Related Experiment Video
Updated: Sep 26, 2026

Hierarchical and Programmable One-Pot Oligosaccharide Synthesis
Published on: September 6, 2019
Alkane-oxidizing consortia produce substantial amounts of disaccharides
Stian Torset1,2,3,4, Lennart Stock3,5,6, Marcus Elvert3,5
1Max Planck Institute for Marine Microbiology, Bremen, Germany.
Abstract:
Consortia of archaea and partner bacteria couple the anaerobic oxidation of alkanes to sulfate reduction. While the catabolic pathways in anaerobic alkane-oxidizing archaea (ANKA) have been extensively studied, their anabolic capacities remain poorly understood. Here, we examined nine enrichment cultures dominated by ANKA and their partner bacteria for small-molecular compounds using solvent extraction and gas chromatographic analysis of derivatized extracts. All alkane-degrading cultures contained substantial amounts of disaccharides in their metabolite pools. Cold-adapted methane-oxidizing cultures dominated by ANME-2c and Seep-SRB2 contained up to 1.5 mg of trehalose per mg soluble protein. Trehalose was also abundant in ethane-oxidizing cultures of Candidatus Ethanoperedens and its distinct partner SRBs, accounting for up to 75% of the extracted metabolites. In contrast, thermophilic ANKA cultures dominated by ANME-1 or Candidatus Syntropharchaeum and Candidatus Desulfofervidus contained an abundant as-yet-unidentified hexose-containing disaccharide. Metagenomic analysis revealed widespread trehalose metabolism genes among partner Desulfobacterota and in ANME-2c and Ca. Ethanoperedens, but lower potential in ANME-1 and Ca. Syntropharchaeum, consistent with metabolite profiles. When exogenous trehalose was added to a thermophilic ethane-oxidizing enrichment, we observed rapid metabolization by heterotrophic microorganisms but poor assimilation by the Ca. Ethanoperedens/Ca. Desulfofervidus core community, indicating that ANKA/SRB consortia do not consume externally supplied trehalose. Instead, Ca. Ethanoperedens/Ca. Desulfofervidus, as well as other ANKA/SRB consortia, may use the disaccharides as energy-storage molecules, osmolytes, or components of the extracellular matrix. The disaccharides produced by the consortia also sustain ancillary heterotrophs, thereby linking alkane oxidation to broader sedimentary carbon cycling.
Related Concept Videos
Oxidation of Alcohols
The process of oxidation in a chemical reaction is observed in any of the three forms:
Preparation of Aldehydes and Ketones from Alcohols, Alkenes, and Alkynes
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Acid-Catalyzed Dehydration of Alcohols to Alkenes
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
Oxidations of Aldehydes and Ketones to Carboxylic Acids
Aldehydes readily undergo oxidation in strong oxidizing agents such as potassium permanganate and chromic acid. The oxidation can also be carried out using mild oxidizing agents such as silver oxide. In fact, aldehydes can be easily oxidized...

