{Reference Type}: Journal Article
{Title}: Characterization of a novel carbohydrate-binding module specifically binding to the major structural units of porphyran.
{Author}: Mei X;Zhang Y;Liu G;Shen J;Han J;Xue C;Xiao H;Chang Y;
{Journal}: Int J Biol Macromol
{Volume}: 253
{Issue}: 0
{Year}: 2023 Dec 31
{Factor}: 8.025
{DOI}: 10.1016/j.ijbiomac.2023.127106
{Abstract}: Porphyran is a promising bioactive polysaccharide majorly composed of 4-linked α-l-galactopyranose-6-sulfate (L6S) and 3-linked β-d-galactopyranose (G) disaccharide repeating units. Carbohydrate-binding modules (CBMs) have been verified to be essential tools for investigating polysaccharides. However, no confirmed CBM binding to porphyran has been hitherto reported. In this study, an unknown domain with a predicted β-sandwich fold from a potential GH86 porphyranase was discovered, and further recombinantly expressed. The CBM protein (named FvCBM99) presented a desired specificity for porphyran tetrasaccharide with an affinity constant of 1.9 × 10-4 M, while it could not bind to agarose tetrasaccharide. The sequence novelty and well-defined function of FvCBM99 and its homologs reveal a new CBM family, CBM99. Besides, the application potential of FvCBM99 in in situ visualization of porphyran was demonstrated. The discovery of FvCBM99 provides a favorable tool for future studies of porphyran.