- Research article
- Open Access
Detection and function of an intramolecular disulfide bond in the pH-responsive CadC of Escherichia coli
© Tetsch et al; licensee BioMed Central Ltd. 2011
Received: 29 November 2010
Accepted: 12 April 2011
Published: 12 April 2011
In an acidic and lysine-rich environment Escherichia coli induces expression of the cadBA operon which encodes CadA, the lysine decarboxylase, and CadB, the lysine/cadaverine antiporter. cadBA expression is dependent on CadC, a membrane-integrated transcriptional activator which belongs to the ToxR-like protein family. Activation of CadC requires two stimuli, lysine and low pH. Whereas lysine is detected by an interplay between CadC and the lysine-specific transporter LysP, pH alterations are sensed by CadC directly. Crystal structural analyses revealed a close proximity between two periplasmic cysteines, Cys208 and Cys272.
Substitution of Cys208 and/or Cys272 by alanine resulted in CadC derivatives that were active in response to only one stimulus, either lysine or pH 5.8. Differential in vivo thiol trapping revealed a disulfide bond between these two residues at pH 7.6, but not at pH 5.8. When Cys208 and Cys272 were replaced by aspartate and lysine, respectively, virtually wild-type behavior was restored indicating that the disulfide bond could be mimicked by a salt bridge.
A disulfide bond was found in the periplasmic domain of CadC that supports an inactive state of CadC at pH 7.6. At pH 5.8 disulfide bond formation is prevented which transforms CadC into a semi-active state. These results provide new insights into the function of a pH sensor.
Escherichia coli uses several strategies to maintain a neutral cytoplasmic pH in an acidic environment helping the bacterium to survive under this unfavorable condition. A number of genes is induced upon exposure of cells to low pH, among them the genes for the degradative amino acid decarboxylase systems adi, gad and cad. The Cad system consists of the cytoplasmic protein CadA and the transmembrane proteins CadB and CadC . CadA is a lysine decarboxylase that catalyzes decarboxylation of lysine to cadaverine whereby one proton is consumed resulting in a relief of the intracellular acid stress. The alkaline product cadaverine is concomitantly excreted by the lysine/cadaverine antiporter CadB [2, 3]. The genes cadA and cadB are organized in an operon [3, 4], which is under the control of the P Cad promoter. Expression of the cadBA operon is induced after external acidification, and simultaneous presence of extracellular lysine. CadC is the positive regulator of cadBA expression , and binds to two sites within the cadBA promoter .
cadC is located upstream of the cadBA operon and encodes a 58 kDa inner membrane protein. CadC, a member of the ToxR-like transcriptional activators , consists of a cytoplasmic N-terminal domain (amino acids 1-158), a single transmembrane domain (amino acids 159-187), and a periplasmic C-terminal domain (amino acids 188-512) [5, 8]. The cytoplasmic domain shows sequence similarity to the ROII-subgroup of DNA-binding domains of response regulators . However, contrary to prototypical response regulators  signal transduction in CadC functions without phosphorylation. Thus, CadC and all other ToxR-like proteins represent a one-component stimulus-response system.
Based on CadC derivatives with altered sensing properties due to single amino acid replacements within the periplasmic domain, it was suggested that this domain is the signal input domain . Recently, it became clear that CadC senses alterations of the external pH directly , but lysine is sensed only indirectly. The lysine-dependent regulation of CadC is exerted by an interplay with the lysine permease LysP, and it is proposed that in the absence of lysine, CadC is inactivated by an interaction with LysP .
Here, we investigated the role of the three cysteine residues in CadC. The best investigated member of the ToxR-like protein family, ToxR of Vibrio cholerae, contains two cysteines within the periplasmic domain. These cysteines were found to be involved in the formation of an intramolecular disulfide bond but also in the formation of intermolecular disulfide bonds between two ToxR molecules and between ToxR and a second transmembrane protein, ToxS [12, 13]. Although it was shown that ToxR binds to the DNA only in a dimeric form , ToxR oligomerization in vivo was independent of environmental changes , and thus evidence for the functional importance of the cysteines in ToxR is still lacking. Our studies indicated that a disulfide bond within the periplasmic domain of CadC is formed at pH 7.6, but these cysteines are in the reduced state at pH 5.8. These results give new insights into the switch between inactive and active states of a pH-responsive protein.
Two periplasmic cysteines are important for the regulation of CadC activity
CadC of E. coli contains three cysteine residues, one in the transmembrane domain (C172), and two in the periplasmic domain (C208 and C272). Amino acid alignment of CadC from all available sequences indicated that C172 is found only in a few species, whereas the two periplasmic cysteines are well conserved in the order of Enterobacteriales (data not shown). In addition, the crystal structure of the periplasmic domain of CadC depicted a close proximity between C208 and C272  predicting an intramolecular disulfide bond. Thus, the role of the cysteines in CadC was studied in detail.
In order to detect intermolecular disulfide bonds, membrane vesicles containing wild-type CadC or CadC derivatives with cysteine replacements were treated with copper phenanthroline, a Cys null crosslinker. Subsequent Western blot analysis revealed that in case of wild-type CadC and CadC with a single Cys at position 172, a fraction of the protein was transformed into an oligomeric form which might be related to the formation of an intermolecular disulfide bond at position 172 (data not shown). Since replacement of Cys172 was without effect on the CadC-mediated cadBA expression (Figure 1), it is concluded that an intermolecular disulfide bond is without functional importance for CadC.
An intramolecular disulfide bond between C208 and C272 is found at pH 7.6 in vivo
To analyze whether a disulfide bond is formed in CadC, an in vivo differential thiol trapping approach with iodoacetamide and PEG-maleimide was used . For simplification, these studies were performed with CadC_C172A which contains only the two periplasmic cysteines. The method is based on the fact that both iodoacetamide and PEG-maleimide react only with free thiol groups. First, E. coli cells producing CadC_C172A were labeled with iodoacetamide during growth at pH 7.6 or pH 5.8. Subsequently, free iodoacetamide was removed, and all disulfide bonds were reduced by treatment with dithiothreitol (DTT). Free thiol groups were labeled with PEG-maleimide in a second step. In consequence, only cysteines that are present in an oxidized form and thus protected from iodoacetamide labeling in the first step, are labeled with PEG-maleimide resulting in a detectable increase of the molecular weight.
The periplasmic disulfide bond can be mimicked by a salt bridge
Importantly, the wild-type like regulation pattern of CadC_C208D,C272K offered the unique opportunity to generate a functional cysteine-free CadC variant required as prerequisite for site-specific labeling studies in future. As expected, the regulation pattern of cells producing the cysteine-free derivative CadC_C172A,C208D,C272K was almost comparable to cells producing the wild-type protein (Figure 4). These data indicate that a salt bridge can take over the function of the disulfide bond in CadC.
The disulfide bond in CadC affects the interaction between sensor and co-sensor
In another experiment CadC_C208A,C272A was introduced into the ΔlysP reporter strain E. coli EP-CD4 (cadC::Tn10, cadA'::lacZ, ΔlysP). In a lysP- background, wild-type CadC activates cadBA expression in a lysine-independent, but pH-dependent manner [11, 19]. As expected, in the lysP- background, CadC_C208A,C272A induced cadBA expression lysine- and pH-independently revealing that LysP is responsible for the inhibition of CadC_C208A,C272A in the absence of lysine at pH 7.6 (data not shown). As discussed below, these experiments revealed that CadC without a disulfide bond is transformed into a semi-active state with respect to both the pH and the lysine stimuli.
Periplasmic disulfide oxidoreductases have no major influence on CadC activation
The results described above led to the hypothesis that at physiological pH CadC contains a disulfide bond which is reduced at low pH. Opening and formation of disulfide bonds requires either the corresponding environment (oxidizing or reducing) or enzymes that catalyze these processes. Therefore, we analyzed whether periplasmic proteins known to be involved in formation and opening of disulfide bonds during the protein folding process such as the Dsb proteins  have an influence on CadC activation. Six gene deletion mutants were constructed lacking the disulfide bond-modifying proteins DsbA, DsbB, DsbC, DsbD, DsbG and CcmG (also known as DsbE). CcmG does not belong to the Dsb system, but is a membrane-anchored protein with a periplasmic thiol:disulfide oxidoreductase domain involved in cytochrome c biogenesis . DsbA is a disulfide oxidase responsible for the formation of disulfide bonds and is recycled by the membrane protein DsbB . DsbC is an isomerase that opens wrongly formed disulfide bonds and introduces the correct ones and as such also exhibits a reductase activity. DsbG is a non-essential isomerase that is able to substitute for DsbC, and seems to protect single cysteines from oxidation that are needed in a reduced state to be catalytically active . Both, DsbC and DsbG, are recycled by DsbD. While DsbB and DsbD are membrane proteins, DsbA, DsbC and DsbG are soluble proteins located in the periplasm.
Cysteines are one of the most rarely used amino acids in proteins of all organisms studied so far . Conserved cysteines usually play crucial roles in the structure and function of proteins because of their ability to form intra- and intermolecular disulfide bonds and to coordinate transition metal ions . Disulfide bonds are often linked to protein stabilization, ligand binding, dimerization and activation. Examples of this are the eukaryotic cytokine receptor GHR  and the OxyR transcriptional factor of E. coli . The ArcB sensor kinase is another example for the participation of disulfide bond formation during signaling [27, 28]. Each ArcB monomer contains two cytosolic cysteines. Quinone-dependent inhibition of ArcB autophosphorylation involves the formation of one or two intermolecular disulfide bonds under aerobic conditions. The V. cholerae activator of virulence gene expression ToxR contains two periplasmic cysteines that are important for the formation of an intramolecular disulfide bond as well as for the formation of intermolecular disulfide bonds between two ToxR molecules and between ToxR and ToxS [12, 13]. ToxR binds to the DNA only in a dimeric form , and dimerization of full-length ToxR was shown in vivo . However, an influence of environmental conditions (pH, osmolarity) on ToxR oligomerization and hence disulfide bond formation in vivo was not detected .
CadC contains three cysteines. Here, we show that cysteines located at positions 208 and 272 are important for the function of CadC, whereas C172 is dispensable. Two stimuli are needed to activate wild-type CadC: low pH and lysine. Replacements of C208 and/or C272 resulted in CadC derivatives that partially induced cadBA expression at pH 7.6 indicating the transformation of CadC into a semi-active state. This discovery and structural data, according to which these residues are in close proximity to each other , prompted experiments to monitor the redox state of the thiol groups of the periplasmic cysteines in CadC in vivo. Differential thiol trapping performed with CadC_C172A producing cells that were grown in minimal medium at pH 7.6 revealed that a disulfide bond is present in CadC. In contrast, at pH 5.8 the periplasmic cysteines of CadC were found to be in the reduced state. These data indicate that CadC contains a functionally important disulfide bond. It is important to note, that CadC is hardly a redox sensor. The differences in the cadBA expression level found for anaerobic and aerobic growth conditions are dependent on H-NS . Therefore, it is proposed that the disulfide bond in CadC provides structural support for the switch of the sensor between the inactive and active state. This assumption is supported by the location of Cys208 within a flexible loop in the N-terminal subdomain .
The question arose, how the disulfide bond might be formed and opened in vivo. Enzymes responsible for these processes might be the periplasmic disulfide oxidoreductases of the Dsb system. CadA activity as indication for cadBA expression was monitored in single dsb and ccmG deletion mutants. However, none of these deletions altered the CadC-mediated induction profile. In all deletion mutants induction of cadBA expression was prevented at pH 7.6, and CadA activity was significantly increased at low pH. These data imply that none of these proteins was essential for the formation or opening of the disulfide bond in CadC. It is worth mentioning, that we found an elevated CadA activity in the dsbA (encoding a disulfide oxidase), dsbB (encoding a protein that regenerates DsbA) and dsbD (encoding a recycling enzyme for an isomerase/reductase) deletion mutants. DsbA/DsbB are responsible for the introduction of disulfide bonds in newly synthesized proteins, thus their lack might support a higher probability of CadC molecules without a disulfide bond and thus the increased CadA activity. The role of DsbD in CadC activation remains unknown. Nevertheless, either these enzymes are functionally redundant, or the spontaneous oxidation by oxygen or low molecular compounds might be responsible for the formation of a disulfide bond in CadC. cadC belongs to the genes/operons with the shortest half-lives of the mRNA . Based on this result and our finding of a transient activation of CadC , we speculate that there is a rapid turnover of CadC and that the disulfide bond is preferentially introduced during de novo synthesis of CadC. The periplasm is accessible for oxygen and therefore allows the spontaneous oxidation of two neighboring cysteines in proteins [32, 33]. Expression of the cadBA operon is induced at low pH, and the induction level is higher in the absence of oxygen . Under these conditions the oxidation of cysteines to cystine is minimized due to the lack of oxygen as well as the surplus of protons which prevents the formation of thiolate anions, the prerequisite for disulfide bond formation . Thus, this shift in the external conditions already dramatically reduces the probability to form a disulfide bond in CadC. Based on these results it is suggested that under non-inducing conditions (pH 7.6) a disulfide bond in the periplasmic domain holds the sensor in an inactive state. Under inducing conditions (pH 5.8) formation of the disulfide bond is either prevented or the disulfide bond is opened by a still unknown mechanism. Concomitantly, CadC undergoes conformational changes due to the protonation of negatively charged amino acids located in a patch at the CadC dimer interface .
This proposal is in accordance with the finding that the disulfide bond could be mimicked by a salt bridge. When C208 was replaced with an aspartate and C272 with a lysine, a CadC derivative was generated that supported cadBA expression comparable to the wild-type protein. Functional substitution of a disulfide bond by a salt bridge in CadC requires formation of the salt bridge at pH 7.6, which is conceivable (aspartate deprotonated, lysine protonated), and an opening of the salt bridge, which might depend on the protonation of aspartate at low pH [36, 37]. In contrast, a CadC derivative in which the cysteines were replaced by the same charged amino acids but at opposite positions (CadC_C208K,C272D) caused deregulation of cadBA expression. It is suggested that a salt bridge was not formed in this derivative due to an unfavorable orientation of the amino acid side chains to each other.
Based on these results, a two step activation mechanism for CadC is proposed (Figure 7). Under non-inducing conditions (no lysine, pH 7.6) CadC-mediated cadBA expression is inhibited by two mechanisms. At pH 7.6 a disulfide bond is formed, and CadC is in an inactive form. Moreover, CadC is inhibited through the interplay with the lysine permease LysP in the absence of lysine . CadC with a disulfide bond remains inactive even when the interaction with LysP is released in the presence of lysine (lysine, pH 7.6). Exposure of CadC to low pH is accompanied by conformational changes and reduction of the cysteines resulting in an active CadC (lysine, pH 5.8). Alternatively, at low pH in the absence of lysine, CadC is still locked in an inactive conformation due to the interplay with LysP (no lysine, pH 5.8). The presence of lysine suspends the interaction with LysP, and CadC is transformed into the active state (lysine, pH 5.8).
In CadC_C208A,C272A formation of a disulfide bond is prevented by amino acid replacements (Figure 7). As consequence, this derivative displays semi-active states at pH 7.6 in the presence of lysine (lysine, pH 7.6) or at low pH in the absence of lysine (no lysine, pH 5.8). Additional pH-dependent conformational changes or the presence of lysine are required to fully activate this CadC derivative (lysine, pH 5.8).
Previously, it was proposed that the two stimuli, lysine and low pH, affect CadC activation independently from each other . Here, we gained new insights into the molecular mechanism how CadC processes these stimuli, particularly that a disulfide bond is involved in the function of CadC.
Bacterial strains and growth conditions
Bacterial strains used in this study.
Source or reference
E. coli JM109
recA1 endA1gyrA96 thi-1 hsdR17 (rK- mK+)
supE44 relA1Δ(lac-proAB) [F' traD36 proAB
E. coli BL21(DE3)pLysS
F- ompT r-B m-B dcm gal tonA (DE3) pLysS (CmR)
E. coli EP314
W3110 Δ(lacIOPZYA) exa-1::Mu
dI1734 Km lac) in cadA] cadC1::Tn10
E. coli EP-CD4
E. coli EP314 lysP::Cm
E. coli MG1655
K12 reference strain
E. coli MG1655ΔdsbA
E. coli MG1655 ΔdsbA::Kan
E. coli MG1655ΔdsbB
E. coli MG1655 ΔdsbB::Kan
E. coli MG1655ΔdsbC
E. coli MG1655 ΔdsbC::Cm
E. coli MG1655ΔdsbD
E. coli MG1655 ΔdsbD::Kan
E. coli MG1655ΔdsbG
E. coli MG1655 ΔdsbG::Kan
E. coli MG1655ΔccmG
E. coli MG1655 ΔccmG::Kan
Plasmids used in this study.
Source or reference
Expression vector, Apr
cadC in pET16b
Amino acid exchange C172A in cadC,
cadC_C172A in pET16b
cadC_C208A in pET16b
cadC_C272A in pET16b
cadC_C172A,C208A in pET16b
cadC_C172A,C272A in pET16b
cadC_C208A,C272A in pET16b
cadC_C172A,C208A,C272A in pET16b
cadC_C208D,C272K in pET16b
cadC_C208K,C272D in pET16b
cadC_C172A,C208D,C272K in pET16b
Expression vector, Cmr
lysP in pBAD33
Generation of plasmids and strains
All cadC derivatives were constructed by polymerase chain reaction (PCR) with mismatch primers either by single step or by two step PCR . To facilitate construction, a cadC gene with two additional unique restriction sites was employed . All site-specific mutations were directed by synthetic oligonucleotide primers containing the required nucleotide exchanges. PCR fragments were cloned into the expression vector pET16b with the restriction enzymes NdeI and BamHI so that all constructs carried the sequence encoding an N-terminal His-Tag of 10 histidine residues. E. coli EP-CD4, E. coli MG1655ΔdsbA, E. coli MG1655ΔdsbB, E. coli MG1655ΔdsbC, E. coli MG1655ΔdsbD, MG1655ΔdsbG and MG1655ΔccmG were constructed by deleting the genes lysP, dsbA, dsbB, dsbC, dsbD, dsbG and ccmG, respectively, via the Quick & Easy E. coli Gene Deletion Kit (Gene Bridges) according to the manufacturer's instructions.
Differential thiol trapping of CadC in vivo
The thiol/disulfide state of the periplasmic cysteines of CadC was monitored in vivo by differential thiol trapping according to . The procedure was modified as follows: E. coli BL21(DE3)pLysS carrying one of the plasmids pET-CadC-C172A, pET-CadC-C172A,C208A or pET-CadC-C172A,C208A,C272A was grown in phosphate buffered minimal medium with a pH of 7.6 or 5.8 to an OD600 of 0.5. Subsequently, overproduction of the CadC derivatives was induced by addition of 0.5 mM IPTG. After an additional hour of growth at 37°C, the OD600 was adjusted to 1, and 5 mM iodoacetamide (dissolved in 0.1 M Tris) was added to 1 ml cell suspension. At pH 7.6, incubation was performed for 15 min (37°C), at pH 5.8 the incubation time was prolonged to 150 min to compensate the lower alkylation rate of iodoacetamide at low pH. This first alkylation procedure irreversibly modified all free thiol groups directly in the living cells. Subsequently, cells were harvested into 100 μl ice-cold 100% (w/v) trichloric acid (TCA) and stored on ice for at least 30 min. The TCA treated cells were centrifuged (16.000 g, 4°C, 15 min), and the resulting pellet was washed with 200 μl of ice-cold 10% (w/v) TCA followed by a wash with 100 μl of ice-cold 5% (w/v) TCA. The supernatant was removed completely, and the pellet was resuspended in 100 μl of denaturing buffer [6 M urea, 200 mM Tris-HCl (pH 8.5), 10 mM EDTA, 0.5% (w/v) SDS] supplemented with 10 mM DTT to reduce disulfide bonds. After one hour of incubation in the dark (37°C, gentle agitation at 1300 rpm), 10 μl ice-cold 100% (w/v) TCA was added, and the sample was stored on ice for at least 30 min. After centrifugation, the resulting pellet was again washed with 200 μl of ice-cold 10% (w/v) TCA followed by a wash with 100 μl of ice-cold 5% (w/v) TCA. Finally, the pellet was resuspended in 50 μl of denaturing buffer containing 10 mM PEG-maleimide (Iris Biotech GmbH, Marktredwitz/Germany) to alkylate all newly reduced cysteines. The reaction (37°C, gentle agitation at 1300 rpm, in the dark) was stopped after one hour by addition of 5 μl ice-cold 100% (w/v) TCA. After precipitation on ice (30 min) and centrifugation, the pellet was washed first with 100 μl of 10% and then with 50 μl of 5% ice-cold (w/v) TCA. After removing the TCA, the pellet was washed twice with 500 μl acetone and resuspended in 50 μl denaturing buffer. Samples were mixed with non-reducing SDS-sample buffer and loaded onto 12.5% SDS-polyacrylamide gels . CadC was detected by Western blot analysis .
Analysis of intermolecular disulfide bonds
For the detection of intermolecular disulfide bonds, wild-type CadC and all available CadC derivatives with Cys replacements (CadC_C172A; CadC_C208A; CadC_C272A; CadC_C172A,C208A; CadC_C172A,C272A; CadC_C208A,C272A; CadC_C172A,C208A,C272A) were overproduced in E. coli BL21(DE3)pLysS, and membrane vesicles were prepared . CadC-containing membrane vesicles [1 mg protein/ml in TG-buffer, 50 mM Tris/HCl, pH 7.5; 10% (v/v) glycerol] were treated with 0.2 mM copper phenanthroline at 25°C for 30 min. The reaction was stopped by addition of 10 mM EDTA. Samples were mixed with non-reducing SDS-sample buffer and loaded onto 7.5% (w/v) SDS-polyacrylamide gels . CadC was detected by Western blot analysis .
Measurement of CadC signal transduction activity in vivo
Signal transduction activity of different CadC derivatives in vivo was probed with a β-galactosidase based reporter gene assay as previously described . Using a pET-based vector in combination with the reporter strain E. coli EP314 that does not possess a T7 polymerase resulted in a low expression that was sufficient to allow complementation but did not lead to overproduction of CadC which would result in stimulus-independent cadBA expression. β-galactosidase activity was determined from at least three independent cultures, and is given in Miller units (MU) calculated as described . The activity of the lysine decarboxylase CadA as a measurement for cadBA expression was determined according to  with the following changes: for the assay cells corresponding to an optical density of 1 (600 nm) were resuspended in 20 mM potassium phosphate buffer (pH 5.6) and lysed by the addition of chloroform. One unit is defined as 1 μmol decarboxylated lysine produced per minute and specific activities were calculated for 1 mg of protein [μmol/(min*mg)]. Insertion of the CadC derivatives into the cytoplasmic membrane was analyzed after overproduction of CadC, isolation of membrane vesicles and subsequent Western blot analysis as previously described [11, 45].
This work was supported by the Deutsche Forschungsgemeinschaft (JU270/5-3 and Exc114/1). We thank Teresa Friedrich for the construction of E. coli MG1655ΔdsbA, MG1655ΔdsbB, MG1655ΔdsbC and MG1655ΔdsbD and Korinna Burdack for technical assistance.
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