Liffourrena Andrés S, Massimelli María J, Forrellad Marina A, Lisa Angela T, Domenech Carlos E, Lucchesi Gloria I
Departamento de Biología Molecular, Facultad de Ciencias Exactas, Fisicoquímicas y Naturales, Universidad Nacional de Río Cuarto, CP5800, Río Cuarto, Córdoba, Argentina.
Curr Microbiol. 2007 Dec;55(6):530-6. doi: 10.1007/s00284-007-9027-2. Epub 2007 Sep 25.
Pseudomonas aeruginosa expresses hemolytic phospholipase C (PlcH) with choline or under phosphate-limiting conditions. PlcH from these conditions were differently eluted from the Celite-545 column after application of an ammonium sulfate linear reverse gradient. The PlcH from supernatants of bacteria grown in the presence of choline was eluted with 30% ammonium sulfate and was more than 85% inhibited by tetradecyltrimethylammonium. PlcH from supernatants of bacteria grown with succinate and ammonium ions in a low-phosphate medium was eluted as a peak with 10% of salt and was less than 10% inhibited by tetradecyltrimethylammonium. PlcH from low phosphate was purified associated with a protein of 17 kDa. This complex was dissociated and separated on a Sephacryl S-200 column with 1% (w/v) sodium dodecyl sulfate. After this dissociation, the resulting protein of 70 kDa, corresponding to PlcH, was inhibited by tetradecyltrimethylammonium, showing a protection effect of the accompanying protein. RT-PCR analyses showed that in choline media, the plcH gene was expressed independently of plcR. In low-phosphate medium, the plcH gene was expressed as a plcHR operon. Because plcR encodes for chaperone proteins, this result correlates with the observation that PlcH from supernatants of bacteria grown in the presence of choline was purified without an accompanying protein. The consequence of the absence of this chaperone was that tetradecyltrimethylammonium inhibited the PlcH activity.
铜绿假单胞菌在有胆碱存在的情况下或在磷酸盐限制条件下表达溶血磷脂酶C(PlcH)。在应用硫酸铵线性反向梯度后,来自这些条件下的PlcH从硅藻土-545柱上以不同方式洗脱。在胆碱存在下生长的细菌上清液中的PlcH用30%硫酸铵洗脱,并且被十四烷基三甲基铵抑制超过85%。在低磷酸盐培养基中以琥珀酸盐和铵离子生长的细菌上清液中的PlcH以10%盐的峰形式洗脱,并且被十四烷基三甲基铵抑制小于10%。低磷酸盐条件下的PlcH与一种17 kDa的蛋白质一起纯化。该复合物在含有1%(w/v)十二烷基硫酸钠的Sephacryl S-200柱上解离并分离。解离后,得到的70 kDa蛋白质(对应于PlcH)被十四烷基三甲基铵抑制,显示出伴随蛋白质的保护作用。逆转录聚合酶链反应(RT-PCR)分析表明,在胆碱培养基中,plcH基因独立于plcR表达。在低磷酸盐培养基中,plcH基因作为plcHR操纵子表达。因为plcR编码伴侣蛋白,该结果与以下观察结果相关:在胆碱存在下生长的细菌上清液中的PlcH在没有伴随蛋白质的情况下被纯化。缺少这种伴侣蛋白的后果是十四烷基三甲基铵抑制了PlcH活性。