Academic Journal
Comparison of three inoculum sources for acetate production and microbial succession in H2/CO2-fed anaerobic system.
| Τίτλος: | Comparison of three inoculum sources for acetate production and microbial succession in H |
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| Συγγραφείς: | Jiang N; College of Environmental Science and Engineering, MOE Key Laboratory of Pollution Processes and Environmental Criteria, Tianjin Key Laboratory of Environmental Remediation and Pollution Control, Academy for Advanced Interdisciplinary Studies, Nankai University, No. 38 Tongyan Road, Jinnan District, Tianjin, 300350, China., Li L; College of Environmental Science and Engineering, MOE Key Laboratory of Pollution Processes and Environmental Criteria, Tianjin Key Laboratory of Environmental Remediation and Pollution Control, Academy for Advanced Interdisciplinary Studies, Nankai University, No. 38 Tongyan Road, Jinnan District, Tianjin, 300350, China., Li X; College of Environmental Science and Engineering, MOE Key Laboratory of Pollution Processes and Environmental Criteria, Tianjin Key Laboratory of Environmental Remediation and Pollution Control, Academy for Advanced Interdisciplinary Studies, Nankai University, No. 38 Tongyan Road, Jinnan District, Tianjin, 300350, China., Li R; College of Environmental Science and Engineering, MOE Key Laboratory of Pollution Processes and Environmental Criteria, Tianjin Key Laboratory of Environmental Remediation and Pollution Control, Academy for Advanced Interdisciplinary Studies, Nankai University, No. 38 Tongyan Road, Jinnan District, Tianjin, 300350, China., Wang G; College of Environmental Science and Engineering, MOE Key Laboratory of Pollution Processes and Environmental Criteria, Tianjin Key Laboratory of Environmental Remediation and Pollution Control, Academy for Advanced Interdisciplinary Studies, Nankai University, No. 38 Tongyan Road, Jinnan District, Tianjin, 300350, China., Li T; College of Environmental Science and Engineering, MOE Key Laboratory of Pollution Processes and Environmental Criteria, Tianjin Key Laboratory of Environmental Remediation and Pollution Control, Academy for Advanced Interdisciplinary Studies, Nankai University, No. 38 Tongyan Road, Jinnan District, Tianjin, 300350, China. tianli1@nankai.edu.cn., Wang X; College of Environmental Science and Engineering, MOE Key Laboratory of Pollution Processes and Environmental Criteria, Tianjin Key Laboratory of Environmental Remediation and Pollution Control, Academy for Advanced Interdisciplinary Studies, Nankai University, No. 38 Tongyan Road, Jinnan District, Tianjin, 300350, China. xinwang1@nankai.edu.cn. |
| Πηγή: | Bioprocess and biosystems engineering [Bioprocess Biosyst Eng] 2026 Aug; Vol. 49 (8), pp. 2133-2145. Date of Electronic Publication: 2026 Jul 02. |
| Τύπος έκδοσης: | Journal Article; Comparative Study |
| Γλώσσα: | English |
| Στοιχεία περιοδικού: | Publisher: Springer-Verlag Country of Publication: Germany NLM ID: 101088505 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1615-7605 (Electronic) Linking ISSN: 16157591 NLM ISO Abbreviation: Bioprocess Biosyst Eng Subsets: MEDLINE |
| Imprint Name(s): | Original Publication: Berlin, Germany : Springer-Verlag, 2001- |
| Ιατρικοί όροι (MeSH): | Carbon Dioxide*/metabolism , Acetates*/metabolism , Hydrogen*/metabolism , Clostridium*/growth & development , Bioreactors*, Sewage/microbiology ; Anaerobiosis ; Fermentation |
| Περίληψη: | Introducing a synthetic H (© 2026. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.) |
| Competing Interests: | Declarations. Conflict of interest: The authors declare no conflicts of interest. Ethical approval: This study did not involve human participants or vertebrate animals. Therefore, ethical approval was not required. |
| References: | Li K, Hu N, Wang L et al (2025) Microbial electrosynthesis for clean utilization and high-value conversion of CO2: A bibliometric review. Int J Hydrog Energy 103:851–866. https://doi.org/10.1016/j.ijhydene.2025.01.226. (PMID: 10.1016/j.ijhydene.2025.01.226) Schuchmann K, Müller V (2014) Autotrophy at the thermodynamic limit of life: a model for energy conservation in acetogenic bacteria. Nat Rev Microbiol 12:809–821. https://doi.org/10.1038/nrmicro3365. (PMID: 10.1038/nrmicro336525383604) Drake HL, Gößner AS, Daniel SL (2008) Old Acetogens, New Light. Ann N Y Acad Sci 1125:100–128. https://doi.org/10.1196/annals.1419.016. (PMID: 10.1196/annals.1419.01618378590) Bian Y, Leininger A, May HD, Ren ZJ (2024) H2 mediated mixed culture microbial electrosynthesis for high titer acetate production from CO2. Environ Sci Ecotechnology 19:100324. https://doi.org/10.1016/j.ese.2023.100324. (PMID: 10.1016/j.ese.2023.100324) Chu N, Wang D, Wang H et al (2023) Flow-Electrode Microbial Electrosynthesis for Increasing Production Rates and Lowering Energy Consumption. Engineering 25:157–167. https://doi.org/10.1016/j.eng.2021.09.015. (PMID: 10.1016/j.eng.2021.09.015) Chen H, Dong F, Minteer SD (2020) The progress and outlook of bioelectrocatalysis for the production of chemicals, fuels and materials. Nat Catal 3:225–244. https://doi.org/10.1038/s41929-019-0408-2. (PMID: 10.1038/s41929-019-0408-2) He Y, Cassarini C, Marciano F, Lens PNL (2021) Homoacetogenesis and solventogenesis from H2/CO2 by granular sludge at 25, 37 and 55°C. Chemosphere 265:128649. https://doi.org/10.1016/j.chemosphere.2020.128649. (PMID: 10.1016/j.chemosphere.2020.12864933109359) Bertsch J, Müller V (2015) Bioenergetic constraints for conversion of syngas to biofuels in acetogenic bacteria. Biotechnol Biofuels. https://doi.org/10.1186/s13068-015-0393-x . 8:. (PMID: 10.1186/s13068-015-0393-x266928974676187) Park S-G, Rhee C, Shin SG et al (2019) Methanogenesis stimulation and inhibition for the production of different target electrobiofuels in microbial electrolysis cells through an on-demand control strategy using the coenzyme M and 2-bromoethanesulfonate. Environ Int 131:105006. https://doi.org/10.1016/j.envint.2019.105006. (PMID: 10.1016/j.envint.2019.10500631330362) Nie E, He P, Zhang H et al (2021) How does temperature regulate anaerobic digestion? Renew Sustain Energy Rev 150:111453. https://doi.org/10.1016/j.rser.2021.111453. (PMID: 10.1016/j.rser.2021.111453) Tsapekos P, Alvarado-Morales M, Angelidaki I (2022) H2 competition between homoacetogenic bacteria and methanogenic archaea during biomethanation from a combined experimental-modelling approach. J Environ Chem Eng 10:107281. https://doi.org/10.1016/j.jece.2022.107281. (PMID: 10.1016/j.jece.2022.107281) Sudiartha GAW, Imai T, Reungsang A (2024) Syntrophic relationship among microbial communities enhance methane production during temperature transition from mesophilic to thermotolerant conditions. J Environ Chem Eng 12:114903. https://doi.org/10.1016/j.jece.2024.114903. (PMID: 10.1016/j.jece.2024.114903) Sudiartha GAW, Imai T, Chairattanamanokorn P, Reungsang A (2024) Unveiling the impact of temperature shift on microbial community dynamics and metabolic pathways in anaerobic digestion. Process Saf Environ Prot 186:1505–1515. https://doi.org/10.1016/j.psep.2024.04.121. (PMID: 10.1016/j.psep.2024.04.121) Schiel-Bengelsdorf B, Dürre P (2012) Pathway engineering and synthetic biology using acetogens. FEBS Lett 586:2191–2198. https://doi.org/10.1016/j.febslet.2012.04.043. (PMID: 10.1016/j.febslet.2012.04.04322710156) Brenner K, You L, Arnold FH (2008) Engineering microbial consortia: a new frontier in synthetic biology. Trends Biotechnol 26:483–489. https://doi.org/10.1016/j.tibtech.2008.05.004. (PMID: 10.1016/j.tibtech.2008.05.00418675483) Wang Y, Qu M, Wang J et al (2024) Recovery of bacterial network complexity and stability after simulated extreme rainfall is mediated by K–/r-strategy dominance. Appl Soil Ecol 203:105657. https://doi.org/10.1016/j.apsoil.2024.105657. (PMID: 10.1016/j.apsoil.2024.105657) Mook A, Herzog J, Walther P et al (2024) Lactate-mediated mixotrophic co-cultivation of Clostridium drakei and recombinant Acetobacterium woodii for autotrophic production of volatile fatty acids. Microb Cell Fact 23. https://doi.org/10.1186/s12934-024-02481-3. Neto AS, Wainaina S, Chandolias K et al (2025) Syngas fermentation for hydrogen and volatile fatty acids production: Effect of inoculum source, pretreatment, and environmental parameters using natural microbial consortia. Bioresource Technol Rep 30:102109. https://doi.org/10.1016/j.biteb.2025.102109. (PMID: 10.1016/j.biteb.2025.102109) Rocamora I, Wagland ST, Villa R et al (2020) Dry anaerobic digestion of organic waste: A review of operational parameters and their impact on process performance. Bioresour Technol 299:122681. https://doi.org/10.1016/j.biortech.2019.122681. (PMID: 10.1016/j.biortech.2019.12268131902638) Dessì P, Rovira-Alsina L, Sánchez C et al (2021) Microbial electrosynthesis: Towards sustainable biorefineries for production of green chemicals from CO2 emissions. Biotechnol Adv 46:107675. https://doi.org/10.1016/j.biotechadv.2020.107675. (PMID: 10.1016/j.biotechadv.2020.10767533276075) Holliger C, Alves M, Andrade D et al (2016) Towards a standardization of biomethane potential tests. Water Sci Technol 74:2515–2522. https://doi.org/10.2166/wst.2016.336. (PMID: 10.2166/wst.2016.33627973356) Raposo F, Fernández-Cegrí V, De la Rubia MA et al (2011) Biochemical methane potential (BMP) of solid organic substrates: evaluation of anaerobic biodegradability using data from an international interlaboratory study. J Chem Technol Biotechnol 86:1088–1098. https://doi.org/10.1002/jctb.2622. (PMID: 10.1002/jctb.2622) Logroño W, Nikolausz M, Harms H, Kleinsteuber S (2022) Physiological Effects of 2-Bromoethanesulfonate on Hydrogenotrophic Pure and Mixed Cultures. Microorganisms 10:355. https://doi.org/10.3390/microorganisms10020355. (PMID: 10.3390/microorganisms10020355352088098877471) Caporaso JG, Lauber CL, Walters WA et al (2010) Global patterns of 16S rRNA diversity at a depth of millions of sequences per sample. Proceedings of the National Academy of Sciences 108:4516–4522. https://doi.org/10.1073/pnas.1000080107. Bolyen E, Rideout JR, Dillon MR et al (2019) Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2. Nat Biotechnol 37:852–857. https://doi.org/10.1038/s41587-019-0209-9. (PMID: 10.1038/s41587-019-0209-9313412887015180) Rognes T, Flouri T, Nichols B et al (2016) VSEARCH: a versatile open source tool for metagenomics. PeerJ 4:e2584. https://doi.org/10.7717/peerj.2584. (PMID: 10.7717/peerj.2584277811705075697) Douglas GM, Maffei VJ, Zaneveld JR et al (2020) PICRUSt2 for prediction of metagenome functions. Nat Biotechnol 38:685–688. https://doi.org/10.1038/s41587-020-0548-6. (PMID: 10.1038/s41587-020-0548-6324833667365738) Oksanen J, Simpson GL, Blanchet FG et al (2022) vegan: Community Ecology Package. Theuerl S, Klang J, Prochnow A (2019) Process Disturbances in Agricultural Biogas Production—Causes, Mechanisms and Effects on the Biogas Microbiome: A Review. Energies 12:365. https://doi.org/10.3390/en12030365. (PMID: 10.3390/en12030365) Okyay TO, Rodrigues DF (2015) Biotic and abiotic effects on CO2 sequestration during microbially-induced calcium carbonate precipitation. FEMS Microbiol Ecol 91. https://doi.org/10.1093/femsec/fiv017. Conrad R (1999) Contribution of hydrogen to methane production and control of hydrogen concentrations in methanogenic soils and sediments. FEMS Microbiol Ecol 28:193–202. https://doi.org/10.1111/j.1574-6941.1999.tb00575.x. (PMID: 10.1111/j.1574-6941.1999.tb00575.x) Raza T, Qadir MF, Khan KS et al (2023) Unraveling the potential of microbes in decomposition of organic matter and release of carbon in the ecosystem. J Environ Manage 344:118529. (PMID: 10.1016/j.jenvman.2023.11852937418912) Boodhoo KVK, Flickinger MC, Woodley JM, Emanuelsson EAC (2022) Bioprocess intensification: A route to efficient and sustainable biocatalytic transformations for the future. Chem Eng Process - Process Intensif 172:108793. https://doi.org/10.1016/j.cep.2022.108793. (PMID: 10.1016/j.cep.2022.108793) Diender M, Stams AJM, Sousa DZ (2016) Production of medium-chain fatty acids and higher alcohols by a synthetic co-culture grown on carbon monoxide or syngas. Biotechnol Biofuels 9. https://doi.org/10.1186/s13068-016-0495-0. Lee CR, Kim C, Song YE et al (2018) Co-culture-based biological carbon monoxide conversion by Citrobacter amalonaticus Y19 and Sporomusa ovata via a reducing-equivalent transfer mediator. Bioresour Technol 259:128–135. https://doi.org/10.1016/j.biortech.2018.02.129. (PMID: 10.1016/j.biortech.2018.02.12929549832) Li C, Hao L, Lü F et al (2022) Syntrophic Acetate-Oxidizing Microbial Consortia Enriched from Full-Scale Mesophilic Food Waste Anaerobic Digesters Showing High Biodiversity and Functional Redundancy. mSystems 7. https://doi.org/10.1128/msystems.00339-22. Guo J, Peng Y, Ni B-J et al (2015) Dissecting microbial community structure and methane-producing pathways of a full-scale anaerobic reactor digesting activated sludge from wastewater treatment by metagenomic sequencing. Microb Cell Fact 14. https://doi.org/10.1186/s12934-015-0218-4. Esquivel-Elizondo S, Delgado AG, Krajmalnik-Brown R (2017) Evolution of microbial communities growing with carbon monoxide, hydrogen, and carbon dioxide. FEMS Microbiol Ecol 93. https://doi.org/10.1093/femsec/fix076. Pan X, Zhao L, Li C et al (2021) Deep insights into the network of acetate metabolism in anaerobic digestion: focusing on syntrophic acetate oxidation and homoacetogenesis. Water Res 190:116774. https://doi.org/10.1016/j.watres.2020.116774. (PMID: 10.1016/j.watres.2020.11677433387947) Zampieri G, Santinello D, Palù M et al (2025) Core cooperative metabolism in low-complexity CO2-fixing anaerobic microbiota. ISME J 19. https://doi.org/10.1093/ismejo/wraf017. Werner JJ, Knights D, Garcia ML et al (2011) Bacterial community structures are unique and resilient in full-scale bioenergy systems. Proceedings of the National Academy of Sciences 108:4158–4163. https://doi.org/10.1073/pnas.1015676108. Shi Z, Zhang C, Tan X et al (2024) Syntrophic microbes involved in the oxidation of short-chain fatty acids in continuous-flow anaerobic digesters treating waste activated sludge with hydrochar. Appl Environ Microbiol 90. https://doi.org/10.1128/aem.02047-23. Stams AJM, Sousa DZ, Kleerebezem R, Plugge CM (2012) Role of syntrophic microbial communities in high-rate methanogenic bioreactors. Water Sci Technol 66:352–362. (PMID: 10.2166/wst.2012.19222699340) Cheng X, Wei Z, Cao W et al (2024) Untangling the interplay of dissolved organic matters variation with microbial symbiotic network in sludge anaerobic fermentation triggered by various pretreatments. Water Res 260:121930. https://doi.org/10.1016/j.watres.2024.121930. (PMID: 10.1016/j.watres.2024.12193038908316) Ragsdale SW, Pierce E (2008) Acetogenesis and the Wood–Ljungdahl pathway of CO2 fixation. Biochimica et Biophysica Acta (BBA) -. Proteins Proteom 1784:1873–1898. https://doi.org/10.1016/j.bbapap.2008.08.012. (PMID: 10.1016/j.bbapap.2008.08.012) Kantzow C, Mayer A, Weuster-Botz D (2015) Continuous gas fermentation by Acetobacterium woodii in a submerged membrane reactor with full cell retention. J Biotechnol 212:11–18. https://doi.org/10.1016/j.jbiotec.2015.07.020. (PMID: 10.1016/j.jbiotec.2015.07.02026239230) Prévoteau A, Carvajal-Arroyo JM, Ganigué R, Rabaey K (2020) Microbial electrosynthesis from CO2: forever a promise? Curr Opin Biotechnol 62:48–57. https://doi.org/10.1016/j.copbio.2019.08.014. (PMID: 10.1016/j.copbio.2019.08.01431593911) Phillips J, Huhnke R, Atiyeh H (2017) Syngas Fermentation: A Microbial Conversion Process of Gaseous Substrates to Various Products. Fermentation 3:28. https://doi.org/10.3390/fermentation3020028. (PMID: 10.3390/fermentation3020028) Artz J, Müller TE, Thenert K et al (2017) Sustainable Conversion of Carbon Dioxide: An Integrated Review of Catalysis and Life Cycle Assessment. Chem Rev 118:434–504. https://doi.org/10.1021/acs.chemrev.7b00435. (PMID: 10.1021/acs.chemrev.7b0043529220170) |
| Grant Information: | 52270042 National Natural Science Foundation of China; 2023C03017 "Pioneer" and "Leading Goose" R&D Program of Zhejiang |
| Contributed Indexing: | Keywords: Acetogenesis; CO2 fixation; H2/CO2 fermentation; Homoacetogenic bacteria; Inoculum source; Microbial community succession |
| Substance Nomenclature: | 142M471B3J (Carbon Dioxide) 0 (Acetates) 7YNJ3PO35Z (Hydrogen) 0 (Sewage) |
| Entry Date(s): | Date Created: 20260702 Date Completed: 20260730 Latest Revision: 20260730 |
| Update Code: | 20260730 |
| DOI: | 10.1007/s00449-026-03381-z |
| PMID: | 42390530 |
| Βάση Δεδομένων: | MEDLINE |
| ISSN: | 1615-7605 |
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| DOI: | 10.1007/s00449-026-03381-z |