Antimicrobial Activity of Dihydroisocoumarin Isolated from Wadi Lajab Sediment-Derived Fungus Penicillium chrysogenum: In Vitro and In Silico Study

被引:11
|
作者
Orfali, Raha [1 ]
Perveen, Shagufta [2 ]
AlAjmI, Mohamed Fahad [1 ]
Ghaffar, Safina [1 ]
Rehman, Md Tabish [1 ]
AlanzI, Abdullah R. [1 ]
Gamea, Saja Bane [1 ]
Khwayri, Mona Essa [1 ]
机构
[1] King Saud Univ, Coll Pharm, Dept Pharmacognosy, POB 2457, Riyadh 11451, Saudi Arabia
[2] Morgan State Univ, Dept Chem, Sch Comp Math & Nat Sci, Baltimore, MD 21251 USA
来源
MOLECULES | 2022年 / 27卷 / 11期
关键词
Penicillium chrysogenum; dihydroisocoumarin; microbial resistance; molecular modeling; ANTIBIOTIC-RESISTANCE; METABOLITES; MECHANISM; GENE;
D O I
10.3390/molecules27113630
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Antibiotic resistance is considered a major health concern globally. It is a fact that the clinical need for new antibiotics was not achieved until now. One of the most commonly prescribed classes of antibiotics is beta-Lactam antibiotics. However, most bacteria have developed resistance against beta-Lactams by producing enzymes beta-Lactamase or penicillinase. The discovery of new beta-Lactamase inhibitors as new antibiotics or antibiotic adjuvants is essential to avoid future catastrophic pandemics. In this study, five dihydroisocoumarin: 6-methoxy mellein (1); 5,6-dihydroxymellein (2); 6-hydroxymellein (3); 4-chloro-6-hydroxymellein (4) and 4-chloro-5,6-di-hydroxymellein (5) were isolated from Wadi Lajab sediment-derived fungus Penicillium chrysogenum, located 15 km northwest of Jazan, KSA. The elucidation of the chemical structures of the isolated compounds was performed by analysis of their NMR, MS. Compounds 1-5 were tested for antibacterial activities against Gram-positive and Gram-negative bacteria. All of the compounds exhibited selective antibacterial activity against Gram-positive bacteria Staphylococcus aureus and Bacillus licheniformis except compound 3. The chloro-dihydroisocoumarin derivative, compound 4, showed potential antimicrobial activities against all of the tested strains with the MIC value between 0.8-5.3 mu g/mL followed by compound 5, which exhibited a moderate inhibitory effect. Molecular docking data showed good affinity with the isolated compounds to beta-Lactamase enzymes of bacteria; NDM-1, CTX-M, OXA-48. This work provides an effective strategy for compounds to inhibit bacterial growth or overcome bacterial resistance.
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页数:15
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