The fnr gene encodes a regulatory protein involved in the response to
oxygen in a variety of bacterial genera. For example, it was previousl
y shown that the anoxygenic, photosynthetic bacterium Rhodobacter spha
eroides requires the fnrL gene for growth under anaerobic, photosynthe
tic conditions, Additionally, the FnrL protein in R. sphaeroides is re
quired for anaerobic growth in the dark with an alternative electron a
cceptor, but it is not essential for aerobic growth. In this study, th
e fnrL locus from Rhodobacter capsulatus was cloned and sequenced. Sur
prisingly, an R. capsulatus strain with the fnrL gene deleted grows li
ke the wild type under either photosynthetic or aerobic conditions but
does not grow anaerobically with alternative electron accepters such
as dimethyl sulfoxide (DMSO) or trimethylamine oxide. It is demonstrat
ed that the c-type cytochrome induced upon anaerobic growth on DMSO is
not synthesized in the R. capsulatus fnrL mutant. In contrast to wild
-type strains, R. sphaeroides and R. capsulatus fnrL mutants do not sy
nthesize the anaerobically, DMSO-induced reductase. Mechanisms that ex
plain the basis for FnrL function in both organisms are are dicussed.