This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Seldin, L.
Right arrow Articles by Paiva, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Seldin, L.
Right arrow Articles by Paiva, E.
Agricola
Right arrow Articles by Seldin, L.
Right arrow Articles by Paiva, E.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, October 1998, p. 3860-3868, Vol. 64, No. 10
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Comparison of Paenibacillus azotofixans Strains Isolated from Rhizoplane, Rhizosphere, and Non-Root-Associated Soil from Maize Planted in Two Different Brazilian Soils

Lucy Seldin,1,* Alexandre Soares Rosado,1 Davi William da Cruz,1 Alberto Nobrega,1 Jan Dirk van Elsas,2 and Edilson Paiva3

Instituto de Microbiologia Prof. Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ,1 and EMBRAPA/CNPMS, Sete Lagoas, MG,3 Brazil, and IPO-DLO, Wageningen, The Netherlands2

Received 31 October 1997/Accepted 28 July 1998

Paenibacillus azotofixans is a nitrogen-fixing bacterium often found in soil and in the rhizospheres of different grasses. In this study, two Brazilian clay soils were planted with cross-hybrid maize (BR-201) and four stages of plant growth were analyzed to characterize the P. azotofixans populations present in the rhizoplanes, rhizospheres, and non-root-associated soils (herein called nonrhizospheres). A total of 106 strains were isolated and identified as P. azotofixans with an API 50CH kit, by classical biochemical tests, and via the use of specific primers based on the 16S rRNA gene in PCRs. To compare the isolated strains, phenotypic characteristics were determined and three different probes were used in hybridization experiments: two nif probes and one probe comprising a 0.58-kb fragment cloned from the P. azotofixans C3L4 genome. These results were used to construct a dendrogram, in which two main clusters could be observed. One cluster contained exclusively strains from Várzea soil, and the other contained the majority of strains from Cerrado soil. The 60 strains from Várzea soil and the 46 strains from Cerrado soil were further analyzed with REP and BOX primers, respectively. Based on the patterns obtained, it was possible to identify 21 different groups among strains from Várzea soil and 4 different groups among strains from Cerrado soil. These different patterns were tested by multivariate analysis of variance, and differences in the populations of P. azotofixans during the four stages of plant growth were demonstrated. Moreover, strains isolated from the rhizoplanes, rhizospheres, and nonrhizospheres of maize planted in Cerrado and Várzea soils were shown to be statistically different; the diversity of P. azotofixans strains was affected by the soil type.


* Corresponding author. Mailing address: Laboratório de Genética Microbiana, Depto. Microbiologia Geral, Instituto de Microbiologia, Universidade Federal do Rio de Janeiro, CCS, Bloco I, Ilha do Fundão, CEP 21941-590, Rio de Janeiro, RJ, Brazil. Phone: 55-21-590 30 93. Fax: 55-21-259 99 57. E-mail: immgsel{at}microbio.ufrj.br.


Applied and Environmental Microbiology, October 1998, p. 3860-3868, Vol. 64, No. 10
0099-2240/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Bertaux, J., Schmid, M., Prevost-Boure, N. C., Churin, J. L., Hartmann, A., Garbaye, J., Frey-Klett, P. (2003). In Situ Identification of Intracellular Bacteria Related to Paenibacillus spp. in the Mycelium of the Ectomycorrhizal Fungus Laccaria bicolor S238N. Appl. Environ. Microbiol. 69: 4243-4248 [Abstract] [Full Text]  
  • van Dillewijn, P., Villadas, P. J., Toro, N. (2002). Effect of a Sinorhizobium meliloti Strain with a Modified putA Gene on the Rhizosphere Microbial Community of Alfalfa. Appl. Environ. Microbiol. 68: 4201-4208 [Abstract] [Full Text]  
  • Mansouri, H., Petit, A., Oger, P., Dessaux, Y. (2002). Engineered Rhizosphere: the Trophic Bias Generated by Opine-Producing Plants Is Independent of the Opine Type, the Soil Origin, and the Plant Species. Appl. Environ. Microbiol. 68: 2562-2566 [Abstract] [Full Text]  
  • Schmalenberger, A., Schwieger, F., Tebbe, C. C. (2001). Effect of Primers Hybridizing to Different Evolutionarily Conserved Regions of the Small-Subunit rRNA Gene in PCR-Based Microbial Community Analyses and Genetic Profiling. Appl. Environ. Microbiol. 67: 3557-3563 [Abstract] [Full Text]  
  • Picard, C., Di Cello, F., Ventura, M., Fani, R., Guckert, A. (2000). Frequency and Biodiversity of 2,4-Diacetylphloroglucinol-Producing Bacteria Isolated from the Maize Rhizosphere at Different Stages of Plant Growth. Appl. Environ. Microbiol. 66: 948-955 [Abstract] [Full Text]  
  • Djordjevic, S. P., Forbes, W. A., Smith, L. A., Hornitzky, M. A. (2000). Genetic and Biochemical Diversity among Isolates of Paenibacillus alvei Cultured from Australian Honeybee (Apis mellifera) Colonies. Appl. Environ. Microbiol. 66: 1098-1106 [Abstract] [Full Text]  
  • Normander, B., Hendriksen, N. B., Nybroe, O. (1999). Green Fluorescent Protein-Marked Pseudomonas fluorescens: Localization, Viability, and Activity in the Natural Barley Rhizosphere. Appl. Environ. Microbiol. 65: 4646-4651 [Abstract] [Full Text]