4.7 Article

Photo-driven heterogeneous microbial consortium reducing CO2 to hydrocarbons fuel

期刊

JOURNAL OF CLEANER PRODUCTION
卷 326, 期 -, 页码 -

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.jclepro.2021.129397

关键词

Bioconversion; CO2; Hydrocarbons; Photosynthesis; Microorganism

资金

  1. National Natural Science Foundation of Tianjin [20JCYBJC01280]
  2. China National Key Research and Development Project [2018YFA0902101]
  3. Key science and technology project of Kar-amay [2019ZD002B]

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This study investigated a photo-driven bioprocess for converting carbon dioxide into small hydrocarbon molecules and developed a versatile consortium-based platform for more efficient CO2 conversion to fuels. The pathway of CO2 bioconversion was revealed through 16S rRNA and metagenomic sequencing, providing important insights for related research.
Carbon dioxide as feedstock for hydrocarbon synthesis attracts numerous efforts via the biological or chemical approaches. With the purpose of constructing a robust and highly-efficient platform for CO2 bioconversion to fuel, we investigated a photo-driven bioprocess of directing CO2 reduction to C-1-C-6 alkanes/alkenes discovered from the enriched microbial consortia. GC-MS analysis revealed that the maximum yield of total gaseous hydrocarbons was 169.66 mu M with the average CO2 reduction rate of 100.87 mu M/day decreasing from 11573.39 mu M to 5905.73 mu M during 50 days culturing. The pathway of CO2 bioconversion was proposed according to the 16S rRNA and metagenomic sequencing that rTCA and Wood-Ljungdahl were mainly contributed to CO2 fixation, and nitrogenase was responsible for the hydrocarbon syntheses. Following these results, a versatile consortium-based platform was developed via the neural network method with the selected Pseudomonas sp., Serratia sp., Candidatus sp., Clostridium sp., Enterococcus sp., Salmonella sp., Rhodospirillum sp., Thalassospira sp., Thioclava sp., Stenotrophomonas sp. and Desulfovibrio sp., which showed the improved CO2 reduction rate of 107.54 mu M/day and the higher selectivity of C-1-C-4 alkanes than the original consortia. This study demonstrated that this artificially constructed consortium could be a promising platform for converting CO2 to the diverse gaseous alkanes and alkenes.

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