在高压厌氧过程中控制产品谱:二氧化碳分压作为生物炼制概念中的新工具。

Pamela Ceron-Chafla, Jo de Vrieze, Korneel Rabaey, Jules B van Lier, Ralph E F Lindeboom
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引用次数: 0

摘要

背景:提高CO2分压(pCO2)已被提出作为混合培养发酵中选择性羧酸盐生产的潜在控制参数。预计中间产物谱和生产速率以及微生物群落的变化将直接受到二氧化碳分压升高的影响。然而,目前尚不清楚pCO2如何与其他操作条件相互作用,即底物特异性、底物与生物质(S/X)比和额外电子供体的存在,以及pCO2对发酵产物的确切组成有什么影响。在这里,我们研究了升高的二氧化碳分压结合(1)混合底物(甘油/葡萄糖)提供可能的转向效应;(2)随后增加底物浓度以增加S/X比;(3)甲酸作为附加的电子给体。结果:代谢物优势,如丙酸与丁酸/醋酸酯,以及细胞密度,取决于pCO2-S/X比和pco2 -甲酸酯之间的相互作用效应。单个底物消耗率受到pCO2-S/X比相互作用的负面影响,并且在降低S/X比和添加甲酸后没有重新建立。产物光谱受微生物群落组成的影响,而微生物群落组成又受底物类型和pco2 -甲酸酯相互作用的影响。高丙酸和丁酸水平分别与阴性菌和梭状芽孢杆菌优势密切相关。在随后的加压发酵阶段,当提供混合底物时,pco2 -甲酸酯之间的相互作用使生产从丙酸转向琥珀酸。结论:总的来说,升高的pCO2、底物特异性、高S/X比和甲酸还原等效物的可得性之间的相互作用,而不是单独的pCO2效应,改变了加压混合底物发酵中丙酸、丁酸和乙酸的比例,代价是消耗速率降低和滞后期增加。以甘油/葡萄糖混合物为底物,提高co2浓度与甲酸盐的相互作用有利于琥珀酸盐的生产和生物量的增长。这种积极作用可能归因于额外的还原等价物的可用性,可能增强了碳固定活性,并由于未解离羧酸浓度的增加而阻碍了丙酸转化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Steering the product spectrum in high-pressure anaerobic processes: CO<sub>2</sub> partial pressure as a novel tool in biorefinery concepts.

Steering the product spectrum in high-pressure anaerobic processes: CO<sub>2</sub> partial pressure as a novel tool in biorefinery concepts.

Steering the product spectrum in high-pressure anaerobic processes: CO<sub>2</sub> partial pressure as a novel tool in biorefinery concepts.

Steering the product spectrum in high-pressure anaerobic processes: CO2 partial pressure as a novel tool in biorefinery concepts.

Background: Elevated CO2 partial pressure (pCO2) has been proposed as a potential steering parameter for selective carboxylate production in mixed culture fermentation. It is anticipated that intermediate product spectrum and production rates, as well as changes in the microbial community, are (in)directly influenced by elevated pCO2. However, it remains unclear how pCO2 interacts with other operational conditions, namely substrate specificity, substrate-to-biomass (S/X) ratio and the presence of an additional electron donor, and what effect pCO2 has on the exact composition of fermentation products. Here, we investigated possible steering effects of elevated pCO2 combined with (1) mixed substrate (glycerol/glucose) provision; (2) subsequent increments in substrate concentration to increase the S/X ratio; and (3) formate as an additional electron donor.

Results: Metabolite predominance, e.g., propionate vs. butyrate/acetate, and cell density, depended on interaction effects between pCO2-S/X ratio and pCO2-formate. Individual substrate consumption rates were negatively impacted by the interaction effect between pCO2-S/X ratio and were not re-established after lowering the S/X ratio and adding formate. The product spectrum was influenced by the microbial community composition, which in turn, was modified by substrate type and the interaction effect between pCO2-formate. High propionate and butyrate levels strongly correlated with Negativicutes and Clostridia predominance, respectively. After subsequent pressurized fermentation phases, the interaction effect between pCO2-formate enabled a shift from propionate towards succinate production when mixed substrate was provided.

Conclusions: Overall, interaction effects between elevated pCO2, substrate specificity, high S/X ratio and availability of reducing equivalents from formate, rather than an isolated pCO2 effect, modified the proportionality of propionate, butyrate and acetate in pressurized mixed substrate fermentations at the expense of reduced consumption rates and increased lag-phases. The interaction effect between elevated pCO2 and formate was beneficial for succinate production and biomass growth with a glycerol/glucose mixture as the substrate. The positive effect may be attributed to the availability of extra reducing equivalents, likely enhanced carbon fixating activity and hindered propionate conversion due to increased concentration of undissociated carboxylic acids.

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