts of the reduced compound were also detected. Compound fragmentation pattern included the neutral loss of GlcNAc, this time in a reduced form (measured and theoretical exact mass loss of 223.106 Da) and generated a compound, as seen in the non-reduced sample, with a m/z identical within error with a MurNAc 6P elimination product (356.072 m/z) (Figure 3B; see also Supplementary Figure 3B). Fragments indicating the loss of phosphate (-79.968 Da, resulting in 499.211 m/z, reduced MurNAc-GlcNAc) were detected also in the reduced sample. However, a fragmentation product indicating the loss of water was absent, as expected for a compound reduced at the anomeric position. These latter results showed that after sample reduction with NaBH4, the mass of the elimination product of MurNAc 6P did not change, but the mass, corresponding to GlcNAc, was changed to the reduced form. Thus, we could conclude that the investigated phosphorylated disaccharide contains a MurNAc at the non-reducing end that is phosphorylated and GlcNAc at the reducing end. Taken together, the fragmentation patterns of the non-reduced and reduced accumulation products, identified the accumulation of MurNAc 6P-GlcNAc disaccharide in the ΔmupG cells.
MurNAc 6P-GlcNAc Is Hydrolyzed by MupG Yielding MurNAc 6P and GlcNAc
To characterize the in vitro functionality of MupG from S. aureus, we overexpressed the enzyme in E. coli BL21(DE3) in the presence of IPTG as a recombinant C-terminal His6-fusion protein (Figure 4A) and purified the recombinant enzyme by Ni2+-affinity and gel filtration chromatography (calculated mass of 41.5 kDa). After purification, a total amount of 3 and 5 mg protein, respectively, was obtained from 1 l bacterial culture in two different experiments and purity of the purified enzyme was confirmed with SDS-PAGE (Figure 4A). Addition of the recombinant MupG enzyme to cytosolic extracts, prepared from wild type and ΔmupG mutant cells revealed the specific cleavage of the ΔmupG recycling product ((M+H)+ = 577.166 m/z, measured in positive ion-mode, and a retention time of 21.2 min), yielding two new masses (M+H)+ = 222.098 m/z and (M+H)+ = 374.083 m/z (Figure 4B). These new masses correspond to the theoretical masses for GlcNAc [(M+H)+ = 222.097 m/z] and MurNAc P [(M+H)+ = 374.085 m/z], respectively. However, MupG did not affect any other compound accumulating in the cytosol of the wild type cells or ΔmupG cells (data not shown). Notably, in extracts of the mutant, we detected a second peak with a mass of (M+H)+ = 577.165 m/z that eluted with a retention time of 25 min (Figure 4B). This compound was only detectable, when the MS analysis was conducted in the positive ion-mode, but was absent when samples were analyzed in negative ion-mode (see Figures 1, 2 for comparison). Recombinant MupG enzyme only diminished the compound with a retention time of 21.2 min but not the compound with the same m/z but a retention time of 25 min (Figure 4B). The identity of this compound is so far unclear, since the MS fragmentation pattern indicated that it is neither composed of non-phosphorylated nor of phosphorylated MurNAc and GlcNAc sugars (data not shown).
FIGURE 4. Production of recombinant MupG and enzymatic digest of MurNAc 6P-GlcNAc extracted from ΔmupG cytosolic fractions. (A) MupG from S. aureus JE2 strain was heterologously expressed in E. coli BL21(DE3) cells. Protein expression, before (-IPTG) and after induction for 3 h (+IPTG), and purity (after purification by Ni2+-affinity and size exclusion chromatography) was controlled by SDS-PAGE (5 μg of the recombinant MupG protein was loaded). MupG-His6 protein has a calculated molecular weight of 41.5 kDa. (B) S. aureus ΔmupG cells were grown in LB medium for 24 h. Acetone extracts of the cytosolic fractions were analyzed by LC-MS in positive ion-mode. Fifty microliter of the cytosolic fraction from ΔmupG was incubated with buffer (no enzyme), with 1 μg recombinant MupG (+MupG) or with MupG and MurNAc 6P etherase MurQ (both 1 μg) for 2.5 h at 37°C. Representative mass spectra of the samples from at least three biological replicates were presented as extracted ion chromatograms (EIC × 104 [cps]) for MurNAc 6P-GlcNAc (observed masses of (M+H)+ = 577.166 m/z) in red, GlcNAc ((M+H)+ = 222.098 m/z) in blue, MurNAc 6P ((M+H)+ = 374.083 m/z) in green and GlcNAc 6P ((M+H)+ = 302.062) in black.
To unequivocally identify MurNAc 6P as the product of MupG cleavage, we incubated the MupG-treated cytosolic fraction, with the MurNAc 6P etherase MurQ, which specifically converts MurNAc 6P to GlcNAc 6P (Borisova et al., 2016). As expected, MurQ reduced the amount of MurNAc 6P about 4 times, at the same time a mass with (M+H)+ = 302.062 m/z, corresponding to the theoretical mass of GlcNAc 6P ((M+H)+ = 302.064 m/z) was generated (Figure 4B). MurQ treatment did not affect amounts of GlcNAc, the second product of MupG action. These results confirmed that the accumulating recycling product is indeed MurNAc 6P-GlcNAc and that the MupG enzyme acts as a MurNAc 6P-GlcNAc glycosidase. The recombinant enzyme was stable for several months at 4°C without losing significant activity, even in the absence of DTT reducing agent.
MurNAc 6P-GlcNAc Accumulation Primarily Occurs in Transition and Stationary Phase and Is Abolished by Plasmid-Based Complementation of MupG
We previously showed that a murQ mutant of S. aureus accumulates intracellularly MurNAc 6P predominantly in transition and stationary phases (Borisova et al., 2016). Here, we examined the growth phase-dependent accumulation of MurNAc 6P-GlcNAc. The time points used for harvesting where mid exponential growth phase (3 h), early stationary phase (9 h) and stationary phase (24 h). These growth phases were defined by a growth kinetics study with S. aureus wild type and ΔmupG mutant cells in LB medium (cf. Figure 1). The accumulation of MurNAc 6P-GlcNAc was low at exponential phase, increased significantly at transition phase and reached the highest level after 24 h of growth (Supplementary Figure 4). Thus, accumulation of MurNAc 6P-GlcNAc in ΔmupG cells confirmed that cell wall sugar recycling occurs predominantly in the transition and stationary phase.
We further investigated, whether accumulation of MurNAc 6P-GlcNAc in the ΔmupG cells can be abolished by expressing MupG on a plasmid. We used stationary phase cells for this study, since highest levels of accumulation were obtained at this stage (Supplementary Figure 4). S. aureus ΔmupG cells were transformed with a plasmid (named pCtufamp-mupG; see Supplementary Data) constitutively expressing MupG, or with empty plasmid (pCtufamp) as a control. Analysis of the cytosolic fractions of the ΔmupG cells showed that MupG expression leads to complete disappearance of MurNAc 6P-GlcNAc amounts in the cytosol after 24 h of growth (Figure 5).
FIGURE 5. LC-MS analysis of cell extract from MupG complemented mutant. S. aureus ΔmupG cells transformed with the control pCtufamp plasmid (ΔmupG + pCtufamp) or with the mupG complementation plasmid pCtufamp-mupG (ΔmupG + pCtufamp-mupG) were grown for 24 h. Cytosolic fractions were analyzed by LC-MS in positive ion-mode. (A) Mass spectra of the samples were presented as base peak chromatograms (BPC × 105 counts per s [cps]) in black and as extracted ion chromatograms (EIC × 105 [cps]) for MurNAc 6P-GlcNAc with observed mass of (M+H)+ = 577.162 m/z in red. (B) MupG complementation experiment was performed in triplicates and the relative amount of the MurNAc 6P-GlcNAc in the cells was determined by calculating the area under the curve (AUC) of the respective EIC spectra.
MurNAc-GlcNAc Accumulates Extracellularly in S. aureus Cells Lacking the MurP Transporter
The PTS transporter MurP of S. aureus was shown to transport and concomitantly phosphorylate MurNAc, yielding MurNAc 6P (Borisova et al., 2016). However, MurNAc-GlcNAc rather than MurNAc is the main sugar released from the peptidoglycan by Atl and other autolysins during cell wall turnover in S. aureus. Thus, we proposed that MurNAc-GlcNAc might be primary the natural substrates of MurP, thereby generating intracellular MurNAc 6P-GlcNAc, the substrate of the MupG hydrolase. To test this hypothesis, we analyzed the extracellular extracts of S. aureus wild type and two murP mutant cells (murP::Tn insertion mutant and ΔmupGmurQPR markerless deletion mutant). The MS analysis of the culture supernatant indeed revealed the accumulation of a disaccharide turnover product with a mass identical to MurNAc-GlcNAc (observed (M+H)+ = 497.197 and 497.195 m/z, respectively, theoretical mass of (M+H)+ = 497.198 m/z), which was lacking in the culture supernatant of the wild type cells (Figure 6). To confirm the identity of the disaccharide, again MS fragmentation analyses before and after reduction were conducted, as summarized in Supplementary Figure 5. A compound with the mass of (M+H)+ = 497.197 m/z was detected also as Na+ and K+ adducts, as well as it was characterized by the neutral loss of GlcNAc (-221.087 Da) and the formation of a MurNAc elimination product [(M+H)+ = 276.111 m/z]. In addition, we identified a fragmentation product in which water was eliminated (-18.004 Da) yielding a dehydration product [(M+H)+ = 479.192 m/z] (Supplementary Figure 5A). After NaBH4 reduction of the culture supernatant from the murP::Tn mutant, the mass of the disaccharide product (M+H)+ = 497.197 m/z disappeared and a product in a reduced form with a mass of (M+H)+ = 499.214 m/z appeared. This product was also detected as Na+ and K+ adducts and, in addition, the fragmentation pattern revealed a mass corresponding to a MurNAc elimination product (observed mass of 276.108 m/z) that lost a neutral mass, corresponding to the exact mass of reduced GlcNAc (-223.107 Da). The absence of a fragmentation product with a loss of water is in agreement with a reduction at the anomeric site, which precludes water elimination. The fragmentation pattern of the non-reduced and reduced extracellular accumulation products indicated that MurNAc-GlcNAc, but not GlcNAc-MurNAc, accumulates in the culture supernantant of ΔmurP deletion mutants. This disaccharide was not cleaved by the recombinant β-1,4-N-acetylglucosaminidase NagZ from B. subtilis (Litzinger et al., 2010a,b) (data not shown), which provides a further evidence that GlcNAc-MurNAc is not the recycling product in S. aureus. The same MS fragmentation pattern was obtained in the culture supernantant of the ΔmupGmurQPR recycling mutant, before and after reduction of the supernatant (data not shown), showing that also in this mutant the recycling product MurNAc-GlcNAc accumulates. Interestingly, in the culture supernatant of the ΔmupGmurQPR mutant also other compounds accumulated and were absent in the supernatant of the wild type cells, which nature could not be identified so far (data not shown).
FIGURE 6. LC-MS analysis from recycling mutants, lacking MurP transporter. S. aureus wild type (wt) cells, a murP transporter mutant (murP::Tn) and a murQ-operon mutant (ΔmupGmurQPR) were grown to stationary phase (24 h) in LB. Bacterial cultures were centrifuged and 1 ml of each supernatant was transferred to 500 μl of ice-cold acetone to remove macromolecules and proteins from the samples. After centrifugation, culture supernatants were dryed in the speedvac, solved in 50 μl of Millipore water and 2 μl of the samples were injected to the HPLC column. MS analysis of the culture supernatants was performed in positive-ion mode and mass spectra are presented as extracted ion chromatograms (EIC × 105 counts per second [cps]) in orange. In the culture supernatants of both mutants, an additional compound accumulates (murP::Tn, observed mass of (M+H)+ = 497.197 m/z; ΔmupGmurQPR, observed mass of (M+H)+ = 497.195 m/z). The mass of this compound in the supernatant corresponds to a disaccharide made of GlcNAc and MurNAc. This compound was further analyzed by MS fragmentation and identified as MurNAc-GlcNAc (see Supplementary Figure 5). MS data are shown as representative from three biological replicates.
To conclude, the extracellular accumulation of MurNAc-GlcNAc in both murP mutants, as well as the intracellular accumulation of MurNAc 6P-GlcNAc in the mupG mutants and the absence of MurNAc 6P-GlcNAc and MurNAc 6P in the cytosol of ΔmupGmurQPR operon mutant revealed that the disaccharide MurNAc-GlcNAc is the natural substrate internalized by the PTS transporter MurP, which intracellularly yields MurNAc 6P-GlcNAc, the substrate of MupG.
We discovered in this study how S. aureus reutilizes the sugar part of the peptidoglycan of its cell wall. The overall scheme of this novel peptidoglycan recycling pathway is depicted in Figure 7. Mass spectrometric analysis of sugars compounds, accumulating in the growth medium of ΔmurP cells (MurNAc-GlcNAc) and in the cytoplasm of ΔmupG cells (MurNAc 6P-GlcNAc), measured directly or after reduction of the sugars, unequivocally demonstrated the chemical nature of these compounds and allowed to establish the pathway. Thus, the principle peptidoglycan turnover product of S. aureus is MurNAc-GlcNAc, which results from the peptidoglycan cleavage by muramoyl-L-Ala amidases and endo-N-acetylglucosaminidases, whereas lysozyme-like endo-N-acetylmuramidases would generate GlcNAc-MurNAc products. Remarkably, the peptidoglycan of S. aureus is frequently O-acetylated at the C6 hydroxyl group of MurNAc, thereby rendered lysozyme-resistant (Bera et al., 2006; Sychantha et al., 2017). An endogenous lysozyme-like muramidase therefore would not be able to cleave the peptidoglycan of S. aureus. Accordingly, S. aureus possesses peptidoglycan-cleaving endo-N-acetylglucosamindases: one of them is the well-studied major autolysin Atl (Sugai et al., 1995; Wheeler et al., 2015; Chan et al., 2016).
FIGURE 7. Scheme of the peptidoglycan sugar recycling in S. aureus. During growth and division, S. aureus cells constantly degrade and resynthesize their peptidoglycan. The major autolysin Atl, a bifunctional muramoyl-L-alanine amidase and endo-N-acetylglucosaminidase, is able to cleave its peptidoglycan, generating MurNAc-GlcNAc and peptide turnover products. MurNAc-GlcNAc disaccharide is reutilized: transported in the cells and concommitantly phosphorylated by the MurP PTS transporter generating intracellularly MurNAc 6P-GlcNAc. Subsequently, the MurNAc 6-phosphate-GlcNAc glycosidase MupG cleaves this compound, generating the products MurNAc 6P and GlcNAc. The D-lactyl ether substituent of MurNAc 6P is specifically cleaved off by the etherase MurQ, previously characterized in our lab, forming GlcNAc 6P and D-lactate (Borisova et al., 2016). It is currently unclear how GlcNAc, the second product of the MupG reaction, is further metabolized in S. aureus cells.
Since only MurNAc-GlcNAc and not MurNAc was found in the spent medium of the murP::Tn and ΔmupGmurQPR mutants during growth, the disaccharide appears to be the general peptidoglycan turnover product of S. aureus and natural substrate of the PTS transporter MurP. However, MurP had been shown previously to take up and phosphorylate also MurNAc, if added to the growth medium (Borisova et al., 2016). Thus, apparently MurP accepts both sugars, MurNAc and MurNAc-GlcNAc as substrates. To our knowledge, this is the first report of a PTS system that is able to take up and to specifically phosphorylate a disaccharide as well as a monosaccharide (Postma et al., 1993). Since murP of S. aureus encodes only the enzyme IIBC components, an enzyme IIA (along with the general components EI and HPr of the PTS) is required to enable MurP functioning (Figure 7). So far, it is unclear which enzyme IIA operates together with MurP.
The most important result of this study is the identification of a novel 6-phosphomuramidase, encoded by SAUSA300_0192 (strain USA300), which we named MupG, for MurNAc-6P glycosidase. MurNAc 6P-GlcNAc accumulated in ΔmupG cells of S. aureus and recombinantly produced MupG cleaved MurNAc 6P-GlcNAc, releasing MurNAc 6P and GlcNAc. The former product is subsequently metabolized and was identified by specific cleavage by the MurNAc 6P etherase MurQ, yielding GlcNAc 6P and D-lactate (Borisova et al., 2016). Moreover, accumulation of MurNAc 6P-GlcNAc in a ΔmupG mutant was abolished by complementation using a MupG-expressing plasmid. Since only accumulation of MurNAc 6P-GlcNAc and not of MurNAc 6P was observed in a ΔmurGmurQ double mutant (please note that MurNAc 6P accumulates in ΔmurQ cells; Borisova et al., 2016), it can be concluded that recycling of the sugar part of the peptidoglycan during growth of S. aureus in LB medium exclusively proceeds via the uptake of MurNAc-GlcNAc disaccharides.
6-phosphoglycosidases commonly act in combination with PTS glycoside transporters. Such systems were characterized with specificities for α-glucosides such as maltose, sucrose, and trehalose (EC 22.214.171.124), or for β-glycosides (EC 126.96.36.199) or β-galactosides (EC 188.8.131.52), such as cellobiose, chitobiose, and lactose (Hengstenberg et al., 1993; Mokhtari et al., 2013). For example, S. aureus (as well as Lactobacillus and Streptococcus sp.) imports lactose via the specific PTS LacE (enzyme IIBC), which phosphorylates the disaccharide at the C6 hydroxyl group of the β-galactose moiety (Hengstenberg et al., 1993). In addition, it possesses a cytoplasmic 6-phospho-β-galactosidase (LacG) that hydrolyzes lactose 6P to galactose 6P and glucose (Staedtler et al., 1995; Yip et al., 2007; Hill and Reilly, 2008). All of the 6P-glycosidases characterized to date are classified within the CAZy glycosidase families 1 and 4 (Davies et al., 2005), which operate by very distinct mechanisms (Witt et al., 1993; Staedtler et al., 1995; Yip et al., 2007; Hill and Reilly, 2008). MupG, however, displays no significant similarity with these glycosidases, instead it founds an entirely new enzyme family. MupG and related proteins so far had been classified as domain of unknown function proteins (IPR008589; DUF871). Although they had been grouped within the glycoside hydrolase (IPR017853) and aldolase-type TIM barrel (IPR013785) superfamilies, no clear attribution to glycosidase function had been made by bioinformatic analyses. The mechanism of members of this novel glycosidase family, i.e., the stereochemical outcome and catalytic residues remain enigmatic. Our results, however, indicate that MupG has no requirement for NAD+ as for family 4 glycosidases (Yip et al., 2007).
Proteins displaying significant amino acid sequence identities with MupG of S. aureus can be found in different bacterial species. Together with MupG these proteins constitute a family (Pfam PF05913) containing domain of unknown function (DUF) 871, with MupG representing the first characterized enzyme of this protein family. The distribution of putative orthologous proteins of MupG is surprisingly narrow and mostly restricted to the phylum firmicutes. The reason for this narrow phylogenetic distribution among the firmicutes and a very selective occurrence within organisms of other phyla, is currently unclear. It may suggest a recent evolutionary event and in addition the distribution by horizontal gene transfer, however, additional studies are required to confirm these assumptions. To learn more about the distribution of MupG orthologs within bacteria, we constructed a phylogenetic tree, based on an alignment of 519 amino acid sequences extracted from the protein family entry Pfam PF05913 (Figure 8) that includes proteins from 115 bacterial genera as well as from five Crenarcheotae and one nematode species (see Supplementary Table 3 for a complete list of species or genera containing putative enzymes orthologous to MupG). Intriguingly, the phylogenetic tree revealed distinct clades of proteins that include close homologs of MupG and more distinct MupG-like proteins (Figure 8). Potential orthologs of MupG of S. aureus are found in various Staphylococcus sp. (red rectangle, Figure 8) and in many other Bacilli, e.g., Bacillales such as Listeria, Paenibacillus, and Bacillus sp., and also in Lactobacillales, e.g., Streptococcus, Lactococcus, Enterococcus, Lactobacillus, and Pediococcus sp., as well as in some Clostridiales. Intriguingly, also some few Fusobacteriales, Chlamydiales and Spirochetales species as well the nematode Trichuris trichiura possess a putative MupG ortholog. Some bacterial species, however, contain up to six putative paralogs of MupG (Supplementary Table 3), indicating that the PF05913/DUF871 protein family besides MupG orthologs might also contain proteins of distinct physiological function and with altered substrate specificity. For example, Coprobacillus cateniformis contains six putative paralogs, Carnobacterium maltaromaticum LMA28 five, Lactobacillus plantarum WCFS1 four, Bacillus anthracis and Enterococcus faecalis V583 three and Lactococcus lactis IL1403, Bacillus megaterium and many other bacteria contain two putative paralogs (cf. Supplementary Table 3). We assume that close homologs of MupG of S. aureus have identical function (MurNAc-6P glycosidases, see protein clade colored red in Figure 8) but more remotely related proteins (colored black in Figure 8) likely contain enzymes of different function. Remarkebly, some archaea (e.g., Sulfolobus solfatorius and Sulfurisphaera tokodaii) contain putative MupG-like orthologs. Since archaea lack a peptidoglycan cell wall it seems likely that these enzymes have a function that differs from the hydrolysis of a peptidoglycan turnover product. Many firmicutes presumably contain a MupG ortholog and supposably possess a recycling pathway for MurNAc-GlcNAc as that presented here for S. aureus. Notably, crystal structures of two putative orthologs of MupG [from Bacillus cereus (1×7f) and Enterococcus faecalis (2P0O)] were deposited to the protein structure database2. We are currently investigating whether these enzymes and MupG have the same specificity and function.
FIGURE 8. Phylogenetic tree showing the relation of MupG orthologs. The phylogenetic tree was constructed with RaxML from an alignment of 519 amino acid sequences, based on the Pfam entry PF05913, which lists putative orthologs of MupG (DUF871 domain proteins). The genus of Staphylococcus is marked by a red rectangle and includes MupG of S. aureus USA300, which was characterized in this study as a MurNAc 6P-glycosidase. Putative MurNAc 6P glycosidase (close orthologs of MupG) constitute a distinct clade, indicated by red lines. More distantly related MupG-like proteins constitute different clades that are indicated by black lines. Bacterial genera are color coded as indicated. See Supplementary Table 3 for a complete list of the proteins within this phylogenetic tree.
For a long time, the need for cell wall recycling in Gram-positive bacteria, and particularly in coccoidal bacteria such as S. aureus, had been questioned. Although, reports from the 1970s revealed a massive turnover of the cell wall in S. aureus (Wong et al., 1974; Blümel et al., 1979; reviewed in Doyle et al., 1988; Reith and Mayer, 2011). Recent studies, showed that the peptidoglycan of the cell wall in S. aureus undergoes a massive rearrangement during growth and division that involves glycan strand trimming by endo-N-acetylglucosaminidases (Wheeler et al., 2015; Chan et al., 2016), peptidoglycan degradation by autolysins such as Atl during cell division and separation (Yamada et al., 1996; Biswas, 2009; Götz et al., 2014) as well as autolysis during biofilm formation (Bose et al., 2012). We recently demonstrated that peptidoglycan recycling proceeds in Gram-positive organisms predominantly occurring during transition and stationary phases (Borisova et al., 2016). The results of the present study confirmed these previous observations. Notably, the mupG mutant and the ΔmupGmurQ double mutant showed a weak disadvantage during growth in stationary phase (cf. Supplementary Figure 2). This growth defect was stronger than previously observed for the ΔmurQ mutant (Borisova et al., 2016), which might be explained by the inability of the former mutants to recycle both sugars of the peptidoglycan, GlcNAc and MurNAc, whereas the latter mutant has a defect only in the recovery of MurNAc. So far, it remains unclear how the GlcNAc part of MurNAc 6P-GlcNAc is recovered, after cleavage by MupG in the cytoplasm. GlcNAc reutilization would require either a GlcNAc kinase, or alternatively the secretion and a re-import by the GlcNAc PTS of S. aureus, in both cases yielding GlcNAc 6P, which can be shuttled into the amino sugar catabolic pathway (Komatsuzawa et al., 2004). Moreover, the fate of the peptide part of the peptidoglycan is currently unknown.
Here we elucidated a novel pathway for the uptake and catabolism of the disaccharide MurNAc-GlcNAc, which is a specific peptidoglycan turnover product generated by the joint action of peptidoglycan amidases and endo-N-acetylglucosamidases, e.g., by the bifunctional autolysin Atl of S. aureus. The pathway in S. aureus involves the PTS transporter MurP, required for the uptake and phosphorylation of the disaccharide yielding MurNAc 6-phosphate-GlcNAc, and MupG, a unique glycosidase with 6-phospho-N-acetylmuramidase activity. MupG is the first characterized representative of a so far unexplored protein family containing domain of unknown function DUF871, which is distributed mostly among firmicutes. As many of these organisms also possess peptidoglycan-cleaving endo-N-acetylglucosaminidases and MurP-like transporters, besides MupG orthologs, recycling of the peptidoglycan turnover product MurNAc-GlcNAc is presumably a common feature among these firmicutes. Peptidoglycan recycling is crucial for stationary phase survival of Gram-positive bacteria (Borisova et al., 2016) and thus, the pathway identified in this study may serve as a novel target to treat persistent infections by S. aureus and selectively other bacteria.
RK, MB, and PE cloned MupG. RK and MB expressed and biochemically characterized MupG. RK and MB performed HPLC-MS experiments and analyzed the data. MA, RK, and NZ aligned the MupG-like protein family, constructed the phylogenetic tree based on this alignment, and prepared the Figure 8. MB and CM formulated the original problem and provided guidance throughout the study. MB, CM, RK, and PE designed the experiments and developed the methodology. MB, CM, and RK wrote the manuscript. MB approved the final version to be published.
This work was financed by the German Research Foundation (DFG; Grants SFB766/A15 and GRK1708/B2 to CM). We further acknowledge support by the DFG and the Open Access Publishing Fund of the University of Tübingen.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We are very grateful to Rosmarie Gaupp, Friedrich Götz, and Heike Brötz-Oesterhelt for providing plasmids, strains, and working space.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmicb.2018.02725/full#supplementary-material
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Keywords: peptidoglycan recycling, cell wall turnover, Staphylococcus aureus, Atl autolysin, peptidoglycan hydrolases, 6-phosphomuramidase, exo-N-acetylmuramidase, MurNAc-GlcNAc
Citation: Kluj RM, Ebner P, Adamek M, Ziemert N, Mayer C and Borisova M (2018) Recovery of the Peptidoglycan Turnover Product Released by the Autolysin Atl in Staphylococcus aureus Involves the Phosphotransferase System Transporter MurP and the Novel 6-phospho-N-acetylmuramidase MupG. Front. Microbiol. 9:2725. doi: 10.3389/fmicb.2018.02725
Received: 04 June 2018; Accepted: 24 October 2018;
Published: 16 November 2018.
Edited by:Marc Bramkamp, Ludwig-Maximilians-Universität München, Germany
Reviewed by:Patrick Joseph Moynihan, University of Birmingham, United Kingdom
Volker F. Wendisch, Bielefeld University, Germany
Copyright © 2018 Kluj, Ebner, Adamek, Ziemert, Mayer and Borisova. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.