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Identification and prioritization of phytochemicals from medicinal plants with inhibitory activity against the transpeptidase enzyme of Streptococcus pyogenes.

Title: Identification and prioritization of phytochemicals from medicinal plants with inhibitory activity against the transpeptidase enzyme of Streptococcus pyogenes.
Authors: Hejazi, Zeynab; Etehadpour, Marzieh; Bagheri, Mahboube
Source: Iranian Journal of Genetics & Plant Breeding (IJGPB); Apr2025, Vol. 14 Issue 1, p9-24, 16p
Subject Terms: PHYTOCHEMICALS; STREPTOCOCCUS pyogenes; ANTIBACTERIAL agents; MOLECULAR docking; PENICILLIN-binding proteins; MOLECULAR dynamics; DRUG resistance in bacteria; MEDICINAL plants
Abstract (English): Antibiotic-resistant bacteria, particularly Streptococcus pyogenes, which is responsible for a wide array of diseases, represent a significant public health threat. Natural therapeutic agents derived from medicinal plants, notably essential oils, have garnered interest due to their potential antimicrobial properties. This study investigated the antibacterial activity of secondary metabolites from sixteen medicinal plants against Streptococcus pyogenes through bioinformatics approaches. A comprehensive insilco analysis was conducted on 890 phytochemicals to evaluate their interactions with the bacterial transpeptidase enzyme via molecular docking and molecular dynamics (MD) simulations. The transpeptidase enzyme sequence was subjected to various analytical procedures, including the ProtParam tool, EMBOSS Antigenic program, and VICMpred server. ProtParam analysis revealed that the enzyme has a molecular weight of 23.54 kDa, comprises 206 amino acids, with an isoelectric point (pI) of 6.24, an instability index of 31.21, and an aliphatic index of 83.25. The EMBOSS Antigenic program predicted eleven potential antigenic sites within the enzyme, with scores indicating cellular process involvement (1.1164), molecular information (-1.5058), molecular metabolism (-0.965), and virulence factors (-0.686). Molecular docking results identified that compounds from licorice, barberry, turmeric, plantain, nettle, cinnamon, aloe vera, and thyme exhibited significant binding affinities, with interaction energies ranging from -7.0 to -9.3 kcal/mol. Nineteen phytochemicals, including methoxyhydnocarpine, linalyl acetate, kaempferol, and glycyrrhizic acid, demonstrated high binding affinity and stability. MD simulations further confirmed that the enzymeligand complexes maintained considerable stability throughout the simulation duration. Additionally, the investigated molecules displayed favorable total interaction energies, spanning from -4.55507 to -90.562 kcal/mol. Collectively, these findings suggest that the identified natural compounds possess promising antibacterial potential, warranting further experimental validation and drug development efforts. [ABSTRACT FROM AUTHOR]
Abstract (Arabic): المقال يركز على تحديد وترتيب الأولويات للمواد الكيميائية النباتية من ستة عشر نباتًا طبيًا تظهر نشاطًا مثبطًا ضد إنزيم الترانسبيبتيداز الخاص بـ *Streptococcus pyogenes*، وهو تهديد كبير للصحة العامة بسبب مقاومة المضادات الحيوية. من خلال طرق المعلوماتية الحيوية، بما في ذلك الربط الجزيئي ومحاكاة الديناميات الجزيئية، قامت الدراسة بتحليل 890 مادة كيميائية نباتية، وكشفت أن المركبات المستخلصة من نباتات مثل العرقسوس، والباربري، والكركم، والزعتر أظهرت تقاربًا قويًا مع الإنزيم، حيث تراوحت طاقات التفاعل بين -7.0 إلى -9.3 كيلو كالوري/مول. تشير النتائج إلى أن هذه المركبات الطبيعية لديها إمكانيات مضادة للبكتيريا واعدة، مما يستدعي مزيدًا من التحقق التجريبي لتطوير الأدوية. تؤكد الدراسة على أهمية استكشاف المركبات المستخلصة من النباتات كبدائل للمضادات الحيوية الاصطناعية في مكافحة مقاومة الميكروبات. [Extracted from the article]
: Copyright of Iranian Journal of Genetics & Plant Breeding (IJGPB) is the property of Imam Khomeini International University and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
Database: Complementary Index