Baldani VLD, Baldani JI, Döbereiner J (1987) Inoculation of field grown wheat (Triticum aestivum) with Azospirillum spp. in Brasil. Biol Fertil Soils 4:37–40
Barbieri P, Galli E (1993) Effect on wheat root development of inoculation with an Azospirillum brasilense mutant with altered indole-3-acetic acid production. Res Microbiol 144:69–75
Barbieri P, Zanelli T, Galli E, Zanetti G (1986) Wheat inoculation with Azospirillum brasilense Sp6 and some mutants altered in nitrogen fixation and indole-3-acetic acid production. FEMS Microbiol Lett 36:87–90
Boddey RM (1987) Methods for quantification of nitrogen fixation associated with Gramineae. CRC Crit Rev Plant Sci 6:209–266
Bottini R, Fulchieri M, Pearce DW, Pharis RP (1989) Identification of gibberellins A1, A3 and iso-A3 in cultures of Azospirillum lipoferum. Plant Physiol 90:45–47
Cacciari I, Lippi D, Pietrosanti T, Pietrosanti W (1989) Phytohormone-like substances produced by single and mixed diazotrophic cultures of Azospirillum and Arthrobacter. Plant Soil 115:151–153
Costacurta A, Keijers V, Vanderleyden J (1994) Molecular cloning and sequence analysis of an Azospirillum brasilense indole-3-pyruvate decarboxylase gene. Mol Gen Genet 243:463–472
Crozier A, Arruda P, Jasmin JM, Monteiro AM, Sandberg G (1988) Analysis of indole-3-acetic acid and related indoles in culture medium from Azospirllum lipoferum and Azospirillum brasilense. Appl Environ Microbiol 54:2833–2837
Dobbelaere S, Croonenborghs A, Thys A, Vande Broek A, Vanderleyden J (1999) Phytostimulatory effect of Azospirillum brasilense wild type and mutant strains altered in IAA production on wheat. Plant Soil 212:155–164
Elmerich C, Newton WE (2007) Associative and endophytic nitrogen-fixing bacteria and cyanobacterial associations. Springer, Dordrecht, p 321
Epstein E, Cohen JD (1981) Microscale preparation of pentofluorobenzyl esters: electron-capture gas chromatographic detection of indole-3-acetic acid in milligram amounts in plant tissue using a benchtop chromatograph-mass spectrometer. Planta 204:1–7
Glickmann E, Dessaux Y (1995) A critical examination of the specificity of the Salkowski reagent for indolic compounds produced by phytopathogenic bacteria. Appl Environ Microbiol 61:793–796
Harari A, Kigel J, Okon Y (1988) Involvement of IAA in the interaction between Azospirillum brasilense and Panicum miliaceum roots. Plant Soil 110:275–282
Horemans S, De Koninck K, Neuray J, Hermans R, Vlassak K (1986) Production of plant growth substances by Azospirillum sp. and other rhizosphere bacteria. Symbiosis 2:341–346
Janzen RA, Rood SB, Dormaar JF, McGill WB (1992) Azospirillum brasilense produces gibberellins in pure culture and chemically-defined medium and in co-culture on straw. Soil Biol Biochem 24:1061–1064
Kloepper JW, Lifshitz R, Zablotowicz RM (1989) Free-living bacterial inocula for enhancing crop productivity. Trends Biotechnol 7:39–43
Okon Y, Kapulnik Y (1986) Development and function of Azospirillum inoculated roots. Plant Soil 90:3–16
Piccoli P, Masciarelli O, Bottini R (1996) Metabolism of 17,17-[2H2]-gibberellins A4, A9 and A20 by Azospirillum lipoferum in chemically-defined culture medium. Symbiosis 21:263–274
Pilet PE, Chollet R (1970) Sur le dosage colorimétrique de l’acide indolylacétique. C R Acad Sci Ser D 271:1675–1678
Prinsen E, Costacurta A, Michiels K, Vanderleyden J, Van Onckelen H (1993) Azospirillum brasilense indole-3-acetic acid biosynthesis: evidence for a non-tryptophan dependent pathway. Mol Plant-Microb Interact 6:609–615
Prinsen E, Van Laer S, Öden S, Van Onckelen H (2000) Auxin analysis. In: Tucker GA, Roberts JA (eds) Plant hormone protocols. Humana, Totowa NJ, USA, pp 49–52
Russo A, Felici C, Toffanin A, Götz M, Collados C, Barea JM, Moënne-Loccoz Y, Smalla K, Vanderleyden J, Nuti M (2005) Effect of Azospirillum inoculants on arbuscular mycorrhiza establishment in wheat and maize plants. Biol Fertil Soils 41:301–309
Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloning: a laboratory manual. Cold Spring Harbor Laboratory, Cold Spring Harbor, New York
Spaepen S, Vanderleyden J, Remans R (2007a) Indole-3-acetic acid in microbial and microorganism-plant signaling. FEMS Microbiol Rev 31:425–448
Spaepen S, Versées W, Gocke D, Pohl M, Steyaert J, Vanderleyden J (2007b) Characterization of phenylpyruvate decarboxylase, involved in auxin production of Azospirillum brasilense. J Bacteriol 189:7626–7633
Steenhoudt O, Vanderleyden J (2000) Azospirillum, a free-living nitrogen-fixing bacterium closely associated with grasses: genetic, biochemical and ecological aspects. FEMS Microbiol Rev 24:487–506
Tien TM, Gaskins MH, Hubbell DH (1979) Plant growth substances produced by Azospirillum brasilense and their effect on the growth of pearl millet (Pennisetum americanum). Appl Environ Microbiol 37:1016–1024
Van Bastelaere E, Lambrecht M, Vermeiren H, Van Dommelen A, Keijers V, Proost P, Vanderleyden J (1999) Characterization of a sugar-binding protein from Azospirillum brasilense mediating chemotaxis to and uptake of sugars. Mol Microbiol 32:703–714
Vande Broek A, Lambrecht M, Eggermont K, Vanderleyden J (1999) Auxins upregulate expression of the indole-3-pyruvate decarboxylase gene from Azospirillum brasilense. J Bacteriol 181:1338–1342
Vande Broek A, Gysegom P, Ona O, Hendrickx N, Prinsen E, Van Impe J, Vanderleyden J (2005) Transcriptional analysis of the Azospirillum brasilense indole-3-pyruvate decarboxylase gene and identification of a cis-acting sequence involved in auxin responsive expression. Mol Plant–Microb Interact 18:311–323
Vanstockem M, Michiels K, Vanderleyden J, Van Gool A (1987) Transposon mutagenesis of Azospirillum brasilense and Azospirillum lipoferum: physiological analysis of Tn5 and Tn5-mob insertional mutants. Appl Environ Microbiol 53:1387–1405
Versées W, Spaepen S, Vanderleyden J, Steyaert J (2007a) The crystal structure of phenylpyruvate decarboxylase from Azospirillum brasilense at 1.5 Å resolution—implications for its catalytic and regulatory mechanism. FEBS J 274:2363–2375
Versées W, Spaepen S, Wood MD, Leeper FJ, Vanderleyden J, Steyaert J (2007b) Molecular mechanism of allosteric substrate activation in a thiamine diphosphate-dependent decarboxylase. J Biol Chem 282:35269–35278
Xi C, Lambrecht M, Vanderleyden J, Michiels J (1999) Bi-functional gfp- and gusA-containing mini-Tn5 transposon derivatives for combined gene expression and bacterial colonization studies. J Microbiol Methods 35:85–92
Zimmer W, Bothe H (1988) The phytohormonal interactions between Azospirillum and wheat. Plant Soil 110:239–247