The bacterial flagellar motor and the ATP-hydrolysing F-1 portion of the F1
F0-ATPase are known to be rotary motors, and it seems highly probable that
the H+-translocating F-0 portion rotates too. The energy source in the case
of F-0 and the flagellar motor is the flow of ions, either H+ (protons) or
Na+, down an electrochemical gradient across a membrane. The fact that ion
s flow in a particular direction through a well-defined structure in these
motors invites the possibility of a type of mechanism based on geometric co
nstraints between the rotor position and the paths of ions flowing through
the motor. The two best-studied examples of such a mechanism are the 'turns
tile' model of Khan and Berg and the 'proton turbine' model of Lauger or Be
rry. Models such as these are typically represented by a small number of ki
netic states and certain allowed transitions between them. This allows the
calculation of predictions of motor behaviour and establishes a dialogue be
tween models and experimental results. In the near future structural data a
nd observations of single-molecule events should help to determine the natu
re of the mechanism of rotary motors, while motor models must be developed
that can adequately explain the measured relationships between torque and s
peed in the flagellar motor.