蜂蜜和标准药物植物配体对金黄色葡萄球菌PBP2a (5M19)的治疗活性

E. David, H. O. Uzoeto, C. Nelson, C. Samuel
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摘要

金黄色葡萄球菌是所有常见葡萄球菌中最危险的。这些革兰氏阳性球形(球菌)细菌通常引起皮肤感染,但也可引起肺炎、心脏瓣膜感染和骨骼感染,并可能对某些抗生素治疗具有耐药性。酚类是蜂蜜中含量最多的植物化学成分,占蜂蜜植物化学成分的25.8%。这些植物化学物质的存在意味着蜂蜜可能具有抗菌、抗癌、抗氧化、利尿和抗炎等治疗特性。6个被测化合物中有2个不符合Lipinski规则5,即氢键供体(HBD) < 5氢键受体(HBA) <10分子量< 500 < 500分子量,< 5氢键供体,<10氢键受体。< 10个可旋转键数,且< 140 Å2 PSA值。总体对接得分在-3.085至-8.724之间,较为有利。绿原酸与合成抑制剂和其他植物配体相比,具有最好的对接分数(最低的结合能)。研究了蜂蜜植物配体与标准药物对金黄色葡萄球菌PBP2a (5M19)的结合方式和几何取向。结果表明,绿原酸与PBP2a具有关键的结合作用,其结合能(-8.724 kcal/mol)优于标准药物(头孢西丁;-5.985千卡/摩尔,奥西林;-5.222千卡/mol和甲基林-3.08千卡/mol)和其他植物配体(原儿茶酸-4.473千卡/mol和橙皮素-4.191千卡/mol)进行了测试。因此,绿原酸可以作为PBP2a的变构效应物进行研究,进一步优化其结构以增强其生物活性,从而合成并测试其实际生物活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic Activity of Phyto Ligands from Honey and Standard Drugs against Staphylococcus aureus PBP2a (5M19)
Staphylococcus aureus is the most dangerous of all of the many common staphylococcal bacteria. These gram-positive, sphere-shaped (coccal) bacteria often cause skin infections but can cause pneumonia, heart valve infections, and bone infections and may be resistant to treatment with some antibiotics. Phenols were the most abundant phytochemical compounds and accounted for 25.8% of the phytochemical composition of the honey. The presence of these phytochemicals implied that the honey could have therapeutic properties like antimicrobial, anticancer, antioxidant, diuretic, and anti-inflammatory activities. two out of the six tested compounds faulted the Lipinski rule of 5 which states that Hydrogen Bond Donor (HBD) < 5 Hydrogen –Bond Acceptor  (HBA) < , 10 Molecular Weight  < 500 < 500 Molecular weight, < 5 H-bond donors, <10 H-bond acceptors.< 10 number of rotatable bonds, and  < 140 Å2 PSA value In this study. favourable overall docking score was observed in the range of -3.085 to -8.724. Chlorogenic acid had the best docked score (lowest binding energy)when compared to the synthetic inhibitors and other phytoligands. The binding manners and geometrical orientation of the studied phyto ligand from Honey and standard drugs against Staphylococcus aureus PBP2a (5M19). The results revealed that, Chlorogenic acid  showed pivotal binding interactions with PBP2a, as it exhibited the best binding energy (-8.724 kcal/mol) compared with to standard drugs (Cefoxitin; -5.985 kcal/mol, Oxacillin; -5.222 kcal/mol and methiclin -3.08 kcal/mol) and other phytoligands (protocatechuic acid -4.473 kcal/mol and Hesperetin -4.191 kcal/mol) tested. Hence, Chlorogenic acid could be studied as promising lead candidates acting as allosteric effectors of PBP2a that might be subjecte d to further structural optimization to enhance their biological activity and hence been synthesized and tested to evaluate their actual biological activity.
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