Debarbouille M, Arnaud M, Fouet A, Klier A, Rapoport G
Unité de Biochimie Microbienne, Centre National de la Recherche Scientifique (URA1300), Institut Pasteur, Paris, France.
J Bacteriol. 1990 Jul;172(7):3966-73. doi: 10.1128/jb.172.7.3966-3973.1990.
The expression of the Bacillus subtilis sacPA operon is induced by sucrose. A DNA fragment containing the upstream region of this operon was cloned. This fragment contains a promoter from which the operon is expressed. This upstream region also contains a palindromic DNA sequence very similar to the transcriptional terminator which regulates the induction of the B. subtilis sacB gene. Of 37 nucleotides in a region partially overlapping the sacP palindromic sequence, 34 were identical to the corresponding region of the sacB gene. A similar motif is also present in the bgl operon of Escherichia coli. The sacT locus controlling sacPA expression had been identified by a single constitutive mutation sacT30 which mapped close to the sacPA operon. DNA fragments containing the sacT+ and sacT30 alleles were cloned and sequenced. The sacT gene product is very similar to the B. subtilis sacY and to the E. coli bglG gene products. The constitutive sacT30 mutation was identified. It corresponds to a Asp-96-to-Tyr missense mutation located in a highly conserved region in SacT and SacY. These results strongly suggest that sacT is a specific regulatory gene of the sacPA operon.
枯草芽孢杆菌sacPA操纵子的表达受蔗糖诱导。克隆了一个包含该操纵子上游区域的DNA片段。该片段含有一个用于表达该操纵子的启动子。此上游区域还包含一个回文DNA序列,与调控枯草芽孢杆菌sacB基因诱导的转录终止子非常相似。在与sacP回文序列部分重叠的区域中的37个核苷酸中,有34个与sacB基因的相应区域相同。类似的基序也存在于大肠杆菌的bgl操纵子中。通过一个位于靠近sacPA操纵子的单个组成型突变sacT30鉴定了控制sacPA表达的sacT位点。克隆并测序了包含sacT⁺和sacT30等位基因的DNA片段。sacT基因产物与枯草芽孢杆菌sacY以及大肠杆菌bglG基因产物非常相似。鉴定出了组成型sacT30突变。它对应于位于SacT和SacY高度保守区域的一个天冬氨酸96到酪氨酸的错义突变。这些结果有力地表明sacT是sacPA操纵子的一个特异性调控基因。