Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/179279
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dc.contributor.authorHuang, Peitianen_US
dc.contributor.authorChen, Yunen_US
dc.contributor.authorLi, Zongen_US
dc.contributor.authorZhang, Baoruien_US
dc.contributor.authorYu, Siweien_US
dc.contributor.authorZhou, Yanen_US
dc.date.accessioned2024-07-24T05:22:18Z-
dc.date.available2024-07-24T05:22:18Z-
dc.date.issued2024-
dc.identifier.citationHuang, P., Chen, Y., Li, Z., Zhang, B., Yu, S. & Zhou, Y. (2024). Ammonia-dependent reducing power redistribution for purple phototrophic bacteria culture-based biohydrogen production. Water Research, 256, 121599-. https://dx.doi.org/10.1016/j.watres.2024.121599en_US
dc.identifier.issn0043-1354en_US
dc.identifier.urihttps://hdl.handle.net/10356/179279-
dc.description.abstractThe global energy crisis has intensified the search for sustainable and clean alternatives, with biohydrogen emerging as a promising solution to address environmental challenges. Leveraging photo fermentation (PF) process, purple phototrophic bacteria (PPB) can harness reducing power derived from organic substrates to facilitate hydrogen production. However, existing studies report much lower H2 yields than theoretical value when using acetate as carbon source and ammonia as nitrogen source, primarily attributed to the widely employed pulse-feeding mode which suffers from ammonia inhibition effect on nitrogenase. To address this issue, a continuous feeding mode was applied to avoid ammonia accumulation in this study. On the other hand, other pathways like carbon fixation and polyhydroxyalkanoate (PHA) formation could compete reducing power with H2 production. However, the reducing power allocation under continuous feeding mode is not yet clear. In this study, the reducing power allocation and hydrogen production performance were evaluated under various ammonia loading, using acetate as carbon source and infrared LED at around 50 W·m-2 as light source. The results show that (a) The absence of ammonia resulted in the best performance for hydrogen production, with 44 % of the reducing power distributed to H2 and the highest H2 volumetric productivity, while the allocation of reducing power to hydrogen production stopped when ammonia loading was above 7.6 mg NH4-N·L-1·d-1; (b) when PPB required to eliminate reducing power under ammonia limited conditions, PHA production was the preferred pathway followed by the hydrogen production pathway, but once PHA accumulation reached saturation, hydrogen generation pathway dominated; (c) under ammonia limited conditions, the TCA cycle was more activated rendering higher NADH (i.e. reducing power) production compared with that under ammonia sufficient conditions which was verified by metagenomics analysis, and all the hydrogen production, PHA accumulation and carbon fixation pathways were highly active to dissipate reducing power. This work provides the insight of reducing power distribution and PPB biohydrogen production variated by ammonia loading under continuous feeding mode.en_US
dc.description.sponsorshipAgency for Science, Technology and Research (A*STAR)en_US
dc.description.sponsorshipMinistry of Education (MOE)en_US
dc.description.sponsorshipNanyang Technological Universityen_US
dc.language.isoenen_US
dc.relationA20H7a0152en_US
dc.relationRT 12/20en_US
dc.relation.ispartofWater Researchen_US
dc.rights© 2024 Elsevier Ltd. All rights reserved.en_US
dc.subjectEngineeringen_US
dc.titleAmmonia-dependent reducing power redistribution for purple phototrophic bacteria culture-based biohydrogen productionen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Civil and Environmental Engineeringen_US
dc.contributor.schoolInterdisciplinary Graduate School (IGS)en_US
dc.contributor.researchNanyang Environment and Water Research Instituteen_US
dc.identifier.doi10.1016/j.watres.2024.121599-
dc.identifier.pmid38615602-
dc.identifier.scopus2-s2.0-85190245129-
dc.identifier.volume256en_US
dc.identifier.spage121599en_US
dc.subject.keywordsPurple non-sulfur bacteriaen_US
dc.subject.keywordsPhotosynthetic bacteriaen_US
dc.description.acknowledgementThe authors would like to thank the Nanyang Environment & Water Research Institute and the Interdisciplinary Graduate Programme, Nanyang Technological University, Singapore, for the award of research scholarship. This work was supported by A*STAR SFS IAF-PP grant (A20H7a0152) and AcRF Tier 1 RT 12/20 awarded to Yan Zhou.en_US
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