Monderer-Rothkoff Galya, Amster-Choder Orna
Department of Molecular Biology, The Hebrew University Medical School, P.O. Box 12272, Jerusalem 91120, Israel.
J Bacteriol. 2007 Dec;189(23):8601-15. doi: 10.1128/JB.01220-07. Epub 2007 Sep 28.
BglF catalyzes beta-glucoside phosphotransfer across the cytoplasmic membrane in Escherichia coli. In addition, BglF acts as a sugar sensor that controls expression of beta-glucoside utilization genes by reversibly phosphorylating the transcriptional antiterminator BglG. Thus, BglF can exist in two opposed states: a nonstimulated state that inactivates BglG by phosphorylation and a sugar-stimulated state that activates BglG by dephosphorylation and phosphorylates the incoming sugar. Sugar phosphorylation and BglG (de)phosphorylation are both catalyzed by the same residue, Cys24. To investigate the coordination and the structural requirements of the opposing activities of BglF, we conducted a genetic screen that led to the isolation of mutations that shift the balance toward BglG phosphorylation. We show that some of the mutants that are impaired in dephosphorylation of BglG retained the ability to catalyze the concurrent activity of sugar phosphotransfer. These mutations map to two regions in the BglF membrane domain that, based on their predicted topology, were suggested to be implicated in activity. Using in vivo cross-linking, we show that a glycine in the membrane domain, whose substitution impaired the ability of BglF to dephosphorylate BglG, is spatially close to the active-site cysteine located in a hydrophilic domain. This residue is part of a newly identified motif conserved among beta-glucoside permeases associated with RNA-binding transcriptional antiterminators. The phenotype of the BglF mutants could be suppressed by BglG mutants that were isolated by a second genetic screen. In summary, we identified distinct sites in BglF that are involved in regulating phosphate flow via the common active-site residue in response to environmental cues.
BglF催化大肠杆菌中β-葡萄糖苷的磷酸转移穿过细胞质膜。此外,BglF作为一种糖传感器,通过可逆地磷酸化转录抗终止子BglG来控制β-葡萄糖苷利用基因的表达。因此,BglF可以以两种相反的状态存在:一种非刺激状态,通过磷酸化使BglG失活;另一种糖刺激状态,通过去磷酸化激活BglG并使进入的糖磷酸化。糖磷酸化和BglG的(去)磷酸化均由同一残基Cys24催化。为了研究BglF相反活性的协调作用和结构要求,我们进行了一次遗传筛选,导致分离出了使平衡向BglG磷酸化方向转变的突变。我们表明,一些在BglG去磷酸化方面受损的突变体保留了催化糖磷酸转移同时发生的活性的能力。这些突变定位在BglF膜结构域的两个区域,根据其预测的拓扑结构,表明与活性有关。通过体内交联,我们表明膜结构域中的一个甘氨酸,其取代损害了BglF使BglG去磷酸化的能力,在空间上靠近位于亲水结构域的活性位点半胱氨酸。该残基是与RNA结合转录抗终止子相关的β-葡萄糖苷通透酶中一个新鉴定的保守基序的一部分。BglF突变体的表型可以被通过第二次遗传筛选分离出的BglG突变体抑制。总之,我们在BglF中鉴定出了不同的位点,这些位点参与通过共同的活性位点残基响应环境线索来调节磷酸盐流动。