Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


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
Right arrow Citation Map
Services
Right arrow Email this article to a friend
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 reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Poysti, N. J.
Right arrow Articles by Oresnik, I. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Poysti, N. J.
Right arrow Articles by Oresnik, I. J.
Agricola
Right arrow Articles by Poysti, N. J.
Right arrow Articles by Oresnik, I. J.
Microbiology 153 (2007), 727-736; DOI  10.1099/mic.0.29148-0
© 2007 Society for General Microbiology

Sinorhizobium meliloti pSymB carries genes necessary for arabinose transport and catabolism

Nathan J. Poysti, Erin D. M. Loewen, Zexi Wang and Ivan J. Oresnik

Department of Microbiology, University of Manitoba, Winnipeg, MB R3T 2N2, Canada

Correspondence
Ivan J. Oresnik
oresniki{at}cc.umanitoba.ca

Arabinose is a known component of plant cell walls and is found in the rhizosphere. In this work, a previously undeleted region of the megaplasmid pSymB was identified as encoding genes necessary for arabinose catabolism, by Tn5-B20 random mutagenesis and subsequent complementation. Transcription of this region was measured by beta-galactosidase assays of Tn5-B20 fusions, and shown to be strongly inducible by arabinose, and moderately so by galactose and seed exudate. Accumulation of [3H]arabinose in mutants and wild-type was measured, and the results suggested that this operon is necessary for arabinose transport. Although catabolite repression of the arabinose genes by succinate or glucose was not detected at the level of transcription, both glucose and galactose were found to inhibit accumulation of arabinose when present in excess. To determine if glucose was also taken up by the arabinose transport proteins, [14C]glucose uptake rates were measured in wild-type and arabinose mutant strains. No differences in glucose uptake rates were detected between wild-type and arabinose catabolism mutant strains, indicating that excess glucose did not compete with arabinose for transport by the same system. Arabinose mutants were tested for the ability to form nitrogen-fixing nodules on alfalfa, and to compete with the wild-type for nodule occupancy. Strains unable to utilize arabinose did not display any symbiotic defects, and were not found to be less competitive than wild-type for nodule occupancy in co-inoculation experiments. Moreover, the results suggest that other loci are required for arabinose catabolism, including a gene encoding arabinose dehydrogenase.


Abbreviations: ABC, ATP-binding cassette; Nm, neomycin; Nal, nalidixic acid; Sm, streptomycin; Tc, tetracycline




This article has been cited by other articles:


Home page
J. Bacteriol.Home page
N. J. Poysti and I. J. Oresnik
Characterization of Sinorhizobium meliloti Triose Phosphate Isomerase Genes
J. Bacteriol., May 1, 2007; 189(9): 3445 - 3451.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2007 Society for General Microbiology.