- Open Access
Regulation of heterologous subtilin production in Bacillus subtilis W168
Microbial Cell Factories volume 21, Article number: 57 (2022)
Subtilin is a peptide antibiotic (lantibiotic) natively produced by Bacillus subtilis ATCC6633. It is encoded in a gene cluster spaBTCSIFEGRK (spa-locus) consisting of four transcriptional units: spaS (subtilin pre-peptide), spaBTC (modification and export), spaIFEG (immunity) and spaRK (regulation). Despite the pioneer understanding on subtilin biosynthesis, a robust platform to facilitate subtilin research and improve subtilin production is still a poorly explored spot.
In this work, the intact spa-locus was successfully integrated into the chromosome of Bacillus subtilis W168, which is the by far best-characterized Gram-positive model organism with powerful genetics and many advantages in industrial use. Through systematic analysis of spa-promoter activities in B. subtilis W168 wild type and mutant strains, our work demonstrates that subtilin is basally expressed in B. subtilis W168, and the transition state regulator AbrB strongly represses subtilin biosynthesis in a growth phase-dependent manner. The deletion of AbrB remarkably enhanced subtilin gene expression, resulting in comparable yield of bioactive subtilin production as for B. subtilis ATCC6633. However, while in B. subtilis ATCC6633 AbrB regulates subtilin gene expression via SigH, which in turn activates spaRK, AbrB of B. subtilis W168 controls subtilin gene expression in SigH-independent manner, except for the regulation of spaBTC. Furthermore, the work shows that subtilin biosynthesis in B. subtilis W168 is regulated by the two-component regulatory system SpaRK and strictly relies on subtilin itself as inducer to fulfill the autoregulatory circuit. In addition, by incorporating the subtilin-producing system (spa-locus) and subtilin-reporting system (PpsdA-lux) together, we developed “online” reporter strains to efficiently monitor the dynamics of subtilin biosynthesis.
Within this study, the model organism B. subtilis W168 was successfully established as a novel platform for subtilin biosynthesis and the underlying regulatory mechanism was comprehensively characterized. This work will not only facilitate genetic (engineering) studies on subtilin, but also pave the way for its industrial production. More broadly, this work will shed new light on the heterologous production of other lantibiotics.
The increasing threat of multidrug-resistant bacteria paired with a small number of emergency antibiotics and empty pipelines in research of new antimicrobials has prompted scientists to search for new antimicrobial agents to fight bacterial infections. In the line of research, a group of ribosomally-synthesized antimicrobial peptides (AMPs), called lantibiotics, has gained great attention as promising alternatives to classic antibiotics [1, 2]. Lantibiotics are characterized by the presence of lanthionine and methyllanthionine bridges [3, 4], and predominantly act against Gram-positive bacteria, including pathogenic organisms, such as methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE) . Many characteristics and chemical properties that lantibiotics hold, like low molecular weights, thermal and protease stability, no or very low toxicity, low tendency to generate resistance and low immunogenicity, render them suitable for potential applications in different healthcare-associated settings such as human and veterinary medicine, and biochemical, pharmaceutical, agricultural or food industries [6, 7]. The ribosomal pathway of lantibiotic biosynthesis also confers clear advantages for bioengineering (to generate variants with improved capability) over the non-ribosomally synthesized compounds because of the direct link between gene sequence and product [6, 8, 9].
Subtilin is a member of class I lantibiotics originally produced by Bacillus subtilis ATCC6633 and was the first lantibiotic produced by Bacillus strain to be described [10, 11]. It shares significant structural and functional similarities to nisin, which is the most prominent and to date the only lantibiotic that has been commercially used in food industry [2, 11]. As with nisin, subtilin shows antimicrobial activity in a nanomolar range against a broad spectrum of Gram-positive bacteria, such as Micrococcus luteus, Lactococcus spp. and Bacillus spp. [12, 13]. It docks on lipid II (an intermediate of cell wall biosynthesis), thus inhibiting bacterial growth, and the aggregation of subtilin-lipid II complex may also result in the permeabilization of the cytoplasmic membrane triggering cell lysis .
The genes involved in subtilin biosynthesis are organized in a gene cluster spaBTCSIFEGRK (spa-locus) (Fig. 1). The structural gene spaS encodes the subtilin precursor, which is subject to post-translational modification by SpaBC and export to the outside of the cell by SpaT [14, 15]. On the trans side of the membrane an N-terminal leader peptide is cleaved off the subtilin precursor by some of the proteases, such as AprE and WprA, produced by B. subtilis ATCC6633, generating the bioactive subtilin [16, 17]. The self-protection of the producing strain is mediated by immunity genes spaIFEG, in which the lipoprotein SpaI acts as subtilin-intercepting protein competing with the formation of subtilin-lipid II complexes, and the SpaFEG transporter expels bioactive subtilin from cell membrane, thus diminishing cell-associated subtilin and protecting the cell . Subtilin biosynthesis and immunity in B. subtilis ATCC6633 are under dual-control of the two-component system (TCS) SpaRK and the transition state regulator AbrB via the alternative sigma factor SigH which positively regulates spaRK expression. During the exponential growth phase, AbrB acts as a repressor of subtilin biosynthesis, and subtilin is basally expressed at a low level . At the end of the exponential phase, AbrB synthesis is repressed, followed by the derepression of SigH and thereby activation of TCS SpaRK. At a threshold concentration of extracellular subtilin, the lantibiotic acts as autoinducing molecule and activates SpaRK, which in turn initiates the transcription of spaIFEG, spaBTC and spaS through the activated response regulator SpaR [20,21,22].
These developments are encouraging for further subtilin study, however, the native producer B. subtilis ATCC6633 is not tractable for genetic modification. Thus, it would be of great advantage if the subtilin gene cluster were available in a strain that is both, amenable to genetic manipulation and suitable for industrial production. With this consideration, B. subtilis 168 strain that is one of the best-characterized Gram-positive model strains, appeared to be the most promising platform. B. subtilis 168 has been the focus of diverse research interest in academic and industrial settings, benefit from the ease of genetic manipulation because of its natural competence and the wealth of available physiological and biochemical data. The rapid growth rate, well-characterized protein secretion ability, excellent fermentation properties and the lack of toxic by-products render B. subtilis 168 indispensable for industrial applications [23,24,25]. B. subtilis 168 was previously explored as a heterologous subtilin producer by transformation with genomic DNA from B. subtilis ATCC6633 . Although subtilin producing transformants were isolated, the limited understanding of spa-locus at the time did not allow further investigation . More recently, van Tilburg et al. used the genome-minimized B. subtilis 168 strain PG10 (MiniBacillus PG10) as a host for subtilin production by introducing the structural gene spaS and modification genes spaBTC, instead of the whole spa-locus, into its genome . However, the lack of extracellular proteases in this strain, required for the maturation of subtilin, meant that additional in vitro proteolytic degradation steps were required to produce bioactive subtilin .
In this study, we sought to exploit B. subtilis W168 (a derivative strain of B. subtilis 168) as a robust workhorse for heterologous subtilin production by integrating the well-characterized subtilin gene cluster spa-locus into its chromosome . Systematic analysis using spa promoter-reporter (lux) fusions revealed the basal expression of spa genes in B. subtilis W168 and the control of subtilin biosynthesis by TCS SpaRK, which strictly relied on subtilin molecule itself for autoregulation. More importantly, we found that AbrB in B. subtilis W168 is a strong inhibitor of subtilin biosynthesis, and its deletion remarkably enhanced the yield of bioactive subtilin to a comparable level as in the native producer B. subtilis ATCC6633. Surprisingly, AbrB was found to regulate subtilin expression in a distinct manner from that found in B. subtilis ATCC6633 . Furthermore, we also developed “online” reporters by incorporating the subtilin-producing system (spa-locus) and subtilin-reporting system (PpsdA/PliaI-lux) together in B. subtilis W168 to monitor the dynamics of subtilin biosynthesis.
Subtilin genes are basally expressed in B. subtilis W168
To get an idea of how spa-locus expression and thereby subtilin production will behave in B. subtilis W168, firstly the basal expression of the spa promoters PspaI, PspaB, PspaS and PspaR was investigated. The four promoter fragments were amplified using the genome DNA of B. subtilis ATCC6633 as template and the primer pairs listed in Additional file 1: Table S3. All of the putative regulatory elements within the promoters based on previous studies have been included [19, 20, 22]. The respective promoter was fused to a luxABCDE cassette as a reporter of promoter activity and integrated into the sacA locus of B. subtilis W168 chromosome (Additional file 1: Table S1). A promoterless Pempty-lux fusion was used as control for background activity of the luciferase.
Three of the promoters, PspaB, PspaS and PspaR, displayed basal activities at different levels (Fig. 2A). PspaR exhibited the strongest activity (26-fold) compared to the control. PspaS and PspaB showed weaker activity with, respectively, 4.7- and 2-fold changes compared to the control. However, no detectable basal activity was observed for PspaI under these conditions. The differing activities of the spa promoters in absence of subtilin was first time reported in our study, in particular the high activity of PspaR. To examine whether the presence of spa-locus would affect the promoter activity in B. subtilis W168, the promoters were further measured in B. subtilis W168 carrying spa-locus, respectively, which revealed the virtually identical behavior of spa promoters in the presence and absence of spa-locus (Additional file 2: Fig. S1). The results suggest that subtilin biosynthesis genes can be basally expressed in B. subtilis W168 even when subtilin molecules are absent. The dynamics of the promoter activity along the cell growth was consistent with the findings that had been observed previously in B. subtilis ATCC6633, i.e., spa promoters were activated at mid-exponential growth phase and reached the maximum activity at the transition point into the stationary growth phase followed by gradually decreasing activity  (Additional file 2: Fig. S2A).
AbrB significantly represses subtilin gene expression in B. subtilis W168
AbrB as a pleiotropic transition state regulator regulates many post-exponentially expressed events, such as antibiotic production and sporulation in B. subtilis . SigH is an alternative sigma factor representing a typical regulator of late-growth activities [29, 30]. The transcription of sigH is under negative control of AbrB, whose synthesis in turn is repressed by Spo0A [31, 32]. In B. subtilis ATCC6633, subtilin biosynthesis is regulated by AbrB via SigH that activates the expression of spaRK .
To unveil the regulation of subtilin expression by AbrB and SigH in B. subtilis W168, abrB and sigH were individually deleted in the strains carrying the different spa promoter-lux fusions. As shown in Fig. 2B, the absence of abrB remarkably enhanced the activity of spa promoters, especially PspaB and PspaS, showing over 60-fold and 16-fold increased activity, respectively. PspaI and PspaR were up-regulated at lower levels compared to PspaB and PspaS. Notably, the effect of AbrB mutation on subtilin gene expression could be observed already in early exponential phase (Additional file 2: Fig. S2B), suggesting a significant repression of AbrB on subtilin biosynthesis during the exponential growth phase.
Unexpectedly, the deletion of SigH did not affect the activity of spa promoters, with the exception of PspaB whose activity was decreased by 2.85-fold (Fig. 2C). The result indicates that, unlike its role as activator of PspaR in B. subtilis ATCC6633, SigH of B. subtilis W168 appeared to solely regulate PspaB. In addition, inactivation of spo0A led to an overall decrease of spa promoter activity by 1.3- to 2.2-fold (Fig. 2D). Presumably, the lack of Spo0A derepressed abrB, which resulted in higher levels of AbrB and consequentially stronger repression of spa gene expression.
SigH solely regulates the expression of spaBTC
The regulatory cascade between SigH, AbrB and Spo0A is clear as mentioned above, but could it be possible that they somehow regulate subtilin gene expression independently of each other, especially with respect to their influence on PspaB? To answer this question, double mutants of ΔabrB ΔsigH and ΔabrB Δspo0A harboring different spa promoter-lux fusions were generated. The response of the spa promoters in the regulator double mutation backgrounds was compared with that in the respective single mutants. As shown in Fig. 3A, PspaI, PspaS and PspaR displayed an identical behavior in the ΔabrB ΔsigH double mutant as in ΔabrB single mutant, suggesting that these three promoters are regulated by AbrB but are independent of SigH. Different from the scenario, the SigH of B. subtilis ATCC6633 directly and only regulates PspaR . In contrast, PspaB again appeared to be an exception by showing obviously lower activity in ΔabrB ΔsigH double mutant than in the ΔabrB single mutant. Additionally, compared to that in wild type, PspaB activity in ΔabrB ΔsigH was still elevated (Fig. 3C). The data suggest that SigH only plays a role in positively regulating PspaB and that AbrB acts as a repressor of sigH in this pathway. However, this does not appear to be the only way in which AbrB regulates PspaB, otherwise PspaB should have shown identical activity in ΔabrB ΔsigH as in ΔsigH. Instead, while deletion of sigH alone led to a marked decrease in PspaB activity, additional deletion of abrB caused an increased activity above wild-type levels, but below those of the abrB single mutant (Fig. 3C). Based on the results, we therefore propose two possible pathways of regulation on PspaB: (I) the regulation by AbrB without the involvement of SigH in between and (II) the regulation by AbrB via SigH.
Furthermore, all spa promoters showed identical behavior in ΔabrB Δspo0A double mutant as in the ΔabrB single mutant (Fig. 3B). This was not surprising, as it confirmed that Spo0A acts upstream of AbrB as a repressor of the abrB gene. Thus, any effect caused by spo0A deletion can be bypassed when abrB gene is deficient. Taken together, the results demonstrate that AbrB regulates subtilin gene expression independently of SigH (except for PspaB) in B. subtilis W168, presenting a distinct regulatory scenario from the regulation of subtilin gene expression by AbrB via SigH in B. subtilis ATCC6633 . Moreover, SigH of B. subtilis W168 solely acted as a positive regulator of spaBTC expression.
Autoregulation of subtilin biosynthesis via two-component system SpaRK
In addition to growth phase-dependent expression, subtilin biosynthesis is also regulated via the two-component regulatory system SpaRK in B. subtilis ATCC6633 . Upon sensing extracellular subtilin at a critical concentration, membrane-spanning SpaK is activated and transfers the signal to the intracellular response regulator SpaR through a phosphorylation cascade. Activated SpaR subsequently binds to target promoters (PspaI, PspaB and PspaS) and initiates gene transcription of subtilin biosynthesis and self-immunity. Subtilin production thereby generates an auto-induction loop that ensures a massive and collective response in the cell community. This process is also termed quorum-sensing, a strategy of cell-to-cell communication generally found in bacteria .
To verify this auto-regulatory mechanism of subtilin biosynthesis in B. subtilis W168, spaRK, encoding the TCS SpaRK, was fused to the xylose-inducible promoter PxylA and integrated into the genome of B. subtilis W168 carrying different spa promoters. The results show that in the absence of subtilin, overexpression of spaRK did not induce the spa promoters under any given conditions, while the addition of subtilin triggered a dramatic activation of PspaI (800-fold), PspaB (311-fold) and PspaS (283-fold), but not PspaR, as shown in Fig. 4A. The data substantiate that the TCS SpaRK mediates the regulatory circuit of subtilin biosynthesis and immunity in B. subtilis W168 and strictly relies on subtilin as autoinducer, but SpaRK does not regulate the expression of its own encoding operon.
It has been reported that overproduction of a TCS response regulator alone can enable its activity, including the OmpR and PhoP of E. coli which belong to the same subfamily of response regulator as SpaR [33,34,35,36,37,38]. To investigate if SpaR alone is sufficient to regulate spa gene expression in B. subtilis W168, spaR was placed under control of the xylose-inducible promoter PxylA and integrated into the genome of B. subtilis W168 strains carrying different spa promoters. However, results indicate that overexpression of SpaR alone in B. subtilis W168 was not sufficient to activate spa promoters in any given conditions (Fig. 4B). This suggests that the histidine kinase SpaK is indispensable for the regulatory function of the TCS SpaRK in subtilin biosynthesis in B. subtilis W168.
Subtilin produced by B. subtilis W168 shows antimicrobial activity
With the understanding of the regulatory mechanism of subtilin biosynthesis, the subtilin gene cluster (spa-locus) from B. subtilis ATCC6633 strain was transferred into B. subtilis W168 by integration into the amyE locus of its chromosome. Given the strong repression of AbrB on subtilin gene expression, abrB was deleted in B. subtilis W168 carrying the spa-locus to examine the actual impact of AbrB on subtilin production, as well as sigH and spo0A.
“Spot-on-lawn” assays were exploited to efficiently evaluate subtilin production. The reporter strain (TMB1617, PliaI-lux) mixed with soft agar was grown on LB plate as “Lawn”, on which the potential subtilin-producing strains were spotted (Fig. 5B). The reporter strain contains the subtilin-sensitive promoter PliaI fused to the lux cassette (Fig. 5A). In the presence of antimicrobially active subtilin, the TCS LiaRS, encoded in the liaIHGFSR operon of B. subtilis W168, is activated through a “damage-sensing” mechanism, which consequentially induces PliaI and the expression of the reporter gene [39, 40]. Thus, the output of bioluminescence at defined time points during the growth course can be indicative of the production of bioactive subtilin.
As shown in Fig. 5C, B. subtilis W168 containing the spa-locus and abrB deletion (TMB3044) produced a comparable amount of active subtilin compared to the positive control (B. subtilis ATCC6633). However, the presence of AbrB strongly inhibited subtilin biosynthesis, as evidenced by the rather weak luminescence signal displayed by the strain TMB3039 containing the wild type abrB gene. No detectable bioluminescence was observed from TMB3057 (B. subtilis W168 spa ΔsigH) and TMB3052 (B. subtilis W168 spa Δspo0A), consistent with the negative effect of sigH and spo0A deletion on subtilin expression explained above. For both TMB3044 (red arrow in Fig. 5C) and B. subtilis ATCC6633 (blue arrow in Fig. 5C), the luminescence signal was detected as early as the 6th hour of growth. The signal intensity gradually increased to a maximum level and sustained for several hours, followed by a gradually decrease in intensity. Notably, the luminescence signal of TMB3044 reached the maximum level earlier than the signal of B. subtilis ATCC6633 (Fig. 5C). Please note that due to the auto-induction of PliaI promoter at the transition point into stationary growth phase , the plate at the 10th and 12th hour of incubation showed a strong background luminescence signal elicited by the “Lawn”. Taken together, the results nicely demonstrate that B. subtilis W168 is compatible with the heterologous subtilin gene cluster and can produce a promising amount of bioactive subtilin when the repressor AbrB is absent.
Quantification and the antimicrobial activity of heterologous subtilin production
Following the preliminary evaluation of subtilin production on solid media, next the subtilin production in liquid was quantified. Here, TMB3044 (W168 spa ΔabrB) was chosen as the most potent B. subtilis W168 subtilin producer, and B. subtilis ATCC6633 strain was used as positive control. Three different growth media: (I) 100% LB, (II) 100% Medium A and (III) mixed medium (50% LB + 50% Medium A) were tested to find the best condition for subtilin production in B. subtilis W168. Samples of the growing TMB3044 and B. subtilis ATCC6633 strains were collected at defined time points and filtered to obtain cell-free subtilin supernatants, which were then evaluated for their ability to induce the reporter strain TMB1617 (PliaI-lux) in microplate reader assays. The activity at the strongest point of induction, as shown in the luminescence curve in Additional file 6: Fig. S5, for each supernatant was depicted in Fig. 6 (left panel) to represent the bioactive subtilin production over the growth.
As shown in Fig. 6 (left panel), TMB3044 was able to produce an amount of bioactive subtilin in both mixed medium and Medium A that was similar to the subtilin amount of B. subtilis ATCC6633 growing in Medium A (positive control). Mixed medium was deemed most suitable for TMB3044 given that subtilin was produced earlier and the maximum production sustained longer than in Medium A alone. No detectable subtilin production was obtained in LB culture (Additional file 7: Fig. S6) indicating that some ingredients contained in Medium A were crucial for subtilin biosynthesis. Moreover, the dynamics of subtilin biosynthesis in TMB3044 cultivated in mixed medium (Fig. 6A, left panel) and B. subtilis ATCC6633 in Medium A (Fig. 6D, left panel) was consistent with that observed from the “spot-on-lawn” assay, i.e., subtilin was produced earlier by TMB3044 than by B. subtilis ATCC6633 and the former reached the maximum of subtilin production more rapidly.
In addition, supernatant samples were tested for their antimicrobial activity against a range of Gram-positive bacteria, including Micrococcus luteus, Staphylococcus aureus and wild type B. subtilis W168, and Gram-negative bacteria including Escherichia coli and Pseudomonas aeruginosa. To do so, the bacterium to be tested was mixed with soft agar and spread on LB plate as “lawn”. Subtilin supernatants were spotted directly on top. The growth inhibition zones indicate the antimicrobial activity of the corresponding subtilin supernatant. The supernatant samples collected from B. subtilis ATCC6633 at the 20th hour of growth in Medium A were used as positive controls. Figure 6 (right panels) shows the results of the growth inhibition assays using M. luteus as the indicator strain. Intriguingly, the antimicrobial activity of subtilin supernatant was shown in good correlation with their corresponding ability to induce the PliaI-reporter strain. Importantly, the supernatants produced by TMB3044 that triggered the same degree of PliaI induction as B. subtilis ATCC6633 samples also triggered the same degree of antibacterial activity as B. subtilis ATCC6633. Furthermore, the antimicrobial activity against other Gram-positive bacteria was also observed, yet to a lesser degree (Additional file 8: Fig. S7). However, not surprisingly, subtilin production was not active against Gram-negative bacteria (data not shown), due to predominantly the outer membrane barrier which bars subtilin from reaching its target lipid II [13, 42].
“Online” monitoring the dynamic of subtilin production
Although manually collecting cell culture along the growth is generally practical to examine the time course of subtilin biosynthesis, no doubt it is labor-demanding and time-consuming. Therefore, the so-called “online” reporters that combine the subtilin-producing system (spa-locus) and subtilin-reporting system (PpsdA-lux/PliaI-lux) within one strain were developed to improve the efficiency of monitoring the dynamics of subtilin production. With this, the subtilin molecule secreted outside of the cell is sensed by the reporter system immediately, fulfilling real-time production detection. In this setting, the PpsdA promoter, which can be induced by AMPs such as nisin and subtilin [43, 44], was chosen in addition to PliaI for the construction of a subtilin-reporting system. Similar to PliaI, the activation of PpsdA relies on TCS-mediated signal transduction, which in this case is the PsdRS TCS (as depicted in Fig. 7A). The “online” reporter strains were evaluated in three different growth conditions, 100% LB, 100% Medium A and mixed medium (50% LB + 50% Medium A), using a microplate reader (please refer to Material and Methods for details of the assay). The results from PpsdA-based “online” reporters were presented here because they produced a better response behavior to subtilin than the PliaI-based reporters (Additional file 9: Fig. S8).
As shown in Fig. 7B (bottom panels), TMB5439 (B. subtilis W168 PpsdA-lux spa ΔabrB, green curves) displayed an induction signal at the transition point to stationary phase in both LB and mixed medium conditions, indicating detectable subtilin production at that point. Notably, the induction increased rapidly to the maximum level, especially in mixed medium (~ 233-fold change within 80 min), which could be a result of the quorum-sensing mechanism of subtilin biosynthesis mediated by TCS SpaRK, leading to a positive feedback on subtilin production . In contrast, TMB4261 (W168 PpsdA-lux spa) that contains native AbrB did not show induction in any cases, showing again that the presence of AbrB strongly inhibited subtilin biosynthesis. Likewise, no activity of PpsdA was elicited in TMB5488 (W168 PpsdA-lux ΔabrB), i.e., a strain lacking the spa locus, which ruled out that the induction of PpsdA activity in strain TMB5439 was caused by abrB deletion.
Induction of subtilin production includes the production of the immunity system (SpaIFEG), whose role it is to diminish cell-associated subtilin . It was therefore conceivable that the removal of subtilin by SpaIFEG interfered with detection by the PsdRS-based reporter system. In a next step, we therefore tried to enhance the sensitivity of the “online” reporter by inactivating the immunity genes spaIFEG. As indicated in black lines in Fig. 7B, the deletion of spaIFEG from TMB5739, resulting in TMB5423 strain (B. subtilis W168 PpsdA-lux spa ΔabrB ΔspaIFEG), increased the induction level compared to that in TMB5739. The induction also appeared earlier around the mid-exponential phase, indicating that subtilin was already present in the culture at that time point, but had previously been masked by the activity of SpaIFEG. Indeed, deficiency of the immunity system in TMB4261 could convert this strain (TMB5721, PpsdA-lux spa ΔspaIFEG, orange curves) into a functional reporter strain in mixed medium despite the presence of AbrB, and the induction was strikingly comparable with that in TMB5723 (black curve). The data suggest that TMB4216 indeed produces subtilin, however the activity of the immunity system SpaIFEG made the small amount of subtilin inaccessible to the sensor of the reporter system, thus failing to produce a detectable signal. The functionality of TMB5721 in mixed medium but not in LB, which was also shown from PliaI-based “online” reporters (Additional file 9: Fig. S8), highlights again the crucial role of Medium A for subtilin biosynthesis. In summary, the concept of incorporating subtilin-producing and -reporting systems in one strain was successfully substantiated by the development of efficient “online” reporters to monitor the dynamics of subtilin biosynthesis.
In the present study, the Gram-positive model organism B. subtilis W168 was successfully modified as subtilin producer by integrating the subtilin gene cluster (spa-locus) into the genome. The transition state regulator AbrB acted as a strong repressor of subtilin biosynthesis in B. subtilis W168. A B. subtilis W168 strain carrying the spa-locus and abrB mutation produced comparable yields of bioactive subtilin as the native producer B. subtilis ATCC6633. However, unlike the AbrB in B. subtilis ATCC6633, which represses subtilin biosynthesis via SigH, which in turn positively regulates spaRK , AbrB in B. subtilisW168 regulates the majority of spa genes in a SigH-independent manner, showing particularly strong control over spaS, encoding the subtilin prepeptide. Expression of spaBTC, which encode proteins involved in post-translational modification and export of the prepeptide, is significantly controlled by AbrB without the involvement of SigH, while additionally it is also positively regulated by SigH with AbrB acting upstream as a repressor of sigH, which turned out to be the only role of SigH in subtilin biosynthesis in B. subtilis W168 (Fig. 8).
The results showed that subtilin genes are basally expressed in a growth phase-dependent manner in B. subtilis W168 even when subtilin is absent and cannot trigger the auto-inducing loop. Notably, the four transcriptional units contained in the spa-locus are expressed at different basal levels in the order, spaIFEG < spaBTC < spaS < spaRK. This observation is consistent with the behavior of PspaI, PspaB and PspaS reported in B. subtilis ATCC6633 [19, 46], while the dynamics of PspaR was for the first time characterized here. As a regulatory system controlling the other three transcriptional units, the high basal expression of SpaRK may enable cells to rapidly respond to the accumulated subtilin in the extracellular space, which most likely indicates high cell densities and thus upcoming adverse living conditions in which subtilin production may provide a competitive advantage for survival. The higher amount of subtilin precursor (encoded by spaS) than the machinery (encoded by spaBTC) for its post-transcriptional modification and export represents a cost-efficient strategy ensuring the amount of substrate exceeds the amount of enzyme. The immunity system-encoding spaIFEG shows very low basal expression, which again may be an energy-saving strategy, as immunity is not required unless subtilin concentrations in the environment increase, at which point the auto-induction loop via SpaRK will ensure sufficient immunity gene expression to provide protection.
Subtilin biosynthesis, i.e., the transcription of spaIFEG, spaBTC and spaS is additionally regulated by the TCS SpaRK, which strictly relies on subtilin peptide as inducer to fulfill the autoregulatory circuit. Furthermore, the three corresponding promoters exhibited distinct responsiveness to the activated response regulator SpaR with PspaI, PspaB and PspaS strikingly induced by ~ 800-fold, ~ 312-fold and ~ 284-fold by SpaR, respectively. This depicts that the cell, once the auto-induction circuit (via SpaRK) is triggered, can quickly adjust the rest of the Spa system. It massively ramps up immunity to ensure protection, and also increases production of the modification machinery to keep up with modifying the concurrently increased level of pre-peptide.
Intriguingly, the remarkable induction behavior of PspaI and its very low basal expression may provide an alternative and more robust setup for the SURE (Subtilin-Regulated Expression) system, which was originally developed based on PspaS and SpaRK controlled by its native promoter PspaR for protein expression in B. subtilis W168 [44, 47]. Furthermore, it should be noted that overproduction of SpaR in B. subtilis W168 alone was not sufficient to activate subtilin gene expression. This is in contrast to a previous study in which it was shown that overproduction of SpaR in Bacillus subtilis MO1099 (also a derivative of B. subtilis 168) could induce subtilin gene expression . Furthermore, overexpression of a TCS response regulator alone to fulfill its functionality seems to be an abundant phenomenon [33,34,35,36,37]. The reason for the infeasibility of SpaR in B. subtilis W168 here is unclear, except for the observed difference regarding the overexpression methods. In this study spaR was encoded in the genome of B. subtilis W168, while in other cases spaR was overexpressed from high-copy number plasmid.
Following establishment of the individual components governing heterologous subtilin production, an “online” reporter tool that combines the producing system (spa-locus) and reporter system (PpsdA/PliaI-lux) in one strain was developed, which can efficiently and easily monitor the dynamic of subtilin biosynthesis. Importantly, the concept employed here may trigger further strategies for tracking the biosynthesis of many AMPs or antibiotics, if the corresponding reporting systems have been characterized.
In summary, this study reported for the first time the successful heterologous expression of the lantibiotic subtilin in the model organism B. subtilis W168 via integrating the complete spa-locus into the genome. The regulatory network of subtilin biosynthesis in this host was systematically characterized. The establishment of B. subtilis W168 as a platform for subtilin expression will facilitate future genetic (engineering) research on subtilin, as well as pave the way for the industrial consideration of subtilin production. Moreover, the concept employed here will likely be applicable to the study of other lantibiotics and ribosomally synthesized AMPs, especially for those the genetic manipulation in their native producers is still a bottleneck to fulfill in-depth research.
Materials and methods
Bacterial strains and growth conditions
Bacterial strains used in this study were routinely grown in Lysogeny Broth (LB) (1% (w/v) tryptone, 0.5% (w/v) yeast extract and 1% (w/v) NaCl) at 37 °C or 30 °C for M. luteus with agitation. The subtilin-producing strain B. subtilis ATCC6633 was cultivated in high sucrose Medium A . It contains (per liter) 100 g of sucrose, 11.7 g of citric acid, 4 g of Na2SO4, 4.2 g of (NH4)2HPO4, 5 g of yeast extract, 100 mL of a salt mixture (7.62 g of KCl, 4.18 g of MgCl2 × 6H2O, 0.543 g of MnCl2 × 4H2O, 0.49 g of FeCl3 × 6H2O, and 0.208 g of ZnCl2 in 1 L of H2O), and sufficient NH4OH to bring the pH to 6.8–6.9 per liter. All solid media additionally contained 1.5% (w/v) agar or 0.75% (w/v) for soft agar. MNGE medium was used for B. subtilis transformation . Selective media for B. subtilis contained kanamycin (10 µg mL−1), chloramphenicol (5 µg mL−1), spectinomycin (100 µg mL−1), tetracycline (12.5 µg mL−1) or erythromycin (1 µg mL−1) combined with lincomycin (25 µg mL−1) for MLS, accordingly. Selective media for E. coli contained kanamycin (50 µg mL−1), chloramphenicol (35 µg mL−1) or ampicillin (100 µg mL−1). All strains used in this study are listed in Additional file 1: Table S1.
DNA manipulation and plasmid construction
General cloning procedure, such as PCR, restriction enzyme digestion and ligation, was performed with enzymes and buffers from New England Biolabs® (NEB, Ipswich, MA, USA) according to the respective instructions. Q5® High-Fidelity DNA polymerase was used for PCRs in case the resulting fragment was further used. Otherwise OneTaq® was the polymerase of choice. PCR-purification was performed using the Hi Yield® PCR Gel Extraction/PCR Clean-up Kit (Süd-Laborbedarf GmbH (SLG), Gauting, Germany). Plasmid preparation was performed using the Hi Yield® Plasmid Mini-kit except for plasmids larger than 10 kb which required the method of alkaline lysis extraction. The E. coli competent cells were chemically prepared and transformed using the standard heat-shock method . All the resulting constructs were verified by sequencing. B. subtilis transformation was performed as described previously . Successful integration of plasmids into the B. subtilis genome was confirmed via colony PCR or on starch plates in the case of amyE locus integration events.
To create the integrative plasmid pBS1C-spaBTCSIFEGRK, the whole spa-locus spaBTCSIFEGRK (GenBank: U09819.1) was first amplified from the genomic DNA of B. subtilis ATCC6633 strain using primers TM4030 and TM3973. The blunt-ended PCR product of spa-locus was then purified and cloned into pCR™-Blunt II-TOPO® vector according to the instruction of Zero Blunt® TOPO® PCR Cloning Kit (Life Technologies). Afterwards, the resulting plasmid pTOPO-spaBTCSIFEGRK was cut using type IIS endonuclease AarI to obtain spa-locus fragment with EcoRI-compatible overhang at the one end and SpeI-compatible overhang at the other end, which was then ligated into vector pBS1C cut with EcoRI and SpeI to generate pBS1C-spaBTCSIFEGRK. The pBS1C is one of the empty vectors in the B. subtilis BioBrick Box and allows the fragment to be integrated into the amyE locus of B. subtilis genome .
To generate the set of spa promoter-lux fusions, the spa promoters were amplified from the genomic DNA of B. subtilis ATCC6633 using respective primer pairs and cloned into pBS3Clux, a reporter vector in the B. subtilis BioBrick Box . The xylose-inducible promoter PxylA was fused to spaRK (spaR) in the pBS2E vector which allows the integration of the fragment into the lacA locus of B. subtilis genome . The vectors and the details of plasmid construction are described in Additional file 1: Table S2. Oligonucleotides are given in Additional file 1: Table S3.
Collection of subtilin-containing supernatant
To prepare subtilin-containing supernatant which was used as inducer across the experiments, 25 mL Medium A was inoculated with a single colony of B. subtilis ATCC6633 and grown at 37 °C with agitation. The culture was collected after 24 h of cultivation and centrifuged at 10,000 rcf for 15 min. The supernatant was then sterilized by filtration using 0.45 µm membrane filter (Sarstedt, Germany) and stored at − 20 °C until use.
The heterologous subtilin production in B. subtilis W168 was evaluated in three different kinds of media, 100% LB, 100% Medium A and 50% LB + 50% Medium A. The overnight culture of tested strains was diluted 1:1000 into 25 mL of the respective medium. During the cultivation at 37 °C with agitation, 1 mL of the culture was collected every 2 h up to 20 h and subsequently in longer intervals every four hours until 32 h. All the culture samples were filtered using 0.45 µm membrane filter and stored at − 20 °C until use.
The luciferase activity of B. subtilis reporter strains carrying luxABCDE operon was assayed using a Synergy™ NEO multi-mode microplate reader from BioTek® (Winooski, VT, USA). The reader was controlled by the software Gen5™ (Version 2.06). Luminescence assays were carried out as followed: 10 mL LB medium (w/o antibiotics) were inoculated 1:1000 from overnight cultures (grown with respective antibiotics) and grown to OD600 of 0.2–0.3. Then, day cultures were diluted to an OD600 of 0.01 and 200 µL were transferred into the wells of a 96-well plate (black wall, clear bottom; Greiner Bio-One, Frickenhausen, Germany). The program was set up for incubation of the plate at 37 °C with agitation (intensity: medium) and the OD600 as well as the luminescence was recorded every 5 min for at least 18 h. Luciferase activity (RLU/OD600) was defined as the raw luminescence output (relative luminescence units, RLU) normalized to OD600 corrected by medium blank at each time point.
If needed, after one hour of incubation, the cells were induced with up to 5 µL of inducer with subtilin supernatant (0.75% (v/v) final concentration) and/or xylose (0.5% (w/v) final concentration). The control samples were treated with the same amount of sterile water. For the “online” reporters, overnight cultures were directly diluted to OD600 of 0.01 for luminescence assay without day cultures.
For this assay, standard LB agar plates were covered with 3.5 mL LB soft agar mixed with 120 µL overnight culture of the reporter strain (as “lawn”) and dried for around 20 min under sterile condition. Afterwards, 6 µL of the overnight culture of the strains (as “spot”) to be tested were spotted on the top of the “lawn” and incubated at 37 °C. Luminescence was evaluated every two hours up to 12 h and subsequently in longer time intervals using a chemiluminescence imaging system FUSION™ (peqlab, VWR International GmbH, Erlangen, Germany). The exposure time was set to 10 min, the aperture was fixed to 0.95 and the full resolution mode was used.
Growth inhibition experiments
To test the antimicrobial activity of subtilin-containing supernatant, the Gram-positive bacteria, B. subtilis W168, M. luteus and S. aureus, and Gram-negative bacteria E. coli and P. aeruginosa were the choices of indicator strains. Standard LB agar plates (square, 10 × 10 cm) were overlaid with 6 mL LB soft agar mixed with 200 µL of the overnight culture of the indicator strain, respectively. Afterwards, 6 µL of subtilin supernatants, harvested from potential subtilin-producing B. subtilis W168 variants and B. subtilis ATCC6633 strain growing in different media, were spotted on the surface of the indicator strain layer. Subsequently, the plates were incubated at 37 °C except for the ones with M. luteus which requires 30 °C. The inhibition zone shown indicates the antimicrobial activity of subtilin supernatant.
Availability of data and materials
All the data generated and analyzed during this study are included in the manuscript and its Additional files.
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Additional file 1: Table S1
. Bacterial strains used in this study. Table S2. Plasmids used in this study. Table S3. Oligonucleotides used in this study
Additional file 2: Fig. S1
. Activity of spa promoters in absence and presence of spa-locus in B. subtilis W168. A represents the dynamics of spa promoter activity in the absence and presence of spa-locus in B. subtilis W168 along growth. B represents the response of spa promoters to the addition of extra subtilin supernatant in both conditions, showing the existing of spa-locus in the strain which caused the SpaRK-mediated autoregulation of subtilin biosynthesis. The color code of the strains is shown on the right side of the respective figure. Luciferase activity was defined as relative luminescence units (RLU) per OD600 (RLU/OD600). The mean values and standard deviations (error bars) of at least replicate measurements are shown.
Additional file 3: Fig. S2
. Activity of spa promoters in wild type B. subtilis W168 and single mutants. A, B, C and D represent the dynamics of spa promoter activities in wild type B. subtilis W168, ΔabrB, ΔsigH, and Δspo0A mutants, respectively, in the absence of subtilin. Each of them contains the growth curves on the top, luminescence curves in the middle and the bar graph (as Fig. 2) at the bottom representing the peak luciferase activity shown in each strain. (The following description also applies to Fig. S3, Fig. S4 and Fig. S5) Luciferase activity was defined as relative luminescence units (RLU) per OD600 (RLU/OD600). The color code of each strain in each panel is depicted at the right side of the growth curves, respectively. The graphs show mean values and standard deviations (error bars) of at least triplicate measurements.
Additional file 4: Fig. S3
. Activity of spa promoters in B. subtilis W168 double mutants. A and B represent the dynamics of spa promoter activities in W168 ΔabrB ΔsigH and W168 ΔabrB Δspo0A double mutants, respectively, in the absence of subtilin. Each of them contains the growth curves on the top, luminescence curves in the middle and the bar graph (as Fig. 3) at the bottom representing the peak luciferase activity in each strain.
Additional file 5: Fig. S4
. Regulation of the two-component system (TCS) SpaRK on subtilin biosynthesis. A and B represent the dynamics of spa promoter activities in B. subtilis W168 PxylA-spaRK and B. subtilis W168 PxylA-spaR under different treatment conditions (untreated, treated with xylose and treated with both xylose and subtilin), respectively. PxylA indicates a xylose-inducible promoter. Each of them contains the growth curves on the top, luminescence curves in the middle and the bar graph (as Fig. 4) at the bottom representing the peak luciferase activity in each strain.
Additional file 6: Fig. S5
. Quantification of subtilin production. The subtilin supernatants collected from TMB3044 (W168 spa ΔabrB) and subtilin native producer B. subtilis ATCC6633 at defined time points of growth as indicated at the right side of the growth curves were tested using reporter strain TMB1617 (PliaI-lux). Mixed medium (50% LB + 50% Medium A) and Medium A were used for the cultivation, respectively, for both strains. The subtilin supernatant was added to the cell culture after 1 hour of growth in a microplate reader. Each of the A, B, C and D contains the growth curves on the top, luminescence curves in the middle and the bar graph (as Fig. 6) at the bottom representing the peak luciferase activity triggered by corresponding subtilin supernatant.
Additional file 7: Fig. S6
. Evaluation of subtilin production of TMB3044 cultured in LB medium. The subtilin supernatants collected at defined time points from TMB3044 (W168 spa ΔabrB) cultured in LB medium were tested using reporter strain TMB1617 (PliaI-lux). Control (-) indicates instead of subtilin supernatant the reporter strain was treated with the same volume of sterile water. Control (+) as the positive control was treated with 0.75% subtilin supernatant collected from B. subtilis ATCC6633 at the 20th hour of growth in Medium A. The upper panel shows the growth curves of the reporter stain under different treatments, and the bottom panel represents the luminescence curves under the corresponding treatments. The graphs show mean values and standard deviations (error bars) of three biological replicates
Additional file 8: Fig. S7
. Antimicrobial activity of subtilin against G+ bacteria S. aureus and B. subtilis W168. The same subtilin supernatant used in Fig. 6 were applied here, including the subtilin supernatant collected from TMB3044 (W168 spa ΔabrB) and B. subtilis ATCC6633 strain growing in mixed medium (50% LB + 50% Medium A), and 100% Medium A at defined time points as labeled on the top left plate in red. The control (indicated as C) was the subtilin supernatant collected from B. subtilis ATCC6633 at the 20th hour of growth in Medium A.
Additional file 9: Fig. S8
. “Online” monitoring the subtilin biosynthesis in B. subtilis W168 (PliaI-lux as the reporting system). The rationale of the response of PliaI to subtilin is given in Fig. 7A. “Online” reporters were examined in LB and mixed medium (50% LB + 50% Medium A), respectively. The genetic background and color-code of the strains are given at the bottom of the figure. The red arrows marked in luminescence graphs indicate the point where the induction starts in TMB5722 strain, while the corresponding arrow in the growth curve indicates the growth situation at the same time point. The mean of at least three replicates is shown with the error bars indicating the standard deviations.
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Zhang, Q., Kobras, C.M., Gebhard, S. et al. Regulation of heterologous subtilin production in Bacillus subtilis W168. Microb Cell Fact 21, 57 (2022). https://doi.org/10.1186/s12934-022-01782-9
- Lantibiotic subtilin
- Heterologous expression
- Bacillus subtilis W168
- Biosynthesis regulation
- Two-component system (TCS)
- Transition state regulator AbrB