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Components of yeast (Sacchromyces cervisiae) extract as defined media additives that support the growth and productivity of CHO cells

机译:酵母(Sacchromyces cervisiae)提取物的成分是确定的培养基添加剂,可支持CHO细胞的生长和生产力

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Yeast and plant hydrolysates are used as media supplements to support the growth and productivity of CHO cultures for biopharmaceutical production. Through fractionation of a yeast lysate and metabolic analysis of a fraction that had bioactivity equivalent to commercial yeast extract (YE), bioactive components were identified that promoted growth and productivity of two recombinant CHO cell lines (CHO-Luc and CHO-hFcEG2) equivalent to or greater than YE -supplemented media. Autolysis of the yeast lysate was not necessary for full activity, suggesting that the active components are present in untreated yeast cells. A bioactive fraction (3KF) of the yeast lysate was isolated from the permeate using a 3 kDa molecular weight cut-off (MWCO) filter. Supplementation of this 3KF fraction into the base media supported growth of CHO-Luc cells over eight passages equivalent to YE -supplemented media. The 3KF fraction was fractionated further by a cation exchange spin column using a stepwise pH elution. Metabolomic analysis of a bioactive fraction isolated at high pH identified several arginine and lysine -containing peptides as well as two polyamines, spermine and spermidine, with 3.5 and 4.5 higher levels compared to a fraction showing no bioactivity. The addition of a mixture of polyamines and their precursors (putrescine, spermine, spermidine, ornithine and citrulline) as well as increasing the concentration of some of the components of the original base medium resulted in a chemically -defined (CD) formulation that produced an equivalent viable cell density (VCD) and productivity of the CHO-Luc cells as the YE -supplemented medium. The VCD of the CHO-hFcEG2 culture in the CD medium was 1.9x greater and with equivalent productivity to the YE-supplemented media. (C) 2016 Elsevier B.V. All rights reserved.
机译:酵母和植物水解产物用作培养基补充剂,以支持用于生物制药生产的CHO培养物的生长和生产力。通过酵母裂解物的分馏和具有与商业酵母提取物(YE)等效的生物活性的馏分的代谢分析,鉴定出了具有生物活性的成分,可以促进两种重组CHO细胞系(CHO-Luc和CHO-hFcEG2)或大于YE补充的媒体。酵母裂解物的自溶不是完整活性所必需的,这表明活性成分存在于未处理的酵母细胞中。使用3 kDa截留分子量(MWCO)过滤器从渗透物中分离出酵母裂解物的生物活性级分(3KF)。向基础培养基中补充此3KF馏分可支持CHO-Luc细胞在相当于YE补充培养基的八次传代中生长。使用逐步pH洗脱,通过阳离子交换离心柱进一步分离3KF级分。在高pH下分离的生物活性部分的代谢组学分析确定了几种精氨酸和赖氨酸的肽,以及两种多胺(精胺和亚精胺),与未显示生物活性的部分相比,其含量分别高3.5和4.5。添加多胺及其前体的混合物(腐胺,精胺,亚精胺,鸟氨酸和瓜氨酸),并增加原始基础培养基中某些成分的浓度,导致产生化学成分确定的(CD)制剂,相当于YE补充培养基的CHO-Luc细胞的等效活细胞密度(VCD)和生产力。 CD培养基中CHO-hFcEG2培养物的VCD比YE培养基高1.9倍,并且具有同等的生产力。 (C)2016 Elsevier B.V.保留所有权利。

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