A lytic transglycosylase connects bacterial focal adhesion complexes to the peptidoglycan cell wall

The Gram-negative bacterium Myxococcus xanthus glides on solid surfaces. Dynamic bacterial focal adhesion complexes (bFACs) convert proton motive force from the inner membrane into mechanical propulsion on the cell surface. It is unclear how the mechanical force transmits across the rigid peptidoglycan (PG) cell wall. Here, we show that AgmT, a highly abundant lytic PG transglycosylase homologous to Escherichia coli MltG, couples bFACs to PG. Coprecipitation assay and single-particle microscopy reveal that the gliding motors fail to connect to PG and thus are unable to assemble into bFACs in the absence of an active AgmT. Heterologous expression of E. coli MltG restores the connection between PG and bFACs and thus rescues gliding motility in the M. xanthus cells that lack AgmT. Our results indicate that bFACs anchor to AgmT-modified PG to transmit mechanical force across the PG cell wall.


Introduction
In natural ecosystems, the majority of bacteria attach to surfaces 1 .Surface-associated motility is critical for many bacteria to navigate and populate their environments 2 .The Gram-negative bacterium Myxococcus xanthus moves on solid surfaces using two independent mechanisms: social (S-) motility and adventurous (A-) motility.S-motility, analogous to the twitching motility in Pseudomonas and Neisseria, is powered by the extension and retraction of type IV pili 3,4 .A-motility, also known as gliding motility, does not depend on conventional motility-related cell surface appendages, such as flagella or pili 2,5 .In M. xanthus, AglR, AglQ, and AglS form a membrane channel that functions as the gliding motor by harvesting proton motive force 6,7 .The motor unit associates with at least fourteen gliding-related proteins that reside in the cytoplasm, inner membrane, periplasm, and outer membrane [8][9][10] .
Recently, the mechanisms for bFAC assembly and the coupling between bFACs and substrate begin to emerge 8,11,12 .In each gliding cell, two distinct populations of gliding complexes coexist: dynamic complexes move along helical paths and static complexes remain fixed relative to the substrate 11,[13][14][15] .Motors transport incomplete gliding complexes along helical tracks but form complete, force-generating complexes at the ventral side of cells that appear fixed to the substrate (Fig. 1) 11,15 .Based on their functional analogy with eukaryotic focal adhesion sites, these complete gliding machineries are called bacterial focal adhesion complexes (bFACs).Despite their static appearance, bFACs are dynamic under single-molecule microscopy.Individual motors frequently display move-stall-move patterns, in which they move rapidly along helical trajectories, join a bFAC where they remain stationary briefly, then move rapidly again toward the next bFAC or reverse their moving directions 13,16,17 .bFACs adhere to the gliding substrate through an outer membrane adhesin 12 .As motors transport bFACs toward lagging cell poles, cells move forward but bFACs remain static relative to the gliding substrate.bFAC assembly can be quantified at nanometer resolution using the single-particle dynamics of gliding motors 13,18 .Single particles of a fully functional, photoactivatable mCherry (PAmCherry)-labeled AglR display three dynamic patterns, stationary, directed motion, and diffusion 13,18 .The stationary population consists of the motors in fully assembled bFACs, which do not move before photobleach.In contrast, the motors moving in a directed manner carry incomplete gliding complexes along helical tracks, whereas the diffusing motors assemble to even less completeness 11,13,15,18 .As motors only generate force in static bFACs 11 , the population of nonmotile motors indicates the overall status of fully assembled bFACs.
However, how bFACs transmit force across the peptidoglycan (PG) cell wall is unclear.PG is a mesh-like single molecule of crosslinked glycan strands that surrounds the entire cytoplasmic membrane.The rigidity of PG defines cell shape and protects cells from osmotic lysis 19,20 .If bFACs physically penetrate PG, their transportation toward lagging cell poles would tear PG and trigger cell lysis.To avoid breaching PG, an updated model proposes that there are two subcomplexes in each bFAC, one on each side of the PG layer.Rather than forming stable and rigid interactions, these two subcomplexes only associate transiently to form a bFAC 11,21 (Fig. 1).
As motors reside in the fluid inner membrane, to transmit force to the cell surface, they must push against two relatively rigid structures, one on each side of the membrane, in opposite directions 21 (Fig. 1).MreB is a bacterial actin homolog that associates with the motors and plays essential roles in gliding 2,5,6,14,18,22 .The motors could push against MreB filaments in the cytoplasm, whereas PG could be the structure that motors push against in the periplasm 11,21 .The interaction between the inner complex and PG not only satisfies the physical requirement for force generation but also supports efficient bFACs assembly.Without this interaction, once the inner subcomplex disassociates from the outer one, it will quickly escape bFACs and no longer contribute to force generation 21 .In this case, the fraction of time each motor generates force (remains in bFACs) will be extremely low 21 .How the inner complex interacts with PG remains unknown.It was speculated that gliding motors in the inner complex could bind PG directly 11 .However, such binding has not been confirmed by experiments.
In this study, we found that AgmT, a lytic transglycosylase (LTG) for PG, is essential for M. xanthus gliding motility.AgmT is required for maintaining PG integrity under the stress from the antibiotic mecillinam.Using single-particle tracking microscopy and coprecipitation assays, we found that AgmT is required for the gliding motors to connect to PG and stall in bFACs.Importantly, expressing Escherichia coli MltG heterologously rescues the connection between PG and bFACs and thus restores gliding motility.Hence, the LTG activity of AgmT anchors bFAC to PG, potentially by modifying PG structure.Our findings reveal the long-sought connection between PG and bFAC that allows mechanical force to transmit across the PG cell wall.

Results
AgmT, a putative LTG, is essential for gliding motility.To elucidate how bFACs interact with PG, we searched for potential PG-binding domains among the proteins that are required for gliding motility.A previous report identified 35 gliding-related genes in M. xanthus through transposon-mediated random mutagenesis 23 .Among these genes, agmT (ORF K1515_04910 24 ) was predicted to encode a protein with a large "periplasmic solute-binding" domain 23 .After careful analysis, we found that AgmT showed significant similarity to the widely conserved YceG/MltG family LTGs.About 70% of bacterial genomes, including firmicutes, proteobacteria, and actinobacteria, encode YceG/MltG domains 25 .Especially, the putative active site, Glu223 (corresponding to E218 in E. coli MltG) 25 , is conserved in AgmT (Fig. 2A).To confirm the function of AgmT in gliding, we constructed an agmT in-frame deletion mutant.To eliminate S-motility, we further knocked out the pilA gene that encodes pilin for type IV pilus.In contrast to the pilA -cells that were still motile with gliding motility, the ∆aglR pilA -cells that lack an essential component in the gliding motor, were unable to move outward from the colony edge.Similarly, the ∆agmT pilA -cells also formed sharp colony edges, indicating that they were nonmotile with gliding (Fig. 2B).As AgmT is a putative LTG for PG, we then tested if its predicted active site, Glu223, is required for gliding.Because the amino acid following Glu223 is also a glutamate (Glu224), we replaced both glutamate residues with alanine (AgmT EAEA ) using site-directed mutagenesis to alter their codons on the chromosome.agmT EAEA pilA -cells were nonmotile (Fig. 2B).Thus, the putative LTG activity of AgmT is essential for M. xanthus gliding motility.
Besides agmT, the genome of M. xanthus contains 13 genes that encode putative LTGs (Table S1).To test if these proteins also contribute to gliding, we knocked out each of these 13 genes in the pilA -background.The resulting mutants all retained gliding motility, indicating that AgmT is the only LTG that is required for M. xanthus gliding (Fig. S1).
AgmT is an LTG.To determine if AgmT is an LTG, we expressed the periplasmic domain (amino acids 25 -339) of wild-type AgmT and AgmT EAEA in E. coli.We purified PG from wild-type M. xanthus cells, labeled it with Remazol brilliant blue (RBB), and tested if the purified AgmT variants hydrolyze labeled PG in vitro and release the dye 26,27 .Similar to lysozyme that specifically cleaves the ®-1,4-glycosidic bonds in PG, wild-type AgmT solubilized dye-labeled M. xanthus PG that absorbs light at 595 nm.In contrast, the AgmT EAEA variant failed to release the dye (Fig. 3A).Hence, AgmT displays LTG activity in vitro.
Whereas AgmT does not affect growth rate (Fig. S2), cells that lacked AgmT or expressed AgmT EAEA maintained rod shape but were slightly shorter and wider than the wild-type ones (Fig. 3B).Nevertheless, altered morphology alone does not likely account for abolished gliding.In fact, a previously reported mutant that lacks all three class A penicillin-binding proteins (⊗3) displays similarly shortened and widened morphology 28 , but is still motile by gliding (Fig. S1).
A recent report revealed that Vibrio cholerae MltG degrades un-crosslinked PG turnover products and prevents their detrimental accumulation in the periplasm 29 .To test if AgmT plays a similar role in M. xanthus, we used mecillinam to induce cell envelope stress.Mecillinam is a ®-lactam that induces the production of toxic, uncrosslinked PG strands 30 .Rather than collapsing the rod shape, mecillinam only causes bulging near the centers of wild-type M. xanthus cells, whereas large-scale cell lysis does not occur and cell poles still maintain rod shape even after prolonged (20 h) treatment (Fig. 3C) 28 .Thus, wild-type M. xanthus can largely mitigate mecillinam stress.In contrast, mecillinam-treated agmT cells increased their width drastically, displayed significant cell surface irregularity along their entire cell bodies, and lysed frequently (Fig. 3C).Cells expressing AgmT EAEA as the sole source of AgmT displayed similar, but even stronger phenotypes under mecillinam stress, growing into elongated, twisted filaments that formed multiple cell poles and lysed frequently (Fig. 3C).These results confirm that similar to V. cholerae MltG, M. xanthus AgmT is important for maintaining cell integrity under mecillinam stress.The different responses from agmT and agmT EAEA cells suggest that AgmT could interact with other PG-related enzymes and that the inactive AgmT variant might still modulate PG through these enzymes.Alternatively, other LTGs could partially substitute AgmT while AgmT EAEA blocks these enzymes from accessing un-crosslinked PG strands.
AgmT is essential for bFACs assembly.How does AgmT support gliding?We first tested if AgmT regulates the function of the gliding motor.For this purpose, we quantified the motor dynamics by tracking single particles of AglR, an essential component of the motor.We spotted the cells that express a fully functional, photoactivatable mCherry (PAmCherry)-labeled AglR 13 on 1.5% agar surface.We used a 405- nm excitation laser to activate the fluorescence of a few labeled AglR particles randomly in each cell and quantified their localization using a 561-nm laser at 10 Hz using single particle tracking photo-activated localization microscopy (sptPALM) under highly inclined and laminated optical sheet (HILO) illumination 13,18,31 .Using this setting, only a thin section of each cell surface that was close to the coverslip was illuminated.To analyze the data, we only chose the fluorescent particles that remained in focus for 4 -12 frames (0.4 -1.2 s).As free PAmCherry particles diffuse extremely fast in the cytoplasm, entering and exiting the focal plane frequently, they usually appear as blurry objects that cannot be followed at 10-Hz close to the membrane 18 .For this reason, the noise from any potential degradation of AglR-PAmCherry was negligible.
To test if other components in the gliding machinery also depend on AgmT to assemble into bFACs, we tested the localization of AglZ, a cytoplasmic protein that is commonly used for assessing bFAC assembly 11,33 .In the cells that expressed wild-type AgmT, yellow fluorescent protein (YFP)-labeled AglZ formed a bright cluster at the leading cell pole and multiple stationary, near-evenly spaced clusters along the cell body, indicating the assembly of bFACs (Fig. 4D).In contrast, AglZ-YFP only formed single clusters at cell poles in the cells that lacked AgmT or expressed AgmT EAEA (Fig. 4D).Taken together, the LTG activity of AgmT is essential for bFACs assembly.
AgmT does not assemble into bFACs.We first hypothesized that AgmT itself could assemble into bFACs, where it could either generate pores in PG that allow the inner and outer gliding complexes interact directly or bind to PG and recruit other components to bFACs through protein-protein interactions.If this is the case, AgmT should localize in bFACs.To test this possibility, we labeled AgmT with PAmCherry on its C-terminus and expressed the fusion protein as the sole source of AgmT using the native promoter and locus of agmT.agmT-PAmCherry pilA -cells displayed gliding motility that was indistinguishable from pilA -cells (Fig. 2B), indicating that the fusion protein is functional.Immunoblot using an anti-mCherry antibody showed that AgmT-PAmCherry accumulated in two bands that corresponded to monomers and dimers of the full-length fusion protein, respectively (Fig. 5A).This result is consistent with the structure of E. coli MltG that functions as homodimers (PDB: 2r1f).Importantly, AgmT-PAmCherry was about 50 times more abundant than AglR-PAmCherry (Fig. 5A).To test if AgmT itself assembles into bFACs, we first expressed AgmT-PAmCherry and AglZ-YFP together using their respective loci and promoter.We exposed agmT-PAmCherry cells to 405-nm excitation (0.2 kW/cm 2 ) for 2 s to visualize the overall localization of AgmT.We found that on a 1.5% agar surface that favors gliding motility, AglZ aggregated into bFACs whereas AgmT localized near evenly along cell bodies without forming protein clusters (Fig. 5B).Thus, AgmT does not localize into bFACs.
These results echo the fact that despite its abundance, AgmT has not been identified as a component in bFACs despite extensive pull-down experiments using various bFAC components as baits AgmT connects bFACs to PG through its LTG activity.We then explored the possibility that AgmT could modify PG through its LTG activity and thus generate the anchor sites for certain components in bFACs.If this hypothesis is true, heterologous expression of a non-native LTG could rescue gliding motility in the ⊗agmT strain.To test this hypothesis, we fused the E. coli mltG gene (mltGEc) to a vanillate-inducible promoter and inserted the resulting construct to the cuoA locus on M. xanthus chromosome that does not interfere gliding 35 .We subjected the ⊗agmT and agmT EAEA cells that expressed MltGEc to mecillinam (100 ⎧g/ml) stress.Induced by 100 ⎧M sodium vanillate, MltGEc restored cell morphology and integrity of the ⊗agmT strain to the wildtype level (Fig. 3C).This result confirmed that MltGEc was expressed and enzymatically active in M. xanthus.In contrast, MltGEc failed to confer mecillinam resistance to the agmT EAEA cells (Fig. 3C).A potential explanation is that AgmT EAEA could still bind to PG and thus block MltGEc from accessing M. xanthus PG.Consistent with its activity, MltGEc restored gliding motility in the agmT pilA cells but not in the agmT EAEA pilA ones (Fig. 2B).As MltGEc substitutes AgmT in gliding motility, it is the LTG activity, rather than specific interactions between AgmT and bFACs, that is required for gliding.
It is challenging to visualize how AgmT facilitates bFAC assembly through its enzymatic activity in vitro.First, the inner complex in a bFAC spans the cytoplasm, inner membrane, and periplasm and contains multiple proteins whose activities are interdependent 8,10,11 .It is hence difficult to purify the entire inner complex in its functional state.Second, Faure et al. hypothesized that AglQ and AglS in the gliding motor could bind PG directly 11 .However, such binding has not been proved experimentally due to the difficulty in purifying the membrane integral AglRQS complex.To overcome these difficulties, we used AglR-PAmCherry to represent the inner complex of bFAC and investigated how bFACs bind PG in their native environment.To do so, we expressed AglR-PAmCherry in different genetic backgrounds as the sole source of AglR using the native aglR locus and promoter.We lysed these cells using sonication, subjected their lysates to centrifugation, isolated the pellets that contained PG, and detected the presence of AglR-PAmCherry in these pellets by immunoblots using a mCherry antibody.Eliminating AgmT and disabling its active site significantly reduced the amounts of AglR in the pellets (Fig. 5B).Because such pellets contain both the PG and membrane fractions, we further eliminated PG in cell lysates using lysozyme before centrifugation and determined the amount of AglR-PAmCherry in the pellets that only contained membrane fractions.Regardless of the presence and activity of AgmT, comparable amounts of AglR precipitated in centrifugation pellets after lysozyme treatment, indicating that AgmT does not affect the expression or stability of AglR (Fig. 5B).Thus, active AgmT facilitates the association between bFACs and PG.Strikingly, the heterologous expression of MltGEc enriched AglR-PAmCherry in the PG-containing pellets from the ⊗agmT cells but not the agmT EAEA ones (Fig. 5B).These results indicate that AgmT connects bFACs to PG through its LTG activity.

Discussion
Gliding bacteria adopt a broad spectrum of nanomachineries.Compared to the transenvelope secretion system that drives gliding in Flavobacterium johnsoniae and Capnocytophaga gingivalis that both contain PG, the gliding machinery of M. xanthus appears to lack a stable structure that transverses cell envelope, especially across the PG layer 2,36,37 .In order to generate mechanical force from the fluid M. xanthus gliding machinery, the inner complex must establish solid contact with PG and push the outer complex to slide 11,21  Then how does AgmT, a protein localized diffusively, facilitate bFAC assembly into near-evenly spaced foci?The actin homolog MreB is the only protein in bFACs that displays quasiperiodic localization independent of other components 18,22 .M. xanthus MreB assembles into bFACs and positions the latter near evenly along the cell body 6,13,18,22,42 .MreB filaments change their orientation in accordance with local membrane curvatures and could hence respond to mechanical cues [43][44][45][46] .Strikingly, M.
xanthus does assemble bFACs in response to substrate hardness (Fig. 4C) and assembled bFACs could distort the cell envelope, generating undulations on the cell surface 6,10,13,47,48 .Taken together, whereas AgmT potentially modifies the entire PG layer, it is still the quasiperiodic MreB filaments that determine the loci for bFAC assembly in response to the mechanical cues from the gliding substrate.S2) could partially explain why it is the only LTG that has been adopted by the gliding machinery.It will be interesting to investigate if other LTGs, once anchored to the inner membrane, could also facilitate bFAC assembly.
using a Nikon Eclipse™ e600 microscope with a 10× 0.30 NA objective and an OMAX™ A3590U camera.

Protein expression and purification
DNA sequences encoding amino acids 25 -339 of AgmT and AgmT EAEA were amplified by polymerase chain reaction (PCR) and inserted into the pET28a vector (Novogen) between the restriction sites of EcoRI and HindIII.The resulting plasmids were transformed into E. coli strain BL21(DE3).Transformed cells were cultured in 20 ml LB (Luria-Bertani) broth at 37 °C overnight and used to inoculate 1 L LB medium supplemented with 1.0% glucose.Protein expression was induced by 0.1 mM IPTG (isopropyl-h-d-thiogalactopyranoside) when the culture reached an OD600 of 0.8.
Cultivation was continued at 16 °C for 10 h before the cells were harvested by centrifugation at 6,000 × g for 20 min.Proteins were purified using the NGC™ Chromatography System (BIO-RAD) and a 5-ml HisTrap™ (Cytiva) 17,53 .Purified proteins were concentrated using Amicon™ Ultra centrifugal filter units (Millipore Sigma) with a molecular cutoff of 10 kDa and stored at -80 °C.

RBB assay
PG was purified following the published protocol 28,54  Ultrasonic Homogenizer (40% output).Unbroken cells and large debris were eliminated by centrifugation (6,000 × g, 10 min, 25 °C).Supernatants were subjected to centrifugation at 21,000 × g for 15 min.Pellets that contain the PG and membrane fractions were resuspended to 1 ml in 1× PBS.To collect the pellets that do not contain PG, supernatants from sonication lysates were incubated with 5 mg/ml lysozyme at 25 °C for 5 h before centrifugation.Resuspended pellets (5 ⎧l each) were mixed with equal volumes of 2× loading buffer and applied to SDS PAGE and immunoblotting.

Microscopy Analysis
For all imaging experiments, 5 ⎧l cells were spotted on an agarose pad.For the treatments with inhibitors, inhibitors were added into both the cell suspension and agarose pads.The length and width of cells were determined from differential interference contrast (DIC) images using a MATLAB (MathWorks) script

Fig. 5. AgmT does not assemble into bFACs but connects bFACs to PG. A)
Immunoblotting using M. xanthus cell lysates and an anti-mCherry antibody shows that PAmCherry-labeled AgmT and AgmT EAEA accumulate as full-length proteins.AgmT is significantly more abundant than the motor protein AglR.The bacterial actin homolog MreB visualized using an MreB antibody is shown as a loading control.B) AgmT does not aggregate into bFACs.C) The LTG activity of AgmT is required for connecting bFACs to PG and expressing the E. coli LTG MltG (MltG Ec ) restores PG binding by bFACs in cells that lack AgmT but not in the ones that express an inactive AgmT variant (AgmT EAEA ).AglR-PAmCherry was detected using an anti-mCherry antibody to mark the presence of bFACs that co-precipitate with PG-containing (lysozyme-) pellets.Lysates from the cells that express AglR-PAmCherry in different genetic backgrounds were pelleted by centrifugation in the presence and absence of lysozyme.
Most bacteria encode multiple LTGs that function in PG growth, remodeling, and recycling.Trans-envelope structures often require highly specialized LTGs to penetrate PG 49 .This work provides an example that macro bacterial machineries domesticate non- specialized LTGs for specialized functions.Other examples include MltD in the Helicobacter pylori flagellum and MltE in the E. coli type VI secretion system 50,51 .Both M. xanthus AgmT and E. coli MltG belong to the YceG family, which is the first identified LTG family that is conserved in both Gram-negative and positive bacteria 39 .LTGs in this family localize to the inner membrane and feature periplasmic transglycosylase domains 39 .Due to their unique localization, the YceG family LTGs are important for determining the length of nascent glycan strands and for degrading the toxic uncrosslinked strands from futile PG synthesis 29,52 .Due to the wide distribution of YceG family LTGs, it is challenging to study how the unique M. xanthus gliding machinery adopts AgmT in evolution.Nevertheless, the fact that AgmT is the only M. xanthus LTG that belongs to this family (Table

Fig.
Fig. 1.Stationary bFACs drive M. xanthus gliding.Motors carrying incomplete gliding complexes either diffuse or move rapidly along helical paths but do not generate propulsion.Motors stall and become nearly static relative to the substrate when they assemble into complete bFACs with other motor-associated proteins at the ventral side of the cell.Stalled motors push MreB and bFACs in opposite directions and thus exert force against outer membrane adhesins.Overall, as motors transport bFACs toward lagging cell poles, cells move forward but bFACs remain static relative to the substrate.IM, inner membrane; OM, outer membrane.

Fig. 4 .
Fig.4.AgmT and its LTG activity are essential for bFAC assembly.A) Overall distribution of AglR-PAmCherry particles on 1.5% agar surface is displayed using the composite of 100 consecutive frames.Single-particle trajectories of AglR-PAmCherry were generated from the same frames.Individual trajectories are distinguished by colors.Deleting agmT or disabling the transglycosylase activity of AgmT (AgmT EAEA ) decrease the stationary population of AglR particles.B) The stationary population of AglR-PAmCherry particles, which reflects the AglR molecules in bFACs, changes in response to substrate hardness (controlled by agar concentration) and the presence and function of AgmT.The total number of particles analyzed is shown on top of each plot.C) AglR fails to assemble into bFACs in the absence of active AgmT, even on 5.0% agar surfaces.D) AgmT and its LTG activity also support the assembly of AglZ into bFACs.White arrows point to bFACs.Scale bars, 5 µm.
R -P A m C hMreB a g m T -P A m C h a g m T E A E A -P A m C h 6,10,34 .We reasoned that if AgmT assembles into bFACs, AgmT and gliding motors should display similar dynamic patterns.To test this possibility further, we used sptPALM to track the movements of AgmT-PAmCherry single particles on 1.5 agar surfaces at 10 Hz.Distinct from the AglR particles of which 32.1% remained stationary, AgmT moved in a diffusive manner, showing no significant immobile population.Importantly, compared to the diffusion coefficients (D) of mobile AglR particles (1.8 ⋅ 10 -2 ± 3.6 ⋅ 10 -3 ⎧m 2 /s (n = 1,833)), AgmT particles diffused much faster (D = 2.9 ⋅ 10 -2 ± 5.3 ⋅ 10 -3 ⎧m 2 /s (n = 8,548)).Taken together, neither the localization nor dynamics of AgmT displayed significant correlation with bFAC components.We thus conclude that AgmT does not assemble into bFACs . In this work, we discovered AgmT as the long-sought factor that connects bFACs to PG.Such connection not only satisfies the requirement for force generation but is also essential for bFAC assembly.
It is rather unexpected that AgmT itself does not assemble into bFACs.Because MltGEc substitutes AgmT in gliding, rather than interacting with bFAC components specifically, AgmT facilitates bFAC assembly through its LTG activity.A few possibilities could explain the function of AgmT.First, LTGs usually break glycan strands and produce unique anhydro caps on their ends 38-41 .Certain components in bFACs could specifically bind to such modified glycan strands in PG and further recruit other components.Second, AgmT could generate small openings all over the PG meshwork that allow the inner and outer subcomplexes in bFACs to interact locally.

1. Stationary bFACs drive M. xanthus gliding.
Motors carrying incomplete gliding complexes either diffuse or move rapidly along helical paths but do not generate propulsion.Motors stall and become nearly static relative to the substrate when they assemble into complete bFACs with other motor-associated proteins at the ventral side of the cell.Stalled motors push MreB and bFACs in opposite directions and thus exert force against outer membrane adhesins.Overall, as motors transport bFACs toward lagging cell poles, cells move forward but bFACs remain static relative to the substrate.IM, inner membrane; OM, outer membrane.AgmT shows significant similarity to a widely conserved PG transglycosylase in YceG/MltG family.The conserved glutamine residue is marked by an asterisk.M_xant, M. xanthus; E_coli, E. coli; M_tube, Mycobacterium tuberculosis; S_coel, Streptomyces coelicolor; A_calc, Acinetobacter calcoaceticus; X_albi, Xanthomonas albilineans; N_meni, Neisseria menningitidis; R_prow, Rickettsia prowazekii; T_aqua, Thermus aquaticus.B) AgmT is required for M. xanthus gliding.Colony edges were imaged after incubating cells on 1.5% agar surface for 24 h.Deleting or Disabling the active site of AgmT abolishes gliding but fusing an PAmCherry (PAmCh) to its C-terminus does not.Heterologous Expression of E. coli MltG restores gliding of ⊗agmT cells but not the cells that express AgmT EAEA .AgmT regulates cell morphology.Compared to wild-type cells, cells that lack AgmT and express AgmT EAEA are significantly shorter and wider.Heterologous expression of E. coli MltG partially restores cell length but not cell width in agmT and agmT EAEA backgrounds.Asterisks, 200 ⎧M sodium vanillate added.p values were calculated using a one-way ANOVA test between two unweighted, independent samples.Whiskers indicate the 25 th -75 th percentiles and red dots the median.The total number of cells analyzed is shown on top of each plot.C) AgmT regulates cell morphology and integrity under mecillinam stress (100 ⎧g/ml).Expressing E. coli MltG by a vanillate-inducible promoter (P van ) restores resistance against mecillinam in agmT cells but not in the cells that express AgmT EAEA .van,.Arrows point to newly lysed cells.Scale bars, 5 µm.
Fig. 3. AgmT regulates cell morphology and integrity under antibiotic stress.A) PurifiedAgmT solubilizes dye-labeled PG sacculi, but AgmT EAEA does not.Lysozyme serves as a positive control.Absorption at 595 nm was measured after 18 h incubation at 25 °C.Data are presented as mean values ± SD from three replicates.B)