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Updated: May 8, 2026

Immobilization of Multi-biocatalysts in Alginate Beads for Cofactor Regeneration and Improved Reusability
Published on: April 22, 2016
Formation of dimers delayed alginate degradation in fecal microbiota fermentation
Dan Yuan1, Wenqian Xiao2, Xingyu Tao2
1Hubei Key Laboratory of Industry Microbiology, Hubei University of Technology, Nanli Road, Wuhan 430068, PR China; Cooperative Innovation Center of Industrial Fermentation (Ministry of Education & Hubei Province), Hubei University of Technology, Nanli Road, Wuhan 430068, PR China; Glyn O. Phillips Hydrocolloid Research Centre, School of Life and Health Sciences, Hubei University of Technology, Nanli Road, Wuhan 430068, PR China.
Abstract:
The present study was to examine the dimer formation of two alginate chains and its degradation in gut microbiota using an in vitro colon fermentation model. The most rapid degradation stage of guluronate in alginate was from 6 h to 24 h (1.68 μg/mL/h), while guluronate in dimers was from 24 h to 36 h (1.69 μg/mL/h). The degradation extent of alginate (97.40 %) was remarkably higher than that of dimers (84.20 %) in 48 h fermentation. Fecal microbiota randomly cleaved alginate into discrete mannuronate blocks (M-blocks), guluronate blocks (G-blocks), or M/G G-blocks. In contrast, dimers were sequentially cleaved into M-blocks before the crosslinked G-blocks. Approximately 25 % of crosslinked G-blocks survived the 48-h fermentation. Furthermore, three Bacteroides spp. strains could collaboratively degrade M-blocks and then crosslinked G-blocks in dimers sequentially. Collectively, the crosslinked G-blocks impeded the dimer degradation by fecal microbiota, presenting a slower degradation rate and a lesser degradation extent.

