Access the full text.
Sign up today, get DeepDyve free for 14 days.
J. Sperber (1958)
The incidence of apatite-solubilizing organisms in the rhizosphere and soilCrop & Pasture Science, 9
D. Boone, Y. Liu, Z. Zhao, D. Balkwill, G. Drake, T. Stevens, H. Aldrich (1995)
Bacillus infernus sp. nov., an Fe(III)- and Mn(IV)-reducing anaerobe from the deep terrestrial subsurface.International journal of systematic bacteriology, 45 3
E. Yabuuchi, I. Yano, H. Oyaizu, Y. Hashimoto, T. Ezaki, Hiroyuki Yamamoto (1990)
Proposals of Sphingomonas paucimobilis gen. nov. and comb. nov., Sphingomonas parapaucimobilis sp. nov., Sphingomonas yanoikuyae sp. nov., Sphingomonas adhaesiva sp. nov., Sphingomonas capsulata comb, nov., and Two Genospecies of the Genus SphingomonasMicrobiology and Immunology, 34
G. Olsen, H. Matsuda, R. Hagstrom, R. Overbeek (1994)
fastDNAmL: a tool for construction of phylogenetic trees of DNA sequences using maximum likelihoodComputer applications in the biosciences : CABIOS, 10 1
T. Phelps, C. Fliermans, T. Garland, S. Pfiffner, D. White (1989)
Methods for recovery of deep terrestrial subsurface sediments for microbiological studiesJournal of Microbiological Methods, 9
E. Stackebrandt, B. Goebel (1994)
Taxonomic Note: A Place for DNA-DNA Reassociation and 16S rRNA Sequence Analysis in the Present Species Definition in BacteriologyInternational Journal of Systematic and Evolutionary Microbiology, 44
R. Gutell (1993)
Collection of small subunit (16S- and 16S-like) ribosomal RNA structures: 1994.Nucleic acids research, 22 17
R. Gutell, N. Larsen, C. Woese (1994)
Lessons from an evolving rRNA: 16S and 23S rRNA structures from a comparative perspective.Microbiological reviews, 58 1
F. Colwell, G. Stormberg, T.J Phelps, S.A Birnbaum, J. McKinley, S. Rawson, C. Veverka, S. Goodwin, P.E Long, B. Russell, T. Garland, D. Thompson, P. Skinner, S. Grover (1992)
Innovative techniques for collection of saturated and unsaturated subsurface basalts and sediments for microbiological characterizationJournal of Microbiological Methods, 15
D. Balkwill (1989)
Numbers, diversity, and morphological characteristics of aerobic, chemoheterotrophic bacteria in deep subsurface sediments from a site in South CarolinaGeomicrobiology Journal, 7
G. Olsen (1988)
Phylogenetic analysis using ribosomal RNA.Methods in enzymology, 164
James Fredrickson, F. Brockman, D. Workman, S. Li, T. Stevens (1991)
Isolation and Characterization of a Subsurface Bacterium Capable of Growth on Toluene, Naphthalene, and Other Aromatic CompoundsApplied and Environmental Microbiology, 57
J. Sinclair, W. Ghiorse (1989)
Distribution of aerobic bacteria, protozoa, algae, and fungi in deep subsurface sedimentsGeomicrobiology Journal, 7
A. Francis, J. Slater, C. Dodge (1989)
Denitrification in deep subsurface sedimentsGeomicrobiology Journal, 7
W. Fitch, E. Margoliash (1967)
Construction of phylogenetic trees.Science, 155 3760
R. Hicks, J. Fredrickson (1989)
Aerobic metabolic potential of microbial populations indigenous to deep subsurface environmentsGeomicrobiology Journal, 7
L. Mcbride, S. Koepf, R. Gibbs, W. Salser, P. Mayrand, M. Hunkapiller, M. Kronick (1989)
Automated DNA sequencing methods involving polymerase chain reaction.Clinical chemistry, 35 11
W. Weisburg, S. Barns, D. Pelletier, S. Goodison (1991)
16S ribosomal DNA amplification for phylogenetic studyJournal of Bacteriology, 173
K. Reed, D. Mann (1985)
Rapid transfer of DNA from agarose gels to nylon membranes.Nucleic acids research, 13 20
K. Pedersen, J. Arlinger, S. Ekendahl, L. Hallbeck (1996)
16S rRNA gene diversity of attached and unattached bacteria in boreholes along the access tunnel to the Äspö hard rock laboratory, SwedenFEMS Microbiology Ecology, 19
K. Pedersen, J. Arlinger, L. Hallbeck, C. Pettersson (1996)
Diversity and distribution of subterranean bacteria in groundwater at Oklo in Gabon, Africa, as determined by 16S rRNA gene sequencingMolecular Ecology, 5
B. Martin, O. Humbert, M. Cámara, E. Guenzi, John Walker, T. Mitchell, P. Andrew, M. Prudhomme, G. Alloing, R. Hakenbeck, D. Morrison, G. Boulnois, J. Claverys (1992)
A highly conserved repeated DNA element located in the chromosome of Streptococcus pneumoniaeNucleic acids research, 20 13
D. Balkwill, G. Drake, R. Reeves, J. Fredrickson, D. White, D. Ringelberg, D. Chandler, M. Romine, D. Kennedy, C. Spadoni (1997)
Taxonomic study of aromatic-degrading bacteria from deep-terrestrial-subsurface sediments and description of Sphingomonas aromaticivorans sp. nov., Sphingomonas subterranea sp. nov., and Sphingomonas stygia sp. nov.International journal of systematic bacteriology, 47 1
R. Reeves, J. Reeves, D. Balkwill (1995)
Strategies for phylogenetic characterization of subsurface bacteriaJournal of Microbiological Methods, 21
James Fredrickson, D. Balkwill, G. Drake, M. Romine, D. Ringelberg, David White (1995)
Aromatic-degrading Sphingomonas isolates from the deep subsurfaceApplied and Environmental Microbiology, 61
D. Lane, B. Pace, G. Olsen, D. Stahl, M. Sogin, N. Pace (1985)
Rapid determination of 16S ribosomal RNA sequences for phylogenetic analyses.Proceedings of the National Academy of Sciences of the United States of America, 82 20
A. Wollum (1982)
Cultural Methods for Soil Microorganisms
G. Olsen, D. Lane, S. Giovannoni, N. Pace, D. Stahl (1986)
Microbial ecology and evolution: a ribosomal RNA approach.Annual review of microbiology, 40
J. Fredrickson, D. Balkwill, J. Zachara, Shu-mei Li, F. Brockman, M. Simmons (1991)
Physiological Diversity and Distributions of Heterotrophic Bacteria in Deep Cretaceous Sediments of the Atlantic Coastal PlainApplied and Environmental Microbiology, 57
J. Brosius, M. Palmer, P. Kennedy, H. Noller (1978)
Complete nucleotide sequence of a 16S ribosomal RNA gene from Escherichia coli.Proceedings of the National Academy of Sciences of the United States of America, 75 10
J. Sambrook, E. Fritsch, T. Maniatis (2001)
Molecular Cloning: A Laboratory Manual
F. Rainey, E. Lang, E. Stackebrandt (1994)
The phylogenetic structure of the genus Acinetobacter.FEMS microbiology letters, 124 3
J. Felsenstein (1985)
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAPEvolution, 39
J. Fredrickson, T. Garland, R. Hicks, J. Thomas, S. Li, K. McFadden (1989)
Lithotrophic and Heterotrophic Bacteria in Deep Subsurface Sediments and Their Relation to Sediment PropertiesGeomicrobiology Journal, 7
T. Jukes (1969)
CHAPTER 24 – Evolution of Protein Molecules
J. Fredrickson, J. Mckinley, S. Nierzwicki-Bauer, D. White, D. Ringelberg, S. Rawson, Shu-mei Li, F. Brockman, B. Bjornstad (1995)
Microbial community structure and biogeochemistry of Miocene subsurface sediments: implications for long‐term microbial survivalMolecular Ecology, 4
E. Boquet, A. Boronat, A. Ramos‐Cormenzana (1973)
Production of Calcite (Calcium Carbonate) Crystals by Soil Bacteria is a General PhenomenonNature, 246
A. Rosado, G. Duarte, L. Seldin (1994)
Optimization of electroporation procedure to transform B. polymyxa SCE2 and other nitrogen-fixing BacillusJournal of Microbiological Methods, 19
K. Sargent, C. Fliermans (1989)
Geology and hydrology of the deep subsurface microbiology sampling sites at the savannah river plant, South CarotinaGeomicrobiology Journal, 7
Ralph Jones, R. Beeman, J. Suflita (1989)
Anaerobic metabolic processes in the deep terrestrial subsurfaceGeomicrobiology Journal, 7
P. Amy, D. Haldeman, D. Ringelberg, D. Hall, Charles Russell (1992)
Comparison of Identification Systems for Classification of Bacteria Isolated from Water and Endolithic Habitats within the Deep SubsurfaceApplied and Environmental Microbiology, 58
F. Louws, D. Fulbright, C. Taylor, Stephens, F. Bruijn (1994)
Specific genomic fingerprints of phytopathogenic Xanthomonas and Pseudomonas pathovars and strains generated with repetitive sequences and PCRApplied and Environmental Microbiology, 60
J. Fredrickson, F. Brockman, B. Bjornstad, P. Long, S. Li, J. Mckinley, J. Wright, J. Conca, T. Kieft, D. Balkwill (1993)
Microbiological characteristics of pristine and contaminated deep vadose sediments from an arid regionGeomicrobiology Journal, 11
W. Ghiorse, John Wilson (1988)
Microbial ecology of the terrestrial subsurface.Advances in applied microbiology, 33
T. Kieft, J. Fredrickson, J. Mckinley, B. Bjornstad, S. Rawson, T. Phelps, F. Brockman, S. Pfiffner (1995)
Microbiological Comparisons within and across Contiguous Lacustrine, Paleosol, and Fluvial Subsurface SedimentsApplied and Environmental Microbiology, 61
V. Boivin-Jahns, A. Bianchi, R. Ruimy, J. Garcin, S. Daumas, R. Christen (1995)
Comparison of phenotypical and molecular methods for the identification of bacterial strains isolated from a deep subsurface environmentApplied and Environmental Microbiology, 61
C. Fliermans, D. Balkwill (1989)
Microbial life in deep terrestrial subsurfacesBioScience, 39
T. Stevens, B. Holbert (1995)
Variability and density dependence of bacteria in terrestrial subsurface samples: implications for enumerationJournal of Microbiological Methods, 21
N. Larsen, G. Olsen, B. Maidak, M. McCaughey, R. Overbeek, T. Macke, T. Marsh, C. Woese (1992)
The ribosomal database projectNucleic acids research, 21 13
D. Balkwill, J. Fredrickson, J. Thomas (1989)
Vertical and Horizontal Variations in the Physiological Diversity of the Aerobic Chemoheterotrophic Bacterial Microflora in Deep Southeast Coastal Plain Subsurface SedimentsApplied and Environmental Microbiology, 55
T. Phelps, E. Raione, D. White, C. Fliermans (1988)
Microbial activities in deep subsurface environmentsGeomicrobiology Journal, 7
S. Ekendahl, J. Arlinger, F. Ståhl, K. Pedersen (1994)
Characterization of attached bacterial populations in deep granitic groundwater from the Stripa research mine by 16S rRNA gene sequencing and scanning electron microscopy.Microbiology, 140 ( Pt 7)
Yitai Liu, T. Karnauchow, K. Jarrell, D. Balkwill, G. Drake, D. Ringelberg, Ronald Clarno, D. Boone (1997)
Description of two new thermophilic Desulfotomaculum spp., Desulfotomaculum putei sp. nov., from a deep terrestrial subsurface, and Desulfotomaculum luciae sp. nov., from a hot springInternational Journal of Systematic and Evolutionary Microbiology, 47
B. Russell, T. Phelps, W. Griffin, K. Sargent (1992)
Procedures for Sampling Deep Subsurface Microbial Communities in Unconsolidated SedimentsGround Water Monitoring and Remediation, 12
AbstractThe Subsurface Microbial Culture Collection (SMCC) was established by the U.S. Dept. of Energy (DOE) and contains nearly 10,000 strains of microorganisms (mostly bacteria) isolated from terrestrial subsurface environments. Selected groups of bacterial isolates from three sample sites situated above geochemically and hydrologically different subsurface environments have been characterized by phylogenetic analysis of 16S ribosomal RNA (rRNA) gene nucleotide sequences. Among these isolates were members of six major phylogenetic groups of bacteria: the high-G+C and low-G+C Gram-positive bacteria; the α-, β-, and γ-subdivisions of the Proteobacteria; and the Flexibacter/Cytophaga/Bacteroides group. A small number of the SMCC strains may be members of new bacterial genera, but most of them could be placed with reasonable confidence into more than 35 previously described genera. The majority of the Gram-positive isolates were species of Arthrobacter, Bacillus, or Streptococcus, whereas Acinetobacter, Comamonas, Pseudomonas, Sphingomonas, and Variovorax were among the most frequently encountered Gram-negative genera. A high proportion of the strains were placed in fewer than 10 genera, implying that there is substantial duplication within the SMCC at the genus level. When groups of isolates assigned to Acinetobacter, Arthrobacter, or Sphingomonas were analyzed in more detail, however, it was found that each group consisted of subgroups of strains that probably differed at the species level. Restriction endonuclease analysis (applied to the strains from one sample site) indicated that additional diversity was present at the strain level. Most of the SMCC isolates assigned to some genera (e.g., Acinetobacter) were very closely related to previously described species in those genera, but most of the isolates assigned to other genera (e.g., Arthrobacter and Sphingomonas) appeared (or were shown) to be new species, thereby indicating that a reasonable amount of novelty is present within the SMCC at the species level.
FEMS Microbiology Reviews – Oxford University Press
Published: Jul 17, 1997
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.