Prevotella bryantii B14 grew faster on glucose than mannose (0.70 versus 0.45 h−1), but these sugars were used simultaneously rather than diauxically. 2‐deoxy‐glucose (2DG) decreased the growth rate of cells that were provided with either glucose or mannose, but 2DG did not completely prevent growth. Cells grown on glucose or mannose transported both 14C‐glucose and 14C‐mannose, but cells grown on glucose had over three‐fold higher rates of 14C‐glucose transport than cells grown on mannose. The 14C‐mannose transport rates of glucose‐ and mannose‐grown cells were similar. Woolf‐Augustinsson‐Hofstee plots were not linear, and it appeared that the glucose/mannose/2DG carrier acted as a facilitated diffusion system at high substrate concentrations. When cultures were grown on nitrogen‐deficient (excess sugar) medium, isolates had three‐fold lower 14C‐glucose transport, but the 14C‐mannose transport did not change significantly. 14C‐glucose and 14C‐mannose transport rates could be inhibited by 2DG and either mannose or glucose, respectively. The 14C‐glucose transport of mannose‐grown cells was inhibited more strongly by mannose and 2DG than those grown on glucose. Cells grown on glucose or mannose had similar ATP‐dependent glucokinase activity, and 2DG was a competitive inhibitor (Ki=0.75 mM). Thin layer chromatography indicated that cell extracts also had ATP‐dependent mannose phosphorylation, but only a small amount of phosphorylated 2DG was detected. Glucose, mannose or 2DG were not phosphorylated in the presence of PEP. Based on these results, it appeared that P. bryantii B14 had: (1) two mechanisms of glucose transport, a constitutive glucose/mannose/2DG carrier and an alternative glucose carrier that was regulated by glucose availability, (2) an ATP‐dependent glucokinase that was competitively inhibited by 2DG but was unable to phosphorylate 2DG at a rapid rate, and (3) virtually no PEP‐dependent glucose, mannose or 2DG phosphorylation activities.