A. Treunerlange et al., THE KDP SYSTEM OF CLOSTRIDIUM-ACETOBUTYLICUM - CLONING, SEQUENCING, AND TRANSCRIPTIONAL REGULATION IN RESPONSE TO POTASSIUM CONCENTRATION, Journal of bacteriology, 179(14), 1997, pp. 4501-4512
The complete sequence of the kdp gene region of Clostridium acetobutyl
icum has been determined. This part of the chromosome comprises two sm
all open reading frames (orfZ and orfY), putatively encoding hydrophob
ic peptides, and the genes kdpA, kdpB, kdpC, and kdyX, followed by an
operon encoding a pair of sensor effector regulatory proteins (KdpD an
d KdpE). Except for orfZ, orfY, and kdpX, all genes showed significant
homology to the kdp genes of Escherichia coli, encoding a high-affini
ty potassium transport ATPase and its regulators. The complete genome
sequence of Synechocystis sp. strain PCC 6803 and a recently published
part of the Mycobacterium tuberculosis genome indicate the existence
of a kdp system in these organisms as well, but all three systems comp
rise neither a second orf upstream of kdpA nor an additional kdpX gene
. Expression of the clostridial kdp genes, including the unique kdpX g
ene, was found to be inducible by low potassium concentrations. A tran
scription start point could be mapped upstream of orfZ. A promoter ups
tream of kdpD was active only under noninducing conditions. Lowering t
he potassium content of the medium led to formation of a common transc
ript (orfZYkdpABCXDE), with a putative internal RNase E recognition si
te, which could be responsible for the instability of the common trans
cript. Except for the two small peptides, all gene products could be d
etected in in vitro transcription-translation experiments.