Transcription factor-based biosensors enlightened by the analyte
- Departamento de Biología Molecular and Instituto de Biomedicina y Biotecnología de Cantabria, Universidad de Cantabria – Consejo Superior de Investigaciones Científicas, Santander, Spain
Whole cell biosensors (WCBs) have multiple applications for environmental monitoring, detecting a wide range of pollutants. WCBs depend critically on the sensitivity and specificity of the transcription factor (TF) used to detect the analyte. We describe the mechanism of regulation and the structural and biochemical properties of TF families that are used, or could be used, for the development of environmental WCBs. Focusing on the chemical nature of the analyte, we review TFs that respond to aromatic compounds (XylS-AraC, XylR-NtrC, and LysR), metal ions (MerR, ArsR, DtxR, Fur, and NikR) or antibiotics (TetR and MarR). Analyzing the structural domains involved in DNA recognition, we highlight the similitudes in the DNA binding domains (DBDs) of these TF families. Opposite to DBDs, the wide range of analytes detected by TFs results in a diversity of structures at the effector binding domain. The modular architecture of TFs opens the possibility of engineering TFs with hybrid DNA and effector specificities. Yet, the lack of a crisp correlation between structural domains and specific functions makes this a challenging task.
General Design of Transcription Factor-Based Whole Cell Biosensors (WCBs)
Whole cell biosensors (WCBs) are devices that use specific biochemical reactions mediated by whole cells to detect chemical compounds usually by optical signals. WCBs are especially useful for environmental monitoring, as they are able to detect a wide range of pollutants in a very specific manner [for a review on methodologies to create WCBs and recent applications see Michelini et al. (2013) and Park et al. (2013)].
Bacteria contain transcription factors (TFs) able to respond to a wide variety of chemical signals. Thus, using genetic engineering, these TFs can be coupled to reporter genes (like fluorescent proteins or luciferases) to create WCBs. Although the use of TF-based biosensors was proposed years ago, few reliable systems have been developed so far. A summary of available TF/analyte pairs can be found in (Landrain et al., 2009). The emergence of synthetic biology, which intends to create synthetic devices able to perform input-sensing and biocomputing functions (Macia and Sole, 2014), has renewed the interest in TF-based bionsensors. In principle, implementing TF-based biosensing in a synthetic circuit is a simple task. Select the chemical analyte for the circuit to respond to, identify the correct TF that responds to that particular analyte, and make the expression of the responding gene (either a reporter gene or the next element in the logical process of the circuit) dependent upon the given TF. Unfortunately, this over – simplistic scheme rarely works, for bacterial TFs employ different mechanisms of analyte recognition and promoter activation/repression, which complicate considerably the development of functional devices. In this review we summarize the mechanisms of analyte recognition and transcriptional control of the most common TF families employed in biosensor development. We have classified them depending on the chemical nature of the analyte detected, thus bringing the input signal to center stage.
Whole cell biosensors are composed of two protein modules that can be combined depending on the analyte to detect and the output signal to obtain. The sensing module is the signal transducer, responsible for recognition of the analyte and transduction of this signal to the reporter module. The reporter module produces a measurable output (typically light, fluorescence, or color changes), depending on the state of the sensing module. Three main reporter modules are used for the construction of WCBs: luminescent enzymes [encoded by eukaryotic luc genes or bacterial lux genes (Wiles et al., 2009)], fluorescent proteins [green fluorescent protein (gfp) and its fluorescent variants (Shimomura, 1979; Chalfie et al., 1994)] and β-galactosidase (lacZ, Fowler and Zabin, 1978; Kalnins et al., 1983). Reporter modules have been extensively analyzed (Ghim et al., 2010; French et al., 2011; Shin et al., 2011; Gutiérrez et al., 2015) and will not be discussed in this review. In general, TF-based signal transducers can be combined with any of the aforementioned reporter systems. A detailed comparison between their usefulness and suitability for different applications can be found in (Hakkila et al., 2002).
In contrast with the limited repertoire of reporter genes, the variety of signal transducers in nature is enormous. Prokaryotes transform environmental signals to cellular responses using one-component or two-component systems. In two-component system, a membrane-bound sensor histidine kinase catalyzes its autophosphorylation and then transfers the phosphoryl group to a response regulator, which regulates gene expression (Laub and Goulian, 2007). The homology of the histidine kinase domains allows swapping of these domains and their cognate regulators to create chimeric systems (Ninfa, 2010). Some whole-cell biosensors were designed by using two-component systems, detecting input signals such as light, oxygen, or osmolarity changes (Zhang and Keasling, 2011). However, because typical two-component systems use kinase phosphorylation for module communication, undesired crosstalk between systems could happen, especially after overexpression of either a chimeric input domain or an unnatural response regulator. Nevertheless, the majority of signal transduction systems in bacteria consist of a single protein that contains both the input and output domains. These one-component systems display a greater domain diversity than two-component systems (Ulrich et al., 2005). One-component TF typically contain a DNA-binding domain (DBD), responsible for recognition and binding of the operator DNA, and an effector-binding domain (EBD), responsible for oligomerization of the regulator and transmission of the effector signal to the DNA-binding domain. Thus, one-component TFs are more versatile than two-component systems although, in the former, it is more complicated to swap EBDs and DBDs to create chimeric systems. Hereafter, TF will be used to refer to one-component TF.
Transcription factors can act as transcriptional repressors or activators (Figure 1). When the effector is not present, transcriptional repressors are bound to their operator sites, which lay in the promoter region of the regulated operon (Figure 1A). When bound to DNA, transcriptional repressors block the association of the RNA polymerase (RNApol) to the promoter, or prevent its progression. Effector binding releases the repressor from its operator, allowing transcription of the operon. A variation of this regulation mode is used by aporepressors, which bind to DNA only if the effector (called corepressor) is present (Figure 1B).
FIGURE 1. Schematic representation of whole cell biosensors (WCBs) based on repressor (A), aporepressor (B), or activator (C) transcription factors (TFs). Binding of TF to its operator (TFO) within the promoter region of the reporter gene affects RNApol activity and thus the signal associated to the reporter protein (green stars). The presence of the analyte (effector molecule) modifies the interaction of TF with TFO and changes the amount of reporter protein produced.
Transcriptional activators bind to their operator sites by recruiting RNApol to the promoter, or inducing the formation of transcriptionally active RNApol-promoter open complexes when the effector is present (Figure 1C). Transcriptional activation is more complex than transcriptional repression, often requiring DNA bending and the establishment of specific contacts with RNApol α-subunit. We will describe these mechanisms in further detail when describing the relevant families of transcription activators.
DNA Binding Domain
Bacteria have evolved a relatively short list of sequence-specific DBDs, commonly displaying one of three basic folds. Most frequently, DBDs contain the helix turn helix (HTH) motif. HTH motif is around 20 amino acids long and comprises two short alpha helices (7–9 amino acids long each). One is the DNA recognition helix while the second, perpendicular to the recognition helix, is the stabilizing helix (Brennan and Matthews, 1989). A short turn connects both helices, with a glycine usually conserved at the start of the turn. HTH DNA binding proteins bind to inverted repeat sequences separated by approximately one turn of helix. Thus, dimerization is required for full activity. Some HTH motifs contain additional alpha helices to stabilize the motif.
A variant of the HTH motif is the winged HTH motif (wHTH). In the canonical wHTH motif, a 3-helical bundle and a 3 strand β-sheet (wing) are arranged in the order: α1-β1-α2-α3-β2-β3 (Gajiwala and Burley, 2000). α2 and α3 form the regular HTH motif, α3 being the recognition helix involved in specific interactions with the major groove of the DNA.
A less frequent DNA binding motif is the ribbon helix helix (RHH) motif. It consists of a two-stranded anti-parallel β-ribbon followed by two α-helices. In RHH DNA binding proteins, two dimers contact each side of their cognate operator. DNA recognition is achieved by insertion of the β-ribbon into the major groove, whereas the two helices constitute most of the hydrophobic core and are involved in dimerization (Schreiter and Drennan, 2007). DNA specific contacts involve polar amino acids of their N-terminal β-sheets.
Effector Binding Domain
While DBDs show a remarkable degree of conservation, EBDs are more variable, because of the chemical diversity of potential effectors. The role of the EBD is to bind the effector and transduce the activating/repressing signal. Signal transduction proceeds via conformational changes transmitted either to the DBD (causing its release from DNA in the case of transcriptional repressors) or to the RNApol (in the case of activators). The chemical specificity of EBD and its ability to produce a robust transcriptional signal is what qualifies a TF as a potential candidate for WCB development.
Structural and phylogenetic analyses identified TF families in prokaryotes. TF families usually share a common regulatory mechanism. Members of each family show sequence homology, with higher sequence conservation at the DBD. Yet, for many TF families, structural homology at the EBD can also be found. In most cases, members of a given TF family bind similar kinds of analytes, allowing a broad classification of TFs based on analyte specificity. There are, however, remarkable exceptions. As we will see, it is not rare to find cases where evolutionary exaptation produced TFs with different analyte specificity than most members of its family.
In general, TFs regulate the transcription of operons somehow related to their cognate analyte. For this reason, most TFs contain EBDs that recognize molecules involved in central metabolism. In nature, there are thousands of TFs with different mechanisms of transcriptional regulation (Figure 1), different effectors, different structural organization, or different DNA binding motifs (Figure 2).
FIGURE 2. Variety of one-component TFs found in nature. (A) ArgR (3LAJ, Cherney et al., 2010) represses the transcription of the biosynthetic genes of the arginine operon. ArgR is a wHTH transcriptional aporepressor activated by the corepressor arginine, so that the regulated operon is not transcribed when the effector is present. (B) LacI (1EFA, Bell et al., 1998) inhibits expression of the lac operon. When the sugar allolactose is present, its binding to the C-terminal domain of dimeric LacI produces a conformational change that inhibits DNA binding by the N-terminal HTH. (C) NikR (2HZV, (Schreiter et al., 2006) is a ligand dependent aporepressor that only binds the operon when Ni+2 is bound. (D) TetR (1QPI, Orth et al., 2000) is a HTH repressor that senses the presence of the antibiotic tetracycline. (E) FadR (1HW2, Xu et al., 2001) contains an N-terminal wHTH motif connected to a C-terminal EBD similar to TetR family EDBs. However, FadR effectors are acyl-CoAs instead of antibiotics. (F) cAMP receptor protein or CRP (1CGP, Schultz et al., 1991) is a transcriptional activator. cAMP allows the binding of the CRP C-terminal HTH motif to the operator of several catabolic operons. There, CRP-cAMP interacts with RNApol, allowing the transcription of the corresponding operons. In this figure, as well as in the following figures, DBDs are colored in green and EBDs in magenta. The number of amino acids of each TF is also shown.
Transcription factors like ArgR, LacI, or CRP constitute the hallmark of transcriptional regulation in bacteria. Most mechanisms that we will describe in the following sections where originally described for these TFs. Unfortunately, these TFs are of little interest for the purpose of WCB development. The role of biosensors is to provide the exquisite chemical specificity of biological components for the detection of compounds that are often hazardous, toxic, and/or contaminating. We will focus our attention in TF families that are used or could be used for the construction of WCBs to detect environmental contaminants such as aromatic compounds, antibiotics, or heavy metals. Depending on the recognized analyte, we grouped TFs in three main groups: TFs that respond to aromatic compounds, TFs for the detection of metal ions and TFs that respond to antibiotics.
Detection of Aromatic Compounds
In the environment, aromatic hydrocarbons are a common source of toxicity. In fact, some aromatic compounds are endocrine disrupting chemicals (EDCs), toxic molecules associated with altered reproductive function, endocrine-related cancers (breast, endometrial, ovarian, prostate, testicular, and thyroid), abnormal growth patterns and neurobehavioral disorders (WHO, 2012). EDCs are found in various materials such as pesticides, additives, or contaminants in food, and personal care products emphasizing the need to detect their presence and concentration in these materials. Most of our knowledge on TFs that respond to aromatic compounds comes from the fields of biorremediation and natural pathways for biodegradation. Due to the toxicity of aromatic compounds, many bacterial species have evolved degradative pathways, often using these compounds as carbon sources for growth. Because exposure to these compounds is not constant, and the production of the enzymes required for degradation is metabolically expensive, the expression of degradative pathways is commonly regulated by the target compounds themselves (Ramos et al., 2009). Thus, many TFs employed by environmental bacteria for detoxification are ideal for the development of WCBs (Galvão and de Lorenzo, 2006).
Most TFs that act as biosensors for aromatic compounds were obtained from bacteria that thrive in polluted environments. Among them, Pseudomonas putida is the most widely used, due to its genetic tractability, culturability, and environmental versatility. Consequently, most data presented in this section comes from experiments performed in this, or closely related species.
Transcription factors for aromatic compound detection usually fall into three major families: XylS-AraC, NahR-LysR, and XylR-NtrC (Table 1). TFs from these families are generally transcriptional activators, although the specific mechanisms employed for transcription activation are different in each case.
Many TFs that respond to aromatic compounds belong to the AraC superfamily of transcriptional regulators. AraC is a transcriptional activator that drives the expression of the arabinose operon in Escherichia coli, and the prototype of a TF family that contains more than 10,000 homologs (Yang et al., 2011). Extensive studies in the last 40 years have unveiled AraC mechanism of action in great detail. AraC is a dual TF, acting as a transcriptional repressor in its apo form, and as a transcriptional activator when bound to arabinose. The canonical AraC “light switch” mechanism of transcriptional control involves two states. In its apo form, AraC forms a dimer and binds to the araBAD promoter via two distant operators (I1 and O2; Figure 3). In this state, DNA is bent forming a loop that prevents transcription initiation. Binding of arabinose to AraC produces an allosteric change in the protein. This allosteric change forces the AraC to bind the adjacent operators I1 and I2, relaxing the DNA loop. The relaxed state of the promoter allows the recruitment of the RNApol by the general regulator CRP, thus promoting transcription. This activation mechanism is similar in other members of the AraC family.
FIGURE 3. XylS-AraC family. (A) Activation mechanism. In the repression state, AraC bound to I1 and O2 at the araBAD promoter forms a DNA loop that prevents transcription initiation. When arabinose is present, each of the AraC monomers bind adjacent operators (I1 and I2), releasing DNA bending and promoting the recruitment of RNApol and subsequent transcriptional activation. XylS activation mechanism is different, being RNApol repressed by apo-XylS bound to operator D and activated by tolune-XylS bound to operator P. (B) XylS-AraC structure. The structure of XylS homolog ToxT (3GBG, Lowden et al., 2010) is shown together with the location of arabinose in the EBD of AraC (2ARC). The two HTH motifs present in the DBD are highlighted. AraC (arabinose) and XylS (toluene) effectors are shown.
Members of the AraC superfamily contain a C-terminal DBD, and an N-terminal EBD (which is also responsible for protein dimerization; Bustos and Schleif, 1993). The DBD contains two HTH motifs (Figure 3B), although only the second one (N-terminal) makes specific contacts with the operator sequence (Gallegos et al., 1997). This DBD is conserved among all members of the AraC superfamily. In contrast, the EBD has suffered a remarkable degree of evolutionary exaptation, producing AraC-like TFs responding to a wide range of different analytes. For WCBs, the most interesting AraC-like TFs belong to a specific sub-family, represented by XylS, a TF from P. putida mt-2.
XylS regulates a degradative pathway present in plasmid pWW0 that allows P. putida mt-2 to degrade toluene and m-xylene. This route is divided in two operons: the upper (ortho) and the lower (meta) operons. XylS is responsible for the transcriptional control of the lower part (the upper part is controlled by XylR, which will be described in the next section). XylS activates transcription in response to benzoate and m-toluate, intermediate metabolites generated by the upper part of the metabolic pathway, and substrates for the enzymes encoded in the meta operon. XylS mechanism of action is slightly different from AraC, since the over expression of XylS can trigger transcriptional activation independently of the inducer (Ramos et al., 1987). Also, the mechanism of activation of XylS upon binding to its inducer is not identical to AraC. In AraC, the apo form of the protein suffers from intermolecular repression (the TF is kept in its inactive form by specific contacts between monomers), while XylS suffers from intramolecular repression (Domínguez-Cuevas et al., 2008).
Regarding analyte specificity, although XylS-AraC family members exhibit substantial sequence identity at the EBD, they recognize widely different analytes. Some, like BenR, exhibit analyte specificities similar to XylS (Pérez-Pantoja et al., 2014). Others participate in the regulation of virulence determinants in different microbial pathogens. These TFs recognize molecules as varied as bicarbonate (RegA from Citrobacter rodentium), cellobiose (TxtR from Streptomyces scabies), urea (UreR from Proteus mirabilis), and bile salts (ToxT from Vibrio cholerae; Yang et al., 2011). Unfortunately the structural basis for this remarkable analyte diversity is poorly understood. Although the crystalline structures of AraC DBD and EBD domains have been obtained (Soisson et al., 1997; Rodgers and Schleif, 2009), the lack of structural information for XylS-like TFs makes the molecular basis of substrate recognition obscure. Even though, PHYRE (Kelley and Sternberg, 2009) predicts XylS structure to be similar to ToxT (3GBG; Lowden et al., 2010), indicating that slight structural changes may result in radical alterations of effector specificity. Despite the lack of structural information for rational engineering, mutagenesis studies have been successful in generating XylS molecules with altered inducer specificity (Michan et al., 1992). Among them, XylS2 mutant stands out for its ability to detect a wide range of inducers, including salicylate (Ramos et al., 1986).
XylR-NtrC Like Transcriptional Regulators
A second group of TFs involved in sensing and degradation of aromatic compounds is the NtrC family. Members of this family are usually involved in the expression of adaptive genes for harsh environmental conditions (Kustu et al., 1989), promoting transcription via σ54 mediated activation of RNApol (Hirschman et al., 1985). σ54 dependent promoters display a -12/-24 architecture that renders the formation of the open complex thermodynamically unfavorable (Hunt and Magasanik, 1985; Thöny and Hennecke, 1989). NtrC-like TFs activate transcription by providing the energy required for the formation of the open complex (Weiss et al., 1991). For this purpose, NtrC-like proteins contain an AAA+ ATPase motif that constitutes a distinct feature of this TF family (De Carlo et al., 2006). Another feature of NtrC-like regulators is the unusual location of their cognate DNA binding sites. These sites, named upstream activator sequences (UASs), are situated up to 200 bp upstream the transcriptional start (Pérez-Martín et al., 1994), resembling eukaryotic enhancers. NtrC activation involves protein multimerization into an ATPAse active form [most commonly into a hexamer, but occasionally into a heptamer (De Carlo et al., 2006; Bush and Dixon, 2012)]. Since UASs are located far up the transcriptional start, activation requires the formation of a DNA loop that allows NtrC to make specific contacts with the σ54-RNApol holoenzyme (Figure 4A). DNA looping is aided either by DNA intrinsic curvature or by other DNA-binding proteins such as IHF (Bush and Dixon, 2012). Once the loop has been formed and contacts between the TF and the σ54-RNApol holoenzyme established, the energy produced by ATP hydrolysis is invested in remodeling the transcription complex from its closed configuration into an open, transcriptionally active form (Rappas et al., 2006).
FIGURE 4. XylR-NtrC family. (A) Activation mechanism. NtrC effector produces NtrC hexamerization to an ATPase active form, in a way that allows NtrC to make specific contacts with the σ54-RNApol holoenzyme and thus remodeling the transcription complex from its closed configuration into an open transcriptionally active form. Activation requires the formation of a DNA loop, aided by IHF. (B) NtrC structure. The crystal structure of the inactive dimer of NtrC1 (1NY5, Lee et al., 2003) is shown. DBD, EDB and AAA+ domains as well as the alpha helix that connects EDB with AAA+ are highlighted.
Structurally, NtrC family TFs (Figure 4B) contain a conserved and a variable region (Bush and Dixon, 2012). The conserved region contains an N-terminal domain that bears the HTH motif responsible for UAS binding (DBD), and a large, central domain that contains the AAA+ fold for ATPase activity (De Carlo et al., 2006). The variable region contains the structural determinants that control oligomerization and ATPase activity. The entire NtrC-like family shows a remarkable degree of variability in this respect, with about 50% of its members containing a regulatory domain for the specific interaction with another protein (two-component systems and protein–protein interactions) while the other 50% exhibit a sensing motif that activates transcription upon binding a small ligand (Bush and Dixon, 2012). NtrC-like proteins involved in aromatic compound sensing and degradation are among the latter, containing a C-terminus region that binds to the effector and regulates oligomerization and ATPase activity (North et al., 1993). For these purposes, the C-terminus of the protein is divided in two domains. The A domain is involved in ligand binding, while the B domain acts as a hinge that brings together the A domain and the AAA+ fold located at the central part of the protein. In this conformation, the A domain suppresses protein oligomerization and ATPase activity. Upon ligand binding, intra-domain repression is relieved, resulting in protein oligomerization and ATPase activation (Pérez-Martín and De Lorenzo, 1995).
Several NtrC-like TFs respond to aromatic compounds, but the model system for this entire group is XylR, the transcriptional regulator of the upper operon for toluene and m-xylene degradation from plasmid pWW0. XylR responds to m-xylene and toluene, substrates for pWW0 upper pathway, but also to a surprising variety of structural analogs (reviewed in Galvão and de Lorenzo, 2006). This versatility was exploited to generate biosensors for BTEX (benzene, toluene, ethylbenzene, and xylene, a common source of contamination resulting from the oil industry) not only in the lab (Mi Na Kim, 2005) but also in situ (de las Heras and de Lorenzo, 2011b). XylR was also engineered to detect nitrotoluenes, a promising approach for the bio-detection of landmines (Garmendia et al., 2008; de Las Heras and de Lorenzo, 2011a). Recently, novel XylR variants that allow the implementation of simple Boolean logic operations were generated (Calles and de Lorenzo, 2013). Similarly, network engineering allowed the generation of sensing circuits based on XylR that display enhanced analyte specificity, overcoming the natural promiscuity of XylR (de Las Heras et al., 2012). These advances turned XylR into a most attractive TF for biosensor development.
Another NtrC-like TF that was successfully turned into a biosensor is DmpR (Campos et al., 2004; Gupta et al., 2012). DmpR is a transcriptional regulator from plasmid pVI150 that confers P. putida the ability to grow on phenols or methyl-phenols (Shingler et al., 1989). DmpR is 65% identical to XylR at the amino acid level, thus the protein structure and mechanism of action are likely to be similar. Yet XylR and DmpR show different analyte specificities (Galvão and de Lorenzo, 2006) protein engineering by domain shuﬄing identified the amino acids involved in this differential specificity (Skärfstad et al., 2000).
LysR-Type Transcriptional Regulators
The LysR family of transcriptional regulators (LTTRs) constitutes the most abundant family of TFs found in bacteria (Pareja et al., 2006). Its members are usually around 300 amino acids long. They display a basic structure consisting of an N-terminal DBD containing an HTH fold, and a C-terminal EBD (Maddocks and Oyston, 2008). LTTRs typically behave as dual transcriptional repressors/activators (Maddocks and Oyston, 2008). Divergent transcription of the regulator and the regulated operon is a common theme among these TFs. LTTRs generally exert a repressive action on their own synthesis (thus engaging in negative feedback loops), while activating transcription of the metabolic pathway upon binding to their cognate effectors (Figure 5A). Transcriptional regulation by LTTRs usually involves two operators, known as the regulatory binding site (RBS) and activating binding site (ABS). In the case of LTTRs involved in aromatic compound metabolism, the RBS is located between the -50 and the -80 position of the promoter, while the ABS is located closer to the transcriptional start (ranging from -50 to -35). The mechanism of action for LTTRs involves a protein tetramer binding simultaneously to both RBS and ABS sites, with one dimer binding RBS and another binding ABS (Figure 5B). This causes the DNA to bend, preventing access of the α-CTD of RNApol to a specific DNA region in the promoter (called UP; Tropel and van der Meer, 2004). Upon binding the effector, the protein slides from the ABS site to an upstream position (ABS″). This movement induces relaxation of DNA bending and directs the α-CTD of RNApol to contact the UP region of the DNA (Devesse et al., 2011). This is the active configuration that promotes transcription.
FIGURE 5. LysR family. (A) Architecture of the LTTR regulator and the regulated operon. LTTRs repress their own synthesis, while activating the transcription of the biodegradative operon. (B) Activation mechanism. Each of the dimers of the tetramer LTTRs binds to the RBS and the activating binding site (ABS), respectively. This causes the DNA to bend, preventing the access of the α-CTD of the RNApol to the promoter. Upon binding to the effector, the protein slides from ABS to ABS″″. This movement directs the α-CTD of RNApol to contact DNA promoting transcription. (C) LTTR structure. The crystal structure of the LTTR CnbR (1IZ1, Muraoka et al., 2003) is shown. The inset shows the location of two benzoic acid molecules within BenM (2F78, Ezezika et al., 2007). The molecular structure of effectors benzoic acid and salicylic acid is also shown.
Several LTTRs are known to respond to aromatic compounds, but unlike XylS and XylR families, there is not a clear prototype for the entire group. Instead, LTTRs involved in the degradation of aromatic compounds can be broadly divided in distinct subgroups according to their effectors (which correlates with sequence similarity at the C-terminal EBD). Among them, two subgroups deserve specific attention. The first comprises LTTRs that respond to cis,cis-muconate or its chlorinated derivative 2-chloro-cis,cis-muconate, intermediates in the degradation pathway of catechol and chlorocatecol, respectively. Main representatives of this subgroup include CnbR, from Ralstonia, ClcR and CatR from Pseudomonas, and BenM from Acinetobacter. Crystal structures of CnbR (1IZ1, Muraoka et al., 2003) and BenM (2F78, Ezezika et al., 2007) shed light on the molecular basis of effector recognition for this group of closely related LTTRs (Figure 5C). CnbR and BenM display 28% amino acid sequence identity and significant structural similarity. Their C-terminus contains two motifs, EBD-I and EBD-II, connected by a hinge (Schell, 1993; Muraoka et al., 2003; Ruangprasert et al., 2010). This arrangement is similar to the prototypic periplasmic binding protein (PBP) fold, in which two globular β/α domains, separated by a hinge, form a clamp that binds a small molecule (Ruangprasert et al., 2010). In the case of CnbR and BenM, the effector binding clamp is formed between EBD-I and EBD-II (Muraoka et al., 2003; Ruangprasert et al., 2010). Characteristic of these proteins is the formation of an asymmetric tetramer (Bundy et al., 2002; Muraoka et al., 2003), resulting from the association of two dimers in different conformations (Muraoka et al., 2003; Ruangprasert et al., 2010). One protein from this group, BenM, shows the distinct property of having two inducers that act synergistically. BenM is induced by cis,cis-muconate and benzoate (Bundy et al., 2002; Clark et al., 2002). The synergistic effect of both inducers is possible because BenM presents two distinct binding sites, one for cis,cis-muconate (present at the clamp between EBD-I and EBD-II domains) and a second one for benzoate (Craven et al., 2009). This dual regulatory input is unique among TFs that respond to aromatic compounds.
A second subgroup of LTTRs involved in the degradation of aromatic compounds is represented by NahR from Pseudomonas and DntR from Burkholderia. These two regulators exhibit a 40.5% identity in their amino acid sequence and they both respond to the inducer salicylate, an intermediate metabolite in the degradation pathway of naphthalene. Although NahR was successfully implemented in functional salicylate biosensors (Werlen et al., 2004; Shin, 2010; Xue et al., 2014), more detailed information about the molecular mechanism of DntR exists in the literature. Among TFs that control degradative pathways of aromatic compounds, DntR is exceptional due to its unusual effector specificity. As mentioned above, DntR responds to salicylate. Yet DntR is associated with a biodegradative pathway for 2,4-dinitrotoluene (DNT), for which salicylate is not an intermediate metabolite. Actually, DntR is unresponsive to DNT or any of its intermediate catabolites. Thus DntR was considered a substrate-blind regulator (de Las Heras et al., 2011). To explain this bizarre situation, de Las Heras et al. (2011) noted that DNT is a xenobiotic compound, not found in the environment. Thus, it is likely that the DNT pathway regulated by DntR represents a recent evolutionary innovation, involving the adaptation of naphthalene degradation genes to mineralization of DNT, with a TF that is still poorly adapted (de Las Heras et al., 2011). Besides representing a beautiful example on how xenobiotic stress drives the evolution of environmental bacteria, the abnormal effector profile of DntR serves also as a cautionary tale for the development of biosensors. It indicates that one cannot take for granted that the transcriptional regulator of a catabolic pathway is going to respond to the substrate or any of the intermediates of the pathway. This is especially likely if the substrate is a xenobiotic compound that has been introduced in the environment in recent times (at the evolutionary scale). Regarding the structural basis of DntR activation by salycilate, crystallographic data indicated that its structure is similar to that of other LTTRs, with a C-terminus consisting of two subdomains linked by a hinge (Devesse et al., 2011). As is the case in BenM and CnbR, the effector binding pocket is located in the interface between these two subdomains (Devesse et al., 2011). Interestingly, DntR shows a second pocket for salicylate binding, which resembles the double binding pocket present in BenM. Although the physiological relevance of the second binding site is not clear (Devesse et al., 2011), it is tempting to speculate that it might represent an intermediate step in the adaptation of DntR to the recognition of DNT or any of its intermediate catabolites. Experimental evolution resulted in DntR variants that show a 10-fold increase in DNT sensitivity, but these mutants also exhibited higher sensitivity for salicylate (Lönneborg et al., 2012).
Detection of Metal Ions
Metal detection is a fundamental goal of WCB development. Some metals, such as Cu, Fe, K, Mg, or Mn are essential nutrients, while others (Ag, Al, Cd, Au, Pb, Hg) serve no known biological function (Bruins et al., 2000). Nevertheless, most metals have toxic effects in biological reactions at high concentrations, regardless of being essential or non-essential. Toxicity is the main reason behind the development of metal biosensors. WCBs were successfully constructed to detect Hg(II) in environmental samples (Bontidean et al., 2004; Priyadarshi et al., 2012). Cadmium is detected using WCBs containing GFP-metallothionein (Amaro et al., 2014) and WCBs with an engineered modular genetic AND logic gate are able to detect As(III), Hg(II), Cu(II), and Zn(II) and distinguish between them (Wang et al., 2013). The economic value of some metals also justified the development of biosensors for mining purposes (Cerminati et al., 2011). Based on their structural homology and analyte specificity, five main families of prokaryotic metal sensing transcriptional regulators can be defined (Pennella and Giedroc, 2005).
The MerR family comprises a group of TFs that generally respond to transition metals and act as transcriptional activators. The main representative of this family is MerR, a TF present in Gram+ and Gram- bacteria, which binds to mercury and regulates the expression of a mercury resistance operon (Barrineau et al., 1985).
MerR is a transcriptional activator that binds to a specific operator located between the -35 and -10 elements of a σ70 promoter. In MerR-responding promoters the space between the -35 and -10 elements is 19–20 bp long, greater than the optimal 17 ± 1 bases required for adequate transcriptional activity (Ross et al., 1989). This elongation causes limited transcriptional activity. Moreover, the apo form of MerR binds to its operator as a dimer, blocking transcription initiation, thus acting as a transcriptional repressor. Upon binding to its effector, MerR causes a slight bend on the operator DNA, approaching the -10 and -35 sequences, thus favoring the association of RNApol (Ansari et al., 1995) and promoting the formation of the transcriptional open complex (Brown et al., 2003).
Structurally, MerR proteins are characterized by three distinct domains: an N-terminal DBD domain, a central linker, and a C-terminal EBD (Figure 6A). The DBD contains a HTH motif formed by the first 44 amino acids of the protein (Brocklehurst et al., 1999). Helices α1 and α2 form the DNA binding HTH motif while the next two helices (α3 and α4) comprise a coupling region that communicates occupancy of the EBD to the DBD (Guo et al., 2010). These helices are followed by a coiled coil region (α5) that is involved in protein dimerization (amino acids 80–128; Zeng et al., 1998). The EBD contains a metal binding pocket formed by three cysteines (Figure 6). Two Cys come from one monomer (Cys117 and Cys126 in E. coli MerR) and one Cys comes from the other monomer (Cys82′ in E. coli MerR; Utschig et al., 1995). This site is essential for metal binding. In MerR the Cys center binds to Hg(II), but other members of the family can bind toxic metals like Br (BmrR) and Pb (PbrR), or micronutrients like Cu (CueR) and Zn (ZntR; Table 2). Although metal binding is always exerted through the Cys coordination, the number of Cys residues involved is not conserved. In some cases MerR regulators can bind to different ions using a distinct subset of these Cys residues. For example, ZntR can be activated by Zn(II), which binds to five Cys residues. However, the same protein can be activated by Pb(II) and Cd(II), which require coordination with only four Cys residues.
FIGURE 6. MerR family. (A) MerR structure. The structure of the MerR member MtaN bound to DNA (1R8D, Newberry and Brennan, 2004) illustrates MerR family binding to its operator. MtaN monomers are shown in green and blue, respectively, while DNA is shown in orange. The inset shows the two cysteines of CueR (1Q05, Changela et al., 2003) involved in Cu (I) coordination. (B) MerR family alignment. The alignment of representative members of MerR family is shown. Residues involved in metal coordination are highlighted in yellow. DNA binding α2 is shown in green.
This Cys center characteristic of MerR regulators is primarily suited for metal binding. Yet evolutionary exaptation has generated MerR regulators where these Cys residues constitutively bind to a metal ion to respond to physichochemical signals. The most paradigmatic example of these type of MerR regulators is the oxidative stress sensor SoxR (Amábile-Cuevas and Demple, 1991). Binding to four metal ions [2Fe-2S], SoxR is able to sense superoxide concentrations (Ding et al., 1996). Other MerR-like regulators are able to sense antibiotics (TipA, Holmes et al., 1993), or even light (LitR, Takano et al., 2011).
The modular structure of MerR-like regulators allowed the construction of chimeric TFs. The proof of principle for this approach is the hybrid MerR-ZntR constructed by Brocklehurst et al. (1999). It comprises the N-terminal region of Tn501 MerR (44 amino acids) and 103 amino acids from the C-terminal region of ZntR. This hybrid MerR-ZntR senses Zn(II) and was expected to regulate the expression of MerR-responding promoters. However, although the hybrid TF is able to bind to its cognate operator, it is not able to activate transcription from this promoter. The hybrid MerR-ZntR TF requires a chimeric promoter that includes the 20 bp spacer of ZntR-responding promoters (Brocklehurst et al., 1999). These results indicate that the conformational changes that promote DNA binding reside in the C-terminal domain, and not in the N-terminal DBD.
The SmtB/ArsR TF family is also involved in metal sensing. They control operons involved in protection against toxic metals, thus constituting an interesting source of TF for metal biosensing. Their mechanism of action is relatively simple. They are repressors that bind their cognate promoters, recognizing an operator located near or overlapping the transcriptional start site. Upon binding the inducer metal ion, ArsR-like TFs are released from the promoter, thus allowing transcription (Eicken et al., 2003). They occur in Gram positive, Gram negative bacteria and also in archaea (Itou et al., 2008). Important members of this family are the As sensor ArsR of E. coli (P15905, Busenlehner et al., 2003), the Cd sensor CadC of Staphylococcus aureus (1U2W, Ye et al., 2005), the Zn sensors SmtB of S. elongatus (1R23, Eicken et al., 2003) and CzrA of S. aureus (1R1V, Eicken et al., 2003) and the Ni sensor NmtR of M. tuberculosis (2LKP, Lee et al., 2012), Table 2.
Structurally, ArsR family members share a similar folding (Itou et al., 2008; Zhao et al., 2010; Mukherjee et al., 2014). They form dimers (Busenlehner et al., 2003) with each monomer exhibiting a α1-α2-α3-αR-β1-β2-α5 organization (Figure 7A, Cook et al., 1998). The dimerization interface is constituted by α1 and α5 helices. The DBD presents a wHTH motif formed by α3 and αR, which is the most conserved region of the protein family (Busenlehner et al., 2003). The effector is bound by two metal coordination sites. The first is located in helix α3, adjacent to the DBD, while the second is found in α5, at the dimerization interface (Shi et al., 1996; Turner et al., 1996; VanZile et al., 2002; Busenlehner et al., 2003). As in the case of MerR-like regulators, metal coordination is exerted by a series of Cys residues. Interestingly, not all members of the ArsR family present both metal coordination sites (Figure 7B): ArsR and Listeria monocytogenes CadC present only α3, CzrA and NmtR present only α5 while CadCs, SmtB, and ZiaR present both (Busenlehner et al., 2003). For those ArsR-like regulators that exhibit two metal coordination sites, only one seems to be involved in signal transduction. SmtB responds through its α5 metal binding motif, while CadC does it through the α3N site (Busenlehner et al., 2003).
FIGURE 7. ArsR family. (A) ArsRF structure. The crystal structure of the dimer SmtB bound to Zn (II) (1R23, Muraoka et al., 2003) is shown. SmtB monomers are shown in green and blue, respectively. The inset shows the residues within α5 involved in metal binding. (B) ArsR family alignment. The alignment of ArsR members of Table 2 is shown. Residues of α3 or α5 involved in metal binding are highlighted in blue and yellow, respectively. DNA binding αR is shown in green.
Biosensors built upon ArsR constitute some of the most successful approaches for the practical use of WCBs. Arsenic contamination in drinking water is a considerable public health problem in several parts of the world (Tchounwou et al., 1999). Because arsenic determination by chemical methods is unaffordable in certain areas, WCBs constitute an appealing low-cost alternative. Field studies have demonstrated the applicability of ArsR biosensing in rural areas (Trang et al., 2005; Siegfried et al., 2012).
DtxR, Fur, and NikR Families
Besides MerR and ArsR families, which comprise TFs associated to metal resistance and detoxification, other TFs are able to bind metals and elicit transcriptional responses. Transition metals are key cofactors for enzymatic catalysis and essential components of many cellular proteins. However, they cannot be accumulated in the cell, since any excess may result in the formation of reactive oxygen species. Thus, bacteria keep a delicate balance of metal homeostasis. Three families of transcriptional repressors, DtxR, Fur, and NikR, are key in this process. These regulators not only have a homeostatic role. Metal deprivation is a common way of fighting infections employed by eukaryotic organisms. Many pathogens have evolved regulatory circuits that link the expression of virulence factors with metal distress (Kehl-Fie and Skaar, 2010). These sensing capabilities make Dtx, Fur, and NikR-like TFs appealing candidates for the development of metal WCBs.
DtxR is the prototype of a family of transcriptional aporepressors involved in metal homeostasis and metal-dependent virulence regulation (Andrews et al., 2003). Members of this family are able to detect iron (DtxR, IdeR, SirR; Hill et al., 1998) and manganese (ScaR, MntR, and TroR; Stoll et al., 2009; Liu et al., 2013) although, like most metal-dependent TFs, they display effector promiscuity, binding other cations with lower affinity (Pennella and Giedroc, 2005). Structurally, DtxR-like repressors present two conserved domains and one variable domain (Stoll et al., 2009). The N-terminal DBD contains a wHTH motif that is conserved among all members of the family, along with a central domain involved in protein dimerization (Figure 8A). SirR, ScaR, and IdeR contain also a FeoA-like C-terminal domain of uncertain function, not present in other members of the family. Domain variability is not related to substrate specificity: ScaR presents three domains, while TroR and MntR present only the first two, yet the three of them recognize primarily Mn(II). IdeR and SirR present a FeoA-like C-terminal domain, but DtxR C-terminus does not, and the three proteins primarily bind iron. The metal binding sites for this family are likely to be not entirely conserved (Qiu et al., 1995; Schiering et al., 1995; Pohl et al., 1999; Feese et al., 2001; Wisedchaisri et al., 2004, 2007; Stoll et al., 2009). In DtxR, two metal binding sites were defined: the primary site, located at the interface between the DBD and the dimerization domain, and the ancillary site, formed between the dimerization domain and the C-terminal part of the protein. In IdeR, occupation of the first site causes dimerization, while binding to the second releases the repressor from its cognate operator (Chou et al., 2004). Mn binding TFs do not generally show equivalent binding sites. MntR contains two binding sites (A and C) located at the interface between the DBD and the dimerization domain (McGuire et al., 2013), while the molecular basis for metal specificity are unclear for TroR and ScaR. Structural data indicates that metal activation is different from DtxR (Hazlett et al., 2003; Stoll et al., 2009). Like in other metal sensory TFs, Ni(II) or Zn(II) binds MntR even with a greater affinity than its cognate metal Mn(II). This observation is in accordance with the Irving-William series for divalent metals, where the stability constant for complex formation follows the order Mg(II) < Mn(II) < Fe(II) < Co(II) < Ni(II) < Cu(II) > Zn(II) (Irving and Williams, 1948). However, in vivo MntR effector is indeed Mn(II), but not Ni(II) or Zn(II). The explanation to this apparent discrepancy is that Ni(II) or Zn(II) activate their specific eﬄux pumps before reaching the levels needed to repress Mn(II) uptake (Spiro and Dixon, 2010). This is something to take into account for the design of synthetic metal-specific WCBs.
FIGURE 8. DtxR, Nur, and NikR families. (A) DtxRF structure. Two DtxR dimers are shown, bound to DtxR operator (1DDN, White et al., 1998). (B) FurF structure. The Ferric uptake regulator (Fur) is bound as a dimer to its operator (2W57, Sheikh and Taylor, 2009). (C) NikRF structure. NikR recognizes its operator sequence by a RHH DBD (2HZV, Schreiter et al., 2006). The location of Ni(II) atoms in DtxR and NikRA and Zn(II) atoms in Fur is shown by red spheres.
A second family of TFs involved in the homeostasis of transition metals and also in the expression of virulence determinants is represented by the ferric uptake regulator Fur. Fur-like TFs are generally transcriptional repressors, although some transcriptional activators can be also found within the family (Delany et al., 2004; Troxell and Hassan, 2013). Other relevant members of Fur family include Mur, Nur, and Zur, which respond to manganese, nickel and zinc, respectively (Troxell and Hassan, 2013). Fur-like regulators are characterized by a simple structure (Fillat, 2014): a wHTH domain with a small C-terminal moiety that serves as metal-binding and dimerization interface (Figure 8B). Metal binding induces conformational changes that promote a tight association of Fur-like TFs with their operators, which are usually inverted repeats (Fillat, 2014). Besides the effector metal, most Fur-like TFs contain a second binding site for zinc, which serves a structural role in the protein (D’Autréaux et al., 2007).
A third family of TFs for transition metals comprises a set of homologous proteins for nickel homeostasis, generally known as NikR proteins (Schreiter et al., 2003; Chivers and Tahirov, 2005; West et al., 2010). NikR are tetramers organized in two domains: a tetramerization domain flanked by two dimeric RHH DNA-binding domains (Figure 8C). NikR contains four high-affinity sites within the tetramerization domain interface and secondary nickel-binding sites between the four subunits that form the tetramer. In E. coli, its proposed mechanism of action includes activation of the tetramer by Ni(II) occupation of the high affinity sites. Binding to secondary sites locks NikR in the closed conformation needed for interaction with DNA and repression of NikR regulated promoters (Chivers and Sauer, 2002; Chivers and Tahirov, 2005; Bahlawane et al., 2010). The operator for E. coli NikR is formed by a dyad-symmetric half-sites 5′-GTATGA-3′ on opposite ends of an imperfect 16–6–16 inverted repeat (Schreiter et al., 2003). When bound to the DNA, the RHH domains of the tetramer rotate around the flexible interdomain linkers to face the DNA binding motif toward the double strand. In this conformation, the antiparallel β-strands occupy the DNA major groove of an operator palindrome half-site (Schreiter et al., 2006). This regulatory mechanism is only partially conserved in other homologs. For example, H. pylori NikR conserves the high and the low affinity binding sites, but the later does not seem to have a regulatory role (Bahlawane et al., 2010; West et al., 2010). Also, despite sequence conservation, H. pylori NikR mechanism of DNA binding and regulation might not be identical to E. coli, since no consensus operator sequence has been identified and, in H. pylori, NikR displays a remarkable pleiotropic action (Bahlawane et al., 2010).
Detection of Antibiotics
Antibiotics are among the most successful drugs used for human therapy. However, since they can challenge microbial populations, they must be considered as important pollutants as well (Martinez, 2009). Antibiotics are likely to be released into the aquatic environment via wastewater eﬄuent and agricultural runoff as a result of incomplete metabolism, ineffective treatment removal or improper disposal. Ultimately, large quantities of antibiotics are used annually in human therapy and in agriculture (Huang et al., 2011). The large excess of antibiotics released by human action into the environment has resulted in rampant levels of antibiotic resistance among bacterial populations, including many pathogens. This situation has triggered efforts to limit the usage of antibiotics in non-essential situations, such as animal husbandry (Andersson and Hughes, 2014). In this context, WCBs could be fundamental tools in containment efforts (Mungroo and Neethirajan, 2014). The TFs that respond to antibiotics are typically involved in the expression of antibiotic resistance genes or, less commonly, antibiotic production. Among these TFs, we distinguish between those that are antibiotic-specific, for which TetR represents the canonical prototype, and those involved in multiple antibiotic resistance, for which MarR constitutes the best characterized example.
TetR family regulators (TFRs), named after the TF that regulates the operon involved in the resistance to tetracycline, represent one of the most common regulatory systems in bacteria. TFRs are mainly associated with antibiotic resistance and the regulation of genes encoding small-molecule exporters, although they also regulate other cellular functions (Ramos et al., 2005; Cuthbertson and Nodwell, 2013). TFRs have been found in almost every prokaryotic genera, usually with several members of the TFR per bacteria.
Structurally, TetR transcriptional regulators comprise an N-terminal DBD and a C-terminal EBD (Figure 9). Nine α helices are conserved in the structure of TFR. DBD, formed by helices 1–3, is highly conserved and contains a HTH motif. α3 is the recognition helix that is inserted in the major groove of the operator DNA. Several structures of TFRs bound to their cognate operators have been solved. The typical TFR operator contains a 15 bp IR with two 6 bp arms separated by 1 bp. The HTH motif of each monomer binds one of the IR arms. Like in other HTH IR DNA binding proteins, dimerization is required for activity. This structure was found in TetR (1QPI, Orth et al., 2000), SimR (2ZQL, Le et al., 2011), TM1030 (4I6Z), DesT (3LSR, Miller et al., 2010) and HrtR (3VOK, Sawai et al., 2012). In QacR, IR is unusually large for an operator sequence bound by a TFR, comprising 15 bp half-sites separated by a 6 bp spacer region (Grkovic et al., 2001). In fact, crystal structure of QacR bound to its 34 bp DNA operator (1JT0, Schumacher et al., 2002) is distinct from TetR and involves the binding of a pair of QacR dimers. Recognition at each IR half-site is mediated by a complement of DNA contacts made by two HTH motifs. Ms6564 (4JL3, Yang et al., 2013) and CgmR (2YVH, Itou et al., 2010) also binds DNA as tetramers. The EBD of TFRs, formed by helices 4–9, regulates DNA binding activity by interacting with its cognate inducer. In general, helices 5–7 form a central triangle, while helices 8 and 9 make up the dimerization interface, forming a four-helix bundle with the same helices from the other monomer (Figures 9A,B). Helices 4 and 6 of the ligand-binding domain link DBD and EDB domains. Effector binding to the EDB provokes a pendulum-like motion of helix 4 in a way that the HTH motifs are badly oriented for DNA binding. In TetR, (and also other homologs like TtgR and ActR) there is a “side entry” opening, distal to the dimerization interface, that seems to be the site of access for the effector (2TRT, Hinrichs et al., 1994); 2VKE, (Palm et al., 2007). Like in most TFs, the EDB is less conserved than the DBD (Ramos et al., 2005; Cuthbertson and Nodwell, 2013). In TFR, the variety of effectors is remarkably high. The structures of TFR bound to more than 100 ligands have been solved.
FIGURE 9. TetR family. (A) TetR family alignment. The alignment of representative TetR members for which effectors are antibiotics is shown. Secondary structure elements forming the DBD and the EDB are colored green and magenta, respectively. Alpha helices described in the text are labeled in the structure and in the alignment. (B) TFR structure. The crystal structure of the TFR TetR bound as a dimer to DNA (1QPI, Orth et al., 2000) is shown. The inset shows the location of a tetracycline derivative (iso-7-chlortetracycline) bound to TetR EDB (2X9D, Volkers et al., 2011). The molecular structure of antibiotic effectors recognized by the aligned proteins is also shown.
Among the spectrum of antibiotics recognized by TRFs, tetracycline and tetracycline-like antibiotics constitute the paradigmatic example, since the description of TetR in transposon Tn10 (Beck et al., 1982). Tetracyclines (Figure 9) are a class of broad-spectrum bacteriostatic antibiotics, as well as against intracellular organisms. They target the small subunit of the bacterial ribosome (Brodersen et al., 2000). TetA mediates tetracyclin detoxification by active eﬄux of the [MeTc]+ cation coupled to the uptake of a proton (Yamaguchi et al., 1991). TetR represses transcription of both its coding gene tetR and the resistance gene tetA. Other tetracycline-like antibiotics such as 7-chlorotetracycline (2TCT, Kisker et al., 1995), 7-iodotetracycline (2XB5, Hinrichs et al., 1994), 6-anhydrotetracycline (2VPR, Aleksandrov et al., 2008), minocycline (2XPV), oxytetracycline (2XPW), or 9-nitrotetracycline (4AUX) are also recognized by TetR.
Two other relevant TFRs, TgtR, and SimR, regulate the expression of antibiotic eﬄux pumps. Chloramphenicol (Figure 9) inhibits protein synthesis by binding reversibly to the 50S subunit of the bacterial ribosome. TtgR represses the transcription of TtgABC, a key eﬄux pump in P. putida, which causes resistance to antibiotics, solvents and toxic plant secondary products. TtgR repression is relieved by binding to Cm (2UXP, Alguel et al., 2007) along with other compounds like phloretin (2UXI), naringenin (2UXU), and quercetin (2UXH). Simocyclinones (Figure 9) are a new class of antibiotics that inhibit bacterial gyrase (Flatman et al., 2005). SimR represses the expression of SimX eﬄux pump. Repression is inhibited by binding of simocyclinone D8 to the EBD of SimR (2Y30, Le et al., 2010). In some cases, TFRs are involved in the control of the biosynthesis and export of antibiotics in producing strains, rather than regulating resistance operons. ActR, present in the biosynthetic gene cluster for the antibiotic actinorhodin (Figure 9) in S. coelicolor, controls the expression of two actinorhodin exporters (Tahlan et al., 2008). Both actinorhodin and its precursor can bind ActR and prevent its interaction with DNA (3B6A, Willems et al., 2008).
The MarR (multiple antibiotic resistance regulator) family of prokaryotic transcriptional regulators (reviewed in Wilkinson and Grove, 2006) includes TFs involved in responses to antibiotic and oxidative stresses, and the catabolism of aromatic compounds. The prototype of the family, MarR, regulates the marRAB gene cluster, which confers resistance to multiple antibiotics (Alekshun and Levy, 1997). While in other TF families the DBD and EDB form structurally different domains, MarR is unique in that DBD and EBD almost completely overlap (Figure 10). The main component of the MarR family is the wHTH motif involved in DNA binding. MarR domain is disposed in the following order α1-α2-β1-α3-α4-β2-β3-α5-α6, being α4 the DNA recognition helix. In general, MarR family TFs are repressors that prevent RNApol recruitment by binding to operators that overlap with the –35 and/or –10 promoter elements. Although some MarR TFs bind directly to antibiotics (Table 3), these TFs tend to be promiscuous, responding to different anionic lipophilic molecules (Wilkinson and Grove, 2006). This relaxed specificity must be taken into account when MarR-like TFs are employed for biosensing purposes. For example, EmrR (MprA) negatively regulates the transcription of the multidrug resistance pump-encoding operon, emrRAB. Although nalidixic acid has been shown to be effector of EmrR, other organic compounds such as carbonyl cyanide, m-chlorophenyldrazone, 2,4-dinitrophenol or tetrachlorosalicylanilide have been shown to activate the emrRAB operon (Xiong et al., 2000). In some cases this effector promiscuity allows the TF to respond to a variety of different antibiotics. TcaR represses the ica locus, involved in poly-N-acetylglucosamine production and biofilm formation in Staphylococcus epidermidis. TcaR structure has been solved bound to salicylate (3KP6) or aminoglycosides and beta-lactam antibiotics such as methicillin (3KP4), kanamycin (3KP5), penicillin G (3KP2), ampicillin (3KP3), or streptomycin (3EJW; Chang et al., 2013).
FIGURE 10. MarR family. (A) MarR family alignment. The alignment of representative MarR members is shown. Secondary structure elements described in the text are labeled in the structure and in the alignment. (B) MarR structure. The structure of S. coelicolor MarA bound to DNA (3ZPL, Chang et al., 2013; Stevenson et al., 2013) is shown as well as the location of kanamycin (4EM0) in the DNA-unbound repressor. The structure of MarR antibiotic effectors is represented.
In this review, we focused on aromatic compounds, metals, and antibiotics because these are common sources of environmental contamination, so they have been amply tested for bacterial sensor devices. Since there is an almost inexhaustible repertoire of different molecules recognized by bacterial TFs, which will provide us with additional sources of synthetic devices, we hope the examples given here will be useful for future mining and characterization. Nature will always provide new mechanisms of action and systems with new properties if mined with an open eye.
The wide number of analytes recognized by TFs is good news for synthetic biology, in that it expands the repertoire of potential input signals that can be used for sensor device construction. We hope our work also clarified that each TF family operates in an idiosyncratic way, so that overall generalizations are difficult and simplifications are likely to produce wrong results. Overall, we identify four main challenges ahead for the systematic employment of TFs in WCBs. The first one involves the quantitative characterization of signal transduction. Robust WCBs demand each TF/analyte pair should be characterized by its transfer function (Fernandez-Lopez et al., 2010) under a number of relevant conditions. The second challenge is to rationally engineer or evolve TFs with enhanced sensitivity and specificity. As we have seen, evolutionary exaptation not always results in highly specific TFs. Most commonly, sensory TFs have a primary effector but also respond to other molecules. In other cases TFs respond to intermediate metabolites of environmental pollutants rather than the pollutant itself. Rational engineering requires further knowledge of the biochemical basis of substrate specificity. Alternatively, directed evolution strategies could be used to select for TFs with the desired specificity profiles. A third challenge involves the development of complex circuits able to perform logic operations. This demands TF/promoter pairs that can be used in a combinatorial fashion. For this purpose, comparative scales should be produced, so the dynamic range of each TF/signal pair can be assessed with respect to each other. This will allow complex circuit building, ensuring that the dynamic range of the upstream output device is within range of the input of the downstream device. In this way, impedance matching problems will be avoided and fine tuning of connected devices will become unnecessary (Yokobayashi et al., 2002; Moon et al., 2012). Finally, the practical applications of WCBs have been hampered by biosafety concerns. WCBs are genetically modified organisms, which require bio-containment strategies to prevent their proliferation in the environment. Thus, regulatory issues will need to be clarified before WCBs can achieve their full potential as highly sensitive, inexpensive sensors for field use (French et al., 2011).
Whole cell biosensors development will critically depend on our ability to develop reliable and secure bacterial chassis, i.e., the generation of bacterial strains with engineered firewalls for biocontainment and prevention of horizontal gene transfer. In this respect, the generation of an engineered E. coli strain that requires non-standard amino acids for survival (Mandell et al., 2015) constitutes a promising development. Resistant to evolutionary escape through mutagenesis and horizontal gene transfer, this strain could be an excellent chassis for biosensor systems. In summary, engineered WCBs produced by synthetic biology constitute one of the pillars for bacterial domestication and thus for the inauguration of a new era in human civilization (Church and Regis, 2012). Ours is a humble attempt to enlighten progress in this direction.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We are grateful to Spanish Ministry of Economy for Grant BIO2010-14809 to GM. Work in FdlC laboratory was financed by the Spanish Ministry of Economy and Competitivity (BFU2011-26608) and by the European Seventh Framework Program [projects 612146/FP7-ICT-2013-10 (PLASWIRES), 289326/KBBE-2011-5 (ST-FLOW) and 282004/FP7-HEALTH-2011-2.3.1-2 (EvoTAR)].
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Keywords: biosensors, transcription factor, effector, aromatic compounds, metal, analyte
Citation: Fernandez-López R, Ruiz R, de la Cruz F and Moncalián G (2015) Transcription factor-based biosensors enlightened by the analyte. Front. Microbiol. 6:648. doi: 10.3389/fmicb.2015.00648
Received: 29 March 2015; Accepted: 15 June 2015;
Published: 01 July 2015.
Edited by:Elisa Michelini, University of Bologna, Italy
Reviewed by:Zhongli Cui, Nanjing Agricultural University, China
Seung Gu Shin, University of Glasgow, UK
Copyright © 2015 Fernandez-López, Ruiz, de la Cruz and Moncalián. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Gabriel Moncalián, Departamento de Biología Molecular and Instituto de Biomedicina y Biotecnología de Cantabria, Universidad de Cantabria – Consejo Superior de Investigaciones Científicas, C/Albert Einstein 22, 39011 Santander, Spain, email@example.com