Isotopic tracing reveals single-cell assimilation of a macroalgal polysaccharide by a few marine Flavobacteria and Gammaproteobacteria
Algal polysaccharides constitute a diverse and abundant reservoir of organic matter for marine heterotrophic bacteria, central to the oceanic carbon cycle. We investigated the uptake of alginate, a major brown macroalgal polysaccharide, by microbial communities from kelp-dominated coastal habitats....
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Veröffentlicht in: | The ISME Journal 2021-10, Vol.15 (10), p.3062-3075 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Algal polysaccharides constitute a diverse and abundant reservoir of organic matter for marine heterotrophic bacteria, central to the oceanic carbon cycle. We investigated the uptake of alginate, a major brown macroalgal polysaccharide, by microbial communities from kelp-dominated coastal habitats. Congruent with cell growth and rapid substrate utilization, alginate amendments induced a decrease in bacterial diversity and a marked compositional shift towards copiotrophic bacteria. We traced
13
C derived from alginate into specific bacterial incorporators and quantified the uptake activity at the single-cell level, using halogen in situ hybridization coupled to nanoscale secondary ion mass spectrometry (HISH-SIMS) and DNA stable isotope probing (DNA-SIP). Cell-specific alginate uptake was observed for
Gammaproteobacteria
and
Flavobacteriales
, with carbon assimilation rates ranging from 0.14 to 27.50 fg C µm
−3
h
−1
. DNA-SIP revealed that only a few initially rare
Flavobacteriaceae
and
Alteromonadales
taxa incorporated
13
C from alginate into their biomass, accounting for most of the carbon assimilation based on bulk isotopic measurements. Functional screening of metagenomic libraries gave insights into the genes of alginolytic
Alteromonadales
active in situ. These results highlight the high degree of niche specialization in heterotrophic communities and help constraining the quantitative role of polysaccharide-degrading bacteria in coastal ecosystems. |
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ISSN: | 1751-7362 1751-7370 |
DOI: | 10.1038/s41396-021-00987-x |