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2
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Optimization and stability of glucoamylase production by recombinant strains of Aspergillus niger in chemostat culture.黑曲霉重组菌株在恒化器培养中生产糖化酶的优化与稳定性
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Recombinant glucoamylase production by Aspergillus niger B1 in chemostat and pH auxostat cultures.黑曲霉B1在恒化器和pH自控培养中生产重组葡萄糖淀粉酶
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凝胶微滴分泌检测:鉴定 CHO 细胞生产人抗体过程中产生的低产量亚群。

The gel microdrop secretion assay: Identification of a low productivity subpopulation arising during the production of human antibody in CHO cells.

机构信息

Department of Molecular Biology, BASF Bioresearch Corporation, 100 Research Drive, Worcester, MA, 01605, U.S.A..

出版信息

Cytotechnology. 2000 Oct;34(1-2):27-37. doi: 10.1023/A:1008186113245.

DOI:10.1023/A:1008186113245
PMID:19003378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3449738/
Abstract

The long-term stability of high-level expression is the mostimportant factor to consider when choosing cell lines for the expression of recombinant proteins. Declining volumetricyields in large-scale fermentation can be caused by changes affecting the cell population as a whole such as loss in viability, depletion of nutrients or accumulation of metabolites affecting cell growth. Alternatively, geneticinstability may lead to the outgrowth of a less productive,metabolically favored sub-population. Currently a variety ofparameters are measured to monitor the condition of cells infermenters including glucose uptake, lactate accumulation andoxygen consumption; in addition, periodic viable cell countsallow the determination of the growth rate and viability of the population. All of these methods measure the condition ofthe cell population as a whole and changes must involve a significantly large proportion of the total culture in orderto be detectable. Here we report on a method that allows theevaluation of the productivity of individual cells. Using the gel microdrop secretion assay, we detected the appearance ofa sub-population of cells with lower productivity. Subsequentanalysis of the culture confirmed the existence of lower productivity cells with a lower vector copy number. Therefore,the single cell secretion assay proved to be a rapid method todetect and isolate a low productivity variant of the producer cell line.

摘要

长期稳定的高水平表达是选择用于表达重组蛋白的细胞系时最重要的考虑因素。在大规模发酵中,体积产率的下降可能是由于整体上影响细胞群体的变化引起的,例如活力丧失、营养物质耗尽或影响细胞生长的代谢物积累。或者,遗传不稳定性可能导致生长效率较低、代谢上有利的亚群的生长。目前,为了监测发酵罐中细胞的状态,测量了各种参数,包括葡萄糖摄取、乳酸积累和耗氧量;此外,定期进行活细胞计数可确定群体的生长速率和活力。所有这些方法都测量细胞群体的整体状态,并且必须涉及总培养物的显著大部分才能被检测到。在这里,我们报告了一种可以评估单个细胞生产力的方法。使用凝胶微滴分泌测定法,我们检测到具有较低生产力的细胞亚群的出现。随后对培养物的分析证实了存在具有较低载体拷贝数的较低生产力细胞。因此,单细胞分泌测定法被证明是一种快速检测和分离生产细胞系低生产力变体的方法。