SUMMARY
Extracytoplasmic function (ECF) sigma factors are a major class of environmentally-responsive transcriptional regulators. In Alphaproteobacteria the ECF sigma factor, σEcfG, activates general stress response (GSR) transcription and protects cells from multiple stressors. A phosphorylation-dependent protein partner switching mechanism, involving HWE/HisKA_2-family histidine kinases, underlies σEcfG activation. The identity of these sensor kinases and the signals that regulate them remain largely uncharacterized. We have developed the aerobic anoxygenic photoheterotrophic (AAP) bacterium, Erythrobacter litoralis DSM 8509, as a comparative genetic model to investigate GSR regulation. Using this system, we sought to define the contribution of visible light and a photosensory HWE kinase, LovK, to GSR transcription. We identified three HWE kinases that collectively regulate GSR: gsrK and lovK are activators, while gsrP is a repressor. GSR transcription is higher in the dark than light, and the opposing activities of gsrK and gsrP are sufficient to achieve light-dependent differential transcription. In the absence of gsrK and gsrP, lovK alone is sufficient to regulate GSR transcription in response to light. This regulation requires a photochemically active LOV domain in LovK. Our studies establish a role for visible light and HWE kinases in light-dependent regulation of GSR transcription in E. litoralis, an AAP species.
ABBREVIATED SUMMARY General stress response (GSR) systems protect bacteria from a diverse range of physical and chemical stressors. We have developed Erythrobacter litoralis as a new genetic model to study GSR in Alphaproteobacteria and show that three HWE-family histidine kinases collectively regulate GSR transcription via σEcfG. Visible light is a GSR regulatory signal in E. litoralis, and LovK is a blue-light photosensor kinase that functions as a dark activated GSR regulator.
INTRODUCTION
LOV-HWE kinases: An overview
Light is a ubiquitous environmental factor that provides energy to support life in many ecosystems. Multiple adaptive responses to light have evolved in bacteria including phototaxis and photoavoidance, photoprotective pigment production, and the regulation of genes required for photosynthesis. These responses are mediated by proteins that sense photons in particular energy ranges across the visible spectrum (Purcell & Crosson, 2008). LOV domains are widely distributed photosensors (Losi et al., 2002) that detect blue light via a bound flavin cofactor (Christie et al., 1999). These photosensory domains are present in an assortment of signal transduction proteins from bacteria, archaea, fungi, protists, and plants (Glantz et al., 2016, Herrou & Crosson, 2011). Though broadly conserved (Losi et al., 2015, Villar et al., 2018), the physiological roles of LOV photosensors in bacteria remain largely undefined.
The class Alphaproteobacteria contains species that inhabit diverse ecological niches, and that have a significant impact on nutrient cycling, agricultural production and human health (Batut et al., 2004). Alphaproteobacteria commonly encode proteins that contain a LOV domain coupled to an HWE/HisKA2-type (Herrou et al., 2017) histidine kinase. Surprisingly, these “LOV-HWE kinases” are often present in heterotrophic species with no evident photobiology (Herrou & Crosson, 2011). Histidine kinases are typically co-expressed with and phosphorylate their cognate response regulators to directly control gene expression (Hoch & Silhavy, 1995), but HWE/HisKA2 kinases are unusual in that they are often orphaned on the bacterial chromosome, or are adjacent to single domain response regulators (SDRR) that lack a regulatory output domain to control gene expression (Herrou et al., 2017).
Early studies of alphaproteobacterial LOV-HWE kinases in Caulobacter crescentus (Purcell et al., 2007) and Rhizobium leguminosarum (Bonomi et al., 2012), demonstrated their influence on cell adhesion and biofilm formation. In the case of C. crescentus, a LOV-HWE kinase (LovK) modulates adhesion by controlling expression of a single downstream gene that regulates surface adhesin biosynthesis (Fiebig et al., 2014, Reyes Ruiz et al., 2019). However, the major effect of deleting or overexpressing genes encoding LOV-HWE kinases appears to be dysregulation of the general stress response (GSR) system (Foreman et al., 2012, Kim et al., 2014), which determines cell survival across a range of stress conditions (Fiebig et al., 2015, Francez-Charlot et al., 2015). There is increasing evidence that multiple HWE/HisKA2-family kinases function as part of complex regulatory networks that regulate the GSR in Alphaproteobacteria by influencing the phosphorylation state of the anti-anti-σ factor, PhyR (Kaczmarczyk et al., 2014, Gottschlich et al., 2018, Lori et al., 2018, Correa et al., 2013). Phospho-PhyR activates an extracytoplasmic function (ECF) σ factor – EcfG – by binding and sequestering its anti-σ factor, NepR (Francez-Charlot et al., 2009) (Figure 1).
Though there is genetic evidence that LOV-HWE kinases control transcription of genes in the GSR regulon (Foreman et al., 2012, Kaczmarczyk et al., 2014, Kim et al., 2014, Sycz et al., 2015), the effects of visible light on LOV-HWE kinase signaling in vivo remain undefined. Therefore, it is important to identify appropriate experimental systems to assess the effect of visible light and other environmental signals on LOV-HWE kinase signaling in living cells.
Erythrobacter litoralis DSM 8509 as a system to study LOV-HWE kinase signaling
We sought to investigate the signaling role of LOV-HWE kinases in the genus Erythrobacter, which was attractive to us for several reasons. Erythrobacter spp. are abundant in the world’s oceans (Sunagawa et al., 2015, Tully et al., 2018, Villar et al., 2018) where they contribute to global nutrient and energy cycling (Koblizek et al., 2007, Kolber et al., 2001). Importantly, LOV-HWE kinases are common in Erythrobacter spp., as evidenced in both sequenced isolates (Oh et al., 2009, Wang et al., 2014) and in a set of metagenome assembled genomes (MAGs) (Delmont et al., 2018) from the Tara oceans sequence datasets (Villar et al., 2018). Though Erythrobacter spp. can be isolated and grown in axenic culture (Lei et al., 2015, Wang et al., 2014), strains have not been extensively cultivated and manipulated. Thus, Erythrobacter spp. are less likely to have acquired lab-adaptive mutations that could potentially skew the effects of light on cell physiology. Most Erythrobacter spp. are aerobic anoxygenic photoheterotrophs (AAP), which carry a photosynthesis gene cluster that encodes production of bacteriochlorophyll a (Bchl a), and other genes required for phototrophy. Therefore, physiological responses to visible light are expected in this genus.
Erythrobacter litoralis strain DSM 8509 was isolated from a cyanobacterial mat in the sublittoral zone off the island of Texel, Netherlands (Yurkov et al., 1994, Yurkov & Van Gemerden, 1993). Draft genome sequence of DSM 8509 indicated the presence of a single LOV-HWE kinase gene (Wang et al., 2014). This distinguishes DSM 8509 from E. litoralis strain HTCC 2594, which encodes multiple LOV-kinases (Oh et al., 2009) that have been previously characterized in vitro (Correa et al., 2013, Dikiy et al., 2019, Rivera-Cancel et al., 2014). HTCC 2594 does not encode the genes required for phototrophy (Oh et al., 2009, Zheng et al., 2016), and though DSM 8509 and HTCC 2594 cluster phylogenetically based on their 16S sequences, they do not group based on amino acid sequence of concatenated core genes (Zheng et al., 2016). As such, it has been suggested that HTCC 2594 should be re-classified as a distinct species, Erythrobacter sp. HTCC 2594 (Jiang et al., 2018).
Here, we report the development of E. litoralis DSM 8509 as an experimental genetic system, which we have used to study the contribution of a LOV-HWE kinase to regulation of the general stress response. Our data show that an ensemble of three HWE kinases, including the LOV-HWE kinase LovK, collectively regulates the general stress response in E. litoralis. The cytoplasmic kinase, GsrK, functions as an activator of GSR transcription in complex medium, while the transmembrane kinase, GsrP, is a repressor. LovK activates GSR transcription, and is a more potent GSR activator under dark conditions. Transcription of the entire GSR regulon is significantly higher in dark conditions than in light. In fact, the set of genes that are differentially transcribed upon shifts in the light environment strongly overlaps the experimentally-defined GSR regulon. While LovK contributes to light-dependent regulation of GSR transcription, it is not strictly required for this response. Our results support a model in which photons directly and indirectly modulate GSR transcription via the HWE kinases GsrK, GsrP, and LovK.
RESULTS
A brief comparison of Erythrobacter litoralis DSM 8509 to other Erythrobacter species
Several partial and complete genome sequences of Erythrobacter isolates have been deposited in public databases (see Table 1 for representative genomes). These genomes have similar characteristics in terms of size and GC content, yet differ in presence/absence of particular genes and pathways. For example, Erythrobacter spp. can encode zero, one, or multiple LOV-HWE kinases, and the total number of HWE/HisKA2-family kinases ranges from two to sixteen (Ulrich & Zhulin, 2010). Although the three LOV kinases present in strain HTCC 2594 have been biochemically characterized (Correa et al., 2013, Dikiy et al., 2019, Rivera-Cancel et al., 2014), we anticipated that the potential functional redundancy of these genes could complicate interpretation of genetic and physiological studies in vivo. In contrast, DSM 8509 encodes only one LOV-HWE kinase. Additionally, when considering our intent to investigate the interplay between multiple HWE/HisKA2-family kinases involved in GSR regulation, we noted that DSM 8509 has a ‘goldilocks’ number of such kinases: more than one, but not too many to complicate genetic analyses (Table 1). Finally, DSM 8509 encodes core genes required for phototrophy, which provides an opportunity to develop genetic tools in a species for which light is likely a central environmental/metabolic signal. For these reasons, we chose to pursue the development of E. litoralis DSM 8509 as a comparative model to study the function of LOV-HWE kinases.
Whole-genome sequencing and development of genetic tools in DSM 8509
To our knowledge, genetic analysis of an Erythrobacter species has not been reported. To support development of Erythrobacter litoralis DSM 8509 as an experimental genetic model, we first completed and closed the genome sequence. Specifically, we re-sequenced DSM 8509 using a PacBio long-read sequencing platform to an average depth of 143X (Table S1). These sequence reads were assembled de novo to a single 3.25 Mb contig, which was deposited and is available to the public under NCBI GenBank accession CP017057. We surveyed the antibiotic sensitivity profile of DSM 8509 to identify useful markers for genetic selection (Table S2), and adapted methods to transform the bacterium with both replicating (pBBR-derived) and integrating (ColE1-derived) plasmids. We successfully transformed E. litoralis DSM 8509 by both electroporation and conjugation (see Materials and Methods). We further identified conditions to generate unmarked gene deletion and allele replacement strains using a two-step recombination and sacB/sucrose counterselection approach, which we applied to our genetic analysis of HWE kinases and GSR signaling described below.
E. litoralis DSM 8509 LovK is a photosensor
Like Caulobacter crescentus (Marks et al., 2010, Purcell et al., 2007), E. litoralis DSM 8509 possesses a single LOV-HWE histidine kinase gene that is located adjacent to a single-domain response regulator gene on the chromosome (locus tags Ga0102493_111685 and 111686). We have named these genes lovK and lovR, respectively (Figure 2). The N-terminal LOV domain of LovK contains a complete flavin binding consensus sequence (Crosson & Moffat, 2001, Herrou & Crosson, 2011), and a conserved cysteine residue required for light-dependent cysteinyl-flavin adduct formation (Salomon et al., 2000). To validate that LovK indeed functions as a bona fide photoreceptor in vitro, we cloned and expressed LovK in a heterologous E. coli system, and purified the protein by affinity chromatography. LovK has a classic LOV domain visible absorption spectrum, with a λmax at 450 nm and vibronic bands at 425 nm and 475 nm. Illumination of the protein with blue light results in loss of these major bands, and a concomitant increase in absorption at 396 nm (Figure 3). This spectral signature is consistent with formation of a covalent cysteinyl-flavin C4(a) adduct upon illumination (Crosson & Moffat, 2002, Salomon et al., 2000, Salomon et al., 2001, Swartz et al., 2001). We further expressed and purified LovK(C73A), in which the conserved cysteine postulated to form a flavin C4(a) adduct is mutated to a non-reactive alanine. LovK(C73A) retains flavin binding as evidenced by its absorption spectrum, but does not undergo the light-dependent bleaching of visible absorption bands that are indicative of cysteinyl-flavin adduct formation (Figure 3). These data provide evidence that E. litoralis DSM 8509 LovK is a photosensor that has the photochemical features of typical LOV proteins.
The E. litoralis DSM 8509 GSR regulon
Before testing whether LovK plays a role in the regulation of general stress response (GSR) transcription, we first sought to define the GSR regulon in E. litoralis DSM 8509 by RNA-sequencing (RNA-seq). To this end, we deleted the predicted orthologs of phyR (locus tag Ga0102493_111538) and the nepR-ecfG operon (locus tags Ga0102493_111536 and 111535) (Figure 2). As discussed in the introduction, these genes encode a protein partner switching system that controls activation of GSR transcription by σEcfG. Deletion of either phyR or ecfG were predicted to result in a strain incapable of activating GSR transcription. We compared the global transcriptional profiles of the ΔphyR and ΔnepR-ecfG deletion strains to wild type (WT) (Table S3). To examine the effects of light, each strain was grown in cool white fluorescent light (60 µmol m−2 s−1) or in darkness (foil-covered tubes) for 24 hours prior to harvesting mRNA.
A shared set of 183 genes were differentially expressed (more than 1.5-fold; false discovery rate (FDR) p-value < 0.01) in ΔphyR and ΔnepR-ecfG compared to wild-type cells (Figure 4, Table S4). With few exceptions, transcript levels in this gene set were lower in the two mutant strains compared to wild type indicating that these differentially regulated genes are transcriptionally activated by σEcfG in wild-type cells. We identified a predicted σEcfG binding motif that matched EcfG motifs from other Alphaproteobacteria (Fiebig et al., 2015, Francez-Charlot et al., 2015, Staron & Mascher, 2010, Staron et al., 2009) in the promoter region of approximately one-quarter of the regulated genes (Figure 4, Table S4). Presence of these motifs predict the subset of genes in the E. litoralis GSR regulon that are directly regulated by the ECF sigma factor, σEcfG.
Genes encoding transporters, cell envelope, and cell surface proteins are broadly represented in the E. litoralis DSM 8509 GSR regulon (Table S4). Transcription of genes encoding the ferritin-like protein DPS, a SOUL heme-binding protein, and superoxide dismutase (sod) are commonly under the control of the GSR system in other Alphaproteobacteria (Alvarez-Martinez et al., 2007, Britos et al., 2011, Foreman et al., 2012, Francez-Charlot et al., 2009, Gourion et al., 2008, Gourion et al., 2009, Jans et al., 2013, Kim et al., 2013, Kim et al., 2014, Lourenco et al., 2011, Martinez-Salazar et al., 2009, Sauviac et al., 2007), and are regulated by nepR-ecfG and phyR in E. litoralis DSM8509 (Table S4). The promoters of dps, sodA, sodC, and a predicted SOUL heme-binding protein gene (Ga0102493_112016) contain EcfG motifs and thus appear to be directly activated by σEcfG. Our transcriptomic data also provide evidence that expression of several DNA photolyases is activated by the GSR system.
Genes directly or indirectly regulated by σEcfG that may be relevant to the photobiology of E. litoralis include a gene encoding a TspO/MBR tryptophan-rich protein (locus Ga0102493_112559). This class of outer membrane protein has been reported to bind tetrapyrroles and promote their photooxidative degradation (Ginter et al., 2013), and to negatively regulate photosynthesis in Rhodobacter (Yeliseev & Kaplan, 1995). Transcripts levels from this particular TspO/MBR gene are highly reduced in strains lacking phyR or nepR-ecfG. Unlike the fungus Aspergillus fumigatus, where TspO/MBR expression is strongly induced by light exposure (Fuller et al., 2013), expression of E. litoralis TspO/MBR (Ga0102493_112559) is lower in light than in dark conditions. Notably, steady-state transcript levels from the bacteriochlorophyll biosynthesis gene, bchC, are higher in both ΔphyR and in ΔnepR-ecfG relative to wild type (Table S4). Transcripts of other bacteriochlorophyll biosynthesis genes including bchF, bchB and bchN are also higher in ΔphyR and ΔnepR-ecfG strains, though to a lesser extent than bchC (Figure S1). These results indicate that the E. litoralis GSR system directly or indirectly represses select genes involved in phototrophy.
Light-dependent regulation of transcription at the genome scale
In wild-type E. litoralis, transcripts in the GSR regulon are more abundant in dark-grown cells (aluminum foil-covered tubes) than in cells illuminated with white light (60 µmol m−2 s−1) (Figure 4). In fact, measured GSR transcript levels from illuminated wild-type cells are only slightly higher than mutant strains lacking either phyR or nepR-ecfG. From this result, we conclude that the GSR is only marginally active when cells are grown in continuous white light (Figure 4 and Table S4). A light versus dark difference in GSR transcripts is not observed in ΔphyR or ΔnepR-ecfG cells.
In wild-type cells, the majority of genes differentially expressed between light and dark conditions are in the GSR regulon. Of the 220 transcripts that change more than 1.4-fold (FDR p-value < 0.01), only 37 are not in the GSR regulon as defined (Figure 5, Table S5). Twenty-five of the differentially-expressed genes outside of the GSR regulon have similar light-dependent changes in the ΔphyR and ΔnepR-ecfG strains, and thus represent a GSR-independent light-regulated gene set. This GSR-independent gene set exhibits modest (less than 2-fold) regulation in response to white light treatment, and includes photosynthesis genes with reduced transcript levels in the light (Figure 5, Figure S1). These genes are distinct from those derepressed in the GSR mutant strains (e.g. bchC) and include bchH, bchL, puhA, and bchM. We conclude that there are genes involved in photosynthesis (e.g. bch, puf, puh) for which expression is influenced by the GSR system, and others for which regulation is independent of GSR (Figure S1).
Reduction in photosynthesis gene expression in E. litoralis in the light is consistent with light repression of reaction center genes in the purple photosynthetic bacterium, Rhodobacter capsulatus (Zhu & Hearst, 1986), and downregulation of photosynthesis-related genes in the aerobic anoxygenic phototrophic bacterium, Dinoroseobacter shibae, upon a shift from heterotrophic growth in the dark to photoheterotrophic growth in the light (Tomasch et al., 2011). An operon of unknown function (Ga0102493_112844-50) involved in acyl-CoA metabolism is repressed by light, independent of the GSR system. Eight metabolic genes of varying function are activated by light, independent of the GSR system (Figure 5).
Regulators of the GSR signaling pathway
Typically, transcription of genes encoding the core GSR regulators NepR, EcfG, PhyR and GSR sensory kinases is activated by σecfG (Foreman et al., 2012, Francez-Charlot et al., 2009, Gourion et al., 2009, Jans et al., 2013, Kim et al., 2013, Kim et al., 2014, Martinez-Salazar et al., 2009, Sauviac et al., 2007). In E. litoralis, a σEcfG-binding motif is positioned directly upstream of the nepR-ecfG operon. As expected, nepR-ecfG transcripts were reduced in the strain lacking phyR and in cells grown in the light (Figure 2C, Table S4).
It was previously noted that conserved nucleotides at −35 and −10 within the σEcfG-binding motif are nearly palindromic, which lead to the hypothesis that a palindromic site might function to drive bi-directional expression of oppositely oriented genes (Staron et al., 2009). The −35 and −10 sites upstream of nepR-ecfG have a strong palindromic character (GGAAC-N17-GTTCC) (Figure 6, Table S4). Our transcriptomic data provide evidence that expression of both nepR-ecfG and the oppositely oriented HWE sensor kinase gene (Ga0102493_111537, gsrP) is activated from this single palindromic site. Both nepR-ecfG and gsrP are part of the GSR regulon as determined by RNA-seq (Figure 2C, Table S4). Moreover, RNA-seq reads corresponding to nepR-ecfG and gsrP transcripts each begin 13-14 bp downstream of either end of this shared promoter motif (Figure 6). While this is not a definitive mapping of transcriptional start sites, these data strongly suggest that this particular motif can functional bi-directionally. The mechanism by which σEcfG could regulate transcription from both strands at this site is not known. We note that the motif oriented toward nepR-ecfG has a stronger score in MEME, and that more RNA-seq reads mapped to nepR-ecfG than gsrP, which together suggest that σEcfG preferentially initiates transcription of nepR-ecfG. Finally, we observed a small number of RNA-seq reads that mapped to the negative strand of this motif and its downstream region (genome positions 619,592-619,621, Figure 6). We speculate that these reads may correspond to transcription initiation from a cryptic or non-ECF σ promoter that would ensure some minimal level of nepR-ecfG expression under conditions in which the GSR was completely inactive.
In contrast to many previously described systems, an EcfG motif was not evident in the phyR promoter and, accordingly, transcript levels for this gene were not affected by deletion of nepR-ecfG or by light conditions (Figure 2C and 6, Table S4). In other words, phyR appears to be constitutively expressed in E. litoralis DSM 8509. Constitutive expression of phyR likely necessitates the presence of a negative PhyR regulator to avoid constitutive activation of the GSR.
HWE/HisKA2-family kinases are associated with the GSR regulatory system in Alphaproteobacteria (Staron & Mascher, 2010, Fiebig et al., 2015, Francez-Charlot et al., 2015). E. litoralis DSM 8509 encodes five HWE/HisKA2-family kinases. Of these, only three are expressed at an appreciable level under our laboratory cultivation conditions, including: 1) the kinase encoded adjacent to nepR-ecfG operon (Ga0102493_111537), 2) lovK, and 3) an orphan sensor kinase (Ga0102493_11718) (Figure 2). Ga0102493_111537 encodes a transmembrane HWE sensor kinase with a periplasmic CHASE (Mougel & Zhulin, 2001) sensory domain; its transcription is activated by phyR and ecfG and by dark conditions (Figure 2C & 6). As noted above, a shared EcfG motif identified between nepR-ecfG and this kinase likely promotes expression of both transcripts. The lovK-lovR promoter also contains an EcfG motif, and transcription of lovK-lovR requires nepR-ecfG and phyR (Figure 2C). The orphan HWE kinase, Ga0102493_11718, lacks an EcfG motif in its promoter and is constitutively expressed in our experimental conditions (Figure 2C). Of the remaining HWE-kinase genes, transcripts corresponding to the orphan kinase gene Ga0102493_112963 are nearly undetectable (RPKM < 10). HWE-kinase gene, Ga0102493_111751, is encoded in an operon with a CRP-family transcription factor and a single domain response regulator. Transcripts for these genes are also low abundance (Figure S2).
The role of three HWE-family sensor kinases in regulation of GSR transcription
To assess the role of HWE-family kinases 111537, 11718, and LovK in regulation of GSR transcription, we constructed strains bearing in-frame unmarked deletions of each kinase gene. We then evaluated GSR transcriptional output in these strains by measuring levels of a GSR-regulated transcript, dps, by qRT-PCR. This transcript was selected because 1) it exhibits a large dynamic range of expression between “GSR-ON” and “GSR-OFF” conditions (Figure S3), 2) it contains an EcfG motif in its promoter suggesting direct regulation by σEcfG (Table S4), and 3) primers to this transcript provided efficient amplification in one-step qRT-PCR reactions (see Materials and Methods). Gene locus Ga0102493_112759, which encodes a methylmalonyl-CoA mutase, was selected as a control gene for normalization (Figure S3). In our RNA-seq data sets, transcripts for this gene were abundant (in the top 20% of all transcripts) and the RPKM coefficient of variation between samples was among the lowest, making this a suitable control gene for normalization. We tested these qRT-PCR primer sets in the same strains evaluated by RNA-seq and patterns of dps expression were consistent between these two methods (Figure S3).
In a strain lacking kinase 111537, steady-state levels of dps transcript increased in cultures grown both in the light and in the dark (Figure 7A). These data are consistent with 111537 functioning as a negative regulator of GSR transcription. Conversely, deletion of the 11718 resulted in decreased dps transcript levels, consistent with this gene functioning as a positive regulator of GSR transcription. Both of these transcriptional phenotypes were complemented by expression of the deleted gene from its native promoter on a replicating plasmid (Figure S4). We have named these genes gsrP and gsrK, for general stress response phosphatase and kinase respectively. We note that the putative phosphatase and/or kinase activity of these proteins has not been established, but our genetic data are consistent with these biochemical activities against PhyR.
Deletion of the lovKR operon did not have a significant effect on dps transcript levels as measured by qRT-PCR (Figure 7A). Moreover, we did not observe large differences in GSR transcription in a ΔlovKR strain at the genome scale compared to wild type in our RNA-seq experiments (Figure 4). Nonetheless, GSR transcripts were uniformly lower in ΔlovKR compared to wild type when strains were grown in the dark (Figure 4D&E). The average log2(fold change) difference in all GSR transcripts between these strains is −0.25, which reflects ∼15% reduction in GSR transcription in the ΔlovKR strain (p < 0.0001). This trend is specific to the GSR regulon: the average log2(fold change) difference for all transcripts is 0.01 reflecting that, on average, the transcriptome at the whole-genome scale remains unchanged. These results provide evidence that lovKR plays a subtle role as an activator of GSR transcription in the dark.
To examine possible redundancy in the functions of these HWE kinases, we evaluated the effect of deleting pairs of kinases, leaving one of the three genes intact. In a ΔgsrK ΔlovKR double deletion strain where gsrP remains, dps transcript levels are lower than either of the single deletion strains in both the light and dark (Figure 7A). This result supports a model in which both GsrK and LovK function as GSR activators; moreover GsrP does not activate GSR transcription in the dark or in the light. In the ΔgsrP ΔlovKR double deletion strain where gsrK remains, dps transcripts are elevated in both the light and the dark, similar to the strain lacking only gsrP. Finally, in the ΔgsrP ΔgsrK strain where lovKR remains, dps transcripts are higher than wild type in both the light and the dark (Figure 7A) and are differentially expressed in response to light treatment. In this strain, dps levels are higher in dark-grown than light-grown cells. To further investigate whether LovK functions as a global activator of GSR, we measured the transcriptome of the ΔgsrP ΔgsrK strain grown in the light and in the dark by RNA-seq. These experiments confirm the single gene (dps) results in this strain. Specifically, GSR transcripts in this strain are broadly elevated compared to wild type in either light condition, and are higher in the dark than the light (Figure 4, Table S4). Together these data support a model in which LovK can function as an activator of GSR transcription that has enhanced activity in the dark.
To test whether LOV domain photochemistry (i.e. cysteinyl-flavin covalent adduct formation) contributes to the light-dark difference in LovK-dependent transcription, we mutated the conserved LOV domain cysteine (C73) to an alanine in the ΔgsrP ΔgsrK strain. Purified LovK(C73A) mutant protein is blind to light (Figure 3), and in the ΔgsrP ΔgsrK lovK(C73A) strain, GSR transcription was no longer sensitive to light (Figure 7B). Specifically, dps levels were comparably high in light and dark grown cultures and similar to dark grown ΔgsrP ΔgsrK lovKR+cultures. From these data, we again conclude that LovK is a more potent activator of GSR in its dark state.
We further tested whether the conserved histidine phosphorylation site in LovK (H161) was required to regulate GSR transcription. dps transcript levels in the ΔgsrP ΔgsrK lovK(H161A) strain are similar to a strain lacking all three kinases (ΔgsrP ΔgsrK ΔlovKR) indicating that a lovK(H161A) mutant behaves like a ΔlovKR deletion. We conclude that LovK phosphorylation is necessary for LovK to activate GSR transcription (Figure 7B). Together, the data provide evidence that gsrP, gsrK and lovK coordinately regulate GSR transcription under our assayed conditions.
DISCUSSION
Regulation of transcription by alternative sigma factors including σS in Gammaproteobacteria (Battesti et al., 2011, Hengge, 2008), σB in select Gram-positive bacteria (Hecker et al., 2007), and σEcfG in Alphaproteobacteria (Fiebig et al., 2015, Francez-Charlot et al., 2015) confers general resistance to a range of physical and chemical stress conditions in vitro. Though these general stress response (GSR) σ factors are conserved within phylogenetic groups, the input signals that cue their activation and the σ-dependent transcriptional outputs vary across species. GSR inputs and outputs presumably reflect the distinct physicochemical challenges that particular species encounter within their niches. In this study, we report the development of the aerobic anoxygenic photoheterotroph (AAP), Erythrobacter litoralis DSM 8509, as a comparative genetic model system to study regulation of GSR transcription by σEcfG. More specifically, we have sought to define the regulatory role of HWE-family sensor histidine kinases (Herrou et al., 2017) — including a photoresponsive LOV-HWE kinase — in σEcfG-dependent transcription in E. litoralis.
Light, LOV, and bacterial stress responses
Proteins containing photosensory LOV domains are widely distributed in archaea, eukarya, and bacteria (Glantz et al., 2016). The possibility that visible light regulates bacterial stress responses via LOV domains was first noted (Losi et al., 2002) after the discovery of the Bacillus subtilis LOV-STAS protein, YtvA, which functions as an activator of σB-dependent transcription (Akbar et al., 2001). It was later shown that blue light can indeed activate σB-dependent transcription in B. subtilis via YtvA (Avila-Perez et al., 2006). Subsequent studies of a related LOV-STAS protein from Listeria monocytogenes support the conclusion that light regulation of σB by LOV proteins occurs more broadly in Gram-positive bacteria (O’Donoghue et al., 2016, Ondrusch & Kreft, 2011). A regulatory link between LOV and σS has also been reported in Pseudomonas syringae, where white light was shown to repress expression of the gene encoding σS (rpoS) via a LOV histidine kinase (Moriconi et al., 2013).
Though the Alphaproteobacterial GSR sigma factor, σEcfG, is not related to σB or σS, studies of Caulobacter crescentus LovK provide evidence that LOV-HWE kinases repress σEcfG-dependent transcription (Foreman et al., 2012). Experiments in Brucella abortus have identified a related LOV-HWE kinase, LovhK, that activates σEcfG-dependent transcription (Kim et al., 2014, Sycz et al., 2015). However, these studies have not provided evidence that visible light is an input signal that influences σEcfG-dependent transcription. In E. litoralis DSM 8509, we have shown that the activity LovK as a regulator of σEcfG is influenced by light. More specifically, LovK functions with two additional HWE-family kinases, GsrP and GsrK, to control GSR output (Figure 8A): GsrK is a strong GSR activator, GsrP is a repressor, and LovK is an activator that can be directly modulated by light (Figure 8A). These data contribute to an emerging model of GSR regulation in Alphaproteobacteria in which consortia of HWE/HisKA2-family kinases regulate σEcfG.
Our RNA-seq experiments show that E. litoralis GSR transcription is highly activated in the dark, and only marginally activated in cells continuously illuminated with white fluorescent light. In contrast, light transiently induces transcription of the core GSR regulators (Dshi_3834-3837) and other stress response genes in the related AAP species, Dinoroseobacter shibae (Tomasch et al., 2011). Similarly, blue light activates rpoE- and rpoH-dependent stress responses in the phototrophic alphaproteobacterium Rhodobacter sphaeroides (Braatsch et al., 2004, Ziegelhoffer & Donohue, 2009). We did not measure transient responses of E. litoralis to light or dark shifts, and the advantage (if any) of elevated GSR transcription in the dark is not known.
LovK functions as part of a consortium of GSR sensor histidine kinases
Although LovK can clearly function as a photoreceptor, it is not explicitly required for light/dark control of GSR transcription. Specifically, transcription from a GSR-regulated promoter remains light-responsive in a gsrK+ gsrP+ ΔlovKR strain. Thus, the combined activities of GsrK and GsrP must be balanced in a manner that leads to higher transcriptional output in dark relative to illuminated conditions (Figure 7A). This light responsiveness could emerge from enhanced activity of GsrK in the dark, enhanced repression by GsrP in the light, or a combination of both. There is no evidence to suggest that photons are a direct signal for either sensor, thus we predict that either GsrK and/or GsrP indirectly sense a metabolic or physiological change that occurs upon shifts in the light environment.
We favor a model in which GsrP is a more potent GSR repressor in cells grown in the light (Figure 8A). In our experimental conditions, gsrK alone strongly activates GSR transcription in light and dark (Figure 7A). This gene is constitutively expressed in both conditions (Figure 2C). While our results suggest that GsrK activity is not affected by light, we cannot entirely exclude the possibility that light conditions influence GsrK. GSR output from the strain bearing only gsrP is equivalently low in light and dark conditions (Figure 7A). While light may influence the activity of GsrP as a repressor, it is difficult to assess this possibility in the absence of a kinase that activates GSR transcription. σEcfG–dependent transcription of gsrP comprises a negative feedback loop that controls GSR transcriptional output; the level of gsrP transcripts is dramatically reduced in light conditions (Figure 2C, Table S4). This regulatory circuitry leads one to predict that the activity of GsrP as a repressor is inversely proportional to its steady-state levels in the cell. The activities of E. litoralis LovK, GsrK, and GsrP likely serve to both counteract and reinforce each other depending on environmental conditions. The possibility that E. litoralis and other Alphaproteobacteria can coordinately perceive multiple environmental inputs through a consortium of HWE-family kinases may endow these species with the ability to execute complex decision-making processes with regard to control of GSR transcription.
Finally, we note that our data support a model in which LovK is active in both the light and dark, though activity of LovK as a positive regulator of σEcfG-dependent transcription is enhanced in the dark. These in vivo data are consistent with in vitro data showing that light does not regulate E. litoralis HTCC 2594 LOV kinases in a binary (i.e. ON-OFF) manner, but rather modulates phosphorylation kinetics (Correa et al., 2013). Though blue light typically enhances the enzymatic activity of LOV kinases in vitro (Correa et al., 2013, Swartz et al., 2007), there is precedent for the unlit, dark state being the active state in vivo. In D. shibae, a short LOV protein is a dark activator of pigment biosynthesis (Endres et al., 2015). In this case, the LOV domain may be thought of as a dark sensor rather than a light sensor.
One may speculate on reasons why LOV proteins are often incorporated into GSR systems in the bacterial kingdom, but the fact remains that we have little understanding of the physiological relevance of LOV-regulated responses to changes in the light or redox environment in bacteria. E. litoralis DSM 8509 is a tractable experimental system with interesting physiological features. This species can now be leveraged as a comparative model to investigate core molecular mechanisms underlying environmental stress responses in Alphaproteobacteria.
MATERIALS AND METHODS
Growth of E. litoralis
Erythrobacter litoralis DSM 8509 was obtained from the American Type Culture Collection (ATCC 700002). For these studies, this organism was grown in Difco Marine Broth 2216. When broth was prepared according to manufacturer’s instructions, cells tended to clump in flocs. Dilution of marine broth to 0.5X reduced flocculation, and thus all cultures were grown at this broth dilution (18.7 g of powder per L). 0.5X marine broth was sterilized by autoclaving and, prior to inoculation with E. litoralis, the medium was passed through a sterile 0.22 µm filter to remove precipitates. Liquid cultures were grown in an Infors air incubator at 30°C in glass culture tubes, inclined at a 45° angle, shaking at 200 RPM. For “light” conditions, a bay of 10 fluorescent Philips and Sylvania T8 lights inside the shaking incubator was switched on. For “dark” conditions glass tubes were carefully wrapped in aluminum foil. For molecular genetic manipulation and isolation of mutants, colonies were grown on 0.5X marine broth solidified with 15 g of agar per L of medium. Agar plates were grown in a 30°C air incubator, or at room temperature in ambient light.
Growth of Escherichia coli strains
E. coli strains were grown in LB Miller medium (10 g peptone, 5 g yeast extract, 10 g NaCl per L) at 37°C. Growth medium was solidified with 1.5% agar. Antibiotics were added at the following concentrations as appropriate: kanamycin, 50 µg/ml; gentamycin 15 µg/ml; chloramphenicol 12 µg/ml.
Antibiotic sensitivity testing
To evaluate the appropriate antibiotic concentrations to use for selection in genetic manipulations, E. litoralis DSM 8509 cells were first grown in a streak on 0.5X marine agar at 30°C for 2-3 days. Cells were scraped from the agar plate into 1 ml of 0.5X marine broth and evenly suspended by pipetting up and down. The optical density (OD) at 660 nm was was adjusted to ∼ 0.1 AU. Cells were then 10-fold serially diluted and 20 µl of each dilution was spotted onto 0.5X marine broth agar that had been supplemented with a range of antibiotics concentrations. The antibiotic concentrations tested were as follows: 200, 100, 50, 25, 10 µg/ml for ampicillin, carbenicillin and tetracycline; 100, 50, 20, 10, 5, 1 µg/ml for gentamycin, spectinomycin, streptomycin, apramycin, and rifampicin. After the liquid absorbed into the agar, the plates were incubated at 30°C for 1 week. The minimal antibiotic concentrations that resulted in at least 4 orders of growth inhibition are reported in Table S2.
Molecular cloning for plasmid generation
Plasmids for expression or allele replacement were generated using routine techniques. Genes or loci of interest were PCR amplified with KOD Xtreme Hot Start polymerase (Millipore Sigma) using the primers listed in Table S6. To aid amplification of these GC-rich sequences, PCR reactions were supplemented with 5% DMSO (final concentration). Primers included a 5’ extension with restriction endonuclease sites or overhangs for overlap extension PCR reactions. Null alleles were generated by first amplifying fragments ∼500 bp upstream and ∼500 bp downstream of the gene of interest. These two fragments were “stitched” together with overlap extension PCR to generate the desired allele. PCR products were cleaned using GeneJet DNA cleanup columns (Thermo Fisher), digested with appropriate restriction endonucleases (NEB) to generate overhang sequences, and ligated into similarly digested plasmids using T4 DNA ligase (NEB). Ligation reactions were transformed into chemically competent TOP10 E. coli by heat shock. Transformants were selected on LB supplemented with the appropriate antibiotic and grown overnight at 37°C. The inserted sequence and cloning junctions of all plasmids were confirmed by PCR amplification with plasmid specific primer sequences, treatment with ExoSapIT (Applied Biosystems) followed by Sanger sequencing (University of Chicago Comprehensive Cancer DNA Sequencing and Genotyping Facility). Plasmids generated for and used in this study are listed in Table S6.
Transformation of E. litoralis
We evaluated and optimized two methods for introducing DNA into E. litoralis DSM8509, electroporation and conjugation. Replicating plasmids (with BBR or RK2 replication origins) could be introduced by electroporation, but this method was not efficient enough to introduce non-replicating (i.e. suicide) plasmids for chromosomal integration. Conjugation, by triparental mating, was used to introduce suicide plasmids containing oriT sequences, and also replicating plasmids containing oriT sequences. Gentamycin (10 µg ml−1) was used to select for clones carrying pBVMCS-4 derived plasmids. Chloramphenicol (1 µg ml−1) was used to select for clones carrying integrated plasmids, which permitted us to generate in-frame deletion or allele replacement strains. Detailed electroporation and conjugation protocols follow.
Electroporation
Cells were scraped from a freshly grown plate that had been grown for 3 days at 30°C. A pellet of 150-200 µl of cells was suspended in 750 µl 0.5x marine broth. Cells were pelleted by centrifugation (1 min at 14,000 × g) at 4°C. The cell pellet was washed 3 times with 750 µl ice cold sterile water with a 1 min centrifugation step at each wash. After the final wash, the cells were resuspended with 140 µl cold water. The total volume of cells and water was ∼200 µl. 60 µl cells were mixed with 0.1-1 µg purified plasmid and placed in a 1 mm electroporation cuvette. Cells were subjected to a single 1.8 kV pulse using the EC1 setting on a MicroPulser (Bio-Rad). Time constants were ∼ 4-5 msec. 450 µl of 0.5x marine broth was added to the cuvette and cells were transferred in this broth to a sterile 13 mm glass culture tube and incubated at 30°C shaking at 200 rpm for 2-4 hours. After this outgrowth, cells were plated on selective medium (about 200 µl per 100 mm petri dish). These plates were incubated at 30°C for about 1 week. After 5 days, pinprick-sized colonies were visible. After 7-8 days, colonies were picked and struck on fresh selective medium to confirm antibiotic resistance and to select away any non-transformed cells. We confirmed that the clones carried the plasmid of interest by colony PCR, amplifying plasmid specific sequences using cells as the template.
Conjugation
Plasmids encoding oriT sequences were transferred from E. coli TOP10 donor strains to E. litoralis using a helper strain (MT607 / pRK600) (Finan et al., 1986) which encodes the pilus required to mobilize oriT containing sequences. E. litoralis recipient strains were inoculated from fresh plates into 2 ml 0.5x marine broth in 13 × 100 mm glass culture tubes and grown shaking at 30°C overnight. The E. coli TOP10 donor strain carrying the plasmid to be transferred was grown in 2 ml LB supplemented with the appropriate antibiotic and the E. coli helper strain was grown in 2 ml LB supplemented with chloramphenicol at 37°C overnight. The three cultures were mixed at a ratio of 1 ml recipient, 200 µl donor, 200 µl helper. The mixed cells were centrifuged for 1 min at 10,000-14,000 × g. The pellet was resuspended in 50-100 µl 0.5x marine broth and then spotted onto a fresh 0.5x marine broth agar plate. After the liquid in the spot of cells absorbed into the agar, the plate was incubated overnight at room temperature or 30°C. The mix of cells was scraped from this non-selective plate and spread on 0.5x marine broth agar supplemented with 1) the appropriate antibiotic to select for acquisition of the plasmid and 2) 100 µg /ml nalidixic acid (Nal) to counterselect against the E. coli donor and helper strains. E. coli strains exhibit increased resistance to Nal when grown on marine broth agar compared to LB, which required increasing the Nal concentration above typical concentrations used for counterselection. These selective plates were incubated for 7-8 days at 30°C. Colonies that emerged were struck on fresh selective 0.5x marine broth agar plates and transformants were checked using the same approach described above for electroporated transformants.
Two-step chromosomal allele replacement
A standard two-step allele replacement approach with sucrose/sacB counterselection (Hmelo et al., 2015, Ried & Collmer, 1987) was optimized for E. litoralis DSM 8509. pNPTS138-derived allele replacement plasmids were introduced by conjugation as described above. Chloramphenicol resistant clones were inoculated into 2 ml 0.5x marine broth and allowed to grow without selection for 8-24 hours. These cells were spread on 0.5x marine broth agar supplemented with 7.5% sucrose to select for clones in which a second recombination event excised the plasmid. After approximately 1 week of growth at 30°C, sucrose resistant colonies were replica patched on agar plates with or without chloramphenicol. From the chloramphenicol sensitive clones (i.e. clones in which the plasmid had excised) the locus of interest was PCR amplified and sequenced to distinguish clones bearing the parental allele from those bearing the desired new allele.
PacBio whole-genome sequencing
E. litoralis DSM 8509 genomic DNA was extracted using guanidium thiocyanate as previously described (Pitcher et al., 1989). Standard Pacific Biosciences (PacBio) large insert library preparation was performed. Briefly, DNA was fragmented to approximately 20kb using Covaris G tubes. Fragmented DNA was enzymatically repaired and ligated to a PacBio adapter to form the SMRTbell template. Templates larger than 10kb were BluePippin (Sage Science) size selected, annealed to sequencing primer, bound to polymerase (P6), bound to PacBio Mag-Beads and SMRTcell sequenced using C4 chemistry. The genome was sequenced using two SMRT cells and was assembled de novo using HGAP3 and polished with quiver. This process yielded a single, closed contig. The genome was automatically annotated using the DOE-JGI pipeline (Huntemann et al., 2015). HWE/HisKA_2-family histidine kinases and the core GSR regulators phyR, ecfG, and nepR were identified manually and annotated before sequence submission to GenBank. Raw PacBio reads can be accessed through the NCBI sequence read archive at accession SRS1630618. The complete, annotated sequence of E. litoralis DSM 8509 is available at GenBank accession CP017057.
RNA extraction
For RNA-seq and qRT-PCR, RNA was extracted using a Trizol reagent based protocol. First, cells were struck from freezer stocks onto fresh 0.5x marine broth agar plates. After 3 days of growth, a scoop of mixed colonies of cells were inoculated into 2 ml 0.5x marine broth in 13 × 100 mm culture tubes and grown for 24 hours 30°C shaking on a 45 degree incline at 200 RPM. Cultures were diluted to 0.005 OD660 in 2 ml fresh 0.5x marine broth and allowed to continue growth at 30°C shaking at 200 RPM. After 20-22 hours, these cultures were diluted to 0.001 OD660 in 6 tubes (for RNA-seq) or 2 tubes (for qRT-PCR) with 2 ml each of 0.5x marine broth. Half of the tubes were placed in the top row of a shaker rack under a bay of 10 T8 fluorescent light bulbs (light conditions). The other half were wrapped in foil (dark conditions) and grown in the bottom row of the same shaker rack. After 22-24 hours of growth in constant light or constant dark conditions, culture densities reached 0.15-0.25 OD660. Cells were harvested by rapid centrifugation in small “genotype-condition” batches to minimize handling time between culture growth and cell lysis. For RNA-seq, the 3 × 2 ml from each genotype-condition set were distributed over 4 × 1.5 ml microfuge tubes and centrifuged for 60-90 seconds at 14,000-17,000 × g. After quickly aspirating the supernatant liquid, the four pellets were resuspended in a total of 1 ml Trizol reagent (Invitrogen). For qRT-PCR, 1.5 ml of culture was harvested as above and resuspended in 1 ml Trizol. Cells lysed in Trizol were immediately stored at −80C until extraction. For RNA-seq, five samples of each genotype-condition were collected, each grown on a different day.
To extract RNA from the Trizol suspended cells, samples were thawed and incubated at 65°C for 10 minutes. After addition of 200 µl of chloroform, samples were vortexed, incubated on the benchtop for 5 minutes, then centrifuged for 12-15 minutes at 14,000-17,000 × g. The aqueous phase (∼500 µl) was transferred to a new 1.5 ml tube and 450 ul isopropanol was added to precipitate the nucleic acid. Samples were frozen overnight at −80°C then centrifuged at 17,000 × g for 30 minutes at 4°C. The pellet was washed twice with 750 µl cold 70% ethanol, suspended in RNase free water (200 µl for RNA-seq samples and 100 µl for qRT-PCR samples), and stored at −80°C.
RNA-seq
RNA was subjected to DNase digestion using TURBO DNase I (Thermo Fisher). RNA samples were bound to an RNAeasy column (Qiagen) and digested on the column by application of 70 µL of DNase coctail (7 µL DNase, 7 µL 10x Buffer, 56 µL diH2O). Digests were incubated at room temperature for 45 minutes. RNA was cleaned and eluted from the column using buffers provided with the RNAeasy columns. DNA removal was confirmed by PCR using the RNA samples as a template and primers that amplify ∼ 100 bp products (set 1: F-GACGGAGAAAAAGGCATCGC, R-GATTCGCCGTGTTCATCTGC; set 2: F-CCCACGAACCGATTTCATGG, R-CCTTCGGGGAGTTTCAAGCA). Absence of amplification confirmed removal of contaminating genomic DNA. Amplification from pre-DNAse samples served as a positive control. rRNA was depleted from the sample using the Gram-negative bacteria Ribo-Zero rRNA Removal Kit (Illumina-Epicentre). RNA-seq libraries were prepared with an Illumina TruSeq stranded RNA kit according to manufacturer’s instructions. The libraries were sequenced on an Illumina HiSeq 4000 by the University of Chicago Functional Genomics Core Facility. Data were analyzed using the RNA-seq workflow in CLC genomics workbench v11.0. RNA-sequencing reads have been deposited in the NCBI GEO database under accession GSE126532.
qRT-PCR
The GSR-dependent transcript, dps (Ga0102493_111653), and an endogenous control transcript (Ga0102493_112759) were evaluated using TaqMan probes and SuperScript III Platinum One-Step qRT-PCR Kit (Invitrogen) with a QuantStudio 5 real time PCR system (Thermo Fisher). The primer-probe sets (dps F – TCTCATCGCCGAACTCAAC; dps R – CGTGCCAGTGGAAATTCTTG; dps probe –/5HEX/CTTCGCGCT/ZEN/GTTCACCAAGACC/3IABkFQ/) and (ctrl F – AGATCGAAATGCTGTTGAAACG; ctrl R – GACCATCCAGAACGACATCC; ctrl probe - /56-FAM/CCGCAACAC/ZEN/CTATATCTACCCGCC/3IABkFQ/) were custom prepared by Integrated DNA Technologies. In control one-step RT-PCR reactions with a dilution series of template, both primer-probe sets exhibit 91-94% efficiency. Primers and probes were mixed to make a 10 µM F, 10 µM R and 5 µM probe stock solution. 0.4 µl primer-probe stock solution was used in each 20 µl reaction. 50 nM ROX served as the reference dye in each reaction. Each RNA sample was diluted to 2.5 ng µl−1; 4 µl were used in each 20 µl reaction. Each sample was assayed in triplicate for each probe set. The average Ct from these technical replicates was considered the Ct for the sample. “No RT” control reactions were conducted on each sample with each probe to ensure that the signal from contaminating genomic DNA was less than 5 % of the signal (i.e. that the Ct from the “No-RT” reaction was at least 4 cycles later than the Ct from the “+RT” reaction. Two control samples (WT – Dark, and WT – Light samples) were diluted to 2.5 ng µl−1 and frozen in 50 µl aliquots. One aliquot was thawed and assayed on each plate to ensure consistency between plates. Reaction parameters were: 50°C 4 min, 95°C 5 min, followed by 40 cycles of 95°C 15 sec, 60°C 30 sec where fluorescence was measured each cycle. For each sample, ΔCt (Ct(dps)-Ct(control)) was calculated. Then the average WT-dark ΔCt was subtracted from each ΔCt to generate a ΔΔCt, which is the same as log2(fold change) compared to WT-dark.
Protein expression and spectroscopy
E. litoralis lovK (gene locus Ga0102493_111685) and a variant of lovK in which the flavin adduct-forming cysteine was mutated to an alanine (C73A) were cloned into the pET28a expression plasmid; see Table S6 for primers. Protein was expressed from these plasmids in E. coli BL21(DE3). Briefly, 2 liters of LB (containing 50 µg ml−1 kanamycin) was inoculated with a 100 ml of an overnight culture. The culture was grown at 37°C / 220 rpm to OD600 ≈0.8 and induced with 0.5 mM IPTG for four hours before cells were pelleted by centrifugation. For purification, the cell pellet was resuspended in 50 ml of resuspension buffer (10 mM Tris (pH 7.6), 150 mM NaCl, 10 mM imidizole) and lysed by two passages through a LV-1 microfluidizer. The lysate was then clarified by centrifugation (15 minutes at 35,000 × g) and applied to 2.5 ml of Ni-NTA resin on a gravity column. The resin had been pre-equilibrated with lysis buffer. The resin was washed with 5 column volumes (CV) of resuspension buffer, followed by a step gradient of buffer with increasing concentrations of imidazole. Specifically, the column was washed with 12 ml resuspension buffer containing 75 mM imidazole, 4 ml buffer with 200 mM imidazole, and finally 5 ml buffer with 500 mM imidazole for elution. The purity of the different fractions was assessed on a 12% SDS-PAGE gel. Peak fractions were desalted with a Zeba spin column (ThermoFisher) with a 7000 kDa MWCO. The visible absorption spectrum of purified LovK and LovK(C73A) was measured in a Tecan Spark 20M. The “lit” state of LovK was generated by illuminating purified protein with a panel of 96 LED bulbs (3 mm bulbs, 430 nm peak wavelength) held 10-20 cm from the sample for 30 seconds (until the visible yellow color was bleached).
AUTHOR CONTRIBUTIONS
Conception and design of the study, AF and SC; acquisition, analysis, or interpretation of the data AF, LV, XAN and SC; writing of the manuscript, AF and SC.
ACKNOWLEDGEMENTS
We dedicate this study to the memory of Winslow Briggs, whose contributions to the field of photobiology cannot be overstated. We thank members of the Crosson lab and Maureen Coleman for helpful discussions throughout this work. We thank Angie Schmoldt at the Great Lakes Genomics Center at UW-Milwaukee for support with PacBio sequencing. The authors have no conflicts of interest to declare.