Most previous studies of bacterial reduction of chromium have been don
e with pure cultures that are not likely to be found in ground water,
and at hexavalent chromium concentrations much greater than typically
present in contaminated ground water. Further, most previous work has
been performed with complex laboratory substrates that would not be su
itable for in situ application. In this study, mixed cultures were enr
iched from three diverse soil sources: surface soil, subsurface soil,
and river sediment. The enrichment medium contained 10 mg Cr6+/L and s
ucrose as the carbon source. The three mixed cultures obtained from th
e diverse soil samples were transferred to batch reactors and exhibite
d similar chromium reduction enzyme kinetics at stationary phase. The
maximum specific reduction rates were between 0.98 and 3.3 mg Cr6+/(g
dry cells.h) and the half velocity constants were between 0.39 and 1.4
8 mg Cr6+/L. The relatively narrow range of values for kinetic paramet
ers suggests that a conservative engineering design for in situ remedi
ation could be applied over a wide range of contaminated sites at the
Cr(VI) concentrations examined.