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Uncoupling Foam Fractionation and Foam Adsorption for Enhanced Biosurfactant Synthesis and Recovery

机译:解耦泡沫分馏和泡沫吸附用于增强的生物活性剂合成和回收

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摘要

The production of biosurfactants is often hampered by excessive foaming in the bioreactor, impacting system scale-up and downstream processing. Foam fractionation was proposed to tackle this challenge by combining in situ product removal with a pre-purification step. In previous studies, foam fractionation was coupled to bioreactor operation, hence it was operated at suboptimal parameters. Here, we use an external fractionation column to decouple biosurfactant production from foam fractionation, enabling continuous surfactant separation, which is especially suited for system scale-up. As a subsequent product recovery step, continuous foam adsorption was integrated into the process. The configuration is evaluated for rhamnolipid (RL) or 3-(3-hydroxyalkanoyloxy)alkanoic acid (HAA, i.e., RL precursor) production by recombinant non-pathogenic Pseudomonas putida KT2440. Surfactant concentrations of 7.5 gRL/L and 2.0 gHAA/L were obtained in the fractionated foam. 4.7 g RLs and 2.8 g HAAs could be separated in the 2-stage recovery process within 36 h from a 2 L culture volume. With a culture volume scale-up to 9 L, 16 g RLs were adsorbed, and the space-time yield (STY) increased by 31% to 0.21 gRL/L·h. We demonstrate a well-performing process design for biosurfactant production and recovery as a contribution to a vital bioeconomy.
机译:通过在生物反应器中过度发泡,生物表面活性剂的产生通常是阻碍的,​​影响系统扩大和下游加工。提出了泡沫分馏,通过用预纯化步骤组合原位产品去除来解决这一攻击。在先前的研究中,泡沫分馏偶联与生物反应器操作,因此在次优参数下操作。在这里,我们使用外部分馏塔从泡沫分馏中脱钩,使能连续的表面活性剂分离,这尤其适用于系统缩放。作为随后的产物回收步骤,将连续泡沫吸附整合到该过程中。通过重组非致病性假单胞菌KT2440评价核醇脂(RL)或3-(3-羟基烷酰氧基)链烷酸(HAA,I.,RL前体)生产的核心醇酸(HAA,即,RL前体)。在分馏的泡沫中获得了7.5GRL / L和2.0GHAA / L的表面活性剂浓度。 4.7g RLS和2.8克HAAs可以在2阶段回收过程中在36小时内分离出2L培养体积。培养体积刻度高达9L,吸附16g RLS,节省时间产率(STY)增加了31%至0.21gL / L·h。我们展示了生物活性剂的生产和恢复的良好过程设计作为对重要生物经济学的贡献。

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