产甲烷
固碳
化学
发酵
甲烷杆菌
乙酸化
丁酸盐
羧酸盐
乙烯
生物反应器
生物化学
有机化学
甲烷
二氧化碳
催化作用
古细菌
基因
作者
Flávio C. F. Baleeiro,Sabine Kleinsteuber,Heike Sträuber
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2022-03-23
卷期号:10 (13): 4073-4081
被引量:11
标识
DOI:10.1021/acssuschemeng.1c05133
摘要
Anaerobic fermentation with mixed cultures has gained momentum as a bioprocess for its promise to produce platform carboxylates from low-value biomass feedstocks. Anaerobic fermenters are net carbon emitters, and their carboxylate yields are limited by electron donor availability. In a new approach to tackle these two disadvantages, we operated two bioreactors at pH 6.0 and 32 °C fed with acetate and lactate as a model feedstock while recirculating H2/CO2 to stimulate concomitant autotrophic activity. After 42 days of operation, hydrogenotrophic methanogenesis was predominant, and ethylene (≥1.3 kPa) was added to one of the reactors, inhibiting methanogenesis completely and recovering net carbon fixation (0.20 g CO2 L–1 d–1). When methanogenesis was inhibited, exogenous H2 accounted for 17% of the consumed electron donors. The lactate-to-butyrate selectivity was 101% (88% in the control without ethylene), and the lactate-to-caproate selectivity was 17% (2.3% in the control). Community analysis revealed that ethylene caused Methanobacterium to be washed out, giving room to acetogenic bacteria. In contrast to 2-bromoethanosulfonate, ethylene is a scalable methanogenesis inhibition strategy that did not collaterally block i-butyrate formation. By favoring the bacterial share of the community to become mixotrophic, the concept offers a way to simultaneously increase the selectivity to medium-chain carboxylates and develop a carbon-fixing chain elongation process.
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