微型生物反应器混合动力学与过渡流态光生物反应动力学的 CFD 预测模拟

IF 3.7 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Bovinille Anye Cho , George Mbella Teke , Godfrey K. Gakingo , Robert William McClelland Pott , Dongda Zhang
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引用次数: 0

摘要

使用微型搅拌生物反应器的高通量系统因其简单和低成本而加速了生物工艺的开发。然而,波动的流体力学给耦合(生物)反应动力学带来了数值挑战,而耦合(生物)反应动力学对于化学和生物工艺行业的优化和放大/缩小至关重要。为了解决这个问题,我们通过对过渡 SST 模型的瞬时 RANS 解进行足够长的时间平均来实现流体力学收敛,从而在第一步中达到统计意义。随后,根据这些收敛场求解了光生物反应器的定向光照和曲率的光生物反应传输模型,以一种以前从未报道过的方法克服了两步耦合的挑战。将该模型应用于通过磁力搅拌器(100-500 rpm)进行机械混合的 0.7 L 肖特瓶光生物反应器中,该模型准确预测了 500 rpm 转速下的漩涡场,模拟示踪剂扩散的误差率为 7%,生物量生长曲线与有关古朴红单胞菌的文献数据一致。然而,并行计算效率并没有随着处理器数量的增加而线性增加,因此时间平均计算的成本很高。此外,改进生物反应器混合可提高生物量生产率,但由于观察到的光照限制,转速超过 300 时需要增加入射光强度(100 Wm-2)。因此,该模型有助于优化搅拌速度,完善放大和缩小工艺的操作参数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CFD predictive simulations of miniature bioreactor mixing dynamics coupled with photo-bioreaction kinetics in transitional flow regime
High-throughput systems using miniaturised stirred bioreactors accelerate bioprocess development due to their simplicity and low cost. However, fluctuating hydrodynamics pose numerical challenges for coupling (bio)reaction kinetics, critical for optimisation and scale-up/down in chemical and bioprocess industries. To address this, hydrodynamic convergence was achieved by time-averaging instantaneous RANS solutions of the transitional SST model over a sufficiently long period to achieve statistical significance in step one. Subsequently, photo-bioreaction transport models, accounting for the photobioreactor’s directional illumination and curvature, were solved based on these converged fields, overcoming two-step coupling challenges in an approach not previously reported. Applied to a 0.7 L Schott bottle photobioreactor mechanically mixed by a magnetic stirrer (100–500 rpm), the model accurately predicted swirly vortex fields at 500 rpm, with a 7 % error margin for simulated tracer diffusion, and aligned biomass growth profiles with literature data on Rhodopseudomonas palustris. However, parallel computing efficiency did not scale linearly with processor count, making time-averaging computationally expensive. Also, improved bioreactor mixing enhanced biomass productivity, but rpms over 300 required increased incident light intensity (>100 Wm−2) due to observed light limitation. Hence, this model facilitates optimising stirring speeds and refining operational parameters for scale-up and scale-down processes.
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来源期刊
Biochemical Engineering Journal
Biochemical Engineering Journal 工程技术-工程:化工
CiteScore
7.10
自引率
5.10%
发文量
380
审稿时长
34 days
期刊介绍: The Biochemical Engineering Journal aims to promote progress in the crucial chemical engineering aspects of the development of biological processes associated with everything from raw materials preparation to product recovery relevant to industries as diverse as medical/healthcare, industrial biotechnology, and environmental biotechnology. The Journal welcomes full length original research papers, short communications, and review papers* in the following research fields: Biocatalysis (enzyme or microbial) and biotransformations, including immobilized biocatalyst preparation and kinetics Biosensors and Biodevices including biofabrication and novel fuel cell development Bioseparations including scale-up and protein refolding/renaturation Environmental Bioengineering including bioconversion, bioremediation, and microbial fuel cells Bioreactor Systems including characterization, optimization and scale-up Bioresources and Biorefinery Engineering including biomass conversion, biofuels, bioenergy, and optimization Industrial Biotechnology including specialty chemicals, platform chemicals and neutraceuticals Biomaterials and Tissue Engineering including bioartificial organs, cell encapsulation, and controlled release Cell Culture Engineering (plant, animal or insect cells) including viral vectors, monoclonal antibodies, recombinant proteins, vaccines, and secondary metabolites Cell Therapies and Stem Cells including pluripotent, mesenchymal and hematopoietic stem cells; immunotherapies; tissue-specific differentiation; and cryopreservation Metabolic Engineering, Systems and Synthetic Biology including OMICS, bioinformatics, in silico biology, and metabolic flux analysis Protein Engineering including enzyme engineering and directed evolution.
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