Abdel-Razik Mahmoud A, Azmy Ahmed F, Dishisha Tarek, El-Gendy Ahmed O, Afzan Adlin, Kamal Nurkhalida, Tawfike Ahmed, Sebak Mohamed
Department of Pharmaceutical Microbiology and Immunology, Faculty of Pharmacy, Beni-Suef University, Beni-Suef, 62514, Egypt.
Phytochemistry Unit, Herbal Medicine Research Centre, Institute for Medical Research, National Institutes of Health, Ministry of Health Malaysia, Shah Alam, Selangor, 40170, Malaysia.
Microb Cell Fact. 2025 Jun 18;24(1):136. doi: 10.1186/s12934-025-02759-0.
In reply to the critical requirement for new anti-infective and anticancer agents, this study explores aquatic actinomycetes as a favorable source of naturally occurring bioactive compounds. Using metabolomics and dereplication analysis, we investigated the chemical profiles of promising eight actinobacterial isolates out of seventy-eight actinomycetes isolated from the Red Sea and the Mediterranean Sea. The eight isolates (6, 10, 12, 35, 42, 43, 45, and 48) demonstrated cytotoxic activity against the breast adenocarcinoma (MCF-7) cell line and broad-spectrum antimicrobial activity against Gram-negative and Gram-positive microbes. Isolate 10 exhibited the broadest antibacterial activity, while isolates 42, 43, and 45 showed moderate to weak cytotoxic potential. Genetic identification via 16S rRNA sequencing classified seven isolates as sp. and one as sp. Multivariate data analysis (MVDA) of the high-resolution mass spectrometry (HRMS) data identified isolate 10 as an outlier, rich in diverse secondary metabolites. Dereplication revealed numerous metabolites with potential antimicrobial and anticancer activity, confirmed by NMR data highlighting their complex chemical profiles. These findings underscore the effectiveness of integrating metabolomics and bioassays to uncover unique bioactive products from aquatic actinobacteria, creating a foundation for further development of novel antimicrobial and antitumor medicines.
The online version contains supplementary material available at 10.1186/s12934-025-02759-0.
为了回应对抗感染和抗癌新药的迫切需求,本研究探索了水生放线菌作为天然生物活性化合物的良好来源。通过代谢组学和去重复分析,我们研究了从红海和地中海分离出的七十八株放线菌中八株有前景的放线菌分离株的化学图谱。这八株分离株(6、10、12、35、42、43、45和48)对乳腺腺癌(MCF-7)细胞系表现出细胞毒性活性,并对革兰氏阴性和革兰氏阳性微生物具有广谱抗菌活性。分离株10表现出最广泛的抗菌活性,而分离株42、43和45显示出中度至弱的细胞毒性潜力。通过16S rRNA测序进行的基因鉴定将七株分离株归类为 属,一株归类为 属。对高分辨率质谱(HRMS)数据的多变量数据分析(MVDA)将分离株10鉴定为异常值,富含多种次生代谢物。去重复揭示了许多具有潜在抗菌和抗癌活性的代谢物,核磁共振(NMR)数据证实了它们复杂的化学图谱。这些发现强调了整合代谢组学和生物测定以从水生放线菌中发现独特生物活性产物的有效性,为新型抗菌和抗肿瘤药物的进一步开发奠定了基础。
在线版本包含可在10.1186/s12934-025-02759-0获取的补充材料。