INTRODUCTION

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Many pseudomonads, including the phytopathogen Pseudomonas syringae, produce the exopolysaccharide alginate, a copolymer of O-acetylated -1,4-linked D-mannuronic acid and its C-5 epimer, L-guluronic acid. P. syringae induces a wide variety of symptoms on plant hosts and can also exist as an epiphyte on plant surfaces without causing disease. Yu et al. (62) used a genetic approach to evaluate the role of alginate in the pathogenicity and epiphytic fitness of P. syringae pv. syringae 3525, which causes bacterial brown spot on beans. Alginate contributed significantly to both virulence and epiphytic survival of P. syringae pv. syringae 3525, perhaps by facilitating colonization and/or dissemination of the bacterium in planta (62).

Alginate has been extensively studied in P. aeruginosa, where it functions as a virulence factor in cystic fibrosis patients (47). An important feature of alginate production by P. aeruginosa is that the alginate biosynthetic genes are normally silent but are activated in the cystic fibrotic lung, which results in a mucoid phenotype. In P. aeruginosa, genes that encode the biosynthesis and regulation of alginate map to four chromosomal locations. With the exception of algC, which is located at 10 min, the structural genes are clustered within an 18-kb region located at 34 min (18, 48). The alginate biosynthetic gene cluster in P. aeruginosa is presumably organized as an operon with transcription initiating at the algD promoter (9).

Genes controlling the regulation of alginate production include algR1 (algR), algR2 (algQ), algR3 (algP), and algB (20, 54). AlgR1 functions as a response regulator and binds to multiple sites upstream of algC and algD (25, 42, 64). The genes which mediate the conversion to constitutive alginate production are located at 68 min on the P. aeruginosa chromosome and include algT (algU), mucA, mucB (algN), mucC (algM), and mucD (algY). The alternative sigma factor encoded by algT, ²², is required for transcription of algD, algR1, and algT (21, 52, 60). Both the algD and algR1 promoters show a consensus sequence at the 35/10 region, a finding which is consistent with recognition by ²², suggesting that an RNAP-²² complex binds to both promoters and positively regulates transcription (52). MucA is a negative regulator of algT transcription and encodes an anti- factor with affinity for ²² (53, 61). MucB is also a negative regulator and is thought to interact with the periplasmic domain of MucA, thereby altering its conformation so that it binds ²² and targets it for degradation (39). MucC and MucD also modulate the expression of algT and have been described elsewhere (6, 7).

As in P. aeruginosa, the alginate biosynthetic genes in other pseudomonads are normally silent (19). Interestingly, an indigenous plasmid designated pPSR12 conferred constitutive alginate production to P. syringae pv. syringae FF5 (29). pPSR12 does not contain homologs of the biosynthetic or regulatory genes which control alginate production in P. aeruginosa; instead, this plasmid presumably contains regulatory genes which have not been characterized (29). Mutagenesis of FF5(pPSR12) with Tn5 resulted in the isolation of several alginate defective (Alg) mutants, including FF5.31 and FF5.32, which contain Tn5 insertions in algL and algR1, respectively (15, 46). The arrangement of the alginate structural gene cluster and the genes flanking algR1 were virtually identical in both P. syringae and P. aeruginosa (15, 46). However, complementation analyses indicated that the structural gene clusters in P. aeruginosa and P. syringae were not functionally interchangeable when expressed from their native promoters (46). Further experiments indicated that P. syringae, unlike P. aeruginosa, does not require a functional copy of algR1 for activation of the algD promoter (15).

In the present study, an Alg mutant of P. syringae pv. syringae FF5(pPSR12) was shown to contain a Tn5 insertion upstream of the algT-mucABCD gene cluster. This region was cloned from P. syringae, and the role of algT in P. syringae was evaluated. An algT mutant was shown to be defective in alginate production, indicating that algT is essential for alginate biosynthesis in P. syringae. The algT mutant was also more susceptible to killing by heat and superoxide-generating redox cycling compounds, indicating that AlgT (²²) regulates genes in P. syringae which respond to environmental stress.

	MATERIALS AND METHODS

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Bacterial strains, plasmids, and media. Table 1 lists the bacterial strains and plasmids used in the present study. P. syringae was routinely maintained at 28°C on King's medium B (30), mannitol-glutamate (MG) (26), or MG supplemented with yeast extract at 0.25 g/liter (MGY). Escherichia coli strains were grown on Luria-Bertani medium (41) at 37°C. Antibiotics were added to media at the following concentrations (µg/ml): ampicillin, 100; tetracycline, 12.5; kanamycin, 25; spectinomycin, 25; chloramphenicol, 25; and gentamicin, 2. 

Molecular genetic techniques. Plasmids were isolated from P. syringae as described by Kado and Liu (24). Restriction enzyme digests, agarose gel electrophoresis, Southern transfers, and isolation of DNA fragments from agarose gels were performed by using standard protocols (50). Genomic DNA was isolated from P. syringae by using established procedures (56), and a genomic library of FF5.36 was constructed in pRK7813 as described previously (2). Clones were mobilized into recipient strains by using a triparental mating procedure and the mobilizer plasmid pRK2013 (4).

Isolation and quantitation of alginate. Selected strains were inoculated by dilution streaking to MGY agar (three plates per strain) and incubated at 28°C for 96 h. Each plate was handled separately for quantitation of alginate. Cells were washed from each plate and resuspended in 0.9% NaCl. Removal of cellular material from the mucoid growth and estimation of total cellular protein were performed as described previously (40). Alginate production was assessed by the carbazole method, an assay which quantifies the total amount of uronic acid polymers (40). In addition to alginate, other uronic acid polymers are detected by this assay, but we previously demonstrated that these are very minor components of the mucoid material isolated from FF5(pPSR12) (29). Alginic acid from seaweed (Macrocystis pyrifera; Sigma Chemical Co., St. Louis, Mo.) was used as a standard in these experiments. Mean values of three replicates were expressed as micrograms of alginate per milligrams of protein.

DNA sequencing and analysis. Nucleotide sequencing reactions were performed by the dideoxynucleotide method (50) with AmpliTaq DNA polymerase (Perkin-Elmer, Foster City, Calif.). Automated DNA sequencing was accomplished by using an ABI 373A apparatus and the ABI PRISM Dye Primer Cycle Sequencing Kit (Perkin-Elmer). Automated sequencing was provided by the Oklahoma State University Recombinant DNA-Protein Resource Facility. The Tn5 insertion in FF5.36 was localized by sequencing the DNA flanking the transposon by using the oligonucleotide 5'-GGTTCCGTTCAGGACGCTAC, which is derived from the border region of IS50 (49). Sequence data were aligned and homology searches were executed by using the University of Wisconsin Genetics Computer Group Sequence Analysis Package (version 9.0) or the National Center for Biotechnology Information BLAST network server.

Construction of an algT mutant of P. syringae. The chloramphenicol resistance (Cm^r) gene in pSL1 was used to construct a nonpolar mutation in algT. pBTB6.5, which contains algT in a 6.5-kb BamHI fragment in pBluescript SK(+), was linearized with NruI, which generates a unique site within algT (Fig. 1A). The Cm^r cassette in pSL1 was excised as a 0.65-kb SmaI fragment and ligated into linearized pBTB6.5, resulting in pBTB.Cm. The 7.15-kb BamHI fragment in pBTB.Cm was then excised and ligated into BamHI-digested pRK415. pRTB.Cm, the construct containing algT::Cm^r in pRK415, was then introduced into P. syringae pv. syringae FF5(pPSR12) by triparental mating, and selection pressure for the vector (Tc^r) was removed to facilitate homologous recombination (4).

View larger version (14K): [in this window] [in a new window]   FIG. 1.   (A) Physical and functional map of the 6.5-kb BamHI fragment in pBTB6.5 and pRTB6.5. The arrows within each open reading frame indicate the direction of translation for each gene. (B) Location and orientation of the algT::uidA transcriptional fusions in palgTA and palgTI. The HindIII site was added during PCR amplification. (C) Expanded view of the 582-bp algT gene from P. syringae FF5(pPSR12). The arrow indicates the location used for insertion of the antibiotic resistance cassette (Cmr). Abbreviations: B, BamHI; C, ClaI; E, EcoRI; K, KpnI; N, NruI; P, PstI.

Heat killing assays. Bacterial cultures were grown to an A₆₀₀ of 0.45 at 28°C and then incubated at 43°C for 0, 15, 30, 45, and 60 min; three replicate cultures were sampled at each time point. Cell dilutions were plated onto MGY agar in triplicate, and viable cells were scored as CFU. Survival was expressed as the percentage of input cells which retained viability.

Susceptibility to killing with ROI. Sensitivity to paraquat or hydrogen peroxide (H₂O₂) was determined by measuring the diameter of the inhibition zone surrounding filters impregnated with reactive oxygen intermediates (ROI)-generating agents. Filter disks (6 mm) were soaked with 5 µl of 1.9% paraquat or 3% H₂O₂ and placed on a layer of soft agar (2 ml of 0.6% agar) containing 100 µl of an overnight culture of P. syringae; this was allowed to gel on 25 ml of MGY containing 1.5% agar. Cells were incubated at 28°C, and inhibition zones were measured 12 to 16 h after inoculation.

Construction of transcriptional fusions. pBBR.Gus, which contains a promoterless glucuronidase gene (uidA) downstream of the polylinker in pBBR1MCS, was used to create algT::uidA transcriptional fusions. To obtain the algT promoter region in transcriptionally active and inactive orientations, a 1-kb PCR product was cloned into the HindIII-PstI or KpnI-HindIII sites of pBBR.Gus, respectively. The promoter region was amplified from pBTB6.5 by using the forward primer 5'-CTGAAGCTTCTGCCCTTGGCGACCAC (the HindIII site is underscored and is followed by nucleotides corresponding to 488 to 472 in Fig. 2) and the reverse primer 5'-CTCTTGGGCTATCGCCGCTGTCTC (the complement of nucleotides 580 to 604 in Fig. 2). After amplification of the 1-kb PCR product, ligation in pCR2.1, and transformation into E. coli DH5, plasmids pCRalgTA and pCRalgT1 were recovered. These were digested with HindIII and PstI (pCRalgTA) or HindIII and KpnI (pCRalgTI) and ligated into pBBR.Gus, resulting in palgTA and palgTI, respectively (Fig. 1B).

View larger version (36K): [in this window] [in a new window]   FIG. 2.   Nucleotide sequence of algT from P. syringae pv. syringae FF5(pPSR12) containing the 5' end of nadB and the nadB-algT intergenic region. The vertical arrow shows the Tn5 insertion site in mutant FF5.36. Potential recognition sequences for 22 are shaded and underlined, and the putative ribosome binding site for algT is underlined. Nucleotides are numbered with respect to the algT translational start site and are indicated on the left; amino acid residues for AlgT are indicated on the right. Translational start sequences are shown in bold italics, and the translational stop codon for algT is indicated by a bold asterisk.

GUS assays. Transcriptional activity was initially screened by spotting bacterial suspensions (A₆₀₀ = 0.1) onto MG agar medium amended with chloramphenicol and 20 µg of X-Gluc (5-bromo-4-chloro-3-indolyl glucuronide) per ml; plates were then incubated at 28°C for 48 h. Prior to quantitative glucuronidase (GUS) assays, all strains were grown overnight in MGY broth containing chloramphenicol. Bacterial concentrations were then adjusted to an A₆₀₀ of 0.1 in MGY broth and incubated at 28°C at 250 rpm. For temporal studies, 1-ml aliquots (three replicates per time point) were removed at 0, 1, 2, 5, 8, 12, 24, and 30 h and analyzed for GUS activity as described previously (44). GUS activity was expressed in units per milligram of protein with 1 U equivalent to 1 nmol of methylumbelliferone formed per min. The effect of salt, sorbitol, and copper sulfate on algT expression was evaluated by adjusting the bacterial concentration to an A₆₀₀ of 0.1 and incubating the cells for 10 h in MGY broth amended with NaCl (0.15, 0.3, or 0.4 M), sorbitol (0.3, 0.6, or 0.8 M), or CuSO₄ (50, 100, or 200 µM). algT transcription was also investigated by preparing bacterial suspensions as described above, growing them to an A₆₀₀ of 0.5, and incubating them at elevated temperature (50°C) or in media amended with H₂O₂ or paraquat (0.001 or 0.01%). Bacterial cells (1 ml) were removed at 0, 15, 30, 60, and 120 min for temperature studies and at 0, 15, 30, and 60 min for assays with H₂O₂ and paraquat.

Nucleotide sequence accession number. The nucleotide sequence for algT in P. syringae pv. syringae has been deposited in the GenBank database under accession no. AF190580.

	RESULTS

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Location of Tn5 insertion in FF5.36. The Tn5 mutant FF5.36 exhibited a leaky phenotype for alginate and produced low amounts of the exopolysaccharide in vitro; this mutant was previously isolated by mutagenesis of FF5(pPSR12), which produces alginate constitutively at high levels (29). To locate the Tn5 insertion in FF5.36, a genomic library of this mutant was constructed in pRK7813, and a cosmid clone containing the Tn5 insertion was recovered and designated pFF5.36. The internal BamHI site in Tn5 and 3 kb of flanking DNA from FF5.36 were cloned from pFF5.36 into pBluescript SK(+), resulting in a clone named pFF5.36B. A primer specific for the border region of IS50 indicated that the Tn5 insertion was located within nadB at nucleotide 61 of the corresponding P. aeruginosa sequence (12). The nadB gene encodes L-aspartate oxidase and is located approximately 400 bp upstream of algT in P. aeruginosa (12). A 600-bp region downstream of the Tn5 insertion was sequenced in pFF5.36B; this region showed 73% nucleotide sequence identity to the first 100 bp of nadB and 65% nucleotide sequence identity to the nadB-algT intergenic region and the 5' end of algT from P. aeruginosa. These results indicated that the location of nadB and algT was conserved in P. syringae and P. aeruginosa.

Cloning of algT from P. syringae. A genomic library of P. syringae FF5(pPSR12) was previously constructed in pRK7813 (46). In the current study, the 6-kb BamHI fragment from pFF5.36B, which contains a portion of algT, was used to screen the library for clones containing the complete algT coding region. One clone designated pLKT5 was chosen for further study and contained a 6.5-kb BamHI fragment which hybridized with the probe. This fragment was subcloned in pBluescript SK(+), resulting in pBTB6.5, and partially sequenced by using the T7 and T3 primers. Sequence analysis indicated that the right border of this fragment contained DNA homologous to mucB (Fig. 1A). Since algT is generally associated with the mucABCD gene cluster (20, 38), we suspected that pBTB6.5 contained a functional copy of algT.

Sequence analysis of algT. A physical map of pBTB6.5 was constructed to further localize the alginate regulatory genes on this fragment (Fig. 1A). Sequence data for the P. syringae algT gene were initially derived by using a primer based on the nucleotide sequence downstream of the Tn5 insertion located in FF5.36 (see vertical arrow, Fig. 2). Additional sequence data was obtained by primer walking, and both DNA strands were sequenced for verification. The P. syringae algT homologue was 582 bp and was highly related to algT from P. aeruginosa (81 and 90% nucleotide and amino acid identities, respectively) (13). The deduced translational product of algT is a protein consisting of 193 amino acids with a predicted mass of 22.3 kDa. A potential ribosome binding site was identified 7 bp upstream of the predicted translational start site. Two putative AlgT (²²) recognition sites were located 60 and 248 bp upstream of the algT translational start site (Fig. 2). The location and sequence of the first ²² recognition site (60 bp upstream of the initiation codon) was conserved in both P. syringae and P. aeruginosa (Fig. 3). The nadB gene in P. syringae was located 516 bp upstream of the algT translational start site and was divergently transcribed with respect to algT (Fig. 1 and 2). Interestingly, nucleotide identity in the 516-bp intergenic region between nadB and algT was only 46% when the P. syringae and P. aeruginosa regions were compared (Fig. 3). Additional sequencing downstream of algT revealed mucA and mucB homologues (Fig. 1) which showed 68 and 70% nucleotide identities, respectively, to the genes previously sequenced in P. aeruginosa (19, 35). In summary, the arrangement of nadB, algT, mucA, and mucB is conserved in P. syringae, P. aeruginosa, and A. vinelandii (12, 35, 38).

View larger version (46K): [in this window] [in a new window]   FIG. 3.   Alignment of the algT promoter sequences from P. syringae pv. syringae FF5(pPSR12) (Ps algT) and P. aeruginosa (Pa algT). The nucleotides for the P. aeruginosa sequence are shown on the left with +1 (see asterisk) corresponding to the transcriptional start site. Nucleotides for the P. syringae pv. syringae algT promoter are shown on the right with +1 corresponding to the translational start site. Gaps (--) were used to maximize the alignment, and identical bases are shaded. The 22 recognition sequences in both species are indicated in boldface type and are double-underscored. The nadB and algT translational start sites are in boldface, and the direction of translation is indicated with an arrow.

Construction of an algT mutant. FF5.36, which contains a Tn5 insertion in nadB, was unstable with respect to alginate production. To avoid potential polar effects on adjacent genes, we constructed an algT mutant with a Cm^r cassette which lacks transcriptional terminators. Recombination of the Cm^r cassette into algT was verified by PCR and sequence analysis. FF5.LK1, the algT mutant resulting from this experiment, produced 61 µg of uronic acid polymers/mg of protein, a level approximately 43-fold lower and significantly less (P = 0.01) than FF5(pPSR12), which synthesized 2,652 µg of uronic acid polymers/mg of protein. Previous work indicated that most of the uronic acid polymers synthesized by FF5(pPSR12) were alginate (29). Furthermore, alginate-defective strains of FF5(pPSR12) still synthesized low amounts of uronic acid polymers in the carbazole assay (15, 29, 46); therefore, we concluded that the algT mutant, FF5.LK1, was defective in alginate production.

Complementation experiments. pRTB6.5, which contains algT, mucA, and mucB in pRK415, was evaluated for its ability to complement P. syringae pv. syringae FF5.LK1 for alginate production. pRTB6.5 did not restore alginate production to FF5.LK1, possibly because this plasmid also contains the negative regulators, mucA and mucB, which could suppress the conversion to mucoidy (19, 36). Consequently, we examined whether palgTA.1, which contains algT but lacks extraneous flanking DNA, could restore alginate production to FF5.LK1. Transconjugants of FF5.LK1 containing palgTA.1 were visibly mucoid and produced 1,086 µg of alginate/mg of protein; this amount was significantly higher (P = 0.01) than the level synthesized by FF5.LK1, indicating that palgTA.1 could partially complement the algT mutant. We also investigated whether pJG309, which contains algT from P. aeruginosa, could complement FF5.LK1 for alginate production. FF5.LK1(pJG309) transconjugants produced 1,081 µg of alginate per mg of protein, a level equivalent to that obtained with FF5.LK1(palgTA.1), which suggests that the two genes may be functionally interchangeable.

Effects of algT on susceptibility to heat and ROI. Previous reports indicate that algT functions as an alternative sigma factor in P. aeruginosa and is involved in the transcriptional activation of heat shock genes (37, 52). Therefore, we evaluated whether the algT mutation in FF5.LK1 resulted in an increased sensitivity to heat killing when compared to the wild-type FF5(pPSR12). Survival after exposure to 43°C was significantly reduced in the algT mutant compared to the wild-type strain (Fig. 4). Within 15 min there was an 85% reduction in the viability of the mutant compared with only 27% in the wild-type (Fig. 4). No difference in viability between the wild-type and mutant strains was apparent after a 60-min incubation at 43°C (Fig. 4).

View larger version (12K): [in this window] [in a new window]   FIG. 4.   Heat-killing curves for P. syringae pv. syringae FF5(pPSR12) (wild-type []) and FF5.LK1 (algT mutant []). The strains were incubated at 43°C for 15, 30, 45, and 60 min, and surviving cells were counted as CFU. Bars indicate standard errors of the means, and survival is expressed as the percentage of input CFU at time zero. The experiment was repeated with similar results.

Kinetics of algT transcription. palgTA, palgTI, and pBBR.Gus were mobilized into P. syringae pv. syringae FF5 and assayed for GUS activity. Colonies of FF5(palgTA) turned blue on media containing X-Gluc, indicating that algT was transcribed at physiological temperatures (28°C). FF5 transconjugants containing palgTI (algT in the transcriptionally inactive orientation) or pBBR.Gus (vector control) remained colorless on X-Gluc media. When FF5 transconjugants containing palgTA, palgTI, or pBBR.Gus were grown in MGY broth at 28°C, growth curves were similar, indicating that the transcriptional fusions had no significant effect on growth (data not shown). A time course experiment at 28°C indicated that algT transcriptional activity increased steadily over time with 960 U of GUS/mg of protein at 30 h; this gradual increase in expression is similar to observations made for algT in P. aeruginosa (13). GUS activity in FF5(palgTI) and FF5(pBBR.Gus) remained low (1 to 14 U) throughout the sampling period and was not significantly different between the two transconjugants; consequently, FF5(pBBR.Gus) was used as a negative control in all subsequent experiments.

algT expression in response to selected factors. GUS activity in FF5(palgTA) was significantly higher (P = 0.01) when the growth medium was amended with 0.15 or 0.3 M NaCl; in contrast, FF5(pBBR.Gus) showed no response to the addition of NaCl (Fig. 5A). To determine whether the effect of NaCl was ionic or osmotic, sorbitol (a nonionic, nonmetabolizable solute) was examined for its effect on algT expression. Sorbitol was added to MGY broth at 0.3, 0.6, and 0.8 M, concentrations which are osmotically equivalent to 0.15, 0.3, and 0.4 M NaCl, respectively. The transcriptional activity of algT was significantly higher (P = 0.01) than the nonsupplemented control when sorbitol was added at all concentrations tested (Fig. 5B). Therefore, the stimulation of algT gene expression by NaCl is due to increased osmolarity rather than an ionic effect.

View larger version (25K): [in this window] [in a new window]   FIG. 5.   GUS activity in P. syringae pv. syringae FF5 derivatives grown in MGY broth containing sodium chloride (A), sorbitol (B), or copper sulfate (C). Prior to the GUS assays, all strains were grown for 20 h in MGY broth containing chloramphenicol. The bacterial concentration was adjusted to an A600 of 0.1, and the cells were incubated at 250 rpm for 10 h at 28°C in MGY broth amended with NaCl, sorbitol, or copper sulfate. palgTA contains the algT promoter in the transcriptionally active orientation, and pBBR.Gus contains a promoterless glucuronidase gene. Values are the mean from one experiment containing three replicates, and the experiment was repeated with similar results. Treatments accompanied by the same lowercase letter were not significantly different at a P of 0.01 as shown by Duncan's multiple-range test.

View larger version (29K): [in this window] [in a new window]   FIG. 6.   GUS activity in P. syringae pv. syringae FF5 derivatives grown in MGY broth containing H2O2 (A) or paraquat (B). Prior to the GUS assays, all strains were initially grown as described in Fig. 5; bacterial concentrations were then adjusted to an A600 of 0.5 and incubated in MGY broth amended with H2O2 or paraquat. palgTA is described in Fig. 5. Values represent the mean from one experiment containing three replicates; the experiment was repeated with similar results. Treatments accompanied by the same lowercase letter were not significantly different at a P of 0.01 as determined by Duncan's multiple-range test.

View larger version (39K): [in this window] [in a new window]   FIG. 7.   GUS activity in P. syringae pv. syringae FF5 subjected to heat shock (temperature shift from 30 to 50°C). Prior to GUS assays, all strains were grown at 30°C as described in Fig. 5. The bacteria were incubated at 30°C until the concentration had an A600 of 0.5 and were then exposed to heat shock by rapid transfer to 50°C. palgTA and pBBR.Gus are described in Fig. 5. Values represent the mean from one experiment containing three replicates, and the experiment was repeated with similar results. Treatments accompanied by the same lowercase letter were not significantly different at a P of 0.01 as determined by Duncan's multiple-range test.

	DISCUSSION

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In the present study, the Alg mutant FF5.36 contained a Tn5 insertion in nadB, which encodes L-aspartate oxidase, a flavoprotein in the pathway for NAD biosynthesis (12). The nadB gene in both P. syringae and P. aeruginosa (12) is encoded upstream of algT and divergently transcribed with respect to algT. In P. aeruginosa, nadB was not essential for NAD production, and a Tn501 insertion in nadB did not affect alginate biosynthesis (12). However, in the present study, the nadB::Tn5 insertion in FF5.36 was unstable with respect to alginate production. Although we could not identify additional Tn5 insertions in FF5.36, it remains possible that additional point mutations may have occurred, leading to a nonmucoid phenotype. Therefore, the algT mutant FF5.LK1 was constructed in the present study, and all subsequent experiments were conducted with this mutant.

The algT genes in P. syringae and P. aeruginosa are highly homologous (81% nucleotide identity) and closely related to rpoE, which encodes ^E, an alternate sigma factor involved in high-temperature gene expression in E. coli (11, 13, 14). Our results show that the algT promoter region in P. syringae contained two motifs conserved in promoters transcribed by the RNAP-^E complex (11) (Fig. 3). In P. aeruginosa, these two promoters were AlgT-dependent and designated P₁ and P₃ (52). The conservation of these promoters in P. syringae and P. aeruginosa and the complementation of FF5.LK1 with algT from both species suggest that the algT homologs in these two pseudomonads may be functionally interchangeable.

In P. aeruginosa, the negative regulatory genes mucA and mucB suppress alginate production, and mutagenesis of these genes results in a mucoid phenotype (19, 36). In the current study, pRTB6.5, which contains algT, mucA, and mucB, did not restore alginate production to the algT mutant FF5.LK1. However, palgTA.1, which contains algT without extraneous flanking DNA, partially restored alginate production to FF5.LK1. Previous studies have shown that MucA physically binds AlgT (²²) and functions as an anti- factor (53, 61), whereas MucB is presumed to alter the conformation of MucA in such a way that it targets ²² for degradation (39). Therefore, a stoichiometric relationship exists between these three proteins and may explain why alginate production was not fully restored to wild-type levels in FF5.LK1(palgTA.1).

There is growing evidence that the algT-mucABCD gene cluster forms a signal transduction system that modulates algT activity in response to environmental stress (13, 37, 51, 52, 63). The algT gene fusion from P. syringae was transcriptionally activated in response to both NaCl and sorbitol (Fig. 5), indicating that osmotic stress is a stimulus for algT activation in both P. syringae and P. aeruginosa (52). Phytopathogenic bacteria are exposed to high osmolarities on the leaf surface (3), and the increased synthesis of alginate is critical to survival during epiphytic colonization (62); therefore, transcriptional activation of algT may enhance epiphytic fitness.

The algT mutant of P. syringae was more sensitive to H₂O₂ and paraquat, and algT expression was activated in response to both compounds. Although an algT mutant of P. aeruginosa showed increased susceptibility to paraquat, no difference in sensitivity to H₂O₂ was detected between the mutant and wild-type strains (37). These results suggest that P. syringae and P. aeruginosa differ in their response to ROIs. Although aspects of the oxidative burst are similar in animal and plant hosts (32), plant cells produce ROIs (mainly H₂O₂) constitutively throughout the defense response (5), and H₂O₂ has an important role in plant disease resistance (1, 8, 59). In animals, alginate production by P. aeruginosa may suppress the oxidative burst in neutrophils and scavenge the ROIs produced by phagocytic cells (22, 55). Therefore, the activation of algT by ROIs and the subsequent production of alginate may help P. syringae evade the plant defense response.

In previous studies, copper sulfate stimulated algD transcriptional activity and alginate production in P. syringae (29, 46). However, copper sulfate was not a signal for algD gene expression or alginate production in clinical strains of P. aeruginosa, possibly because these strains are not repeatedly exposed to toxic levels of copper sulfate (29, 46). In the current study, the algT promoter in P. syringae pv. syringae FF5 was stimulated by exposure to copper sulfate (Fig. 5C), which is consistent with earlier studies showing algD activation in response to copper sulfate (46). In agriculture, bactericidal sprays containing copper sulfate are frequently used for the control of P. syringae and other phytopathogenic bacteria, and copper-mediated stress is high. Because copper is known to generate free radicals (58), the increased production of alginate in response to copper sulfate may be caused by oxidative stress. Alternatively, the sequence divergence in the nadB-algT intergenic regions of P. syringae and P. aeruginosa may reflect the unique activation of the algT promoter in P. syringae by copper sulfate.

The algT mutant of P. syringae was more sensitive to elevated temperature (Fig. 4), and algT expression was activated in response to heat shock (Fig. 7). In contrast to human and animal pathogens, little is known about how phytopathogenic bacteria respond to temperature stress. We recently demonstrated that P. syringae responds to heat shock by producing DnaK (28), a molecular chaperone that facilitates the disassembly of proteins that have been damaged by heat stress (34). The present study expands our knowledge of the temperature stress response in P. syringae and clearly shows that algT increases the heat tolerance of this bacterium. The increased production of alginate in response to elevated temperatures could be advantageous since the alginate capsule could provide some protection from the dehydration and desiccation which develop during heat stress.

In P. syringae, algT is required for alginate production and increases the survival of the bacterium during environmental stress. Copper and H₂O₂ are toxic compounds that P. syringae encounters during colonization of host plant tissues, and these substances may be unique signals for algT activation in this bacterium. However, heat shock is a conserved signal for activation of algT expression in both P. aeruginosa (52) and P. syringae. In P. aeruginosa, AlgT (²²) is required for transcription of algD, which encodes GDP-mannose dehydrogenase, the first committed step in the alginate biosynthetic pathway (10). In P. syringae, the algD promoter region contains a putative recognition site for ²² (15), but the requirement of ²² for algD transcription has not yet been demonstrated. However, the transcriptional activation of the algT and algD (46) promoters in response to heat, osmotic stress, and copper sulfate supports the hypothesis that algT may control activation of algD transcription in P. syringae. Studies are currently under way to examine this hypothesis and other possible roles for algT in the pathogenicity and fitness of P. syringae.