It is shown that fucoidans are degraded through synergistic interactions between specialized bacteria with complementary metabolic functions, providing a mechanistic framework for understanding carbon cycling in the ocean and for engineering synthetic microbial consortia to degrade recalcitrant polysaccharides.
Abstract
Fucoidans, a class of complex polysaccharides produced by brown algae and diatoms, contribute to long-term carbon sequestration owing to their resistance to microbial degradation1,2. Although individual microorganisms can break down portions of these polysaccharides3-5, it remains unclear whether complete breakdown is possible in nature and, if so, by what mechanisms. Here we show that fucoidans are degraded through synergistic interactions between specialized bacteria with complementary metabolic functions. Using metabolomic analysis of a reconstructed marine consortium, we uncovered metabolic guilds of bacteria that preferentially degrade either the sulfated fucose backbone or the side branches of rare monomers. This functional division of labour leads to an unexpectedly high number of synergistic interactions between different degraders that enhanced degradation efficiency up to 97.1%. Despite varying fucoidan structures across different types of algae6, the metabolic functions of degraders remained conserved, enabling quantitative prediction of degradation outcomes based on community and substrate composition. The frequent co-occurrence of functionally complementary fucoidan degraders in ocean metagenomes suggests that synergistic degradation is a globally relevant strategy. Our findings suggest that the environmental turnover of complex biopolymers depends not only on individual metabolic capabilities of degraders but also on ecological interactions shaped by substrate architecture. This work provides a mechanistic framework for understanding carbon cycling in the ocean and for engineering synthetic microbial consortia to degrade recalcitrant polysaccharides.
Brown macroalgae secrete complex carbohydrate polymers, their extracellular matrix, as protection against microbial degradation, which can contribute to marine carbon sequestration, though mechanisms, extent, and timescales remain unknown.
Inga Hellige, H. Buck-Wiese, M. Bligh et al.· bioRxiv· 0 citations
Fucoidans, also known as fucose-containing sulfated polysaccharides (FCSPs), are abundant and structurally complex glycans found in the cell wall of brown algae. These compounds have been shown to have fundamental roles in the development and physiology of these organisms, to provide a major contribution to marine carb...
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A wide range of microorganisms produce storage biopolymer polyhydroxyalkanoates (sPHAs) as carbon and energy reserves. However, only bacteria and fungi are known to degrade microbial sPHAs, using enzymes called polyhydroxyalkanoate depolymerases (PHADs). Here we show that some animals also have PHADs that can degrade s...
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The "labor division" during glycan degradation is characterized across four bacterial fractions: cytoplasm, outer membrane, extracellular vesicles, and supernatant, revealing a synergistic multicomponent strategy for glycan degradation in Bacteroides.
Ying He, Ziyang Yu, Qi-Qiong Li et al.· Journal of Agricultural and...· 0 citations
The enrichment and expression of polyphenol degradation pathways define a previously underappreciated metabolic niche for SAR116 and provides new evidence emphasizing the importance of polyphenol metabolism in the marine carbon cycle.
Jordan T. Coelho, M. Borton, J. Thrash· bioRxiv· 0 citations
It is revealed that a globally distributed clade of symbiotic SRB has a conserved core metabolism that diverges from free-living relatives, and these endosymbionts retain key traits of SRB such as sulfate reduction, complete oxidation of acetate to CO2, amino acid degradation for nitrogen acquisition, and transport of...
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