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Azospírillum VI and Related Microorganisms Genetics - Physiology - Ecology Edited by István Fendrik Maddalena del Gallo Jos Vanderleyden Miklos de Zamaroczy NATO ASI Series Series G: Ecological Sciences, Vol. 37 jced bacteria. in the infectíon of cercáis wilh R.PastorelU, A.Gori and F.Favilli Dipartimento di Scienze e Tecnologie Alimentari Sez. di Microbiología Applícata, University of Flo Piazzale delle Cascine, 27 - 50144 Firenze, Itaty. pirillum inoculation technology: iol 36: 591-608 ic responses in plant growth, yield ilion with Azospirillum brasilense (1986) Effect of inoculation of vn wheat. Plant Soil 95: ME, Littell RC, Galaher NR, Is and hybrids to inoculation with ) Establishment of Azospirillum .¡ochen. 21:59-64 Genotype-dependent response to in Brassica júncea L. Curr. Sci. 88) Field inoculation of sorg'hum •edicae. Plant Soil. 110: Abstract Several bacterial strains were isolated from the rh classifíed in the genera Enterobacter, Pseudomo on the basis of their morphological and biochem of colonizatíon and adhesión of these bacteria to microscopy have been carried out. Keywords: rhizosphere, adhesión, root surface, S biofertilizer in intensive wheat ilion of Azospirillum spp. Appl. Introduction ig roots of nonleguminous plañís. Is) Nauka Moscow (in Russian) Chmeleva ZV (1989) Bacteria of ivily of nonhomologous plañís. The ability of rhizobacteria to colonize roots is competition of the bacterium in the rhizosphere. ;arl millet cultivars to inoculation that are important to promote competitiveness, surface. Living firmty anchored to root, bacteria (Mentéis e/a/., 1989). In this work we have investigated the capacity t bacterial strains isolated from the rhizosphere of i described by Bazzicalupo et al. (1985). Plañís to root surface of maize and w th cabinet (16h light, 21°C; 8h dark, 17°C) for Figure 1A shows how most epidemial cells in tiie root-hair r washed inoculated-roots were fixed for 18h at connected to root surface an jhosphate buffer (pH 7.0), washed three times, coíonization was observed near le and dehydrated in a grade series of ethanol. to be attached to the cell surfac al Point Dryer 020 Balzers) mounted on stubs, while the other strains along the i05 scanning electrón microscope (Haahtela et The majority of the bacterial c aggregations, with the exception the surface of roots (Fig. ID). Azospirillum snáBacittus strain observations provided evidence pecies zospirittum lipoferum zospirillum lipoferum 'nteróbacter cloacae 'nterobacter sakazakii seudomonas sp. zotobacter chroococcum acillus subtilis acüius megaiherium Conclusión* Bacteria tested prefer to colon exúdales; the modality of adhe seems to be supported by fibrilla Internal root coíonization has b Azospirillum strains are able Á2ospirillum penetraíion into i understood (Bashan and Levan penetraíion of bacteria in root in Figure 1. Scanning electrón micrographs: (A) EnunAp3 adherec ~ maize root, X655; (B) EnunB12 anchored to root surface fibrillar materal, X5000; (C) EnunEtS anchored to maize roer bj a single pole of the bacterial cell, X2500, (D) EnunB12 femé: aggregations on maize root surface, X600; (E) EnunAp2 ad'r.= r^~ to root hair surface, X2620; (F) internal colonization of r = _ : ^ root by EnunAp3, X1250. Azospirülum as a challenge for agriculture. Can Bazácalupo M, Cresta E and Favilli F (1985) An i wheat association. In Azospirülum DI: Genetic Springer-Verlag, pp. 139-146 de Freitas JR and Germida JJ (1990) A root ti rhizobacteria interactíons. Appl Microbiol Biote Haahtela K, Laakso T, Nurmiaho-Lassila EL and of Poa pratensis and Triticum aestivum Enterobacter máAzospirillum. Plant and Soil Holt JG (1984) Bergey's manual of systematic ba Wilkins Co. Baltimore. Michiels K, Vanderleyden J and Van Gool A (1 review. Biol Fértil Soils 8:356-363 (A) EnunAp3 adhered to to root surface by hored to maize root by 30, (D) EnunB12 formad ; (E) EnunAp2 adhered colonization of maize