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杆状病毒-昆虫细胞系统中的细胞密度效应:能量代谢的定量分析

Cell density effect in the baculovirus-insect cells system: a quantitative analysis of energetic metabolism.

作者信息

Bernal Vicente, Carinhas Nuno, Yokomizo Adriana Y, Carrondo Manuel J T, Alves Paula M

机构信息

Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa (ITQB-UNL/IBET), Oeiras, Portugal.

出版信息

Biotechnol Bioeng. 2009 Sep 1;104(1):162-80. doi: 10.1002/bit.22364.

Abstract

The cell density effect (i.e., the drop in the specific productivity in the baculovirus-insect cells expression system when cells are infected at high cell densities) has been extensively described in the literature. In this article, a model for the central metabolism of serum-free suspension cultures of Spodoptera frugiperda Sf9 cells is proposed and used to investigate the metabolic basis for this phenomenon. The main metabolic pathways (glycolysis, pentose phosphate pathway, tricarboxylic acids cycle, glutaminolysis, and amino acids metabolism), cellular growth and energetics were considered. The analysis of the stoichiometric model allowed further understanding of the interplay of the consumption of carbon and nitrogen sources in insect cells. Moreover, metabolic flux analysis revealed that Sf9 cells undergo a progressive inhibition of central metabolism when grown to high cell densities, for which the incorporation of amino acids carbon backbones into the TCA cycle (mainly glutamine) and the down-regulation of glycolysis are partially responsible. Following infection by baculovirus and cellular division arrest, central energy metabolism depended on the infection strategy chosen (cell concentration at the moment of infection and multiplicity of infection), inhibition being observed at high cell densities. Interestingly, the energetic status of the culture correlated with the decrease in cellular production of baculovirus, meaning that there is room for process optimization through the application of metabolic engineering techniques.

摘要

细胞密度效应(即杆状病毒 - 昆虫细胞表达系统中当细胞在高细胞密度下被感染时比生产率下降)在文献中已有广泛描述。在本文中,提出了一种针对草地贪夜蛾Sf9细胞无血清悬浮培养物中心代谢的模型,并用于研究这一现象的代谢基础。考虑了主要代谢途径(糖酵解、磷酸戊糖途径、三羧酸循环、谷氨酰胺分解和氨基酸代谢)、细胞生长和能量学。对化学计量模型的分析有助于进一步理解昆虫细胞中碳源和氮源消耗之间的相互作用。此外,代谢通量分析表明,Sf9细胞在生长至高密度时会经历中心代谢的逐步抑制,其中氨基酸碳骨架掺入三羧酸循环(主要是谷氨酰胺)以及糖酵解的下调对此负有部分责任。在杆状病毒感染和细胞分裂停滞之后,中心能量代谢取决于所选择的感染策略(感染时的细胞浓度和感染复数),在高细胞密度下会观察到抑制现象。有趣的是,培养物的能量状态与杆状病毒细胞产量的下降相关,这意味着通过应用代谢工程技术进行工艺优化存在空间。

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