Growth and indole-3-acetic acid biosynthesis of Azospirillum brasilense Sp245 is environmentally controlled

FEMS Microbiology Letters

Volumn 246, Issue 1, 2005, Pages 125-132

  Ona, Ositadinma ^a   Van Impe, Jan ^a   Prinsen, Els ^b   Vanderleyden, Jos ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

Azospirillum brasilense; Fermentor; Indole 3 acetic acid

Indexed keywords

INDOLEACETIC ACID; MALIC ACID; TRYPTOPHAN;

AERATION; ARTICLE; AZOSPIRILLUM BRASILENSE; BACTERIAL GROWTH; BATCH CELL CULTURE; BIOLOGICAL MONITORING; BIOREACTOR; BIOSYNTHESIS; CARBON SOURCE; CONCENTRATION (PARAMETERS); CULTURE MEDIUM; ENVIRONMENTAL FACTOR; FED BATCH CULTURE; GENE EXPRESSION; GROWTH DISORDER; NONHUMAN; PRIORITY JOURNAL; TEMPERATURE DEPENDENCE;

AZOSPIRILLUM BRASILENSE;

EID: 18144373469     PISSN: 03781097     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.femsle.2005.03.048     Document Type: Article

References (46)

1. Y. Okon, and J. Vanderleyden Root-associated Azospirillum species can stimulate plants ASM News 63 1997 366 370
2. S. Dobbelaere, A. Croonenborghs, A. Thys, D. Ptacek, Y. Okon, and J. Vanderleyden Effect of inoculation with wild type A. brasilense and A. irakense strains on development and N-content of spring wheat and grain maize Biol. Fert. Soils 36 2002 284 297
3. R. Barbieri, and E. Galli Effect on wheat root development of inoculation with an Azospirillum brasilense mutant with altered indole-3-acetic acid production Res. Microbiol. 144 1993 69 75
4. N.G. Buckley, and G.J. Pugh Auxin production by phylloplane fungi Nature 231 1971 332
5. M. Rudy, S. Haskin, H. Levi-Kedmi, and A. Sharon In planta production of indole-3-acetic acid by Colltotrichum gloeosporiodes f. sp. Aeschynomene Appl. Environ. Microbiol. 70 2004 1852 1854
6. N. Mohammed, R. Onodera, and R.I. Khan Tryptophan biosynthesis and production of other related compounds from indole and l-serine by mixed ruminal bacteria, protozoa, and their mixture in vitro Curr. Microbiol. 39 4 1999 200 204
7. A. Costacurta, and J. Vanderleyden Synthesis of phytohormones by plant-associated bacteria Crit. Rev. Microbiol. 21 1995 1 18
8. C.L. Patten, and B.R. Glick Bacterial biosynthesis of indole-3-acetic acid Can. J. Microbiol. 42 1996 207 220
9. N.A. Eckardt New insights into auxin biosynthesis Plant Cell 13 2001 1 3
10. O. Steenhoudt, and J. Vanderleyden Azospirillum, a free-living nitrogen fixing bacterium closely associated with grasses: genetic, biochemical and ecological aspects FEMS Microbiol. Rev. 24 2000 487 506
11. E. Prinsen, A. Costacurta, K. Michiels, J. Vanderleyden, and H. van Onckelen Azospirillum brasilense indole-3-acetic acid biosynthesis: evidence for a non-tryprophan dependent-dependent pathway Mol. Plant-Microbe Interact. 6 1993 609 615
12. A. Vande Broek, M. Lambrecht, K. Eggermont, and J. Vanderleyden Auxins up-regulate expression of the indole-3-pyruvate decarboxylase gene in Azospirillum brasilense J. Bacteriol. 181 1999 1338 1342
13. T. Bar, and Y. Okon Tryptophan conversion to indole-3-acetic acid via indole-3-acetamide in Azospirillum brasilense Sp7 Can. J. Microbiol. 39 1993 81 86
14. J. Koga, T. Adachi, and H. Hidaka Molecular cloning of the gene for indolepyruvate decarboxylase from Enterobacter cloacae Mol. Gen. Genet. 226 1991 10 16
15. M.T. Brandl, and S.E. Lindow Cloning and characterization of a locus encoding an indolepyruvate decarboxylase involved in indole-3-acetic acid synthesis in Erwinia herbicola Appl. Environ. Microbiol. 62 1996 4121 4128
16. E. Sergeeva, A. Liaimer, and B. Bergman Evidence for production of the phytohormone indole-3-acetic acid by cyanobacteria Planta 215 2002 229 238
17. K. Yagi, T. Chujo, H. Nojiri, T. Omori, M. Nishiyama, and H. Yamane Evidence for the presence of DNA-binding proteins involved in regulation of the gene expression of indole-3-pyruvic acid decarboxylase, a key enzyme in indole-3-acetic acid biosynthesis in Azospirillum lipoferum FS Biosci. Biotechnol. Biochem. 65 2001 1265 1269
18. Y. Bashan Inoculants of plant growth promoting bacteria for use in agriculture Biotechnol. Adv. 16 1998 729 770
19. M.L.E. Reed, and B.R. Glick Applications of free living plant growth-promoting rhizobacteria Antonie van Leeuwenhoek 86 1 2004 1 25
20. H. Bolton, J.K. Fredrickson, S.A. Bentjen, D.J. Workman, S.W. Lis, and J.M. Thomas Field calibration of soil core macrocosms: fate of a genetically altered rhizobacterium Microb. Ecol. 21 1991 163 173
21. M. Vanstockem, K. Michiels, J. Vanderleyden, and A.P. van Gool Transposon mutagenesis of Azospirillum brasilense and Azospirillum lipoferum: physical analysis of Tn5 and Tn5 mob insertion mutants Appl. Environ. Microbiol. 53 1987 410 415
22. E. Prinsen, S. van Laer, S. Öden, and H. van Onckelen Auxin analysis G.A. Tucker Plant hormone protocols 2000 Humana Press Totowa, NJ 49 65
23. E. Epstein, and J.D. Cohen Microscale preparation of pentafluorobenzyl esters: electron-capture gas chromatographic detection of indole-3-acetic acid in milligram amounts of plant tissue using a benchtop chromatograph-mass spectrometer Planta 204 1981 1 7
24. R.A. Jefferson Assaying chimeric genes in plants: the GUS gene fusion system Plant Mol. Biol. Rep. 5 1987 387 405
25. J.H. Miller Experiments in molecular genetics 1972 Cold Spring Harbor Laboratory New York
26. P.K. Jjemba, and M. Alexander Possible determinants of rhizosphere competence of bacteria Soil Biol. Biochem. 31 1999 623 632
27. W. Cheng, Q. Zhang, D.C. Coleman, C.R. Carrroll, and C.A. Hoffman Is available carbon limiting microbial respiration in the rhizosphere Soil Biol. Biochem. 28 1996 1283 1288
28. R. Barak, I. Nur, Y. Okon, and Y. Henis Aerotactic response of Azospirillum brasilense J. Bacteriol. 152 1982 643 649
29. I.B. Zhulin, V.A. Bespalov, M.S. Johnson, and B.L. Taylor Oxygen taxis and proton motive force in Azospirillum brasilense J. Bacteriol. 178 1996 5199 5204
30. Y. Okon, T. Bar, S. Tal, and E. Zaddy Physiological properties of Azospirillum brasilense involved in root growth promotion M. Polsinelli R. Naterassi M. Vincenzini Nitrogen fixation 1991 Kluwer Academic Publishers Norwell, MA 113 125
31. M.T. Brandl, and S.E. Lindow Environmental signals modulate the expression of an indole-3-acetic acid biosynthetic gene in Erwinia herbicola. Mol Plant Microb. Intract. 10 1997 499 505
32. S.S. Saleh, and B.R. Glick Involvement of gacS and rpoS in enhancement of the plant growth-promoting capabilities of Enterobacter cloacae CAL2 and UW4 Can. J. Microbiol. 47 2001 698 705
33. C.L. Patten, and B.R. Glick Regulation of indoleacetic acid production in Pseudomonas putida GR12-2 by tryptophan and the stationary-phase sigma factor RpoS Can. J. Microbiol. 48 2002 635 642
34. E. Fallik, and Y. Okon The response of maize (Zea mays) to Azospirillum inoculation in various types of soil in the field World J. Microbiol. Biotechnol. 12 1996 511 515
35. W. Zimmer, and H. Bothe The phytohormonal interaction between Azospirillum and wheat F.A. Skimmer R.M. Boddey I. Fendrik Nitrogen fixation with non legumes 1989 Kluwer Academic Dordrecht 137 145
36. R.R. Bouknight, and H.L. Sadoff Tryptophan catabolism in Bacillus megaterium J. Bacteriol. 121 1975 70 76
37. K.O. Oleg, L. Jablonski, P. Boris, P. Dorrestien, T. Begley, and A. Osterman Aerobic trytophan degradation pathway in bacteria: novel kynurenine formamidase FEMS Microbiol. Lett. 227 2003 219 227
38. J.C. Vederas, E. Schleicher, M.D. Tsai, and H.G. Floss Stereochemistry and mechanism of reactions catalyzed by tryptophanase in Escherichia coli J. Biol. Chem. 253 1978 5350 5354
39. M. Nozaki, and Y. Ishimura Tryptophan metabolism in micro-organisms Biochem. J. 128 1972 24 25
40. O. Salcher, and F. Lingens Metabolism of tryptophan by Pseudomonas aureofaciens and its relationship to pyrrolnitrin biosynthesis J. Gen. Microbiol. 121 1980 465 471
41. W. Zimmer, M. Wesche, and L. Timmermans Identification and isolation of indole-3-pyruvate decaboxylase gene from Azospirillum brasilense Sp7: sequencing and functional analysis of the gene locus Curr. Microbiol. 36 1998 327 331
42. R. Prusty, P. Grisafi, and R. Fink The plant growth indoleacetic acid induces invasive growth in Saccharomyces cerevisiae Proc. Natl. Acad. Sci. USA 101 2004 4153 4157
43. G. Holguin, and Y. Bashan Nitrogen fixation by Azospirillum brasilense CD is promoted when co-cultured with a mangrove rhizosphere bacterium (Staphylococcus sp.) Soil Biol. Biochem. 28 1996 1651 1660
44. A. Vande Broek, J. Michiels, A. Van Gool, and J. Vanderleyden Spatial-temporal colonization patterns of Azospirillum brasilense on the wheat root surface and expression of bacterial nifH gene during association Mol. Plant-Microbe Interact. 6 1993 592 600
45. O. Hojberg, and J. Sorensen Microgradients of microbial oxygen consumption in a barley rhizosphere model system Appl. Environ. Microbiol. 59 1993 431 437
46. H.A. Tobert, and C.W. Wood Effects of soil compaction and water-filled pore space on soil microbial activity and N losses Commun. Soil Sci. Plant Anal. 23 1992 1321 1331