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首页> 外文期刊>Applied and Environmental Microbiology >Possible Association of GroES and Antigen 85 Proteins with Heat Resistance of Mycobacterium paratuberculosis
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Possible Association of GroES and Antigen 85 Proteins with Heat Resistance of Mycobacterium paratuberculosis

机译:GroES和抗原85蛋白可能与副结核分枝杆菌的耐热性相关

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Conflicting reports on the heat resistance of Mycobacterium paratuberculosis prompted an examination of the effect of culture medium on this property of the organism. M. paratuberculosis was cultured in three types of media (fatty acid-containing medium 7H9-OADC (oleic acid-albumin-dextrose-catalase supplement) and glycerol-containing media WR-GD and 7H9-GD [glycerol-dextrose supplement]) at pH 6.0. M. paratuberculosis grown under these three culture conditions was then tested for heat resistance in distilled water at 65°C. Soluble proteins and mycolic acids of M. paratuberculosis were evaluated by two-dimensional electrophoresis (2-DE) and thin-layer chromatography (TLC), respectively. The type of culture medium used significantly affected the heat resistance of M. paratuberculosis. The decimal reduction times at 65°C (D65°C values; times required to reduce the concentration of bacteria by a factor of 10 at 65°C) for M. paratuberculosis strains grown in 7H9-OADC were significantly higher than those for the organisms grown in WR-GD medium (P D65°C value was significantly lower than that for the organism grown in 7H9-OADC medium (P = 0.022) but higher than that when it was cultured in WR-GD medium (P = 0.005). Proteomic analysis by 2-DE of soluble proteins extracted from M. paratuberculosis grown without heat stress in the three media (7H9-OADC, 7H9-GD, and WR-GD) revealed that seven proteins were more highly expressed in 7H9-OADC medium than in the other two media. When the seven proteins were subjected to matrix-assisted laser desorption ionization-mass spectrometric analysis, four of the seven protein spots were unidentifiable. The other three proteins were identified as GroES heat shock protein, alpha antigen, and antigen 85 complex B (Ag85B; fibronectin-binding protein). These proteins may be associated with the heat resistance of M. paratuberculosis. Alpha antigen and Ag85B are both trehalose mycolyltransferases involved in mycobacterial cell wall assembly. TLC revealed that 7H9-OADC medium supported production of more trehalose dimycolates and cell wall-bound mycolic acids than did WR-GD medium. The present study shows that in vitro culture conditions significantly affect heat resistance, cell wall synthesis, and protein expression of M. paratuberculosis and emphasize the importance of culture conditions on in vitro and ex vivo studies to estimate heat resistance.
机译:关于副结核分枝杆菌耐热性的报道相互矛盾,促使人们研究了培养基对生物体这种特性的影响。在三种类型的培养基(含脂肪酸的培养基7H9-OADC(油酸-白蛋白-葡萄糖-过氧化氢酶补充剂)和含甘油的培养基WR-GD和7H9-GD [甘油-葡萄糖补充剂])中培养副结核分枝杆菌。 pH值6.0。然后在这三种培养条件下生长的副结核分枝杆菌在65℃的蒸馏水中进行耐热性测试。分别通过二维电泳(2-DE)和薄层色谱法(TLC)评估副结核分枝杆菌的可溶性蛋白和霉菌酸。使用的培养基类型显着影响副结核分枝杆菌的耐热性。在7H9-OADC中生长的副结核分枝杆菌菌株在65°C时的十进制减少时间(D65°C值;在65°C时将细菌浓度降低10倍所需的时间)显着高于生物体在WR-GD培养基中生长的细菌(P D65°C值显着低于在7H9-OADC培养基中生长的生物(P = 0.022),但高于在WR-GD培养基中培养的生物(P = 0.005)。通过2-DE蛋白质组学分析从副结核分枝杆菌中提取的可溶蛋白,在三种培养基(7H9-OADC,7H9-GD和WR-GD)中在没有热应激的情况下生长,其中7种蛋白质在7H9-OADC培养基中的表达高于在另外两种介质中,当这7种蛋白质进行基质辅助激光解吸电离质谱分析时,这7种蛋白质斑点中有4种是无法鉴定的,其他3种蛋白质被鉴定为GroES热激蛋白质,α抗原和抗原。 85复合物B(Ag85B;纤连蛋白结合蛋白质)。这些蛋白质可能与副结核分枝杆菌的耐热性有关。 α抗原和Ag85B都是分枝杆菌细胞壁组装中涉及的海藻糖麦考糖基转移酶。 TLC显示,与WR-GD培养基相比,7H9-OADC培养基支持产生更多的海藻糖二甲酸酯和细胞壁结合的霉菌酸。本研究表明,体外培养条件显着影响副结核分枝杆菌的耐热性,细胞壁合成和蛋白质表达,并强调了培养条件在体外和离体研究中评估耐热性的重要性。

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