Controlling H2S and CH4 emissions is critical for ensuring the safety of sewer systems. Bioaugmentation offers a cost-effective and environmentally friendly alternative to chemical dosing, yet its performance and mechanisms in sewers remain unclear. This study investigated a bioaugmentation strategy by inoculating laboratory-scale sewer reactors with Bacillus subtilis and Saccharomyces cerevisiae. A 7-day inoculation (10⁷ CFU/mL) reduced H2S and CH4 emissions by 86.1% and 62.9%, respectively, with half-recovery times of 12 and 22 days. The strategy extended the duration of effective H2S control by 20-300% compared with chemical dosing. Life-cycle assessment and cost analyses further indicated a 7.4% reduction in operating costs and a 60.6% reduction in greenhouse-gas emissions compared with a typical chemical dosing strategy. Bioaugmentation-induced assimilatory sulfate reduction was the primary pathway for H2S mitigation. By diverting sulfate into the biosynthesis of sulfur-containing amino acids (an 859.3% increase), B. subtilis and S. cerevisiae reduced the electron acceptor available for sulfate-reducing bacteria (SRB), thereby reducing the relative abundance of SRB from 17.5% to 0.2% and suppressing H2S emissions. Meanwhile, bioaugmentation-induced chain elongation was the dominant pathway for CH4 mitigation. The inoculum selectively enriched lactic acid bacteria and Clostridium spp., which converted acetate to medium-chain fatty acids (increased by 150.5%) that are not utilized by methanogenic archaea (MA). This limited electron-donor availability reduced MA relative abundance (17.4% to 0.5%). These findings support the potential of bioaugmentation for sustained control of H2S and CH4 in sewers.
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| Evidence ID | Analyze ID | Gene/Complex | Systematic Name/Complex Accession | Qualifier | Gene Ontology Term ID | Gene Ontology Term | Aspect | Annotation Extension | Evidence | Method | Source | Assigned On | Reference |
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| Evidence ID | Analyze ID | Gene | Gene Systematic Name | Phenotype | Experiment Type | Experiment Type Category | Mutant Information | Strain Background | Chemical | Details | Reference |
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| Evidence ID | Analyze ID | Gene | Gene Systematic Name | Disease Ontology Term | Disease Ontology Term ID | Qualifier | Evidence | Method | Source | Assigned On | Reference |
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| Evidence ID | Analyze ID | Regulator | Regulator Systematic Name | Target | Target Systematic Name | Direction | Regulation of | Happens During | Regulator Type | Direction | Regulation Of | Happens During | Method | Evidence | Strain Background | Reference |
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| Site | Modification | Modifier | Source | Reference |
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| Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Allele | Assay | Annotation | Action | Phenotype | SGA score | P-value | Source | Reference | Note |
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| Evidence ID | Analyze ID | Interactor | Interactor Systematic Name | Interactor | Interactor Systematic Name | Assay | Annotation | Action | Modification | Source | Reference | Note |
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| Complement ID | Locus ID | Gene | Species | Gene ID | Strain background | Direction | Details | Source | Reference |
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| Evidence ID | Analyze ID | Dataset | Description | Keywords | Number of Conditions | Reference |
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