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铁和锰结合的辅因子对口腔致病性微生物变形链球菌中超氧化物歧化酶性质的调节

Regulation of the properties of superoxide dismutase from the dental pathogenic microorganism Streptococcus mutans by iron- and manganese-bound co-factor.

作者信息

De Vendittis Alberto, Amato Massimo, Mickniewicz Andzelika, Parlato Giuseppe, De Angelis Amalia, Castellano Immacolata, Rullo Rosario, Riccitiello Francesco, Rengo Sandro, Masullo Mariorosario, De Vendittis Emmanuele

机构信息

Dipartimento di Biochimica e Biotecnologie Mediche, Università di Napoli Federico II, Via S. Pansini 5, 80131 Napoli, Italy.

出版信息

Mol Biosyst. 2010 Oct;6(10):1973-82. doi: 10.1039/c003557b. Epub 2010 Jul 30.

Abstract

Streptococcus mutans, the main pathogen involved in the development of dental caries, is an aerotolerant microorganism. The bacterium lacks cytochromes and catalase, but possesses other antioxidant enzymes, such as superoxide dismutase (SmSOD). Previous researches suggested that SmSOD belongs to the 'cambialistic' group, functioning with Fe or Mn in the active site. A recombinant SmSOD (rSmSOD) with a His-tail has been produced and characterised. Studies on metal uptake and exchange proved that rSmSOD binds either Fe or Mn as a metal co-factor, even though with a consistent preference for Fe accommodation. The analysis of several enzyme samples with different values of the Mn/Fe ratio in the active site proved that the type of metal is crucial for the regulation of the activity of rSmSOD. Indeed, differently from the significant preference for Fe displayed by the enzyme in the binding reaction, its Mn-form was 71-fold more active compared to the Fe-form. The rSmSOD was endowed with a significant thermostability, its half-inactivation occurring after 10 min exposure at 71 or 73 degrees C, depending on the bound metal. Moreover, the enthalpic and entropic contribution to the heat inactivation process of rSmSOD were strongly regulated by the Mn content of the enzyme. The effect of typical inhibitors/inactivators has been investigated. rSmSOD was inhibited by sodium azide, and its sensitivity increased in the presence of higher Mn levels. Concerning two physiological inactivators, the enzyme displayed a different behaviour, being quite resistant to hydrogen peroxide and significantly sensitive to sodium peroxynitrite. Furthermore, the Mn co-factor had an amplifying role in the regulation of this different sensitivity. These results confirm the cambialistic nature of SmSOD and prove that its properties are regulated by the different metal content. The adaptative response of S. mutans during its aerobic exposure in the oral cavity could involve a different metal uptake by SmSOD.

摘要

变形链球菌是参与龋齿形成的主要病原体,是一种兼性厌氧菌。该细菌缺乏细胞色素和过氧化氢酶,但拥有其他抗氧化酶,如超氧化物歧化酶(SmSOD)。先前的研究表明,SmSOD属于“兼性”组,在活性位点与铁或锰一起发挥作用。一种带有His尾的重组SmSOD(rSmSOD)已被制备并表征。对金属摄取和交换的研究证明,rSmSOD作为金属辅因子结合铁或锰,尽管它始终优先结合铁。对活性位点中锰/铁比值不同的几种酶样品的分析证明,金属类型对于调节rSmSOD的活性至关重要。事实上,与酶在结合反应中对铁的明显偏好不同,其锰形式的活性比铁形式高71倍。rSmSOD具有显著的热稳定性,根据结合的金属不同,在71或73摄氏度下暴露10分钟后其活性会减半。此外,rSmSOD热失活过程中的焓和熵贡献受酶中锰含量的强烈调节。已经研究了典型抑制剂/失活剂的作用。rSmSOD被叠氮化钠抑制,在较高锰水平存在时其敏感性增加。关于两种生理性失活剂,该酶表现出不同的行为,对过氧化氢相当耐受,对过氧亚硝酸钠则非常敏感。此外,锰辅因子在调节这种不同敏感性方面具有放大作用。这些结果证实了SmSOD的兼性本质,并证明其性质受不同金属含量的调节。变形链球菌在口腔中需氧暴露期间的适应性反应可能涉及SmSOD摄取不同的金属。

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