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pH dependent effects of sodium ions on dextransucrase activity in Streptococcus mutans

机译:pH依赖的钠离子对变形链球菌葡聚糖酶活性的影响

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摘要

Dextransuccrase (E.C 2.4.1.5) is a key enzyme in S. mutans for the metabolism of sucrose which helps in the adherence and accumulation of bacteria on tooth surface leading to the formation of dental caries. Dextransuccrase resembles in its catalytic properties with the brush boarder sucrase and exhibits pH dependent inhibitory and stimulatory effects in response to Na+. In this communication we studied the effect of monovalent cations on the activity of dextransuccrase from S. mutans. The percentage inhibition of dextransuccrase was 65% at 0.5 mM NaCl which enhanced to 90% at 20 mM sodium concentration. However there was no effect on dextransucrase activity in presence of other monovalent cations (Rb+, Cs+, and K+) tested. Enzyme activity was enhanced 20–24% in acidic pH but was strongly inhibited (59–89%) around neutral and alkaline pH by 0.5–2.0 mM sodium chloride. Upon dialysis, 86% of enzyme activity was restored to control values. There was no effect of 2 mM NaCl on glucosyltransferase activity of the enzyme. Kinetic studies revealed that enzyme showed biphasic effects in response to Na+ ions. At acidic pH the enzyme exhibited mixed type of activation affecting both Vmax and Km, while in alkaline pH, the enzyme showed V- type effect reducing Vmax by 74% without affecting Km. The effects of sodium ions on dextransuccrase activity were specific, thus it can be useful to block its catalytic activity, and reducing the cariogenic potential of S. mutans.
机译:葡聚糖(E.C 2.4.1.5)是变形链球菌中蔗糖代谢的关键酶,它有助于细菌在牙齿表面的附着和积累,从而导致龋齿的形成。葡聚糖蔗糖酶的催化性能与刷糖蔗糖酶相似,并表现出对Na + 响应的pH依赖性抑制和刺激作用。在本交流中,我们研究了单价阳离子对变形链球菌葡聚糖酶活性的影响。右旋糖酐酶在0.5µmM NaCl中的抑制百分比为65%,在钠浓度为20µmM时增加至90%。但是,在测试的其他单价阳离子(Rb + ,Cs + 和K + )存在下,对葡聚糖酶的活性没有影响。在中性和碱性pH值附近,酶的活性在酸性pH值下可提高20–24%,但在0.5–2.0μmMM的氯化钠附近则被强烈抑制(59–89%)。透析后,酶活性的86%恢复到对照值。 2 mM NaCl对酶的葡萄糖基转移酶活性没有影响。动力学研究表明,酶对Na + 离子具有双相作用。在酸性pH下,酶表现出混合的活化类型,同时影响Vmax和Km,而在碱性pH下,酶显示出V型作用,将Vmax降低74%,而不影响Km。钠离子对葡聚糖转移酶活性的影响是特异的,因此可以有效地阻止其催化活性,并降低变形链球菌的致癌潜力。

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