Aitian Tian, Hongliang Gao, Yanfang Sun, Jingyu Zhang, Shuchang Wang, Yanning Niu, Chunjing Zou, Caifeng Jia, Zhongyi Chang, Jing Huang, Deming Jiang
Sulfated polysaccharides with significant biological activities were widely applied in functional food, cosmetic, biomedical and pharmaceutical industries. In this study, we established a practical high-throughput screening workflow for sulfated polysaccharide-producing bacteria and applied it to natto-derived isolates. Using this approach, a sulfated polysaccharide produced by Bacillus subtilis var. natto GX10-35 with the yield of 0.86 mg/mL was isolated and a purified polysaccharide fraction, GX10-35-P1, was obtained from its fermentation broth. Chemical analyses showed the sulfate content of the sulfated polysaccharide GX10-35-P1 was 12.02%. Spectroscopic analyses suggests that GX10-35-P1 is a sulfated exopolysaccharide with distinct structural features, with a proposed backbone consisting of α-D-Galp-(1→6)-α-D-Glcp-(1→→6)-α-D-Glcp-(1→→6)-α-D-Glcp-(1→6)-α-D-Galp3S-(1→6)-α-D-Glcp-(1→6)-α-D-Glcp-(1→6)-α-D-Glcp-(1→, indicating it could be classified as an unreported type of water-soluble sulfated exopolysaccharide from bacteria. Moreover, GX10-35-P1 could induce murine macrophage cells RAW264.7 to proliferation, phagocytic, release nitric oxide and promote the mRNA expression of TNF-α, IL-1β, IL-6 and IL-10 cytokines. These results indicate that GX10-35-P1 is a promising bacterial sulfated polysaccharide with potential for further investigation as an immunomodulatory agent.