The Kil Peptide of Bacteriophage λ Blocks Escherichia coli Cytokinesis via ZipA-Dependent Inhibition of FtsZ Assembly

Assembly of the essential, tubulin-like FtsZ protein into a ring-shaped structure at the nascent division site determines the timing and position of cytokinesis in most bacteria and serves as a scaffold for recruitment of the cell division machinery. Here we report that expression of bacteriophage λ kil, either from a resident phage or from a plasmid, induces filamentation of Escherichia coli cells by rapid inhibition of FtsZ ring formation. Mutant alleles of ftsZ resistant to the Kil protein map to the FtsZ polymer subunit interface, stabilize FtsZ ring assembly, and confer increased resistance to endogenous FtsZ inhibitors, consistent with Kil inhibiting FtsZ assembly. Cells with the normally essential cell division gene zipA deleted (in a modified background) display normal FtsZ rings after kil expression, suggesting that ZipA is required for Kil-mediated inhibition of FtsZ rings in vivo. In support of this model, point mutations in the C-terminal FtsZ-interaction domain of ZipA abrogate Kil activity without discernibly altering FtsZ-ZipA interactions. An affinity-tagged-Kil derivative interacts with both FtsZ and ZipA, and inhibits sedimentation of FtsZ filament bundles in vitro. Together, these data inspire a model in which Kil interacts with FtsZ and ZipA in the cell to prevent FtsZ assembly into a coherent, division-competent ring structure. Phage growth assays show that kil+ phage lyse ∼30% later than kil mutant phage, suggesting that Kil delays lysis, perhaps via its interaction with FtsZ and ZipA.


Introduction
The replication and lytic functions of bacteriophage l rapidly diminish Escherichia coli viability and lead to ultimate host death by lysis [1]. Decades-old research uncovered a secondary mode of linduced host cell death using a defective prophage containing only the immunity region and the P L operon. Under derepressed conditions, E. coli cells containing this defective prophage filament and eventually die.
The P L operon ( Figure 1A, top) contains no genes essential for lytic growth except N, but consists of accessory genes that may be essential in certain circumstances, such as the red recombination genes (exo, bet, and gam) [2]. A series of nested deletions beginning at attL and int, and removing successive prophage genes toward P L , initially defined the region of this secondary, lysis-independent killing function [3]. These deletions identified a putative gene located in this region named kil (host killing by an induced l prophage) responsible for host cell filamentation, loss of viability, and ultimate death. However, because kil overlaps the gam and cIII genes [4], some questions remained concerning the exact identity of kil and the possible influence of gam and cIII on host killing [2,5]. Later experiments further mapped Kil activity to the annotated kil open reading frame [6]. Additionally, separate experiments inducing expression of the annotated kil open reading frame from a plasmid verified that this region was responsible for causing cell filamentation and a loss of viability [7].
Although assumed to encode a protein, the product of the annotated kil gene has not been identified. Likewise, the host cell target of the kil gene product (Kil) is unknown. Given the strong cell filamentation and loss-of-viability phenotypes associated with kil expression, we reasoned that Kil likely targets a component of the E. coli cell division apparatus.
Cytokinesis in most bacteria studied to date involves assembly of the highly conserved prokaryotic tubulin-homolog FtsZ into a ring-shaped structure at the nascent site of divison [8]. FtsZ undergoes GTP-dependent polymerization into single stranded polymers in vitro, which in turn are able to bundle together through lateral interactions that are enhanced by certain buffer conditions or bundling agents [9].
In E. coli, the assembly of the FtsZ ring at mid-cell prior to division is stabilized and linked to the membrane through the formation of a 'proto-ring' that includes the essential transmembrane-anchored ZipA and membrane-associated FtsA proteins [10]. Once the proto-ring is formed, a coterie of both essential and non-essential proteins is recruited in a partially step-wise fashion to form a mature complex termed the divisome. The divisome contains all the components necessary to divide the cell through a combination of constriction, a switch from lateral cell wall growth to septum (crosswall) formation, and cell separation [11].
Cell survival requires proper coordination of division with other cell cycle events, such as growth, DNA replication, and chromosome segregation. This coordination is largely controlled by precisely regulating the timing and position of FtsZ ring formation by altering FtsZ assembly dynamics [12]. In E. coli, this regulation is chiefly controlled through the combined activities of the Min system (MinCDE) and the nucleoid-occlusion factor SlmA [8,13]. SlmA is a protein that binds specific regions of the chromosome and prevents FtsZ from assembling over unsegregated nucleoids [14,15,16,17,18]. The Min system functions to prevent FtsZ from assembling in DNA-free regions of cell poles through the inhibitory activity of MinC, whose localization is controlled by MinD and MinE [13,19,20,21]. Another welldescribed inhibitor of FtsZ assembly is SulA, which is activated following DNA damage as part of the SOS response to inhibit cell division until genetic errors are corrected [22,23,24].
Whereas numerous additional host factors that regulate cell division have been described in several species [11,25], little work has been done characterizing potential regulation by phage factors. Rac prophage and bacteriophage Mu each contain a gene also named kil [26,27]. Despite their identical names, however, these kil genes and their predicted peptide products have no significant similarity to one another or to l kil. Rac kil expression prevents FtsZ ring formation, which blocks cell division resulting in filamentation; no details on the direct target or the mechanism of its activity have been reported [26]. In contrast, expression of the Mu kil gene results in spherical E. coli cells [27], indicative of inhibiting cell elongation by this temperate member of the Myoviridae. The cryptic lambdoid prophage Qin (Kim) and its widespread relatives also contain two factors known to affect cell division [28]: DicB, which acts in place of MinD to bring MinC into position to inhibit FtsZ ring formation [29,30], and dicF, which encodes an antisense RNA that inhibits ftsZ translation [31]. Finally, the cryptic e14 phage-like element of E. coli contains the sfiC gene, which inhibits FtsZ assembly following SOS induction similarly to SulA (SfiA) [32,33,34].
Here, we report that l kil expression from a defective prophage, from a plasmid, or during induction of a complete, lytic-competent l lysogen inhibits cell division due to a block in FtsZ ring formation. We verify that Kil encodes a peptide, and show that it acts independently of well-characterized host systems of FtsZ assembly regulation. We further identify and characterize Kilresistant ftsZ and zipA mutant alleles, demonstrate inhibition of FtsZ assembly in vitro by an affinity-tagged Kil derivative, and discuss potential models for Kil activity on FtsZ assembly. Finally we address the relevance of kil to l biology, demonstrating that Kil acts during normal lytic growth of l phage and suggesting that this activity can delay cell lysis.

Expression of kil interferes with E. coli cell division
To investigate the role of kil expression on E. coli cell division, we first used a bacterial strain (CC4506) harboring a defective l prophage in which a modified operon is under control of a temperature-sensitive (ts) allele (cI857) of the phage CI repressor. In this kil + strain, a point mutation destroys the start codon of cIII, a cat cassette replaces sieB to ea10, and a tet cassette replaces gam through int ( Figure 1A). Consistent with previous findings [6], CC4506 cells formed long, non-dividing filaments after derepression of the P L operon by thermo-inactivation of the CI857 repressor at 42uC ( Figure 1B), and lost viability ( Figure 1C). In contrast, an isogenic strain with the start codon of kil destroyed by a point mutation (CC4512), continued to divide normally following induction of the prophage and retained viability, similar to the W3110 background strain ( Figure 1B & C).
The loss of cell viability, presumably caused by the division blockage elicited by kil expression, could be rescued in the short term by returning E. coli filaments to low temperature conditions that restored CI857 repressor activity ( Figure 1C, bottom left). However, prolonged kil expression at 42uC (,6 hours) prevented restoration of growth even after returning cells to conditions that repress kil expression ( Figure 1D).
To identify the potential target of kil expression, we screened a pBR322 library of E. coli chromosomal fragments for multi-copy suppression of kil-induced toxicity at 42uC. Consistent with kil expression targeting cell division, multi-copy expression of an ,5.4-kb fragment including the ftsQAZ operon completely suppressed toxicity. Similarly, low-copy (pSC101) expression of the ftsQAZ operon alone suppressed kil-induced toxicity, but less efficiently ( Figure 1E). Analysis of the kil-expressing strain containing pSC101 with ftsQZ, ftsQA, or ftsZ alone confirmed that this suppression derives specifically from ftsZ (but not ftsQA) overexpression. Further supporting the link between the toxicity of kil expression and cell division, an independent multi-copy suppressor screen identified sdiA ( Figure 1E), whose product increases ftsQAZ operon transcription [35].

Kil inhibits FtsZ ring formation
Filamentation of E. coli cells could arise either from a failure to form FtsZ rings at the nascent division site, or from a defect in divisome maturation and septal synthesis after FtsZ ring assembly. Over-expression of ftsZ could conceivably help suppress either of these mechanisms to permit Kil-resistance. We therefore

Author Summary
Bacterial antibiotic resistance is a serious concern, particularly its role in hospital-acquired infection. Viruses that infect bacteria (bacteriophage) can kill their host, and some prevent the bacterial cell from reproducing during that process. Since their discovery, phage have been considered a potential tool against bacterial infection, but little is known regarding how phage-encoded factors may inhibit bacterial cell division. Understanding the interaction between phage factors and the targeted host systems is therefore a critical research goal. Our report focuses on E. coli and l, a well-studied phage that infects it. l contains a gene, kil, whose expression prevents E. coli from dividing, causing cells to grow into long filaments that die. Here we report that Kil protein prevents an essential bacterial protein, FtsZ, from properly assembling into the structure needed for cell division. Our data show that Kil can inhibit FtsZ assembly directly in vitro, but that ZipA, another essential cell division protein, enhances its activity on FtsZ in vivo. The results of our study elucidate one way that a phage naturally inhibits bacterial reproduction, which could serve as a target for rational antibiotic design. Figure 1. Induction of l kil interferes with E. coli cell division, but is suppressed by ftsZ overexpression. Strains: W3110 = wild type, CC4506 = kil + , CC4512 = kil 2 . (A) Location of kil in the l genome and the defective prophage used for this study. The l kil gene overlaps cIII and gam as part of the operon under P L control (top schematic). P L expression of kil in the defective prophage (CC4506) is under control of the temperaturesensitive cI857 repressor, allowing repression at 30uC (middle schematic) and expression at 42uC (bottom schematic). (B) Induction of kil causes cell filamentation. Differential interference contrast (DIC) microscopy of E. coli strains back-diluted from a mid-log 30uC culture to low optical density (OD 600 ,0.025) and grown to late-log in LB at 30uC (top panels) or 42uC (bottom panels). Scale bar = 5 mm. (C) Induction of kil leads to a loss in cell viability. Serial spot dilutions of cells grown in LB at 30uC (top panels) or 42uC for 90 minutes (bottom panels) and then plated onto LB agar incubated at 30uC (left panels) or 42uC (right panels) overnight. (D) Prolonged induction of kil leads to an irreversible loss of viability. Bacterial titers of CC4506, expressed as colony-forming units (cfu) per mL, after indicated time of kil induction. Time points with error bars represent the average and standard determined by immunofluorescence microscopy whether FtsZ rings continued to form in E. coli cells following derepression of kil under P L control.
At 30uC, when P L is repressed, both CC4506 (kil + ) and CC4512 (kil 2 ) cells were normal-sized on average (3.160.1 and 3.160.2 mm, respectively) compared to W3110 wild-type control cells (3.160.2 mm) (Figure 2A, top). Immunofluorescence microscopy (IFM) with antibody against E. coli FtsZ demonstrated that cells of each strain contained a single band of FtsZ signal localized at midcell in the majority (92.461.3% to 94.061.5%) of the populations, on average ( Figure 2B, top).
However, upon a shift to growth at 42uC and the resulting kil expression, CC4506 cells continued to grow at a normal rate into nondividing filaments (.10 mm), before reaching stationary phase (Figure 2A, bottom). In contrast, W3110 and CC4512 control strains still displayed normal average cell lengths at 42uC (3.360.55 and 3.260.48 mm, respectively). Kil induction also led to a rapid (,5 minutes) loss in FtsZ rings observable by IFM, leaving only a few cells with normal FtsZ localization on average (8.362.2%). FtsZ localization in W3110 cells was unaffected on average (92.161.7%) until 90 minutes post-temperature-shift when cells entered stationary phase and FtsZ ring frequency decreased sharply ( Figure 2B, bottom).
Notably, although CC4512 (kil 2 ) cells displayed normal cell lengths during growth at 42uC (Figure 2A, bottom), this strain background still showed a small, but significant, effect on FtsZ ring formation in the first minutes following temperature shift, with ring frequency dropping to an average of 73.064.6%. However, by 20 minutes, these cells had recovered normal FtsZ ring frequencies (92.760.07%), unlike the CC4506 kil + counterpart strain where FtsZ ring frequency remained below 10% ( Figure 2B, bottom). This suggests that some other factor in CC4512 has a minor and transient effect on FtsZ assembly upon shift to high temperature.
IFM micrographs corresponding to the data in Figure 2A & B showed normal medial FtsZ localization in both W3110 and CC4512 kil 2 strains after five minutes post temperature shift to 42uC ( Figure 2C) and all time points observed thereafter (data not shown). CC4506 kil + cells showed normal FtsZ localization at 30uC, but FtsZ immunostaining became patchy and diffuse after only five minutes of kil induction at 42uC. This mislocalization continued throughout growth at 42uC, sometimes forming into broad, unproductive FtsZ foci (possibly helices) along the cell filament ( Figure 2C). This pattern, typical upon FtsZ ring formation inhibition in vivo, suggests that FtsZ is unable to form a coherent ring-shaped structure in the presence of Kil, thus preventing septum formation and cell division.
Due to the observed kil-independent, transient effect on FtsZ ring formation ( Figure 2B, bottom), we chose to study the effects of kil outside of any phage context by expressing the gene from a plasmid. This enabled us to be certain that any observed effects were caused by Kil alone, and eliminated the need to expose E. coli cells to temperature shock. We cloned the kil gene downstream of the arabinose-inducible promoter in pBAD33 and transformed the resulting plasmid (pDH104) into W3110. W3110 pDH104 cells grown in non-inducing conditions divided normally, comparable to the W3110 background containing empty vector, indicating that uninduced levels of Kil are low. Consistent with the prophage results, expression of kil from the plasmid proved sufficient to induce cell filamentation through a rapid loss of FtsZ ring formation ( Figure 2D). Similar results were also obtained by cloning kil under P lac (IPTG-inducible) control in pRR48 (data not shown).
Kil does not alter FtsZ levels or act through wellcharacterized endogenous systems of FtsZ assembly inhibition Proper FtsZ assembly and subsequent cell division in E. coli is dependent on levels of FtsZ relative to other division components [36]. Though alterations in FtsZ levels are not a normal part of division regulation in E. coli [37], conditions that artificially elevate or reduce available FtsZ result in FtsZ mislocalization and cell filamentation [38]. A trivial explanation for the loss of FtsZ ring formation upon the induction of l kil is that its product, the presumed Kil peptide (see below), somehow alters FtsZ protein levels. A known example of this occurs with the cryptic prophagederived dicF, which encodes a small RNA that blocks ftsZ mRNA translation by an antisense mechanism [31]. However, quantitative immunoblotting of FtsZ in CC4506 cells induced for kil expression showed levels of FtsZ approximately equivalent to those in uninduced CC4506 counterparts or in W3110 and CC4512 controls ( Figure 3A). Furthermore, induction of kil from pBAD33 or pRR48 in W3110 similarly had no effect on FtsZ compared to levels seen in uninduced cells or cells with empty plasmid (data not shown). These results suggest that the kil product does not act by altering FtsZ levels.
To investigate a possible contribution of the SOS-inducible protein, SulA, in Kil activity, we examined the effects of kil induction from pBAD33 in a WM1074 DsulA::kan background. WM1074 is a wild-type derivative of MG1655, whereas the characterizations of Kil presented above utilized the K12 derivative W3110. Expression of kil from pBAD33 in WM1074 caused filamentation and inhibition of FtsZ ring formation ( Figure 3B) comparable to that seen in W3110 ( Figure 2D). Addition of 0.2% arabinose to sulA 2 cells resulted in cell filamentation ( Figure 3C) indistinguishable from that seen for the sulA + background, verifying that Kil does not act through SulA and that it confers a similar phenotype in a different strain background.
As with the DsulA::kan background, induction of kil from pBAD33 in DminCDE::kan or DslmA::kan backgrounds also increased cell filamentation ( Figure 3C), arguing that neither MinC nor SlmA are involved in Kil activity. As shown previously, minCDE mutant cells already have division defects due to the presence of extra FtsZ rings, and are elongated. Upon kil induction all FtsZ rings disappear into irregular patchy localization, and the already-long minCDE mutant cells grow into even longer filaments. Together these data demonstrate that unlike dicF or DicB, the kil deviation between three replicate experiments. (E) Over-expression of the E. coli cell division gene ftsZ suppresses the loss of cell viability caused by kil induction. Plating efficiencies expressed as survivor ratios (cfu/mL surviving at 42uC divided by total cells) for CC4506 with indicated plasmids containing different combinations of the genes in the ftsQAZ operon. Error bars represent the standard deviation between three replicate experiments. doi:10.1371/journal.pgen.1004217.g001 Figure 2. Induction of l kil rapidly blocks FtsZ ring formation. (A) Induction of kil causes cell filamentation. Average cell lengths (mm) at various time points (min) following temperature shift to 42uC (bottom panel) or continued incubation (control) at 30uC (top panel), measured from IFM micrographs. Error bars represent standard deviation between average length measurements from three separate images. (B & C) Midcell FtsZ ring localization is rapidly lost upon kil induction. (B) FtsZ ring frequency (%) at various time points (min) following temperature shift to 42uC (bottom panel) or continued incubation (control) at 30uC (top panel), counted from IFM micrographs. Error bars represent standard deviation between FtsZ ring frequency counts from three separate images. Cell length and ring frequency measurements at each point were obtained using a minimum number of 100 cells. (C) Representative IFM micrographs of indicated strains at indicated times and temperature from images used for measurements/counts in (A) & (B). Cell wall signal is from rhodamine-conjugated wheat-germ agglutinin, FtsZ signal is from AlexaFluor 488conjugated, goat a-rabbit recognition of rabbit a-FtsZ, and DNA signal is from 49,6-diamidino-2-phenylindole (DAPI). Scale bar = 5 mm. (D) Induction of kil from pBAD33 in W3110 (lacking l phage) blocks FtsZ ring formation and leads to cell filamentation. Shown are representative IFM micrographs of W3110 cells containing indicated plasmid under indicated induction conditions. Signals and scale bar are as in (C). doi:10.1371/journal.pgen.1004217.g002 product does not act through any of the well-characterized endogenous host systems that regulate FtsZ assembly.

Isolation and characterization of ftsZ alleles resistant to kil expression
The preceding results suggest that Kil inhibits FtsZ ring formation, potentially through direct interaction with FtsZ. To further investigate this interaction, we generated ftsZ mutant alleles by recombineering with randomly mutagenized ftsZ PCR fragments, selecting for those that allowed survival at 42uC in a thermo-inducible kil + and thermo-sensitive ftsZ (ftsZ84) strain (see Materials and Methods). This strategy identified two mutant alleles of ftsZ with increased resistance to kil expression, ftsZ V208A and ftsZ L169R ( Figure 4A). According to a recently reported Mycobacterium tuberculosis FtsZ crystal structure [45], both of these residues are located in the subunit interface of FtsZ protofilaments. Specifically, FtsZ V208 lies in the conserved T7-loop region, which during polymerization inserts into the nucleotide-binding region near the FtsZ L169 residue in the N-terminal domain of an adjacent subunit ( Figure 4B).
To verify that these alleles confer Kil resistance, we replaced the wild-type ftsZ gene of a fresh kil + strain with each mutant allele. Spot dilutions of the resulting strains verified that the ftsZ V208A or ftsZ L169R alleles conferred resistance to Kil compared to the wildtype ftsZ allele control, although the appearance of the spots suggests that the strains acquired suppressors fairly readily at 42uC ( Figure 4C).
IFM on the kil + strains harboring ftsZ V208A or ftsZ L169R in place of the native wild type allele showed normal-sized cells with FtsZ rings present at 30uC when kil expression is repressed ( Figure 4D). However, in addition to normal medial ring localization, FtsZ V208A appeared to also form frequent rings or puncta at cell poles (marked by arrowheads) and occasional ring doublets (marked by an asterisk). Similarly, FtsZ L169R sometimes formed aberrant FtsZ structures (marked by asterisks), along the long axis of the cell. These observations suggest that although these FtsZ mutants are competent for assembly and cell division, they seem to be overly stable and insensitive to endogenous regulators of FtsZ assembly.
Unlike in the wild-type ftsZ allele background, short-term exposure to kil expression at 42uC did not cause cell filamentation in ftsZ V208A or ftsZ L169R backgrounds ( Figure 4D), consistent with their partial resistance to Kil as seen in spot dilutions ( Figure 4C). The apparent insensitivity of the mutant FtsZ V208A and FtsZ L169R proteins to endogenous regulation seen at 30uC is even more obvious at 42uC upon P L operon derepression. For example, FtsZ V208A localizes predominantly to one cell pole at higher temperature (only ,14% midcell localization after 40 min of kil induction). FtsZ L169R , in contrast, forms multiple rings throughout the length of cells at higher temperatures, likely contributing to their slightly longer cell lengths. These cells also contain apparent inclusions visible by DIC microscopy ( Figure 4D), which may be from high levels of non-interactive Kil. Importantly, the inclusion bodies and mutant FtsZ localization abnormalities did not arise from inappropriate FtsZ levels in the cell, as both mutant FtsZs were present at levels comparable to the wild-type control ( Figure 4E).
The above spot dilution and IFM data demonstrate that the isolated ftsZ V208A and ftsZ L169R mutant alleles confer partial resistance to kil as expressed from P L upon de-repression at 42uC, permitting FtsZ assembly, albeit aberrant, and preventing cell filamentation. To further address the Kil-resistance of these mutant ftsZ alleles and avoid the mutant FtsZ mislocalization seen at higher temperatures, the above strains were transformed with pRR48-kil and investigated by expressing kil by IPTG induction at 30uC.
In contrast to the resistance of the ftsZ mutant alleles to kil expressed at 42uC from P L , they were unable to confer resistance to short-term induction of kil from plasmid pRR48 (1 mM IPTG). Rings formed by FtsZ WT , FtsZ V208A , or FtsZ L169R were all rapidly lost upon pRR48-kil induction ( Figure 4F, top and center panels), leading to cell filamentation ( Figure 4F, bottom panels). It is possible that the levels of Kil obtained from plasmid expression were higher than those obtained from its native P L context, but we noticed that longer inductions of kil from P L also ultimately overcame the initial resistance of FtsZ V208A or FtsZ L169R (data not shown). These results suggest that although these ftsZ alleles confer partial resistance to Kil from their abnormal assembly characteristics, Kil is still able to overcome these mutant FtsZ proteins under some conditions.

FtsZ alleles resistant to inhibition by Kil are also resistant to inhibition by MinC or SulA
The abnormal localization of FtsZ V208 and FtsZ L169R , such as to cell poles, suggested that these mutants may have increased filament stability and a certain general resistance to endogenous FtsZ assembly inhibitors, not just the action of l Kil. Additionally, WM1074 cells transduced from ftsZ WT to ftsZ V208A or ftsZ L169R had a minicell-producing phenotype (data not shown), further implicating resistance to FtsZ assembly inhibition by MinC.
To determine whether the ftsZ V208A and ftsZ L169R alleles make the strains generally resistant to FtsZ assembly inhibitors, we monitored resistance to over-expression of sulA or to a his-minCD translational fusion (minCD). We transformed the kil + (under chromosomal P L control) strains harboring ftsZ V208A or ftsZ L169R with either pDSW210-his-minCD or pBAD33-sulA and grew them at 30uC, where kil is not expressed whether or not the plasmids are induced. Induction of either minCD or sulA caused FtsZ WT cell filamentation and a loss of FtsZ ring formation after 40 min. However, in the presence of FtsZ V208 or FtsZ L169R , high levels of SulA or MinCD had no apparent effect on cell length in the same time frame ( Figure 5A & B). Consistent with prior results, FtsZ V208 and FtsZ L169R localized normally at 30uC in non-inducing conditions for either plasmid. Similar to observations for the FtsZ mutants upon kil expression at 42uC ( Figure 4C), induction of sulA, and particularly minCD, at 30uC caused both FtsZ V208 and FtsZ L169R to mislocalize, often at cell poles ( Figure 5A & B). This suggests that, in contrast to FtsZ WT , both FtsZ mutants are able to assemble in the presence of high SulA or MinCD levels, but that this assembly is abnormal and persists at new cell poles following division, similar to what was seen for these FtsZ mutant proteins in the presence of Kil.
The continued growth and division of ftsZ V208A or ftsZ L169R mutant cells upon short-term induction of either minCD or sulA suggests that these cells remain more viable than wild-type cells, despite many mislocalized FtsZ rings. Spot dilutions of ftsZ WT , ftsZ V208A , or ftsZ L169R cells carrying pDSW210-his-minCD or pBAD33-sulA onto plates with relevant inducers at 30uC (to ensure no kil expression) verified that both ftsZ V208A and ftsZ L169R increased cell viability upon sulA over-expression ( Figure 5C). Although minCD over-expression blocked wild-type FtsZ ring formation and led to cell filamentation ( Figure 5A), these cells remained partially viable in spot dilutions upon full induction with IPTG (1 mM). However, ftsZ V208A and ftsZ L169R conferred an approximately 10-fold improvement in that viability ( Figure 5C). As expected, cell growth was normal in the absence of inducer (data not shown). As with kil resistance (Figure 4D), the ftsZ V208A The ftsZ V208A and ftsZ L169R mutants are Kil-resistant alleles. Shown are cfu at 32uC and 42uC and resulting survivor frequencies (cfu/mL at 42uC divided by cfu/mL at 32uC) for kil-expressing strains with ftsZ WT , ftsZ V208A , or ftsZ L169R . (B) Location of L170 and V209 in the crystal structure of Pseudomonas aeruginosa FtsZ [92], corresponding to L169 and V208 of E. coli FtsZ, generated by allele showed somewhat stronger resistance to minCD and sulA over-expression compared to the ftsZ L169R allele ( Figure 5C).
Previously characterized ftsZ mutant alleles, ftsZ9 (ftsZ 18VV-G -a two residue insertion) and ftsZ114 (ftsZ F268C ), show general resistance to both MinC and SulA [46,47,48]. We therefore tested whether these alleles were also resistant to l kil expression. For these experiments we utilized the original PB143 ftsZ 2 background strains that contain ftsZ WT , ftsZ9, or ftsZ114 on a low-copy number plasmid under constitutive expression (pBEF0, pBEF9, and pBEF114) and transformed each with pBAD33-kil. FtsZ WT and FtsZ114, which displays ,50% GTPase activity of the wild-type FtsZ, were unable to resist inhibition by Kil and failed to form detectable FtsZ rings in the presence of Kil. However, FtsZ9, which is nearly devoid of GTPase activity (10% of normal) more strongly resisted Kil inhibition and was able to form some detectable FtsZ rings ( Figure 5D). This result in the presence of Kil is comparable to the partial, weak resistance of FtsZ114 (and the relatively strong resistance of FtsZ9) to inhibition by SulA or MinC [46,47,48]. The ability of these strains to form colonies with or without kil induction correlates well with their Kil resistance by IFM ( Figure 5E).

Kil activity requires ZipA in vivo
The ftsA R286W (ftsA*) gain of function mutation can bypass the loss of several normally essential cell division proteins, including ZipA or FtsK, as well as partially suppress an ftsQ ts mutant [49,50,51,52]. This ability to stabilize the divisome prompted us to ask whether ftsA R286W cells might be more resistant to Kil. However, we found that ftsA R286W conferred no resistance to Kil produced from pRR48, as cells formed extensive filaments (data not shown). As a control, we also tested a ftsA R286W DzipA::aph double mutant for resistance to Kil, expecting similar results. Strikingly, these double mutant cells were entirely resistant to kil expression from pRR48, manifesting neither filamentation nor a loss of FtsZ ring localization following induction ( Figure 6A). This strain background was also resistant to induction of kil from pBAD33 (data not shown). These results suggested that the absence of zipA, not the presence of ftsA R286W , imparts resistance to Kil. Note that zipA + ftsA R286W cells are slightly shorter, while DzipA ftsA R286W cells are slightly longer than their wild-type counterparts [49].
To verify that the observed kil-resistance is specifically caused by an absence of zipA, we added the gene back in trans by introducing the compatible plasmid pKG110-zipA into the DzipA ftsA R286W strain containing pRR48-kil. Uninduced levels of zipA expressed from pKG110 in these cells did not perturb cell division on their own but were sufficient to restore kil-sensitivity ( Figure 6B). Cells with the empty vector or expressing another early division protein, zapA [53,54,55], did not restore Kil-sensitivity in this DzipA ftsA R286W strain ( Figure 6B). Unlike the isolated Kil-resistant ftsZ alleles, DzipA ftsA R286W cells remained sensitive to both SulA and MinC inhibition ( Figure 6C), arguing that the Kil resistance of the DzipA ftsA R286W strain is not a general effect on FtsZ. Taken together, these results strongly suggest that ZipA is specifically required for the effect of Kil on FtsZ assembly and subsequently cell division.

Additional Kil-resistant isolates map to zipA
If ZipA were required for Kil-mediated inhibition of FtsZ as inferred from the above genetic experiments, we reasoned that it should be possible to isolate mutations in the essential zipA gene that confer Kil-resistance in a wild-type ftsA background without abrogating ZipA's normal function in the divisome. The powerful phenotype of Kil-induced cell filamentation and death allowed us to isolate spontaneous Kil-resistant mutants. To discourage the isolation of mutations that simply reduce kil expression or inactivate the kil product itself, we constructed a 'double kil' strain harboring both pBAD33-kil and pRR48-kil in WM1074. We isolated spontaneous Kil-resistant colonies by plating cultures of this strain on LB agar with both IPTG and arabinose ( Figure 7A). Several independent isolates were saved and their zipA loci amplified for DNA sequencing.
All isolated kil resistant strains contained one of two mutations in zipA, encoding ZipA L286Q and ZipA L286R , respectively. The Cterminal domain of ZipA containing this residue (ZipA C ) directly interacts with the C terminus of FtsZ [56,57,58] ( Figure 7B). As both alleles seemed to have similar properties, we chose ZipA L286Q for further investigation.
To assess the general activity of ZipA L286Q in cell division, we first cloned it into pKG110 and transformed the resulting plasmid into a WM1074 wild-type background. We then introduced the DzipA::aph allele by P1 transduction. The transduction efficiencies into cells harboring pKG110-zipA L286Q or pKG110-zipA WT were similar, verifying that ZipA L286Q functions normally in cell division in place of the essential ZipA WT . Low-level induction of either zipA WT or zipA L286Q from pKG110 (with 0.5 mM sodium salicylate) in the WM1074 DzipA::aph background resulted in cellular levels of ZipA comparable to those in wild-type cells ( Figure 7C) and caused no discernable differences in growth or division phenotypes. Additionally, overproduction of ZipA WT [59] or ZipA L286Q caused cell filamentation with multiple FtsZ rings present (data not shown).
To verify the Kil-resistance of zipA L286Q , we replaced the zipA WT gene of the W3110 strain harboring kil under P L control with zipA L286Q (or zipA L286R ) by recombineering. The resulting strains displayed normal cell division phenotypes and resistance to kil upon derepression of promoter at 42uC ( Figure 7D and data not shown). Finally, a fresh WM1074 wild-type background transduced with zipA L286Q linked to a ptsH,.tet marker was resistant to kil expression from pRR48, but remained sensitive to both SulA Chimera (http://www.cgl.ucsf.edu/chimera/). a-helices are red and b-sheets are purple. The L170 sidechain, adjacent to the GTP-binding pocket, is indicated in green and the V209 sidechain, within the T7 loop, is indicated in blue. (C) Placement of isolated ftsZ alleles in a fresh background confers resistance to kil expression. Spot dilutions of indicated ftsZ alleles in a CC4506 background strain under conditions where kil is not expressed (30uC, left) and expressed (42uC, right). (D) Expression of kil in strains harboring ftsZ V208A or ftsZ L169R does not result in cell filamentation and permits FtsZ ring formation, although mutant FtsZ ring localization is not completely normal upon kil expression at 42uC. Representative DIC (top) or a-FtsZ (top & bottom) micrographs of fixed cells are shown with indicated ftsZ alleles in the CC4506 background at 30uC (left) and after 40 minutes of kil expression at 42uC (right). a-FtsZ signal is as described in Figure 2. Scale bar = 5 mm. For ftsz V208A cells, arrowheads mark rings or puncta at cell poles and asterisks mark ring doublets. For ftsZ L169R cells, asterisks mark aberrant FtsZ structures. (E) FtsZ V208A and FtsZ L169R are synthesized at comparable levels to FtsZ WT . Shown are immunoblots against FtsZ (upper panels) from whole cell extracts of indicated strains harvested after 40 minutes of growth at 30uC (left panels) or 42uC (right panels). Relative levels of total protein are shown as a cropped segment of Coomassie-stained lanes (bottom panels). and MinCD inhibition ( Figure 7E), demonstrating that this zipA allele is specific for resistance to Kil. Finally, random mutagenesis of zipA by PCR generated a mutation in a nearby residue, Q290R,  The kil gene encodes a protein that interacts with ZipA and FtsZ Early research on the kil gene identified a putative and abundantly produced protein product [60]. However, subsequent research established that this protein was actually l Ea10, and that kil is likely expressed at only low levels from the P L promoter of l phage ( [2] and see below). Initial attempts to identify, purify, or chemically synthesize the protein product of the kil gene failed, prompting us to investigate whether the kil gene truly encodes a protein. Previous work established that insertion of a stop codon within the 59 portion of kil or disruption of its stop codon abolishes Kil activity ([6] and Figure 1), but did not definitely show whether the loss of activity was caused by changes at the protein level or the nucleotide alterations themselves.
To test this definitively, we inserted an amber stop mutation into the thirty-first codon (normally encoding tyrosine) of kil (kil tyr31UAG ) to terminate translation prematurely. Cells harboring the kil tyr31UAG allele under P L control survived at 42uC. To determine if cell survival was due to interrupted translation or due to a mutation in the RNA, we introduced the supF gene, which encodes a suppressor tRNA that would supply the originally encoded tyrosine amino acid at the amber mutation. The presence of supF restored Kil activity, confirming the product of kil functions as a protein ( Figure 8A).
To obtain purified Kil protein, we cloned the kil gene into a pET vector, adding an N-terminally encoded FLAG-tag to create a his 6 -flag-kil fusion for expression and protein purification by cobalt-affinity chromatography. Purification of His 6 -FLAG-Kil yielded a single prominent band on Coomassie-stained SDS polyacrylamide gels that migrates near its predicted ,10.5 kDa molecular weight with an estimated purity of .95% ( Figure 8B). Induction of his 6 -flag-kil in BL21(DE3) cells inhibited cell division, indicating that the tagged fusion is active (data not shown). We found that optimal induction occurred in the absence of zipA and in the presence of extra FtsZ; we therefore preferentially expressed his 6 -flag-kil in a BL21(DE3) ftsA R286W DzipA::aph pBS58 background.
Surprisingly, his 6 -flag-kil expression seemed to augment Kil activity in vivo, blocking cell division even in the absence of zipA (data not shown). Notably, this phenotype occurs with all tested Kil fusion derivatives, and no instances of complete suppression of any fusions have been isolated to date. With no antibody against Kil, we cannot know if this effect is merely because Kil fusions permit higher protein levels compared to wild-type untagged Kil, or if this effect arises from the increased length/size of a tagged Kil fusion.
Nonetheless, because ZipA is required for the activity of normal, untagged Kil on FtsZ assembly in vivo, we investigated whether Kil interacts directly with ZipA or FtsZ. We incubated purified, renatured His 6 -FLAG-Kil (see Materials and Methods) in the presence of a-FLAG M2 affinity resin with or without purified FtsZ and/or purified, His-tagged ZipA C-terminal domains (denoted ZipA C for wild type zipA and ZipA* C for zipA L286Q ). Following binding of the resin by His 6 -FLAG-Kil, samples were washed extensively and retained proteins bound to the resin and/ or His 6 -FLAG-Kil were visualized on Coomassie-stained SDSpolyacrylamide gels ( Figure 8C). As expected, His 6 -FLAG-Kil remained bound to the resin following the washes, whereas FtsZ, ZipA C , or ZipA* C were not resin-associated when incubated on their own without any His 6 -FLAG-Kil. However, FtsZ and each ZipA C remained in samples following washes in the presence of His 6 -FLAG-Kil, arguing in favor of direct specific interactions between His 6 -FLAG-Kil and FtsZ, and between His 6 -FLAG-Kil and either ZipA C . In support of this, bovine serum albumin added to all the input mixtures at concentrations similar to those of FtsZ and ZipAc showed no specificity for the resin. Notably, His 6 -FLAG-Kil -ZipA C interacts similarly with wild-type ZipA C and the mutant ZipA* C , and the His 6 -FLAG-Kil -FtsZ interaction does not seem to be significantly augmented by either ZipA C under the conditions of this experiment. Together these data suggest that Kil is capable of interacting independently with either FtsZ or the C-terminal domain of ZipA, and the L286Q mutation in ZipA does not prevent it from interacting with His 6 -FLAG-Kil.

Purified Kil inhibits FtsZ bundling in vitro
Our in vivo evidence suggests that Kil inhibits FtsZ assembly, and that this activity normally requires the presence of ZipA. To test whether Kil could directly act to inhibit FtsZ assembly, we used sedimentation assays with purified FtsZ and His 6 -FLAG-Kil purified from the BL21(DE3) ftsA R286W DzipA::aph pBS58 background to ensure that little ZipA would be present in reactions. Not surprisingly, purified FtsZ does contain a small amount of copurified ZipA (data not shown), barely detectable by immunoblotting and not visible at the FtsZ concentrations used for sedimentation reactions.
We initiated FtsZ assembly with the addition of 1 mM GTP and then sedimented polymer bundles of FtsZ by centrifugation. Sedimentation primarily detects polymer bundles of FtsZ, and in our buffer conditions; little FtsZ sedimented in the presence of GTP alone, consistent with the relatively poor bundling capability  of E. coli FtsZ [61]. Addition of calcium increased FtsZ polymer bundling and thus sedimentation, as previously reported [62,63]. Strikingly, addition of His 6 -FLAG-Kil to FtsZ assembly reactions greatly reduced the amount of polymer sedimentation in the presence of calcium ( Figure 8D), suggesting that the purified tagged Kil can directly inhibit FtsZ assembly in vitro.
To address the potential contribution of ZipA to Kil activity on FtsZ, we added purified ZipA C or ZipA* C to additional sedimentation reactions. As previously reported [56], ZipA C increased polymer bundling, measured as sedimentation, similar to the effect of calcium. ZipA* C also enhanced FtsZ sedimentation to similar levels. As with calcium, addition of His 6 -FLAG-Kil to the assembly reactions greatly reduced polymer sedimentation in the presence of either ZipA C or ZipA* C ( Figure 8E). His 6 -FLAG-Kil co-sedimented with the small fraction of FtsZ polymer bundles that assembled in its presence, either with calcium ( Figure 8D) or the ZipA C domains, but did not sediment on its own ( Figure 8E). This suggests that Kil may multimerize in the presence of FtsZ and/or form stable Kil-FtsZ complexes. Together, these data demonstrate that His 6 -FLAG-Kil interacts with FtsZ and inhibits its assembly in vitro, and suggest that the normal importance of ZipA in vivo for this activity is bypassed by the in vitro conditions.
To test the effect of Kil on FtsZ GTP hydrolysis rates, we performed GTPase activity assays under conditions identical to the sedimentation assays. GTP hydrolysis by FtsZ is induced by monomer-monomer interactions within a newly formed protofilament. If Kil inhibits FtsZ assembly by sequestering monomers, similar to SulA, it should strongly inhibit FtsZ GTP hydrolysis activity. If instead Kil severs FtsZ protofilaments or decreases FtsZ polymer bundling, this would increase the pools of monomers available to make new protofilaments, which should increase GTP hydrolysis.
The background GTPase activity signal from His 6 -FLAG-Kil, ZipA C , or ZipA* C was negligible (,0.5 GTP/min/FtsZ), and FtsZ displayed a rate of ,3.2-4.1 GTP/min/FtsZ independent of bundling agent ( Figure 8F). The presence of Kil in assembly reactions caused a small but significant increase in FtsZ GTP hydrolysis to 4.3-5.3 GTP/min/FtsZ. The effect of Kil was most pronounced in the presence of calcium (a 1.4-fold increase) and least pronounced in the presence of ZipA* C ( Figure 8F). Though modest, the across-the-board increase in GTP hydrolysis in the presence of Kil is consistent with either inhibition of FtsZ protofilament extension, severing protofilaments, or inhibition of FtsZ protofilament bundling.

Kil-mediated inhibition of host cell division during phage infection
Our data inspire a model in which Kil interacts with FtsZ in a ZipA-dependent manner in vivo to inhibit FtsZ ring assembly and cause cell filamentation. The location of kil in the l genome ( Figure 1A) suggests that it would be expressed transiently during initial establishment of lysogeny and then upon exit of lysogeny when entering the lytic cycle. Normally, induction of a l lysogen leads to rapid host cell lysis, but the potential role and importance of kil in this process is unknown. We therefore chose to investigate kil in its native context in intact E. coli l lysogens, with the cI857 allele to facilitate universal l lysogen activation.
Induction of a l lysogen by a shift to 42uC led to an increase in cell length up to 40 minutes post-induction ( Figure 9A), at which time cells began to lyse. This increase in cell length is similar to that observed upon similar P L derepression in a defective prophage (Figure 2A), but does not proceed as rapidly or reach the point of extreme filamentation seen during kil expression. Induction of the l lysogen also led to a rapid loss of FtsZ rings ( Figure 9B).
The observed increase in cell length and rapid, complete loss of FtsZ ring assembly following induction of the l lysogen did not occur in an isogenic kil 2 mutant. Although kil 2 cells still entered the lytic cycle with no observable delay, cell length did not increase significantly in the absence of kil ( Figure 9A). Although FtsZ ring formation was partially inhibited under these conditions, perhaps by other l components or through indirect effects on host cell physiology, the majority of kil 2 cells still contained FtsZ rings sufficient to maintain division ( Figure 9B). These data indicate that kil expression has a dramatic effect on FtsZ ring formation, and subsequently on cell length, during the induction of a l lysogen into the lytic cycle.
Finally, to ask whether kil 2 phage are compromised for reproduction, we monitored a single cycle of phage growth of cI857 and a nonpolar deletion of kil, cI857kilD7, in MG1655 at 39uC ( Figure 9C). Overall phage yields were not significantly affected by the absence of kil, although we observed a reproducibly shorter lysis time for the cI857 kilD7 phage relative to kil. Kil effects on host cell lysis have been previously reported [7,64].

Discussion
The results reported here establish that the Kil protein of bacteriophage l blocks host cell division by rapidly ablating FtsZ rings. In reactions with FtsZ purified from ZipA-deficient cells, purified tagged Kil prevents sedimentation of FtsZ bundled either by calcium or purified ZipA C . In addition, purified tagged Kil interacts with FtsZ in the presence or absence of ZipA. Together, these results suggest that Kil can interact directly with FtsZ in vitro to disrupt FtsZ protofilament bundling. However, ZipA is required for wild-type Kil to disrupt FtsZ rings normally in vivo, and point mutations in either FtsZ or ZipA can effectively resist FtsZ ring disruption by Kil. Excess FtsZ can also protect against inhibition by Kil in vivo, presumably by enhancing protofilament assembly and/or titrating out the inhibitor.

A model for Kil-mediated inhibition of FtsZ ring assembly
The normal involvement of ZipA in vivo suggests that Kil may interact with both FtsZ and ZipA in the cell, a possibility supported by our in vitro interaction data. One explanation for the in vivo ZipA requirement is that ZipA may act specifically to recruit Kil to FtsZ protofilaments (Fig. 9D). The location of the mutations FtsZ, ZipA C , and ZipA* C in pull down assays. Various protein samples as indicated were incubated with a-FLAG resin and extensively washed, followed by SDS-PAGE and Coomassie staining. Proteins associated with His 6 -FLAG-Kil should be strongly enriched in the gels. Bovine serum albumin (BSA) was added to all input samples at the level shown and migrates immediately above the IgG heavy chain (IgG H.C.) in gels after pull downs (bottom strip). (D) Kil inhibits in vitro FtsZ assembly as assayed by sedimentation of calcium-bundled FtsZ polymer bundles. FtsZ and His 6 -FLAG-Kil bands are shown from Coomassie-stained gels of supernatant and pellet samples, following sedimentation of FtsZ assembly reactions in the presence of 1 mM GTP and other indicated components. (E) Kil inhibits FtsZ bundling by purified ZipA WT or ZipA L286Q C-terminal domains (ZipA C or ZipA* C ). Shown are FtsZ and His 6 -FLAG-Kil bands from Coomassie-stained gels of supernatant and pellet samples as in (D). (F) Kil slightly increases the GTPase activity of FtsZ. Rates of GTP hydrolysis are expressed as average GTP/min/FtsZ for the indicated combination of purified components in the presence of 1 mM GTP as in the sedimentation reactions in (D). Kil refers to His 6 -FLAG-Kil and ZipA or ZipA L286Q refer to His-tagged C-terminal domains. Error bars represent the range of values between two replicate experiments. doi:10.1371/journal.pgen.1004217.g008 in ZipA that confer resistance to Kil is consistent with this idea. Although these mutations are in the FtsZ-binding domain of ZipA, the mutated L286 residue is not predicted to interact directly with the C-terminus of FtsZ, facing away from it in the co-crystal structure [58]. The L286 mutations could have an allosteric effect on ZipA-FtsZ interactions, but cells carrying zipA L286Q divide normally, so these interactions cannot be grossly altered. Moreover, over-expression of zipA L286Q causes cell division defects similar to that seen with zipA WT (data not shown), further arguing that the mutant is not dysfunctional in its effects on FtsZ assembly. According to this model, ZipA L286Q would be less able to recruit Kil to midcell than ZipA WT , presumably because of decreased ZipA-Kil interactions. However, our in vitro interaction data suggest no difference between His 6 -FLAG-Kil interaction with ZipA C or ZipA* C . This disparity could stem from the additional length/size of the His 6 -FLAG-Kil fusion (that seems to act independently of ZipA in vivo unlike untagged Kil), or from the absence of full-length ZipA in the in vitro experiments. Additionally, results from the sedimentation experiment suggest that the high concentrations of Kil present in reactions might cause it to multimerize in the presence of FtsZ. Further work is required to clarify the precise mechanism of Kil activity and the role of ZipA in this activity.
The proposed ZipA-mediated recruitment of Kil to FtsZ in vivo is reminiscent of mechanisms proposed for other FtsZ inhibitors. For example, the cryptic prophage-derived DicB protein uses ZipA to recruit the DicB/MinC complex to the membraneassociated FtsZ ring [65]. However, unlike DicB, Kil inhibits FtsZ directly and does not require MinC for its inhibitory activity ( Figure 3). The B. subtilis EzrA protein is related to ZipA in that it binds FtsZ and shares ZipA's unusual topology of N-terminal integral membrane domain and C-terminal cytoplasmic domain. A mutant of EzrA lacking this N-terminal transmembrane domain is able to inhibit FtsZ assembly directly in vitro, but in vivo this mutant does not localize to the membrane, thus lowering the local concentration of EzrA to a point where its interaction with FtsZ is no longer inhibitory [66]. By analogy, ZipA might serve to concentrate Kil near the membrane where FtsZ is located, enhancing its inhibition of FtsZ assembly (a function no longer needed in vitro). Kil is predominantly hydrophobic, and although it is not predicted to contain any transmembrane segment, it is predicted to have peripheral membrane association [67]. If this is the case, interactions with ZipA could still enhance localization of Kil specifically to midcell and/or position Kil optimally to interfere with FtsZ assembly within the in vivo environment that is absent in our in vitro FtsZ assembly assays.
Normal FtsZ assembly dynamics ensure that FtsZ rings properly form both temporally and spatially to link cell division with other cell cycle events [12]. Kil acts independently of the wellcharacterized host-derived systems of regulation, but may act on FtsZ assembly in a generally similar fashion. In support of this notion, our two Kil-resistant ftsZ alleles, ftsZ V208A and ftsZ L169R , display a general resistance to multiple forms of FtsZ assembly inhibition, and ftsZ alleles previously reported for SulA and MinCresistance [46,47,48] also show similar degrees of resistance to Kil. Despite having lesions in the conserved T7-loop and near the nucleotide-binding region, these two mutant FtsZs are capable of FtsZ ring assembly in vivo, although many rings form at potential division sites other than midcell, including cell poles. This is consistent with a bias away from disassembly and towards stabilization. Such a bias would lead to resistance to disassembly factors such as MinC, even if Kil inhibits by a different mechanism. This resistance is incomplete, because Kil produced from a plasmid rapidly ablates FtsZ V208A and FtsZ L169R rings, and even Kil produced from the P L operon eventually overwhelms their ability to form rings and encourages acquisition of suppressors.
Recent publication of a crystal structure for a GDP-bound protofilament of FtsZ from Mycobacterium tuberculosis implicates residues adjacent to those corresponding to V208 and L169 of E. coli FtsZ as being involved in conformational changes at the subunit interface between straight, GTP-bound filament and curved, GDPbound filament forms [45]. The general resistance of the FtsZ V208A and FtsZ L169R mutants to disassembly factors suggests that they may favor the GTP-bound form and have reduced GTP hydrolysis. The properties of other inhibitor-resistant FtsZ mutants fit this idea. The FtsZ9 mutant has extremely low GTPase activity and is highly resistant to SulA, MinC or Kil. In contrast, the FtsZ114 mutant, which has ,50% of normal GTPase activity, confers only partial resistance to Kil or MinC [48]. The inhibitory activity of His 6 -FLAG-Kil on FtsZ filament bundling would be predicted to induce greater FtsZ subunit turnover and thus increase GTP hydrolysis, which is what we observe, and is similar to the effects of some other factors that inhibit FtsZ bundling such as EzrA [66,68]. Consistent with Kil blocking FtsZ bundling, FtsZ localization in the presence of Kil becomes patchy and diffuse, possibly into broad helices, suggesting that FtsZ filaments still assemble, but fail to condense into a mature, bundled ring. An alternative explanation for the increased GTPase activity is that Kil may also prevent FtsZ protofilament elongation, which would increase the pool of free FtsZ monomers available to form dimers and oligomeric filaments capable of hydrolyzing GTP.

Role of bacteriophage-encoded cell division inhibitors
A handful of other phage-encoded factors have been identified that block bacterial cell division, including a newly-described T7 gene product that also acts on FtsZ [69]. Other factors act through host-cell regulation of FtsZ assembly (DicB and dicF [28,29]) or through an unknown mechanism (Kil of prophage Rac [26]). The lytic SPO1 phage of Bacillus subtilis encodes a peptide that inhibits host division prior to lysis [70], but acts at a stage following FtsZ ring formation (Haeusser and Margolin, unpublished data). Therefore, it seems that a variety of phage are able to target host cell division through unique peptides that act by diverse mechanisms. Suppression of host cell division by cryptic prophage-encoded factors has previously been implicated in increasing host adaptation to stress and resistance to antibiotics [71], and it is possible that kil benefits the host in some way during the lysogenic state.
In contrast to inhibiting FtsZ ring formation, a recent report described the role of B. subtilis W29 p1 in promoting phage replication through association with assembled FtsZ [72]. This temperatures are listed. Cell wall and a-FtsZ signals are as described in Figure 2. Scale bar = 5 mm. (C) A one-step growth curve of kil + phage (solid circles) and kil 2 phage (open circles) showing plaque forming units (pfu) per mL over time in MG1655 at 39uC. (D) A model (with key to shapes on right) for Kil activity on FtsZ ring formation (top cartoons) is depicted for the indicated strain genotypes, and the resulting effects on cellular phenotype (lower cartoons). The top left cartoon illustrates the kil 2 condition alone, not all Kil-resistant conditions. The recruitment of Kil to midcell inhibits FtsZ assembly by completely blocking normal FtsZ ring assembly. FtsZ blobs and spirals seen by IFM suggest that FtsZ assembles aberrantly in the presence of Kil in vivo, unable to resolve into a closed ring structure. See discussion for the potential role of ZipA. Cell filamentation may increase lysis time in an un-compartmentalized host. doi:10.1371/journal.pgen.1004217.g009 strategy allows W29 to utilize an existing host cell scaffold to organize and optimize viral DNA production, but how a phage would benefit from perturbing FtsZ ring formation and inhibiting cell division is less clear. The original studies on kil 2 l phage suggested that they still replicate, assemble, and lyse the host comparably to kil + counterparts, with similar burst sizes [3,6,73]. However, these studies used cIII67 mutant phage, which may be more prone to lysogeny and mask a kil 2 growth phenotype. Here, we show that Kil activity is evident upon lytic induction of l, and demonstrate that, in a single cycle of growth, the kil 2 mutant phage has a shorter latent period and causes earlier cell lysis. Although we did not observe a decrease in yield for the kil mutant phage, in some circumstances a shorter latent period may result in lower phage yieldl. The larger average volume of kil + cells relative to kil 2 cells might translate into a longer time to induce lysis. Cell size changes may also affect the lysis-lysogeny decision [74].
ln addition to affecting the timing of lysis, kil could benefit phage by creating a non-compartmentalized host that permits easier and more accurate phage reproduction. In this scenario, activation of cell division and construction of a septum could interfere with excision of the l lysogen, its replication, or its packaging. Previous studies with kil from the lambdoid P22 phage of Salmonella found that kil expression was required for efficient lytic growth of abc 2 mutants lacking anti-RecBCD activity, increasing burst size by eight fold [75]. This suggests Kil activity becomes important during conditions of high recombination frequency. By analogy, B. subtilis Maf induces a temporary block in cell division during natural competence development that permits efficient, uninterrupted DNA recombination [76].
The lack of an obvious kil 2 phenotype for l phage in original studies [3] and the subtle defects reported here could arise from biased, unnatural laboratory growth conditions, or an overlapping function with other phage components, such as gam. The abrupt but temporary loss of FtsZ rings upon P L derepression in the absence of kil and the relatively large percentage of cells that lose FtsZ ring formation even in an otherwise complete kil 2 l lysogen suggest that Kil may not act completely independently. Future experiments will focus on clarifying the molecular mechanism of Kil-mediated FtsZ ring disruption and uncovering its role in l phage biology.

Strains and growth conditions
All E. coli strains used are listed in Table 1. Standard genetic methods including transformation and P1 vir transduction were used for strain construction. Recombineering methods for strain construction [77,78] are described in a section below.

DNA and protein manipulation and analysis
Standard protocols or manufacturers' instructions were used to isolate plasmid DNA, as well as for restriction endonuclease, DNA ligase, PCR, and other enzymatic treatments of plasmids and DNA fragments. Enzymes were purchased from New England BioLabs, Inc. (NEB) or Invitrogen. Plasmid DNA was prepared using the Wizard Plus SV Minipreps DNA Purification Kit, PCR and digest reactions were cleaned up using the Wizard SV Gel and PCR Clean-up System, and chromosomal DNA was prepared using the Wizard Genomic DNA Purification Kit (Promega). KAPA HiFi HotStart DNA polymerase (Kapa Biosystems) or Phusion High-Fidelity DNA polymerase (Thermo Scientific -NEB) or Platinum Taq (Invitrogen) were used for PCR reactions in a MyCycler Thermal Cycler (Bio-Rad). Oligonucleotides were purchased from Sigma-Aldrich or IDT and their sequences are listed in Table S1. The final versions of all cloning products were sequenced to verify their construction. DNA sequencing was performed by GeneWiz (South Plainfield, NJ), SeqWright (Houston, TX) or SAIC-Frederick, Inc. (Frederick, MD). DNA bands were visualized using an AlphaImager Mini System (ProteinSimple) and DNA concentrations were estimated with a NanoDrop ND-1000 Spectrophotometer (Thermo Scientific). Protein concentrations were determined using the Coomassie Plus Assay (Themo Scientific -Pierce). Molecular graphics and analyses were performed with the UCSF Chimera package (http://www.cgl.ucsf.edu/chimera). Chimera is developed by the Resource for Biocomputing, Visualization, and Informatics at the University of California, San Francisco (supported by NIGMS P41-GM103311).

Plasmid construction
All plasmids are listed in Table 2. Kil expression plasmids: For pRR48-kil, the kil coding sequence was amplified from CC4506 chromosomal DNA with primers DPH199 and 200; the PCR product was digested with PstI and SpeI, then ligated into a pRR48-derivative where the original multiple cloning site had been replaced (NdeI to SalI) with that of pKG110. For pDH104 (pBAD33-kil), the kil coding sequence with its native ribosome-binding site was amplified from CC4506 chromosomal DNA with primers DPH217 and 202; the PCR product was digested with XmaI and PstI, then ligated into pBAD33.
Plasmids for protein purifications: For pET28-zipA C the Cterminal ZipA domain coding sequence was amplified by Tushar Beuria with primers WM269 & 268; the PCR product was digested with BamHI and XhoI, then ligated into pET28a. As primer WM268 did not include a stop codon, this construct produces His 6 -ZipA C -His 6 . Construction of pDH146 Plasmid pDH149 (pET15-flag-kil) was constructed by digesting pDH139 with NcoI and XhoI, then ligating the his 6 -flag-kil insert into identically-digested pET15b.

General recombineering methods
Recombineering was done using published methods [77,78]. Briefly, the Red functions were expressed either from the defective prophage or from a recombineering plasmid such as pSIM18, a hygromycin resistant plasmid encoding the temperature-sensitive CI857 repressor and a portion of the P L operon containing gam, exo, and bet. Log phase cells propagated at 32uC were subjected to a 15 minute heat pulse in a 42uC shaking water bath to induce the Red functions, quickly chilled in an ice-water slurry, and prepared for electroporation by washing. DNA, either double-or singlestranded, was introduced into the cells by electroporation. When a drug marker was selected, the cells were allowed to recover for several hours in 1 mL broth before plating. When point mutations were introduced with ,70 base oligonucleotides, the cells were plated non-selectively on LB agar plates after a 30 minute recovery time, either at 42uC for direct selection of Kil-resistant alleles or at 32uC for screening by PCR, as described below. In some cases oligonucleotides with additional sequence changes in third positions (wobble positions) were used to create mutations. As described [83], these additional wobble changes were placed near the change of interest, creating a configuration of mispairs that is not recognized by the E. coli mismatch repair system, without changing the amino acid sequence. This allows both highefficiency recombineering and detection of recombinant chromosomes with PCR. When wobble changes were introduced, between 12-20 colonies were analyzed, using one oligonucleotide that hybridized specifically to the recombinant sequence, paired with a second nearby oligonucleotide; this primer pair should not yield product with the parental sequence. Positive candidates were purified to single colonies and about a dozen of these single colonies were again subjected to the same PCR analysis. The region of interest from positive candidates identified in the second round of PCR screening was sequenced. Sequences for oligonucleotides used are listed in Table S1.
Construction of a non-polar deletion of kil in l cI857 phage A seven-codon in-frame deletion within kil, removing codons 20-26, was initially constructed in XTL241 (HME6 gam,.cat-sacB) and then moved to a phage. The deletion was built into a hybrid oligonucleotide, LT793, which along with an oligonucleotide to the downstream gam gene, LT795, were used to amplify a PCR product containing the deletion and spanning the region containing the counter-selectable marker. Recombineering was used to replace the cat-sacB. After introduction of the PCR product into electrocompetent XTL241 induced for the Red functions, cultures were grown overnight and recombinants were selected on sucrose plates at 32uC. Candidate colonies were purified on sucrose and confirmed to be chloramphenicol-sensitive. Primers AW24 and LT795 were used to amplify the region containing the deletion, which was confirmed by sequencing. In contrast to the kil + control, cells containing the deletion did not filament after several hours of growth at 42uC, and formed colonies after overnight growth at 42uC. A lysate of l cI857red3 was grown on cells containing the seven-codon deletion to allow marker rescue from the defective prophage onto the phage. The lysate was plated on LT352. Plaques were picked into 0.5 mL TMG (10 mM Tris base, 10 mM MgS0 4 0.01% gelatin) and 2 ml of the pickate was used for PCR with oligonucleotides AW24 and LT795: the difference in size between the deletion and the wild-type alleles was resolvable on a 1.2% agarose gel. The deletion phage was purified by another round of plating on LT352 and a high titer plate lysate was grown from a purified plaque on C600.
Isolation of multicopy suppressors of kil CC4506 was transformed with a pBR322-based library containing 1.5-5 kb Sau3A fragments of LE392 genomic DNA cloned into pHDB3 [84] and transformants were selected on LB ampicillin agar at 42uC. Ampicillin-resistant colonies that survived Kil induction were pooled, plasmid DNA was isolated and CC4506 was transformed with this enriched plasmid population to confirm suppression. The Sau3A library was kindly provided by Nadim Magdalani (NIH). Plasmid pJP10 was isolated by this procedure. Plasmid pNB15 was isolated by a similar procedure except the pBR322-based library was constructed by cloning 2-4 Kb Sau3A fragments of JS549 genomic DNA into pBR322 cut with BamHI.

Isolation of Kil-resistant ftsZ alleles
The ftsZ gene was amplified from W3110 with oligonucleotides XMZ325 and XMZ326, using standard PCR conditions. This ftsZ PCR product was used as a template for mutagenic PCR [85] with the same oligonucleotides. This randomly mutagenized pool of ftsZ PCR fragments was used for recombineering into strain AW34, which carries the thermo-sensitive ftsZ84 allele (G105S) linked to leuD::Tn10, a defective l prophage with thermo-inducible kil expression, and a mutS,.amp allele to prevent host mismatch repair during recombination. After a 30 minute recovery in broth at 30uC, aliquots were plated on nitrocellulose filters on LB plates and incubated at 32uC for 3 hours. Filters were then transferred to 42uC pre-warmed LB plates and these plates were subsequently incubated overnight at 42uC to select for growth. This procedure simultaneously selects for recombinants that replace ftsZ84 with the wild type allele and for resistance to l Kil expression. A lysate of P1 vir was grown on a pool of the temperature-resistant isolates. This lysate was used to transduce the Kil-expressing strain AW41, selecting tetracycline resistance at 42uC. Thermo-resistant colonies were purified and their ftsZ gene was amplified with colony PCR; the resulting PCR products were sequenced. Several isolates of the ftsZ V208A mutation were obtained, and only one isolate of ftsZ L169R . One isolate of each of the mutant types was chosen for further characterization. The mutations were introduced into a fresh background by P1 transduction at 32uC, selecting for the linked leuD,.Tn10 and screening for temperature resistance.

Isolation of Kil-resistant zipA alleles
Competent WM1074 cells were sequentially transformed with pBAD33-kil and pRR48-kil and the resulting strain was verified to have a kil + phenotype upon induction of kil from either plasmid. A culture of this 'double kil' strain was grown to mid-logarithmic phase and induced with IPTG and arabinose simultaneously. 100 mL of stationary phase culture was plated on LB agar supplemented with appropriate antibiotics, IPTG, and arabinose and grown overnight at 37uC. All resulting colonies were purified, then grown in liquid media to freeze samples. Chromosome purification and PCR amplification of the zipA locus in the saved isolates showed that all contained a zipA L286Q mutation, while the original WM1074 pBAD33-kil pRR48-kil strain contained zipA WT sequence.
A second isolation of spontaneous Kil-resistant mutants was carried out using a similar protocol, with the only difference being that cells were grown in liquid culture under non-inducing conditions into stationary phase, then plated on medium containing IPTG and arabinose. All isolated colonies from this second experiment contained a zipA L286R mutation.
Using ssDNA recombination to isolate, map and confirm suppressor mutations Recombineering using ssDNA can be very efficient with up to 75% of the cells being recombinants [83]. Therefore, recombineering with ssDNA can be used to isolate and map mutations, and these techniques were used throughout this work. For example, when mutagenic PCR was used to isolate zipA mutations, in one case sequencing revealed a double mutation, zi-pA A245T,Q290R . We designed and ordered oligonucleotides to make each mutation separately via recombineering. Recombineeringproficient cells prepared on CC4506 were transformed with each oligonucleotide separately or both together, outgrown for 30 minutes, then diluted and spot-titered on LB plates at 30uC and 42uC. We found that only one of the oligonucleotides, MH82, was necessary and sufficient to create a mutation that suppressed Kil-dependent killing.

Spot titers
Cells used for spot titers were taken from the same cultures used for fixation unless as noted below. A ten-fold dilution of these cultures was taken approximately forty minutes after induction (or control conditions), unless otherwise noted, and then serially diluted into fresh LB media in a 96-well plate using a multichannel pipette. A flame-sterilized and cooled, metal-pronged tool was then used to replica-plate spots of serially diluted culture onto LB plates with added components and incubation conditions as indicated in the text and figures. Photos of plates were taken in a FluoroChem 8800 system with its accompanying camera and software (Alpha Innotech).
Spot titers in Figures 4C and 7D were done as follows: An overnight culture was diluted 100-fold and cells were grown at 30u for 2 hours in LB. Ten-fold serial dilutions of these cultures were made in TMG (see above) and 10 ml was spotted on pre-warmed LB plates and incubated at the indicated temperatures.

Determining loss of viability after exposure to Kil
To generate the data in Figure 1D, an overnight culture of CC4506 was diluted 70-fold into 15 mL of LB broth and grown to an OD 600 ,0.25 at 32u. The culture was diluted in 10-fold increments from 10 0 to 10 25 . At time ''0'', 0.1 mL samples of appropriate dilutions were spread on prewarmed 42u LB plates on which we had placed a sterile 82 mm (diameter) nitrocellulose filter. After the indicated time, sterile forceps were used to move the filter to a 32u plate. These LB plates were incubated overnight at 32u and colonies counted.

Cell fixation, microscopy, and analysis
Overnight cultures were started from 280uC strain stocks and grown under appropriate antibiotic selection and permissive conditions. Overnight cultures were diluted into fresh medium, grown to mid-logarithmic phase, then the OD 600 of individual cultures was adjusted to a uniform OD 600 = 0.025 with fresh medium. Cultures were grown for approximately 2 doublings at permissive conditions and then shifted to non-permissive conditions (or kept as permissive controls) at time point zero. Unless otherwise indicated, samples of culture for microscopy were taken approximately 40 minutes after shifting to non-permissive conditions.
Cells were fixed with methanol and processed for immunofluorescence microscopy (IFM) as previously published [86] using lysozyme (Sigma) treatment for 5 minutes and antibodies diluted in bovine serum albumin (Fisher Scientific). Primary polyclonal rabbit a-FtsZ [87] was used at 1/2500, secondary goat a-rabbit-AlexaFluor 488 (Molecular Probes) and wheat germ agglutinin conjugated to rhodamine (Molecular Probes), to visualize cell wall, were used at 1/200. For DNA staining, 49,6-diamidino-2phenylindole (DAPI) (Molecular Probes) was used at 0.5 mg/mL. Micrograph images were captured on an Olympus BX60 microsope with a Hamamatsu C8484 camera using HC Image software (Hamamatsu). Cell length and ring frequency measurements were taken with the ObjectJ extension [88] (http://simon. bio.uva.nl/objectj/) of ImageJ [89] (National Institutes of Health) using a minimum number of 100 cells and images were minimally adjusted for brightness/contrast using Adobe Photoshop CS4. Microsoft Excel 2008 for Mac (v. 12.3.6) was used for data tabulation and calculatio

Immunoblot analysis
Samples were prepared, subjected to SDS-PAGE on 20% acrylamide gels, and transferred as published [90]. Transfer of His 6 -FLAG-Kil samples was done in 10 mM CAPS pH 10.0, 10% methanol transfer buffer with a two-hour transfer time. Mouse monoclonal a-His primary antibody (Sigma-Aldrich) and affinitypurified rabbit polyclonal a-FtsZ [87] were used at 1/5000. Affinity-purified rabbit polyclonal a-ZipA [49] was used at 1/ 1000. Goat a-mouse and a-rabbit secondary antibodies conjugated to horseradish peroxidase (HRP) (Sigma-Aldrich) were used at 1/10,000. A SuperSignal West Pico Chemiluminescent Substrate Kit (Thermo Scientific -Pierce) was used for HRP detection; blots were exposed to film and developed using a Konica SRX101A Film Processor (Konica Minolta).

Protein purification
Proteins were induced for purification from pET vectors (Novagen -EMD Millipore) in BL21(DE3) [91] backgrounds as 2 L cultures that were grown to OD 600 ,0.7 at 30uC, at which point 1 mM IPTG was added. (Volumes in this and subsequent steps were scaled down by a factor of 10 for copurification assays). Cultures were left overnight at 30uC to induce protein and were harvested in the morning by spinning in a Beckman J2-21 centrifuge with a JA-17 rotor at 7,000 rpm. Cell pellets were then washed in buffer (50 mM sodium phosphate pH 8.0; 300 mM NaCl), re-centrifuged, and stored as cell pellets at 280uC.
For purifications, cell pellets were thawed on ice, resuspended in 30 mL of the sodium phosphate wash buffer (except for His-tagged Kil, see below) with 1 mg/mL lysozyme and an EDTA-Free c0mplete Protease Inhibitor Cocktail Tablet (Roche), and incubated on ice for 30 minutes. Cells were disrupted by sonication on ice (Branson Sonifier 250; 50% level, output 4) in a series of six alternating 30-second periods of sonication and 30-second rest periods. Cell lysates were clarified of debris by spinning at 40,000 rpm at 4uC for 45 minutes in an 80 Ti rotor with an Optima XL-100K Ultracentrifuge (Beckman).
His-tagged ZipA C proteins were purified by gravity flow over water-washed and buffer-equilibrated cobalt-conjugated resin with a 5 mL bed volume at 4uC. Imidazole at pH 8.0 was added to 10 mM in cell lysates for loading onto the column. Following loading, columns were washed successively in ten-column volumes of purification buffer (50 mM HEPES pH 7.5; 300 mM NaCl) with 10 mM, 25 mM, and 50 mM imidazole. His-tagged ZipA C s were eluted in 10 mL purification buffer+250 mM imidazole. Eluted proteins were concentrated and subjected to buffer exchange into polymerization buffer using Amicon Ultra-10K Centrifugal Filter Devices (Millipore), flash-frozen in liquid nitrogen, and stored at 280uC.
His 6 -FLAG-Kil was primarily induced in, and purified from, BL21(DE3) ftsA R286W DzipA::aph pBS58 cells. The exception was for copurification experiments, where the fusion was also prepared from zipA WT + or zipA L286Q + backgrounds, as noted. Following induction, His 6 -FLAG-Kil was found to be predominantly associated in insoluble inclusion bodies, leading to very low yields under native conditions, even in an ftsA R286W DzipA::aph background. We therefore purified His 6 -FLAG-Kil under denaturing conditions according to the QIAexpressionist Handbook (QIAGEN, 2003) protocol, followed by renaturation by dialysis. Purity was estimated at .95% by Coomassie staining.
Lysates from His 6 -FLAG-Kil-expressing cells were prepared similarly as described above, except cell pellets were resuspended in denaturing lysis buffer (100 mM sodium phosphate, pH 8.0, 10 mM Tris-Cl, 6M guanidine hydrochloride) with an EDTA-Free c0mplete Protease Inhibitor Cocktail Tablet (Roche), but without lysozyme. After incubation for 30 minutes at room temperature, cells were sonicated as described above.
These His 6 -FLAG-Kil-containing lysates were then loaded by gravity flow onto water-washed and denaturation lysis bufferequilibrated cobalt-conjugated resin with a 5 mL bed volume at room temperature. Columns were washed in ten-column volumes of freshly prepared denaturing wash buffer (100 mM sodium phosphate, pH 6.3, 10 mM Tris-Cl, 8 M urea). Denatured His 6 -FLAG-Kil was eluted in 10 mL freshly prepared denaturing elution buffer (100 mM sodium phosphate, pH 4.5, 10 mM Tris-Cl, 8 M urea). The eluted protein was then renatured by dialysis into polymerization buffer overnight and through the following day (three 2 L changes of buffer in total). Renatured His 6 -FLAG-Kil was concentrated using Amicon Ultra-3K Centrifugal Filter Devices (Millipore), flash-frozen in liquid nitrogen, and stored at 2 80uC.

Interaction and sedimentation assays
To assay interaction between purified proteins, 200 mL samples were prepared in polymerization buffer containing 6 mM bovine serum albumin. FtsZ at 5 mM, His 6 -FLAG-Kil at 10 mM, and/or His 6 -tagged ZipA C domains (WT and L286Q) at 5 mM were included as indicated. 50 mL of 50% buffer-equilibrated a-FLAG M2 affinity resin (Sigma-Aldrich) were added and samples were incubated at room temperature, mixing, for one to three hours for binding. Samples were then loaded onto gravity flow columns and the resin was washed with 25 mL polymerization buffer. Following washes, resin was recovered in 250 mL buffer, SDS-PAGE sample buffer was added and samples were boiled and separated by 20% SDS-PAGE followed by Coomassie blue staining.
Sedimentation assays were performed essentially as previously described [66] in a Beckman TL-100 Ultracentrifuge, but using a TLA 100.3 rotor at 70,000 rpm with appropriate adaptors and speed-resistant tubes (Beckman). 100 mL samples were prepared in polymerization buffer with FtsZ at 5 mM, His 6 -FLAG-Kil at 10 mM, His 6 -tagged ZipA C domains (WT and L286Q) at 5 mM, and GTP at 1 mM. Components were added in the following order: polymerization buffer, Kil buffer or Kil, FtsZ, ZipA C , and GTP. For reactions with calcium-induced bundling, CaCl 2 was added to 1 mM after GTP addition.

GTPase activity assay
GTPase activities were determined using the EnzChek Phosphate Assay Kit (Molecular Probes) in reactions set up with the same concentrations and buffers as for sedimentation assays, but in a 96 well plate and with the required purine nucleoside phosphorylase enzyme and 7-Methyl-6-thio-D-guanosine (MESG) substrate components. Reactions were initiated by adding one half the reaction volume as buffer with FtsZ alone, simultaneously via multi-channel pipette, into the other half of the reaction volume that contained all other components. (For reactions without FtsZ, buffer with GTP alone was used to simultaneously initate reactions). OD 360 readings were taken every 30 seconds using a Synergy Mx Microplate Reader (BioTek). GTP hydrolysis rates were calculated based on a phosphate standard curve.
Phage one-step growth assay One-step growth was done according to Frank Stahl (unpublished). Briefly, 10 mL MG1655 was growth at 39uC in tryptone broth to OD 600 = 0.4 (,1.5610 8 per mL). The cells were pelleted and suspended in TMG (see above) and incubated at 37uC for 30 minutes to starve the cells. NaCN was added at 2610 23 M and 1.8 mL was dispensed to two small glass-plating tubes. To initiate the growth curve, 0.2 mL phage stock at 1.5610 8 per mL was added to the cell suspension. Phage adsorption was monitored over a 30 minute period by mixing 0.1 mL infected cells into 4.9 mL tryptone broth containing 0.25 mL chloroform and plating appropriate dilutions on C600 host cells. After a 30 minute adsorption the infected cells were diluted 100-fold into tryptone broth and two further dilutions were made into 39uC tryptone broth, one 100-fold and one 5610 3 -fold. At various times, 0.1 mL samples were taken from these dilutions and plated immediately on C600.

Supporting Information
Table S1 Oligonucleotides used in this study. (DOCX)