AEM
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Other Versions of this Article:
AEM.01892-06v1
73/22/7308    most recent
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 arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Flores-Mireles, A. L.
Right arrow Articles by Holguin, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Flores-Mireles, A. L.
Right arrow Articles by Holguin, G.
Agricola
Right arrow Articles by Flores-Mireles, A. L.
Right arrow Articles by Holguin, G.
Applied and Environmental Microbiology, November 2007, p. 7308-7321, Vol. 73, No. 22
0099-2240/07/$08.00+0     doi:10.1128/AEM.01892-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Molecular Characterization of Diazotrophic and Denitrifying Bacteria Associated with Mangrove Roots{triangledown}

Ana L. Flores-Mireles,1,2* Stephen C. Winans,2 and Gina Holguin1

Centro de Investigaciones Biológicas del Noroeste CIBNOR, Mar Bermejo no. 195, Colonia Playa Palo de Santa Rita, La Paz, BCS 23090, México,1 Department of Microbiology, Cornell University, Ithaca, New York 148532

Received 8 August 2007/ Accepted 27 August 2007

An analysis of the molecular diversity of N2 fixers and denitrifiers associated with mangrove roots was performed using terminal restriction length polymorphism (T-RFLP) of nifH (N2 fixation) and nirS and nirK (denitrification), and the compositions and structures of these communities among three sites were compared. The number of operational taxonomic units (OTU) for nifH was higher than that for nirK or nirS at all three sites. Site 3, which had the highest organic matter and sand content in the rhizosphere sediment, as well as the lowest pore water oxygen concentration, had the highest nifH diversity. Principal component analysis of biogeochemical parameters identified soil texture, organic matter content, pore water oxygen concentration, and salinity as the main variables that differentiated the sites. Nonmetric multidimensional scaling (MDS) analyses of the T-RFLP data using the Bray-Curtis coefficient, group analyses, and pairwise comparisons between the sites clearly separated the OTU of site 3 from those of sites 1 and 2. For nirS, there were statistically significant differences in the composition of OTU among the sites, but the variability was less than for nifH. OTU defined on the basis of nirK were highly similar, and the three sites were not clearly separated on the basis of these sequences. The phylogenetic trees of nifH, nirK, and nirS showed that most of the cloned sequences were more similar to sequences from the rhizosphere isolates than to those from known strains or from other environments.


* Corresponding author. Mailing address: Cornell University, Department of Microbiology, 360 Wing Hall, Ithaca, NY 14853. Phone: (607) 255-2037. Fax: (607) 255-3904. E-mail: alf38{at}cornell.edu

{triangledown} Published ahead of print on 7 September 2007.


Applied and Environmental Microbiology, November 2007, p. 7308-7321, Vol. 73, No. 22
0099-2240/07/$08.00+0     doi:10.1128/AEM.01892-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. Microbiol. Mol. Biol. Rev. Eukaryot. Cell All ASM Journals

Copyright © 2007 by the American Society for Microbiology. All rights reserved.