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LDH-C can be differentially expressed during fermentation of CHO cells

机译:LDH-C可以在CHO细胞发酵过程中差异表达

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Expression of CHO mRNA was measured with special microarrays from the Consortium for Chinese Hamster Ovary (CHO) Cell Genomics led by Prof. Wei-Shou Hu of the University of Minnesota and Prof. Miranda Yap of the Bioprocess Technology Institute of A*STAR, Singapore ( http://hugroup.cems.umn.edu/CHO/cho_index.html ). Cultivation experiments were performed in small scale 2L stirred tank bioreactors. During fermentation a temperature shift of -3°C was performed. This was accompanied by a reduction of the cell specific lactate production rate. The analysis of transcriptome samples before and after the temperature shift with microarrays showed several changes in the expression of available gene markers. LDH-C expression raised about 2 fold after temperature shift. LDH-A did not change. As LDH-C is known to be a specialized isoenzyme in sperm cells for consuming lactate in a lactate containing milieu, LDH-C could be proposed as a target for genetic engineering, facilitating lactate consumption in the late phase of high cell density cultures and prolonging longevity of CHO production cultures by reducing lactate and base accumulation.
机译:CHO mRNA的表达由明尼苏达大学的胡维寿教授和新加坡A * STAR生物工艺技术研究所的Miranda Yap教授领导的中国仓鼠卵巢(CHO)细胞基因组学联盟的特殊微阵列测量。 (http://hugroup.cems.umn.edu/CHO/cho_index.html)。培养实验在小型2L搅拌釜生物反应器中进行。在发酵期间,进行了-3℃的温度变化。这伴随着细胞特异性乳酸产生速率的降低。用微阵列对温度变化前后的转录组样品进行的分析显示,可用基因标记的表达发生了一些变化。温度变化后,LDH-C表达升高约2倍。 LDH-A不变。由于已知LDH-C是精子细胞中的一种专门的同工酶,用于消耗含环境的乳酸中的乳酸,因此LDH-C可以作为基因工程的靶标,促进高细胞密度培养后期乳酸的消耗并延长通过减少乳酸和碱基积累,延长CHO生产文化的寿命。

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