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Marine Planktonic Archaea Take Up Amino Acids

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Date 2000 Oct 31
PMID 11055931
Citations 103
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Abstract

Archaea are traditionally thought of as "extremophiles," but recent studies have shown that marine planktonic Archaea make up a surprisingly large percentage of ocean midwater microbial communities, up to 60% of the total prokaryotes. However, the basic physiology and contribution of Archaea to community microbial activity remain unknown. We have studied Archaea from 200-m depths of the northwest Mediterranean Sea and the Pacific Ocean near California, measuring the archaeal activity under simulated natural conditions (8 to 17 degrees C, dark and aerobic [corrected]) by means of a method called substrate tracking autoradiography fluorescence in situ hybridization (STARFISH) that simultaneously detects specific cell types by 16S rRNA probe binding and activity by microautoradiography. In the 200-m-deep Mediterranean and Pacific samples, cells binding the archaeal probes made up about 43 and 14% of the total countable cells, respectively. Our results showed that the Archaea are active in the uptake of dissolved amino acids from natural concentrations (nanomolar) with about 60% of the individuals in the archaeal communities showing measurable uptake. Bacteria showed a similar proportion of active cells. We concluded that a portion of these Archaea is heterotrophic and also appears to coexist successfully with Bacteria in the same water.

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References
1.
Delong E . Archaea in coastal marine environments. Proc Natl Acad Sci U S A. 1992; 89(12):5685-9. PMC: 49357. DOI: 10.1073/pnas.89.12.5685. View

2.
Brock T, Brock M . Autoradiography as a tool in microbial ecology. Nature. 1966; 209(5024):734-6. DOI: 10.1038/209734a0. View

3.
Cottrell M, Kirchman D . Natural assemblages of marine proteobacteria and members of the Cytophaga-Flavobacter cluster consuming low- and high-molecular-weight dissolved organic matter. Appl Environ Microbiol. 2000; 66(4):1692-7. PMC: 92043. DOI: 10.1128/AEM.66.4.1692-1697.2000. View

4.
Braun-Howland E, Danielsen S, Nierzwicki-Bauer S . Development of a rapid method for detecting bacterial cells in situ using 16S rRNA-targeted probes. Biotechniques. 1992; 13(6):928-34. View

5.
Brunk C, Avaniss-Aghajani E, Brunk C . A computer analysis of primer and probe hybridization potential with bacterial small-subunit rRNA sequences. Appl Environ Microbiol. 1996; 62(3):872-9. PMC: 167853. DOI: 10.1128/aem.62.3.872-879.1996. View