Alginate, a copolymer of D-mannuronic acid and L-guluronic acid, is produced by a variety of pseudomonads, including Pseudomonas syringae. Alginate biosynthesis has been most extensively studied in P. aeruginosa, and a number of structural and regulatory genes from this species have been cloned and characterized. In the present study, an alginate-defective (Alg ؊ ) mutant of P. syringae pv. syringae FF5 was shown to contain a Tn5 insertion in algL, a gene encoding alginate lyase. A cosmid clone designated pSK2 restored alginate production to the algL mutant and was shown to contain homologs of algD, alg8, alg44, algG, algX (alg60), algL, algF, and algA. The order and arrangement of the structural gene cluster were virtually identical to those previously described for P. aeruginosa. Complementation analyses, however, indicated that the structural gene clusters in P. aeruginosa and P. syringae were not functionally interchangeable when expressed from their native promoters. A region upstream of the algD gene in P. syringae pv. syringae was shown to activate the transcription of a promoterless glucuronidase (uidA) gene and indicated that transcription initiated upstream of algD as described for P. aeruginosa. Transcription of the algD promoter from P. syringae FF5 was significantly higher at 32°C than at 18 or 26°C and was stimulated when copper sulfate or sodium chloride was added to the medium. Alginate gene expression was also stimulated by the addition of the nonionic solute sorbitol, indicating that osmolarity is a signal for algD expression in P. syringae FF5.The phytopathogenic bacterium Pseudomonas syringae produces two well-characterized extracellular polysaccharide (EPS) molecules: levan, a polymer of fructofuranan, and alginate, a copolymer of O-acetylated ␤-1,4-linked D-mannuronic acid and its C-5 epimer, L-guluronic acid (21, 29). Possible roles for the EPS molecules produced by P. syringae are varied and include avoidance of host plant cell recognition, resistance of bacterial cells to desiccation, and enhancement of epiphytic fitness (33, 41). Furthermore, alginate has been implicated in a symptom known as water soaking, where the intercellular tissues of infected plants become filled with water (20, 29). However, a role for alginate in the symptomology or virulence of P. syringae has not been proven.Alginate biosynthesis has been extensively studied in Pseudomonas aeruginosa, where it functions as a major virulence factor in strains infecting the lungs of cystic fibrosis patients (56). 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, most of the structural genes are located at 34 min. The regulatory genes map at 10 and 13 min, and the loci responsible for the genotypic switch to alginate production are located at 68 min (46). Most of the structural genes for alginate biosynthesis are clustered within an 18-kb region in the P. aeruginosa chromosome (16). Structural genes that have...

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Plant-associated pseudomonads are commonly exposed to copper bactericides, which are applied to reduce the disease incidence caused by these bacteria. Consequently, many of these bacteria have acquired resistance or tolerance to copper salts. We recently conducted a survey of 37 copper-resistant (Cu r) Pseudomonas spp., including P. cepacia, P. fluorescens, P. syringae, and P. viridiflava, and found that a subset of the P. syringae strains showed a dramatic increase in exopolysaccharide (EPS) production on mannitol-glutamate medium containing CuSO 4 at 250 g/ml. A modified carbazole assay indicated that the EPS produced on copperamended media contained high levels of uronic acids, suggesting that the EPS was primarily alginic acid. Uronic acids extracted from selected strains were further confirmed to be alginate by demonstrating their sensitivity to alginate lyase and by descending paper chromatography following acid hydrolysis. Subinhibitory levels of arsenate, cobalt, lithium, rubidium, molybdenum, and mercury did not induce EPS production, indicating that alginate biosynthesis is not induced in P. syringae cells exposed to these heavy metals. A 200-kb plasmid designated pPSR12 conferred a stably mucoid phenotype to several P. syringae recipients and also increased their resistance to cobalt and arsenate. A cosmid clone constructed from pPSR12 which conferred a stably mucoid phenotype to several P. syringae strains but not to Pseudomonas aeruginosa was obtained. Results obtained in this study indicate that some of the signals and regulatory genes for alginate production in P. syringae differ from those described for alginate production in P. aeruginosa.

Carbon assimilation rate (A) and stomatal conductance (g) are highly correlated. However, the slope of the A versus g relationship differs among species and environments resulting in differences in gas exchange efficiency which should reflect water use efficiency. The objective of this research was to determine the genetic variation for A and g in grain sorghum (Sorghum bicolor [L.] Moench.). Field experiments were conducted using 30 sorghum hybrids with four water supply treatments. A, g, and leaf water potential ( ¶',) of individual leaves were monitored every 15 to 20 days. Significant genetic variation existed among the hybrids for A and g. Plant age and water supply also affected A and g as expected. When A was regressed on g for each hybrid, large and significant differences existed among the slopes, implying differences in intrinsic gas exchange efficiency. The regression analysis of A and g versus ',, suggested that A was more sensitive than g to increasing water stress. Genetic differences in the rate of change in A as water stress increased were observed. Regression analysis was used to evaluate the individual hybrid response relative to other hybrids. Twofold difference in slopes existed for A. These results provide evidence for genetic variation in gas exchange rates which might directly contribute to whole plant water use efficiency and productivity.

As the use of genetically engineered microorganisms for agricultural tasks becomes more frequent, the ability of bacteria to exchange genetic material in the agricultural setting must be assessed. Transduction (bacterial virus-mediated horizontal gene transfer) is a potentially important mechanism of gene transfer in natural environments. This study investigated the potential of plant leaves to act as surfaces on which transduction can take place among microorganisms. Pseudomonas aeruginosa and its generalized transducing bacteriophage F116 were used as a model system. The application of P. aeruginosa lysogens of F116 to plant leaves resulted in genetic exchange among donor and recipient organisms resident on the same plant. Transduction was also observed when these bacterial strains were inoculated onto adjacent plants and contact was made possible through high-density planting.