Enzymology and Fungal Biotechnology Lab, Botany and Microbiology Department, Faculty of Science, Zagazig University, Zagazig, 44519, Egypt.
Biochemistry Department, Faculty of Agriculture, Zagazig University, Zagazig, 44519, Egypt.
Microb Cell Fact. 2024 Jan 5;23(1):15. doi: 10.1186/s12934-023-02270-4.
Attenuation of camptothecin (CPT) productivity by fungi with preservation and subculturing is the challenge that halts fungi to be an industrial platform of CPT production. Thus, screening for novel endophytic fungal isolates with metabolic stability for CPT production was the objective. Catharanthus roseus is one of the medicinal plants with diverse bioactive metabolites that could have a plethora of novel endophytes with unique metabolites. Among the endophytes of C. roseus, Aspergillus terreus EFBL-NV OR131583.1 had the most CPT producing potency (90.2 μg/l), the chemical identity of the putative CPT was verified by HPLC, FT-IR, NMR and LC-MS/MS. The putative A. terreus CPT had the same molecular mass (349 m/z), and molecular fragmentation patterns of the authentic one, as revealed from the MS/MS analyses. The purified CPT had a strong activity against MCF7 (5.27 μM) and UO-31 (2.2 μM), with a potential inhibition to Topo II (IC value 0.52 nM) than Topo 1 (IC value 6.9 nM). The CPT displayed a high wound healing activity to UO-31 cells, stopping their metastasis, matrix formation and cell immigration. The purified CPT had a potential inducing activity to the cellular apoptosis of UO-31 by ~ 17 folds, as well as, arresting their cellular division at the S-phase, compared to the control cells. Upon Plackett-Burman design, the yield of CPT by A. terreus was increased by ~ 2.6 folds, compared to control. The yield of CPT by A. terreus was sequentially suppressed with the fungal storage and subculturing, losing ~ 50% of their CPT productivity by 3rd month and 5th generation. However, the productivity of the attenuated A. terreus culture was completely restored by adding 1% surface sterilized leaves of C. roseus, and the CPT yield was increased over-the-first culture by ~ 3.2 folds (315.2 μg/l). The restoring of CPT productivity of A. terreus in response to indigenous microbiome of C. roseus, ensures the A. terreus-microbiome interactions, releasing a chemical signal that triggers the CPT productivity of A. terreus. This is the first reports exploring the potency of A. terreus, endophyte of C. roseus" to be a platform for industrial production of CPT, with an affordable sustainability with addition of C. roseus microbiome.
真菌在保存和传代过程中对喜树碱(CPT)产量的衰减是阻碍真菌成为 CPT 生产工业平台的挑战。因此,筛选具有代谢稳定性的新型内生真菌分离株以生产 CPT 是目标。长春花是具有多种生物活性代谢物的药用植物之一,可能有大量具有独特代谢物的新型内生真菌。在长春花的内生真菌中,曲霉 EFBL-NV OR131583.1 具有最强的 CPT 产生能力(90.2μg/l),通过 HPLC、FT-IR、NMR 和 LC-MS/MS 验证了推定 CPT 的化学身份。从 MS/MS 分析可知,推定的曲霉 CPT 具有相同的分子量(349m/z)和分子碎片模式与真实 CPT 相同。纯化的 CPT 对 MCF7(5.27μM)和 UO-31(2.2μM)具有很强的活性,对 Topo II(IC 值 0.52nM)的抑制作用强于 Topo 1(IC 值 6.9nM)。CPT 对 UO-31 细胞具有很高的伤口愈合活性,阻止其转移、基质形成和细胞迁移。与对照细胞相比,纯化的 CPT 对 UO-31 细胞的细胞凋亡具有潜在的诱导活性,约增加 17 倍,并在 S 期阻止其细胞分裂。在 Plackett-Burman 设计中,与对照相比,曲霉产生的 CPT 产量增加了约 2.6 倍。曲霉的 CPT 产量随着真菌的储存和传代而依次受到抑制,到第 3 个月和第 5 代时,其 CPT 产量损失约 50%。然而,通过添加 1%表面消毒的长春花叶片,可以完全恢复失活曲霉培养物的 CPT 生产力,CPT 产量比第一代培养物增加了约 3.2 倍(315.2μg/l)。对内生菌的 CPT 生产能力的恢复曲霉响应长春花的本土微生物组,确保了曲霉-微生物组的相互作用,释放出一种化学信号,触发曲霉的 CPT 生产能力。这是首次探索曲霉的潜力,长春花的内生菌"作为 CPT 工业生产的平台,通过添加长春花微生物组实现具有成本效益的可持续性。