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. 2011 Apr 11;108(17):7194–7199. doi: 10.1073/pnas.1014125108

Fig. 4.

Fig. 4.

ATP-dependent 3H-l-fucose phosphorylation and GTP-dependent 3H-l-fucose activation. Whole-cell lysates (100 μg) of the indicated strains grown in the presence or absence of [3H]-l-fucose (as indicated) for 24 h and assayed for their potential to fucose under the indicated assay conditions. Ec, E. coli K12 wild-type; ΔEcfucK, E. coli K12 fucK mutant; Cj, C. jejuni NCTC11168 wild-type; Δcj0486, C. jejuni NCTC11168 Δ0486; Bt, B. thetaiotaomicron wild-type. The presence or absence of ATP and GTP are indicated by (+) and (−). Formation of modified 3H-l-fucose was found to be linear over the first 10 min of the assay. SDs are displayed by error bars. 3H-l-fucose alone did not show any significant binding to the column material.