Kocabay Samet, Alagöz M Abdullah, Akkaya Birnur
Department of Molecular Biology and Genetics, Faculty of Science and Literature, İnönü University, Malatya, Turkiye.
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, İnönü University, Malatya, Turkiye.
Turk J Biol. 2025 Jan 8;49(1):92-101. doi: 10.55730/1300-0152.2727. eCollection 2025.
BACKGROUND/AIM: produces glucansucrase, an enzyme that converts sucrose into lactic acid, which lowers the pH in the oral environment and leads to tooth enamel demineralization, a key factor in dental caries. Additionally, glucansucrase facilitates the formation of extracellular polysaccharides, which promote bacterial adhesion to tooth surfaces. This study investigates the inhibitory effects of carvacrol, a natural compound, on glucansucrase activity both in vitro and in silico.
Glucansucrase enzyme was purified from . The inhibitory effects of carvacrol against glucansucrase enzyme were investigated both in vitro and in silico.
In the presence of 50 mM carvacrol, glucansucrase and salivary amylase activities were reduced by 51.25% and 14.85%, respectively. Carvacrol did not significantly inhibit (4.73%) the salivary amylase enzyme at 10 mM. Glucansucrase activity decreased by 51.63% in the presence of 10 mM acarbose, which was used as a positive control in glucansucrase enzyme studies. Acarbose inhibited salivary amylase with 82.54% loss of enzyme activity in the presence of 1 mM acarbose. The docking score obtained for carvacrol was -5.262 kcal/mol, while that obtained for acarbose was -6.084 kcal/mol. We carried out molecular dynamics simulation studies for 100 ns to determine the stability of carvacrol in the active site of the protein. Carvacrol demonstrated stable binding to glucansucrase with hydrogen bonds and interactions at key residues (ASP477, GLN960, and ASP909), confirmed by molecular dynamics simulations. Carvacrol remained stable between 16 and 100 ns.
Carvacrol selectively inhibits glucansucrase without significantly affecting salivary amylase, making it a more targeted inhibitor compared to acarbose, which inhibits both enzymes. Docking studies indicated that while carvacrol has a lower binding affinity than acarbose, its stable interaction with the enzyme suggests sustained inhibitory action. These findings highlight carvacrol as a promising natural compound for preventing dental caries, offering a more selective alternative to traditional inhibitors. Further in vivo studies are necessary to assess its therapeutic efficacy and safety in clinical applications for oral health.
背景/目的:产生葡聚糖蔗糖酶,该酶可将蔗糖转化为乳酸,从而降低口腔环境的pH值,导致牙釉质脱矿,这是龋齿的一个关键因素。此外,葡聚糖蔗糖酶有助于细胞外多糖的形成,促进细菌黏附于牙齿表面。本研究调查了天然化合物香芹酚在体外和计算机模拟中对葡聚糖蔗糖酶活性的抑制作用。
从……中纯化葡聚糖蔗糖酶。在体外和计算机模拟中研究了香芹酚对葡聚糖蔗糖酶的抑制作用。
在存在50 mM香芹酚的情况下,葡聚糖蔗糖酶和唾液淀粉酶的活性分别降低了51.25%和14.85%。在10 mM时,香芹酚对唾液淀粉酶的抑制作用不显著(4.73%)。在葡聚糖蔗糖酶研究中用作阳性对照的10 mM阿卡波糖存在时,葡聚糖蔗糖酶活性降低了51.63%。在1 mM阿卡波糖存在时,阿卡波糖对唾液淀粉酶的抑制率为82.54%,酶活性丧失。香芹酚的对接分数为-5.262 kcal/mol,而阿卡波糖的对接分数为-6.084 kcal/mol。我们进行了100 ns的分子动力学模拟研究,以确定香芹酚在蛋白质活性位点的稳定性。分子动力学模拟证实,香芹酚通过氢键和与关键残基(ASP477、GLN960和ASP909)的相互作用与葡聚糖蔗糖酶表现出稳定结合。香芹酚在16至100 ns之间保持稳定。
香芹酚选择性抑制葡聚糖蔗糖酶,而对唾液淀粉酶无显著影响,与同时抑制两种酶的阿卡波糖相比,它是一种更具针对性的抑制剂。对接研究表明,虽然香芹酚的结合亲和力低于阿卡波糖,但其与酶的稳定相互作用表明具有持续的抑制作用。这些发现突出了香芹酚作为一种有前景的预防龋齿的天然化合物,为传统抑制剂提供了一种更具选择性的替代物。有必要进行进一步的体内研究,以评估其在口腔健康临床应用中的治疗效果和安全性。