IDENTIFICATION OF A BACILLUS-THURINGIENSIS GENE THAT POSITIVELY REGULATES TRANSCRIPTION OF THE PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE-C GENE AT THE ONSET OF THE STATIONARY-PHASE
D. Lereclus et al., IDENTIFICATION OF A BACILLUS-THURINGIENSIS GENE THAT POSITIVELY REGULATES TRANSCRIPTION OF THE PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE-C GENE AT THE ONSET OF THE STATIONARY-PHASE, Journal of bacteriology, 178(10), 1996, pp. 2749-2756
A transcriptional analysis of the phosphatidylinositol-specific phosph
olipase C (plcA) gene of Bacillus thuringiensis indicated that its tra
nscription was activated at the onset of the stationary phase in B. th
uringiensis but was not activated in B. subtilis. The B. thuringiensis
gene encoding a transcriptional activator required for plcA expressio
n was cloned by using a B. subtilis strain carrying a chromosomal plcA
'-'lacZ fusion as a heterologous host for selection. This trans activa
tor (designated PlcR) is a protein of a calculated molecular weight of
33,762 which appears to be distantly related to PreL and NprA, regula
tor proteins enhancing transcription of neutral protease genes during
the stationary phase of a Lactobacillus sp. and B. stearothermophilus,
respectively. plcR gene transcription was analyzed in B. thuringiensi
s and in B. subtilis. PlcR positively regulated its own transcription
at the onset of the stationary phase. There is a highly conserved DNA
sequence (17 bp) 34 nucleotides upstream from the plcR transcriptional
start site and 49 nucleotides upstream from the plcA transcriptional
start site. As PlcR positively regulates its own transcription and plc
A transcription, this conserved DNA sequence may be the specific recog
nition target for PlcR activation.