- Research article
- Open Access
The MetJ regulon in gammaproteobacteria determined by comparative genomics methods
© Augustus and Spicer; licensee BioMed Central Ltd. 2011
- Received: 18 August 2011
- Accepted: 14 November 2011
- Published: 14 November 2011
Whole-genome sequencing of bacteria has proceeded at an exponential pace but annotation validation has lagged behind. For instance, the MetJ regulon, which controls methionine biosynthesis and transport, has been studied almost exclusively in E. coli and Salmonella, but homologs of MetJ exist in a variety of other species. These include some that are pathogenic (e.g. Yersinia) and some that are important for environmental remediation (e.g. Shewanella) but many of which have not been extensively characterized in the literature.
We have determined the likely composition of the MetJ regulon in all species which have MetJ homologs using bioinformatics techniques. We show that the core genes known from E. coli are consistently regulated in other species, and we identify previously unknown members of the regulon. These include the cobalamin transporter, btuB; all the genes involved in the methionine salvage pathway; as well as several enzymes and transporters of unknown specificity.
The MetJ regulon is present and functional in five orders of gammaproteobacteria: Enterobacteriales, Pasteurellales, Vibrionales, Aeromonadales and Alteromonadales. New regulatory activity for MetJ was identified in the genomic data and verified experimentally. This strategy should be applicable for the elucidation of regulatory pathways in other systems by using the extensive sequencing data currently being generated.
The advent of fast sequencing techniques over the past few decades has led to an exponential increase in the number of fully sequenced organisms, particularly bacteria with their smaller genomes. Although a great deal of data is being generated, much of it is in the form of annotations based on automated similarity searches. It is important to validate these annotations and extend the use of the databases by organizing the genes into coherent pathways.
Functions of the genes involved in methionine utilization
AdoMet-dependent transcriptional repressor
homocysteine-dependent transcriptional activator
aspartokinase II/homoserine dehydrogenase II
methionine synthase (B12-dependent)
methionine synthase (B12-independent)
S-adenosylmethionine (AdoMet) synthetase
Methionine salvage pathway genes
~MTR transporter (ATPase subunit)
~MTR transporter (permease subunit)
~MTR transporter (substrate-binding subunit)
5-methylthioribose (MTR) kinase
methionine transporter (ATPase subunit)
methionine transporter (permease subunit)
methionine transporter (substrate-binding subunit)
~methionine transporter (Na+/H+ antiporter family)
vitamin B12 (cobalamin) outer membrane transporter
~cobalt transporter (substrate-binding subunit)
~cobalt transporter (ATPase subunit)
~cobalt transporter (permease subunit)
Other regulated genes
S-methylmethionine : homocysteine methyltransferase
~transporter (substrate-binding subunit)
~transporter (permease subunit)
~transporter (permease subunit)
~transporter (ATPase subunit)
~amino acid permease
~methionine synthetase (B12-independent)
Various unregulated genes
aspartate semialdehyde dehydrogenase
10-formyltetrahydrofolate : L-methionyl-tRNAfMet N-formyltransferase
GTP cyclohydrolase I
methylthioadenosine (MTA) nucleosidase/S-adenosylhomocysteine (AdoHcy) nucleosidase
Previously, genes in the regulon were recognized on an individual basis by identifying DNA binding sites for MetJ, called metboxes, or by showing regulation via MetJ, methionine or its derivative S-adenosylmethionine (AdoMet) which is the co-factor for MetJ. Efforts to do large-scale, undirected searches for MetJ-regulated genes have been limited to E. coli [5, 6]. By expanding our search to all sequenced bacteria, the dataset we had available for this study included 206 sequenced organisms representing 41 genera in 5 orders.
In this study, we have identified the conserved members that form the core of the regulon in all the organisms. While each species has a unique spectrum of regulated genes, the over-all regulon includes all the genes involved in methionine biosynthesis, salvage and transport. We have identified some previously unknown members of the regulon and, in addition, have experimentally confirmed that some of these are regulated by MetJ in vivo.
MetJ homologs and metboxes
Composition of the MetJ regulon for the five orders
For the entire complement of the MetJ regulon, most organisms regulate 70-80% of the genes, particularly Ent, Vib and Alt. For the Aeromonads, A. hydrophila regulates 94% of its genes, while Tolumonas only does 57%. The Pasteurellales are also highly variable, with repression percents ranging from 27% for Aggregatibacter to 69% for Pasteurella. Among the Ent symbiotes, only two species, Hamiltonella defensa and Baumannia cicadellinicola, have MetJ homologs, and it is a pseudogene in the latter. (We note that the classification of genes as pseudogenes in this paper is based on the genome annotation and therefore could be affected by sequencing errors. However in the case of symbiotic species, pseudogenization and gene loss are common features of reductive genome evolution .) These species are also the only symbiotes with metboxes, although with a limited distribution; in H. defensa only metNIQ has them, while in B. cicadellinicola only metE/R have them. The metbox regions for these genes are highly similar to those of other Ent species (70% identical to the corresponding regions of E. coli) and appear to be conserved from the common ancestor.
In addition to the Ent symbiotes, Sodalis glossinidius (Ent) and Haemophilus ducreyi (Pas) show a great deal of attrition in the MetJ regulon. S. glossinidius lives as a symbiote of tsetse flies but unlike the other symbiotic species, it has not reduced its genome significantly. However, while the genome is about the same size as E. coli, S. glossinidius has only about half as many intact genes. For our genes of interest, metE2a, metH, metL, mtnK, mtnA, mtnC, mtnE and btuB are identifiable as (unannotated) pseudogenes. Other than metH and metL, it retains the full complement of biosynthetic enzymes. In the case of H. ducreyi, an obligate pathogen, almost all genes of the MetJ regulon have been lost and it retains only metJ, metK and metNIQ. Of these, only metK retains its metboxes, so we may be seeing the first stage of the loss of metJ from this organism.
Regulation by MetJ
In order to confirm their regulation by MetJ, some of the candidate genes were chosen for further study. The ability of MetJ to regulate the genes was assessed in vivo using an ONPG assay where the native operators (400 base pairs upstream of the coding sequence) were used to direct expression of lacZ. We cannot assume all foreign promoters will be functional in E. coli, but we are interested only in the expression of the gene in the presence of MetJ relative to the expression without MetJ, i.e. the repression ratio (RR). (We also note that we had difficulty transforming constructs containing H. influenzae operators into E. coli, although constructs from the other species could be readily transformed.)
In addition to MetJ, some genes of the MetJ regulon are also regulated by MetR, a transcriptional activator of the LysR family. This protein primarily controls the expression of genes at the end of the pathway: metF, metE and metH, but also metA, glyA, luxS and metR itself. This gene is well represented in 91% of the species, and has metboxes in 89% of those. It almost always co-occurs with metE and they are divergently transcribed from a common intergenic region with common metboxes. In Alteromonas macleodii, an Alt species which lacks metE, metR is instead located 1 kilobase away from metH.
Methionine biosynthesis genes: homocysteine formation
In the canonical biosynthetic pathway, the backbone of methionine comes from aspartate, which is also the precursor to lysine, threonine and isoleucine (Figure 1). Consequently, the three steps to convert aspartate to homoserine are catalyzed by the isoforms MetL (aspartokinase II, homoserine dehydrogenase II), ThrA (aspartokinase I, homoserine dehydrogenase I) and LysC (aspartokinase III), as well as the unique enzyme Asd (aspartate semialdehyde dehydrogenase). We note that all organisms without metL (mostly symbiotes and Pasteurellales) have thrA (distinguishable because it clusters with thrB and thrC) so it is possible that thrA provides the necessary function in those species. In almost every species of interest, the metL gene forms an operon with metB, and thus is regulated by the metB promoter (Figure 5). The only exceptions are Idiomarina, where metB has been lost, and Kangiella, where the operon has been expanded to include metX2 and metF.
The immediate precursor to methionine is homocysteine which can be made in multiple ways. Homoserine, created by MetL, is first activated by either succinylation or acetylation, and this represents the first committed step in methionine biosynthesis. These reactions are normally carried out by the unrelated proteins MetA (homoserine O-succinyltransferase) and MetX (homoserine O-acetyltransferase), however the two proteins do not have strict specificities . Homocysteine can then be generated by either direct sulfhydrylation, a single step using inorganic sulfur, or by transsulfuration, a two step process using cystathionine as an intermediate with cysteine as the sulfur donor. The first reaction is usually catalyzed by MetY (O-acetylhomoserine (thiol)-lyase), while the second set of reactions is carried out by MetB (cystathionine gamma-synthase) and MetC (cystathionine beta-lyase). However, just as with MetA and MetX, there is a certain amount of promiscuity in the functions of MetY, MetB and MetC , particularly since they all belong to the same transsulfuration family of pyridoxal-dependent enzymes (Additional file 4 Figure S2).
For the first step of homoserine activation, almost all our species of interest use MetA (83%), and it has metboxes in most of them (86%). In addition, the E. coli protein is known to be feedback inhibited by methionine and AdoMet, and to be regulated at the level of transcription by MetR as well as MetJ. In most Ent and some Alt and Aer it occurs close in the genome to metH, the B12-dependent methionine synthase, even seeming to form an operon in Pseudoalteromonas and Alteromonas species.
The species without MetA either lack de novo biosynthesis (Ent symbiotes and H. ducreyi) or use MetX homologs (Pas and the Alt species Idiomarina and Kangiella). These genes all have metboxes. In addition, five Alt (three Pseudoalteromonas, Alteromonas and Idiomarina) and one Ent (Pantoea sp. At-9b) have a MetX homolog even though they also have MetA (or MetX1 in the case of Idiomarina). These genes do not have metboxes. The few metX genes that exist seem to have arisen from horizontal gene transfer; metX in Pas likely came from Listeria or a close relative .
In addition to replacing MetA with MetX, Pas species also replaced MetB with MetB2 from Gram-positives . These two genes are not located close to each other on the chromosome so they may represent independent transfers. Possibly the native MetB was not capable of or efficient at recognizing the acetylated product of MetX; E. coli MetB can act on acetyl-homocysteine although not as efficiently as the succinylated substrate . MetC remains to convert cystathionine to homocysteine. One of the H. influenzae strains (PittGG) lacks MetB2 and MetX is a pseudogene so it may have lost the ability to synthesize methionine. While all the Pas metX genes have metboxes and they were shown to be functional in H. influenzae, albeit weakly (RR = 0.52), only one of the metB2 genes has potential metboxes.
With the notable exception of Pas, succinylation by MetA and transsulfuration using MetB and MetC appears to be the ancestral pathway for homocysteine synthesis as these genes are well represented in all the orders. In almost all cases (98%) metB has metboxes, while metC has metboxes only in about half the Ent and a handful of Alt. Among the Ent symbiotes, only Baumannia and Blochmannia have the three genes, but none of them have metboxes. metB is a pseudogene in Yersinia pestis strains, which explains its known methionine auxotrophy . Although it relies on transport to meet its methionine needs, Y. pestis has not yet lost any of the other genes associated with biosynthesis, or the metboxes that regulate them.
MetY homologs, which create homocysteine via direct sulfhydrylation, are eclectically represented in the five orders, but unlike MetA, MetB and MetC, the distribution of the MetY homologs does not match the phylogeny, so they are probably not inherited. There are metboxes in most of the Aer and Alt species and the gene from Shewanella is strongly repressed by MetJ (RR = 0.11). Almost all the species with MetY also have MetA, MetB and MetC so they may be able to use both pathways for homocysteine synthesis. The Alt Idiomarina is unique in that it lacks MetA, MetB and MetC and only has MetX1 and MetY, which form an operon and therefore presumably function together. Kangiella is odd in that it has metB, but not metY or metC. Probably MetB in this organism is capable of converting the MetX2 product directly to homocysteine through direct sulfhydrylation, a secondary function that E. coli MetB also has .
Methionine biosynthesis genes: methionine formation
Homocysteine is converted to methionine using one of two unrelated enzymes: MetH, which requires vitamin B12 (cobalamin) as co-factor, and MetE. For organisms which have both proteins (~70% of our species), MetH is preferred when B12 is available since it is a much more efficient enzyme than MetE. MetH has metboxes in Vib, Aer and Alt species, but rarely in Ent or Pas. MetE, on the other hand, has metboxes in almost every species. This is probably because, in the absence of repression, the metE gene is very highly expressed to overcome the fact that it is such an inefficient enzyme . In E. coli, this expression also requires MetR so it is not surprising that, with the exception of symbiotes, all species with metE also have metR, although the reverse is not true. As said before, metE typically shares a locus with metR, with the two genes being divergently transcribed from a common intergenic region in almost all species.
The terminal methyl group for methionine comes from the donor 5-methyltetrahydrofolate which is made by the enzyme MetF (5,10-methylenetetrahydrofolate reductase) and is usually in a glutamylated form. MetF has metboxes in almost all species (85%), the primary exception being Pas. In addition, there are four Alt species (Psychromonas ingrahamii, Shewanella piezotolerans, Colwellia psychrerythraea and Pseudoalteromonas haloplanktis) that lack the ortholog of E. coli metF, but instead have a gene we will refer to in this paper as metF2. This is only weakly similar to metF, but contains the same conserved domain (cd00537; PF02219). Because it occurs in species without metF, and because 3 of the 4 genes have metboxes, this gene likely performs the same function.
All but seven organisms have one or both of metE and metH, along with metF and thus can presumably synthesize methionine from homocysteine. Four of these deficient species are the symbiotes Hamiltonella, Wigglesworthia, Riesia and the Pas H. ducreyi which also lack the pathway for homocysteine synthesis. The Pas A. succinogenes and Alt Idiomarina lack metE, metH and metF while retaining the genes necessary for homocysteine synthesis. In the case of Idiomarina, it was shown that it is capable of growing in the absence of methionine  so it must have another pathway for its creation. It does not have any close homologs of metH or metE, but A. succinogenes has homologs of both metH (MHT2) and metE (metE2b and metE2c) so possibly one or more of these can complement the loss. The Aer A. salmonicida lacks only metF while retaining the synthases, so only its methyl donor is unknown.
Methionine can be further converted into S-adenosylmethionine (AdoMet) by the essential enzyme MetK. AdoMet is primarily used as a methyl donor but is also required for synthesis of polyamines, autoinducers and other molecules [18, 19]. Crucially for the MetJ regulon, AdoMet is the co-factor for MetJ, which thus detects methionine levels only indirectly. The metK gene has metboxes in most Ent and Pas, but only a handful of Vib and Alt and no Aer. In many Gram-positive bacteria, which all lack MetJ, methionine biosynthesis is regulated by an AdoMet riboswitch [20, 21]. Thus it seems that AdoMet synthesis is usually coordinately regulated as a part of methionine metabolism.
The methionine salvage (MS) pathway allows the recycling of methylthioadenosine (MTA), produced during polyamine synthesis and other reactions, back to methionine (reviewed in ). MTA, which is a potent inhibitor of its parent reaction, is cleaved to methylthioribose (MTR) by the ubiquitous nucleosidase MtnN (5'-methylthioadenosine/S-adenosylhomocysteine nucleosidase). In E. coli, which lacks the MS pathway, MTR is excreted  and this may be true for other species which lack the pathway.
The enzymes which convert MTR to methionine in Enterobacteria are (in order of reaction): MtnK (5-methylthioribose kinase), MtnA (S-methyl-5-thioribose-1-phosphate isomerase), MtnB (methylthioribulose-1-phosphate dehydratase), MtnC (2,3-diketo-5-methylthio-1-phosphopentane phosphatase), MtnD (1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase) and MtnE (methionine aminotransferase). The pathway is illustrated in Figure 1. The final step can actually be catalyzed by multiple aminotransferases, such as tyrB in Klebsiella , while mtnV, the aminotransferase in Bacillus subtilis, was found to be dispensable . Nevertheless, the mtnE gene is special because it only occurs in species that have (or whose ancestors had) the MS pathway, it clusters with other MS genes, and it is the only aminotransferase with metboxes. There are also some alternate proteins used by other species. For instance the single enzyme MtnP (methylthioadenosine phosphorylase) can be used in place of MtnN and MtnK, while MtnW (2,3-diketo-5-methylthiopentyl-1-phosphate enolase) and MtnX (2-hydroxy-3-keto-5-methylthiopentenyl-1-phosphate phosphatase) can be used in place of the bifunctional enzyme MtnC. None of these alternate enzymes have close homologs in our species of interest however.
In addition, these genes co-occur with a probable MTR transporter initially identified in Bacillus cereus . It has not been functionally characterized yet, but is similar to other sugar transporters and has an S-box (AdoMet riboswitch) in B. cereus as well as metboxes in gammaproteobacteria. We will refer to the three components of this ABC transporter as mtrACB. The mtrB gene is usually closely followed by a gene of unknown function (COG5276) which we refer to as mtrY since its role is a mystery. Another gene, called mtnU, is closely associated with the MS genes. It is a nitrilase (from conserved domain cl11424) but its specificity is unknown. It was proposed to have a regulatory function in B. subtilis because it was produced at much lower levels than the other proteins . Finally, another protein of unknown function, the putative alcohol dehydrogenase ybdH, also co-occurs with the MS genes and shares regulation by common intergenic metboxes.
The full complement of genes exists only in the Enterobacteria, although individual species have suffered various rearrangements and losses. In Klebsiella, the mtnB gene was inverted and moved to the middle of a cluster of ~15 genes that were inserted between mtnA and mtnD. In the branch leading to E. coli, Salmonella and Citrobacter the entire cluster has been deleted, causing the flanking genes, ybdH and mtnE, to come together and share common regulation by the group 4 metboxes. In C. rodentium, even ybdH and mtnE were lost, but the upstream and downstream genes are the same as in the other species in that branch indicating that this was a localized deletion. In C. koseri, the entire MS cluster has then apparently been re-acquired, causing a duplication of the group 4 metboxes. For Yersinia pestis, all the strains except for Angola and Pestoides have lost the enzymes. They retain ybdH and the mtrACBY cluster, but mtrA is a pseudogene in all of them.
Oddly enough, one of the three Pantoea species (strain At-9b) has two mtrB genes. Pat9b_0820 occurs next to mtrAC, just like in other Pantoea and closely related Erwinia strains, while Pat9b_3290 occurs separate from the other MS genes in a cluster with ybdH and mtrY, which otherwise do not occur in Pantoea and Erwinia. Of all the other species with the MS pathway, only Serratia shares this pattern for the three genes. This suggests that in Pantoea sp. At9b, and maybe Serratia as well, the genes were re-acquired as a group. We note that none of the flanking genes are the same for these two species so the synteny only includes this 3-gene cluster. Since these genes also have different trees than the other MS genes, we distinguish them as ybdH2-mtrB2-mtrY2.
In addition, 3 of the 51 Escherichia/Shigella strains (UMN026, S88 and SE15) have acquired genes for mtnK and mtnA, apparently from alphaproteobacteria which have the most similar homologs. These genes form a cluster with a gene that is weakly similar to mtnB, but is most similar to the native fucA (D-ribulose-phosphate aldolase). We will refer to it as mtnB2. The insertion of the cluster was presumably phage-mediated as the genes are adjacent to a KpLE2 prophage. The genes co-occur with a fourth gene that is only found in these three E. coli strains and is annotated as a sugar permease. It is possible this cluster of genes is involved in the transport and enzymatic alteration of a sugar with unknown specificity. None of these genes have metboxes.
Enterobacteria at the base of the tree, Edwardsiella, Photorhabdus, Proteus and Xenorhabdus, lack all the genes associated with the MS cluster. The pathway is also lacking in the other orders, although some genes do unexpectedly show up in a handful of other species, e.g. an mtnK homolog in one Vib species (Aliivibrio). Among the Alt we find mtnE in two Shewanella species; mtnC in Ferrimonas and all 20 Shewanella species; mtnB and mtnU in Pseudoalteromonas haloplanktis; and the entire mtn cluster in Pseudoalteromonas sp. SM9913. Although we initially believed this was a result of horizontal gene transfer, phylogenetic trees for the genes match those of the organisms. Furthermore the metboxes, which are only preserved in the two Pseudoalteromonas, appear quite divergent from the Ent examples in the same context. This suggests that these genes have been in their genomes for a long time.
There are two known systems for methionine transport in the gammaproteobacteria. The most widespread is the ABC transporter MetNIQ which has been characterized in E. coli [3, 4]. Except for two Alt species (Psychromonas and Ferrimonas), this transporter only occurs in Aer, Vib, Pas and Ent. The other transporter was recently identified in Gram-positive bacteria, as well as homologs in Vibrio and Shewanella, called MetT . This is a member of the NhaC Na+/H+ antiporter family and only occurs in Alt, Aer and Vib species. Thus metT appears to be the ancestral transporter that was lost at the time Pas branched off (see Figure 2), while metNIQ may be a newcomer that was introduced after most of the Alt species had already speciated. About 68% of Aer and Vib species retain both transporter systems. In almost all cases the transporter genes have metboxes and all the genes that were tested showed repression by MetJ: Ec.metN (RR = 0.05), Vc.metT (0.08) and Sh.metT (0.21). Thus all species, except for some symbiotes and two Alteromonads (Alteromonas and Kangiella), have methionine-specific transporters. In the case of Alteromonas, the only transporter with metboxes is MADE_2464 which is a putative polysaccharide transporter (conserved domain cl10513) and thus seems unlikely. In the case of Kangiella, one uncharacterized gene with potential metboxes has some similarity to dipeptide transporters: Kkor_1992 (DUF1302 superfamily). Homologs of this gene occur in other Alt species, but not with metboxes.
Vitamin B12, or cobalamin, is the necessary co-factor for the methionine synthase MetH, as well as some other enzymes. It is transported across the outer membrane by BtuB. Expression of this gene is known to be regulated by a riboswitch [28, 29]. Regulation by MetJ was not suspected because E. coli and Salmonella lack metboxes. However, btuB genes in a third of our species of interest do have potential metboxes and the Yersinia ones we tested are functional (RR = 0.06 for Y. pseudotuberculosis, 0.25 for Y. pestis but 1.01 for E. coli which lacks the metboxes). The metboxes are located at the start of transcription, which includes the sizeable riboswitch, thus they are on average ~300 bp away from the start of translation. There are no other genes for which the metboxes are typically so far away. If it is the case the metboxes must precede riboswitches, then this suggests that no other gene in our study is also regulated by a riboswitch.
Another candidate transporter is similar to mtsABC, a metal transporter from Streptococcus . This was also identified as part of the methionine regulon in Gram-positives . Among our species, it only exists in Vib but has metboxes 60% of the time. It is annotated as a potential cobalt transporter which may link it to cobalamin utilization, just like btuB.
Finally, there is an NhaP Na+/H+ antiporter family member in Pas, Vib, Aer and one Alt species. This is a transporter of unknown specificity. It has metboxes in some Vib and Aer species, but only when it shares an operator with metH. Although this pattern suggested that these metboxes should be specific to metH, when tested with the ONPG assay the nhaP gene from V. cholerae had the same level of repression as metH (0.46 vs. 0.50).
Other regulated genes
There are various other genes that do not fit into the main categories of synthesis, salvage and transport. The mmuPM operon is composed of two genes: mmuP codes for an S-methylmethionine permease while mmuM codes for a specialized homocysteine methyltransferase that uses S-methylmethionine as its substrate [31, 32]. MmuP is similar to other amino acid permeases like AroP and LysP while MmuM belongs to the same family as MetH. These genes exist in a random handful of Ent species. Among the 51 sequenced Escherichia/Shigella strains, only six K12 strains have homologs, and in those species they occur as part of the CP4-6 prophage. In strain BW2952, a subsequent deletion of ~100 kb led to the loss of mmuM and the fusion of the N-terminus of mmuP with the C-terminus of mhpD. This has happened recently enough that the metboxes have not been lost yet. For the other species, however, the homologs are not associated with a phage insertion. Furthermore, except for Pectobacterium the metboxes appear to be the same for all the species (≥60% identity to Klebsiella), suggesting a common origin for them. The mmuPM metboxes are unusual in that they occur very close to the start of translation, only 2 bases away in E. coli. For the other metboxes in this study, the average gap is ~75 bases. It was previously shown by immunoblotting that MmuM expression was reduced by high methionine concentrations . We tested the operators for Ec.mmuP and Kp.mmuP and both were highly repressed (RR = 0.02) in the presence of MetJ.
MetE belongs to the CIMS-C-terminal-like family (conserved domain cd03311) and Figure 7C shows the other homologous genes. These proteins are half the size of MetE, which probably arose from an ancient duplication event . Genes in the MetE1 group have no metboxes and occur downstream of a protein of unknown function (pfam08908) which only occurs with MetE1, suggesting these two proteins share a related function. None of the genes in the MetE2 cluster occur in a conserved environment, or adjacent to any putative transporter. Most of the genes in the MetE2a subgroup have metboxes. We tested Klebsiella pneumoniae and found that it was strongly repressed (RR = 0.02) by MetJ. Since all the organisms with MetE2a also have MetE, it is not clear what role this enzyme plays in metabolism.
In addition to the main MetNIQ cluster, there are various other components of this transporter system. There are six other 3-gene clusters with varying gene orders: metNIQ, metIQN and metQNI. These are referred to as metD2-7 in Table S2. There are two 2-gene clusters (metNI) and four isolated metQ homologs. (The number of homologs of metN was on the order of several thousand, so only those that cluster with metI or metQ are included in Table S2.) None of these genes are very common and very few of them have metboxes. MetQ is the periplasmic substrate-binding component and since MetNIQ can transport both D- and L-methionine, it was proposed that metQ and its only homolog in E. coli, called nlpA, could be specific for the different enantiomers ; unfortunately this was shown to be unlikely. However, some of the MetQ homologs in other species may show specificity.
Except for NlpA, none of the other MetNIQ homologs occur in E. coli, even though it is known to have a second methionine-specific transporter . The high-affinity transporter, which can transport both D- and L-methionine, was called metD and was subsequently identified as metNIQ. The low-affinity transporter, which is specific to L-methionine, was called metP and is still unknown, although it was shown to not be mmuP, the S-methylmethionine permease [3, 35]. Among the E. coli genes with metboxes, the only uncharacterized transporter is yjhF which is similar to gluconate transporters, but was shown not to be able to transport gluconate .
All the genes described above are likely members of the MetJ regulon. In addition, there are three other potential members that have functions related to methionine metabolism, but which we consider to be unlikely. The operon mtcBC encodes the genes involved in reverse transsulfuration -- the conversion of methionine to cysteine. MtcB is a cystathionine beta-synthase and is related to the cysteine synthases CysK and CysM. MtcC is a member of the transsulfuration family of enzymes, related to MetB, MetC and MetY. In our species of interest, these two genes only occur in 20 Ent and 2 Alt where they always occur together. Another potential member of the regulon is MegL. This is another transsulfuration family protein and is similar to methionine-gamma-lyase which is involved in methionine degradation [38, 39]. There are several MegL-like genes, but only one group has metboxes. This group always clusters with an oxygenase similar to isopenicillin N synthase (PcbC, COG349).
For all these genes the number of homologs with metboxes is small. In the case of MegL only a few closely related Shewanella species have them. In addition to the paucity of metboxes, if the functional prediction is correct then it seems unlikely that they would be repressed by MetJ. They act to reduce methionine concentrations, so during times of MetJ activation (high methionine), these proteins should also be activated to allow for recyling of the sulfur group. Nevertheless, in Klebsiella mtcBC seem to be upregulated by MetJ, although the mechanism is not clear . We include them as potential members of the regulon until they can be tested for actual regulation.
The various regulons
The genes in the MetJ regulon in E. coli make up the core of the regulon that is consistently repressed in other gammaproteobacteria species. This includes all the genes involved in methionine biosynthesis and transport, although not every gene is regulated in every species. In addition, comparative genomics methods have identified other genes, such as the methionine salvage pathway, which does not occur in E. coli, but which is consistently regulated in all the species where it is found. With only a few exceptions, the methionine utilization genes that form the MetJ regulon in gammaproteobacteria are the same as those in Gram-positive bacteria, despite major differences in regulatory mechanisms .
Novel members of the regulon that we were able to verify experimentally are btuB (vitamin B12 transporter), metX (homoserine O-acetyltransferase), metY (possible O-acetylhomoserine sulfhydrylase), metH (B12-dependent methionine synthase), metE2a (possible methionine synthase), mtnKADCB (methionine salvage pathway enzymes), and the transporters mtrACB, metT and nhaP. We also identified some potential members that we were not able to test at this time: metF2 (possible 5,10-methylenetetrahydrofolate reductase), MHT1 and MHT2 (possible methionine synthases), mtcBC (reverse transsulfuration enzymes), megL (possible methionine gamma-lyase) and mtsABC (metal transporter). These novel genes highlight one of the major advantages of genomics-based methods since most of these genes do not exist in E. coli, and the others, like btuB and metH, are not regulated by MetJ.
There are some genes that appear never to have metboxes in the species we studied. These include asd, glyA and folE which are peripheral genes in the methionine biosynthetic pathway; mtnN, luxS and ahcY which are involved in recycling S-adenosylhomocysteine back to homocysteine; metG, fmt, def and map which generate methionyl-tRNA, formylate it, deformylate it and remove initial methionine from translated proteins; and the genes involved in cysteine metabolism. We note that folE was previously identified as a possible target for MetJ based on microarray data . We could not identify metboxes for any of the folE homologs in the five orders and a gel-shift assay performed with E. coli folE showed no binding under our conditions (Figure S1). However, in the ONPG assay folE had weak repression so it may be indirectly regulated.
The various organisms
The spectrum of regulated genes is undoubtedly related to the particular environments these organisms live in, as sulfur, and thus methionine, concentrations can vary a great deal . One observation we can make from this study is that organisms which have developed an endosymbiotic (e.g. Buchnera aphidicola and Sodalis glossinidius) or obligate pathogenic (e.g. Haemophilus ducreyi and Yersinia pestis) lifestyle tend to lose regulon genes, as well as MetJ itself and the metbox sites. There are a variety of patterns of loss that likely reflect the degree of symbiosis as well as the time-scale involved. For instance the Ent symbiotes which lack MetJ have also lost all their metboxes and most regulon genes, while Yersinia pestis has a largely intact regulon with loss of only a few genes and no change in metbox distribution.
For free-living organisms there is likely to be a synergistic effect from the environmental niche in which the bacteria find themselves. For instance many Enterobacteria have a methionine salvage pathway which can utilize MTR as a sulfur source. In addition to endogenous production of MTR, these species likely can transport it from organisms like E. coli which excrete it into the common milieu. Likewise, S-methylmethionine is commonly produced by plants, and organisms with the mmuPM genes, like the plant pathogen Pectobacterium, can utilize this as a substrate for methionine synthesis.
The various pathways
There are a variety of biosynthetic pathways on display in Figure 1, but there is clearly an ancestral pattern for methionine biosynthesis via MetA, MetB, MetC and the synthases MetE and MetH. Some organisms have replaced these with alternate pathways, such as MetX and MetB2 in Pas, or have acquired additional genes that may function in parallel, such as the many transsulfuration enzymes with unknown specificities. In particular, the spectrum of present, absent, regulated, and unregulated genes in Table S2 provides a rich resource for identifying non-canonical pathways or filling gaps in known ones. Alternate routes for methionine production may include reliance on transport of precursors, such as MTR and S-methylmethionine as well as homocysteine, or recycling pathways, such as methionine salvage which regenerates methionine molecules that derive their backbone from ribose rather than aspartate. For each species, a delineation of the full pathway would be necessary to understand the place of methionine biosynthesis within the metabolism of the whole organism. Such system-wide information is useful in metabolic engineering for production of organic molecules , as well as in the development of drugs for prokaryotic-specific proteins such as those of the methionine salvage pathway  and the cobalamin-independent methionine synthase MetE .
This study is designed to use data from bacterial genome sequencing projects to gain a more complete understanding of the regulon controlled by MetJ in all the organisms in which it is found. We have identified over 2000 binding sites for ~35 genes and operons from 206 gammaproteobacteria species. Among these are genes expected from the E. coli MetJ regulon, as well as some new ones. For some of these genes we were also able to verify their regulation by MetJ experimentally.
The genomes (and plasmids) for all sequenced species within the five orders containing MetJ homologs (Enterobacteriales, Pasteurellales, Vibrionales, Aeromonadales and Alteromonadales) were accessed from the Genome Information Broker [43, 44] website in January, 2011. This was a total of 206 species. Orthologous genes were identified using BLAST searches , as well as consideration of the genomic environment. In most cases this identification was straight-forward since we were only interested in a subset of the gammaproteobacteria. However in some cases, particularly metR (part of the LysR family) and btuB (part of the TonB family), it was not always possible to confidently identify orthologs. For determining entire gene families (e.g. metE and metH in Figure 7), an e-value of e-25 was used as the threshold. Gene alignments were made using ClustalW within MEGA5 . Trees were made in MEGA5 using Neighbor-Joining with 500 bootstrap replicates. Data for the phylogenetic tree of gammaproteobacteria in Figure 2 was downloaded from the Orthologous Matrix Project [7, 47] and manipulated in MEGA5.
Since the binding site is palindromic the data was symmetrized for each half-metbox.
Information weight matrix used to search for metboxes
Riw (bits per base)2
0 > 13
lacZ reporter and ONPG assay
A reporter plasmid was made from pBR322  by: removing the ampicillin resistance gene; making a silent mutation in the tetracycline resistance gene to remove an NheI site; and adding NsiI and KpnI sites by primer-amplification of the plasmid. The full-length E. coli lacZ gene sequence was amplified from strain W3110 with flanking NheI and KpnI sites, then cloned into the modified pBR322. This construct is referred to as pBZT. Operator sequences were cloned between the NheI and NsiI sites.
The candidate operators were cloned from one of eight bacteria: Escherichia coli W3110 and Haemophilus influenzae Rd KW20 (both courtesy C. Raetz, Duke University), Klebsiella pneumoniae and Yersinia pestis KIM (both courtesy S. Abraham, Duke University), Yersinia pseudotuberculosis YPIII and Yersinia enterocolitica 8081 (both courtesy V. Miller, University of North Carolina at Chapel Hill), Vibrio cholerae N16961 (courtesy M. Kuehn, Duke University) and Shewanella oneidensis MR-1 (courtesy J. Frederickson, Pacific Northwest National Laboratory).
When necessary, genomic DNA was prepared by centrifuging an overnight culture of bacteria (1.5 ml) and resuspending the cells in 500 μl buffer containing 100 mM Tris, pH 8 and 50 mM EDTA. SDS was added to 1% to lyse the cells. 250 μl of 7.5 M ammonium acetate was added, then 500 μl phenol-chloroform. After spinning the sample down, the top 500 μl was removed and 1 ml isopropanol was added to precipitate the DNA. The DNA was washed with 70% ethanol, air-dried, then resuspended in 50 μl TE (10 mM Tris, pH 8, 1 mM EDTA).
Operator sequences were amplified by PCR from the genomic DNA using PfuUltra II HotStart 2× (Stratagene) with primers that produced flanking NsiI and NheI sites. (For operators which contained these sites, PstI and SpeI, respectively, were used instead to produce compatible ends.) These operators were cut and gel-purified then inserted into pBZT. All insertions were verified by sequencing. In cases where the insertion differed from the published sequence, a second independent construct was prepared to verify the polymorphism. In no case were these changes in the proposed metboxes. We note that our Klebsiella strain does not match any of the published genomes, but is most similar to K. pneumoniae NTUH-K2044.
For each construct in each strain, at least two colonies were chosen, and triplicate samples were assayed for each colony. Results are represented as the ratio of the activity during repressed conditions (MC4100) to that during derepressed conditions (ΔmetJ), and shown with the standard deviation for the six measurements.
Gel shift assay
Operators were tested directly for MetJ binding using a gel-shift assay. For each plasmid, primers in the vector were used with MangoMix (Bioline) to amplify a 636-bp fragment incorporating the 400-bp operator. 50 μl PCR reactions were cleaned up using SureClean Plus (Bioline) and the precipitated DNA was resuspended to the same starting volume with TES Buffer (20 mM Tris, pH 8, 1 mM EDTA, 150 mM NaCl). 1 μl of the PCR mix (approximately 10 ng DNA) was used in a 30 μl reaction with 0 or 50 nM MetJ. Samples were run on a 7.5% TGE gel (25 mM Tris, 192 mM glycine, and 2 mM EDTA) containing 250 μM AdoMet, then stained with Vistra Green (GE Healthcare) and imaged with a Typhoon 9410 phosphorimager using a 520 BP 40 fluorescence filter.
We thank Drs. S. Abraham, J. Frederickson, R. Greene, M. Kuehn, V. Miller, and C. Raetz for generously providing bacterial strains or genomic DNA. Financial support for this work was in part from NIH Grant RR-022854 and Duke University.
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