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Improved purification and characterization of hemolysin BL a hemolytic dermonecrotic vascular permeability factor from Bacillus cereus.

机译:改善了溶血素BL(一种蜡状芽孢杆菌的溶血性皮肤坏死性血管通透性因子)的纯化和特性。

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摘要

Bacillus cereus causes diarrheal and emetic food poisoning syndromes as well as a variety of mild to severe infections. A dermonecrotic vascular permeability (VP) factor has been implicated as a virulence factor in these illnesses. Hemolysin BL was previously identified as a unique tripartite hemolysin possessing VP activity. In this study, a high-yield purification scheme, which allowed quantitative characterization of hemolysin BL activity and determination of the molecular weight, pI, and N-terminal sequence of each component, was developed. Milligram quantities of the B, L1, and L2 components were highly purified by a combination of anion-exchange and hydroxylapatite chromatographies. The combined components had VP activity at low doses and were necrotic at higher doses. The toxin exhibited an unusual dose-response zone phenomenon in turbidometric hemolysis assays. Activity increased at doses up to 200 ng/ml, then decreased at doses up to 350 ng/ml, and was constant at doses up to at least 2,500 ng/ml. This behavior may provide an explanation for the unusual discontinuous pattern typical of hemolysin BL in gel diffusion assays. At high concentrations of one or two components, the presence of low amounts of the complementary component(s) resulted in full hemolytic activity. Erythrocytes were protected from lysis by Zn2+ at micromolar concentrations but not by Ca2+ and Mg2+ at concentrations up to 25 mM. These data provide guidelines for future work on this toxin and indicate that hemolysin BL is the dermonecrotic VP factor implicated as a B. cereus virulence factor.
机译:蜡状芽孢杆菌引起腹泻和呕吐食物中毒综合症以及各种轻度至重度感染。在这些疾病中,皮肤坏死性血管通透性(VP)因子被认为是一种致病因子。溶血素BL以前被鉴定为具有VP活性的独特的三方溶血素。在这项研究中,开发了一种高产量的纯化方案,该方案允许对溶血素BL活性进行定量表征,并确定每种组分的分子量,pI和N端序列。毫克数量的B,L1和L2组分通过阴离子交换和羟基磷灰石色谱的结合进行了高度纯化。合并的成分在低剂量时具有VP活性,而在高剂量时则坏死。在浊度溶血分析中,毒素表现出不寻常的剂量反应区现象。在最高200 ng / ml的剂量下活性增加,然后在最高350 ng / ml的剂量下活性降低,在最高2500 ng / ml的剂量下活性保持恒定。这种行为可以解释溶血素BL在凝胶扩散测定中的典型不连续模式。在一种或两种组分的高浓度下,少量互补组分的存在导致充分的溶血活性。红摩尔浓度的Zn2 +可保护红细胞免于裂解,而浓度高达25 mM的Ca2 +和Mg2 +则不能保护红细胞。这些数据为该毒素的进一步研究提供了指导,并表明溶血素BL是一种皮肤坏死性VP因子,与蜡状芽孢杆菌致病因子有关。

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