Germination-Arrest Factor (GAF): 3. Determination that the herbicidal activity of GAF is associated with a ninhydrin-reactive compound and counteracted by selected amino acids

Biological Control

Volumn 51, Issue 1, 2009, Pages 181-190

  Armstrong, Donald ^a   Azevedo, Mark ^b   Mills, Dallice ^a   Bailey, Bonnie ^a   Russell, Brian ^a   Groenig, Aleta ^a   Halgren, Anne ^b   Banowetz, Gary ^b   McPhail, Kerry ^a  

^a OREGON STATE UNIVERSITY   (United States)

^b AGRICULTURAL RESEARCH SERVICE   (United States)

Author keywords

Amino acids; Annual bluegrass; Biocontrol; Grassy weeds; Herbicide; Poa annua; Pseudomonas fluorescens; Rhizobacteria

Indexed keywords

BACTERIA (MICROORGANISMS); POA; POA ANNUA; PSEUDOMONAS FLUORESCENS; RHIZOBIALES;

EID: 68949099463     PISSN: 10499644     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biocontrol.2009.06.004     Document Type: Article

References (25)

1. Banowetz G.M., Azevedo M.D., Armstrong D.J., Halgren A.B., and Mills D.I. Germination-Arrest Factor (GAF): biological properties of a novel, naturally-occurring herbicide produced by selected isolates of rhizosphere bacteria. Biological Control 46 (2008) 380-390
2. Banowetz G.M., Azevedo M.D., Armstrong D.J., and Mills D.I. Germination-Arrest Factor (GAF): part 2. Physical and chemical properties of a novel, naturally-occurring herbicide produced by selected isolates of rhizosphere bacteria. Biological Control 50 (2009) 103-110
3. Bolton H., Elliott L.F., Gurusiddaiah S., and Fredrickson J.K. Characterization of a toxin produced by a rhizobacterial Pseudomonas species that inhibits wheat growth. Plant and Soil 114 (1989) 279-287
4. Braun S.D., Vollksch B., Nuske J., and Spiteller D. 3-Methylarginine from Pseudomonas syringae pv. syringae 22d/93 suppresses the bacterial blight caused by its close relative Pseudomonas syringae pv. glycinea. ChemBioChem 9 (2008) 1913-1920
5. Compeau G., Al-Achi B.J., Platsouka E., and Levy S.B. Survival of rifampicin-resistant mutants of Pseudomonas fluorescens and in soil systems. Applied Environmental Microbiology 54 (1988) 2432-2438
6. De Sousa C.A.F., and Sodek L. Alanine metabolism and alanine aminotransferase activity in soybean (Glycine max) during hypoxia of the root system and subsequent return to normoxia. Environmental and Experimental Botany 50 (2003) 1-8
7. Dowling D.N., and O'Gara F. Metabolites of Pseudomonas involved in the biocontrol of plant disease. Trends in Biotechnology 12 (1994) 133-141
8. Fredrickson J.K., and Elliott L.F. Effects on winter wheat seedling growth by toxin-producing rhizobacteria. Plant and Soil 83 (1985) 399-409
9. Good A.G., and Crosby W.L. Anaerobic induction of alanine aminotransferase in barley root tissue. Plant Physiology 90 (1989) 1305-1309
10. Gurusiddaiah S., Gealy D.R., Kennedy A.C., and Ogg Jr. A.G. Isolation and characterization of metabolites from Pseudomonas fluorescens D7 for control of downy brome (Bromus tectorum). Weed Science 42 (1994) 492-501
11. Howell C.R., and Stipanovic R.D. Control of Rhizoctonia solani on cotton seedlings with Pseudomonas fluorescens and with an antibiotic produced by the bacterium. Phytopathology 69 (1979) 480-482
12. Kennedy A.C., Elliott L.F., Young F.L., and Douglas C.L. Rhizobacteria suppressive to the weed downy brome. Soil Science Society of America Journal 55 (1991) 22-727
13. Kennedy A.C., Johnson B.N., and Stubbs T.L. Host range of a deleterious rhizobacterium for biological control of downy brome. Weed Science 49 (2001) 792-797
14. Lesinger T., and Margraff R. Secondary metabolites of the fluorescent Pseudomonads. Microbiological Reviews 43 (1979) 422-442
15. Loper J.E., and Gross H. Genomic analysis of antifungal metabolite production by Pseudomonas fluorescens Pf-5. European Journal of Plant Pathology 119 (2007) 265-278
16. Matthysse A.G., Stretton S., Dandie C., McClure N.C., and Goodman A.E. Construction of GFP vectors for use in gram-negative bacteria other than Escherichia coli. FEMS Microbiology Letters 145 (1996) 87-94
17. Mavrodi D.V., Blankenfeldt W., and Thomashow L.S. Phenazine compounds in fluorescent Pseudomonas spp.: biosynthesis and regulation. Annual Review of Phytopathology 44 (2006) 417-445
18. Nehl D.B., Allen S.J., and Brown J.F. Deleterious rhizosphere bacteria: an integrating perspective. Applied Soil Ecology 5 (1996) 1-20
19. Nielsen T.H., Sorensen D., Tobiasen C., Andsersen J.B., Christophersen C., Givskov M., and Sorensen J. Antibiotic and biosurfactant properties of cyclic lipopeptides produced by fluorescent Pseudomonas spp. from the sugar beet rhizosphere. Applied and Environmental Microbiology 68 (2002) 3416-3423
20. Pedras M.S.C., Ismail N., Quail J.W., and Boyetchko S.M. Structure, chemistry and biological activity of pseudophomins A and B, new cyclic lipodepsipeptides isolated from the biocontrol bacterium Pseudomonas fluorescens. Phytochemistry 62 (2003) 1105-1114
21. Raaijmakers J.M., de Bruijn I., and de Kock M.J.D. Cyclic lipopeptide production by plant-associated Pseudomonas spp.: diversity, activity, biosynthesis, and regulation. Molecular Plant-Microbe Interactions 19 (2006) 699-710
22. Sambrook J., and Russell D.W. Molecular Cloning: A Laboratory Manual. third ed. (2001), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
23. Sands D.C., and Rovira A.D. Isolation of fluorescent Pseudomonads with a selective medium. Applied Microbiology 20 (1970) 513-514
24. Simon A., Rovira A.D., and Sands D.C. An improved selective medium for isolating fluorescent pseudomonads. Journal of Applied Bacteriology 36 (1973) 141-145
25. Wilson M., and Lindow S.E. Interactions between the biological control agent Pseudomonas fluorescens strain A506 and Erwinia amylovora in pear blossoms. Phytopathology 83 (1993) 117-123