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Photo-driven heterogeneous microbial consortium reducing CO2 to hydrocarbons fuel

文献类型： 外文期刊

作者： Xia, Wenjie 1 ; Chen, Rui 2 ; Li, Yang 3 ; Gao, Peike 4 ; Li, Chihong 5 ; Jin, Tianzhi 1 ; Ma, John 6 ; Ma, Ting 1 ;

作者机构： 1.Nankai Univ, Coll Life Sci, Minist Educ, Key Lab Mol Microbiol & Technol, Tianjin 300071, Peoples R China

2.Tianjin Acad Agr Sci, Biotechnol Res Inst, Tianjin 300381, Peoples R China

3.Tianjin Med Univ Canc Inst & Hosp, Tianjin Canc Inst, Tianjin 300060, Peoples R China

4.Qufu Normal Univ, Sch Life Sci, Jining 273165, Peoples R China

5.CCC SDC Green Environm Engn Co, Shanghai 200120, Peoples R China

6.CALTECH, Mat & Proc Simulat Ctr, Pasadena, CA 91125 USA

关键词： Bioconversion; CO2; Hydrocarbons; Photosynthesis; Microorganism

期刊名称：JOURNAL OF CLEANER PRODUCTION （ 影响因子：11.072； 五年影响因子：11.016 ）

ISSN： 0959-6526

年卷期： 2021 年 326 卷

页码：

收录情况： SCI

摘要： 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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