1887

Abstract

The 16S rRNA sequence of sp. strain NIBB 1067 was determined and used for the construction of a distance tree and bootstrap analysis. The tree shows that, among the available cyanobacterial 16S rRNA sequences, NIBB 1067 has PCC 7515 as its closest relative, presenting 94.9% of sequence similarity with the latter strain. This is in contrast to a difference of 9 mol% G + C in mean genomic DNA base composition between the two organisms. Nevertheless, the genotypic heterogeneity presented by a number of strains assigned to the genus hinders a taxonomic decision on the separate existence of the genera and The sequence of the internal transcribed spacer (ITS) between the 16S and 23S rRNA genes was also determined, as a possible marker to study inter- and intraspecific variability. The ITS contains the genes coding for tRNA and tRNA and its total length is 547 nucleotides. In six out of eight sequenced clones, there is a duplication of 29 nucleotides, surrounding the 5′ end of the tRNA.

Loading

Article metrics loading...

/content/journal/micro/10.1099/13500872-140-8-2159
1994-08-01
2024-04-19
Loading full text...

Full text loading...

/deliver/fulltext/micro/140/8/mic-140-8-2159.html?itemId=/content/journal/micro/10.1099/13500872-140-8-2159&mimeType=html&fmt=ahah

References

  1. Anagnostidis K., Komarek J. Modern approach to the classification system of cyanophytes 3-Oscillatoriales. Arch Hydrobiol/Suppl 1988; 80:1–4 Algological Studies 50/53, 327-472
    [Google Scholar]
  2. Britschgi T.B., Giovannoni S.J. Phylogenetic analysis of a natural marine bacterioplankton population by rRNA gene cloning and sequencing. Appl Environ Microbiol 1991; 57:1707–1713
    [Google Scholar]
  3. Brosius J., Dull T.J., Sleeter D.D., Noller H.F. Gene organization and primary structure of a ribosomal RNA operon from Eschericbia coli. J Mol Biol 1981; 148:107–127
    [Google Scholar]
  4. Capone D.G., Carpenter E.J. Nitrogen fixation in the marine environment. Science 1982; 217:1140–1142
    [Google Scholar]
  5. Castenholz R.W. Subsection III, order Oscillatoriales. In Bergey's Manual of Systematic Bacteriology 1989 Edited by Staley J.T., Bryant M.P., Pfennig N., Holt J.G. Baltimore : Williams & Wilkins; pp 1710–1806
    [Google Scholar]
  6. Drews G., Weckesser J. Function, structure and composition of cell walls and external layers. In The Biology of Cyanobacteria 1982 Edited by Carr N.G., Whitton B.A. Oxford : Blackwell Scientific Publications; pp 333–357
    [Google Scholar]
  7. Felsenstein J. Confidence limits on phylogenies: an approach using the bootstrap. Evolution 1985; 39:783–791
    [Google Scholar]
  8. Fogg G.E. Marine planktonic cyanobacteria. In The Cyanobacteria 1987 Edited by Fay P., Van Baalen C. Amsterdam: Elsevier; pp 393–414
    [Google Scholar]
  9. Gantt E., Okhi K., Fujita Y. Trichodesmium thiebautii\ structure of a nitrogen-fixing marine blue-green alga (Cyanophyta). Protoplasma 1984; 119:188–196
    [Google Scholar]
  10. Geitler L. Cyanophyceae. In Rabenhorsf s Kryptogamenflora von Deutschland, Osterreich und der Schweiy 1932 Leipzig: Akademische Verslagsgesellschaft; 14: pp 1–1196 Reprinted 1971, New York: Johnson
    [Google Scholar]
  11. Giovannoni S.J., Turner S., Olsen G.J., Barns S., Lane D.J., Pace N.R. Evolutionary relationships among cyanobacteria and green chloroplasts. J Bacteriol 1988; 170:3584–3592
    [Google Scholar]
  12. Giovannoni S.J., Britschgi T.B., Moyer C.L., Field K.G. Genetic diversity in Sargasso Sea bacterioplankton. Nature 1990; 345:60–63
    [Google Scholar]
  13. Golubic S. Speciation in Trichodesmium: occupation of an oceanic pelagic niche. Schweiy Z Hydrol 1977; 39:141–143
    [Google Scholar]
  14. Gomont M. Monographic des Oscillariees (Nostocaceae homocystees). Ann Sci Nat Ser Bot 1892; 15:265–368 16, 91-264. Reprinted 1962, Weinheim, Germany: Cramer
    [Google Scholar]
  15. Graf L., Kossel H., Stutz E. Sequencing of 16S-23S spacer in a ribosomal RNA operon of Euglena gracilis chloroplast DNA reveals two tRNA genes. Nature 1980; 286:908–910
    [Google Scholar]
  16. Herdman M., Janvier M., Waterbury J.B., Rippka R., Stanier R.Y., Mandel M. Deoxyribonucleic acid base composition of cyanobacteria. J Gen Microbiol 1979; 111:63–71
    [Google Scholar]
  17. Holton T.A., Graham M.W. A simple and efficient method for direct cloning of PCR products using ddT-tailed vectors. Nucleic Acids Res 1991; 19:1156
    [Google Scholar]
  18. International Union of Biochemistry, Nomenclature Committee Nomenclature for incomplete specified bases in nucleic acid sequences. European Journal of Biochemistry 1985; 150:1–5
    [Google Scholar]
  19. Jukes T.H., Cantor C.R. Evolution of protein molecules. In Mammalian Protein Metabolism 1969 Edited by Munro H.N. New York: Academic Press; 3 pp 21–132
    [Google Scholar]
  20. Ligon P.J.B., Meyer K.G., Martin J.A., Curtis S.E. Nucleotide sequence of a 16S rRNA gene from Anabaena sp strain PCC7120. Nucleic Acids Rw 1991; 19:4553
    [Google Scholar]
  21. Neefs J.-M., Van De Peer Y., De Rijk P., Chapelle S., De Wachter R. Compilation of small ribosomal subunit RNA structures. Nucleic Acids 1993; 21:3025–3049
    [Google Scholar]
  22. Nichols J.M., Foulds I.J., Crouch D.H., Carr N.G. The diversity of cyanobacterial genomes with respect to ribosomal RNA cistrons. J Gen Microbiol 1982; 128:2739–2746
    [Google Scholar]
  23. Ohki K., Rueter J.G., Fujita Y. Cultures of the pelagic cyanophvtes Trichodesmium erythraeum and T. thiebautii in synthetic medium. Mar Biol 1986; 91:9–13
    [Google Scholar]
  24. Ohyama K., Fukuzawa H., Kohchi T., Shirai H., Sano T., Sano S., Umesono K., Shiki Y., Takeuchi M., Chang Z., Aota S.I., Inokuchi H., Ozeki H. Chloroplast gene organization deduced from complete sequence of liverwort Marchantia polymorpha chloroplast DNA. Plant Mol Biol Rep 1986; 4:148–175
    [Google Scholar]
  25. Rippka R., Deruelles J., Waterbury J.B., Herdman M., Stanier R.Y. Generic assignments, strain histories and properties of pure cultures of cyanobacteria. J Gen Microbiol 1979; 111:1–61
    [Google Scholar]
  26. Rossau R., Michielsen A., Jannes G., Duhamel M., Kersters K., Van Heuverswijn H. DNA probes for Bordetella species and a colorimetric reverse hybridization assay for the detection of Bordetella pertussis. Mol Cell Probes 1992; 6:281–289
    [Google Scholar]
  27. Saitou N., Nei M. The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 1987; 4:406–425
    [Google Scholar]
  28. Sournia A. La cyanophycee Oscillatoria (= Trichodesmium) dans le plancton marin: taxonomie, et observations dans le canal de Mozambique. Nova Hedwigia 1968; 15:1–12
    [Google Scholar]
  29. Tomioka N., Sugiura M. The complete nucleotide sequence of a 16S ribosomal RNA gene from a blue-green alga, Anacystis nidulans. Mol & Gen Genet 1983; 191:46–50
    [Google Scholar]
  30. Tomioka N., Sugiura M. Nucleotide sequence of the 16S-23S spacer region in the rrnA operon from a blue-green alga, Anacystis nidulans. Mol & Gen Genet 1984; 193:427–430
    [Google Scholar]
  31. Turner S., Burger-Wiersma T., Giovannoni S.J., Mur L.R., Pace N.R. The relationship of a prochlorophyte, Prochlorothrix hollandica, to green chloroplasts. Nature 1989; 337:380–382
    [Google Scholar]
  32. Umezaki I. On the taxonomy of the genus Trichodesmium. Bull Plankton Soc Jpn 1974; 20:93–99
    [Google Scholar]
  33. Urbach E., Robertson D.L., Chisholm S.W. Multiple evolutionary origins of prochlorophytes within the cyanobacterial radiation. Nature 1992; 355:267–270
    [Google Scholar]
  34. Van Baalen C., Brown R.M. The ultrastructure of the marine blue green alga, Trichodesmium erythraeum, with special reference to the cell wall, gas vacuoles, and cylindrical bodies. Arch Mikrobiol 1969; 69:79–91
    [Google Scholar]
  35. Van De Peer Y., De Wachter R. treecon : a software package for the construction and drawing of evolutionary trees. Comput Appl Biosci 1993; 9:177–182
    [Google Scholar]
  36. Van De Peer Y., Neefs J.M., De Wachter R. Small ribosomal subunit RNA sequences, evolutionary relationships among different life forms, and mitochondrial origins. J Mol Evol 1990; 30:463–476
    [Google Scholar]
  37. Walsby A. Cyanobacteria: planktonic gas-vacuolate forms. In The Prokaryotes 1981 Edited by Starr M.P., Stolp H., Triiper H.G., Balows A., Schlegel H.G. Berlin: Springer-Verlag; pp 224–235
    [Google Scholar]
  38. Wayne L.G., Brenner D.J., Colwell R.R., Grimont P.A.D., Kandler O., Krichevsky M.I., Moore L.H., Moore W.E.C., Murray R.G.E., Stackebrandt E., Starr M.P., Triiper H.G. Report of the ad hoc committee on reconciliation of approaches to bacterial systematics. Int J Syst Bacteriol 1987; 37:463–464
    [Google Scholar]
  39. Weller R., Walsh Weller J., Ward D.M. 16S rRNA sequences of uncultivated hot spring cyanobacterial mat inhabitants retrieved as randomly primed cDNA. Appl Environ Microbiol 1991; 57:1146–1151
    [Google Scholar]
  40. Weller R., Bateson M.M., Heimbuch B.K., Kopczinski E.D., Ward D.M. Uncultivated cyanobacteria, Chloroflexus-like inhabitants, and spirochete-like inhabitants of a hot spring microbial mat. Appl Environ Microbiol 1992; 58:3964–3969
    [Google Scholar]
  41. Williamson S.E., Doolittle W.F. Gene for tRNAIle and tRNAAla in the spacer between the 16S and 23S rRNA genes of a blue-green alga: strong homology to chloroplast tRNA genes and tRNA genes of E. coli rrnD cluster. Nucleic Acids Res 1983; 11:225–235
    [Google Scholar]
  42. Wilmotte A., Turner S., Van De Peer Y., Pace N.R. Taxonomic study of marine oscillatoriacean strains (cyanobacteria) with narrow trichomes. II. Nucleotide sequence analysis of the 16S ribosomal RNA. J Phycol 1992; 28:828–838
    [Google Scholar]
  43. Wilmotte A., Van der Auwera G., De Wachter R. Structure of the 16S ribosomal RNA of the thermophilic cyanobacterium Chlorogloeopsis HTF ('Mastigocladus laminosus HTF') strain PCC7518, and phylogenetic analysis. FEBS Eett 1993; 317:96–100
    [Google Scholar]
  44. Zehr J.P., Limberger R.J., Ohki K., Fujita Y. Antiserum to nitrogenase generated from an amplified DNA fragment from natural populations of Trichodesmium spp Appl. Environ Microbiol 1990; 56:3527–3531
    [Google Scholar]
  45. Zehr J.P., Ohki K., Fujita Y. Arrangement of nitrogenase structural genes in an aerobic filamentous non-heterocystous cyanobacterium. J Bacteriol 1991a; 173:7055–7058
    [Google Scholar]
  46. Zehr J.P., Ohki K., Fujita Y., Landry D. Unique modification of adenine in genomic DNA of the marine cyanobacterium Trichodesmium sp strain NIBB 1067. J Bacteriol 1991b; 173:7059–7062
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/micro/10.1099/13500872-140-8-2159
Loading
/content/journal/micro/10.1099/13500872-140-8-2159
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error