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首页> 外文期刊>Biotechnology and Bioengineering >Influence of intracellular nucleotide and nucleotide sugar contents on recombinant interferon-gamma glycosylation during batch and fed-batch cultures of CHO cells
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Influence of intracellular nucleotide and nucleotide sugar contents on recombinant interferon-gamma glycosylation during batch and fed-batch cultures of CHO cells

机译:CHO细胞分批和补料分批培养过程中细胞内核苷酸和核苷酸糖含量对重组干扰素-γ糖基化的影响

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摘要

Both the macroheterogeneity of recombinant human IFN-gamma produced by CHO cells and intracellular levels of nucleotides and sugar nucleotides, have been characterized during batch and fed-batch cultures carried out in different media. Whereas PF-BDM medium was capable to maintain a high percentage of the doubly-glycosylated glycoforms all over the process, mono-glycosylated and non-glycosylated forms increased during the batch culture using SF-RPMI medium. Intracellular level of UTP was higher in PF-BDM all over the batch culture compared to the SF-RPMI process. UDP-Gal accumulated only during the culture performed in PF-BDM medium, probably as a consequence of the reduced UDP-Glc synthesis flux in SF-RPMI medium. When the recombinant CHO cells were cultivated in fed-batch mode, the UTP level remained at a relatively high value in serum-containing RPMI and its titer increased during the fed-phase indicating an excess of biosynthesis. Besides, an accumulation of UDP-Gal occurred as well. Those results all together indicate that UTP and UDP-Glc syntheses in CHO cells cultivated in SF-RPMI medium in batch process, could be limiting during the glycosylation processes of the recombinant IFN-gamma. At last, the determination of the energetic status of the cells over the three studied processes suggested that a relationship between the adenylate energy charge and the glycosylation macroheterogeneity of the recombinant IFN-gamma may exist.
机译:在不同培养基中分批和补料分批培养的过程中,均已表征了CHO细胞产生的重组人IFN-γ的宏观异质性以及细胞内核苷酸和糖核苷酸的水平。 PF-BDM培养基能够在整个过程中维持高百分比的双糖基化糖型,而在使用SF-RPMI培养基的分批培养过程中,单糖基化和非糖基化的形式有所增加。与SF-RPMI过程相比,在整个分批培养中,PF-BDM中UTP的细胞内水平较高。仅在PF-BDM培养基中进行培养时才会积累UDP-Gal,这可能是SF-RPMI培养基中UDP-Glc合成流量降低的结果。当以补料分批方式培养重组CHO细胞时,UTP水平在含血清的RPMI中保持相对较高的值,并且在补料阶段其滴度增加,表明生物合成过多。此外,也发生了UDP-Gal的积累。这些结果一起表明,在SF-RPMI培养基中分批培养的CHO细胞中的UTP和UDP-Glc合成可能在重组IFN-γ的糖基化过程中受到限制。最后,在三个研究过程中确定细胞的能量状态表明,腺苷酸能电荷与重组IFN-γ糖基化宏观异质性之间可能存在关系。

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