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Phosphatidylcholine-Specific Phospholipase C and Sphingomyelinase Activities in Bacteria of the Bacillus cereus Group

机译:蜡状芽孢杆菌组细菌中的磷脂酰胆碱特异性磷脂酶C和鞘磷脂酶活性

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摘要

Bacillus anthracis is nonhemolytic, even though it is closely related to the highly hemolytic Bacillus cereus. Hemolysis by B. cereus results largely from the action of phosphatidylcholine-specific phospholipase C (PC-PLC) and sphingomyelinase (SPH), encoded by the plc and sph genes, respectively. In B. cereus, these genes are organized in an operon regulated by the global regulator PlcR. B. anthracis contains a highly similar cereolysin operon, but it is transcriptionally silent because the B. anthracis PlcR is truncated at the C terminus. Here we report the cloning, expression, purification, and enzymatic characterization of PC-PLC and SPH from B. cereus and B. anthracis. We also investigated the effects of expressing PlcR on the expression of plc and sph. In B. cereus, PlcR was found to be a positive regulator of plc but a negative regulator of sph. Replacement of the B. cereus plcR gene by its truncated orthologue from B. anthracis eliminated the activities of both PC-PLC and SPH, whereas introduction into B. anthracis of the B. cereus plcR gene with its own promoter did not activate cereolysin expression. Hemolytic activity was detected in B. anthracis strains containing the B. cereus plcR gene on a multicopy plasmid under control of the strong B. anthracis protective antigen gene promoter or in a strain carrying a multicopy plasmid containing the entire B. cereus plc-sph operon. Slight hemolysis and PC-PLC activation were found when PlcR-producing B. anthracis strains were grown under anaerobic-plus-CO2 or especially under aerobic-plus-CO2 conditions. Unmodified parental B. anthracis strains did not demonstrate obvious hemolysis under the same conditions.
机译:炭疽芽孢杆菌是非溶血性的,即使它与高度溶血的蜡状芽孢杆菌密切相关。蜡状芽孢杆菌的溶血作用主要是由磷脂酰胆碱特异性磷脂酶C(PC-PLC)和鞘磷脂酶(SPH)分别由plc和sph基因编码引起的。在蜡状芽孢杆菌中,这些基因在由全局调节子PlcR调节的操纵子中组织。炭疽芽孢杆菌含有高度相似的溶细胞素操纵子,但是由于炭疽芽孢杆菌PlcR在C末端被截短,因此它在转录上是沉默的。在这里,我们报告了来自蜡状芽孢杆菌和炭疽芽孢杆菌的PC-PLC和SPH的克隆,表达,纯化和酶促表征。我们还研究了表达PlcR对plc和sph表达的影响。在蜡状芽孢杆菌中,发现PlcR是plc的正调节剂,但是sph的负调节剂。蜡状芽孢杆菌plcR基因被炭疽芽孢杆菌的截短的直向同源物取代,消除了PC-PLC和SPH的活性,而将蜡状芽孢杆菌plcR基因以其自身的启动子引入炭疽芽孢杆菌中并不能激活蜡质溶素的表达。在强炭疽芽孢杆菌保护性抗原基因启动子的控制下,在多拷贝质粒上含有蜡状芽孢杆菌plcR基因的炭疽芽孢杆菌菌株中,或在携带包含整个蜡状芽孢杆菌plc-sph操纵子的多拷贝质粒的菌株中检测到溶血活性。 。当产生PlcR的炭疽芽孢杆菌菌株在厌氧+ CO2或特别是在好氧+ CO2条件下生长时,发现轻微溶血和PC-PLC活化。在相同条件下,未经修饰的亲本炭疽芽孢杆菌菌株未显示出明显的溶血现象。

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