Zhu Marie M, Goyal Asti, Rank Douglas L, Gupta Sunil K, Vanden Boom Thomas, Lee Steven S
Biotechnology Development, Bristol-Myers Squibb Company, PO Box 4755, Syracuse, New York 13221-4755, USA.
Biotechnol Prog. 2005 Jan-Feb;21(1):70-7. doi: 10.1021/bp049815s.
Partial pressure of CO2 (pCO2) and osmolality as high as 150 mmHg and 440 mOsm/kg, respectively, were observed in large-scale CHO cell culture producing an antibody-fusion protein, B1. pCO2 and osmolality, when elevated to high levels in bioreactors, can adversely affect cell culture and recombinant protein production. To understand the sole impact of pCO2 or osmolality on CHO cell growth, experiments were performed in bench-scale bioreactors allowing one variable to change while controlling the other. Elevating pCO2 from 50 to 150 mmHg under controlled osmolality (about 350 mOsm/kg) resulted in a 9% reduction in specific cell growth rate. In contrast, increasing osmolality resulted in a linear reduction in specific cell growth rate (0.008 h(-1)/100 mOsm/kg) and led to a 60% decrease at 450 mOsm/kg as compared to the control at 316 mOsm/kg. This osmolality shift from 316 to 445 mOsm/kg resulted in an increase in specific production rates of lactate and ammonia by 43% and 48%, respectively. To elucidate the effect of high osmolality and/or pCO2 on the production phase, experiments were conducted in bench-scale bioreactors to more closely reflect the pCO2 and osmolality levels observed at large scale. Increasing osmolality to 400-450 mOsm/kg did not result in an obvious change in viable cell density and product titer. However, a further increase in osmolality to 460-500 mOsm/kg led to a 5% reduction in viable cell density and a 8% decrease in cell viability as compared to the control. Final titer was not affected as a result of an apparent increase in specific production rate under this increased osmolality. Furthermore, the combined effects from high pCO2 (140-160 mmHg) and osmolality (400-450 mOsm/kg) caused a 20% drop in viable cell density, a more prominent decrease as compared to elevated osmolality alone. Results obtained here illustrate the sole effect of high pCO2 (or osmolality) on CHO cell growth and demonstrate a distinct impact of high osmolality and/or pCO2 on production phase as compared to that on growth phase. These results are useful to understand the response of the CHO cells to elevated pCO2 (and/or osmolality) at a different stage of cultivation in bioreactors and thus are valuable in guiding bioreactor optimization toward improving protein production.
在大规模生产抗体融合蛋白B1的中国仓鼠卵巢(CHO)细胞培养中,观察到二氧化碳分压(pCO₂)和渗透压分别高达150 mmHg和440 mOsm/kg。当生物反应器中的pCO₂和渗透压升高到高水平时,会对细胞培养和重组蛋白生产产生不利影响。为了了解pCO₂或渗透压对CHO细胞生长的单独影响,在实验室规模的生物反应器中进行了实验,允许一个变量变化,同时控制另一个变量。在渗透压受控(约350 mOsm/kg)的情况下,将pCO₂从50 mmHg提高到150 mmHg,导致比细胞生长速率降低9%。相比之下,渗透压升高导致比细胞生长速率呈线性下降(0.008 h⁻¹/100 mOsm/kg),与316 mOsm/kg的对照相比,在450 mOsm/kg时下降了60%。渗透压从316 mOsm/kg转变为445 mOsm/kg导致乳酸和氨的比生产率分别提高了43%和48%。为了阐明高渗透压和/或pCO₂对生产阶段的影响,在实验室规模的生物反应器中进行了实验,以更密切地反映大规模观察到的pCO₂和渗透压水平。将渗透压提高到400 - 450 mOsm/kg不会导致活细胞密度和产物滴度明显变化。然而,与对照相比,将渗透压进一步提高到460 - 500 mOsm/kg导致活细胞密度降低5%,细胞活力降低8%。由于在这种升高的渗透压下比生产率明显提高,最终滴度没有受到影响。此外,高pCO₂(140 - 160 mmHg)和渗透压(400 - 450 mOsm/kg)的联合作用导致活细胞密度下降20%,与单独升高渗透压相比下降更为显著。此处获得的结果说明了高pCO₂(或渗透压)对CHO细胞生长的单独影响,并证明了高渗透压和/或pCO₂对生产阶段的影响与对生长阶段的影响不同。这些结果有助于了解CHO细胞在生物反应器培养的不同阶段对升高的pCO₂(和/或渗透压)的反应,因此对于指导生物反应器优化以提高蛋白质生产具有重要价值。