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PMID: 10742262 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Natural assemblages of marine proteobacteria and members of the Cytophaga-Flavobacter cluster consuming low- and high-molecular-weight dissolved organic matter.

Applied and environmental microbiology ·Vol. 66 ·No. 4 ·2000-04-00 ·Pages 1692-7

Cottrell MT, Kirchman DL

Abstract

We used a method that combines microautoradiography with hybridization of fluorescent rRNA-targeted oligonucleotide probes to whole cells (MICRO-FISH) to test the hypothesis that the relative contributions of various phylogenetic groups to the utilization of dissolved organic matter (DOM) depend solely on their relative abundance in the bacterial community. We found that utilization of even simple low-molecular-weight DOM components by bacteria differed across the major phylogenetic groups and often did not correlate with the relative abundance of these bacterial groups in estuarine and coastal environments. The Cytophaga-Flavobacter cluster was overrepresented in the portion of the assemblage consuming chitin, N-acetylglucosamine, and protein but was generally underrepresented in the assemblage consuming amino acids. The amino acid-consuming assemblage was usually dominated by the alpha subclass of the class Proteobacteria, although the representation of alpha-proteobacteria in the protein-consuming assemblages was about that expected from their relative abundance in the entire bacterial community. In our experiments, no phylogenetic group dominated the consumption of all DOM, suggesting that the participation of a diverse assemblage of bacteria is essential for the complete degradation of complex DOM in the oceans. These results also suggest that the role of aerobic heterotrophic bacteria in carbon cycling would be more accurately described by using three groups instead of the single bacterial compartment currently used in biogeochemical models.

MeSH Terms
Cytophaga/metabolism Ecosystem Flavobacterium/metabolism In Situ Hybridization, Fluorescence/methods Organic Chemicals/metabolism Phylogeny Proteobacteria/metabolism Seawater/microbiology Water Microbiology
Chemicals
Organic Chemicals
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Cottrell M T
College of Marine Studies, University of Delaware, Lewes, Delaware 19958, USA.
Kirchman D L
References (13)
13 references, click to expand
  1. Regulation of Bacterial Growth Rates by Dissolved Organic Carbon and Temperature in the Equatorial Pacific Ocean
    Microb Ecol. 1997 Jan;33(1):11-20 PMID: 9039761
  2. Impact of culture-independent studies on the emerging phylogenetic view of bacterial diversity.
    J Bacteriol. 1998 Sep;180(18):4765-74 PMID: 9733676
  3. Genetic diversity in Sargasso Sea bacterioplankton.
    Nature. 1990 May 3;345(6270):60-3 PMID: 2330053
  4. Bacterioplankton compositions of lakes and oceans: a first comparison based on fluorescence in situ hybridization.
    Appl Environ Microbiol. 1999 Aug;65(8):3721-6 PMID: 10427073
  5. Phylogenetic identification and in situ detection of individual microbial cells without cultivation.
    Microbiol Rev. 1995 Mar;59(1):143-69 PMID: 7535888
  6. Combination of 16S rRNA-targeted oligonucleotide probes with flow cytometry for analyzing mixed microbial populations.
    Appl Environ Microbiol. 1990 Jun;56(6):1919-25 PMID: 2200342
  7. Determination of Active Marine Bacterioplankton: a Comparison of Universal 16S rRNA Probes, Autoradiography, and Nucleoid Staining.
    Appl Environ Microbiol. 1997 Apr;63(4):1208-13 PMID: 16535563
  8. Combined microautoradiography-16S rRNA probe technique for determination of radioisotope uptake by specific microbial cell types in situ.
    Appl Environ Microbiol. 1999 Apr;65(4):1746-52 PMID: 10103276
  9. Bacterial diversity in Adirondack mountain lakes as revealed by 16S rRNA gene sequences.
    Appl Environ Microbiol. 1997 Jul;63(7):2957-60 PMID: 9212443
  10. Combination of fluorescent in situ hybridization and microautoradiography-a new tool for structure-function analyses in microbial ecology.
    Appl Environ Microbiol. 1999 Mar;65(3):1289-97 PMID: 10049895
  11. In situ probing of gram-positive bacteria with high DNA G + C content using 23S rRNA-targeted oligonucleotides.
    Microbiology. 1994 Oct;140 ( Pt 10):2849-58 PMID: 8000548
  12. Application of a suite of 16S rRNA-specific oligonucleotide probes designed to investigate bacteria of the phylum cytophaga-flavobacter-bacteroides in the natural environment.
    Microbiology. 1996 May;142 ( Pt 5):1097-106 PMID: 8704951
  13. Bacterial diversity among small-subunit rRNA gene clones and cellular isolates from the same seawater sample.
    Appl Environ Microbiol. 1997 Mar;63(3):983-9 PMID: 9055415
Article Info
Journal
Applied and environmental microbiology
Abbr.
Appl Environ Microbiol
ISSN
0099-2240
Published
2000-04-00
Pages
1692-7
Language
English
Region
United States
NLM ID
7605801
PMCID
PMC92043
Subset
IM
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