The plasmid-encoded arsenical resistance (ars) operon of plasmid R773
produces resistance to trivalent and pentavalent salts of the metalloi
ds arsenic and antimony in cells of Escherichia coli, The first two ge
nes in the operon, arsR and arsD, were previously shown to encode tran
s-acting repressor proteins, ArsR controls the basal level of expressi
on of the operon, while ArsD controls maximal expression. Thus, action
of the two repressors form a homeostatic regulatory circuit that main
tains the level of ars expression within a narrow range. In this study
, we demonstrate that ArsD binds to the same site on the ars promoter
element as ArsR but with 2 orders of magnitude lower affinity, The res
ults of gel shift assays demonstrate that ArsD is released from the ar
s DNA promoter by phenylarsine oxide, sodium arsenite, and potassium a
ntimonyl tartrate (in order of effectiveness), the same inducers to wh
ich ArsR responds, Using the quenching of intrinsic tryptophan fluores
cence to measure the affinity of the repressor for inducers, apparent
K-d values for Sb(III) and As(III) of 2 and 60 mu M, respectively, wer
e obtained, These results demonstrate that the arsR-arsD pair provide
a sensitive mechanism for sensing a wide range of environmental heavy
metals.