Wildfeuer A, Heymer B, Schleifer K H, Haferkamp O
Appl Microbiol. 1974 Nov;28(5):867-71. doi: 10.1128/am.28.5.867-871.1974.
Lysates obtained from amoebocytes of Limulus polyphemus, the horseshoe crab, showed gel formation after the addition of bacterial endotoxin. In contrast to living gram-negative bacteria, viable gram-positive microorganisms did not cause gelation of lysate. Nevertheless, peptidoglycan isolated from the cell walls of various gram-positive organisms did induce the reaction. However, the activity of peptidoglycan was 1,000 to 400,000 times less than that of Escherichia coli lipopolysaccharide. After exposure to lysozyme, peptidoglycan no longer gelled amoebocyte lysate, therefore apparently excluding endotoxin contamination. Gelation of amoebocyte lysate by endotoxin or peptidoglycan was inhibited by different concentrations of sodium polystyrolsulfonate. Whereas these studies confirm the specificity of the Limulus test for bacterial endotoxins, they also indicate that other substances of bacterial origin should be investigated for their ability to gel amoebocyte lysate.
从鲎(Limulus polyphemus)的变形细胞中获得的裂解物,在添加细菌内毒素后会形成凝胶。与活的革兰氏阴性菌不同,活的革兰氏阳性微生物不会导致裂解物凝胶化。然而,从各种革兰氏阳性生物体细胞壁中分离出的肽聚糖确实能引发该反应。但是,肽聚糖的活性比大肠杆菌脂多糖低1000至400000倍。暴露于溶菌酶后,肽聚糖不再使变形细胞裂解物凝胶化,因此显然排除了内毒素污染。不同浓度的聚苯乙烯磺酸钠可抑制内毒素或肽聚糖使变形细胞裂解物凝胶化。虽然这些研究证实了鲎试剂检测细菌内毒素的特异性,但它们也表明,对于其他细菌来源的物质,应研究其使变形细胞裂解物凝胶化的能力。