INTRODUCTION

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The toluene degradation pathway determined by the TOL plasmid pWW0 of Pseudomonas putida mt-2 is both an enzymatic and regulatory paradigm for the metabolism of recalcitrant compounds in the environment (reviewed in reference 42). The key event in the activation of the whole pathway is the substrate-dependent transcription of the cognate catabolic operons encoded by the plasmid. Expression of the upper-pathway TOL operon for bioconversion of toluene and xylenes into the corresponding carboxylic acids (22) is driven by the ⁵⁴-dependent promoter Pu. This promoter is activated at a distance by the enhancer-binding and toluene-responsive protein XylR with the structural assistance of the integration host factor (IHF). In addition, the cells must be in an adequate metabolic status for Pu activity, since an excess of certain carbon sources (10, 11, 24) or rapid growth in rich medium (8, 16, 17, 25, 29) entirely inhibits promoter output in vivo even if the compound to be degraded is present in the culture. This behavior, which is phenomenologically akin to catabolic repression (16, 17, 27, 29), is by no means exclusive to the Pu promoter. Expression of many other biodegradative pathways of Pseudomonas is also inhibited by a number of growth conditions which adjust the activity of specific catabolic promoters to a given metabolic and physiological status (9).

More than one mechanism may cause the down-regulation of Pu in certain growth scenarios. Glucose and other carbohydrates (24) decrease Pu activity through a process involving the ptsN gene (11, 38). However, rapid growth in rich medium also results in a separate negative signal in the system through the control of the activity of ⁵⁴ (8). In addition, full activity in vivo of ⁵⁴ requires (at least in Escherichia coli) the participation of the FtsH product (6), a protein with both protease and chaperone activities which is involved in the turnover of the heat shock factor ³² (23) and other regulators. In spite of all these observations, the specific instruments for the physiological control of Pu remain unknown.

A case similar to the Pu promoter of the TOL plasmid is that of the Po promoter of the dimethylphenol (dmp)-degrading pathway of plasmid pVI150 of Pseudomonas sp. strain CF600. Po is a ⁵⁴ promoter which is activated at a distance by the phenol-responsive protein DmpR, which has high similarity to XylR (35). Although the sequence of the Pu and Po promoters are different, the upstream activating motifs (UAS) are similar enough to be recognized by both proteins as binding sites (19). On this basis, DmpR and XylR behave more as variants of the same protein than as two distinct proteins. Like Pu, the activation of Po by DmpR is also subjected to a tight metabolic control by certain carbon sources and by the growth rate (47). A recent study by Shingler's laboratory (48) has traced the physiological down-regulation of Po to the need for (p)ppGpp, the signal molecule which triggers the stringent response to amino acid starvation (12). This is a very attractive possibility, since many metabolic conditions are reflected in the intracellular levels of this alarmone molecule (reviewed in reference 12).

The present study was undertaken to examine whether the observed physiological control of the Pu promoter of the TOL plasmid could also be connected to the direct or indirect effects of (p)ppGpp. The results in vivo an in vitro, given below, clearly demonstrate that although Pu activity is indeed stimulated by ppGpp, the effect is insufficient to account for the inhibition of Pu during exponential growth. In addition, our data suggest that the moderate effect of ppGpp on Pu is the result of a direct stimulation of the transcription initiation complex by the alarmone.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results and Discussion References

Strains, plasmids, and general procedures. The strains and plasmids used in this work are listed in Table 1. Recombinant DNA techniques were carried out by published methods (43). All plasmids used in the transcription assays were derived from vector pTE103, which adds a strong T7 terminator downstream of the promoter under study (18). Plasmid pEZ10 carries Pu and has been described previously (7, 36). Plasmid pTE103-Po carries a 481-bp DNA insert spanning positions 471 to +10 of the Po promoter sequence (39). Similarly, plasmid pTE103-PlacUV5 bears an insert with this control promoter between positions 117 and +12. All cloned inserts and DNA fragments were verified through automated DNA sequencing in an Applied Biosystems device. All the supercoiled plasmid DNA templates used for in vitro transcription were prepared with the Qiagen plasmid purification system.

Growth and induction conditions. Bacteria were generally grown at 30°C in rich Luria-Bertani (LB) medium (32). M9 minimal medium (43) supplemented with 0.2% succinate was supplemented, where indicated, with 0.2% Casamino Acids. When required, media were also supplemented with 150 µg of ampicillin per ml, 50 µg of streptomycin per ml, 50 µg of spectinomycin per ml, 30 µg of chloramphenicol per ml, and isopropyl-1-thio--D-galactopyranoside (IPTG). Promoter activity in vivo was monitored in all cases by assaying the accumulation of -galactosidase in cells permeabilized with chloroform and sodium dodecyl sulfate (SDS) as described by Miller (32) under the conditions specified in each case. To measure the accumulation of -galactosidase, overnight cultures of each of the strains under study were diluted twice 50-fold in the same medium to suppress the -galactosidase accumulated by stationary-phase bacteria. Fresh exponential cells were then further regrown with aeration, and samples were taken at the stages indicated in each experiment. Where needed, the cultures were exposed to saturating vapors of the upper TOL pathway inducer 3-methyl benzylalcohol (1). The -galactosidase activity values given throughout this paper represent the average of at least three independent experiments in duplicate samples.

Proteins and protein techniques. Purified factor ⁵⁴ and core RNA polymerase (RNAP) from E. coli were the kind gift of B. Magasanik. IHF was obtained from H. Nash. The ⁷⁰-RNAP holoenzyme was purchased from Amersham. The XylR variant called XylRA is identical to the wild-type protein except for the deletion of its N-terminal module (called the A domain). This variant is fully constitutive and can thus activate transcription from Pu in the absence of any aromatic inducer (20, 36). XylRA was purified to apparent homogeneity by metalloaffinity purification of the His-tagged protein as described by Pérez-Martín and de Lorenzo (36). His-tagged RelA in crude extracts was detected as previously described (20). To this end, whole E. coli cells were disrupted in sample buffer containing 2% SDS and 5% -mercaptoethanol and run in 10% polyacrylamide gels containing SDS (26). Samples were then blotted on a Immobilon-P membrane (Millipore) and probed with a 1:5,000 dilution of an anti-His monoclonal antibody from Clontech. The band corresponding to the protein was identified with anti-mouse immunoglobulin G IgG conjugated to horseradish peroxidase and developed with an H₂O₂-luminol-luciferin system.

Construction of a His-tagged RelA expression plasmid and purification of the protein. To obtain a variant of the relA gene of E. coli encoding a product amenable to affinity purification, the NdeI insert of plasmid pCNB0118 (30), which bears the relA sequence, was cloned in His fusion and Plac/lacI^q/pT7 expression vector pET19-b (Novagen), to generate plasmid pCNB0209R. Depending on the host strain, the resulting hybrid gene was expressed through the Plac promoter upon addition of IPTG, through the T7 promoter, or through both. This is the case when pCNB0209R was transformed in E. coli BL21(DE3)(pLys) (46), since the strain bears a chromosomal Plac-based system for expression of the T7 polymerase. For purification of the His-tagged RelA protein, an overnight culture of E. coli BL21(DE3) cotransformed with both pLys and pCNB0209R was grown at 37°C in 2YT medium (43), diluted 1:30 in fresh medium, and regrown under the same conditions to an optical density at 600 nm of approximately 0.7. Expression of the His-tagged RelA was then induced by addition of 0.3 mM IPTG, and the culture was given a further incubation for 3 h. The cells were then harvested by centrifugation, washed with ice-cold buffer A (20 mM Tris-acetate [pH 8.5], 5 mM imidazole, 500 mM NaCl, 0.5 mM phenylmethylsulfonyl fluoride), and stored in aliquots of approximately 0.5 g at 70°C. When needed, cells (0.5 g) were suspended in 5 ml of buffer A and disrupted by sonication. After addition of magnesium acetate to 5 mM, the crude lysate was cleared by centrifugation (4,000 × g for 15 min at 4°C). The supernatant was recentrifuged at 25,000 × g for 30 min at 4°C, and the cleared sample was loaded onto a 2-ml Ni²⁺-nitrilotriacetic acid column (Novagen, Madison, Wis.), which had been precharged with NiSO₄ (as recommended by the manufacturer), and equilibrated in A buffer. After the protein sample was loaded, the column was washed with 15 ml of buffer A and then with 20 ml of buffer A containing 60 mM imidazole. Then a 30-ml linear gradient of this metal chelator was run to a final concentration of 1 M imidazole. Fractions (2 ml) were collected at a flow rate of 0.3 ml min¹ and tested for the presence of the desired protein by SDS-polyacrylamide gel electrophoresis analysis and by assays of (p)ppGpp-synthesizing activity (see below). The main peak of His-tagged RelA protein eluted at 250 to 350 mM imidazole. The corresponding fractions were pooled and used for large-scale synthesis of ppGpp. Protein concentrations were determined (5) using bovine serum albumin as the standard. This procedure yielded up to 4 mg of His-tagged RelA per g of cells, with an apparent enzyme purity of 98%.

In vitro synthesis and purification of ppGpp. Preparative-scale synthesis of ppGpp was performed using the His-tagged RelA protein prepared as described above. The standard reaction was carried out at 30°C in a final volume of 5 ml containing 1.5 ml of the His-tagged RelA preparation (stock at 0.1 to 0.3 mg/ml), 2 mM ATP, 2 mM GDP, and 1× buffer RB (50 mM Tris-acetate [pH 8.0], 15 mM magnesium acetate, 60 mM potassium acetate, 30 mM ammonium acetate, 0.2 mM EDTA, 0.5 mM phenylmethylsulfonyl fluoride, 15% methanol). The progress of the reaction was monitored by ascending thin-layer chromatography on fluorescence-labeled polyethyleneimine cellulose plates, using 1.5 M KH₂PO₄ (pH 3.4) as chromatographic buffer. When no further increase in the level of ppGpp could be detected (5 to 12 h later), the reaction was stopped by adding formic acid to 1 M. After removal of precipitated protein by centrifugation (2 min at 9,000 × g, the resulting supernatant was diluted at least threefold with 50 mM triethylammonium acetate (pH 7.7) and applied to a 25-ml DEAE-Bio-Gel column (Bio-Rad), previously equilibrated in the same buffer. After being loaded, the column was eluted with 50, 100, and 150 mM triethylammonium acetate (pH 7.7) (25, 25, and 35 ml, respectively) and finally with 150 ml each of 200 and 400 mM triethylammonium acetate (pH 7.7) or with a 300-ml linear gradient of the same buffer to a final triethylammonium acetate concentration of 400 mM. Fractions (5 ml) were collected in each case, and the elution of ppGpp was analyzed by UV spectroscopy and polyethyleneimine thin-layer chromatography. Fractions containing ppGpp were frozen in an ethanol bath, lyophilized, and dissolved in a small volume of water. The ppGpp concentration was determined at 252 nm (₂₅₂ = 13,100 M¹ cm¹) (49), and aliquots were frozen and stored at 20°C. The overall yield of ppGpp, calculated on the basis of the GDP initially added to the reaction was 80%. The purity of ppGpp (>95%) was assessed by high-performance liquid chromatography analysis in a Waters 600S system fitted with a 996 Photodiode array detector. For analyses, samples were injected into a C₁₈ 100 Nucleosil column (4.6 mm by 20 cm) (Sugelabor) and run at a flow rate of 0.7 ml min¹ with a 10-min KH₂PO₄ (pH 7) linear gradient (5 to 30 mM) in 20 mM tetrabutylammonium bromide-20% methanol (solution A), followed by a 10-min KH₂PO₄ linear gradient (30 to 100 mM) in solution A and a 5-min isocratic elution with 200 mM KH₂PO₄ in the same solution.

In vitro transcription assays. Transcription assays were performed by a published procedure (14). Supercoiled DNA templates were used at 5 nM. Samples (50 µl) of reaction mixtures were placed at 37°C in a buffer consisting of 50 mM Tris-HCl (pH 7.5), 50 mM KCl, 10 mM MgCl₂, 0.1 mM bovine serum albumin, 10 mM dithiothreitol, and 1 mM EDTA. Unless indicated otherwise, each DNA template was premixed with 25 nM core RNAP, 100 nM ⁵⁴, 25 nM IHF, and 100 nM XylRA. The DNA templates and the proteins were supplemented with purified ppGpp at the concentration indicated in each case and then incubated at 37°C with 4 mM ATP for 20 min to allow open-complex formation. For multiple-round assays, transcription was then initiated by adding a mixture of ATP, CTP, GTP (400 µM each), UTP (50 µM) and 5 µCi of [-³²P]UTP (3,000/mmol). For single-round experiments, heparin (0.1 mg/ml) was added along with the nucleoside triphosphate mixture to prevent reinitiation. After incubation for 10 min at 37°C, the reactions were stopped with an equal volume of a solution containing 50 mM EDTA, 350 nM NaCl, and 0.5 mg of carrier tRNA per ml. Transcription assays with placUV5 templates were carried out with 0.5 nM supercoiled plasmid pTE103-placUV5 mixed with 25 nM ⁷⁰-containing E. coli RNAP holoenzyme (Amersham) in the transcription buffer described above and incubated for 15 min at 37°C. The transcription rounds were initiated, as above, by the addition of the same mixture of nucleoside triphosphates, and the mixtures were incubated for 15 min at 37°C. In any case, the mRNA was extracted from the reaction products, precipitated with ethanol, electrophoresed on a denaturing 7 M urea-4% polyacrylamide gel, and visualized by autoradiography. Transcript levels were quantified with a Bio-Rad Molecular Imager FX system.

	RESULTS AND DISCUSSION

Top Abstract Introduction Materials and Methods Results and Discussion References

Reproducing the inhibition of Pu by Casamino Acids in an E. coli reporter system. For an adequate genetic assay to examine the physiological conditions that regulate Pu, we employed the low-copy-number plasmid pMCP1 (6), which includes a transcriptional Pu-lacZ fusion and the wild-type xylR gene. As shown in Fig. 1A, this fusion appears to grossly reproduce in E. coli the physiological down-regulation undergone by Pu in rich medium (24), which has been named exponential silencing (8). This is characterized by the lack of significant activity of Pu while cells grow exponentially in LB despite the presence of a XylR effector (such as 3-methyl benzylalcohol) in the medium. In contrast, when the same reporter cells were grown in a minimal mineral medium with a nonrepressive carbon source such as succinate (24), Pu activity was quickly elicited following exposure to the inducer (Fig. 1B). Finally, the presence of 0.2% Casamino Acids in the minimal medium (Fig. 1C) restored the inhibition of Pu during exponential-phase growth of induced cells. The results in Fig. 1 not only validated the use of an E. coli host for the genetic analyses discussed below but also demonstrated the inhibitory effect of an excess of Casamino Acids on the outcome of Pu activity already described in P. putida (29). Since the abundance of amino acids in the medium restrains the stringent response mediated by (p)ppGpp, these results encouraged us to explore the connection between Pu activity and this physiological phenomenon.

View larger version (24K): [in this window] [in a new window]   FIG. 1.   Physiological control of the Pu promoter of P. putida reproduced in an E. coli host. E. coli strain CC118 harboring plasmid pMCP1 (xylR+/Pu-lacZ), which encodes the wild-type XylR protein, was grown at 30°C in LB rich medium (A), M9 minimal medium with 0.2% succinate (panel B), or M9-succinate medium with 0.2% Casamino Acids (C). At an early growth stage, the cultures were exposed to saturating vapors of the XylR effector 3-methyl benzylalcohol (3mBA), and the accumulation of -galactosidase activity (expressed in Miller units) was monitored during subsequent growth. The enzymatic activities shown are the average of duplicate samples as explained in the text. Note the repressive effect of Casamino Acids during exponential growth. The organization of the reporter system encoded by pMCP2 is sketched (not to scale) at the top of the figure.

Pu performance in a (p)ppGpp-deficient genetic background. One attractive explanation for the data above described could be that ppGpp is required for Pu performance in vivo. Therefore, the lack of enough intracellular levels of (p)ppGpp brought about by the availability of amino acids in the medium during the earlier stages of growth (12) could inhibit promoter activity. This possibility was easy to test, since production of (p)ppGpp depends of genes relA and spoT in E. coli (50). Should ppGpp be needed for Pu activity, the promoter must become silent in a (p)ppGpp-deficient [(p)ppGpp⁰] background. To reduce the number of variables, we tested this notion with plasmid pMCP2 as the reporter system. Similarly to pMCP1, pMCP2 also bears a Pu-lacZ fusion, but xylR is present in the form of a truncated gene encoding the variant XylRA, with the N-terminal domain deleted. Such a deletion results in the constitutive activity of the protein independently of effector addition (20). XylRA makes Pu nonresponsive to aromatic inducers, but the promoter still maintains its metabolic control (8). Therefore, this reporter system reflects the physiological regulation of Pu as a phenomenon different from its activation by XylR inducers. Both the wild-type E. coli MG1655 and its isogenic relA spoT derivative E. coli CF1693 were transformed with pMCP2, and the accumulation of -galactosidase was monitored during growth in LB medium. As shown in Fig. 2A, the pattern of LacZ expression in the two strains was very similar, with only relatively minor differences. Not only were -galactosidase levels comparable, but also Pu displayed the same extent of exponential silencing in the (p)ppGpp⁰ strain as in its wild-type counterpart. Similar results were obtained when plasmid pMCP1, bearing the wild-type xylR gene, was transformed in the same strains and the cultures were induced by 3-methyl benzylalcohol (data not shown). These results sufficed by themselves to rule out the possibility that the alarmone was the predominant signal which mediates the physiological control of Pu. However, it was also found that the levels of -galactosidase accumulated by the relA spoT strain were systematically 20 to 30% lower than those in the ppGpp⁺ cells; therefore, the signal may be playing a minor role in Pu activity.

View larger version (24K): [in this window] [in a new window]   FIG. 2.   Pu performance in vivo in the absence of (p)ppGpp or with an excess of the alarmone. (A) The wild-type strain E. coli MG1655 and its ppGpp0 isogenic derivative E. coli CF1693 (relA spoT) harboring the reporter plasmid pMCP2 (xylRA+/Pu-lacZ) were grown in LB medium at 30°C and assayed for -galactosidase activity (expressed in Miller units). The growth rates of the two strains were indistinguishable. There was a moderate decrease in accumulation of the reporter product in the relA spoT host. The reporter system encoded by pMCP2, bearing the constitutive xylR alele xylRA, is sketched at the top of the figure. (B) The wild-type strain E. coli MG1655 was cotransformed with pMCP2 (xylRA+/Pu-lacZ) and pCNB0209R (expressing a His-tagged RelA product under the control of a lacI/Plac system) (see the text). The cotransformant was grown in LB medium, and the accumulation of -galactosidase was monitored throughout growth after the addition of 0.1 mM IPTG. The expression levels of the RelA product were revealed by the protein blot, shown at the top of the figure, which was probed with an anti-poly His monoclonal antibody (the last lane corresponds to advanced stationary-phase cells not plotted in the graph). The significant increase in Pu activity upon relA overexpression is evident.

Overexpression of relA improves Pu performance. To ascertain whether the small effect of (p)ppGpp in Pu detected with the relA spoT strain could be exacerbated by artificially increasing the intracellular levels of the alarmone, we contransformed compatible plasmids pMCP2 (xylRA⁺/Pu-lacZ) and pCNB0209R in host strain E. coli MG1655. Plasmid pCNB0209R carries a His-tagged variant of the relA gene of E. coli (see Materials and Methods), whose expression is tightly controlled by a lacI/Plac system. Intracellular levels of (p)ppGpp can thus be artificially elevated even in the presence of amino acids by the addition of 0.1 mM IPTG to the medium (44) because of the increased activity of the relA product. Figure 2B shows the course of -galactosidase accumulation of E. coli MG1655(pMCP2, pCNB0209R) during growth in LB medium with or without the addition of IPTG. It is worth mentioning that under the assay conditions, overproduction of the His-tagged RelA product (as detected with a Western blot assay [Fig. 2B]) did not significantly affect the growth rate. The data in Fig. 2B show that overexpression of RelA, predicted to result in higher intracellular levels of ppGpp, appeared both to increase the overall activity of Pu threefold and to cause an induction pattern devoid of growth stage regulation. These results suggested that the partial dependency of Pu activity on (p)ppGpp indicated by the experiments in Fig. 2 could indeed be genuine, albeit somewhat minor under normal physiological conditions. However, since (p)ppGpp also regulates the intracellular levels of IHF (2) and since the binding sites for this protein are not saturated during exponential growth (34), it is also possible that the (p)ppGpp-dependent increase in Pu activity in vivo reflects an indirect effect on IHF levels. In fact, we have observed that overproduction of IHF also causes an increase of Pu activity and a partial relief of exponential silencing (data not shown). These observations encouraged us to test directly the effect of ppGpp in an in vitro transcription system for Pu as explained below.

ppGpp directly stimulates the ⁵⁴-dependent transcriptional machinery of Pu. To ascertain unequivocally whether the influence of ppGpp on Pu suggested by the data above reflected a direct or an indirect effect, we exploited the in vitro transcription system developed previously in our laboratory for this promoter (7, 36). This includes not only the purified core RNAP, the ⁵⁴ factor, and the XylRA protein but also the IHF, which is required for the assembly of an optimal geometry of the DNA region (15) and for the recruitment of the enzyme to the promoter sequences (4). In addition, we used the supercoiled DNA template named pEZ10 (36), which contains the promoter region as a 301-bp fragment spanning positions 208 to +93 of Pu, cloned upstream of a strong T7 terminator. We used also the ⁷⁰-dependent promoter lacUV5 as a control basically independent of ppGpp (13, 40, 41). This promoter was assembled in the same transcription template as Pu. For the experiments described below, it was of the utmost importance to use preparations of ppGpp which had been purified shortly before use. We had noticed early in this project that this compound is often inactive when shipped from distant origins or after storage for long periods. This problem encouraged us to develop a simplified and very efficient procedure for the production of large amounts of ppGpp. The method, which is described in detail in Materials and Methods, uses an in vitro reaction between ATP and GDP catalyzed by the purified His-tagged RelA protein in solution.

View larger version (28K): [in this window] [in a new window]   FIG. 3.   Effect of ppGpp on the transcriptional activity of Pu in vitro. (A) Results of multiple-round transcription reactions with 5 nM Pu-containing template pEZ10, 100 nM XylRA, 25 nM IHF, 25 nM core RNAP, 100 nM 54, and increasing concentrations of purified ppGpp as indicated. Under these conditions, pEZ10 produces an mRNA of 394 nucleotides. The levels of transcript found in each case are plotted below the autoradiograph of the gel. The baseline value starts at 50 arbitrary units. (B) Control with the placUV5 promoter. The transcription reaction mixtures contained 5 nM supercoiled pTE103-PlacUV5 template mixed with 25 nM E. coli 70 RNAP holoenzyme and different amounts of ppGpp. In this system, PlacUV5 produces an mRNA of 313 nucleotides.

Comparison of the responsiveness of Pu and Po to ppGpp. As mentioned above, the ⁵⁴ promoter Po drives the expression of a phenol-degrading pathway in Pseudomonas sp. strain CF600 in a fashion very similar to that of Pu for the upper TOL pathway (45, 47). The two promoters have identical UASs for their respective activators, DmpR and XylR (19). Furthermore, we have shown previously (37) that XylRA binds the Po enhancer with the same affinity as it binds to the cognate promoter Pu. This is not surprising, since the two proteins have identical recognition surfaces (33) in the helix-turn-helix motif of their DNA-binding D domain (35). This provided an opportunity to examine the effect of ppGpp on a different ⁵⁴ template whose only difference was the promoter sequence. To this end, we used the same in vitro transcription setup described above but with the Po sequence from 471 to + 10 as the insert in the pTE103 transcription vector that was used with Pu and with PlacUV5. The result of the experiment is shown in Fig. 4, which gives the data for four independent assays. Under the conditions (300 nM ppGpp) at which we saw the best stimulation of Pu, we detected a dramatic but dissimilar responsiveness of Po to the alarmone. Consistent with the data in Fig. 3A, ppGpp did not increase Pu activity by more than 40 to 60%, an increase based on an already efficient production of transcripts. In contrast, the activity of Po was very low in the absence of ppGpp but was stimulated by four- to eightfold on addition of this compound. These results provided a rationale for the different behavior of Po (48) and Pu in vivo. They also suggested that such differences could be ultimately dictated by specific sequences of each promoter.

View larger version (23K): [in this window] [in a new window]   FIG. 4.   Comparison of the effects of the ppGpp on the transcriptional activity of Pu and Po in vitro. The result of a typical multiple-round transcription experiment run in parallel with 5 nM Pu-containing template pEZ10 or Po-containing template pTE103-Po is shown at the top of the figure. Assays were carried out under standard conditions (100 nM XylRA, 25 nM IHF, 25 nM core RNAP, 100 nM 54), and 350 nM purified ppGpp was added or omitted as indicated. Note the different sizes of the transcripts arising from Pu (394 nucleotides) or Po (311 nucleotides) due to the different distances from the promoter to the T7 terminator in the vector plasmid (see Materials and Methods). The average stimulation of Pu and Po activity by ppGpp on the basis of four independent experiments is represented below the autoradiograph.

The target of ppGpp in the ⁵⁴-dependent transcription machinery. The mechanism by which ppGpp affects (mostly inhibiting) the performance of many promoters during the stringent response is not yet fully understood and is not devoid of controversy (12, 13). ppGpp seems to bind a distinct site of the  subunit of the ⁷⁰ RNAP (13), thereby decreasing the affinity of the sigma factor for the core enzyme (3). Depending on the specific promoter, this results in the enzyme failing to form productive preelongation complexes or to form abortive transcripts (3, 21, 51). However, since ⁵⁴ and ⁷⁰ are quite different from one another (31), the mechanisms involved in the control of cognate promoters by ppGpp are likely to be dissimilar as well.

View larger version (31K): [in this window] [in a new window]   FIG. 5.   Effect of ppGpp on activation of Pu with increasing concentrations of 54-RNAP. The upper part of the figure shows the result of multiple-round transcription reactions containing 5 nM Pu-containing plasmid template pEZ10. To this was added 100 nM XylRA, 25 nM IHF, and increasing concentrations of 54-RNAP with or without 300 nM ppGpp as indicated. The intensity of the bands was quantified in a Bio-Rad Molecular Imager FX system and plotted in arbitrary units as a function of RNAP concentration (shown in the lower part of the figure). The effect of ppGpp on the transcriptional output appears to be constant throughout the entire range of enzyme concentrations used, and therefore it does not appear to stimulate binding of the promoter by the 54-RNAP (see the text for an explanation).

ppGpp contributes to, but does not determine, the physiological control of the Pu promoter. The work reported above establishes a connection between the behavior of the Pu promoter of the TOL plasmid in vivo and the stringent response mediated by ppGpp. Such an association is, however, relatively minor compared the dramatic dependence of Po, a second ⁵⁴-dependent system for which the issue has been examined in detail (48). The differences between the two promoters, Po and Pu, in this respect seem to be authentic even though they share so many genetic elements and physiological behaviors. Although we have not yet made a rigorous comparison between the two systems under all conditions, the published data on Po (48) and the results presented here suggest that most of the physiological down-regulation of Po, but not of Pu, can be attributed to the effect of ppGpp. Since the only major difference between the two promoters is the nucleotide composition of the sequences interspaced within the major shared motifs (UAS, -12/-24), it is tempting to speculate that these sequences may determine the type of metabolic signals which are entered into the promoter. This adds one more nonanticipated degree of regulatory flexibility to ⁵⁴-dependent promoters, accounting for their evolutionary success in systems, such as biodegradative pathways, whose expression requires fine-tuning with the overall metabolic status of the cells (9).