Wang L, Bender C L, Ullrich M S
Max-Planck-Institut für terrestrische Mikrobiologie, AG Okophysiologie, Marburg, Germany.
Mol Gen Genet. 1999 Sep;262(2):250-60. doi: 10.1007/s004380051081.
A modified two-component regulatory system consisting of the histidine protein kinase CorS and two highly homologous response regulators, CorR and CorP, controls biosynthesis of the polyketide phytotoxin coronatine (COR) by Pseudomonas syringae pv. glycinea PG4180 in a temperature-dependent manner. COR synthesis is maximal at 18 degrees C but does not occur at 28 degrees C. Fusions of CorR and CorP to the maltose-binding protein (MBP) were overproduced in Escherichia coli and P. syringae PG4180, and tested for functionality by complementation of corR and corP mutants of PG4180, respectively. The cmaABT promoter region was defined by deletion mapping, and the DNA-binding capability of CorR and CorP was examined by gel retardation assays. When overproduced in P. syringae at 18 degrees C and purified, MBP-CorR was shown to bind specifically to a 218-bp DNA fragment corresponding to positions -841 to -623 bp upstream of the transcriptional start site of the cmaABT operon. In contrast, MBP-CorP and MBP itself, when overproduced in P. syringae and E. coli at 18 degrees C and 28 degrees C, respectively, did not bind to the 218-bp fragment or to any other DNA fragment analyzed. The CorP protein lacks typical DNA-binding motifs, suggesting that it might modulate the function of CorR. However, addition of purified MBP-CorP did not alter the DNA-binding activity of MBP-CorR. On the other hand, this activity was completely abolished when MBPCorR was overproduced at 28 degrees C or in a corS mutant, indicating that the binding of CorR depended on the growth temperature at which it was produced and was controlled by CorS. In addition, overproduction of MBP-CorR in a corP mutant of PG4180 also yielded inactive protein, underlining the importance of CorP for CorR activation. We propose that CorR is activated by CorS at low temperature and that CorP is required for this activation before CorR can bind to DNA.
一种由组氨酸蛋白激酶CorS和两个高度同源的响应调节因子CorR和CorP组成的改良双组分调节系统,以温度依赖的方式控制丁香假单胞菌大豆致病变种PG4180中聚酮植物毒素冠菌素(COR)的生物合成。COR合成在18℃时最大,但在28℃时不发生。将CorR和CorP与麦芽糖结合蛋白(MBP)的融合体在大肠杆菌和丁香假单胞菌PG4180中过量表达,并分别通过互补PG4180的corR和corP突变体来测试其功能。通过缺失定位确定了cmaABT启动子区域,并通过凝胶阻滞试验检测了CorR和CorP的DNA结合能力。当在18℃的丁香假单胞菌中过量表达并纯化时,MBP-CorR被证明能特异性结合一个218 bp的DNA片段,该片段对应于cmaABT操纵子转录起始位点上游-841至-623 bp的位置。相比之下,分别在18℃和28℃的丁香假单胞菌和大肠杆菌中过量表达的MBP-CorP和MBP本身,均不与218 bp片段或任何其他分析的DNA片段结合。CorP蛋白缺乏典型的DNA结合基序,这表明它可能调节CorR的功能。然而,添加纯化的MBP-CorP并没有改变MBP-CorR的DNA结合活性。另一方面,当MBP-CorR在28℃或corS突变体中过量表达时,这种活性完全丧失,这表明CorR的结合取决于其产生时的生长温度,并受CorS控制。此外,在PG4180的corP突变体中过量表达MBP-CorR也产生了无活性的蛋白,强调了CorP对CorR激活的重要性。我们提出,CorR在低温下被CorS激活,并且在CorR能够结合DNA之前,这种激活需要CorP。