Hastie A T, Hingley S T, Kueppers F, Higgins M L, Tannenbaum C S, Weinbaum G
Infect Immun. 1983 May;40(2):506-13. doi: 10.1128/iai.40.2.506-513.1983.
The temporal appearance of extracellular proteases produced by Pseudomonas aeruginosa was analyzed by pH 9 and pH 4 polyacrylamide gel electrophoresis (PAGE) and sodium dodecyl sulfate-PAGE. Ammonium sulfate precipitates of culture supernatants from various stages of growth revealed a time-dependent increase in number and amount of proteolytically active proteins. One mucoid P. aeruginosa clinical isolate and its derived nonmucoid variant, as well as two other nonmucoid variant P. aeruginosa strains (all from cystic fibrosis patients), showed similar production of five differently migrating proteases (P1 to P5, numbered according to increasing net negative charge) in pH 9 PAGE and one protease in pH 4 PAGE. P2, P3, and P5 increased to maximum concentrations at 24 to 48 h, decreasing thereafter, whereas P4 continued increasing even at 83 h, and P1 fluctuated. P3 was identified as an elastase. P2 was possibly composed of polypeptide chains bridged by disulfide bonds, since without reduction it migrated in sodium dodecyl sulfate-PAGE as a single protein, and with reduction it migrated as three protein bands. Two-dimensional PAGE revealed multiple molecular weight species within protease-positive bands in pH 9 gel strips. Isoelectric focusing gave a pattern of protein separation that correlated with two-dimensional PAGE analysis. Thus, greater heterogeneity of active proteases than previously reported has been demonstrated in all P. aeruginosa clinical isolates studied by sensitive two-dimensional PAGE analysis.
通过pH 9和pH 4聚丙烯酰胺凝胶电泳(PAGE)以及十二烷基硫酸钠 - PAGE分析了铜绿假单胞菌产生的细胞外蛋白酶的时间出现情况。来自不同生长阶段培养上清液的硫酸铵沉淀物显示,蛋白水解活性蛋白的数量和量呈时间依赖性增加。一株黏液型铜绿假单胞菌临床分离株及其衍生的非黏液型变体,以及另外两株非黏液型变体铜绿假单胞菌菌株(均来自囊性纤维化患者),在pH 9 PAGE中显示出五种迁移不同的蛋白酶(P1至P5,根据净负电荷增加编号)以及在pH 4 PAGE中一种蛋白酶的相似产生情况。P2、P3和P5在24至48小时达到最大浓度,此后下降,而P4即使在83小时仍继续增加,P1则波动。P3被鉴定为弹性蛋白酶。P2可能由通过二硫键桥接的多肽链组成,因为在不还原的情况下它在十二烷基硫酸钠 - PAGE中作为单一蛋白质迁移,而在还原时它迁移为三条蛋白带。二维PAGE揭示了pH 9凝胶条带中蛋白酶阳性条带内的多种分子量种类。等电聚焦给出了与二维PAGE分析相关的蛋白质分离模式。因此,通过灵敏的二维PAGE分析,在所研究的所有铜绿假单胞菌临床分离株中都证明了活性蛋白酶的异质性比以前报道的更大。