Sage A E, Vasil M L
Department of Microbiology, University of Colorado Health Sciences Center, Denver 80262, USA.
J Bacteriol. 1997 Aug;179(15):4874-81. doi: 10.1128/jb.179.15.4874-4881.1997.
Expression of the hemolytic phospholipase C (PlcH) of Pseudomonas aeruginosa is induced under phosphate starvation conditions or in the presence of the osmoprotectants choline and glycine betaine. Because choline and glycine betaine may serve as carbon and energy sources in addition to conferring osmoprotection to P. aeruginosa, it seemed possible that induction of plcH is subject to catabolite repression control (CRC) by tricarboxylic cycle intermediates such as succinate. Total phospholipase (PLC) activity in osmoprotectant-induced cultures of P. aeruginosa PAO1 supplemented with 20 mM succinate was three- to fourfold lower than the levels in cultures supplemented with the non-catabolite-repressive substrate lactate. Analyses of osmoprotectant-dependent plcH expression in a derivative of strain PAO1 containing a plcH::lacZ operon fusion showed that (i) succinate prevented induction of plcH expression by osmoprotectants; and (ii) addition of succinate reduced or shut down further expression of plcH in osmoprotectant-induced bacteria, while cultures supplemented with lactate had little or no change in plcH expression. RNase protection analysis confirmed that repression of plcH occurs at the transcriptional level. However, a P. aeruginosa mutant decoupled in CRC exhibited a phenotype similar to that of the wild-type strain (PAO1) with respect to succinate-dependent repression of plcH expression. Osmoprotectant-induced total PLC activities, levels of expression of plcH measured with the same plcH::lacZ fusion, and levels of plcH transcription in a CRC-deficient strain reflected those seen in strain PAO1. This indicates that CRC of plcH functions by a distinct mechanism which differs from that regulating the glucose or mannitol catabolic pathway. A strain carrying a mutation in vfr, which encodes the Escherichia coli Crp homolog in P. aeruginosa, still exhibited a wild-type phenotype with respect to osmoprotectant-dependent expression and CRC of plcH. These data indicate that there is a novel CRC system that regulates the expression of plcH in P. aeruginosa.
铜绿假单胞菌溶血磷脂酶C(PlcH)的表达在磷酸盐饥饿条件下或存在渗透保护剂胆碱和甘氨酸甜菜碱时被诱导。由于胆碱和甘氨酸甜菜碱除了赋予铜绿假单胞菌渗透保护作用外,还可作为碳源和能源,因此plcH的诱导似乎可能受到三羧酸循环中间体(如琥珀酸)的分解代谢物阻遏控制(CRC)。在补充有20 mM琥珀酸的铜绿假单胞菌PAO1的渗透保护剂诱导培养物中,总磷脂酶(PLC)活性比补充有非分解代谢物阻遏底物乳酸的培养物中的水平低三到四倍。对含有plcH::lacZ操纵子融合的PAO1菌株衍生物中渗透保护剂依赖性plcH表达的分析表明:(i)琥珀酸阻止了渗透保护剂对plcH表达的诱导;(ii)添加琥珀酸会降低或关闭渗透保护剂诱导的细菌中plcH的进一步表达,而补充有乳酸的培养物中plcH表达几乎没有变化。核糖核酸酶保护分析证实plcH的阻遏发生在转录水平。然而,在CRC中解偶联的铜绿假单胞菌突变体在plcH表达的琥珀酸依赖性阻遏方面表现出与野生型菌株(PAO1)相似的表型。渗透保护剂诱导的总PLC活性、用相同的plcH::lacZ融合测定的plcH表达水平以及CRC缺陷菌株中plcH的转录水平反映了PAO1菌株中的情况。这表明plcH的CRC通过一种不同于调节葡萄糖或甘露醇分解代谢途径的机制发挥作用。携带vfr突变的菌株,vfr在铜绿假单胞菌中编码大肠杆菌Crp同源物,在plcH的渗透保护剂依赖性表达和CRC方面仍表现出野生型表型。这些数据表明存在一种新的CRC系统,可调节铜绿假单胞菌中plcH的表达。