Metabolic profiling and biological potential of the marine sponge associated Nocardiopsis sp. UR67 along with docking studies

被引:2
|
作者
Ibrahim, Alyaa Hatem [1 ]
Attia, Eman Zekry [2 ]
Hofny, Heba A. [3 ]
Alsenani, Faisal [4 ]
Zayed, Ahmed [5 ,6 ]
Rateb, Mostafa E. [7 ]
Abdelmohsen, Usama Ramadan [2 ,8 ]
Desoukey, Samar Yehia [2 ]
Fouad, Mostafa Ahmed [2 ]
Kamel, Mohamed Salah [2 ,8 ]
机构
[1] Sohag Univ, Fac Pharm, Dept Pharmacognosy, Sohag, Egypt
[2] Minia Univ, Fac Pharm, Dept Pharmacognosy, Al Minya, Egypt
[3] Sohag Univ, Fac Pharm, Dept Pharmaceut Chem, Sohag, Egypt
[4] Umm Al Qura Univ, Coll Pharm, Dept Pharmacognosy, Mecca, Saudi Arabia
[5] Tanta Univ, Coll Pharm, Dept Pharmacognosy, Tanta, Egypt
[6] Tech Univ Kaiserslautern, Inst Bioproc Engn, Kaiserslautern, Germany
[7] Univ West Scotland, Sch Comp Engn & Phys Sci, Paisley, Renfrew, Scotland
[8] Deraya Univ, Fac Pharm, Dept Pharmacognosy, New Minia City, Egypt
关键词
Nocardiopsis; marine sponges; metabolomics; anti-infective; cytotoxicity; STREPTOMYCES; ANTIBIOTICS; DERIVATIVES;
D O I
10.1080/14786419.2022.2084396
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This work was performed to dig into the phytochemical composition and bioactivities of Nocardiopsis sp. UR67 associated with the marine sponge Callyspongia sp. It was fermented in suspension and immobilised in calcium alginate bead cultures. The ethyl acetate extracts, afforded from the broth in each case named EG49 and J-48g, respectively, revealed 16 chemical principles mostly belonging to polyketides, macrolides, and peptides. EG-49 and J-48g displayed anti-Candida albicans activity with IC50 values of 8.1 and 8.3 mu g/mL, and a substantial cytotoxic effect against lung adenocarcinoma H1650 at IC 50 12.6 and 13.7 mu g/mL, respectively. However, only EG-49 exhibited a noteworthy anti-trypanosomal activity at 7.5 mu g/mL. Molecular docking of the characterised compounds against Trypanosoma brucei trypanothione reductase demonstrated the highest binding models of griseochelin-methyl ester (9) and filipin-II (11), which drew considerable significance of the metabolites derived from Nocardiopsis sp. UR67 developing potential T. brucei trypanothione reductase inhibitors.
引用
收藏
页码:3531 / 3537
页数:7
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