Ramos Gisele da Costa, Silva-Silva João Victor, Watanabe Luciano Almeida, Siqueira José Edson de Sousa, Almeida-Souza Fernando, Calabrese Kátia S, Marinho Andrey Moacir do Rosario, Marinho Patrícia Santana Barbosa, Oliveira Aldo Sena de
Post-Graduate Program in Chemistry, Federal University of Pará, Belém 66075-110, Brazil.
Laboratory of Immunomodulation and Protozoology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro 81310-020, Brazil.
Antibiotics (Basel). 2022 Sep 29;11(10):1332. doi: 10.3390/antibiotics11101332.
The present work reports the isolation and biological evaluation of three dimeric xanthones from sp. EJC01.1 isolated as endophytic from , a typical plant of the Amazon. The compounds phomoxanthone A (), phomoxanthone B () and dicerandrol B () were isolated by chromatographic procedures and identified by spectroscopic methods of 1D and 2D NMR and MS. The extracts and compound showed antimicrobial activities against , , , and . The compound phomoxanthone A () showed greater inhibitory activity against (MIC of 7.81 µg mL); in addition, it also pronounced inhibitory effect against promastigote forms of (IC of 16.38 ± 1.079 µg mL) and epimastigote forms (IC of 28.61 ± 1.071 µg mL). To provide more information about the antibacterial activity of compound 1, an unprecedented molecular docking study was performed using S-ribosyl-homocysteine lyase (LuxS) (PDB ID 2FQO), which showed a possible interaction of phomoxanthone A with two of the residues (His58 and Cys126) that are fundamental for the catalysis mechanism in , which may be associated with the higher activity, when compared to other bacteria, observed in experimental studies. Additionally, quantum studies (DFT) were performed, for which a low gap value (5.982 eV) was observed, which corroborates the reactivity of phomoxanthone A. Thus, phomoxanthone A can be a good agent against pathogenic bacteria.
本研究报道了从亚马逊地区一种典型植物中分离出的内生菌EJC01.1中三种二聚口山酮的分离及生物学评价。通过色谱法分离得到化合物异戊二烯口山酮A()、异戊二烯口山酮B()和双丝兰醇B(),并通过一维和二维核磁共振及质谱等光谱方法进行鉴定。提取物和化合物对、、、和显示出抗菌活性。化合物异戊二烯口山酮A()对(最低抑菌浓度为7.81 µg/mL)表现出更强的抑制活性;此外,它对前鞭毛体形式的(半数抑制浓度为16.38±1.079 µg/mL)和上鞭毛体形式(半数抑制浓度为28.61±1.071 µg/mL)也有显著的抑制作用。为了提供更多关于化合物1抗菌活性的信息,使用S-核糖基高半胱氨酸裂解酶(LuxS)(蛋白质数据银行编号2FQO)进行了一项前所未有的分子对接研究,结果表明异戊二烯口山酮A与中的两个对催化机制至关重要的残基(His58和Cys126)可能存在相互作用,这可能与实验研究中观察到的该化合物相对于其他细菌更高的活性有关。此外,还进行了量子研究(密度泛函理论),观察到其低能隙值(5.982 eV),这证实了异戊二烯口山酮A的反应活性。因此,异戊二烯口山酮A可能是一种对抗病原菌的良好药物。