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Genetic diversity in Sargasso Sea bacterioplankton.

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TLDR
The phylogenetically analysed clone libraries of eubacterial 16S ribosomal RNA genes amplified from natural populations of Sargasso Sea picoplankton indicate the presence of a novel microbial group, the SAR 11 cluster, which appears to be a significant component of this oligotrophic bacterioplankton community.
Abstract
BACTERIOPLANKTON are recognized as important agents of biogeochemical change in marine ecosystems, yet relatively little is known about the species that make up these communities. Uncertainties about the genetic structure and diversity of natural bacterioplankton populations stem from the traditional difficulties associated with microbial cultivation techniques. Discrepancies between direct counts and plate counts are typically several orders of magnitude, raising doubts as to whether cultivated marine bacteria are actually representative of dominant planktonic species1–3. We have phylogenetically analysed clone libraries of eubacterial 16S ribosomal RNA genes amplified from natural populations of Sargasso Sea picoplankton by the polymerase chain reaction4. The analysis indicates the presence of a novel microbial group, the SAR 11 cluster, which appears to be a significant component of this oligotrophic bacterioplankton community. A second cluster of lineages related to the oxygenic phototrophs—cyanobacteria, prochlorophytes and chloroplasts—was also observed. However, none of the genes matched the small subunit rRNA sequences of cultivated marine cyanobacteria from similar habitats. The diversity of 16S rRNA genes observed within the clusters suggests that these bacterioplankton may be consortia of independent lineages sharing surprisingly distant common ancestors.

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Citations
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Molecular microbial diversity of an anaerobic digestor as determined by small-subunit rDNA sequence analysis.

TL;DR: The bacterial community structure of a fluidized-bed reactor fed by vinasses (wine distillation waste) was analyzed and four small-subunit (SSU) rDNA clone libraries of Bacteria, Archaea, Procarya, and Eucarya populations were established.
Journal ArticleDOI

Bacterioplankton compositions of lakes and oceans: a first comparison based on fluorescence in situ hybridization.

TL;DR: FISH with rRNA-targeted oligonucleotide probes was used to investigate the phylogenetic composition of bacterioplankton communities in several freshwater and marine samples, finding that Beta subclass proteobacteria constituted a dominant fraction in freshwater systems and members of the Cytophaga-Flavobacterium cluster were the most abundant group detected in the marine systems.
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Typical freshwater bacteria: an analysis of available 16S rRNA gene sequences from plankton of lakes and rivers

TL;DR: It is shown that rivers and lakes have a specific planktonic bacterial community distinct from bacteria in neighboring environments such as soil and sediments, and it is pointed out that these planktonics bacteria are distributed in diverse fresh- water ecosystems around the world.
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Microbial Evolution, Diversity, and Ecology: A Decade of Ribosomal RNA Analysis of Uncultivated Microorganisms

TL;DR: This review provides an outline of the main methods used in molecular microbial ecology, and their limitations, with reference to morphologically distinctive, uncultivated bacteria; an important biotechnological process (wastewater treatment); and symbiotic relationships between Bacteria, Archaea and Eukarya.
Journal ArticleDOI

Ecology and exploration of the rare biosphere

TL;DR: The ecology of rare microbial populations is discussed, molecular and computational methods for targeting taxonomic 'blind spots' within the rare biosphere of complex microbial communities are highlighted, and the value of studying the biogeography of microorganisms is highlighted.
References
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Journal ArticleDOI

DNA sequencing with chain-terminating inhibitors

TL;DR: A new method for determining nucleotide sequences in DNA is described, which makes use of the 2',3'-dideoxy and arabinon nucleoside analogues of the normal deoxynucleoside triphosphates, which act as specific chain-terminating inhibitors of DNA polymerase.
Journal ArticleDOI

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

TL;DR: A thermostable DNA polymerase was used in an in vitro DNA amplification procedure, the polymerase chain reaction, which significantly improves the specificity, yield, sensitivity, and length of products that can be amplified.
Journal ArticleDOI

Site-directed mutagenesis by overlap extension using the polymerase chain reaction.

TL;DR: In this paper, complementary oligodeoxyribonucleotide (oligo) primers and the polymerase chain reaction are used to generate two DNA fragments having overlapping ends, and these fragments are combined in a subsequent 'fusion' reaction in which the overlapping ends anneal, allowing the 3' overlap of each strand to serve as a primer for the three' extension of the complementary strand.
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