TABLE 1.
Sample name | Monomer yields |
Total yields | Molar ratios | |||
H | G | S | S/G | |||
+ddH2O | TRV:00 | 5.5 ± 0.9 | 67.8 ± 9.5 | 66.7 ± 8.3 | 140 | 0.98 |
TRV:CAD35 | 4.6 ± 0.5 | 59.5 ± 7.2 | 61.5 ± 8.8 | 125.6 | 1.03 | |
TRV:CAD45 | 6.1 ± 0.3 | 55.6 ± 5.0 | 57.3 ± 5.2 | 119 | 1.03 | |
TRV:CAD43 | 4.7 ± 0.2 | 61.8 ± 6.0 | 58.5 ± 9.7 | 125 | 0.95 | |
+V. dahliae | TRV:00 | 5.1 ± 0.2 | 62.1 ± 4.9 | 46.9 ± 5.2 | 114.1 | 0.76 |
TRV:CAD35 | 5.0 ± 0.2 | 52.0 ± 8.8 | 25.0 ± 4.5 | 75 | 0.48 | |
TRV:CAD45 | 5.5 ± 0.7 | 51.9 ± 4.7 | 31.2 ± 3.6 | 88.6 | 0.6 | |
TRV:CAD43 | 5.9 ± 0.6 | 55.5 ± 7.0 | 39.2 ± 5.3 | 100.6 | 0.71 |
Yields (μmol/g of Klason Lignin) of Lignin-Derived Thioacidolysis Monomers from Various Lignocellulosic Materials, Measured by GC–MS.
H, p-hydroxyphenyl monomer; G, guaiacyl monomer; S, syringyl monomer.