Klipstein F A, Engert R F
Infect Immun. 1976 Feb;13(2):373-81. doi: 10.1128/iai.13.2.373-381.1976.
The enterotoxic material in cell-free growth preparations of Klebsiella pneumoniae serotype 5 was purified by sequential ultrafiltration and gel filtration (GF) procedures and the fractions were assayed for enterotoxic activity by determining their ability to induce in vivo net water secretion in the rat jejunum. Whole-cell lysates were inactive. Anaerobic broth culture conditions yielded a 10-fold increase in toxin production over aerobic conditions. Enterotoxic activity was absent in the UM-10 retentate of the broth filtrate but present in both the retentate and filtrate of the UM-2 membrane. GF of the two UM-2 ultrafiltration fractions through a Sephadex G-25 column yielded an active eluate, whose potency was increased by 10- or 200-fold, in or adjacent to the void volume. When subsequently passed through a G-50 column, these pools eluted at a Kav of between 0.4 and 0.6 and were further increased in potency by two- or fivefold. A second equally potent fraction was also recovered in the void volume of the G-50 eluate of the UM-2 filtrate; this may represent a polymer. Progressive purification by GF was associated with an increased protein and decreased carbohydrate content of the most active fractions. The most active G-50 eluate of the UM-2 retentate had a minimal effective enterotoxic dose of 5 mug/ml and that of the filtrate was less than 0.1 mug/ml. Heating the active GF eluates to 100 C for 30 min did not abolish enterotoxic activity and lowering the pH to 1 or incubation with either Pronase or trypsin had no effect on activity. These observations indicate that K. pneumoniae heat-stable enterotoxin is probably a single toxin with an apparent molecular weight in the range of 5,000. The elution characteristics during GF as well as the chemical composition of the most purified enterotoxin fractions indicate that the toxin is not associated with endotoxin.
通过连续超滤和凝胶过滤(GF)程序对肺炎克雷伯菌5型无细胞生长制剂中的肠毒素物质进行了纯化,并通过测定各组分在大鼠空肠中诱导体内净水分分泌的能力来检测其肠毒素活性。全细胞裂解物无活性。厌氧肉汤培养条件下的毒素产量比需氧条件下增加了10倍。肉汤滤液的UM - 10截留物中没有肠毒素活性,但UM - 2膜的截留物和滤液中均有活性。通过Sephadex G - 25柱对两个UM - 2超滤组分进行凝胶过滤,得到一个活性洗脱液,其效力在空体积或空体积附近增加了10倍或200倍。随后通过G - 50柱时,这些组分在Kav为0.4至0.6之间洗脱,效力进一步提高了2倍或5倍。在UM - 2滤液的G - 50洗脱液的空体积中还回收了第二个效力相当的组分;这可能代表一种聚合物。通过凝胶过滤进行的逐步纯化与最具活性组分的蛋白质含量增加和碳水化合物含量降低有关。UM - 2截留物的最具活性的G - 50洗脱液的最小有效肠毒素剂量为5微克/毫升,滤液的最小有效肠毒素剂量小于0.1微克/毫升。将活性凝胶过滤洗脱液加热至100℃ 30分钟不会消除肠毒素活性,将pH值降至1或与链霉蛋白酶或胰蛋白酶一起孵育对活性也没有影响。这些观察结果表明,肺炎克雷伯菌热稳定肠毒素可能是一种表观分子量在5000左右的单一毒素。凝胶过滤过程中的洗脱特性以及最纯的肠毒素组分的化学成分表明,该毒素与内毒素无关。