Evidence map›Paper›PMID 30116038›Full record

ArticleThe ISME journal2019

Biphasic cellular adaptations and ecological implications of Alteromonas macleodii degrading a mixture of algal polysaccharides.

Hanna Koch, Alexandra Dürwald, Thomas Schweder, Beatriz Noriega-Ortega, Silvia Vidal-Melgosa, Jan-Hendrik Hehemann, Thorsten Dittmar, Heike M Freese, Dörte Becher, Meinhard Simon and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The ISME journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
6.6field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 89 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Hanna KochInstitute for Chemistry and Biology of the Marine Environment, University of Oldenburg, Oldenburg, Germany.
Alexandra DürwaldInstitute of Marine Biotechnology, Greifswald, Germany.
Thomas SchwederInstitute of Marine Biotechnology, Greifswald, Germany.ORCID http://orcid.org/0000-0002-7213-3596
Beatriz Noriega-OrtegaICBM-MPI Bridging Group for Marine Geochemistry, University of Oldenburg, Oldenburg, Germany.
Silvia Vidal-MelgosaMARUM-MPI Bridge Group for Marine Glycobiology, University of Bremen, Bremen, Germany.
Jan-Hendrik HehemannMARUM-MPI Bridge Group for Marine Glycobiology, University of Bremen, Bremen, Germany.
Thorsten DittmarICBM-MPI Bridging Group for Marine Geochemistry, University of Oldenburg, Oldenburg, Germany.ORCID http://orcid.org/0000-0002-3462-0107
Heike M FreeseLeibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Dörte BecherInstitute of Marine Biotechnology, Greifswald, Germany.
Meinhard SimonInstitute for Chemistry and Biology of the Marine Environment, University of Oldenburg, Oldenburg, Germany.
Matthias WietzInstitute for Chemistry and Biology of the Marine Environment, University of Oldenburg, Oldenburg, Germany. matthias.wietz@uni-oldenburg.de.ORCID http://orcid.org/0000-0002-9786-3026
Carl von Ossietzky Universität Oldenburg · DEUniversitätsmedizin Greifswald · DEUniversity of Bremen · DELeibniz Institute DSMZ – German Collection of Microorganisms and Cell Cultures · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Algal polysaccharides are an important bacterial nutrient source and central component of marine food webs. However, cellular and ecological aspects concerning the bacterial degradation of polysaccharide mixtures, as presumably abundant in natural habitats, are poorly understood. Here, we contextualize marine polysaccharide mixtures and their bacterial utilization in several ways using the model bacterium Alteromonas macleodii 83-1, which can degrade multiple algal polysaccharides and contributes to polysaccharide degradation in the oceans. Transcriptomic, proteomic and exometabolomic profiling revealed cellular adaptations of A. macleodii 83-1 when degrading a mix of laminarin, alginate and pectin. Strain 83-1 exhibited substrate prioritization driven by catabolite repression, with initial laminarin utilization followed by simultaneous alginate/pectin utilization. This biphasic phenotype coincided with pronounced shifts in gene expression, protein abundance and metabolite secretion, mainly involving CAZymes/polysaccharide utilization loci but also other functional traits. Distinct temporal changes in exometabolome composition, including the alginate/pectin-specific secretion of pyrroloquinoline quinone, suggest that substrate-dependent adaptations influence chemical interactions within the community. The ecological relevance of cellular adaptations was underlined by molecular evidence that common marine macroalgae, in particular Saccharina and Fucus, release mixtures of alginate and pectin-like rhamnogalacturonan. Moreover, CAZyme microdiversity and the genomic predisposition towards polysaccharide mixtures among Alteromonas spp. suggest polysaccharide-related traits as an ecophysiological factor, potentially relating to distinct 'carbohydrate utilization types' with different ecological strategies. Considering the substantial primary productivity of algae on global scales, these insights contribute to the understanding of bacteria-algae interactions and the remineralization of chemically diverse polysaccharide pools, a key step in marine carbon cycling.

Indexed as

AcclimatizationAdaptation, PhysiologicalAlginatesAlteromonasEcosystemPolysaccharidesProteomicsAlginatesPolysaccharides

Identifiers

PMID30116038
PMCPMC6298977
OpenAlexW2887944254

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.