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Comparison Between Simple Batch and Fed-Batch Bioreactor Cultivation of Recombinant BCG

生物反应器 重组DNA 简单(哲学) 生物技术 微生物学 化学 制浆造纸工业 生物 食品科学 生物化学 工程类 植物 基因 认识论 哲学
作者
Sofia Mendes,Maria Carolina Pereira Gonçalves,Vitoria A. P. Aiex,Ryhára Dias Batista,Patrícia Zorzete,Luciana C. C. Leite,Viviane Maimoni Gonçalves
出处
期刊:Pharmaceutics [Multidisciplinary Digital Publishing Institute]
卷期号:16 (11): 1433-1433
标识
DOI:10.3390/pharmaceutics16111433
摘要

Background/Objectives: Tuberculosis continues to be a significant global health concern, causing 1.3 million deaths in 2022, particularly affecting children under 5 years old. The Bacillus Calmette-Guérin (BCG) vaccine, developed in 1921, remains the primary defense against tuberculosis but requires modernized production methods. The recombinant BCG-pertussis strain shows potential in providing dual protection against tuberculosis and whooping cough, especially for vulnerable newborns, and enhanced efficacy against bladder cancer. Implementing submerged cultivation techniques for rBCG-pertussis production can offer increased productivity and standardization. Methods: This study explores a fed-batch cultivation strategy with pH-stat control to feed L-glutamic acid through the acid pump into 1 L bioreactor. Three pH values were evaluated for fed-batch and a simple batch without pH control was done for comparison. The viable cell concentration was compared before and after freeze-drying samples harvested during the cultures. Results: L-glutamic acid was identified as the preferred substrate for rBCG-pertussis. While the fed-batch strategy did not enhance the maximum specific growth rate compared to simple batch cultivation, it did improve the specific growth rate after day 4 in the pH 7.4-controlled fed-batch cultures, thereby reducing the cultivation time. Fed-batch cultures controlled at three pH levels exhibited lower optical density than the simple batch, although the viable cell counts were similar. Notably, samples harvested after day 8 from the simple batch cultures showed a reduction in CFU/mL after freeze-drying, whereas all fed-batch samples exhibited high recovery of viable cell counts post lyophilization. Conclusions: The additional glutamate supplied to the fed-batch cultures may have protected the cells during the lyophilization process.

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