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采用响应面法对金黄色葡萄球菌生物法生产 staphyloxanthin 的营养优化:靶向表皮生长因子受体抑制的有前景的抗癌支架。

Nutritional optimization for bioprocess production of staphyloxanthin from Staphylococcus aureus with response surface methodology: promising anticancer scaffold targeting EGFR inhibition.

作者信息

Nosair Ahmed M, Abdelaziz Ahmed A, Abo-Kamer Amal M, Al-Madboly Lamiaa A, Farghali Mahmoud H

机构信息

Department of Microbiology and Immunology, Faculty of Pharmacy, Tanta University, Tanta, Egypt.

出版信息

Microb Cell Fact. 2025 May 6;24(1):99. doi: 10.1186/s12934-025-02717-w.

Abstract

BACKGROUND

Staphyloxanthin (STX) is a secondary metabolite pigment associated with membrane structures, recognized for its significant antioxidant properties. It plays a crucial role in combating reactive oxygen species (ROS), positioning it as a promising and effective alternative in cancer treatment. This study focused on enhancing the production of STX pigment by employing statistical optimization of media components, alongside the evaluation of its safety and anticancer properties.

RESULTS

A total of 59 Staphylococcus aureus isolates were screened and quantitatively estimated for STX production. The best pigment-producing isolate was identified based on molecular phylogenetic analysis as S. aureus A2, with accession number PP197164. A Box-Wilson central composite design was employed to evaluate the intricate interactions among six variables affecting the pigment yield. The most optimal conditions resulted in the highest production of STX of OD = 0.328, which is approximately 1.5-fold greater than the yield (OD = 0.215) obtained from OFAT optimization. The final response surface model fitting the data achieved a R² of 0.8748. STX exhibited marked cytotoxicity against the A549 NSCLC cell line with IC50 of 57.3 µg/mL, a safe dose in normal Vero cells. The anticancer activity of STX was predominantly mediated by the apoptotic pathway, as confirmed by confocal microscopy, the annexin V-FITC apoptosis assay, and the overexpression of caspase-3. Moreover, STX disrupted cell cycle at pre-G1 and G0/G1 phases in lung cancer. Intriguingly, STX exhibited its antitumor activity through reducing the EGFR expression. The molecular docking study revealed the potential binding interactions and affinities within the active sites of both wild-type and mutant EGFR.

CONCLUSION

The bioprocess for optimized production, combined with the biological profiling and low cytotoxicity, substantiates the potential application of STX pigment in combating lung cancer.

摘要

背景

金黄色葡萄球菌黄素(STX)是一种与膜结构相关的次生代谢产物色素,以其显著的抗氧化特性而闻名。它在对抗活性氧(ROS)方面发挥着关键作用,使其成为癌症治疗中有前景且有效的替代物。本研究聚焦于通过对培养基成分进行统计优化来提高STX色素的产量,并评估其安全性和抗癌特性。

结果

共筛选了59株金黄色葡萄球菌分离株,并对其STX产量进行了定量估计。基于分子系统发育分析,鉴定出最佳色素产生分离株为金黄色葡萄球菌A2,登录号为PP197164。采用Box-Wilson中心复合设计评估影响色素产量的六个变量之间的复杂相互作用。最优化条件下STX的最高产量为OD = 0.328,比单因素试验优化获得的产量(OD = 0.215)高出约1.5倍。拟合数据的最终响应面模型的R²为0.8748。STX对A549非小细胞肺癌细胞系表现出显著的细胞毒性,IC50为57.3 μg/mL,在正常Vero细胞中为安全剂量。共聚焦显微镜、膜联蛋白V-FITC凋亡检测和caspase-3的过表达证实,STX的抗癌活性主要通过凋亡途径介导。此外,STX在肺癌中使细胞周期在G1期前和G0/G1期受阻。有趣的是,STX通过降低表皮生长因子受体(EGFR)表达发挥其抗肿瘤活性。分子对接研究揭示了野生型和突变型EGFR活性位点内的潜在结合相互作用和亲和力。

结论

优化生产的生物过程,结合生物学特性分析和低细胞毒性,证实了STX色素在对抗肺癌方面的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2bd/12054202/2d0fd2655b52/12934_2025_2717_Fig1_HTML.jpg

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