4 and reveals nine Deforolimus major and three minor cross-peaks. The 1H,13C-coupled version of this experiment was used to obtain one-bond 1H,13C-coupling constants that contain information about the anomeric configuration. Thus, the 13C anomeric resonances with chemical shifts <103 p.p.m. all had 1JC,H values >170 Hz, indicating α-anomeric configurations. Major cross-peaks

were present at δH/δC 4.92/100.3, 5.07/102.9, 5.08/102.9, 5.08/99.1, 5.11/99.2, 5.16/102.9, 5.18/102.9 and 5.28/101.4; two minor cross-peaks were observed at δH/δC 5.05/99.3 and 5.46/96.9. The residue having its anomeric proton resonating at 4.53 p.p.m. had 3JH1,H2=8.0 Hz and its anomeric carbon observed at 103.5 p.p.m. showed 1JC,H≈160 Hz, indicative of the β-anomeric configuration. A series of 1D 1H,1H-TOCSY experiments starting from the anomeric proton of this residue revealed the complete spin system of a hexose residue, viz., δH 4.53 (H1), 3.36 (H2), 3.52 (H3), 3.47 (H4), 3.64 (H5), 3.87 (H6a) and 4.22 (H6b), which according to its chemical shifts, should be a glucosyl residue substituted at O6 (Jansson et

al., 1994). The 1H,13C-HMBC spectrum revealed a trans-glycosidic correlation between H1 and C6 at 69.8 p.p.m. and an intraresidue one between C1 and H2, indicating that the material contains a chain of 6)-β-d-Glcp-(1residues. In the 1H,13C-HSQC selleck products spectrum, a minor cross-peak was also present at δH/δC 4.36/103.9. The 1H,13C-HMBC spectrum revealed correlations at δH/δC 4.36/57.8 and 103.9/3.57, consistent with a 1H,13C-HSQC cross-peak at δH/δC 3.57/57.8. These results suggest the presence of an aminosugar, such as N-acetylglucosamine, which could be the primer from which the exopolysaccharide biosynthesis is started. The residues having their anomeric 13C chemical shifts <103 p.p.m. are consequently suggested to originate from mannosyl residues. Aided by the computer program CASPER (Jansson et al., 2006), which is used for the prediction of 1H and 13C NMR chemical shifts

and for the structural analysis of oligo- and polysaccharides, Adenosine further analysis was carried out. The chemical shifts of the anomeric 1H,13C-HSQC cross-peaks were in accord with different combinations of 2- and/or 6-substituted mannosyl residues. This conclusion was corroborated by correlations in the 1H,13C-HMBC spectrum at, inter alia, δH/δC 4.92/66.6, 5.07/79.4, 5.08/66.5, 5.08/79.0, 5.11/66.6, 5.11/79.4, 5.16/78.7 and 5.28/79.3. Thus, the major structural part is reminiscent of mannan structures present in oligo- and polysaccharides of bacterial and other origins (Briken et al., 2004; Lee et al., 2005; Omarsdottir et al., 2006; Prieto et al., 2007). In addition, the translational diffusion of the exopolysaccharide material was carried out and resulted in Dt=6.8 × 10−11 m2 s−1.