Pharmacognosy Department, Faculty of Pharmacy, Zagazig University, Zagazig, 44519, Egypt.
Enzymology and Fungal Biotechnology Lab, Botany and Microbiology Department, Faculty of Science, Zagazig University, Zagazig, 44519, Egypt.
Microb Cell Fact. 2024 Mar 12;23(1):78. doi: 10.1186/s12934-024-02356-7.
The biosynthetic potency of Taxol by fungi raises their prospective to be a platform for commercial production of Taxol, nevertheless, the attenuation of its productivity with the fungal storage, is the challenge. Thus, screening for a novel fungal isolate inhabiting ethnopharmacological plants, with a plausible metabolic stability for Taxol production could be one of the most affordable approaches. Aspergillus niger OR414905.1, an endophyte of Encephalartos whitelockii, had the highest Taxol productivity (173.9 μg/L). The chemical identity of the purified Taxol was confirmed by HPLC, FTIR, and LC-MS/MS analyses, exhibiting the same molecular mass (854.5 m/z) and molecular fragmentation pattern of the authentic Taxol. The purified Taxol exhibited a potent antiproliferative activity against HepG-2, MCF-7 and Caco-2, with IC values 0.011, 0.016, and 0.067 μM, respectively, in addition to a significant activity against A. flavus, as a model of human fungal pathogen. The purified Taxol displayed a significant effect against the cellular migration of HepG-2 and MCF-7 cells, by ~ 52-59% after 72 h, compared to the control, confirming its interference with the cellular matrix formation. Furthermore, the purified Taxol exhibited a significant ability to prompt apoptosis in MCF-7 cells, by about 11-fold compared to control cells, suppressing their division at G2/M phase. Taxol productivity by A. niger has been optimized by the response surface methodology with Plackett-Burman Design and Central Composite Design, resulting in a remarkable ~ 1.6-fold increase (279.8 μg/L), over the control. The biological half-life time of Taxol productivity by A. niger was ~ 6 months of preservation at 4 ℃, however, the Taxol yield by A. niger was partially restored in response to ethyl acetate extracts of E. whitelockii, ensuring the presence of plant-derived signals that triggers the cryptic Taxol encoding genes.
真菌产生紫杉醇的生物合成能力使其成为紫杉醇商业生产的平台,然而,真菌储存过程中生产力的衰减是一个挑战。因此,筛选一种新型的真菌分离株,其代谢稳定性合理,能够生产紫杉醇,可能是最具成本效益的方法之一。内生真菌 Aspergillus niger OR414905.1 是 Encephalartos whitelockii 的一种,其紫杉醇产量最高(173.9μg/L)。通过 HPLC、FTIR 和 LC-MS/MS 分析,确认了纯化紫杉醇的化学结构,其分子量(854.5m/z)和分子碎片模式与紫杉醇一致。纯化的紫杉醇对 HepG-2、MCF-7 和 Caco-2 具有很强的增殖抑制活性,IC50 值分别为 0.011、0.016 和 0.067μM,此外对 A. flavus 也有显著的抑制作用,A. flavus 是一种人类真菌病原体模型。纯化的紫杉醇对 HepG-2 和 MCF-7 细胞的细胞迁移有显著的抑制作用,72 小时后抑制率约为 52-59%,与对照组相比,证实了其对细胞基质形成的干扰。此外,与对照组相比,纯化的紫杉醇对 MCF-7 细胞的凋亡有显著的促进作用,约增加 11 倍,抑制其在 G2/M 期的分裂。通过 Plackett-Burman 设计和中心复合设计的响应面法对黑曲霉紫杉醇的生物合成进行了优化,产量比对照提高了约 1.6 倍(279.8μg/L)。黑曲霉紫杉醇的生物半衰期约为 4℃保存 6 个月,然而,黑曲霉紫杉醇的产量在响应白鳞铁角蕨的乙酸乙酯提取物时部分恢复,这确保了植物衍生信号的存在,这些信号触发了隐藏的紫杉醇编码基因。