IJSEM Journal of Bacteriology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
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 Wright, D.
Right arrow Articles by Potts, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wright, D.
Right arrow Articles by Potts, M.
Agricola
Right arrow Articles by Wright, D.
Right arrow Articles by Potts, M.

International Journal of Systematic and Evolutionary Microbiology, Vol 51, 1839-1852, Copyright © 2001 by Society for General Microbiology


Form species Nostoc commune (Cyanobacteria)

D Wright, T Prickett, RF Helm and M Potts
Virginia Tech Center for Genomics (VIGEN), Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA

The form species concept for the Cyanobacteria was evaluated using a comprehensive set of Nostoc samples that were collected during the past two centuries, from all continents, including regions from the Tropics to the Poles. Phylogenies were constructed based upon the conserved regions of tRNA(Leu) (UAA) group I intron DNA sequences. Thirty-four forms contained a tRNA(Leu) (UAA) intron of 284 nt. These 284-nt introns contained 200 nt of conserved sequence that, in most cases, shared 100% sequence identity, they had three variable regions (I, II and III) amounting to 84 nt, contained no hypervariable region and formed a discrete cluster in phylogenetic analysis. These forms represented 31 independent populations in both hemispheres and constitute examples of form species Nostoc commune. Multiple introns were obtained from several of the populations. Ten populations contained introns of 287--340 nt with a hypervariable region, 8 to 59 nt in length, located between variable regions I and II. Alignments identified 15 examples where 5'-AAAAUCC-3' occurred at the hypervariable region--variable region II boundary; this sequence is identical to the conserved sequence at the 3' intron--exon boundary (splice site) within the tRNA(Leu) (UAA) gene. The possibility that hypervariable regions were removed from the primary intron through secondary splicing was tested in vitro but proved to be negative under the experimental conditions used. Shared morphologies of genetically different strains, dissimilar morphologies in strains that share identical genetic markers, incorrect naming of culture collection strains and genetic drift in cultured strains emphasize that the successful delineation of cyanobacterial species requires the application of multiple taxonomic criteria.


This article has been cited by other articles:


Home page
J Exp BotHome page
J. Rikkinen and V. Virtanen
Genetic diversity in cyanobacterial symbionts of thalloid bryophytes
J. Exp. Bot., March 5, 2008; (2008) ern003v1.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
D. J. Wright, S. C. Smith, V. Joardar, S. Scherer, J. Jervis, A. Warren, R. F. Helm, and M. Potts
UV Irradiation and Desiccation Modulate the Three-dimensional Extracellular Matrix of Nostoc commune (Cyanobacteria)
J. Biol. Chem., December 2, 2005; 280(48): 40271 - 40281.
[Abstract] [Full Text] [PDF]


Home page
Int. J. Syst. Evol. Microbiol.Home page
A. Oren
A proposal for further integration of the cyanobacteria under the Bacteriological Code
Int J Syst Evol Microbiol, September 1, 2004; 54(5): 1895 - 1902.
[Abstract] [Full Text] [PDF]


Home page
Int. J. Syst. Evol. Microbiol.Home page
I. Oksanen, K. Lohtander, K. Sivonen, and J. Rikkinen
Repeat-type distribution in trnL intron does not correspond with species phylogeny: comparison of the genetic markers 16S rRNA and trnL intron in heterocystous cyanobacteria
Int J Syst Evol Microbiol, May 1, 2004; 54(3): 765 - 772.
[Abstract] [Full Text] [PDF]


Home page
Appl. Environ. Microbiol.Home page
E. Shaw, D. R. Hill, N. Brittain, D. J. Wright, U. Tauber, H. Marand, R. F. Helm, and M. Potts
Unusual Water Flux in the Extracellular Polysaccharide of the Cyanobacterium Nostoc commune
Appl. Envir. Microbiol., September 1, 2003; 69(9): 5679 - 5684.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
B. Shirkey, N. J. McMaster, S. C. Smith, D. J. Wright, H. Rodriguez, P. Jaruga, M. Birincioglu, R. F. Helm, and M. Potts
Genomic DNA of Nostoc commune (Cyanobacteria) becomes covalently modified during long-term (decades) desiccation but is protected from oxidative damage and degradation
Nucleic Acids Res., June 15, 2003; 31(12): 2995 - 3005.
[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 © 2001 by the International Union of Microbiological Societies.