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. 2010 Nov 5;193(2):449–459. doi: 10.1128/JB.00737-10

TABLE 3.

1H- and 13C-NMR parameters established from COSY, NOESY, and HSQCa

Product H Shift (ppm) J coupling (Hz) C Shift (ppm)
GlcNAcα-PP-(CH2)11-OPh
    GlcNAc H-1 5.53 (5.64) C-1 96
H-2 3.97 C-2 55
H-3 3.75 C-3 72.9
H-4 3.33 (3.45) C-4 71.9
GlcNAcα-PP-decanol (7)
    GlcNAc H-1 5.45 3.2, 7.2 C-1 94.5
Galβ1-4GlcNAc-PP-(CH2)11-OPh (WfeD)
    GlcNAc H-1 5.561 C-1 94.7
H-2 4.027 C-2 53.1
H-3 3.846 C-3 69.4
H-4 3.626 C-4 79.1
    Gal H-1 4.345 7.6 C-1 103.4
H-2 3.538 6.9, 10.1 C-2 70.8
H-3 3.465 2.9, 9.5 C-3 73.1
H-4 3.792 2.5 C-4 68.8
Galβ1-3GlcNAc-PP-(CH2)11-OPh (17)
    GlcNAc H-1 5.58 C-1 94.8
H-2 4.14 C-2 52.4
H-3 3.84 C-3 80.3
    Gal H-1 4.35 C-1 104.0
Glcβ1-3GlcNAc-PP-(CH2)11-OPh (6)
    GlcNAc H-1 5.54 C-1 95.0
H-2 4.14 C-2 54.0
H-3 3.87 C-3 82.8
H-4 3.42 C-4 70.3
    Glc H-1 4.41 C-1 105.0
H-2 3.18 C-2 74.5
H-3 3.37 C-3 77.6
H-4 3.33
a

Shown is a comparison of NMR parameters between substrates and β3-GalT, β4-GalT, and β3-Glc-transferase enzyme products. NOESY, nuclear Overhauser enhancement spectroscopy.