Cell Fate Regulation Governed by a Repurposed Bacterial Histidine Kinase

The pathway that regulates asymmetric cell division in Caulobacter involves a signaling kinase whose catalytic output domain has been repurposed as an input sensor of the phosphorylation state of the response regulator – a reversal of the conventional direction of information flow; this allows wiring of simple linear signaling pathways into complex eukaryote-like networks.


Introduction
Cell fate decisions driven by the spatial organization of signaling proteins are a hallmark of asymmetric divisions in systems as diverse as stem cells and bacteria. Caulobacter, a model system for localization-dependent signaling network studies, divides asymmetrically yielding two distinct daughter cells: a motile swarmer cell and a replication-competent stalked cell ( Figure 1). Cell division in Caulobacter is a stepwise process that includes a cytoplasmic compartmentalization stage [1] during which the inner membrane closes to form a barrier between the incipient swarmer and stalked cell compartments ( Figure 1A) [2,3]. This event segregates crucial signaling proteins [2,4,5] and culminates in the swarmer cell-specific activation of the global transcriptional regulator CtrA ( Figure 1B) [6], which controls the expression of more than 100 genes involved in cell division and asymmetric polar organelle development [7]. The two daughter cells are distinguished by a compartment-sensing module composed of the response regulator (RR) DivK and two histidine kinases (HKs), DivJ and PleC, which differentially regulate the CtrA signaling pathway upon compartmentalization. DivJ and PleC respectively occupy the old and new cell poles ( Figure 1A) [4,5]. Prior to cell division, the cytoplasm contains a homogeneous mixture of phosphorylated (DivK,P) and unphosphorylated DivK [8]. In pre-divisional cells, however, PleC (positioned at the new pole) functions as a DivK phosphatase, while DivJ (positioned at the old pole) functions as a DivK kinase [4,5,9]. In this way, compartmentalization promotes accumulation of unphosphorylated DivK in the incipient swarmer cell and DivK,P in the incipient stalked cell [10,11], providing unique cell-type markers.
In Caulobacter, the DivK phosphorylation state provides the basis for a regulatory switch that underlies divergent cell-fates upon cell division [12][13][14][15]. This switch is achieved through the activity of the pseudokinase DivL, which activates the CckA-ChpT-CtrA phosphorelay pathway in the uncomplexed state and inhibits this phosphorelay when bound to DivK,P ( Figure 1B) [13]. Previous in vitro work has shown that DivL has a binding preference for DivK,P over unphosphorylated DivK, and genetic evidence suggests that the DivL-DivK,P interaction leads to inhibition of the hybrid-HK CckA activity [13]. Additionally, DivL appears to play a role in the regulation of CckA polar localization and autokinase activity [13,16]. Thus, DivL functions as a critical link that couples two distinct signaling pathways ( Figure 1B).
DivL has a predicted domain architecture that is typical of many HKs, consisting of multiple PAS domains fused to a C-terminal HK module that contains dimerization and histidine phosphotransfer (DHp) and catalytic and ATP-binding (CA) domains ( Figure 1C). In contrast to typical HKs, a conserved tyrosine (Tyr550) appears in place of the predicted phosphorylatable histidine throughout DivL homologs in a-proteobacteria [17], with the exception of the Magnetospirillum magneticum DivL that contains a non-phosphorylatable alanine ( Figure 1C). Furthermore, DivL's essential functions in vivo do not require a phosphorylated DHp domain [12,13,16], and the CA domain is dispensable for activity [12,18]. Divergent a-proteobacteria that lack a DivK ortholog also frequently lack the catalytic domains (DHp-CA) of their DivL orthologs ( Figure 1C) [19]. The co-evolution of DivK with the DHp-CA domains of DivL suggests that DivL and DivK may work together as a regulatory module within the cell-cycle [19]. Despite the apparent connection between DivK and DivL in cell fate signaling, the molecular nature of the interaction between this unconventional HK-RR pair is poorly understood. To gain insight into this signaling system, we solved the crystal structure of the HK region of DivL at 2.5 Å resolution and interrogated the interaction between DivL and both DivK and DivK,P. Our results show that Caulobacter has repurposed a conserved HK as a highly specific sensor module for a phosphorylated RR,P.

Results
DivL Binds Specifically to DivK,P within the Core Cell-Cycle Signaling Circuit Previous experiments [13,14], and our results obtained from in vivo co-immunoprecipitation analysis ( Figure S1) all support an interaction between DivL and DivK. We employed a fluorescence polarization assay [20] to measure the binding affinities between DivL and DivK, as well as between DivK and other HKs in the compartment sensing signaling modules ( Figure 1B, PleC and DivJ) and the differentiation module (Figures 1B, CckA and the ChpT histidine phosphotransfer protein, and 2). We fluorescently labeled DivK with a BODIPY dye and measured binding by mixing 10 mM of HK with 250 nM of labeled DivK or DivK,P (see Materials and Methods). As shown in Figures 2 and S1, DivJ bound with similar affinity to both phosphorylated (K d = 1663.2 mM) and unphosphorylated (K d = 862.1 mM) forms of DivK, whereas PleC preferentially bound to DivK,P (K d = 2.460.9 mM) over DivK (K d = 26630 mM). DivL(152-769) bound exclusively to DivK,P with an apparent K d of 1164.2 mM, and very limited binding to unphosphorylated DivK ( Figure S1). No binding of DivK to CckA or ChpT was observed regardless of the DivK phosphorylation state, even when the RR was present at concentrations as high as 100 mM. Thus, DivK or DivK,P binds specifically to DivJ, PleC, and DivL with affinities within an order of magnitude of values reported for canonical HK-RR pairs (,1 mM), while non-cognate pairs have binding affinities greater than ,75 mM [21]. Thus, DivK impacts the CckA-ChpT-CtrA pathway without directly interacting with this set of signaling proteins.

Structure of DivL's HK region
To define the structural basis for the phosphorylation-dependent binding of DivK to DivL, we determined the crystal structure of DivL's HK region (residues 523-769, Figures 1C and 3) by the multiple-wavelength anomalous diffraction (MAD) method using a gold derivative. The final model (PDB code 4q20) was refined to an R cryst of 20.2% and an R free of 23.2% using native data up to 2.5 Å resolution (Table S2). The model of DivL displays good geometry with an overall quality score that ranks in the 100th percentile compared to other structures with similar resolution, as calculated by MolProbity [22]. The asymmetric unit contains a DivL dimer ( Figure 3A), which is consistent with size exclusion chromatography showing dimeric DivL in solution (observed MW = 50615 kDa, predicted dimer MW = 47.3 kDa).
Overall, the DivL structure resembles other characterized HKs, such as the Thermotoga maritima HKs: HK853 [23,24] and ThkA [25], although the DivL dimer is asymmetric. Asymmetric dimers were also observed in several recent HK structures (additional discussion included in Text S1) [26][27][28][29]. The dimer interface buries ,3,900 Å 2 total surface area. Each DivL monomer (DivL-A and DivL-B) consists of a DHp domain with two helices, a1 and a2 (residue range 526-608; since the a1-a2 loop is disordered in the crystal structure we assigned the connectivity of the two DHp helices in each monomer as in other class I HKs [23]), and a Cterminal CA domain with a highly conserved fold (residue range 609-758). The functionally important residue Tyr550 (colored in yellow in Figure 3A and 3B) is located at the middle of the first DHp helix (a1). Except for the substitution of a normally phosphorylatable histidine with tyrosine, DivL appears to retain all of the characteristic HK motifs, such as H, N, G1, F, and G2 boxes ( Figure S2). A highly conserved patch of residues located near Tyr550 was revealed by mapping the degree of sequence conservation of DivL orthologs onto the DivL structure ( Figure  S2). We note with interest that this surface is typically involved in the RR recognition [23,30].

DivL Forms an Asymmetric Dimer
The CA domains of the DivL dimer are almost identical (RMSD of 0.64 Å for 144 C a atoms). However, the DHp domains

Author Summary
Across all kingdoms of life the generation of cell-type diversity is the consequence of asymmetry at the point of cell division. The bacterium Caulobacter crescentus divides asymmetrically to produce daughter cells that have distinct morphology and behavior. As in eukaryotes, an unequal distribution of signaling proteins in daughter Caulobacter cells triggers the differential read-out of identical genomes. A critical interaction between two protein molecules -a protein kinase (DivL) and a response regulator (DivK) -is known to occur exclusively in one daughter cell and to thereby regulate differentiation. However, mapping the observed signaling interconnections that drive asymmetric division has been difficult to reconcile with traditional models of bacterial signaling. Here we determine how DivL detects and processes this DivK signal. Although DivL has an architecture that is typical of histidine kinases, which normally act by regulating the phosphorylation state of the appropriate response regulator, DivL's essential functions do not require kinase activity and DivL does not add or remove phosphate from DivK. Instead we find that DivL has converted its output kinase domain into an input sensor domain that specifically detects phosphorylated DivK, and we identify key features of DivL that underlie this specificity. This novel reassignment of sensory functions reverses the conventional kinase-to-response-regulator signaling flow and logically couples linear signaling pathways into complex eukaryote-like networks to regulate cell development. display significant structural differences (RMSD of 3.4 Å for 80 Ca atoms), indicating that the DivL dimer is asymmetric. The conformational differences between two DivL monomers are best described as rigid-body movements of substructures ( Figure 3B-3D). Three rigid substructures can be identified in each monomer ( Figure 3B), with each substructure representing a functional module. The largest substructure (residue range 591-758) consists of the CA domain and the ''output helix,'' which contains the Cterminal portion of a2 (a2C). The interface between a2C and CA is stabilized by clusters of highly conserved hydrophobic residues ( Figure S3). A highly conserved CA domain and a very similar arrangement between a2C and CA can be identified in DivL, HK853, ThkA, and QseC ( Figure S3), suggesting that this structural arrangement is a conserved HK feature. The second substructure (''RR docking module'') consists of the C-terminal portion of a1 (a1C) and the N-terminal portion of a2 (a2N) ( Figure 3B); the equivalent region in HK853 is involved in its cognate RR recognition. [23]. The third substructure (''input helix'') consists of the first portion of a1 (a1N), which is connected to the N-terminal PAS sensor domains. To promote cell differentiation, Caulobacter employs three distinct signaling modules: a compartment sensing module consisting of DivJ (HK), DivK (RR), and PleC (phosphatase), a differentiation module consisting of CckA (hybrid HK), ChpT (phosphotransferase), and CtrA (RR), and a cellfate-switch module comprising the DivL pseudokinase that connects the compartment-sensing and differentiation modules. DivL activates the differentiation module when unbound (via CckA), but represses this module when bound to DivK,P. (C) The domain organization of DivL in select a-proteobacteria that contain a putative DivK ortholog versus DivL domain organization in a-proteobacteria that do not contain a putative DivK ortholog [19]. Based on comparative analysis, DivL(523-769) containing only the DHp-CA domains was selected as a minimal DivK interacting unit for crystallization trials. doi:10.1371/journal.pbio.1001979.g001 Fluorescence polarization binding assay of BODIPY dye labeled DivK under unphosphorylated (gray) versus phosphorylated (black) conditions mixed with the following HKs at 10 mM PleC, DivJ, DivL, CckA, and ChpT. PleC and DivL binds to phosphorylated DivK specifically, while DivJ binds to both phosphorylated and unphosphorylated DivK. Numerical data used to generate manuscript graphs or histograms can be found in Table S1. doi:10.1371/journal.pbio.1001979.g002 When two DivL monomers are superimposed about the RR docking module, the relative movements between the other two substructures become apparent ( Figure 3C and 3D). The input helix in DivL-B is kinked more significantly around Tyr550 compared to DivL-A, resulting in a conformational change with respect to the Tyr550 side chain. This bending of the DHp helices is a common feature in many HKs [23,26,31,32], due to the conserved residue Pro555 [32]. The ''output helix+CA'' module interacts and moves in tandem with the input helix, with a pivot point at the ATP binding site (proximal to Leu722). As a result, the bending of the input helix repositions the output+CA module with respect to the RR docking module, which may reflect HK conformational changes crucial for propagating long-range signals from the sensor domain to the catalytic domain or vise visa (Movies S1 and S2 illustrates the ''morphing'' between the two DivL conformations) and illustrated as a cartoon in Figure 3D.
The structural movements produce an additional contact interface between DHp and CA in DivL-A, resulting in an increase in the buried surface area (1,730 Å 2 total) compared to that of DivL-B (1,400 Å 2 total) ( Figure S3). The asymmetry of the DivL dimer likely reflects some inherent conformational flexibility of DivL in solution, even though it could be induced by the crystal packing. The temperature factor (i.e., B-values) distribution supports the assertion that the DivL structure is highly flexible, save for the central four-helix bundle near Tyr550 where there is less conformational freedom ( Figure S3).

DivL Interacts with DivK,P Via the RR Docking Interface
To build a computational model of the DivL-DivK,P interaction, we compared the primary sequence of these proteins to the T. maritima HK-RR co-crystal structure of HK853-RR468 [23]. DivL's HK region shares 27% sequence identity with HK853, while DivK shares 36% sequence identity with RR468, the cognate RR for HK853. Strikingly, the surface of HK853 that directly interacts with RR468 is highly conserved in DivL, suggesting that the interaction between DivL and DivK is comparable to that observed between HK853 and RR468. Hence, we modeled a DivL-DivK,P complex based on the HK853-RR468 co-complex ( Figures 4A and S4). The resulting model places complementary surfaces of DivL and DivK,P together with favorable interactions, supporting the model's feasibility. In this model, Leu565 and Gly561of DivL interact with a hydrophobic patch on the DivK,P surface formed by Leu17, Leu21, Pro106, and Ile107. Furthermore, Ala582 of DivL makes an additional hydrophobic contact with Leu13 of DivK,P. Potential hydrogen bonds between DivL and DivK are also predicted, such as Tyr562OH with Leu13O and Leu17N, Arg553N1 and Ala84O, and His579Ne2 with Asp20Od2.
To interrogate the predicted interface, we introduced targeted mutations (R553A, T557N, Y562A, H579E, and Y550H) within DivL at the putative DivK,P docking site ( Figure 4A, highlighted in green) and measured the effect of each mutation on the DivL-DivK,P interaction. Each mutant was selected based upon introducing a significant side-chain perturbation, with the exception of T557N, which was selected based upon the presence of Asn (N) at this position in the DivJ kinase sequence. Each of these mutant proteins was purified and subjected to gel-filtration, which indicated that each variant formed dimers in solution. Four mutations (R553A, T557N, Y562A, and H579E) resulted in significant loss of DivK,P binding ( Figure 4B), with apparent dissociation constants measured to be 8-15-fold less than observed for wild-type DivL ( Figure S5), highlighting the importance of these residues for binding of DivK,P to DivL and supporting the validity of the DivL-DivK,P computational model. The Y550H substitution did not reduce the affinity of DivL for DivK,P. Intriguingly, T557N did not improve DivL's binding affinity for unphosphorylated DivK and instead diminished affinity for both forms of DivK. This indicates that DivL may bind DivK in a slightly different manner than DivJ. We also did not discover any mutations within this binding surface that switched binding specificity from DivL-DivK,P to DivL-DivK.
Due to the asymmetric nature of the DivL dimer, Tyr550 of the DivL-A subunit (green in Figure 4A) is situated above the canonical phosphotransfer site (where the hydroxyl group may form hydrogen bond[s] with the phosphoryl group on Asp53 of DivK,P), while in DivL-B (cyan in Figure 4A), both Tyr550 and the CA domain are displaced from the DivK active site (see Figure  S4). This observation implies that conformational changes in DivL may impact affinity for DivK,P. As a result, the asymmetric DivL dimer presents two different RR binding sites that share a common core surface but vary in the surface aspect involving Tyr550 and the ATP lid.

PAS Sensor Domains Enhance Binding Specificity towards DivK,P
DivL exhibits extensive structural homology with the PASlinked HK ThkA [25], and comparative analysis suggests that a conserved surface-exposed patch on the DivL CA domain ( Figure  S2) could participate in a similar PAS domain interaction as observed in the ThkA structure. Because a PAS-CA interaction potentially restricts CA domain movement, we analyzed binding of DivK to DivL in the presence and absence of one or more DivL PAS domains to determine whether they influence the interaction between DivK and DivL. For these studies, we constructed DivL mutants containing 3, 2, 1, or 0 PAS domains and measured DivL-DivK or DivL-DivK,P binding for each construct as a function of DivL concentration (0-120 mM). To our surprise, removal of all DivL PAS domains almost completely eliminated specificity for DivK,P: DivL containing three PAS domains (residues 152-769) was highly selective for DivK,P (K d = 11 mM for DivK,P and . 150 mM for DivK), whereas a DivL variant with no PAS domains (i.e., crystallization construct) bound phosphorylated and unphosphorylated DivK with similar affinity (K d = 15 mM for DivK and 7 mM for DivK,P) ( Figure 5A). DivL constructs containing three, and two PAS domains bind specifically to DivK,P, while the DivL variants R553A, T557N, Y562A, and H579E disrupt the binding to DivK, while DivL variant Y550H has no impact on DivK,P binding. Numerical data used to generate manuscript graphs or histograms can be found in Table S1. doi:10.1371/journal.pbio.1001979.g004 1-PAS domain DivL construct did not bind DivK,P and may be less stable than other DivL constructs ( Figure 5B). These results indicate that DivL's PAS sensor domains play a critical role in DivK,P selectivity.
Previously, a DivL mutant (A601L) was shown to disrupt the DivL-DivK,P interaction and thereby leading to the upregulation of CckA kinase activity in vivo [13]. Residue Ala601 lies at the interface between the input and output helices and away from the DivK,P binding site ( Figure 5C), indicating that the A601L mutation may impact DivL-DivK,P binding through an allosteric effect rather than by modifying the docking site. Critically, this interface includes the C-terminal end of the DHp domain that has been shown to alter its structure by helical unwinding or bending to activate sensor kinases upon receiving a signal in the Bacillus subtillus HK KinA [33]. To determine whether the disruption of DivK,P binding is due to perturbation of the RR module itself or of the arrangement of the PAS and CA domains with respect to the RR docking module, we evaluated the impact of A601L and a bona fide RR docking surface mutation (R553A) on DivK,P binding to DivL that either contains or lacks PAS domains. We found that the R553A substitution disrupts DivK,P binding regardless of whether the PAS domains are present. The DivL(A601L) variant binds DivK,P and weakly to unphosphorylated DivK, but only when the PAS domains are deleted ( Figure 5D). The observed PAS-domain-sensitive DivK,P binding to DivL(A601L) suggests that interdomain interactions influence the binding of DivK,P to DivL and explains in part the requirement for the PAS domains in DivK,P selectivity. Specifically, in the DivL-A conformation the output helix forms a three-helix bundle in association with the two input helices ( Figure 5C), whereas the output helix is isolated from the input domain in the DivL-B conformation ( Figure 5C). Therefore,  Table S1. doi:10.1371/journal.pbio.1001979.g005 modulations of interactions at the input-output helix interface likely alters the PAS and CA inter-domain arrangement with respect to the DivK,P binding site.

DivL Lacks Kinase and Phosphatase Activities
Consistent with in vivo studies that indicate DivL's kinase activity is not essential for viability [12,13,16], we observed in vitro that DivL does not exhibit autokinase activity and that a Y550H mutation could not rescue activity ( Figure S6). Loss of autokinase activity may be rooted in poor ATP binding as we found that DivL binds weakly to the ATP analog TNP-ATP with an apparent binding constant of 5768 mM ( Figure S7) [34]. DivL binds to TNP-ATP greater than 196 weaker than most prototypical HKs that exhibit binding constants in the range of 0.5-3 mM [34][35][36][37], with the exception of one study that reported a 294 mM Kd for the catalytic domains of PhoQ [38]. We also crystallized DivL in presence of various nucleotide analogs, but no nucleotide or magnesium ion could be identified in the density map ( Figure S7). Structural analysis of the crystallized DivL conformation shows that both nucleotide-binding sites are either inaccessible or too small to accommodate ATP ( Figure S7). Compared to other HKs, the DivL ATP lid mobility is more restricted since it is sandwiched between Tyr550 and the remainder of the CA domain. These results suggest that DivL has little intrinsic kinase activity compared to functional HK controls, which is consistent with our structural and nucleotide binding data.
We also asked if DivL functions as a DivK phosphatase in a manner similar to PleC ( Figure 6A and 6B). DivK,P was generated by addition of His-DivJ, which was then purified by metal affinity chromatography. The remaining ATP in the DivK,P reaction mixture was converted to ADP by incubation with hexokinase and glucose. DivK,P phopho-aspartate stability was then compared over a 4 hour time frame in the presence of either PleC or DivL. We found that PleC reduced the DivK,P halflife from 126 min to 8 min. However, the DivK,P stability was increased in the presence of DivL (half-life .700 min). Furthermore, restoration of a phosphorylatable histidine on DivL (DivL Y550H) has no impact on DivK,P phosphostability. Therefore, we conclude that DivL does not function as a DivK,P phosphatase.
It has been established that DivK allosterically activates the kinase activity of DivJ and PleC [9]. In light of these findings, we questioned whether any autokinase activity of DivL could be stimulated by DivK using a coupled-enzyme assay which assays ATPase activity (see Materials and Methods). Consistent with previous reports, we observed stimulation of DivJ autokinase activity in the presence of DivK. In contrast, no DivL autophosphorylation was observed upon addition of DivK or DivK,P ( Figure 6C). However, we did observe phosphate accumulation on DivL Y550H in the presence of DivK,P and ATP ( Figure 6D). In the absence of ATP no significant accumulation of phosphate signal was observed upon DivL Y550H ( Figure S8), indicating that DivK,P likely stimulate DivL autokinase activity in the presence of a canonical phosphate acceptor (i.e., His550). We do note it is formally possible DivK,P has the ability to back transfer to DivL Y550H, but only in an ATP-dependent manner. Taken together, our results suggest that DivL does not act on DivK by modifying the RR phosphorylation state. Instead, based on previous genetic studies [13,16], it appears the consequence of the DivL-DivK,P interaction is to allosterically modulate DivL's regulatory functions towards CckA ( Figure 1B).

Disruption of DivL-DivK,P Binding Impacts Cell Fitness
Previous genetic experiments have indicated that excess CtrA,P can impact cell growth, motility, replication, cell division [7], and DivL localization ( Figure 7A) [39]. Since the DivL-DivK,P interaction is known to result in inhibition of the CckA phosphorelay [13], we predicted that the DivL mutations characterized here, which impact binding of DivK,P to DivL, should consequently reduce cell fitness through dysregulation of CtrA signaling. Therefore, we generated translational fusions of each divL mutant allele described above to the coding region for eYFP and introduced the fusion constructs into the Caulobacter genome at the xylX locus under control of the xylose inducible P xylX promoter [40]. The strain background employed in each experiment contained a previously constructed divL depletion construct in which the wild-type divL ORF was placed under the control of the vanillate-inducible P vanA promoter at the chromosomal vanA locus [16]. In the resulting merodiploid strains, wildtype and mutant divL alleles could be conditionally expressed through the addition of vanillate or xylose, respectively, to the growth medium.
We expressed multiple divL-eyfp mutant alleles (Y550H, R553A, and A601L) grown in peptone yeast extract (PYE) media supplemented with xylose. Cell lengths were significantly longer in cells expressing Y550H, R553A, and A601L, while Y562A exhibited no obvious cell morphology defects ( Figure 7B). Plating efficiency assays indicated growth defects ranging from very mild (Y562A) or moderate (Y550H) to severe in A601L cells ( Figure 7C). Interestingly, the R553A mutant was similar to Y550H on PYE plates with no xylose, but additional expression of the mutant by addition of xylose further inhibited the growth of the R553A mutant specifically, suggesting a dominant negative effect (compare Figures 7C with S9). Monitoring growth in liquid culture by optical density also revealed additional xylose induced expression of R553A was toxic ( Figure S9). In a mixed population of cells grown in minimal media, we observe that 42% of cells expressing DivL-eYFP exhibit an observable monopolar DivL population ( Figure S9), whereas only 20% of cells containing DivL-DivK,P binding mutations (Y550H, R553A, and A601L) had an observable monopolar focus and the Y562A DivL mutant had a mild reduction (32%) in the proportion of cells with monopolar DivL ( Figure S9). Overall, these results demonstrate that two DivL-DivK,P binding mutants, A601L and R553A, have severe impacts on cell fitness, while the Y562A mutation has a relatively mild effect even though DivK,P binding is similarly affected by that substitution in vitro. Intriguingly, the strain containing the Y550H mutation exhibits clear growth and morphology defects despite the fact that DivK,P binding to DivL is not disrupted in that background, suggesting that Y550H perturbs the activity of DivL in a distinct manner.

Transmitter Core Converted to a Sensory Module
Our structural and biochemical analysis showed that DivL lacks both kinase and phosphatase activity but still retains its ability to dimerize and bind DivK,P specifically. The DivL mutant Y550H supports viability but impacts cell morphology, doubling time, and the subcellular localization of DivL. These defects suggest that the replacement of histidine by tyrosine is critical for optimal DivL function. We observed that DivL Y550H bound to DivK,P with similar affinity as the wild type, indicating that the tyrosine substitution neither enhances nor diminishes DivK,P binding. The Y550H mutation did not rescue autonomous autokinase activity in vitro, however, DivL(Y550H) autokinase activity can be stimulated by DivK,P in the presence of ATP ( Figure 6D). Thus, the H to Y substitution in DivL does not perturb HK-RR binding but abrogates kinase activity. From these studies, we propose that or DivK,P with PleC (orange), or DivL (green), or DivL Y550H (red). (C) DivK stimulates DivJ ATP consumption, but has no impact on DivL ATP consumption. ATP consumption rates for DivJ, DivJ-DivK, DivL alone, and DivL-DivK are shown. (D) DivK,P stimulates DivL Y550H autophosphorylation but has no impact on the phosphorylation state of wild-type DivL. Purified DivK,P and [c-32 P]ATP were incubated with 5 mM PleC, with 5 mM DivL, or with 5 mM DivL Y550H for 0, 0.5, 1, 2, 5, and 20 minutes. (E) Cartoon illustrating the functional differences between the PleC phosphatase and the DivL phosphospecific DivK,P sensor. Samples were transferred into SDS sample buffer and subjected to electrophoresis followed by phosphorimaging. Numerical data used to generate manuscript graphs or histograms can be found in Table S1. doi:10.1371/journal.pbio.1001979.g006 the DivL pseudokinase has repurposed its catalytic HK fold to function primarily as a sensory module for a phosphorylated RR. Loss of catalytic function ensures orthogonal sensor function while preventing unwanted signal modification (i.e., inter-conversion of DivK and DivK,P) that would compromise asymmetric cell division.

A Role for Histidine Kinase PAS Domains in Phosphospecific RR Recognition
Previous studies of two-component systems have highlighted the critical role of the RR docking module in determining HK-RR phosphotransfer specificity [21,[41][42][43][44][45]. Consistent with these studies, we identified four point mutations within the RR docking module that disrupt DivK,P binding to DivL (Figure 4). Thus, our results support the notion that DivL binds DivK,P in a conserved manner similar to a canonical HK-RR pair [23,[41][42][43][44]. However, a key question remains: how does DivL specifically recognize DivK,P? The tyrosine or histidine side chain at position 550 could contribute to the specific recognition of the phosphoryl group on DivK directly, by forming a hydrogen bond. However, we do note that Y550F has been previously shown to specifically bind phosphorylated DivK over unphosphorylated DivK [13]. Furthermore, the DivL RR docking surface, which includes Tyr550, may be tuned to specifically recognize structural changes in DivK that are induced by phosphorylation. Here, we observed that the PAS sensor domain plays an unexpected role in phosphospecific discrimination of DivK,P over DivK ( Figure 5). One possible role of the PAS sensor domain could be to directly sterically block unphosphorylated DivK binding while permitting DivK,P binding, or perhaps more likely the DivL PAS domains could indirectly reconfigure the DivK binding site to promote phosphospecific binding. The PAS domain's role in phosphospecific RR binding is consistent with the finding that optimal WalK [46] and ThkA [25] phosphatase activity requires a PAS module. More generally, it appears that PAS sensor domains may regulate kinase/phosphatase activity by influencing the phosphospecific binding preference of an HK for its cognate RR.

Models for the DivL Cell-Fate Switch
Several recent biochemical studies of HKs have revealed that HKs transmit signaling information over a long-range through large-scale conformational changes in order to regulate activity. DHp conformational rearrangements, such as ''twisting'' (cogwheeling or rotation) and ''bending'' (kinking), can produce unique functional states that are crucial for HK regulation [24,[26][27][28]32,[47][48][49][50]. Our rigid-body structural analysis of DivL suggests that interhelical bending could alter the relative position of domains that regulate DivL function. Indeed, our binding studies indicate that a mutation at the interface between two rigid bodies (A601L), disrupts DivK,P binding in a PAS-domain-dependent manner ( Figure 5C). Furthermore, the A601L mutation causes a more severe phenotype than does the direct RR docking mutation Y562A. This suggests that A601L may be pleiotropic, perhaps simultaneously affecting upstream (i.e., DivK,P binding) and downstream events (i.e., CckA inhibition). Residue Arg553 may also serve a switch-like role triggering conformational changes upon DivK,P binding by interacting with DivK,P in the complexed state, and in the uncomplexed state interacting with the output-helix residue Asp595 ( Figure 5). Taken together, this model may explain why A601L and R553A have stronger impacts on cell fitness than the Y562A variant. Additionally, DivK,P-dependent rescue of DivL autokinase activity in the presence of Y550H suggests that DivK,P binding triggers conformational changes in DivL that are necessary for ATP binding and autokinase activity.
Thus, we propose a model in which the interaction between Tyr550 and the phosphorylation site of DivK,P induces bending in the a1 helix of DHp, which is then propagated to the rest of the Morphology assay of Caulobacter strains grown in PYE indicates that Y550H, R553A and A601L display cell filamentation and cell division defects, while the Y562A variant is similar in morphology to a wild-type strain. (C) An efficiency of plating assay indicates a reduction in growth rates of Y550H, R553A, and A601L, while Y562A displayed a mild reduction in growth rate relative to wild-type. doi:10.1371/journal.pbio.1001979.g007 structure via rigid-body movements. As a result of the conformational change, the CA and PAS domains of DivL may re-position to allow formation of additional contacts with bound DivK,P. In the absence of catalytic functions, we suggest that DivL exploits the underlying large-scale conformational re-arrangements of the HK-fold to function as a DivK,P-modulated two-state molecular switch (Figure 8). Asymmetric dimers have been proposed to represent important activation intermediates [26][27][28][29]51], and it is conceivable that DivL undergoes a symmetric-asymmetric conformational switch upon DivK,P binding. However, the mechanism by which DivK,P-dependent conformational changes in DivL impact the CckA-ChpT-CtrA phosphorelay [12,13,15,39,52] remains unclear. It is plausible that DivL interacts directly or indirectly with CckA in the multi-protein polar complex, thus allowing the structural changes in DivL induced by DivK,P to propagate to changes in CckA activity. Future experiments will focus on dissecting DivL's essential regulation of the CckA-ChpT-CtrA pathway.

Broadening the Wiring Possibilities of Two-Component Systems
A common bacterial signaling strategy is to wire two-component systems as simple orthogonal linear signaling arrays to limit crosstalk and maintain the integrity of signaling information [43,44]. Phosphorelay pathways offer a way to branch signaling pathways in order to enable multiple signaling inputs [30] or outputs [45,53]. Signaling directionality in the two-component systems from a kinase to a response regulator apparently limits bacterial signal processing capacity relative to more complex eukaryotic systems. Here, we demonstrated an exception to this paradigm in which loss of HK catalytic activity repurposes an output module as a phosphospecific RR input sensor, thereby reversing the flow of information observed in conventional HK-RR systems. This reversal allows DivL to couple two distinct signaling pathways by serving as an ''output'' for a compartment sensing pathway and an ''input'' for the differentiation phosphorelay ( Figure 8). The extent to which nature utilizes this reversed signaling warrants further investigation. For example, it could allow transmission cytosolic stress signals to the periplasm via membrane-bound HKs. The presence of pseudokinases in two-component signaling systems therefore offers a general mechanism for coupling signaling pathways, reminiscent of complex eukaryotic signaling networks.

Construction of Plasmids and Strains
DNA primers, plasmids, plasmid construction methods, and bacteria strains used in this study are listed in Tables S3, Table S4,  Table S5, and Table S6, and detailed cloning methods are included in Text S2. The domain architecture of DivL was annotated using the HHpred structure prediction algorithm [54]. For the DHp-CA construct we retained a significant portion of the N-terminal input helix that connects the sensor domains to the DHp domain to generate DivL(523-769). Constructs with Nterminal start codons at: 411 containing one PAS domain, 281 containing two PAS domains, and 152 containing three PAS domains. DivL residues 1-53, which were predicted to form a transmembrane helix followed by a coiled-coil region, were not included to improve in vitro solubility.

Protein Expression and Purification
Protein expression of all DivL variants, DivJ, PleC, and DivK followed the same protocol and is described in detail below for the crystallization construct DivL(523-769). Protein expression of ChpT, CckA, and CckA H322A were performed as described previously [45]. Plasmid pWSC8 was then transformed into chemically competent Rosetta (DE3) pLysS cells, and plated onto selective LB media (30 mg/ml chloramphenicol and 50 mg/ml kanamycin plates), and grown overnight at 37uC. From a single colony, an overnight 25 ml LB (chloramphenicol: 20 mg/ml; kanamycin: 30 mg/ml) culture was inoculated and grown to saturation overnight. From this saturated culture a 2L LB culture was inoculated and grown to mid-log phase (,0.6 OD).  MBP-DivK expression and purification followed the same protocol, however after elution from the Ni-NTA agarose TEV protease was used to cleave off the His-MBP-TEV site tag of DivK. Briefly, His 6 -MBP-DivK was diluted to 2 mg/ml and mixed with His 6 -TEV protease and the solution was dialyzed overnight at 4uC in two 12 ml Slide-A-Lyzer 10 k MWCO dialysis cassettes against 2L dialysis buffer (20 mM HEPESáKOH [pH 8.0], 100 mM KCl, 0.5 mM EDTA, 10% glycerol, 1 mM DTT). The following day, the His6-tagged unreacted protein impurities were removed by subtractive Ni-NTA affinity purification with 6 ml of 50% slurry of Ni-NTA agarose affinity resin (5Prime) equilibrated in dialysis buffer; the eluate containing cleaved DivK was collected.

Crystallization
The initial crystallization conditions for DivL were obtained using the sparse matrix screening method (Hampton Research). The conditions were subsequently optimized manually to improve the quality of the crystals. The crystals used for structure solution were obtained using the hanging-drop vapor diffusion method at 22.5uC. The reservoir well contained 500 ml 0.1 M HEPES (pH 7.5) and 18% PEG 10000, while the drop contained 1.2 ml of DivL (concentration 5.8 mg/ml) mixed with 1.2 ml of the reservoir solution. For cryoprotection, the crystals were gradually transferred to a series of reservoir solutions containing incrementally higher concentration of PEG 4000, up to a final concentration of 30% prior to flash freezing in liquid nitrogen. The data were indexed and processed in the trigonal space group P3 1 21 with unit cell dimensions of a = 69.5 Å and c = 194.4 Å .
To obtain heavy atom derivatives, crystals were soaked in cryo solution containing 10 mM KAu(CN) 2 for 10 min. For cocrystallization with nucleotides, MgCl 2 and each nucleotide (ATP, ADP, AMP-PNP, AMP-PSP, and TNP-ATP) were added in ,10 molar excess to the protein before crystallization. In addition, attempts were made to soak the native crystals in the presence of nucleotides and magnesium.

Data Collection, Structure Determination, and Refinement
Native data and multiwavelength anomalous diffraction (MAD) data for the gold derivative, and data for crystals obtained in the presence of different nucleotides were collected at the SSRL Beamline 12-2. The datasets were collected at 100 K using a Pilatus 6M pixel array detector (Dectris). Each dataset was integrated using XDS and then scaled with the program XSCALE [55]. Gold sites were located with SHELXD [56] using the data corresponding to the peak wavelength (1.0397 Å ) of the Au-MAD experiment. Phase refinement (FOM = 0.32 for three Au sites) and automatic model building were performed using autoSHARP [57] and BUCCANEER [58]. Model completion and refinement were performed with COOT [59] and BUSTER [60]. Additional CCP4 programs [61] were used to for data conversion and other calculations. Data reduction and refinement statistics are summarized in Table S2. Atomic coordinates and experimental structure factors for DivL at 2.5 Å resolution have been deposited in the PDB (http://www.rcsb.org) under accession code 4q20.

Gel Filtration
A gel filtration standard (Bio-rad) containing thyroglobulin (bovine), c-globulin (bovine), ovalbumin (chicken), myoglobulin (horse), and vitamin B12 were used to generate a molecular weight standard plot using a Superdex 200 10/300 GL column (GE Healthcare). A 2 mg/ml sample of His 6 -DivL(523-769) was loaded onto the column and eluted after 14.2 ml, corresponding to a molecular weight of 50615 kDa (dimer = 57.4 kDa). Error bars for molecular weight estimated as the full width at half maximum (FWHM) for the eluting peak.

Co-immunoprecipitation Assay
Immunoprecipitations were performed as previously described [62]. A 500 ml culture of wild type Caulobacter cells (strain LS101) and a strain carrying divL-m2 (LS4468) [16] were grown in PYE media at 28uC to mid-log phase. The cells were harvested in a centrifuge at 4uC, 15 min, and 7,800 rpm. Cells were then washed with CO-IP buffer (20 mM HEPES pH 7.5, 100 mM NaCl, 20% glycerol), and pelleted in a centrifuge at 4uC, 15 min, and 9,000 rpm. Cells were resuspended in 29.2 ml PBS (pH 6.8) containing 1% formaldehyde and allowed to cross-link at room temperature for 30 minutes. Cells were pelleted in a centrifuge at 4uC, 15 min, 9,000 rpm and then resuspended in 30 ml of CO-IP buffer supplemented with protease inhibitors. The pellet was snap frozen with liquid nitrogen and stored at 280uC. The cell suspension was thawed and lysed with three passes through a French Press at 20,000 psi. After lysis, 2 mM EDTA and 1% Triton X-100 were added and allowed to incubate on ice for 60 min. Insoluble cell debris was pelleted via centrifugation (9,000 rpm, 10 min at 4uC). Lysate was incubated with 50 ml of FLAG-M2 agarose (FLAGIPT-1 kit; Sigma) overnight on a nutator at 4uC. Beads were washed twice with co-IP buffer supplemented with 0.05% NP-40, then washed five times with wash buffer (50 mM Tris-HCl, 150 mM NaCl, protease inhibitors, 0.05% NP-40) and proteins were eluted by incubating with 36 FLAG peptides. Western blots were performed as previously described [62]. Antibody dilutions were as follows: a-FLAG (Sigma) 1:1,000,) and a-DivK (1:5,000). Films were scanned and processed with Adobe Photoshop.

Fluorescence Polarization Assay
DivK was labeled at Cys-99 using thiol-reactive BODIPY FL Naminoethyl malemide (Invitrogen). DivK was mixed together with 10-fold excess BODIPY FL N-aminoethyl malemide and allowed to react for 2 hours at room temperature, and unreacted dye was quenched with mercaptoethanol. BODIPY-DivK was purified via dialysis to remove unreacted fluorescent dye. BODIPY-DivK,P was generated by mixing 250 nM DivJ with 1 mM ATP and 5 mM MgCl 2 and incubated for 40 min. Mock binding assays were done in the presence of [c-32 P]ATP, and under these reaction conditions scintillation counting combined with Bradford assay estimate .75% of DivK was in the phosphorylated state.
Upon phosphorylation of BODIPY-DivK by 250 nM DivJ no change in fluorescence polarization was observed. This finding indicates that BODIPY-DivK,P was likely a monomer under reducing buffer conditions (1 mM DTT) and that no significant DivJ was bound to DivK.
For binding assays using unphosphorylated DivK, 1 mM nonhydrolyzable AMP-PNP and 5 mM MgCl 2 were included in the buffer. BODIPY-DivK,P or BODIPY-DivK was then incubated with varying kinase concentrations for 45 minutes to reach binding equilibrium. Fluorescent DivK was excited at 470 nm and emission polarization was measured at 530 nm in a Molecular Devices SpectraMax M5 plate reader. Fluorescent polarization measurements were performed in triplicates, and three independent trials were averaged with error bars representing the standard deviation. We extensively screened buffer conditions to optimize DivL-DivK binding by exploring KCl concentration, % glycerol, and pH. Of these parameters, DivL-DivK binding was most sensitive to KCl concentration and low KCl (50 mM) promoted the DivL-DivK interaction ( Figure S1). Interestingly, ATP appeared to promote the interaction between DivL-DivK and DivL-DivK,P ( Figure S1).

Coupled-Enzyme Activity Assay
ATPase activity of DivL constructs was measured using a coupled-enzyme assay [63,64]. Proteins were mixed in kinase buffer supplemented with 1 mM ATP, 10 mM MgCl 2 , 1 mM phosphoenolpyruvate, 0.2 mM NADH, 2 units of pyruvate kinase, and 6.6 units of lactate dehydrogenase. Reactions were performed in triplicate in 200 ml volumes and loaded into a clear, polystyrene 96-well plate. Reactions were initiated by the addition of protein, and absorbance at 340 nm was recorded every 10 seconds for a 30 minute period. The slope of a stable linear absorbance decay was measured to calculate ATP hydrolysis rates, using a NADH Kpath value of 3,248 OD M 21 [63]. Background rates of ATP hydrolysis and NADH oxidation were measured and subtracted from observed ATP hydrolysis rates of all DivL constructs.

Autophosphorylation Reactions
CckA(70-691) and DivL(152-769) constructs at 5 mM were incubated for one hour at room temperature in kinase buffer supplemented with 0.5 mM ATP, 0.167 mCi/ml [c-32 P]ATP, and 5 mM MgCl 2 in a total reaction volume of 50 ml. Reactions were stopped by the addition of 26Laemmli sample buffer, then loaded onto 12% Tris-HCl gels for electrophoresis. The radioactivity in wet gels was recorded on phosphor storage plate for 3 h, and then imaged on a Typhoon fluorescence imager (Molecular Dynamics). Quantitation of band intensities was measured using ImageJ and band intensities for three individual experiments were averaged. The mean intensity and standard deviation were plotted using Prism 6 software (GraphPad).

DivK,P Dephosphorylation Assays
For DivK,P phosphatase assays, DivK was incubated with 250 nM His-DivJ, 1 mM ATP, and 5 mM MgCl 2 on Ni-NTA agarose resin for 40 min. DivK,P was eluted and purified away from His-DivJ, followed by a second round of Ni-NTA purification. Purified DivK,P was then incubated with excess hexokinase and glucose for 10 minutes to convert remaining ATP into ADP. Purified DivK,P was then incubated with either PleC, DivL(152-769), or DivL(152-769) Y550H for varying amounts of time. Reactions were quenched with 46 SDS-PAGE sample buffer. Gels were processed as described above in the autophosphorylation section. The mean intensity and standard deviation from three independent experiments were plotted using Prism 6 software (GraphPad).

TNP-ATP Binding Assay
A solution of 1 mM TNP-ATP [34] was compared with a solution of 2 mM TNP-ATP with 10 mM DivL(523-769) in 50 mM HEPES6KOH (pH 8.0), 200 mM KCl, 0.1 mM EDTA, 10% (v/v) glycerol. Solutions were allowed to reach equilibrium for 30 min at room temperature, prior to fluorescence measurements. An emission profile was collected over a wavelength range of 475-750 nm. Presented curves in Figure S7 are average values of three replicates.

Filter Binding Assays
Filter binding assays were designed to capture transiently bound [c-32 P] ATP [65,66]. Solutions of DivL(523-769), DivL(523-769) Y550A, CckA (70-691) H322A, ChpT, and BSA at 10 mM protein concentration was mixed with 27.5 fmol of [c-32 P] ATP in kinase buffer at room temperature. Empirically, we found a 30minute period allowed adequate time for equilibration, while minimizing hydrolysis and release of ATP. Solutions were passed over a nitrocellulose membrane filter and washed three times with 1 ml of kinase buffer. Bradford assays indicated .95% of protein remained bound to the nitrocellulose. Subsequently, nitrocellulose filters were submerged into scintillation fluid and scintillation counted to quantify bound [c-32 P] ATP. [c-32 P] ATP standard solutions were used to determine the specific activity and convert scintillation counts in fmol bound to the nitrocellulose. [c-32 P] ATP only solutions were passed through nitrocellulose membranes to quantify non-specific binding.

Growth and Morphology Assays of DivL-DivK Binding Mutants
Each of the pXYFPC-divL mutant strains were transformed into Caulobacter NA1000 strain AA871 that is DdivL vanA::divL. In these strains the impact of divL mutant expression was evaluated by removal of vanillate from media to deplete wild-type divL from cells, and addition of xylose to express divL-yfp mutants. Mutant divL genes were examined in a strain where the native copy of divL was deleted, the WT divL placed under vanillate induction at the vanA locus, and a mutant divL-yfp was placed at the xylose-inducible xylX locus of the chromosome. Cells were grown for 24 h in PYE containing no vanillate and no xylose. Cells were then diluted in fresh, xylose-containing media to optical density at 600 nm (OD-600) of 0.02 (diluted to approximately 0.06 for efficiency of plating assays). The cells were then allowed to grow for several hours in the xylose until either being plated or imaged. For efficiency of plating assays, cells grew for either 0 or 6 hours after addition of xylose. Cells were spotted on PYE-agar plates in 3 ml volumes. The first, leftmost spot was spotted from the 0.06 OD-600 culture, and subsequent dilutions were made serially in 5-fold steps. The xylose content of the plates was varied from 0 to 0.3% w/v, and cells were plated from liquid media containing an equal amount of xylose. The plates were then grown at 28uC for 2 days and subsequently imaged. For liquid culture growth curves, we measured the OD-600 every 1-2 hours for 10 hours or until the culture reached saturation.

Microscopy
DdivL vanA::divL xylX::divL-yfp WT, Y550H, R553A, Y562A, and A601L strains (WSC399, WSC308, WSC310, WSC312, and WSC314) were cultured overnight in M2G supplemented with 5 mM vanillate and sub-cultured into fresh media containing 0.03% xylose for 6 hours or until they reached an OD600 of 0.4 for divL localization assays. Cell suspensions were then dried onto agarose pads (1.5% agarose in M2G) and imaged on a Leica DM 6000 B microscope with a HCX PL APO 100u-/1.40 Oil PH3 CS objective, Hamamatsu EM-CCD 15 C9100 camera and Metamorph (Molecular Devices). Both phase-contrast and fluorescence images were recorded. Images were processed in Adobe Photoshop, and quantitative analysis of images was performed using ImageJ's cell-counter. For morphology assays, the cells were grown overnight in PYE and switched into fresh PYE with xylose. After 6 hours of xylose induction, cells were placed on a PYE-agar pad for imaging. Images were processed in Adobe Photoshop. Figure S1 Interaction between DivK and DivL, DivJ, or PleC. (A) Multiple sequence alignment of the DHp domains of three known DivK binding partners, DivL, DivJ, and PleC. The predicted residues involved in the interactions with DivK are highlighted at the bottom (orange, hydrophobic contacts; blue, hydrogen bonds involving side-chains). (B) In-vivo co-immunoprecipitation of DivK with DivL-m2 from Caulobacter lysates. (C-E) DivK (black) and DivK,P (red) binding curves for DivJ, PleC, and DivL using a fluorescence polarization assay. Influence of buffer conditions upon the interaction between DivL-DivK,P using the DivL(523-769) construct by varying the concentration of (F) KCl, (G) pH, and (H) % glycerol. (I) Examination of the impact of ATP binding upon the interaction of DivL-DivK (unphosphorylated). Numerical data used to generate manuscript graphs or histograms can be found in Table S1. (TIF) Figure S2 Sequence conservation of DivL orthologs mapped on the DivL structure. (A) The sequence of the HK region of DivL mapped with the secondary structures. The sequence is colored in gradient by degrees of sequence conservation, calculated from top 40 DivL homologs with sequence identity between 35% and 90%, from not conserved (white background) to strictly conserved (black background). The relative solvent accessibility of each residue (ratio of solvent accessible surfaces of each residue in the structure and in solution) is shown by blue boxes above the sequence. The residues that are near the DHp-CA interface in the structure shown in Figure S3 are marked by orange dots below the sequence. The five sequence motifs (H, N, G1, F, and G2) defined by Parkinson and Kofoid [67]  cyan. An ADP molecule, shown as sticks, was modeled into the ATP binding site based on the structure of KinB. The ATP lid is colored in red. Tyr550 is colored in yellow. An ADP molecule, shown in spheres in the same scale, highlights the size of ADP compared to the opening for ATP entry. Numerical data used to generate manuscript graphs or histograms can be found in Table S1. (TIF) Figure S8 DivL(152-769) Y550H accumulates phosphate in a DivK,P and ATP-dependent manner. Comparison of reaction mixtures of DivL(152-769) Y550H with phosphorylated DivK,P in the presence and absence of ATP. (TIF) Figure S9 Effects on Caulobacter growth and DivL localization by site-directed mutations disrupting DivL-DivK interaction. (A) Growth curves of strains containing divL point mutants. Growth was measured by optical density for 10 hours or until culture saturation. Mutants were binned depending on their location on the RR binding surface or based on allostery involving the input-output helix of DivL. Growth curves were consistent across triplicate measurements, and one representative curve is shown for each mutant grown with and without xylose. Curves were fitted to a single exponential model. Inset: cartoon of DivL depicting the approximate location of each mutant. (B) Cell growth assayed by efficiency of plating. Prior to plating, cells were grown in PYE liquid media to OD-600 of 0.2 in the absence of xylose for 6 h. The culture was diluted 10-fold for the left-most inoculation, and 5-fold for subsequent dilutions. Plating was performed in duplicate using no xylose concentrations or vanillate. A representative plate is shown. (C-E) DivL-DivK binding mutants impact DivL-yfp subcellular localization. divL-yfp mutant strains were grown in M2G supplemented with 0.003% xylose. (C) Fluorescent images of divL-yfp mutant strains were grown in M2G supplemented with 0.003% xylose for DivL-DivK binding mutants: Y550H, R553A, Y562A, and A601L relative to wild-type divL-yfp. (D) Cell population analysis characterizing the percentage of cells with an observable monopolar focus. (E) Singlecell analysis of the fraction of DivL-yfp signal localized at the cell pole in cells with an observable monopolar focus. Numerical data used to generate manuscript graphs or histograms can be found in Table S1. (TIF)    Text S1 Supplementary discussion of the DivL structure.

(DOCX)
Text S2 Detailed methods for Construction of plasmids and strains.

(DOCX)
Movie S1 A movie clip of a DivL dimer that illustrates ''morphing'' between the two observed DivL monomer conformations. The monomeric subunits DivL-A and DivL-B are colored in violet and cyan, respectively. The ATP lid in each monomeric subunit is colored red, and Tyr550 is shown in yellow sticks.

(MOV)
Movie S2 A movie clip of a DivL monomeric subunit (shown in cyan) that illustrates ''morphing'' between the two observed DivL monomer conformations. The ATP lid is shown in red and Tyr550 is shown in magenta sticks. (MOV)