Bacillus licheniformis Contains Two More PerR-Like Proteins in Addition to PerR, Fur, and Zur Orthologues.

The ferric uptake regulator (Fur) family proteins include sensors of Fe (Fur), Zn (Zur), and peroxide (PerR). Among Fur family proteins, Fur and Zur are ubiquitous in most prokaryotic organisms, whereas PerR exists mainly in Gram positive bacteria as a functional homologue of OxyR. Gram positive bacteria such as Bacillus subtilis, Listeria monocytogenes and Staphylococcus aureus encode three Fur family proteins: Fur, Zur, and PerR. In this study, we identified five Fur family proteins from B. licheniformis: two novel PerR-like proteins (BL00690 and BL00950) in addition to Fur (BL05249), Zur (BL03703), and PerR (BL00075) homologues. Our data indicate that all of the five B. licheniformis Fur homologues contain a structural Zn2+ site composed of four cysteine residues like many other Fur family proteins. Furthermore, we provide evidence that the PerR-like proteins (BL00690 and BL00950) as well as PerRBL (BL00075), but not FurBL (BL05249) and ZurBL (BL03703), can sense H2O2 by histidine oxidation with different sensitivity. We also show that PerR2 (BL00690) has a PerR-like repressor activity for PerR-regulated genes in vivo. Taken together, our results suggest that B. licheniformis contains three PerR subfamily proteins which can sense H2O2 by histidine oxidation not by cysteine oxidation, in addition to Fur and Zur.

Introduction

The <span class="Chemical">ferric uptake regulator (<span class="Chemical">Fur) protein is an iron-sensing transcriptional regulator which controls the expression of genes involved in intracellular iron homeostasis [1]. Under iron-replete conditions, Fur mediates the repression of genes involved in intracellular iron increase to prevent iron overload. Since its first recognition in Escherichia coli, Fur family proteins have been found and characterized in a variety of organisms ranging from bacteria to archaea [1, 2]. Fur family proteins are not only responsible for the acquisition and storage of iron, but also involved in the oxidative stress response as well as in the acquisition and storage of other metal ions. Now it is appreciated that there are various subgroups of Fur family proteins, which include zinc uptake regulator (Zur), manganese uptake regulator (Mur), nickel uptake regulator (Nur), heme-dependent iron response regulator (Irr) and metal-dependent peroxide regulon repressor (PerR), in addition to Fur itself [1, 2].

<span class="Chemical">Fur family proteins are homo dimeric DNA binding proteins, and each monomer is composed of two domains, a winged-helix DNA-binding domain at the N-terminus and a dimerization domain at the C-terminus, connected by a loop. The available structures of <span class="Chemical">Fur family proteins indicate that many, but not all, of these proteins have at least two metal binding sites in each monomer: a structural Zn2+-binding site and a regulatory metal-binding site [3-9]. The structural Zn2+ is usually coordinated by four Cys residues arranged in two CXXC motifs and stabilizes the dimerization domain. The regulatory metal binding site, located in the hinge region between the DNA binding domain and the dimerization domain, engages amino acids from both domains. In Fur and PerR proteins, the regulatory metal binding site is penta- or hexa-coordinated by three His residues and two Asp/Glu residues [4, 6, 8, 9], whereas this site is tetra-coordinated by two His residues, one Asp/Glu residue, and one Cys residue in Zur proteins [3, 5, 7].

While <span class="Chemical">Fur and Zur are widely distributed in both Gram positive and Gram negative bacteria, PerR is mainly found in Gram positive bacteria as a functional homologue of <span class="Chemical">OxyR [10]. PerR regulates genes involved in oxidative stress response like OxyR. However, unlike cysteine-thiol based peroxide sensor OxyR, PerR senses H2O2 by Fe-mediated histidine oxidation [11]. Reaction of H2O2 with Fe2+ leads to a rapid oxidation of either one of the two His residues involved in Fe2+-coordination (His37 and His91 in B. subtilis PerR), resulting in the loss of repressor activity. However, Fur does not react with H2O2, despite the strong similarity of regulatory metal binding site [11, 12].

<span class="Species">B. licheniformis is a Gram-positive, spore-forming soil bacterium which is closely related to the well-studied model organism <span class="Species">B. subtilis [13]. B. licheniformis is an industrially important organism widely used for the manufacture of enzymes, peptide antibiotics and specialty chemicals. Despite the importance of stress physiology during the fermentation process, little is known about the physiology and stress response of B. licheniformis compared with its close relative B. subtilis [14].

Here we investigated the <span class="Chemical">Fur family proteins from <span class="Species">B. licheniformis. B. licheniformis genome encodes five Fur family proteins, with three of them clustering in the PerR group. We have unequivocally identified BL00075, BL03703, and BL05249 as PerR, Zur, and Fur, respectively, using B. subtilis promoter fusion reporter systems. In addition, we provide several lines of evidence that two novel PerR-like proteins, BL00690 and BL00950, are also able to sense H2O2 by histidine oxidation, and that BL00690 has a transcriptional repressor activity for PerR-regulated genes.

Materials and Methods

Bacterial strains and culture conditions

The bacterial strains used in t<span class="Chemical">his study are described in Table 1. <span class="Species">E. coli and B. subtilis strains were routinely grown in Luria-Bertani (LB) media at 37°C with appropriate antibiotics. MOPS buffered minimal medium was used for the metal-limited minimal media (MLMM) as described previously [15]. Ampicillin (100 μg/ml) and chlorampenicol (34 μg/ml) were used for the selection of E. coli strains. Spectinomycin (100 μg/ml), erythromycin (1 or 5 μg/ml), neomycin (25 μg/ml), kanamycin (20 μg/ml), chlorampenicol (10 μg/ml), tetracyclin (10 μg/ml), and lincomycin (8 μg/ml) were used for the selection of B. subtilis strains. For the induction of xylA promoter, 1% xylose (w/v) was used.

Table 1

Bacterial strains used in this study.

Strains	Relevant genotype or purpose	Reference or source
B. subtilis
HB9700	CU1065 zur::tet	[26]
HB9703	CU1065 perR::tet	[15]
HBL100	CU1065 fur::kan	This study
LB1066	CU1065 fur::kan, zur::tet, perR::cat	This study
LB1532	HB9703 amyE::spc, SPβ2Δ2::Tn917::Φ(mrgA-cat-lacZ)	[17]
HB9738	HB9703 amyE::perRBS-FLAG, SPβ2Δ2::Tn917::Φ(mrgA-cat-lacZ)	[15]
LB1023	HB9703 amyE::bl00075-FLAG, SPβ2Δ2::Tn917::Φ(mrgA-cat-lacZ)	This study
LB1034	HB9700 amyE::spc, SPβ2Δ2::Tn917::Φ(yciC-cat-lacZ)	This study
LB1035	HB9700 amyE::zurBS-FLAG, SPβ2Δ2::Tn917::Φ(yciC-cat-lacZ)	This study
LB1036	HB9700 amyE::bl03703-FLAG, SPβ2Δ2::Tn917::Φ(yciC-cat-lacZ)	This study
LB1040	HBL100 amyE::spc, SPβ2Δ2::Tn917::Φ(feuA-cat-lacZ)	This study
LB1041	HBL100 amyE::furBS-FLAG, SPβ2Δ2::Tn917::Φ(feuA-cat-lacZ)	This study
LB1042	HBL100 amyE::bl05249-FLAG, SPβ2Δ2::Tn917::Φ(feuA-cat-lacZ)	This study
LB1227	LB1066 thrC::spc	This study
LB1287	LB1066 thrC::PxylA-bl00950-FLAG	This study
LB1288	LB1066 thrC::PxylA-bl00690-FLAG	This study
LB1490	LB1066 thrC::PxylA-perRBS-FLAG	This study
LB1491	LB1066 thrC::PxylA-furBS-FLAG	This study
LB1493	LB1066 thrC::PxylA-zurBS-FLAG	This study
LB1233	LB1227 SPβ2Δ2::Tn917::Φ(mrgA-cat-lacZ)	This study
LB1234	LB1227 SPβ2Δ2::Tn917::Φ(feuA-cat-lacZ)	This study
LB1235	LB1227 SPβ2Δ2::Tn917::Φ(yciC-cat-lacZ)	This study
LB1297	LB1287 SPβ2Δ2::Tn917::Φ(mrgA-cat-lacZ)	This study
LB1288	LB1287 SPβ2Δ2::Tn917::Φ(feuA-cat-lacZ)	This study
LB1299	LB1287 SPβ2Δ2::Tn917::Φ(yciC-cat-lacZ)	This study
LB1300	LB1288 SPβ2Δ2::Tn917::Φ(mrgA-cat-lacZ)	This study
LB1301	LB1288 SPβ2Δ2::Tn917::Φ(feuA-cat-lacZ)	This study
LB1302	LB1288 SPβ2Δ2::Tn917::Φ(yciC-cat-lacZ)	This study
LB4031	LB1490 SPβ2Δ2::Tn917::Φ(mrgA-cat-lacZ)	This study
LB4065	LB1491 SPβ2Δ2::Tn917::Φ(feuA-cat-lacZ)	This study
LB4066	LB1493 SPβ2Δ2::Tn917::Φ(yciC-cat-lacZ)	This study
LB1010	HB9703 amyE::spc	This study
LB2128	HB9703 amyE::PperR-NdeI-perRBS-FLAG	This study
LB4034	HB9703 amyE::PperR-NdeI-bl00690-FLAG	This study
LB4106	HB9703 amyE::PperR-NdeI-bl00950-FLAG	This study
E. coli
LE0001	BL21(DE3)pLysS pET-11a::bl00950	This study
LE0002	BL21(DE3)pLysS pET-16b::bl00690	This study
LE0008	BL21(DE3)pLysS pET-11a::bl00075	This study
LE0009	BL21(DE3)pLysS pET-11a::bl05249	This study
LE0010	BL21(DE3)pLysS pET-11a::bl03703	This study
LE1374	BL21(DE3)pLysS pET-15b::His6-bl00950	This study

Construction of E. coli strains overexpressing Fur family proteins

The open reading frames (ORFs) of bl05249, <span class="CellLine">bl03703, bl00075, bl00950 and, bl00690 were PCR-amplified with <span class="Species">B. licheniformis ATCC14580 chromosomal DNA as template. The PCR fragments of bl05249, bl03703, bl00075, and bl00950 were individually cloned into the NdeI and BamHI sites of expression vector pET-11a (Novagen) resulting in plasmids named pJL303, pJL304, pJL302, and pJL201, respectively. The PCR fragments of bl00690 were cloned into the NcoI and BamHI sites of expression vector pET-16b (Novagen) resulting in plasmid named pJL202. For the purification of N-terminally His-tagged BL00950, the PCR-fragments of bl00950 were cloned into NdeI and BamHI sites of pET-15H-oxyR [16] resulting in plasmids named pJL853. The plasmids were introduced into E. coli BL21 (DE3) pLysS cells for the overexpression of encoded proteins.

Each <span class="Species">E. coli <span class="CellLine">BL21 (DE3) pLysS strain carrying pJL303, pJL304, pJL302, pJL853, or pJL202 was grown in 1 L of LB medium containing 0.4% (w/v) glucose, chloramphenicol, and ampicillin. At OD600 of ~0.4, isopropyl-β-D-thiogalactopyranoside (IPTG) was added to a final concentration of 1 mM (with additional final 50 μM ZnSO4 for cells expressing BL03703), and the cells were allowed to grow for an additional 2 h. The cells were harvested by centrifugation, and lysed by sonication for protein purification. BL00075, BL05249, and BL03703 were purified by heparin-Sepharose and MonoQ chromatography using buffer A (20 mM Tris-HCl, pH 8.0, 0.1 M NaCl, and 5% glycerol (v/v)) containing 10 mM EDTA for BL00075 and BL05249, or 2 mM EDTA for BL03703 with the application of a linear gradient of 0.1–1 M NaCl as described previously [15]. BL00690 was purified by heparin-Sepharose and SP-Sepharose chromatography using buffer A containing 10 mM EDTA with the application of a linear gradient of 0.1–1 M NaCl. Since BL00950 did not bind to heparin-Sepharose resin unlike other Fur family proteins, we used His-tagged BL00950 for this study. His-tagged BL00950 was first purified by Ni-NTA chromatography, and subsequently by SP-Sepharose chromatography using buffer A containing 10 mM EDTA with the application of a linear gradient of 0.1–1 M NaCl. All the proteins were further purified using a Superdex 200 HiLoad 16/60 column (GE Healthcare) equilibrated with Chelex-100-treated buffer A. Note that BL00950 was purified as monomer whereas all the other proteins were purified as dimers as judged by elution profiles from Superdex 200 HiLoad gel filtration chromatography. The purities of all of the purified proteins were checked by SDS-PAGE, and their concentrations were determined by measuring A280 nm using the calculated values of molar extinction coefficient of each protein (BL05249: 11,460 M-1cm-1, BL03703: 10,430 M-1cm-1, BL00075: 8,940 M-1cm-1, BL00690:10,430 M-1cm-1, BL00950: 8,940 M-1cm-1).

Electrophoretic mobility shift assay

The 431 bp DNA fragment containing <span class="Species">B. subtilis mrgA promoter region was generated by PCR, and su<span class="Species">bsequently digested with EcoRI, resulting in a 273 bp fragment containing PerR box and a 154 bp fragment used for a non-specific control. The DNA fragments were end-labelled with [γ-32P] ATP using T4 polynucleotide kinase (NEB) and unincorporated labels were removed using nucleotide removal kit (Qiagen). Protein (BL00690 or BL00950) and a labelled probe were mixed in binding buffer (20 mM Tris-HCl pH 8.0, 50 mM KCl, and 5% glycerol (v/v), 50 μg/ml BSA and 100 μM MnCl2), and separated by 6% PAGE with a 45 mM Tris-borate buffer containing 100 μM MnCl2. After 2 h at 120 V, the gel was dried and exposed to X-ray film with an intensifying screen (Kodak) at -80°C.

Measurement of Zn2+ release by H2O2 using PAR

Measurement of <span class="Chemical">Zn2+ release by <span class="Chemical">H2O2 was performed as described previously [15, 17]. 5 μM protein in buffer A was treated with 0, 1, 10, or 100 mM H2O2 in the presence of 100 μM 4-(2-pyridylazo)resorcinol (PAR), and Zn2+-release was measured by monitoring the Zn2+-PAR complex at 494 nm every 1 s for 30 min. The Zn2+ content of purified proteins by PAR assay was determined using a molar extinction coefficient of 85,000 M-1cm-1 at 494 nm for Zn2+-PAR complex.

MALDI-TOF MS and LC-ESI MS/MS analysis

The analysis of protein oxidation after overexpression in <span class="Species">E. coli was performed as previously described [17, 18]. Briefly, aliquots of <span class="Species">E. coli cells (1.8 ml of culture of LE0001, LE0002, LE0008, LE0009, or LE0010) were either treated with 1 mM H2O2 (final concentrations) for 1 min or not. Cells harvested by centrifugation after the addition of 200 μM of trichloroacetic acid (TCA) were sonicated in 500 μl of 10% TCA. The pellets obtained by centrifugation were resuspended with 20 μl IA buffer (50 mM iodoacetamide, 0.5 M Tris pH 8.0, 5% glycerol, 100 mM NaCl, 1 mM EDTA, 2% SDS) and incubated for 1 h in the dark to alkylate free thiols. After separation on 13.3% Tris-Tricine SDS-PAGE and staining with Coomassie Brilliant Blue R-250, protein bands were cut and analyzed by MALDI-TOF MS using a Voyager-DE STR instrument (Applied Biosystems) after in-gel tryptic digestion. The sites of oxidation were identified by LC-MS/MS analyses using an Agilent nanoflow-1200 series HPLC system connected to a linear ion trap mass spectrometer (Thermo Scientific).

Construction of deletion mutant, complementation, and reporter fusion strains

The <span class="Species">B. subtilis <span class="Chemical">fur deletion mutant strain (HBL100) was constructed using long-flanking homology PCR as described previously [19]. The fur zur double mutant strain (HBL112) was generated by transformation of HBL100 with zur::tet cassette, and the perR fur zur triple mutant strain (LB1066) was generated by transformation of HBL112 with perR::cat cassette.

For the expression of FLAG fusion proteins from their own promoter in <span class="Species">B. subtilis, the PCR fragments containing ORF and about 200 bp upstream region (bl00075, bl05249, <span class="CellLine">bl03703, bl00690, bl00950, fur, zur) were individually cloned into BamHI and EagI sites of pJL070. For the expression of FLAG fusion proteins from xylA promoter in B. subtilis, the pXT plasmid which can fuse a xylose-inducible promoter to the gene of interest was used. The PCR fragments containing ribosome binding sequence and perR ORF from pJL070 were cloned into BamHI and EcoRI sties of pXT, generating pJL240. Then, the PCR fragments containing consensus ribosome binding sequence and ORF (perR, fur, zur, bl00690, and bl00950) were each cloned into BamHI and EagI sites of pJL240. For the expression of PerRBS-FLAG, BL00690-FLAG, and BL00950-FLAG from B. subtilis perR promoter in B. subtilis (for the construction of LB2128, LB4034, and LB4106 strains), NdeI site was introduced at the beginning of perR ORF in pJL070 by QuikChange site-directed mutagenesis (Stratagene) generating pJL448. Then, the PCR amplified bl00690 and bl00950 ORFs were each cloned into NdeI and EagI sites of pJL448. The ScaI digest of each plasmid was introduced to the corresponding B. subtilis strain to generate a transformant containing FLAG-fused gene in the amyE (pJL070-derived plasmids) or thrC (pJL240-derived plasmids) locus. The reporter fusion strains were constructed by transduction with SPβ phages, and β-galactosidase assays were performed, as described previously [15].

Results

Identification of five Fur family proteins in B. licheniformis

Many Gram positive bacteria such as <span class="Species">B. subtilis, <span class="Species">L. monocytogenes and S. aureus encode three Fur family proteins: Fur, Zur, and PerR [20-22]. Interestingly, the BLAST homology searches of the B. licheniformis ATCC14580 genome sequence [13] with each one of the B. subtilis Fur family proteins revealed the presence of five putative genes encoding Fur family proteins. BL00075, BL03703, and BL05249 of B. licheniformis show the highest similarity to PerRBS, ZurBS, and FurBS from B. subtilis, respectively, and all these proteins cluster with their homologues from L. monocytogenes and S. aureus as well as B. subtilis (Fig 1A). Although the sequence identity between BL00690 and BL00950 is not high (33%), both proteins cluster with PerR proteins with sequence identities ranging between 41 and 44% for BL00690 and between 41 and 46% for BL00950 (Fig 1B). In comparison, BL00690 and BL00950 exhibit sequence identities of ~25% to Fur and Zur proteins (Fig 1B), which are comparable to those between PerR and Fur or between PerR and Zur [1, 2, 22, 23].

Fig 1

Sequence analysis of five Fur family proteins from B. licheniformis.

(A) Phylogenetic tree of Fur-like proteins. The tree was constructed based on a multiple sequence alignment of Fur-like proteins from Bacillus subtilis (BS), Bacillus licheniformis (BL), Listeria monocytogenes (LM), and Staphylococcus aureus (SA), using CLUSTALW. Note that BL00690 and BL00950 cluster with PerR proteins. The scale bar represents an estimated distance of 0.1 amino acid substitution/site. (B) Amino acid identity matrix for BL00690 and BL00950. The amino acid sequences of BL00690 and BL00950 were compared with other Fur family proteins. The sequence identity values were shown as %. (C) Sequence alignment of Fur family proteins. The predicted structural Zn2+-binding site (blue) and regulatory metal binding site (red) are highly conserved in all five Fur-like proteins from B. licheniformis. The numbers above each sequence alignment group correspond to the sequence numbers of PerRBS, ZurBS, and FurBS, respectively.

(A) Phylogenetic tree of <span class="Chemical">Fur-like proteins. The tree was constructed based on a multiple sequence alignment of <span class="Chemical">Fur-like proteins from Bacillus subtilis (BS), Bacillus licheniformis (BL), Listeria monocytogenes (LM), and Staphylococcus aureus (SA), using CLUSTALW. Note that BL00690 and BL00950 cluster with PerR proteins. The scale bar represents an estimated distance of 0.1 amino acid substitution/site. (B) Amino acid identity matrix for BL00690 and BL00950. The amino acid sequences of BL00690 and BL00950 were compared with other Fur family proteins. The sequence identity values were shown as %. (C) Sequence alignment of Fur family proteins. The predicted structural Zn2+-binding site (blue) and regulatory metal binding site (red) are highly conserved in all five Fur-like proteins from B. licheniformis. The numbers above each sequence alignment group correspond to the sequence numbers of PerRBS, ZurBS, and FurBS, respectively.

As shown in Fig 1C, all the five <span class="Chemical">Fur family proteins from <span class="Species">B. licheniformis retain four highly conserved Cys residues corresponding to Cys96, Cys99, Cys136, and Cys139 of B. subtilis PerR. These four Cys residues arranged in two CXXC motifs are involved in high affinity structural Zn2+-binding in most Fur family proteins including PerRBS [9, 15]. In addition to this structural Zn2+-binding site, Fur family proteins also have a regulatory metal binding site. For PerRBS, this site is composed of His37, Asp85, His91, His93 and Asp104 [9, 11]. These five residues are conserved in BL00690 as well as PerR proteins including BL00075. Although Fur proteins and BL00950 also have conserved N-donor ligands (corresponding to His37, His91, and His93 of PerRBS), these proteins have a Glu residue in place of Asp104 (for Fur proteins) or Asp85 (for BL00950) as an O-donor ligand. Zur proteins are known to use S-donor ligand corresponding to Cys84 of ZurBS instead of O-donor ligand corresponding to Asp85 of PerRBS for regulatory Zn2+-binding, and do not have a conserved N-donor ligand corresponding to His37 of PerRBS [3, 5, 7]. Based on their repressor activities as described below as well as their sequence similarity and conserved amino acid residues involved in putative structural and regulatory metal binding, we functionally annotate BL00075, BL03703, and BL05249 as PerRBL, ZurBL, and FurBL, respectively. And, the new Fur homologues, BL00690 and BL00950, were annotated as PerR2 and PerR3, respectively, based on their sequence similarity to the PerR proteins and their ability to sense peroxide by histidine oxidation as described below.

All the five Fur family proteins from B. licheniformis contain structural Zn2+

The sequence analysis indicates that all the <span class="Chemical">Fur family proteins from <span class="Species">B. licheniformis have conserved cysteine residues putatively involved in structural Zn2+-binding. To investigate the involvement of cysteine residues in Zn2+ coordination, we purified all the five Fur family proteins after overexpression in E. coli (Fig 2A), and measured Zn2+-release from each protein upon H2O2 treatment by monitoring the formation of PAR-Zn2+ complex (Fig 2B) as described previously [15, 17]. Interestingly, unlike other Fur family proteins PerR3 did not bind to heparin-Sepharose (which is widely used for the purification of DNA-binding proteins). Furthermore, PerR3 was purified as monomeric protein by a gel filtration chromatography, whereas the other four Fur family proteins were purified as dimeric proteins (see Materials and Methods).

Fig 2

Zn2+-contents of Fur family proteins from B. licheniformis.

(A) Purified Fur family proteins from B. licheniformis. B. licheniformis Fur-like proteins were purified after overexpression in E. coli, and analyzed by SDS-PAGE after alkylation by iodoacetamide. (B) H2O2-dependent Zn2+-release. Release of Zn2+ from proteins (5 μM) was measured by monitoring Zn2+-PAR complex at 494 nm every 1 sec for 30 min after treatment of 0, 1, 10, and 100 mM H2O2. Data for experiments with 100 mM H2O2 are only shown for clarity. The Zn2+-content of proteins was calculated using a molar extinction coefficient of 85,000 M-1cm-1 at 494 nm for Zn2+-PAR complex.

(A) Purified <span class="Chemical">Fur family proteins from <span class="Species">B. licheniformis. B. licheniformis Fur-like proteins were purified after overexpression in E. coli, and analyzed by SDS-PAGE after alkylation by iodoacetamide. (B) H2O2-dependent Zn2+-release. Release of Zn2+ from proteins (5 μM) was measured by monitoring Zn2+-PAR complex at 494 nm every 1 sec for 30 min after treatment of 0, 1, 10, and 100 mM H2O2. Data for experiments with 100 mM H2O2 are only shown for clarity. The Zn2+-content of proteins was calculated using a molar extinction coefficient of 85,000 M-1cm-1 at 494 nm for Zn2+-PAR complex.

<span class="Chemical">PAR-Zn2+ complex formation was not detected for 30 min without <span class="Chemical">H2O2 treatment, and the rate of Zn2+-release was dependent on added H2O2 concentrations (Fig 2B). These results indicate that all the Fur family proteins from B. licheniformis, including PerR3 purified as monomers, have stably bound Zn2+ which cannot easily be removed by high affinity Zn2+-chelator PAR (Kapp ~ 1013 M-2 for PAR2-Zn2+ complex, [24]) in the absence of H2O2. Furthermore, the dependence of Zn2+-release on H2O2 strongly suggests that Zn2+ is coordinated by conserved cysteine residues as observed with PerR proteins [15, 17]. The second-order rate constants of Zn2+ release by H2O2 were determined to be ~0.03 M-1s-1 for PerR2, PerR3, and FurBL, ~0.04 M-1s-1 for PerRBL, and ~0.01 M-1s-1 for ZurBL. The slow rates of H2O2-mediated Zn2+ release for Fur family proteins from B. licheniformis, which are comparable to those observed with B. subtilis and S. aureus PerR proteins (~0.05 M-1s-1) [15, 17], suggest that the Zn2+ sites play a structural rather than a H2O2 sensing role. The Zn2+ contents of the purified proteins per monomer were determined to be ~0.8 for PerR2, ~0.9 for PerR3, ~0.5 for FurBL, ~0.7 for PerRBL, and ~0.5 for ZurBL. The retention of ~0.5–0.9 Zn2+ per monomer, despite the use of strong metal chelator EDTA during protein purification (see Materials and Methods), also supports the notion that all the Fur family proteins from B. licheniformis have a structural Zn2+ site. Altogether, these data indicate that all the five Fur family proteins from B. licheniformis contain a structural Zn2+ presumably coordinated by conserved cysteine residues like many other Fur proteins.

PerR2 (BL00690) and PerR3 (BL00950) as well as PerRBL can sense H2O2 by protein oxidation

Previously we have shown that the oxidation of PerR proteins can be easily and efficiently evaluated using <span class="Species">E. coli system [17, 18]. To investigate the oxidation of <span class="Chemical">Fur family proteins from B. licheniformis, we analyzed protein oxidation by MALDI-TOF MS after overexpression in E. coli with or without H2O2 treatment (Fig 3) as described previously [17, 18]. As noted for PerRBS, PerRBL showed H2O2-dependent oxidation at two tryptic peptides, T5 (His25 to Lys45, m/z = 2401.19) containing His37 and T11* (Phe84 to Arg98, m/z = 1910.85) containing His91, befitting its role as PerR (Fig 3A). In contrast, FurBL and ZurBL displayed no detectable changes in tryptic peptide peaks after H2O2 treatment (Fig 3D and 3E). Interestingly, PerR2 exhibited significant degree of oxidation at T8 peptide (Asn38 to Arg50, m/z = 1506.80) containing His39 (corresponding to His37 in PerRBS) even without H2O2 treatment, and further oxidation at T8 peptide and T13* peptide (Phe85 to Lys102, m/z = 2170.99) containing His92 (corresponding to His91 in PerRBS) after H2O2 treatment (Fig 3B). PerR3 also displayed H2O2-dependent oxidation, although less when compared with PerRBL and PerR2, at T7 peptide (Thr27 to Arg42, m/z = 1660.84) containing His34 (corresponding to His37 in PerRBS) and T13* peptide (Tyr77 to Lys90, m/z = 1824.87) containing His84 (corresponding to His91 in PerRBS) (Fig 3C). As expected, the sites of oxidation responsible for the 16 Da mass increase were mapped to be His37 and His91 for PerRBL, His39 and His92 for PerR2, and His34 for PerR3 (S1–S5 Figs). The site of oxidation for T13*+16 from PerR3 could not be exactly mapped partially due to the weak signal intensity. The presence of significantly oxidized T8 peptide (T8+16) from PerR2 as compared to that (T5+16) from PerRBL in the absence of H2O2 treatment suggests that PerR2 is more sensitive than PerRBL to oxidation by H2O2 encountered during aerobic growth of E. coli [17]. In addition, no detectable oxidation without external H2O2 treatment and the inefficient oxidation by H2O2 treatment for PerR3 suggest that PerR3 is less sensitive to oxidation by H2O2 than PerRBL or PerR2.

Fig 3

H2O2-dependent oxidation of Fur family proteins from B. licheniformis.

Oxidation of PerRBL (A), PerR2 (B), PerR3 (C), FurBL (D), and ZurBL (E) before and after H2O2 treatment. E. coli cells expressing PerRBL (LE0008), PerR2 (LE0002), PerR3 (LE0001), FurBL (LE0009), or ZurBL (LE0010), were treated with or without 1 mM H2O2 for 1 min. Oxidation status of proteins was analyzed by MALDI-TOF MS after SDS-PAGE fractionation and in-gel tryptic digestion. Asterisks represent peptides containing one (PerRBL and PerR3), two (PerR2 and FurBL), or three (ZurBL) carboxyamidomethylated cysteine residues.

Oxidation of PerRBL (A), PerR2 (B), PerR3 (C), <span class="Chemical">FurBL (D), and ZurBL (E) before and after <span class="Chemical">H2O2 treatment. E. coli cells expressing PerRBL (LE0008), PerR2 (LE0002), PerR3 (LE0001), FurBL (LE0009), or ZurBL (LE0010), were treated with or without 1 mM H2O2 for 1 min. Oxidation status of proteins was analyzed by MALDI-TOF MS after SDS-PAGE fractionation and in-gel tryptic digestion. Asterisks represent peptides containing one (PerRBL and PerR3), two (PerR2 and FurBL), or three (ZurBL) carboxyamidomethylated cysteine residues.

All the <span class="Chemical">peptides (T11* <span class="Chemical">peptide of PerRBL, T13* peptide of PerR2, and T13* peptide of PerR3) containing putative Zn2+-binding motif CXXC motif (corresponding to C96XXC99 in PerRBS) were detected in their fully alkylated form (Fig 3, S2 and S4 Figs). Note that the small amount of T13 peptide of PerR2, which is detected without alkylation even in the absence of H2O2 treatment, underwent no further oxidation after H2O2 treatment (Fig 3B). This observation that the cysteine residues are refractory to oxidation by H2O2 treatment is consistent with the idea that these cysteine residues are involved in structural Zn2+-binding. All these data together suggest that PerR2 and PerR3 as well as PerRBL can sense H2O2 with differential sensitivity, by histidine oxidation but not by cysteine oxidation.

Functional annotation of PerRBL (BL00075) as PerR, FurBL (BL05249) as Fur, and ZurBL (BL03703) as Zur

The function of PerR, Zur, and <span class="Chemical">Fur have intensively been studied both structurally and molecular genetically in <span class="Species">B. subtilis [11, 25–28], a close relative of B. licheniformis. Thus, B. subtilis provides an excellent model system for the characterization of Fur family proteins from B. licheniformis. To investigate whether PerRBL (BL00075) functions as PerR, FurBL (BL05249) as Fur, and ZurBL (BL03703) as Zur, heterologous complementation studies were performed using B. subtilis. For this, PerRBL-FLAG, FurBL-FLAG, or ZurBL-FLAG was expressed from its own promoter (with ~200 nucleotide sequence upstream of ORF) in a B. subtilis strain lacking a functional perR, zur, or fur gene, respectively (Fig 4). Since the FLAG epitope-tagged B. subtilis Fur family proteins are fully functional and the epitope tag provides a convenient means of monitoring protein levels in vivo, C-terminal FLAG-tagged proteins were used for activity analyses in vivo [11, 17, 26, 29].

Fig 4

, Fur, and Zur (A) Repressor activities of PerRBS and PerRBL for P-lacZ reporter fusion. B. subtilis cells expressing no PerR orthologue (LB1532), PerRBS-FLAG (HB9738), or PerRBL-FLAG (LB1023) were treated without or with 100 μM H2O2 for 30 min, and β-galactosidase activities were measured using P-lacZ reporter fusion. (B) Repressor activities of FurBS and FurBL for P-lacZ reporter fusion. B. subtilis cells expressing no Fur orthologue (LB1040), FurBS-FLAG (LB1041), or FurBL-FLAG (LB1042) were treated without or with 100 μM H2O2 for 30 min, and β-galactosidase activities were measured using P-lacZ reporter fusion. (C) Repressor activities of ZurBS and ZurBL for P-lacZ reporter fusion. B. subtilis cells expressing no Zur orthologue (LB1034), ZurBS-FLAG (LB1035), or ZurBL-FLAG (LB1036) were treated without or with 100 μM H2O2 for 30 min, and β-galactosidase activities were measured using P-lacZ reporter fusion. (D-F) Western blot analyses of FLAG-fused PerR orthologues (D), Fur orthologues (E), and Zur orthologues (F). The FLAG-fused proteins were probed by anti-FLAG antibody. (G) Fe-dependent repressor activities of FurBS and FurBL for P-lacZ reporter fusion. B. subtilis cells expressing no Fur orthologue (LB1040), FurBS-FLAG (LB1041), or FurBL-FLAG (LB1042) were grown in MLMM supplemented with or without 10 μM FeSO4, and β-galactosidase activities were measured using P-lacZ reporter fusion. (H) Zn-dependent repressor activities of ZurBS and ZurBL for P-lacZ reporter fusion. B. subtilis cells expressing no Zur orthologue (LB1034), ZurBS-FLAG (LB1035), or ZurBL-FLAG (LB1036) were grown in MLMM supplemented with or without 10 μM ZnCl2, and β-galactosidase activities were measured using P-lacZ reporter fusion.

, <span class="Chemical">Fur, and Zur (A) Repressor activities of PerR<span class="Species">BS and PerRBL for P-lacZ reporter fusion. B. subtilis cells expressing no PerR orthologue (LB1532), PerRBS-FLAG (HB9738), or PerRBL-FLAG (LB1023) were treated without or with 100 μM H2O2 for 30 min, and β-galactosidase activities were measured using P-lacZ reporter fusion. (B) Repressor activities of FurBS and FurBL for P-lacZ reporter fusion. B. subtilis cells expressing no Fur orthologue (LB1040), FurBS-FLAG (LB1041), or FurBL-FLAG (LB1042) were treated without or with 100 μM H2O2 for 30 min, and β-galactosidase activities were measured using P-lacZ reporter fusion. (C) Repressor activities of ZurBS and ZurBL for P-lacZ reporter fusion. B. subtilis cells expressing no Zur orthologue (LB1034), ZurBS-FLAG (LB1035), or ZurBL-FLAG (LB1036) were treated without or with 100 μM H2O2 for 30 min, and β-galactosidase activities were measured using P-lacZ reporter fusion. (D-F) Western blot analyses of FLAG-fused PerR orthologues (D), Fur orthologues (E), and Zur orthologues (F). The FLAG-fused proteins were probed by anti-FLAG antibody. (G) Fe-dependent repressor activities of FurBS and FurBL for P-lacZ reporter fusion. B. subtilis cells expressing no Fur orthologue (LB1040), FurBS-FLAG (LB1041), or FurBL-FLAG (LB1042) were grown in MLMM supplemented with or without 10 μM FeSO4, and β-galactosidase activities were measured using P-lacZ reporter fusion. (H) Zn-dependent repressor activities of ZurBS and ZurBL for P-lacZ reporter fusion. B. subtilis cells expressing no Zur orthologue (LB1034), ZurBS-FLAG (LB1035), or ZurBL-FLAG (LB1036) were grown in MLMM supplemented with or without 10 μM ZnCl2, and β-galactosidase activities were measured using P-lacZ reporter fusion.

The repressor activity of PerRBL-FLAG was monitored using a <span class="Species">B. subtilis mrgA promoter-lacZ reporter fusion (P-lacZ) which is under the control of PerR<span class="Species">BS. As reported previously [11], the P-lacZ was repressed in cells expressing PerRBS-FLAG but derepressed in the perR null mutant cells. The P-lacZ was also fully repressed by PerRBL-FLAG, and the repression was relieved upon H2O2 treatment as observed with PerRBS-FLAG (Fig 4A). FurBL showed a full repressor activity for FurBS-regulated feuA promoter-lacZ reporter fusion (P-lacZ) (Fig 4B). ZurBL-FLAG exhibited a full repressor activity for B. subtilis yciC promoter-lacZ reporter fusion (P-lacZ) which is under the control of ZurBS, despite the lower levels of expression when compared to ZurBS-FLAG (Fig 4C). We also examined the metal-dependent repressor activities of FurBL and ZurBL using a metal-limited minimal medium (MLMM). As expected, FurBL fully repressed the P-lacZ in the presence of Fe like FurBS, and ZurBL fully repressed the P-lacZ in the presence of Zn like ZurBS (Fig 4G and 4H).

These results imply that PerRBL (BL00075), <span class="Chemical">FurBL (BL05249), and ZurBL (<span class="CellLine">BL03703) may function as PerR, Fur, and Zur, respectively, in B. licheniformis, and that each protein can be expressed from its own promoter located in ~200 nucleotide sequence upstream of each ORF.

PerR2 (BL00690), but not PerR3 (BL00950), has a PerR-like repressor activity

PerR2-FLAG and PerR3-FLAG could not be expressed with ~200 nucleotide sequence upstream of their ORFs, thus it is likely that the genes encoding these proteins do not have their own promoters. To express PerR2-FLAG and PerR3-FLAG and investigate the roles of these proteins in vivo, we used the pXT system which fuses a <span class="Chemical">xylose-inducible promoter to the gene of interest, and a triple mutant <span class="Species">B. subtilis strain which lacks all of the three fur family genes (Fig 5). Despite the use of same xylA promoter along with the consensus ribosome binding site, the expression levels of Fur family proteins were not identical possibly by differences in mRNA and/or protein stability (Fig 5A). However, as observed with single mutant background with their own promoters (Fig 4), PerRBS-FLAG, FurBS-FLAG, and ZurBS-FLAG expressed from xylA promoter fully repressed the P-lacZ, P-lacZ, and P-lacZ, respectively (Fig 5B). Although PerR3-FLAG was highly expressed under the control of xylA promoter, PerR3-FLAG showed no repressor activity for PerR-regulated reporter fusion as well as for Fur- and Zur-regulated reporter fusions. Interestingly, PerR2-FLAG exhibited repressor activity for the PerR-regulated P-lacZ, but no repressor activity for the Fur-regulated P-lacZ nor the Zur-regulated P-lacZ. This specific repressor activity of PerR2 for the known PerR-regulated promoters, along with its H2O2-dependent histidine oxidation, suggest that PerR2 may act as a second PerR in B. licheniformis.

Fig 5

Repressor activity of PerR2.

(A) Western blot analysis of FLAG-fused Fur family proteins expressed from xylA promoter. B. subtilis perR fur zur triple mutant cells expressing no Fur family protein (LB1227), PerR3 (LB1287), PerR2 (LB1288), PerRBS (LB1490), FurBS (LB1491), and ZurBS(LB1493) were used. (B) Repressor activities of PerR2 and PerR3. Repressor activities of PerR3 and PerR2 were measured using P-lacZ, P-lacZ, and P-lacZ reporter fusions. As a control, repressor activities of PerRBS, FurBS, and ZurBS were also measured using P-lacZ, P-lacZ, and P-lacZ reporter fusions, respectively. The reporter fusion strains were constructed from the strains used in Fig 5A (Table 1). (C) Effects of PerR2 and PerR3 on the growth of the B. subtilis perR deletion mutant strain. The B. subtilis perR deletion mutant cells expressing no PerR (LB1010), PerRBS (LB2128) PerR2 (LB4034), or PerR3 (LB4106) were grown on LB agar plate for 1 day. (D) DNA binding activities of PerR2 and PerR3. DNA binding activities of PerR2 and PerR3 were measured by EMSA in the presence of 100 μM MnCl2.

(A) Western blot analysis of FLAG-fused <span class="Chemical">Fur family proteins expressed from xylA promoter. <span class="Species">B. subtilis perR fur zur triple mutant cells expressing no Fur family protein (LB1227), PerR3 (LB1287), PerR2 (LB1288), PerRBS (LB1490), FurBS (LB1491), and ZurBS(LB1493) were used. (B) Repressor activities of PerR2 and PerR3. Repressor activities of PerR3 and PerR2 were measured using P-lacZ, P-lacZ, and P-lacZ reporter fusions. As a control, repressor activities of PerRBS, FurBS, and ZurBS were also measured using P-lacZ, P-lacZ, and P-lacZ reporter fusions, respectively. The reporter fusion strains were constructed from the strains used in Fig 5A (Table 1). (C) Effects of PerR2 and PerR3 on the growth of the B. subtilis perR deletion mutant strain. The B. subtilis perR deletion mutant cells expressing no PerR (LB1010), PerRBS (LB2128) PerR2 (LB4034), or PerR3 (LB4106) were grown on LB agar plate for 1 day. (D) DNA binding activities of PerR2 and PerR3. DNA binding activities of PerR2 and PerR3 were measured by EMSA in the presence of 100 μM MnCl2.

It is known that a <span class="Species">B. subtilis perR null mutant strain grows very poorly in nonstressed conditions due to <span class="Disease">Fe deficiency resulting from elevated levels of FurBS and KatA [19]. To examine whether PerR2 can complement the perR null mutant strain and rescue the small colony phenotype, complementation experiments were performed (Fig 5C). As expected, the perR null mutant strain expressing PerRBS-FLAG showed a wild-type like colony phenotype. The perR null mutant strain expressing PerR2 also exhibited significantly increased colony size, indicating that PerR2 can rescue the Fe-deficiency presumably by reducing the levels of KatA and/or FurBS. In contrast, the perR null mutant strain expressing PerR3 still exhibited the small colony phenotype (Fig 5C) consistent with the lack of repressor activity for the PerR-regulated gene (Fig 5B).

To investigate the interaction of PerR2 with DNA, we performed electrophoretic mobility shift assays using the <span class="Species">B. subtilis mrgA promoter regions as probe. As shown in Fig 5D, PerR2 specifically shifted the DNA fragment containing PerR box but not the DNA fragment lacking PerR box. T<span class="Chemical">his result indicates that the repressor activity of PerR2 observed with the PerR-regulated promoter fusion is due to direct interaction of PerR2 with PerR box. However, it should be noted that the apparent K value of PerR2 for DNA binding was measured to be ~ 70 nM. This rather weak DNA binding activity of PerR2, as compared to that of PerRBS (K ~ 10 nM) [29], is likely to reflect the higher oxidation (inactivation) levels of PerR2 as shown in Fig 3B. In contrast, consistent with the lack of repressor activity for the PerR regulated promoter fusion, PerR3 showed no DNA binding activity (Fig 5D).

Discussions

Proteins with <span class="Chemical">Fur-like domain architecture are widespn>read in prokaryotes with ~20,000 homologues in EMBL-EBI InterPro database (IPR002481). Depending on signals they respn>ond, <span class="Chemical">Fur family proteins are classified as Fur (Fe), Zur (Zn), Mur (Mn), Nur (Ni), PerR (peroxide), and Irr (heme) [1, 2]. Among these, Fur is the most ubiquitous, and Zur, albeit not as ubiquitous as Fur, is also widespread in Gram negative and Gram positive bacteria. In contrast, PerR is mainly found in Gram positive bacteria as a functional substitute for OxyR, although it is also found in some Gram negative bacteria, and, in some cases, coexists with OxyR [1, 10]. Mur and Irr have been found in some α-proteobacteria including Rhizobiales and Rhodobacterales [30], and Nur has been only found in Streptomyces genus [31]. Although four Fur paralogues (Fur orthologue FurA, PerR orthologue CatR, Zur, and Nur) have been found and characterized in S. coelicolor [3, 31–33], many bacteria contains up to three Fur family proteins, usually two or three. For example, Gram negative bacteria E. coli and V. cholerae contain two (Fur and Zur) [4, 7], and Gram positive bacteria B. subtilis and S. aureus contain three (Fur, Zur, and PerR) [20, 22]. In this study, we found that B. licheniformis, a close relative of B. subtilis, contains five Fur family proteins. Like many other Fur family proteins, all these proteins retain a tightly bound Zn2+ presumably coordinated by highly conserved cysteine residues. Three of them were identified as Fur, Zur, and PerR orthologues of B. subtilis based on their repressor activity. The other two were identified as PerR-like proteins based on their sequence similarity to PerR proteins and their H2O2-dependent oxidation of histidine residues.

The <span class="Chemical">H2O2-sensing mechanism of PerR has only been extensively studied in <span class="Species">B. subtilis and S. aureus, despite its wide distribution in most Gram positive bacteria and in some Gram negative bacteria [10, 11, 17, 25]. Unlike OxyR which utilizes the oxidation of cysteine thiol, PerR uses a distinct Fe-dependent histidine oxidation mechanism for H2O2 sensing, where H2O2 oxidizes the histidine ligands of the Fe2+ at the regulatory site to 2-oxo-histidine. Our results indicate that PerRBL also uses a histidine oxidation mechanism for H2O2 sensing. Furthermore, we found that H2O2 can also oxidize the two other PerR-like proteins, PerR2 and PerR3, but not FurBL and ZurBL. MALDI-TOF MS and ESI-MS/MS analyses of the tryptic peptides, along with sequence analyses, of PerR2 and PerR3 indicate that the oxidation events occur at histidine residues rather than cysteine residues. Despite the high similarity between the regulatory metal binding sites of PerR and Fur, Fur does not react with H2O2 under conditions where PerR does [11]. Recently, it has been suggested that O-donor ligand corresponding to Asp104 of PerRBS or Glu108 of FurBS is the key residue which determines the accessibility of H2O2 to Fe2+-coordination site [12]. It is noteworthy that PerR2 and PerR3, as well as other PerR proteins, also contain a conserved Asp at this position, whereas Fur proteins have a Glu (Fig 1C).

Despite the presence of bona fide PerRBL, PerR2 also showed specific repressor activity on the representative PerR-regulated gene but not on <span class="Chemical">Fur- or Zur-regulated gene, and the perR null mutant small colony phenotype could be rescued by PerR2 (Fig 5). Thus, it is reasonable to speculate that PerR regulon in <span class="Species">B. licheniformis is under the control of both PerRBL and PerR2. In the simplest scenario, the two proteins would exert influence on the PerR regulon genes simultaneously. Alternatively, each protein may regulate genes under different conditions. The higher sensitivity of PerR2 than PerRBL seems to suggest the differential role of these proteins under different oxidation conditions.

Unlike PerR2, no repressor activity of PerR3 was o<span class="Species">bserved for any genes under the control of PerR, <span class="Chemical">Fur, and Zur using B. subtilis reporter fusion assays. And, PerR3 was purified as monomer after overexpression in E. coli, whereas all the other four Fur family proteins from B. licheniformis were purified as dimer. Considering that all the biochemically characterized Fur family proteins are dimeric DNA binding proteins, PerR3 may not be a canonical Fur family protein. However, the oxidation of PerR3 by H2O2, albeit less sensitive as compared to PerRBL or PerR2, suggests that PerR3 may play a role as a H2O2 sensor in B. licheniformis. It has been previously reported that the transcription of perR3 (bl00950, bli04114) is massively induced after H2O2 treatment [34]. Interestingly, the genes encoding for PerR3 and BL00949 (BLi04115, putative ferrochelatase) are located directly downstream of katA gene (bl00951, bli04113). Furthermore, in contrast to B. subtilis katA gene which is monocistronically transcribed under the control of PerRBS, B. licheniformis katA gene is cotranscribed with perR3 and bl00949 after H2O2 treatment [34]. These imply that PerR3 may have some role especially under conditions of H2O2 stress.

In summary, we have shown that <span class="Species">B. licheniformis contains a total of five <span class="Chemical">Fur family proteins: two novel PerR-like proteins in addition to the canonical PerR, Fur, and Zur. The presence of two additional Fur family proteins in B. licheniformis, in contrast to its close relative B. subtilis, may indicate that the metal ion regulation and peroxide stress response under the control of Fur family proteins are far more complex than previously reported for B. subtilis. Further study is required to identify distinct roles of PerR2 and PerR3 along with their relevance to other Fur family proteins in B. licheniformis.

Identification of His37 as an oxidation site in T5 peptide (His25 to Lys45) from PerRBL by ESI MS/MS analysis.

(A) Predicted m/z values of b- and y-ions of unmodified T5 <span class="Chemical">peptide of PerRBL. <span class="Chemical">His37 is shown in red. (B) Tandem MS spectrum of T5 peptide. Triple charged precursor ion ([T5+3H]3+ = 801.85, shown in green) was analyzed by tandem MS. The b- and y-ions are shown in purple and blue, respectively. (C) Tandem MS spectrum of T5+16 peptide. Triple charged precursor ion ([T5+16+3H]3+ = 806.82, shown in green) was analyzed by tandem MS. The b- and y-ions are shown in purple and blue, respectively. The y-ions not containing His37 (y4-y8) appear at the predicted m/z values, whereas the subsequent y-ions containing His37 (y9-y20) have a +16 Da mass shift. Note that almost all the y9- and y10-ions (containing His37 but not Met35) have a +16 Da mass shift. The b-ions not containing His37 (b5-b12) appear at the predicted m/z values, whereas the subsequent b-ions containing His37 (b13-b20) have a +16 Da mass shift. Note that almost all the b10- and b11-ions (containing Met35 but not His37) appear at the predicted m/z values. Taken together, these data indicate that most of the oxidation in T5+16 peptide occurred at His37 rather than Met35.

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Identification of His91 as an oxidation site in T11* peptide (Phe84 to Arg98) from PerRBL by ESI MS/MS analysis.

(A) Predicted m/z values of b- and y-ions of T11* <span class="Chemical">peptide (containing carboxyamidomethylated <span class="Chemical">Cys96 residue) of PerRBL. His91 is shown in red. (B) Tandem MS spectrum of T11* peptide. Double charged precursor ion ([T11*+2H]2+ = 956.06, shown in green) was analyzed by tandem MS. The b- and y-ions are shown in purple and blue, respectively. (C) Tandem MS spectrum of T11*+16 peptide. Double charged precursor ion ([T11*+16+2H]2+ = 964.42, shown in green) was analyzed by tandem MS. The b- and y-ions are shown in purple and blue, respectively. The y-ions not containing His91 (y3-y7) appear at the predicted m/z values, whereas the subsequent y-ions containing His91 (y8-y14) have a +16 Da mass shift. The b-ions not containing His91 (b3-b7) appear at the predicted m/z values, whereas the subsequent b-ions containing His91 (b8-b14) have a +16 Da mass shift. These data indicate that the oxidation in T11*+16 peptide occurred at His91.

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Identification of His39 as an oxidation site in T8 peptide (Asn38 to Arg50) from PerR2 by ESI MS/MS analysis.

(A) Predicted m/z values of b- and y-ions of T8 <span class="Chemical">peptide of PerR2. <span class="Chemical">His39 is shown in red. (B) Tandem MS spectrum of T8 peptide. Triple charged precursor ion ([T8+3H]3+ = 503.20, shown in green) was analyzed by tandem MS. The b- and y-ions are shown in purple and blue, respectively. (C) Tandem MS spectrum of T8+16 peptide. Triple charged precursor ion ([T8+16+3H]3+ = 509.16, shown in green) was analyzed by tandem MS. The b- and y-ions are shown in purple and blue, respectively. The y-ions not containing His39 (y1-y11) appear at the predicted m/z values, whereas the subsequent y-ions containing His39 (y12-y13) have a +16 Da mass shift. The b-ions containing His39 (b2-b13) have a +16 Da mass shift. These data indicate that the oxidation in T8+16 peptide occurred at His39.

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Identification of His92 as an oxidation site in T13* peptide (Phe85 to Lys102) from PerR2 by ESI MS/MS analysis.

(A) Predicted m/z values of b- and y-ions of T13* <span class="Chemical">peptide (containing carboxyamidomethylated <span class="Chemical">Cys97 and Cys100 residues) of PerR2. His92 is shown in red. (B) Tandem MS spectrum of T13* peptide. Triple charged precursor ion ([T13*+3H]3+ = 724.93, shown in green) was analyzed by tandem MS. The b- and y-ions are shown in purple and blue, respectively. (C) Tandem MS spectrum of T13*+16 peptide. Triple charged precursor ion ([T13*+16+3H]3+ = 730.05, shown in green) was analyzed by tandem MS. The b- and y-ions are shown in purple and blue, respectively. The y-ions not containing His92 (y3-y10) appear at the predicted m/z values, whereas the subsequent y-ions containing His92 (y11-y17) has a +16 Da mass shift. The b-ions not containing His92 (b3-b7) appear at the predicted m/z values, whereas the subsequent b-ions containing His92 (b8-b16) has a +16 Da mass shift. These data indicate that the oxidation in T8+16 peptide occurred at His92.

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Identification of His34 as an oxidation site in T7 peptide (Thr27 to Arg42) from PerR3 by ESI MS/MS analysis.

(A) Predicted m/z values of b- and y-ions of T7 <span class="Chemical">peptide of PerR3. <span class="Chemical">His34 is shown in red. (B) Tandem MS spectrum of T7 peptide. Double charged precursor ion ([T7+2H]2+ = 831.40, shown in green) was analyzed by tandem MS. The b- and y-ions are shown in purple and blue, respectively. (C) Tandem MS spectrum of T7+16 peptide. Double charged precursor ion ([T7+16+2H]2+ = 839.29, shown in green) was analyzed by tandem MS. The b- and y-ions are shown in purple and blue, respectively. The y-ions not containing His34 (y3-y8) appear at the predicted m/z values, whereas the subsequent y-ions containing His34 (y9-y15) has a +16 Da mass shift. The b-ions not containing His34 (b5-b7) appear at the predicted m/z values, whereas the subsequent b-ions containing His34 (b8-b16) has a +16 Da mass shift. These data indicate that the oxidation in T7+16 peptide occurred at His34.

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