A nutrient-dependent division antagonist is regulated post-translationally by the Clp proteases in Bacillus subtilis
Changes in nutrient availability have dramatic and well-defined impacts on both transcription and translation in bacterial cells. At the same time, the role of post-translational control in adaptation to nutrient-poor environments is poorly understood. Previous studies demonstrate the ability of the glucosyltransferase UgtP to influence cell size in response to nutrient availability. Under nutrient-rich medium, interactions with its substrate UDP-glucose promote interactions between UgtP and the tubulin-like cell division protein FtsZ in Bacillus subtilis, inhibiting maturation of the cytokinetic ring and increasing cell size. In nutrient-poor medium, reductions in UDP-glucose availability favor UgtP oligomerization, sequestering it from FtsZ and allowing division to occur at a smaller cell mass.
Intriguingly, in nutrient-poor conditions UgtP levels are reduced ~ 3-fold independent of UDP-glucose. B. subtilis cells cultured under different nutrient conditions indicate that UgtP accumulation is controlled through a nutrient-dependent post-translational mechanism dependent on the Clp proteases. Notably, all three B. subtilis Clp chaperones appeared able to target UgtP for degradation during growth in nutrient-poor conditions.
Together these findings highlight conditional proteolysis as a mechanism for bacterial adaptation to a rapidly changing nutritional landscape.
KeywordsCell cycle Cell size Cell division ClpP UgtP UDP-glucose
- Minimal Glucose
S750 + 1% Glucose
- Minimal Glycerol
S750 + 1% Glycerol
- Minimal Sorbitol
S750 + 1% Sorbitol
Osmoregulated Periplasmic Glucan
As single-celled organisms, bacteria constantly alter their physiology to adapt to their environment. Nutrients in particular can dramatically impact bacterial growth and morphology. Escherichia coli, Salmonella, and Bacillus subtilis cells grow several times faster and are up to three times larger when cultured in nutrient-rich medium than when cultured in nutrient-poor medium [1, 2, 3]. Nutrient-dependent increases in cell size appear to be a means of accommodating the concomitant increase in macromolecular biosynthesis at faster growth rates, particularly the additional DNA generated by multifork replication [4, 5].
The nutrient-dependent regulation of biosynthesis has been an area of intense interest for many years. Numerous studies have explored how changes in nutrient composition and growth rate impact transcription and translation, which in large part is a response mediated via accumulation of the signaling molecule guanosine pentaphosphate ((p)ppGpp) [6, 7, 8, 9]. Although post-translational regulation has been implicated in adaptation to changes in growth phase (e.g. carbon starvation [10, 11]), how fluctuations in nutritional content and growth rate impact post-translational regulation at the molecular level is poorly defined.
In previous work, we identified a class of division antagonists responsible for coordinating cell size with nutrient availability in B. subtilis and E. coli [4, 5]. Both organisms employ unrelated, yet functionally similar, glucosyltransferases—UgtP in B. subtilis and OpgH in E. coli—to inhibit division and increase size during growth in carbon-rich medium [12, 13]. In both cases, binding to their substrate, UDP-glucose, stimulates interaction between UgtP and OpgH and the tubulin-like cell division protein FtsZ. The net result of these interactions is a delay the maturation of the cytokinetic ring and an increase cell size. Loss-of-function mutations in ugtP or opgH and in genes required for UDP-glucose biosynthesis reduce cell size by as much as 35% during growth in nutrient-rich conditions.
UgtP and OpgH both have additional roles as glucosyltransferases that contribute to cell envelope biogenesis. UgtP transfers glucose from UDP-glucose to diacylglycerol to form the diglucosyl-diacylglycerol membrane anchor for lipoteichoic acid (LTA) . OpgH transfers glucose from UDP-glucose to the periplasm as an initial step toward the synthesis of osmoregulated periplasmic glucans (OPGs) . LTA and OPGs are proposed to have similar functions  based on the conservation of enzymes involved in their synthesis, their location within the cellular envelope [17, 18], and their contribution to osmoprotection [13, 19].
In B. subtilis, UDP-glucose increases UgtP’s affinity for FtsZ . During growth in nutrient-rich conditions UgtP is localized throughout the cytoplasm, where the largest pool of FtsZ is located, and can also be found at the cytokinetic ring and at cell poles . During growth in carbon-poor conditions or when synthesis of UDP-glucose is disrupted, UgtP self-assembles into large oligomers, sequestering it from FtsZ and permitting division to occur at a reduced cell size . In vitro studies suggest UDP-glucose acts as a molecular rheostat, precisely modulating UgtP’s affinity for itself and FtsZ to coordinate size with growth rate and nutrient availability . Curiously, while the UgtP homolog in the Gram-positive pathogen Staphylococcus aureus interacts with FtsZ and other divisome proteins, it does not exhibit the same dynamic localization pattern it does in B. subtilis nor does it appear to make a significant contribution to cell size .
In addition to UDP-glucose-dependent changes in its affinity for FtsZ, UgtP is also subject to nutrient-dependent changes in concentration. UgtP levels are reduced several-fold during growth in nutrient-poor conditions . Defects in the UDP-glucose biosynthesis pathway have no discernable impact on the intracellular concentration of UgtP, suggesting that nutrient-dependent changes in accumulation are independent of the signaling molecule .
The striking difference in UgtP levels, together with previous work suggesting protein turnover might be increased in nutrient-poor conditions , prompted us to investigate the mechanism underlying this additional layer of UgtP regulation. Here we report that UgtP nutrient-dependent accumulation is governed by a post-translational mechanism involving all three substrate recognition components of the B. subtilis Clp protease system. We find that some of the clp chaperone genes are upregulated during growth in nutrient-poor medium, suggesting a possible mechanism for increased UgtP degradation under these conditions. These findings suggest an important role for conditional proteolysis in the nutrient-dependent regulation of cellular processes.
UgtP accumulation is subject to nutrient-dependent post-translational regulation
In our initial investigation, we observed that the intracellular concentration of a UgtP-6XHis fusion protein was three to four-fold lower when cells were cultured under carbon-poor conditions, but unaffected by the absence of UDP-glucose . Nutrient-dependent changes in concentration contrast strongly with FtsZ, whose levels are essentially constant across a wide range of growth conditions . The net result is a reduction in the UgtP:FtsZ ratio from ~ 1:2 in LB to as low as ~ 1:8 in minimal medium based on previous calculations of absolute FtsZ and UgtP concentrations per cell [4, 22]. To expand on this observation we measured levels of the same UgtP-His fusion across four different nutrient conditions: Lysogeny Broth [LB], S750 + 1% glucose (minimal glucose), S750 + 1% glycerol (minimal glycerol), and S750 + 1% sorbitol (minimal sorbitol). Under each condition, the respective mass doubling time of this strain (P ugtP -ugtP-his) was 22′, 39′, 58′, and 78′.
To determine if UgtP is subject to transcriptional or post-transcriptional modes of regulation, we generated two ugtP-lacZ fusion constructs. In the first construct, a reporter for ugtP transcription, the 700 base pairs immediately upstream of the ugtP start codon were fused to lacZ, leaving the lacZ Shine-Dalgarno sequence intact. In the second construct, a reporter for UgtP translation, lacZ was fused in-frame downstream of the first 30 codons of the ugtP open reading frame that included the native ugtP Shine-Dalgarno sequence.
The Clp proteases are responsible for UgtP degradation under carbon-poor conditions
To understand the mechanism responsible for the post-translational regulation of UgtP, we sought to identify the protease responsible for its degradation. As an initial step, we screened B. subtilis strains defective in five well-studied proteases: YluC, CptA, ClpP, YvjB, and Lon for aberrant UgtP regulation. We rationalized that if one of these proteases were responsible for the growth rate-dependent degradation of UgtP, then UgtP would inappropriately accumulate in its absence during growth in carbon-poor conditions. For this experiment we used the P xyl -ugtP-his construct described above to enhance our ability to detect UgtP by semi-quantitative immunoblot. During growth in LB medium and in the presence of the inducer, xylose, this construct raises intracellular UgtP levels ~ 8.5-fold (changing the UgtP:FtsZ ratio from ~ 1:2 to ~ 4:1) and increases cell length by ~ 22% . (P xyl is generally insensitive to nutrient availability .)
ClpP is a processive serine protease widely conserved throughout bacteria. Ineffective on its own, ClpP functions in tandem with AAA+ ATPase Clp chaperones . The Clp chaperones are responsible for recognizing target proteins, unfolding them using the energy of ATP hydrolysis, and translocating the unfolded polypeptide into the ClpP proteolytic chamber [25, 26]. In B. subtilis, there are three Clp chaperones: ClpC, ClpE, and ClpX. Since each chaperone identifies a unique set of substrates with limited target overlap, we reasoned that either ClpC, ClpE, or ClpX would be responsible for growth rate-dependent degradation of UgtP. To distinguish the Clp chaperone involved, we examined accumulation of UgtP-His from a xylose-inducible promoter in ∆clpC, ∆clpE, and ∆clpX cells cultured in minimal sorbitol.
Deletion of clpC, clpE, and clpX alone or in pairwise combination had little impact on UgtP-His levels in minimal sorbitol. UgtP-His accumulated to levels similar to that observed in the ∆clpP mutant only in a strain defective for all three chaperones (Fig. 3B). These data suggest that all three Clp chaperones function redundantly to control UgtP accumulation in a growth rate-dependent manner.
To confirm that the Clp proteases are indeed responsible for degradation of UgtP, as our data suggested, we employed an in vivo proteolysis assay similar to that described in . Briefly, we cultured P xyl -ugtP-his and the congenic ∆clpP strains in minimal sorbitol with xylose to an A600 of ~ 0.2. We then added chloramphenicol to inhibit new protein synthesis and sampled cells every 30 min for 2 h. UgtP-His levels were determined via semi-quantitative immunoblot. Consistent with UgtP being directly targeted by ClpP, UgtP-His levels decreased rapidly in clpP + cells over time, but were stable in the absence of the protease (Fig. 3C and Additional file 2: Figure S2).
Consistent with the Clp proteases serving as nutrient-dependent regulators of protein stability, expression of clpC and clpE were elevated in minimal sorbitol (Fig. 3D). qRT-PCR indicated that expression of clpC and clpE are upregulated > 4-fold, while clpX and clpP are marginally upregulated (~ 1.5-fold) in minimal sorbitol, our poorest carbon source, relative to LB. These findings are consistent with those of the Hecker lab who observed ClpXP and ClpCP drive proteolysis of a large group of proteins, most notably enzymes involved in central carbon metabolism, upon glucose starvation (UgtP was not identified as a Clp substrate in this study) .
Defects in UgtP’s hexose-binding site increases susceptibility to proteolysis in vivo
In an attempt to identify regions of UgtP required for recognition by the Clp chaperones, we screened a series of UgtP mutants for sensitivity to Clp-mediated degradation in vivo. Of particular interest were regions of UgtP that mediate interaction with UDP-glucose, FtsZ, or itself. To test the impact of UDP-glucose binding and oligomerization on Clp-dependent degradation, we employed three UgtP mutants, generated based on structural data from the UgtP homologue, mongalactosyldiacylglycerol (MGDG) synthase : one defective in its putative uracil-binding site (URA-: F112A V117A), one defective in the putative hexose-binding site (HEX-: E306A N309A), and one in the predicted dimerization/oligomerization domain (OLI-: I142A E146A).
For analysis of UgtP mutant accumulation, His-tagged versions of all three UgtP variants (URA-, HEX- and OLI-) were expressed from an ectopic locus under the control of a xylose-inducible promoter in a ugtP null background. UgtP mutant accumulation under nutrient-rich (LB) and carbon-poor conditions (minimal sorbitol) was monitored by semi-quantitative immunoblot in early exponential phase. For reasons that are unclear, both UgtPURA--His and UgtPHEX--His exhibited migration patterns different from wild type UgtP-His when separated by SDS-PAGE prior to immunoblotting (Fig. 4). This difference may reflect conformational changes in mutant protein structure.
Of the three mutants, only UgtPHEX--His exhibited ClpP-dependent differential in accumulation compared to wild type UgtP-His, suggesting hexose binding might protect UgtP from proteolysis. UgtPHEX--His accumulated to only ~ 35% of UgtP-His (WT) levels during growth in LB (Fig. 4B). Even in minimal sorbitol, UgtPHEX--His levels were ~ 65% of UgtP-His (Fig. 4C). UgtPURA--His and UgtPOLI--His were indistinguishable from wild type UgtP-His with regard to ClpP-dependent changes in accumulation, arguing against a role for interaction with FtsZ or homo-oligomerization in shielding UgtP from Clp recognition. Importantly, each of the constructs exhibited congruent mRNA levels measured by qRT-PCR and UgtPHEX--His is at WT levels in a ∆clpP background strain in both LB and minimal sorbitol, indicating that the change in stability is directly due to ClpP-mediated degradation (Additional file 4: Figure S4).
Together these data suggest that interaction with the hexose moiety of UDP-glucose, which we have measured as being more prevalent when cultured in nutrient-rich conditions (Additional file 5: Figure S5), may provide some protection from Clp-mediated proteolysis. At the same time, however, this observation is inconsistent with our previous observation that UgtP accumulation is independent of UDP-glucose synthesis , a point we address in the discussion.
UgtP is targeted by ClpXP for proteolysis in vitro
To clarify whether Clp recognition of UgtP is direct or reliant on a nutrient-dependent adaptor protein, we next determined if UgtP could be degraded directly by ClpXP in vitro. Although our genetic data indicate all three Clp chaperones are capable of degrading UgtP (Fig. 3B), we focused on ClpX as the most prevalent chaperone (there are an estimated 1400 ClpX, 250 ClpC, and 100 ClpE hexamers per cell during growth in LB) .
For these experiments, we expressed and purified ClpX and ClpP as previously described and a His-UgtP we constructed for this study . We employed the well-characterized ClpXP substrate Spx  as a positive control, and a non-targeted protein, Thioredoxin-His, as a negative control. As expected, Spx was subject to robust ATP-dependent ClpXP mediated degradation, while Thioredoxin-His was retractile to ClpXP proteolysis (Additional file 6: Figure S6). Due to the size-similarity between His-UgtP and ClpX used in the degradation assays (44 kDa vs 46 kDa), we could not distinguish between the two when separated by standard SDS-PAGE. Instead, we employed a monoclonal anti-His antibody to distinguish between His-UgtP and ClpX via immunoblot. Please note that because we detected UgtP by immunoblot and the anti-His antibody (monoclonal THE™ antibody, Genscript) interacted strongly with nanogram amounts of the His-UgtP fusion protein, we found it necessary to utilize significantly lower concentrations of His-UgtP relative to the Spx and Thioredoxin-His control proteins to remain in linear range. While His-UgtP levels were monitored by immunoblot, Spx and Thioredoxin-His were monitored by Coomassie staining.
Based on our in vivo data supporting a model in which hexose binding may shield UgtP from Clp-mediated proteolysis (Fig. 4), we speculated that adding UDP-glucose or simply glucose to the ClpXP proteolysis assays might hinder UgtP degradation. To test this model we added UDP-glucose or glucose 6-phosphate in excess to the ClpXP in vitro proteolysis reactions described above. However, we saw no difference in UgtP proteolysis in the presence of either sugar (Fig. 5B).
Clp-mediated UgtP degradation during growth in minimal sorbitol medium does not significantly impact cell size or diglucosyl-diacylglycerol production
In an effort to illuminate the potential “rationale” for Clp mediated degradation of UgtP during growth in carbon-poor medium we examined the impact of Clp activity on cell size and production of diglucosyl-diacylglycerol (DGD), the anchor for LTA. UgtP exhibits a high affinity for FtsZ (38 nM) even in the absence of UDP-glucose . Nutrient-dependent degradation may thus serve as an additional control to prevent UgtP-mediated division inhibition during growth in carbon-poor conditions.
For these experiments, we took advantage of two strains capable of producing a range of UgtP concentrations in minimal sorbitol: BH736 (∆ugtP; P xyl -ugtP-his) and BH12 (P ugtP -ugtP-his; P xyl -ugtP-his). Semi-quantitative immunoblots indicate that non-induced BH736 produces no detectible UgtP-His, induced BH736 and non-induced BH12 produce similar levels of UgtP-His, and induced BH12 produces approximately 60% more UgtP-His than BH12 non-induced (Additional file 7: Figure S7). If cell size under carbon-poor conditions is sensitive to UgtP concentration, then we would expect to see a gradient of cell sizes with cell size increasing in proportion to UgtP concentration. We opted not to measure the impact of ClpP on cell size since clpP is highly pleotropic and deletion could feasibly alter cell length independent of UgtP degradation.
Cell length in response to differential UgtP levels in minimal sorbitol
Cell Length [μm]
BH736 – xylose
(∆ugtP; P xyl -ugtP-his)
2.63 ± 0.27
BH736 + xylose
(∆ugtP; P xyl -ugtP-his)
99 ± 45
2.72 ± 0.11
(P ugtP -ugtP-his; P xyl -ugtP-his)
BH12 – xylose
100 ± 24
3.07 ± 0.20
(P ugtP -ugtP-his; P xyl -ugtP-his)
BH12 + xylose
155 ± 33
2.95 ± 0.25
Another possible explanation for the degradation of UgtP in carbon-poor conditions is the preservation of intracellular glucose by curtailing production of UgtP’s product, diglucosyldiacylglycerol . To test this possibility we measured DGD levels in wild type and ∆clpP strains, as well as their isogenic P xyl -ugtP counterparts, cultured in minimal sorbitol (with xylose added when growing P xyl -ugtP strains). Briefly, we purified membranes from these strains, performed a methanol:chloroform lipid extraction, separated the lipids using thin-layer chromatography, stained for DGD using iodine gas, and quantified DGD. Lipids were also extracted from ∆ugtP cells for use as a negative control.
Despite the 3-fold difference in UgtP concentration, DGD levels were not significantly different between WT/∆clpP cells (p = 0.78) or induced P xyl -ugtP cells ± clpP (p = 0.30) (Fig. 6B). As expected, ∆ugtP cells produced no detectible DGD (Additional file 8: Figure S8). These data suggest that while UgtP is necessary for DGD production, degradation of UgtP via the Clp proteases is irrelevant for modulating DGD concentration. It is therefore unlikely that degradation of UgtP occurs in carbon-poor conditions as a means of conserving glucose, as production of glucose-rich DGD is not affected by UgtP degradation.
Our results indicate UgtP accumulation is controlled in a nutrient-dependent manner via a post-translational, Clp-dependent mechanism. This additional layer of regulation governing UgtP activity, distinct from UDP-glucose-mediated changes in UgtP’s affinity for itself and FtsZ, ensures that active UgtP accumulates only under nutrient-rich growth conditions when it antagonizes cell division. While there are several prominent examples of conditional proteolysis coupled to growth phase [31, 32, 33], there are only a handful of examples in which proteolysis has been linked to growth rate and/or nutrient availability. Two such examples are from the Narberhaus lab: 1) The DNA-binding replication inhibitor CspD is selectively proteolyzed by the Lon protease during growth in nutrient-rich medium  and 2) LpxC, a deacetylase involved in lipid A biosynthesis, is degraded only when cultured at slower growth rates by the protease FtsH .
We were somewhat surprised by our finding that UgtP proteolysis in vivo is accomplished via the redundant activity of ClpCP, ClpEP, and ClpXP (Fig. 3B). While ZapC is recognized and degraded by ClpXP and ClpAP in E. coli, to our knowledge UgtP is the first published example of a Clp substrate recognized by all the Clp chaperone proteins in B. subtilis . Further, we find that genes encoding two of the clp chaperones, clpC and clpE, are expressed at higher levels during slower growth, which likely contributes toward the growth medium-dependent regulation of UgtP (Fig. 3D). It is noteworthy that ClpX, previously identified as a direct inhibitor of FtsZ assembly in B. subtilis independent of its role in proteolysis, also modulates the stability of an entirely different FtsZ inhibitor .
Since AAA+ proteases exhibit distinct substrate-binding repertoires with only minor overlap in target specificity , it is curious how and why all three Clp chaperones are able to target UgtP. These chaperones either recognize unstructured peptide sequence tags (known as degrons) within a client protein or adaptor proteins bound to target substrates. ClpC exclusively uses adaptor proteins (MecA, YpbH, and McsB) to recognize substrate as well as to promote the activation of the ClpC hexamer [38, 39, 40, 41]. Although ClpXP is capable of degrading UgtP in vitro (Fig. 5), we were unable to identify putative degrons for any of the three Clp chaperone proteins within the UgtP primary sequence through comparison with other verified and putative B. subtilis Clp substrates [10, 42, 43]. It thus remains an open question whether ClpXP, ClpCP, and ClpEP share a common degron or adaptor protein, or use distinct mechanisms, to target UgtP for degradation.
UgtP degradation was enhanced in vivo by two point mutations (E306A N309A) in its putative hexose-binding site suggesting ligand binding might afford some protection from ClpP-specific proteolysis (Fig. 4). While there is precedent in both prokaryotic and eukaryotic systems of small molecule ligands governing proteolytic susceptibility [44, 45, 46], our data do not cohesively support that UDP-glucose shields UgtP from degradation. Neither defects in UDP-glucose biosynthesis  nor mutations disrupting the putative nucleotide binding site (URA-, F112A V117A) had an impact on UgtP accumulation (Fig. 4). Instead, these data suggest ligand binding is largely irrelevant to UgtP stability and the hexose-binding mutation (E306A N309A) may simply lead to a conformation that exposes a Clp recognition sequence. Although we are unaware of any literature supporting a negative relationship between clp expression or activity and cell size, enrichment of the Clp proteases—particularly ClpC and ClpE—under nutrient-poor conditions as the most parsimonious, albeit still theoretical, explanation for UgtP degradation under these conditions (Fig. 3D).
As a whole, our data point to UgtP being subject to an elaborate set of multilayered controls. Not only is it unclear why three Clp chaperones would be needed for UgtP degradation in minimal medium, it is also not readily apparent why a carbon-starved cell would spend energy to transcribe and translate ugtP only to immediately have it proteolyzed, consuming ATP at each step. We were unable to identify a phenotypic explanation for the nutrient-dependent degradation of UgtP. Given the myriad of conditions under which B. subtilis is able to grow, it may very well be that we are looking in the wrong place and for the wrong phenotypes. Alternatively, UgtP may simply be one of a large cohort of proteins that have a shorter half-life during growth in carbon-poor conditions . If so, growth medium-dependent changes in Clp protease activity may simply serve as a crude means of supporting B. subtilis’ uncanny ability to adapt rapidly to a wide range of environments while ensuring cells retain a relatively robust supply of biosynthetic building blocks even during growth in carbon-poor conditions.
Strains and general methods
All B. subtilis strains are derivatives of JH642 . Details of their construction and a list of strains used for this study are described in (Additional file 9 and Additional file 10: Table S1). All cloning was done using the E. coli strain AG1111 . Either Vent (NEB) or Phusion (NEB) DNA polymerases were used for PCRs. Cells were cultured in either Lysogeny Broth (LB) or minimal S750 defined media  supplemented with either 1% glucose, glycerol, or sorbitol as carbon sources and appropriate amino acid supplements. For strains containing ∆clpP or ∆clpCEX, cells were always first cultured in LB prior to growth in other growth media.
Bacterial cells cultured to A600 0.20–0.40 were lysed by centrifuging 1 mL of culture then re-suspending in 50 μL lysis buffer (20 mM tris pH 8.0, 12.5 mM MgCl2, 1 mM CaCl2, 2 mg/mL lysozyme, 1X Halt™ Protease Inhibitor Cocktail), incubating 10 min at 42 °C, then adding SDS to 1% (v/v). Laemmli buffer was added to 1X, lysates were incubated 10 min at 100 °C, then lysate was normalized to OD and subjected to SDS-PAGE. Proteins were transferred to PVDF membranes using Bio-Rad Trans-Blot® Turbo™ instrument as described on pg. 15 of the operation manual. Subsequent to transfer, but prior to blocking PVDF membranes were stained with 1X Ponceau S solution in 5% acetic acid for 5 min and total protein per lane used as a loading control . Membranes were then blocked with 5% nonfat milk in PBS for 1 h.
Two different Anti-His antibodies to detect His-tagged UgtP were employed in this study: 1) His-probe monoclonal antibody (Santa Cruz Biotechnology) used at 1:1000 (used in Fig. 3), and 2) monoclonal THE™ His Tag (Genscript) α-His antibodies incubated at 1:1000. Rabbit polyclonal (Genscript) α-GFP antibodies incubated (at 1:1000) were used to detect YFP-tagged UgtP. FtsZ was detected using an affinity-purified polyclonal rabbit α-FtsZ antibody (at 1:5000) . Cognate goat α-rabbit or goat α-mouse (Genscript) HRP secondary antibodies were used (at 1:5000). The membranes were developed using ECL substrate (Bio-Rad #1705060) and imaged using a Li-COR Odyssey FC instrument that detected saturation and autocorrected exposure time. Loading was first normalized to cell density measured by A600, then total protein per lane was calculated using Ponceau-S prior to blocking. Blot density was quantified using ImageJ (NIH) by subtracting background and normalizing to total protein (Ponceau S staining). In some cases, FtsZ is shown as the loading control because it was largely invariant with Ponceau-S staining.
In vivo UgtP degradation assay
Protocol was adapted from . Strains were cultured in 5 mL LB + 0.5% xylose at 37 °C with shaking until A600 = 0.20–0.40. These cultures were then diluted into 20 mL minimal sorbitol + 0.5% xylose to A600 = 0.005. Once A600 reached 0.20–0.40, spectinomycin was added to 200 μg/mL. Cultures were sampled (1 mL) at 0, 30, 60, 90, and 120 min after spectinomycin addition, and the samples were frozen at − 80 °C for future use. These samples were then subjected to semi-quantitative immunoblotting for UgtP-His, the protein was quantified using ImageJ (NIH) and processed in Microsoft Excel.
β-galactosidase activity in liquid cultures
Specific activity was calculated essentially as described in . Strains encoding lacZ fusions were cultured at 37 °C to early/mid-log (A600 0.30–0.40). Prior to sampling, the cultures were diluted 1:2 in their respective medium and absorbance at A600 was recorded. 30 μl of toluene and 30 μl of a 0.1% sodium dodecyl sulfate solution were added to 2 ml of bacterial culture to permeabilize cells. Incubating cells at 37 °C for 45 min then evaporated the toluene. Cells were then mixed with Z-buffer (60 mM Na2HPO4, 40 mM NaH2PO4, 10 mM KCl, 1 mM MgSO4, 50 mM β-mercaptoethanol) and tubes were incubated at 25 °C for 5′. Reactions were started by adding 0.25 ml of 0.4% o-nitrophenol-β-galactoside in Z-buffer and stopped by adding 0.5 ml of 1 M Na2CO3. A420 was then recorded. The specific unit value was calculated using the equation: = 200 × (A420 of the culture − A420 in the control tube)/minutes of incubation × dilution factor.
Quantitative real-time polymerase chain reaction
RNA was harvested from B. subtilis cells in early-log (A600 = 0.20–0.40) with RiboPure™ Kit (Ambion), treated with the Turbo DNA-Free Kit™ (Ambion), and reverse transcribed for 1 h at 42 °C using the RETROscript® Kit (Ambion). Template was diluted 10-fold, added to iTaq SYBR Green Supermix (Bio-Rad) with appropriate oligonucleotide pairs. Oligonucleotides used in this study are described in (Additional file 11: Table S2). Data were acquired using an Applied Biosystems model 7500 thermocycler. Results were analyzed using the comparative Pfaffl method .
All plasmids encoding genes used for purification were mini-prepped from storage E. coli strain AG1111 and freshly transformed into C41(DE3) cells and consequently used for expression of protein (no frozen stocks were used). Briefly, 1 L of LB medium was inoculated 1:100 with overnight culture from a single colony. Cells were grown at 37 °C with the exception of ClpP and ClpX, which were grown at room temperature. When A600 ~ 0.6, cells were induced with isopropyl 1-thio-β-D-galactopyranoside to a final concentration of 1 mM. Cells were grown for an additional 4-8 h and then cells were harvested by centrifugation, and cell pellets were stored at − 80 °C.
ClpP and ClpX were purified using the IMPACT System (NEB) as described previously . Spx was also purified as previously described  with the following modifications: Spx-His was purified from a Ni-NTA column with a 50-500 mM imidazole gradient and peak fractions pooled. An N-terminal 6X–His tag was then removed by cleavage with AcTev protease (Life Technologies). Spx was further purified using size exclusion chromatography over an S-300 column in buffer containing 50 mM Tris pH 7.5, 50 mM KCl, and 10% glycerol. Peak fractions were collected, pooled, and concentrated using an Amicon-10 kDa centrifugation column, flash frozen on liquid nitrogen, and stored at − 80 °C.
His-UgtP in pET28a(+) (PL3521) was purified as follows: Starting from frozen pellets, cells were thawed on ice and re-suspended in Buffer A (50 mM Tris pH 8.0, 500 mM NaCl, 10 mM Imidazole, 10% glycerol). Pefabloc-SC (Sigma) was then added as a protease inhibitor. Re-suspended cells were then lysed by three times by French press at a pressure of 10,000 psi. The lysed cells were then cleared by centrifugation, spinning at 120,000×g for 45 min at 4 °C. The resulting supernatant was brought up to a volume of 50 mL and loaded onto a DynaLoop connected to a DuoFlow F10 FPLC system (Bio-Rad). The supernatant was then applied over two 5 mL Bio-Scale Mini Profinity IMAC cartridges connected in series (Bio-Rad). The columns were then washed with 10 column volumes of Buffer A followed by 5 column volumes of Buffer B (50 mM Tris pH 8.0, 500 mM NaCl, 20 mM Imidazole, 10% glycerol). Protein was then eluted off of the columns with 5 column volumes of Buffer C (50 mM Tris pH 8.0, 500 mM NaCl, 500 mM Imidazole, 10% glycerol). Peak fractions were collected and concentrated to a volume of ~ 1 mL using an Amicon-10KDa centrifugation column. The concentrated protein was loaded onto a 1 mL loop and applied over a HiPrep 16/60 Sephacryl S-300 HR size exclusion column (GE Healthcare). The column was washed and protein was then eluted off the column in Buffer D (50 mM HEPES pH 7.5, 100 mM KCl, 10% glycerol). Peak fractions were checked by SDS-PAGE and then aliquot, flash frozen on liquid nitrogen and stored at − 80 °C.
In vitro ClpXP proteolysis assay
Reactions were carried out in 50 mM HEPES pH 7.6, 50 mM KCl, 15 mM Mg acetate, 5 mM DTT, 5 mM ATP, 10 mM creatine phosphate, and 0.1 μg/μl creatine kinase (Sigma). 500 ng of His-UgtP was incubated at 37 °C in the presence of ClpP (6 μM) and ClpX (3 μM) in a 100 μl reaction mixture. Each reaction was initiated by the addition of 5 mM ATP. At 0 and 30 or 45 min, samples of the reactions were taken containing what corresponded to 125 ng His-UgtP at the start of the reaction. Samples were then diluted to 2.5 ng/μl with 2X sample buffer. 50 ng of His-UgtP was then loaded per lane on a 10% SDS-PAGE. After electrophoresis, proteins were transferred via Western blot to a PVDF membrane. Membranes were blocked, then incubated with mouse monoclonal THE™ His Tag (Genscript) at a 1:4000 dilution overnight at 4 °C. Control reactions with Spx and Thio-His were performed as with His-UgtP except at a concentration of 3 μM. At 0 and 60 min, 15 μl of the samples was collected and analyzed on a 15% SDS-PAGE followed by staining with Coomassie blue.
Fluorescence microscopy and cell length measurements
Samples were first fixed as previously described . Briefly, cells were fixed by treating with 2.575% paraformaldehyde and 0.0008% glutaraldehyde. Fixed samples were permeabilized with 0.01 mg/mL lysozyme for two minutes, and then treated with 10 μg/mL wheat germ agglutinin tetramethylrhodamine conjugate (WGA-Rhod, ThermoFisher #W849) in PBS to stain cell wall septa for 10 min. 5 μL of prepared samples were applied to 1% agarose in PBS pads, allowed to dry, and then covered with a coverslip. Cells were imaged using a Nikon TI-E microscope equipped with a Texas Red/mCherry/AlexaFluor 594 filter set for fluorescence microscopy (Chroma # 39010).
Cell length was determined using Nikon Elements by measuring the distance between the midpoints of adjacent cell wall septa for cells stained with WGA-Rhod. T-test analysis was employed to test for significant differences between conditions.
Bacterial cultures (1 L volumes) were centrifuged at 15,000 x g for 1 min, decanted, and then resuspended in 100 mL 100 mM sodium citrate pH 4.7. Cells were lysed using a French press. Lysates were centrifuged at 12,000 g for 20 min to pellet membranes. Pellets were weighed and resuspended to 0.4 g/mL in 100 mM sodium citrate pH 4.7. Methanol and chloroform were added to obtain a ratio of 2:1:0.8 methanol:chloroform:sodium citrate. Mixture was vortexed 30 s every 15 min for 2 h. Chloroform and sodium citrate were added to obtain a ratio of 1:1:0.9 methanol:chloroform:sodium citrate. The mixture was vortexed for 1 min and centrifuged at 4000 x g for 10 min. Bottom chloroform layer was transferred to a new tube. Methanol and sodium citrate were added to obtain a ratio of 1:1:0.9 methanol:chloroform:sodium citrate. Mixture was vortexed for 1 min and centrifuged at 4000 x g for 10 min. Bottom chloroform layer was transferred to new tube and allowed to dry in fume hood. Dried lipids were weighed and resuspended in 1:1 methanol:chloroform to a final concentration of 600 mg/mL and stored at − 20 °C.
Lipid thin-layer chromatography and diglucosyl-diacylglycerol quantification
140 mL chloroform and 60 mL methanol were added to a glass TLC development chamber. Placed filter paper into developing solution, thoroughly wetted blot paper, and then placed the paper along the chamber walls. A TLC plate (Analtech #p46021) was pre-run in developing solution by placing it in the chamber, covering the chamber with its glass lid, and allowing the solvent to run to the top of the plate. The plate was dried at 100 °C for 10 min. Using a pencil, a line was drawn across the width of the plate approximately 1 cm from the bottom. Lipid samples (2 μL) were spotted along this line and allowed to dry. Samples were repeatedly spotted and allowed to dry 5 additional times. Once the spots were dry, the plate was placed back into the chamber, the lid was placed on top, and the solvent was allowed to run to 1 cm from the top of the plate. The plate was taken out of the development chamber, the solvent line was quickly marked with pencil, and the plate was dried. The plate was then placed inside a polystyrene container with a few iodine crystals, sealed, and stained for 16 h with iodine gas. The stained plate was scanned to acquire images. The stained plate was scanned to acquire images. ImageJ was used to quantify the amount of DGD present, and another band (indicated in Additional file 8: Figure S8) was used as a loading control. T-test analysis was employed to test for significant differences between conditions.
Statistical parameters and significance are reported in the figures and the figure legends. Asterisks designate statistical significance as: *, p < 0.05; **, p < 0.01; ***, p < 0.001; ****, p < 0.0001. Statistical analysis was performed in GraphPad PRISM 6.
We are indebted to Richard Losick, Peter Zuber, and David Dubnau for the kind gift of strains and reagents. We thank EKB, MAH, OJB, and RSM for their critical reading. Finally, we thank all members of the Levin lab for thoughtful discussions. This work was supported by a National Institutes of Health grant (NIH GM64671) to PAL.
This work was supported by a National Institutes of Health grant (NIH GM64671) to PAL. The funding agency had no role in design of this study, collection, analysis, and interpretation of data, nor writing of this manuscript.
Availability of data and methods
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
NH designed and performed all aspects of the experimentation except as noted below, analyzed data, and drafted the manuscript. JZ performed and analyzed data for the in vivo UgtP-His proteolysis assay in (Fig. 3C), cell measurements and membrane lipid TLC in (Fig. 6 and Table 1), Western blots of YFP-UgtP in (Additional file 1: Figure S1), Western blots to demonstrate differences in UgtP-His expression in (Additional file 7: Figure S7). JZ also designed the cell measurement experiment in (Fig. 6A and Table 1) and assisted in drafting the manuscript. PB performed, designed, and analyzed the in vitro His-UgtP proteolysis assay in (Fig. 5 and Additional file 6: Figure S6) including the purification of ClpXP and UgtP. PB also assisted in drafting the manuscript. AC constructed the hexose/uracil/oligomerization mutant forms of ugtP used in (Fig. 4 and Additional file 4: Figure S4). PAL helped design experiments and draft the manuscript. All authors read and approved the final manuscript.
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