Table I.
Glycosyl Residue | B Normala | B-Deficientb | 10B-Treatedc |
---|---|---|---|
mol %b | |||
Rha | 9 | 8 | 9 |
Fuc | 2 | 2 | 2 |
Ara | 18 | 17 | 19 |
Xyl | 7 | 11 | 11 |
Man | 1 | 1 | 1 |
Gal | 13 | 11 | 10 |
Glc | 27 | 30 | 30 |
GalA | 23 | 19 | 19 |
μm g−1 dry wt AIR | |||
mRG-IId | 0.6 | 4.3 | 2.3 |
dRG-II-Bd | 1.8 | 0 | 1.0 |
Be | 1.6 | <0.1 | 1.0 |
The values given are for those glycosyl residue that accounted for >1 mol % of the AIR. The glycosyl residues that are diagnostic of RG-II (2-O-Me Fuc, 2-O-Me Xyl, and apiose) each accounted for <0.5 mol % of the AIR.
B, AIR from cells grown in the presence of 11B boric acid (100 μm).
AIR from cells grown in the absence of added boric acid.
AIR from B-deficient cells grown for 10 min in the presence of 10B boric acid (100 μm).
The RG-II content was estimated from the 2-O-Me Fuc and 2-O-Me Xyl contents of the AIR. The relative proportions of dRG-II-B and mRG-II were determined by SEC of the phosphate-buffer-soluble extracts of the AIR (see Fig. 3), and these values were used to estimate the mRG-II and dRG-II-B contents using molecular masses of 5 and 10 kD, respectively (O'Neill et al., 1996).
The B content of the AIR was determined by ICP-AES.