Suppr超能文献

开发工业规模的微流化为细胞破碎、生物分子释放和提高 Chlorella pyrenoidosa 的生物利用度。

Developing industry-scale microfluidization for cell disruption, biomolecules release and bioaccessibility improvement of Chlorella pyrenoidosa.

机构信息

State Key Laboratory of Food Science and Resources, Nanchang University, Nanchang 330047, Jiangxi, PR China.

State Key Laboratory of Food Science and Resources, Nanchang University, Nanchang 330047, Jiangxi, PR China.

出版信息

Bioresour Technol. 2023 Nov;387:129649. doi: 10.1016/j.biortech.2023.129649. Epub 2023 Aug 7.

Abstract

To facilitate biomolecules extraction and bioaccessibility of Chlorella pyrenoidosa, a novel industry-scale microfluidization (ISM) was used to disrupt cells effectively. Microscope images showed ISM damaged cell integrity, disorganized cell wall structure, pulverized cell membrane and promoted the release of intracellular components. The decrease of particle size and the increase of ζ-potential also confirmed the cell disruption. The cell breakage ratio of sample treated at 120 MPa was 98%. Compared with untreated samples, total soluble solid content and protein extraction rate of the sample treated at 120 MPa increased by 2 °Brix and 12%. Protein was degraded by ISM, the release of intracellular protein and the reduction of molecular weight increased protein digestibility by 20% in in vitro gastric phase. Lipid yield and chlorophyll b content were also increased by ISM. These results provided a new solution to cell disruption of microalgae and expanded the application field of ISM.

摘要

为了促进蛋白核小球藻生物分子的提取和生物利用度,采用新型工业化微射流(ISM)技术有效地破坏细胞。显微镜图像显示 ISM 破坏了细胞完整性,打乱了细胞壁结构,粉碎了细胞膜并促进了细胞内成分的释放。粒径的减小和 ζ-电位的增加也证实了细胞的破坏。在 120 MPa 下处理的样品的细胞破碎率为 98%。与未处理的样品相比,在 120 MPa 下处理的样品的总可溶性固体含量和蛋白质提取率分别增加了 2 度 Brix 和 12%。ISM 使蛋白质降解,细胞内蛋白质的释放和分子量的降低使蛋白质在体外胃阶段的消化率提高了 20%。脂质产率和叶绿素 b 含量也随着 ISM 的作用而增加。这些结果为微藻的细胞破碎提供了新的解决方案,并扩展了 ISM 的应用领域。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验