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用于海洋海绵珍珠拟海牛原代细胞培养的基础培养基的配方。

Formulation of a basal medium for primary cell culture of the marine sponge Hymeniacidon perleve.

作者信息

Zhao Quanyu, Zhang Wei, Jin Meifang, Yu Xingju, Deng Maicun

机构信息

Marine Bioproducts Engineering Group, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.

出版信息

Biotechnol Prog. 2005 May-Jun;21(3):1008-12. doi: 10.1021/bp050029c.

Abstract

Marine sponge cell culture is a potential route for the sustainable production of sponge-derived bioproducts. Development of a basal culture medium is a prerequisite for the attachment, spreading, and growth of sponge cells in vitro. With the limited knowledge available on nutrient requirements for sponge cells, a series of statistical experimental designs has been employed to screen and optimize the critical nutrient components including inorganic salts (ferric ion, zinc ion, silicate, and NaCl), amino acids (glycine, glutamine, and aspartic acid), sugars (glucose, sorbitol, and sodium pyruvate), vitamin C, and mammalian cell medium (DMEM and RPMI 1640) using MTT assay in 96-well plates. The marine sponge Hymeniacidon perleve was used as a model system. Plackett-Burman design was used for the initial screening, which identified the significant factors of ferric ion, NaCl, and vitamin C. These three factors were selected for further optimization by Uniform Design and Response Surface Methodology (RSM), respectively. A basal medium was finally established, which supported an over 100% increase in viability of sponge cells.

摘要

海洋海绵细胞培养是可持续生产海绵衍生生物产品的一条潜在途径。开发基础培养基是海绵细胞在体外附着、铺展和生长的先决条件。鉴于对海绵细胞营养需求的了解有限,人们采用了一系列统计实验设计,通过在96孔板中进行MTT分析,来筛选和优化关键营养成分,包括无机盐(铁离子、锌离子、硅酸盐和氯化钠)、氨基酸(甘氨酸、谷氨酰胺和天冬氨酸)、糖类(葡萄糖、山梨醇和丙酮酸钠)、维生素C以及哺乳动物细胞培养基(DMEM和RPMI 1640)。海洋海绵皱皮软海绵被用作模型系统。采用Plackett-Burman设计进行初步筛选,确定了铁离子、氯化钠和维生素C这些显著因素。分别通过均匀设计和响应面法(RSM)对这三个因素进行进一步优化。最终建立了一种基础培养基,该培养基能使海绵细胞的活力提高超过100%。

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