Interactions between proteolytic and non-proteolytic Pseudomonas fluorescens affect protein degradation in a model community

FEMS Microbiology Ecology

Volumn 32, Issue 2, 2000, Pages 103-109

  Worm, Jakob ^a   Jensen, Linda E ^a   Hansen, Thomas S ^a   Søndergaard, Morten ^b   Nybroe, Ole ^a  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

^b UNIVERSITY OF COPENHAGEN   (Denmark)

Author keywords

Interaction; Model community; Proteinase activity; Pseudomonas fluorescens

Indexed keywords

PROTEIN HYDROLYSATE; PROTEINASE;

BACTERIUM; DEGRADATION; ECOLOGICAL MODELING; INTERSPECIFIC INTERACTION; METABOLISM; MICROBIAL COMMUNITY; PROTEIN;

ARTICLE; BACTERIAL GROWTH; BACTERIAL METABOLISM; BIOLUMINESCENCE; ECOSYSTEM; ENZYME ACTIVITY; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN TRANSPORT; PSEUDOMONAS FLUORESCENS;

PSEUDOMONAS FLUORESCENS;

EID: 0034097287     PISSN: 01686496     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-6496(00)00019-2     Document Type: Article

References (39)

1. Coffin R.B. Bacterial uptake of dissolved free and combined amino acids in estuarine waters. Limnol. Oceanogr. 34:1989;531-542.
2. Rosenstock B., Simon M. Use of dissolved combined and free amino acids by planktonic bacteria in Lake Constance. Limnol. Oceanogr. 38:1993;1521-1531.
3. Kroer N., Jørgensen N.O.G., Coffin R.B. Utilization of dissolved nitrogen by heterotrophic bacterioplankton: a comparison of three ecosystems. Appl. Environ. Microbiol. 60:1994;4116-4123.
4. Cousin, M.A. (1989) Physical and biochemical effects on milk component. In: Enzymes of Psychrotrophs in Raw Food (McKellar, R.C., Ed.), pp. 205-225. CRC, Boca Raton, FL.
5. Kunji E.R.S., Mierau I., Hagting A., Poolman B., Konings W.N. The proteolytic systems of lactic acid bacteria. Antonie van Leeuwenhoek Int. J. Gen. Mol. Microbiol. 70:1996;187-221.
6. Payne J.W., Smith M.W. Peptide transport by micro-organisms. Adv. Microb. Physiol. 36:1994;1-80.
7. McFall, E. and Newman, E.B. (1996) Amino acids as carbon sources. In: Escherichia coli and Salmonella (Neidhardt, F.C., Curtiss III, R., Ingraham, J.L., Lin, E.C.C., Low, D.B., Magasanik, B., Reznikoff, W.S., Riley, M., Schaechter, M. and Umbarger, H.E., Eds.), pp. 358-379. American Society for Microbiology, Washington, DC.
8. Fox, P.F., Power, P. and Cogan, T.M. (1989) Isolation and molecular characteristics. In: Enzymes of Psychrotrophs in Raw Food (McKellar, R.C., Ed.), pp. 57-120. CRC, Boca Raton, FL.
9. Givskov M., Eberl L., Molin S. Control of exoenzyme production, motility and cell differentiation in Serratia liquefaciens. FEMS Microbiol. Lett. 148:1997;115-122.
10. McKellar, R.C. (1989) Regulation and control of synthesis. In: Enzymes of Psychrotrophs in Raw Food (McKellar, R.C., Ed.), pp. 153-172. CRC, Boca Raton, FL.
11. Juillard V., Foucaud C., Flambard B., Furlan S., Bellengier P., Richard J. Interactions entre bactéries lactiques mésophiles dans le lait: rôle des facteurs nutritionnels. Lait. 78:1998;91-97.
12. Chróst R.J., Wcislo R., Halemejko G.Z. Enzymatic decomposition of organic matter by bacteria in an eutrophic lake. Arch. Hydrobiol. 107:1986;145-165.
13. Vetter Y.A., Deming J.W., Jumars P.A., Krieger-Brockett B.B. A predictive model of bacterial foraging by means of freely released extracellular enzymes. Microb. Ecol. 36:1998;75-92.
14. Marshall D.L., Schmidt R.H. Physiological evaluation of stimulated growth of Listeria monocytogenes by Pseudomonas species in milk. Can. J. Microbiol. 37:1991;594-599.
15. Verheul A., Rombouts F.M., Abee T. Utilization of oligopeptides by Listeria monocytogenes Scott A. Appl. Environ. Microbiol. 64:1998;1059-1065.
16. de Lorenzo V., Herrero M., Sánchez J.M., Timmis K.N. Mini-transposons in microbial ecology and environmental biotechnology. FEMS Microbiol. Ecol. 27:1998;211-224.
17. Christoffersen K., Nybroe O., Jürgens K., Hansen M. Measurement of bacterivory by heterotrophic nanoflagellates using immunofluorescence labelling of ingested cells. Aquat. Microb. Ecol. 13:1997;127-134.
18. Andersen J.B., Sternberg C., Poulsen L.K., Bjørn S.P., Givskov M., Molin S. New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria. Appl. Environ. Microbiol. 64:1998;2240-2246.
19. Smibert, R.M. and Krieg, N.R. (1994) Phenotypic characterization. In: Methods for General and Molecular Bacteriology (Gerhardt, P., Murray, R.G.E., Wood, W.A. and Krieg, N.R., Eds.), pp. 607-654. American Society for Microbiology, Washington, DC.
20. Kragelund L., Christoffersen B., Nybroe O., de Bruijn F.J. Isolation of lux reporter gene fusions in Pseudomonas fluorescens DF57 inducible by nitrogen or phosphorus starvation. FEMS Microbiol. Ecol. 17:1995;95-106.
21. Jensen, L.E., Koch, B. and Nybroe, O., unpublished.
22. Jensen L.E., Nybroe O. Nitrogen availability to Pseudomonas fluorescens DF57 is limited during decomposition of barley straw in bulk soil and in barley rhizosphere. Appl. Environ. Microbiol. 65:1999;4320-4328.
23. Kragelund L., Nybroe O. Culturability and expression of outer membrane proteins during carbon, nitrogen, or phosphorus starvation of Pseudomonas fluorescens DF57 and Pseudomonas putida DF14. Appl. Environ. Microbiol. 60:1994;2944-2948.
24. Hoppe, H. (1993) Use of flourogenic model substrates for extracellular enzyme activity (EEA) measurement of bacteria. In: Handbook of Methods in Aquatic Microbial Ecology (Kemp, P.F., Sherr, B.F., Sherr, E.B. and Cole, J.J., Eds.), pp. 423-431. Lewis, Boca Raton, FL.
25. Stead D. A fluorimetric method for the determination of Pseudomonas fluorescens AR11 lipase in milk. J. Dairy Res. 50:1983;491-502.
26. Blouin K., Walker S.G., Smit J., Turner R.F.B. Characterization on in vivo reporter systems for gene expression and biosensor application based on luxAB luciferase genes. Appl. Environ. Microbiol. 62:1996;2013-2021.
27. Hansen M., Kragelund L., Nybroe O., Sørensen J. Early colonization of barley roots by Pseudomonas fluorescens studied by immunofluorescence technique and confocal laser scanning microscopy. FEMS Microbiol. Ecol. 23:1997;353-360.
28. Clarke R.G., Pinder A.C. Improved detection of bacteria by flow cytometry using a combination of antibody and viability markers. J. Appl. Microbiol. 84:1998;577-584.
29. Sokal, R.G. and Rohlf, F.J. (1995) Biometry, 3rd. edn., W.H. Freemann and Company, New York.
30. Liao C.-H., McCallus D.E. Biochemical and genetic characterization of an extracellular protease from Pseudomonas fluorescens CY091. Appl. Environ. Microbiol. 64:1998;914-921.
31. Duong F., Soscia C., Lazdunski A., Murgier M. The Pseudomonas fluorescens lipase has a C-terminal secretion signal and is secreted by a three-component bacterial ABC-exporter system. Mol. Microbiol. 11:1994;1117-1126.
32. Unge A., Tombolini R., Mølbak L., Jansson J.K. Simultaneous monitoring of cell number and metabolic activity of specific bacterial populations with a dual gfp-luxAB marker system. Appl. Environ. Microbiol. 65:1999;813-821.
33. Pesci E.C., Pearson J.P., Seed P.C., Iglewski B.H. Regulation of las and rhl quorum sensing in Pseudomonas aeruginosa. J. Bacteriol. 179:1997;3127-3132.
34. Juillard V., Richard J. Mixed cultures in milk of a proteinase-positive and a proteinase-negative variant of Lactococcus lactis subsp. lactis influence of initial percentage of proteinase-positive cells on the growth parameters of each strain and on the rate of acidification. Lait. 74:1994;3-12.
35. Juillard V., Furlan S., Foucaud C., Richard J. Mixed cultures of proteinase-positive and proteinase-negative strains of Lactococcus lactis in milk. J. Dairy Sci. 79:1996;964-970.
36. Winkel S.A., Richardson G.H. Cell mass and acid production of proteinase-positive and proteinase-negative lactic cultures in buffered non-fat milk. J. Dairy Sci. 67:1984;2856-2859.
37. Søndergaard M., Middelboe M. A cross-system analysis of labile dissolved organic carbon. Mar. Ecol. Prog. Ser. 118:1995;283-294.
38. Chróst, R.J. (1991) Microbial ectoenzymes in aquatic environments. In: Aquatic Microbial Ecology. Biochemical and molecular approaches (Overbeck, J. and Chróst, R.J., Eds.), pp. 47-78. Springer-Verlag, New York.
39. Martinez J., Smith D.C., Steward G.F., Azam F. Variability in ectoenzyme activities of pelagic marine bacteria and its significance for substrate processing in the sea. Aquat. Microb. Ecol. 10:1996;223-230.