Table 3. Determination of regiospecificity and substrate specificity for hydrolysis of natural oligosaccharides and glycans.
Mfuc1 | Mfuc2 | Mfuc3 | Mfuc4 | Mfuc5 | Mfuc6 | Mfuc7 | Thma | |
---|---|---|---|---|---|---|---|---|
2’-FL | 76 ±1% | 88±1% | 2 ±1% | 47±1% | 87±1% | 2 ±2% | 94±1% | 71±1% |
3-FL | 11 ±2% | 4±2% | 0 ±2% | 3 ±2% | 34 ±3% | 0 ±2% | 12 ±2% | 1 ±2% |
Citrus XG | 4% | 1% | 1% | 3% | 39% | 4% | 3% | 0% |
Arabidopsis XG | 100% | 84% | 7% | 78% | 100% | 7% | 43% | 13% |
Sambucus XG | 100% | 85% | 7% | 91% | 100% | 5% | 44% | 9% |
The reactions were performed using 1 mM of substrate at 30°C for 150 min and the fraction of fucose released from the substrates under the reaction conditions employed is given in %. For hydrolysis of 2’-FL, 3-FL and citrus xyloglucan, the fucose content was determined by HPAEC-PAD. The hydrolysis of fucose from Arabidopsis thaliana and Sambucus nigra xyloglucan was measured using immuno-glycan arrays (S2 File), and 0% corresponds to the signal from untreated samples whereas 100% corresponds to the complete α-L-fucosidase-mediated removal of the antibody fucosyl epitope detected by the antibody.