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首页> 外文期刊>Biochemical Engineering Journal >Effects of phosphatidic acid on recombinant protein production by chinese hamster ovary cells in serum-free culture
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Effects of phosphatidic acid on recombinant protein production by chinese hamster ovary cells in serum-free culture

机译:磷脂酸对无血清培养中国仓鼠卵巢细胞产生重组蛋白的影响

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摘要

When recombinant Chinese hamster ovary (CHO) cells (ATCC CRL-8200) producing human interferon-#gamma# (hIFN-#gamma#) were incubated with exogenously supplied phosphatidic acid (PA) from egg yolk lecithin in a serum-free medium, PA induced increases in both the density of viable cells and concentration of hIFN-#ganna# secreted into the medium. Dispersion of PA with a non-ionic surfactant, Tween 80, further enhanced both cell growth and hIFN-#gamma# production. Replacement of the culture medium containing PA by fresh medium without PA in the course of a static culture did not influence cell growth indicating that PA is required to be continuously present in a serum-free medium to stimulate cell growth. Using a fresh medium containing PA for replacement resulted in significant enhancement of both cell density and hIFN-#gamma# yield. These results suggest that PA is a promising constituent of low-protein serum-free media for the effective production of recombinant proteins.
机译:将产生人干扰素-#γ#(hIFN-#γ#)的重组中国仓鼠卵巢(CHO)细胞(ATCC CRL-8200)与来自蛋黄卵磷脂的外源磷脂酸(PA)在无血清培养基中孵育时, PA诱导的活细胞密度和分泌到培养基中的hIFN-#ganna#浓度均增加。 PA与非离子表面活性剂Tween 80的分散进一步增强了细胞生长和hIFN-#γ#的产生。在静态培养过程中,用不含PA的新鲜培养基替换含PA的培养基不会影响细胞生长,这表明PA必须连续存在于无血清培养基中以刺激细胞生长。使用含有PA的新鲜培养基进行置换可显着提高细胞密度和hIFN-γ产量。这些结果表明PA是有效生产重组蛋白的低蛋白无血清培养基的有希望的组成部分。

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