CAJ | 학술논문

氨基酸的浓度与配比对细胞生长和产物表达有重要作用。在自主研发无血清培养基的基础上，通过单纯型格子实验设计优化氨基酸浓度及配比后发现，优化的无血清培养基明显促进了细胞生长。生物反应器批式培养中，最高活细胞密度达52.6×105 cells?mL-1，抗体融合蛋白产量52.2 mg?L-1，相对于商业培养基Ex-cell 302，分别提高了26.7%和11.5%。在此基础上，通过部件搜索的方法确认具有显著正影响的氨基酸为谷氨酰胺、脯氨酸和甲硫氨酸。基于上述研究工作，在2L反应器采用自主研发的优化无血清培养基，以葡萄糖为关键控制参数，进行两阶段动态流加培养过程， CHO细胞最大活细胞密度达94.6×105 cells?mL-1，抗体融合蛋白终产量600 mg?L-1，相对于商业培养基Ex-cell 302批式培养，分别提高了2.75倍和11.8倍。本研究工作为抗体融合蛋白的高效工业化生产奠定了基础。
안기산적농도여배비대세포생장화산물표체유중요작용。재자주연발무혈청배양기적기출상，통과단순형격자실험설계우화안기산농도급배비후발현，우화적무혈청배양기명현촉진료세포생장。생물반응기비식배양중，최고활세포밀도체52.6×105 cells?mL-1，항체융합단백산량52.2 mg?L-1，상대우상업배양기Ex-cell 302，분별제고료26.7%화11.5%。재차기출상，통과부건수색적방법학인구유현저정영향적안기산위곡안선알、포안산화갑류안산。기우상술연구공작，재2L반응기채용자주연발적우화무혈청배양기，이포도당위관건공제삼수，진행량계단동태류가배양과정， CHO세포최대활세포밀도체94.6×105 cells?mL-1，항체융합단백종산량600 mg?L-1，상대우상업배양기Ex-cell 302비식배양，분별제고료2.75배화11.8배。본연구공작위항체융합단백적고효공업화생산전정료기출。
Based on statistical analysis, cell growth was improved in optimized serum-free media via the optimization of the concentration and proportion of amino acids using simplex lattice and elements dialogue design methods. Using the optimized serum-free media, the maximum viable cell density (MVCD) and the maximum antibody concentration are 52.6×105 cells?mL-1 and 52.2 mg?L-1, respectively, and these values are increased by 26.7% and 11.5% respectively comparing to those obtained by using the commercial medium Ex-cell302. Glutamine, proline and methionine are confirmed to have positive effects through the elements dialogue experiment. Moreover, two-stage dynamic fed-batch culture for CHO cells was studied in a 2 L bioreactor. The feeding strategy was based on using the glucose concentration as the key controlling parameter. The maximum viable cell density reaches to 94.6×105 cells?mL-1, and 600 mg?L-1 antibody concentration was achieved within 10 days of cultivation. The maximum cell concentration and antibody production are improved by 2.75 and 11.8 times comparing to the results obtained by commercial medium cultivation. This research is useful for efficient industrial production of antibody fusion proteins.