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Journal ArticleDOI

Genetic diversity in Sargasso Sea bacterioplankton.

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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Journal ArticleDOI

Rapid detection and quantification of members of the archaeal community by quantitative PCR using fluorogenic probes.

TL;DR: A rapid, reproducible, and sensitive method for detection and quantification of archaea in naturally occurring microbial communities and is applicable to culture-independent molecular analysis of microbial communities in various environments is described.
Journal ArticleDOI

Marine biodiversity: patterns, threats and conservation needs

TL;DR: Marine biodiversity is higher in benthic rather than pelagic systems, and in coasts rather than the open ocean since there is a greater range of habitats near the coast as mentioned in this paper.
Journal ArticleDOI

Bacterial Endophytes: Potential Role in Developing Sustainable Systems of Crop Production

TL;DR: Bacterial endophytes have been implicated in supplying biologically fixed nitrogen in non-legumes, and these associations can increase the nitrogen economy of a crop, reducing the requirement for N fertilizers.
Book ChapterDOI

In situ identification of micro-organisms by whole cell hybridization with rRNA-targeted nucleic acid probes

TL;DR: The sequencing of 16S and 23S ribosomal RNA molecules is currently the gold standard for the classification of new microbial isolates and microbial ecologists who want to apply this approach to investigate correlations between community structures and functions should be aware of this fact and design or apply rRNA-targeted probes accordingly.
Journal ArticleDOI

Physiology and molecular phylogeny of coexisting Prochlorococcus ecotypes

TL;DR: Direct evidence supporting the coexistence and distribution of multiple ecotypes permits the survival of the population as a whole over a broader range of environmental conditions than would be possible for a homogeneous population is reported.
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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