4.7 Article

Production of a Novel Fucoidanase for the Green Synthesis of Gold Nanoparticles by Streptomyces sp and Its Cytotoxic Effect on HeLa Cells

期刊

MARINE DRUGS
卷 13, 期 11, 页码 6818-6837

出版社

MDPI
DOI: 10.3390/md13116818

关键词

fucoidan; fucoidanase; Streptomyces; gold nanoparticles; HeLa cells

资金

  1. Marine Biotechnology Program - Ministry of Oceans and Fisheries, Korea [20150220]
  2. Korea Institute of Marine Science & Technology Promotion (KIMST) [201502202] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Marine actinobacteria-produced fucoidanases have received considerable attention as one of the major research topics in recent years, particularly for the medical exploitation of fucoidans and their degradation products. The present study describes the optimization and production of a novel fucoidanase for the green synthesis of gold nanoparticles and its biological applications. The production of fucoidanase was optimized using Streptomyces sp. The medium components were selected in accordance with the Plackett-Burman design and were further optimized via response surface methodology. The fucoidanase was statistically optimized with the most significant factors, namely wheat bran 3.3441 g/L, kelp powder 0.7041 g/L, and NaCl 0.8807 g/L, respectively. The biosynthesized gold nanoparticles were determined by UV-vis spectroscopy and were further characterized by X-ray diffraction analysis, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, energy dispersive X-ray analysis, and high-resolution transmission electron microscopy. Furthermore, the biosynthesized gold nanoparticles exhibited a dose-dependent cytotoxicity against HeLa cells and the inhibitory concentration (IC50) was found to be 350 mu g/mL at 24 h and 250 mu g/mL at 48 h. Therefore, the production of novel fucoidanase for the green synthesis of gold nanoparticles has comparatively rapid, less expensive and wide application to anticancer therapy in modern medicine.

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