The phosphatidylcholine synthase of Pseudomonas putida A ATCC 12633 is responsible for the synthesis of phosphatidylcholine, which acts as a temporary reservoir for Al3+

Microbiology

Volumn 158, Issue 5, 2012, Pages 1249-1257

  Boeris, Paola S ^a   Lucchesi, Gloria I ^a  

^a DEPARTAMENTO DE QUÍMICA   (Argentina)

Author keywords

[No Author keywords available]

Indexed keywords

ALUMINUM; BACTERIAL ENZYME; PHOSPHATIDYLCHOLINE; PHOSPHATIDYLCHOLINE SYNTHASE; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ARTICLE; BACTERIAL GENE; BACTERIAL GROWTH; BACTERIAL STRAIN; BACTERIUM MUTANT; CONTROLLED STUDY; GENE EXPRESSION; GENE IDENTIFICATION; GENE INSERTION; GENE SEQUENCE; MOLECULAR CLONING; NONHUMAN; NUCLEOTIDE SEQUENCE; PHOSPHOLIPID SYNTHESIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PSEUDOMONAS PUTIDA; SEQUENCE HOMOLOGY; THIN LAYER CHROMATOGRAPHY; WILD TYPE;

ALUMINUM; AMINO ACID SEQUENCE; BACTERIAL PROTEINS; CLONING, MOLECULAR; MOLECULAR SEQUENCE DATA; MUTATION; PHOSPHATIDYLCHOLINES; PSEUDOMONAS PUTIDA; TRANSFERASES (OTHER SUBSTITUTED PHOSPHATE GROUPS);

PSEUDOMONAS PUTIDA;

EID: 84860537229     PISSN: 13500872     EISSN: None     Source Type: Journal    
DOI: 10.1099/mic.0.054072-0     Document Type: Article

References (46)

1. Albelo, S. T. & Domenech, C. E. (1997). Carbons from choline present in the phospholipids of Pseudomonas aeruginosa. FEMS Microbiol Lett 156, 271-274.
2. Ames, G. F. (1968). Lipids of Salmonella typhimurium and Escherichia coli: structure and metabolism. J Bacteriol 95, 833-843.
3. Bernal, P., Muñoz-Rojas, J., Hurtado, A., Ramos, J. L. & Segura, A. (2007). A Pseudomonas putida cardiolipin synthesis mutant exhibits increased sensitivity to drugs related to transport functionality. Environ Microbiol 9, 1135-1145.
4. Bligh, E. G. & Dyer, W. J. (1959). A rapid method of total lipid extraction and purification. Can J Biochem Physiol 37, 911-917.
5. Boeris, P. S., Domenech, C. E. & Lucchesi, G. I. (2007). Modification of phospholipid composition in Pseudomonas putida A ATCC 12633 induced by contact with tetradecyltrimethylammonium. J Appl Microbiol 103, 1048-1054.
6. Boeris, P. S., Liffourrena, A. S., Salvano, M. A. & Lucchesi, G. I. (2009). Physiological role of phosphatidylcholine in the Pseudomonas putida A ATCC 12633 response to tetradecyltrimethylammonium bromide and aluminium. Lett Appl Microbiol 49, 491-496.
7. Bradford, M. M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72, 248-254.
8. Browne, B. A., McColl, J. C. & Driscoll, C. T. (1990). Aluminium speciation using morin. Morin and its complexes with aluminium. J Environ Qual 19, 65-72.
9. Comerci, D. J., Altabe, S., de Mendoza, D. & Ugalde, R. A. (2006). Brucella abortus synthesizes phosphatidylcholine from choline provided by the host. J Bacteriol 188, 1929-1934.
10. Conde-Alvarez, R., Grilló, M. J., Salcedo, S. P., de Miguel, M. J., Fugier, E., Gorvel, J. P., Moriyón, I. & Iriarte, M. (2006). Synthesis of phosphatidylcholine, a typical eukaryotic phospholipid, is necessary for full virulence of the intracellular bacterial parasite Brucella abortus. Cell Microbiol 8, 1322-1335.
11. Conover, G. M., Martinez-Morales, F., Heidtman, M. I., Luo, Z. Q., Tang, M., Chen, C., Geiger, O. & Isberg, R. R. (2008). Phosphatidylcholine synthesis is required for optimal function of Legionella pneumophila virulence determinants. Cell Microbiol 10, 514-528.
12. Daiyasu, H., Kuma, K. I., Yokoi, T., Morii, H., Koga, Y. & Toh, H. (2005). A study of archaeal enzyme involved in polar lipid synthesis linking amino acid sequence information, genomic context and lipid composition. Archea 1, 399-410.
13. de Rudder, K. E. E., Thomas-Oates, J. E. & Geiger, O. (1997). Rhizobium meliloti mutants deficient in phospholipid N-methyltransferase still contain phosphatidylcholine. J Bacteriol 179, 6921-6928.
14. de Rudder, K. E. E., López-Lara, I. M. & Geiger, O. (2000). Inactivation of the gene for phospholipid N-methyltransferase in Sinorhizobium meliloti: phosphatidylcholine is required for normal growth. Mol Microbiol 37, 763-772.
15. Duque, E., García, V., de la Torre, J., Godoy, P., Bernal, P. & Ramos, J. L. (2004). Plasmolysis induced by toluene in a cyoB mutant of Pseudomonas putida. Environ Microbiol 6, 1021-1031.
16. Fiske, C. H. & Subbarow, Y. (1925). The colorimetric determination of phosphorus. J Biol Chem 66, 375-400.
17. Hanada, T., Kashima, Y., Kosugi, A., Koizumi, Y., Yanagida, F. & Udaka, S. (2001). A gene encoding phosphatidylethanolamine Nmethyltransferase from Acetobacter aceti and some properties of its disruptant. Biosci Biotechnol Biochem 65, 2741-2748.
18. Hanahan, D. (1983). Studies on transformation of Escherichia coli with plasmids. J Mol Biol 166, 557-580.
19. Higgins, J. A. (1987). Separation and analysis of membrane lipid components. In Biological Membranes: a Practical Approach, pp. 103-137. Edited by J. B. C. Findlay & W. H. Evans. Oxford, UK: IRL Press.
20. Kaniga, K., Delor, I. & Cornelis, G. R. (1991). A wide-host-range suicide vector for improving reverse genetics in Gram-negative bacteria: inactivation of the blaA gene of Yersinia enterocolitica. Gene 109, 137-141.
21. Kovach, M. E., Elzer, P. H., Hill, D. S., Robertson, G. T., Farris, M. A., Roop, R. M., II & Peterson, K. M. (1995). Four new derivatives of the broad-host-range cloning vector pBBR1MCS, carrying different antibiotic-resistance cassettes. Gene 166, 175-176.
22. Liffourrena, A. S., López, F. G., Salvano, M. A., Domenech, C. E. & Lucchesi, G. I. (2008). Biodegradation of tetradecyltrimethylammonium in Pseudomonas putida A ATCC 12633 improved by aluminium ions. J Appl Microbiol 2, 396-402.
23. López-Lara, I. M. & Geiger, O. (2001). Novel pathway for phosphatidylcholine biosynthesis in bacteria associated with eukaryotes. J Biotechnol 91, 211-221.
24. Lucchesi, G. I., Lisa, T. A. & Domenech, C. E. (1989). Choline and betaine as inducer agents of Pseudomonas aeruginosa phospholipase C activity in high phosphate medium. FEMS Microbiol Lett 57, 335-338.
25. Lucchesi, G. I., Liffourrena, A. S., Boeris, P. S. & Salvano, M. A. (2010). Adaptative response and degradation of quaternary ammonium compounds by Pseudomonas putida A ATCC 12633. In Current Research, Technology and Education Topics in Applied Microbiology and Microbial Biotechnology, pp. 1297-1303. Edited by A. Méndez-Vilas. Badajoz, Spain: Formatex.
26. 31P NMR spectroscopic studies. Chem Phys Lipids 132, 23-36.
27. 31P NMR spectroscopy. Chem Phys Lipids 139, 85-95.
28. Martínez-Morales, F., Schobert, M., López-Lara, I. M. & Geiger, O. (2003). Pathways for phosphatidylcholine biosynthesis in bacteria. Microbiology 149, 3461-3471.
29. Medeot, D. B., Bueno, M. A., Dardanelli, M. S. & de Lema, M. G. (2007). Adaptational changes in lipids of Bradyrhizobium SEMIA 6144 nodulating peanut as a response to growth temperature and salinity. Curr Microbiol 54, 31-35.
30. Minder, A. C., de Rudder, K. E. E., Narberhaus, F., Fischer, H. M., Hennecke, H. & Geiger, O. (2001). Phosphatidylcholine levels in Bradyrhizobium japonicum membranes are critical for an efficient symbiosis with the soybean host plant. Mol Microbiol 39, 1186-1198.
31. Nelson, K. E., Weinel, C., Paulsen, I. T., Dodson, R. J., Hilbert, H., Martins dos Santos, V. A. P., Fouts, D. E., Gill, S. R., Pop, M. & other authors (2002). Complete genome sequence and comparative analysis of the metabolically versatile Pseudomonas putida KT2440. Environ Microbiol 4, 799-808.
32. Palleroni, N. J. (1992). Taxonomy and identification. In Pseudomonas, Molecular Biology and Biotechnology, pp. 105-115. Edited by E. Galli, S. Silver & B. Witholt. Washington, DC: American Society for Microbiology.
33. Pinkart, H. C. & White, D. C. (1997). Phospholipid biosynthesis and solvent tolerance in Pseudomonas putida strains. J Bacteriol 179, 4219-4226.
34. Ramos, J. L., Duque, E., Rodríguez-Herva, J. J., Godoy, P., Haïdour, A., Reyes, F. & Fernández-Barrero, A. (1997). Mechanisms for solvent tolerance in bacteria. J Biol Chem 272, 3887-3890.
35. Rock, C. O., Jackowski, S. & Cronan, J. E. (1996). Lipid metabolism in prokaryotes. In Biochemistry of Lipids, Lipoproteins and Membranes, pp. 35-74. Edited by D. E. Vance & J. Vance. Amsterdam: Elsevier.
36. Russell, N. J. (1992). Physiology and molecular biology of psychrophylic microorganisms. In Molecular Biology and Biotechnology of Extremophiles, pp. 203-224. Edited by R. A. Herbert & R. J. Sharp. Glasgow, London: Blackie.
37. Sambrook, J. & Russell, D. R. (2001). Molecular Cloning: a Laboratory Manual, 2nd edn. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory.
38. Schäfer, A., Tauch, A., Jäger, W., Kalinowski, J., Thierbach, G. & Pühler, A. (1994). Small mobilizable multi-purpose cloning vectors derived from the Escherichia coli plasmids pK18 and pK19: selection of defined deletions in the chromosome of Corynebacterium glutamicum. Gene 145, 69-73.
39. Sohlenkamp, C., de Rudder, K. E. E., Rohrs, V., López-Lara, I. M. & Geiger, O. (2000). Cloning and characterization of the gene for phosphatidylcholine synthase. J Biol Chem 275, 18919-18925.
40. Sohlenkamp, C., López-Lara, I. M. & Geiger, O. (2003). Biosynthesis of phosphatidylcholine in bacteria. Prog Lipid Res 42, 115-162.
41. Studier, F. W., Rosenberg, A. H., Dunn, J. J. & Dubendorff, J. W. (1990). Use of T7 RNA polymerase to direct expression of cloned genes. Methods Enzymol 185, 60-89.
42. Tang, Y. & Hollingsworth, R. I. (1998). Regulation of lipid synthesis in Bradyrhizobium japonicum: low oxygen concentrations trigger phosphatidylinositol biosynthesis. Appl Environ Microbiol 64, 1963-1966.
43. Wessel, M., Klüsener, S., Gödeke, J., Fritz, C., Hacker, S. & Narberhaus, F. (2006). Virulence of Agrobacterium tumefaciens requires phosphatidylcholine in the bacterial membrane. Mol Microbiol 62, 906-915.
44. Wilderman, P. J., Vasil, A. I., Martin, W. E., Murphy, R. C. & Vasil, M. L. (2002). Pseudomonas aeruginosa synthesizes phosphatidylcholine by use of the phosphatidylcholine synthase pathway. J Bacteriol 184, 4792-4799.
45. Williams, J. G. & McMaster, C. R. (1998). Scanning alanine mutagenesis of the CDP-alcohol phosphotransferase motif of Saccharomyces cerevisiae cholinephosphotransferase. J Biol Chem 273, 13482-13487.
46. Xia, W. & Dowhan, W. (1995). In vivo evidence for the involvement of anionic phospholipids in initiation of DNA replication in Escherichia coli. Proc Natl Acad Sci U S A 92, 783-787.