Cited by 53Microbial Metabolic Engineering and BioproductionMicrobial bioremediation and biosurfactantsMicrobial Fuel Cells and Bioremediation

Top-down and bottom-up microbiome engineering approaches to enable biomanufacturing from waste biomass

Open access
Lyu, Xuejiao, Nuhu, Mujaheed, Candry, Pieter, Wolfanger, Jenna, Betenbaugh, Michael, Saldivar, Alexis, Zuniga, Cristal, Wang, Ying +1 more·2024·Journal of Industrial Microbiology and Biotechnology

Abstract

Growing environmental concerns and the need to adopt a circular economy have highlighted the importance of waste valorization for resource recovery. Microbial consortia-enabled biotechnologies have made significant developments in the biomanufacturing of valuable resources from waste biomass that serve as suitable alternatives to petrochemical-derived products. These microbial consortia-based processes are designed following a top-down or bottom-up engineering approach. The top-down approach is a classical method that uses environmental variables to selectively steer an existing microbial consortium to achieve a target function. While high-throughput sequencing has enabled microbial community characterization, the major challenge is to disentangle complex microbial interactions and manipulate the structure and function accordingly. The bottom-up approach uses prior knowledge of the metabolic pathway and possible interactions among consortium partners to design and engineer synthetic microbial consortia. This strategy offers some control over the composition and function of the consortium for targeted bioprocesses, but challenges remain in optimal assembly methods and long-term stability. In this review, we present the recent advancements, challenges, and opportunities for further improvement using top-down and bottom-up approaches for microbiome engineering. As the bottom-up approach is relatively a new concept for waste valorization, this review explores the assembly and design of synthetic microbial consortia, ecological engineering principles to optimize microbial consortia, and metabolic engineering approaches for efficient conversion. Integration of top-down and bottom-up approaches along with developments in metabolic modeling to predict and optimize consortia function are also highlighted. One-Sentence Summary: This review highlights the microbial consortia-driven waste valorization for biomanufacturing through top-down and bottom-up design approaches and describes strategies, tools, and unexplored opportunities to optimize the design and stability of such consortia.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1093/jimb/kuae025

Cites

5 of 5 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 168

  1. Adav S. S., Lee D.-J. (2008). Aerobic granulation of pure bacterial strain Bacillus thuringiensis. Frontiers of Environmental Science & Engineering in China, 2 (4), 461– 467. 10.1007/s11783-008-0066-0 · DOI
  2. Aggarwal N., Pham H. L., Ranjan B., Saini M., Liang Y., Hossain G. S., Ling H., Foo J. L., Chang M. W. (2023). Microbial engineering strategies to utilize waste feedstock for sustainable bioproduction. Nature Reviews Bioengineering, 2 (2), 155– 174. 10.1038/s44222-023-00129-2 · DOI
  3. Albright M. B. N., Louca S., Winkler D. E., Feeser K. L., Haig S.-J., Whiteson K. L., Emerson J. B., Dunbar J. (2022). Solutions in microbiome engineering: Prioritizing barriers to organism establishment. The ISME Journal, 16 (2), 331– 338. 10.1038/s41396-021-01088-5 34420034 PMC8776856 · DOI
  4. Altschul S. F., Gish W., Miller W., Myers E. W., Lipman D. J. (1990). Basic local alignment search tool. Journal of Molecular Biology, 215 (3), 403–410. 10.1016/S0022-2836(05)80360-2 2231712 · DOI · Paper page
  5. Alves A. A., Siqueira E. C., Barros M. P. S., Silva P. E. C., Houllou L. M. (2023). Polyhydroxyalkanoates: A review of microbial production and technology application. International Journal of Environmental Science and Technology, 20 (3), 3409– 3420. 10.1007/s13762-022-04213-9 · DOI
  6. An Z., Jin Q., Zhang X., Huang H., Wang Z.-W. (2021). Anaerobic granulation of single culture Clostridium beijerinckii. Food and Bioproducts Processing, 130, 164– 170. 10.1016/j.fbp.2021.09.012 · DOI
  7. Andraskar J., Yadav S., Kapley A. (2021). Challenges and control strategies of odor emission from composting operation. Applied Biochemistry and Biotechnology, 193 (7), 2331– 2356. 10.1007/s12010-021-03490-3 33635490 · DOI
  8. Aoyagi T., Inaba T., Aizawa H., Mayumi D., Sakata S., Charfi A., Suh C., Lee J. H., Sato Y., Ogata A., Habe H., Hori T. (2020). Unexpected diversity of acetate degraders in anaerobic membrane bioreactor treating organic solid waste revealed by high-sensitivity stable isotope probing. Water Research, 176, 115750. 10.1016/j.watres.2020.115750 32272322 · DOI
  9. Arora J., Mars Brisbin M. A., Mikheyev A. S. (2020). Effects of microbial evolution dominate those of experimental host-mediated indirect selection. PeerJ, 8, e9350. 10.7717/peerj.9350 32676220 PMC7334978 · DOI
  10. Balagurunathan B., Jonnalagadda S., Tan L., Srinivasan R. (2012). Reconstruction and analysis of a genome-scale metabolic model for Scheffersomyces stipitis. Microbial Cell Factories, 11 (1), 27. 10.1186/1475-2859-11-27 22356827 PMC3310799 · DOI
  11. Barlow J. T., Bogatyrev S. R., Ismagilov R. F. (2020). A quantitative sequencing framework for absolute abundance measurements of mucosal and lumenal microbial communities. Nature Communications, 11 (1), 2590. 10.1038/s41467-020-16224-6 PMC7244552 32444602 · DOI
  12. Bernstein D. B., Sulheim S., Almaas E., Segrè D. (2021). Addressing uncertainty in genome-scale metabolic model reconstruction and analysis. Genome Biology, 22 (1), 64. 10.1186/s13059-021-02289-z 33602294 PMC7890832 · DOI
  13. Beun J. J., Hendriks A., Van Loosdrecht M. C. M., Morgenroth E., Wilderer P. A., Heijnen J. J. (1999). Aerobic granulation in a sequencing batch reactor. Water Research, 33 (10), 2283– 2290. 10.1016/S0043-1354(98)00463-1 11831218 · DOI
  14. Bioproducts to Enable Biofuels Workshop Summary Report. (2015). U.S. Department of Energy. https://www.energy.gov/eere/bioenergy/articles/bioproducts-enable-biofuels-workshop-summary-report (accessed April 8, 2024).
  15. Blair E. M., Dickson K. L., O'Malley M. A. (2021). Microbial communities and their enzymes facilitate degradation of recalcitrant polymers in anaerobic digestion. Current Opinion in Microbiology, 64, 100– 108. 10.1016/j.mib.2021.09.008 34700124 · DOI
  16. Bodor A., Bounedjoum N., Vincze G. E., Erdeiné Kis Á., Laczi K., Bende G., Szilágyi Á., Kovács T., Perei K., Rákhely G. (2020). Challenges of unculturable bacteria: Environmental perspectives. Reviews in Environmental Science and Bio/Technology, 19 (1), 1– 22. 10.1007/s11157-020-09522-4 · DOI
  17. Bokinsky G., Peralta-Yahya P. P., George A., Holmes B. M., Steen E. J., Dietrich J., Soon Lee T., Tullman-Ercek D., Voigt C. A., Simmons B. A., Keasling J. D. (2011). Synthesis of three advanced biofuels from ionic liquid-pretreated switchgrass using engineered Escherichia coli. Proceedings of the National Academy of Sciences, 108 (50), 19949– 19954. 10.1073/pnas.1106958108 PMC3250153 22123987 · DOI
  18. Boob A. G., Chen J., Zhao H. (2024). Enabling pathway design by multiplex experimentation and machine learning. Metabolic Engineering, 81, 70– 87. 10.1016/j.ymben.2023.11.006 38040110 · DOI
  19. Borenstein E., Kupiec M., Feldman M. W., Ruppin E. (2008). Large-scale reconstruction and phylogenetic analysis of metabolic environments. Proceedings of the National Academy of Sciences, 105 (38), 14482– 14487. 10.1073/pnas.0806162105 PMC2567166 18787117 · DOI
  20. Brophy J. A. N., Voigt C. A. (2014). Principles of genetic circuit design. Nature Methods, 11 (5), 508– 520. 10.1038/nmeth.2926 24781324 PMC4230274 · DOI
  21. Burmeister A., Grünberger A. (2020). Microfluidic cultivation and analysis tools for interaction studies of microbial co-cultures. Current Opinion in Biotechnology, 62, 106– 115. 10.1016/j.copbio.2019.09.001 31715386 · DOI
  22. Cai C., Xu Z., Li J., Zhou H., Jin M. (2022). Developing rhodococcus opacus and sphingobium sp. Coculture systems for valorization of lignin-derived dimers. Biotechnology and Bioengineering, 119 (11), 3162– 3177. 10.1002/bit.28215 36030484 · DOI
  23. Cai F., Lin M., Wang L., Song C., Jin Y., Liu G., Chen C. (2023). Enhancing acidification efficiency of vegetable wastes through heat shock pretreatment and initial pH regulation. Environmental Science and Pollution Research, 31 (1), 1079– 1093. 10.1007/s11356-023-31025-2 38030843 · DOI
  24. Cai J., Tan T., Chan S. H. J. (2021). Predicting nash equilibria for microbial metabolic interactions. Bioinformatics, 36 (24), 5649– 5655. 10.1093/bioinformatics/btaa1014 33315094 · DOI
  25. Candry P., Godfrey B. J., Wang Z., Sabba F., Dieppa E., Fudge J., Balogun O., Wells G., Winkler M.-K. H. (2022). Tailoring polyvinyl alcohol-sodium alginate (PVA-SA) hydrogel beads by controlling crosslinking pH and time. Scientific Reports, 12 (1), 20822. 10.1038/s41598-022-25111-7 36460678 PMC9718846 · DOI
  26. Cao Z., Yan W., Ding M., Yuan Y. (2022). Construction of microbial consortia for microbial degradation of complex compounds. Frontiers in Bioengineering and Biotechnology, 10, 1051233. 10.3389/fbioe.2022.1051233 36561050 PMC9763274 · DOI · Paper page
  27. Carr A., Baliga N. S., Diener C., Gibbons S. M. (2024). Personalized Clostridioides difficile engraftment risk prediction and probiotic therapy assessment in the human gut. bioRxiv: the preprint server for biology, 2023.04.28.538771. 10.1101/2023.04.28.538771 · DOI
  28. Carr A., Diener C., Baliga N. S., Gibbons S. M. (2019). Use and abuse of correlation analyses in microbial ecology. The ISME Journal, 13 (11), 2647– 2655. 10.1038/s41396-019-0459-z 31253856 PMC6794304 · DOI
  29. Carvajal-Arroyo J. M., Candry P., Andersen S. J., Props R., Seviour T., Ganigué R., Rabaey K. (2019). Granular fermentation enables high rate caproic acid production from solid-free thin stillage. Green Chemistry, 21 (6), 1330– 1339. 10.1039/C8GC03648A · DOI
  30. Cha S., Lim H. G., Kwon S., Kim D., Kang C. W., Jung G. Y. (2021). Design of mutualistic microbial consortia for stable conversion of carbon monoxide to value-added chemicals. Metabolic Engineering, 64, 146– 153. 10.1016/j.ymben.2021.02.001 33571657 · DOI
  31. Chang C.-Y., Vila J. C. C., Bender M., Li R., Mankowski M. C., Bassette M., Borden J., Golfier S., Sanchez P. G. L., Waymack R., Zhu X., Diaz-Colunga J., Estrela S., Rebolleda-Gomez M., Sanchez A. (2021). Engineering complex communities by directed evolution. Nature Ecology & Evolution, 5 (7), 1011– 1023. 10.1038/s41559-021-01457-5 33986540 PMC8263491 · DOI
  32. Chen Y., Gin J. W., Wang Y., De Raad M., Tan S., Hillson N. J., Northen T. R., Adams P. D., Petzold C. J. (2023). Alkaline-SDS cell lysis of microbes with acetone protein precipitation for proteomic sample preparation in 96-well plate format. PLoS ONE, 18 (7), e0288102. 10.1371/journal.pone.0288102 37418444 PMC10328223 · DOI
  33. Chen Y., Kim J. K., Hirning A. J., Josić K., Bennett M. R. (2015). Emergent genetic oscillations in a synthetic microbial consortium. Science, 349 (6251), 986– 989. 10.1126/science.aaa3794 26315440 PMC4597888 · DOI
  34. Chi X., Li J., Wang X., Zhang Y., Antwi P. (2018). Hyper-production of butyric acid from delignified rice straw by a novel consolidated bioprocess. Bioresource Technology, 254, 115– 120. 10.1016/j.biortech.2018.01.042 29413911 · DOI
  35. Cleveland C. J., Morris C. (2014). Section 45—Climate change. In Handbook of Energy (pp. 805– 820). Elsevier. 10.1016/B978-0-12-417013-1.00045-5. · DOI
  36. De Bernardini N., Basile A., Zampieri G., Kovalovszki A., De Diego Diaz B., Offer E., Wongfaed N., Angelidaki I., Kougias P. G., Campanaro S., Treu L. (2022). Integrating metagenomic binning with flux balance analysis to unravel syntrophies in anaerobic CO2 methanation. Microbiome, 10 (1), 117. 10.1186/s40168-022-01311-1 35918706 PMC9347119 · DOI
  37. De Groof V., Coma M., Arnot T., Leak D. J., Lanham A. B. (2019). Medium chain carboxylic acids from complex organic feedstocks by mixed culture fermentation. Molecules (Basel, Switzerland), 24 (3), 398. 10.3390/molecules24030398 30678297 PMC6384945 · DOI
  38. De Raad M., Li Y. V., Kuehl J. V., Andeer P. F., Kosina S. M., Hendrickson A., Saichek N. R., Golini A. N., Han L. Z., Wang Y., Bowen B. P., Deutschbauer A. M., Arkin A. P., Chakraborty R., Northen T. R. (2022). A defined medium for cultivation and exometabolite profiling of soil bacteria. Frontiers in Microbiology, 13, 855331. 10.3389/fmicb.2022.855331 35694313 PMC9174792 · DOI
  39. De Souza Moraes B., Mary Dos Santos G., Palladino Delforno T., Tadeu Fuess L., José Da Silva A. (2019). Enriched microbial consortia for dark fermentation of sugarcane vinasse towards value-added short-chain organic acids and alcohol production. Journal of Bioscience and Bioengineering, 127 (5), 594– 601. 10.1016/j.jbiosc.2018.10.008 30420331 · DOI
  40. Diao W., Guo L., Ding Q., Gao C., Hu G., Chen X., Li Y., Zhang L., Chen W., Chen J., Liu L. (2021). Reprogramming microbial populations using a programmed lysis system to improve chemical production. Nature Communications, 12 (1), 6886. 10.1038/s41467-021-27226-3 PMC8617184 34824227 · DOI
  41. Díaz-García L., Huang S., Spröer C., Sierra-Ramírez R., Bunk B., Overmann J., Jiménez D. J. (2021). Dilution-to-stimulation/extinction method: A combination enrichment strategy to develop a minimal and versatile lignocellulolytic bacterial consortium. Applied and Environmental Microbiology, 87 (2), e02427– 20. 10.1128/AEM.02427-20 33127812 PMC7783344 · DOI
  42. Diender M., Parera Olm I., Sousa D. Z. (2021). Synthetic co-cultures: Novel avenues for bio-based processes. Current Opinion in Biotechnology, 67, 72– 79. 10.1016/j.copbio.2021.01.006 33517194 · DOI
  43. Diener C., Gibbons S. M., Resendis-Antonio O. (2020). MICOM: Metagenome-scale modeling to infer metabolic interactions in the gut microbiota. MSystems, 5 (1), e00606– 19. 10.1128/mSystems.00606-19 31964767 PMC6977071 · DOI
  44. Doloman A., Besteman M. S., Sanders M. G., Sousa D. Z. (2024). Methanogenic partner influences cell aggregation and signalling of syntrophobacterium fumaroxidans. Applied Microbiology and Biotechnology, 108 (1), 127. 10.1007/s00253-023-12955-w 38229305 PMC10787695 · DOI
  45. Du P., Zhao H., Zhang H., Wang R., Huang J., Tian Y., Luo X., Luo X., Wang M., Xiang Y., Qian L., Chen Y., Tao Y., Lou C. (2020). De novo design of an intercellular signaling toolbox for multi-channel cell–cell communication and biological computation. Nature Communications, 11 (1), 4226. 10.1038/s41467-020-17993-w PMC7445162 32839450 · DOI
  46. Duncker K. E., Holmes Z. A., You L. (2021). Engineered microbial consortia: Strategies and applications. Microbial Cell Factories, 20 (1), 211. 10.1186/s12934-021-01699-9 34784924 PMC8597270 · DOI · Paper page
  47. Dzulkarnain E. L. N., Audu J. O., Wan Dagang W. R. Z., Abdul-Wahab M. F. (2022). Microbiomes of biohydrogen production from dark fermentation of industrial wastes: Current trends, advanced tools and future outlook. Bioresources and Bioprocessing, 9 (1), 16. 10.1186/s40643-022-00504-8 38647867 PMC10991117 · DOI
  48. Eng A., Borenstein E. (2019). Microbial community design: Methods, applications, and opportunities. Current Opinion in Biotechnology, 58, 117– 128. 10.1016/j.copbio.2019.03.002 30952088 PMC6710113 · DOI
  49. Flemming H.-C., Wingender J., Szewzyk U., Steinberg P., Rice S. A., Kjelleberg S. (2016). Biofilms: An emergent form of bacterial life. Nature Reviews Microbiology, 14 (9), 563– 575. 10.1038/nrmicro.2016.94 27510863 · DOI · Paper page
  50. Fonoll X., Shrestha S., Khanal S. K., Dosta J., Mata-Alvarez J., Raskin L. (2021). Understanding the anaerobic digestibility of lignocellulosic substrates using rumen content as a cosubstrate and an inoculum. ACS ES&T Engineering, 1 (3), 424– 435. 10.1021/acsestengg.0c00164 · DOI
  51. Fonoll X., Zhu K., Aley L., Shrestha S., Raskin L. (2024). Simulating rumen conditions using an anaerobic dynamic membrane bioreactor to enhance hydrolysis of lignocellulosic biomass. Environmental Science & Technology, 58 (3), 1741– 1751. 10.1021/acs.est.3c06478 38184844 · DOI
  52. Ghosh P., Kumar M., Kapoor R., Kumar S. S., Singh L., Vijay V., Vijay V. K., Kumar V., Thakur I. S. (2020). Enhanced biogas production from municipal solid waste via co-digestion with sewage sludge and metabolic pathway analysis. Bioresource Technology, 296, 122275. 10.1016/j.biortech.2019.122275 31683109 · DOI
  53. Gildemyn S., Molitor B., Usack J. G., Nguyen M., Rabaey K., Angenent L. T. (2017). Upgrading syngas fermentation effluent using Clostridium kluyveri in a continuous fermentation. Biotechnology for Biofuels, 10 (1), 83. 10.1186/s13068-017-0764-6 28367228 PMC5372331 · DOI
  54. Gilmore S. P., Lankiewicz T. S., Wilken S.t. E., Brown J. L., Sexton J. A., Henske J. K., Theodorou M. K., Valentine D. L., O'Malley M. A. (2019). Top-down enrichment guides in formation of synthetic microbial consortia for biomass degradation. ACS Synthetic Biology, 8 (9), 2174– 2185. 10.1021/acssynbio.9b00271 31461261 · DOI
  55. Gonzalez J. E., Antoniewicz M. R. (2017). Tracing metabolism from lignocellulosic biomass and gaseous substrates to products with stable-isotopes. Current Opinion in Biotechnology, 43, 86– 95. 10.1016/j.copbio.2016.10.002 27780112 · DOI
  56. Göpfrich K., Platzman I., Spatz J. P. (2018). Mastering complexity: Towards bottom-up construction of multifunctional eukaryotic synthetic cells. Trends in Biotechnology, 36 (9), 938– 951. 10.1016/j.tibtech.2018.03.008 29685820 PMC6100601 · DOI
  57. Gottshall E. Y., Bryson S. J., Cogert K. I., Landreau M., Sedlacek C. J., Stahl D. A., Daims H., Winkler M. (2021). Sustained nitrogen loss in a symbiotic association of comammox nitrospira and anammox bacteria. Water Research, 202, 117426. 10.1016/j.watres.2021.117426 34274897 · DOI
  58. Grootscholten T. I. M., Steinbusch K. J. J., Hamelers H. V. M., Buisman C. J. N. (2013). Chain elongation of acetate and ethanol in an upflow anaerobic filter for high rate MCFA production. Bioresource Technology, 135, 440– 445. 10.1016/j.biortech.2012.10.165 23228455 · DOI
  59. Haruta S., Yamamoto K. (2018). Model microbial consortia as tools for understanding complex microbial communities. Current Genomics, 19 (8), 723– 733. 10.2174/1389202919666180911131206 30532651 PMC6225455 · DOI
  60. Heinken A., Hertel J., Acharya G., Ravcheev D. A., Nyga M., Okpala O. E., Hogan M., Magnúsdóttir S., Martinelli F., Nap B., Preciat G., Edirisinghe J. N., Henry C. S., Fleming R. M. T., Thiele I. (2023). Genome-scale metabolic reconstruction of 7,302 human microorganisms for personalized medicine. Nature Biotechnology, 41 (9), 1320– 1331. 10.1038/s41587-022-01628-0 PMC10497413 36658342 · DOI
  61. Heinken A., Magnúsdóttir S., Fleming R. M. T., Thiele I. (2021). DEMETER: Efficient simultaneous curation of genome-scale reconstructions guided by experimental data and refined gene annotations. Bioinformatics, 37 (21), 3974– 3975. 10.1093/bioinformatics/btab622 34473240 PMC8570805 · DOI
  62. Henry C. S., Bernstein H. C., Weisenhorn P., Taylor R. C., Lee J., Zucker J., Song H. (2016). Microbial community metabolic modeling: A community data-driven network reconstruction. Journal of Cellular Physiology, 231 (11), 2339– 2345. 10.1002/jcp.25428 27186840 PMC5132105 · DOI
  63. Hess M., Sczyrba A., Egan R., Kim T.-W., Chokhawala H., Schroth G., Luo S., Clark D. S., Chen F., Zhang T., Mackie R. I., Pennacchio L. A., Tringe S. G., Visel A., Woyke T., Wang Z., Rubin E. M. (2011). Metagenomic discovery of biomass-degrading genes and genomes from cow rumen. Science, 331 (6016), 463– 467. 10.1126/science.1200387 21273488 · DOI · Paper page
  64. Hirschi S., Ward T. R., Meier W. P., Müller D. J., Fotiadis D. (2022). Synthetic biology: Bottom-up assembly of Molecular systems. Chemical Reviews, 122 (21), 16294– 16328. 10.1021/acs.chemrev.2c00339 36179355 · DOI
  65. Hu H., Wang M., Huang Y., Xu Z., Xu P., Nie Y., Tang H. (2022). Guided by the principles of microbiome engineering: Accomplishments and perspectives for environmental use. mLife, 1 (4), 382– 398. 10.1002/mlf2.12043 38818482 PMC10989833 · DOI
  66. Ibrahim M., Raajaraam L., Raman K. (2021). Modelling microbial communities: Harnessing consortia for biotechnological applications. Computational and Structural Biotechnology Journal, 19, 3892– 3907. 10.1016/j.csbj.2021.06.048 34584635 PMC8441623 · DOI
  67. Imajo U., Tokutomi T., Furukawa K. (2004). Granulation of Anammox microorganisms in up-flow reactors. Water Science and Technology, 49 (5-6), 155– 164. 10.2166/wst.2004.0749 15137419 · DOI
  68. Janga S., Babu M. M. (2008). Network-based approaches for linking metabolism with environment. Genome Biology, 9 (11), 239. 10.1186/gb-2008-9-11-239 19040774 PMC2614483 · DOI
  69. Jenior M. L., Glass E. M., Papin J. A. (2023). Reconstructor: A COBRApy compatible tool for automated genome-scale metabolic network reconstruction with parsimonious flux-based gap-filling. Bioinformatics, 39 (6), btad367. 10.1093/bioinformatics/btad367 37279743 PMC10275916 · DOI
  70. Jiang M.-Z., Zhu H.-Z., Zhou N., Liu C., Jiang C.-Y., Wang Y., Liu S.-J. (2022). Droplet microfluidics-based high-throughput bacterial cultivation for validation of taxon pairs in microbial co-occurrence networks. Scientific Reports, 12 (1), 18145. 10.1038/s41598-022-23000-7 36307549 PMC9616874 · DOI
  71. Jiang W., Hernández Villamor D., Peng H., Chen J., Liu L., Haritos V., Ledesma-Amaro R. (2021). Metabolic engineering strategies to enable microbial utilization of C1 feedstocks. Nature Chemical Biology, 17 (8), 845– 855. 10.1038/s41589-021-00836-0 34312558 · DOI · Paper page
  72. Jiang Y., Wu R., Zhang W., Xin F., Jiang M. (2023). Construction of stable microbial consortia for effective biochemical synthesis. Trends in Biotechnology, 41 (11), 1430– 1441. 10.1016/j.tibtech.2023.05.008 37330325 · DOI · Paper page
  73. Johnston T. G., Yuan S.-F., Wagner J. M., Yi X., Saha A., Smith P., Nelson A., Alper H. S. (2020). Compartmentalized microbes and co-cultures in hydrogels for on-demand bioproduction and preservation. Nature Communications, 11 (1), 563. 10.1038/s41467-020-14371-4 PMC7000784 32019917 · DOI
  74. Joseph C., Zafeiropoulos H., Bernaerts K., Faust K. (2024). Predicting microbial interactions with approaches based on flux balance analysis: An evaluation. BMC Bioinformatics [Electronic Resource], 25 (1), 36. 10.1186/s12859-024-05651-7 38262921 PMC10804772 · DOI
  75. Kapoore R. V., Padmaperuma G., Maneein S., Vaidyanathan S. (2022). Co-culturing microbial consortia: Approaches for applications in biomanufacturing and bioprocessing. Critical Reviews in Biotechnology, 42 (1), 46– 72. 10.1080/07388551.2021.1921691 33980092 · DOI
  76. Karlsen E., Schulz C., Almaas E. (2018). Automated generation of genome-scale metabolic draft reconstructions based on KEGG. BMC Bioinformatics [Electronic Resource], 19 (1), 467. 10.1186/s12859-018-2472-z 30514205 PMC6280343 · DOI
  77. Karp P. D., Paley S., Krummenacker M., Kothari A., Wannemuehler M. J., Phillips G. J. (2022). Pathway tools management of Pathway/genome data for microbial communities. Frontiers in Bioinformatics, 2, 869150. 10.3389/fbinf.2022.869150 36304298 PMC9580912 · DOI
  78. Kawai R., Toya Y., Miyoshi K., Murakami M., Niide T., Horinouchi T., Maeda T., Shibai A., Furusawa C., Shimizu H. (2022). Acceleration of target production in co-culture by enhancing intermediate consumption through adaptive laboratory evolution. Biotechnology and Bioengineering, 119 (3), 936– 945. 10.1002/bit.28007 34914093 · DOI
  79. Kehe J., Kulesa A., Ortiz A., Ackerman C. M., Thakku S. G., Sellers D., Kuehn S., Gore J., Friedman J., Blainey P. C. (2019). Massively parallel screening of synthetic microbial communities. Proceedings of the National Academy of Sciences, 116 (26), 12804– 12809. 10.1073/pnas.1900102116 PMC6600964 31186361 · DOI
  80. Khandelwal R. A., Olivier B. G., Röling W. F. M., Teusink B., Bruggeman F. J. (2013). Community flux balance analysis for microbial consortia at balanced growth. PLoS ONE, 8 (5), e64567. 10.1371/journal.pone.0064567 23741341 PMC3669319 · DOI
  81. Kim J., Coradetti S. T., Kim Y.-M., Gao Y., Yaegashi J., Zucker J. D., Munoz N., Zink E. M., Burnum-Johnson K. E., Baker S. E., Simmons B. A., Skerker J. M., Gladden J. M., Magnuson J. K. (2021). Multi-omics driven metabolic network reconstruction and analysis of lignocellulosic carbon utilization in rhodosporidium toruloides. Frontiers in Bioengineering and Biotechnology, 8, 612832. 10.3389/fbioe.2020.612832 33585414 PMC7873862 · DOI
  82. Kim M., Sung J., Chia N. (2022). Resource-allocation constraint governs structure and function of microbial communities in metabolic modeling. Metabolic Engineering, 70, 12– 22. 10.1016/j.ymben.2021.12.011 34990848 · DOI
  83. Kim S. Y., Yang Y.-H., Choi K.-Y. (2020). Bioconversion of plant hydrolysate biomass into biofuels using an engineered Bacillus subtilis and Escherichia coli mixed-whole cell biotransformation. Biotechnology and Bioprocess Engineering, 25 (3), 477– 484. 10.1007/s12257-019-0487-6 · DOI
  84. Kotay S. M., Das D. (2010). Microbial hydrogen production from sewage sludge bioaugmented with a constructed microbial consortium. International Journal of Hydrogen Energy, 35 (19), 10653– 10659. 10.1016/j.ijhydene.2010.03.059 · DOI
  85. Kucek L. A., Nguyen M., Angenent L. T. (2016). Conversion of l-lactate into n-caproate by a continuously fed reactor microbiome. Water Research, 93, 163– 171. 10.1016/j.watres.2016.02.018 26905795 · DOI
  86. Kundu P., Manna B., Majumder S., Ghosh A. (2019). Species-wide metabolic interaction network for understanding natural lignocellulose digestion in termite gut microbiota. Scientific Reports, 9 (1), 16329. 10.1038/s41598-019-52843-w 31705042 PMC6841923 · DOI
  87. Lawson C. E., Harcombe W. R., Hatzenpichler R., Lindemann S. R., Löffler F. E., O'Malley M. A., García Martín H., Pfleger B. F., Raskin L., Venturelli O. S., Weissbrodt D. G., Noguera D. R., McMahon K. D. (2019). Common principles and best practices for engineering microbiomes. Nature Reviews Microbiology, 17 (12), 725– 741. 10.1038/s41579-019-0255-9 31548653 PMC8323346 · DOI
  88. Lee D.-J., Show K.-Y., Wang A. (2013). Unconventional approaches to isolation and enrichment of functional microbial consortium—A review. Bioresource Technology, 136, 697– 706. 10.1016/j.biortech.2013.02.075 23566469 · DOI
  89. Lee J. A., Baugh A. C., Shevalier N. J., Strand B., Stolyar S., Marx C. J. (2021). Cross-feeding of a toxic metabolite in a synthetic lignocellulose-degrading microbial community. Microorganisms, 9 (2), 321. 10.3390/microorganisms9020321 33557371 PMC7914493 · DOI
  90. Levy R., Borenstein E. (2013). Metabolic modeling of species interaction in the human microbiome elucidates community-level assembly rules. Proceedings of the National Academy of Sciences, 110 (31), 12804– 12809. 10.1073/pnas.1300926110 PMC3732988 23858463 · DOI
  91. Li B., Godfrey B. J., RedCorn R., Candry P., Abrahamson B., Wang Z., Goel R., Winkler M.-K. H. (2023). Mainstream nitrogen removal from low temperature and low ammonium strength municipal wastewater using hydrogel-encapsulated comammox and anammox. Water Research, 242, 120303. 10.1016/j.watres.2023.120303 37419028 · DOI
  92. Li D., Yin F., Ma X. (2020). Towards biodegradable polyhydroxyalkanoate production from wood waste: Using volatile fatty acids as conversion medium. Bioresource Technology, 299, 122629. 10.1016/j.biortech.2019.122629 31881436 · DOI
  93. Li W., Zhou Z., Li X., Ma L., Guan Q., Zheng G., Liang H., Yan Y., Shen X., Wang J., Sun X., Yuan Q. (2022). Biosynthesis of plant hemostatic dencichine in Escherichia coli. Nature Communications, 13 (1), 5492. 10.1038/s41467-022-33255-3 PMC9485241 36123371 · DOI
  94. Li Z., Wang X., Zhang H. (2019). Balancing the non-linear rosmarinic acid biosynthetic pathway by modular co-culture engineering. Metabolic Engineering, 54, 1– 11. 10.1016/j.ymben.2019.03.002 30844431 · DOI
  95. Liang J., Nabi M., Zhang P., Zhang G., Cai Y., Wang Q., Zhou Z., Ding Y. (2020). Promising biological conversion of lignocellulosic biomass to renewable energy with rumen microorganisms: A comprehensive review. Renewable and Sustainable Energy Reviews, 134, 110335. 10.1016/j.rser.2020.110335 · DOI
  96. Lin L. (2022). Bottom-up synthetic ecology study of microbial consortia to enhance lignocellulose bioconversion. Biotechnology for Biofuels and Bioproducts, 15 (1), 14. 10.1186/s13068-022-02113-1 35418100 PMC8822760 · DOI
  97. Lindemann S. R., Bernstein H. C., Song H.-S., Fredrickson J. K., Fields M. W., Shou W., Johnson D. R., Beliaev A. S. (2016). Engineering microbial consortia for controllable outputs. The ISME Journal, 10 (9), 2077– 2084. 10.1038/ismej.2016.26 26967105 PMC4989317 · DOI
  98. Liu T., Li J., Hao X., Meng J. (2024). Efficient caproic acid production from lignocellulosic biomass by bio-augmented mixed microorganisms. Bioresource Technology, 399, 130565. 10.1016/j.biortech.2024.130565 38461870 · DOI
  99. Lopes A. M., Ferreira Filho E. X., Moreira L. R. S. (2018). An update on enzymatic cocktails for lignocellulose breakdown. Journal of Applied Microbiology, 125 (3), 632– 645. 10.1111/jam.13923 29786939 · DOI
  100. Louie T., Golan Y., Khanna S., Bobilev D., Erpelding N., Fratazzi C., Carini M., Menon R., Ruisi M., Norman J. M., Faith J. J., Olle B., Li M., Silber J. L., Pardi D. S. (2023). VE303, a defined Bacterial Consortium, for prevention of recurrent clostridioides difficile infection: A randomized clinical trial. JAMA, 329 (16), 1356. 10.1001/jama.2023.4314 37060545 PMC10105904 · DOI
  101. Machado D., Andrejev S., Tramontano M., Patil K. R. (2018). Fast automated reconstruction of genome-scale metabolic models for microbial species and communities. Nucleic Acids Research, 46 (15), 7542– 7553. 10.1093/nar/gky537 30192979 PMC6125623 · DOI
  102. Machado D., Maistrenko O. M., Andrejev S., Kim Y., Bork P., Patil K. R., Patil K. R. (2021). Polarization of microbial communities between competitive and cooperative metabolism. Nature Ecology & Evolution, 5 (2), 195– 203. 10.1038/s41559-020-01353-4 33398106 PMC7610595 · DOI
  103. Madill M. B. W., Luo Y., Sampara P., Ziels R. M. (2021). Activity-based cell sorting reveals resistance of functionally degenerate nitrospira during a press disturbance in nitrifying activated sludge. mSystems, 6 (4), e00712– 21. 10.1128/mSystems.00712-21 34282936 PMC8407113 · DOI
  104. Massot F., Bernard N., Alvarez L. M. M., Martorell M. M., Mac Cormack W. P., Ruberto L. A. M. (2022). Microbial associations for bioremediation. What does “microbial consortia” mean? Applied Microbiology and Biotechnology, 106 (7), 2283– 2297. 10.1007/s00253-022-11864-8 35294589 · DOI · Paper page
  105. McDaniel E. A., Scarborough M., Mulat D. G., Lin X., Sampara P. S., Olson H. M., Young R. P., Eder E. K., Attah I. K., Markillie L. M., Hoyt D. W., Lipton M. S., Hallam S. J., Ziels R. M. (2023). Diverse electron carriers drive syntrophic interactions in an enriched anaerobic acetate-oxidizing consortium. The ISME Journal, 17 (12), 2326– 2339. 10.1038/s41396-023-01542-6 37880541 PMC10689502 · DOI
  106. Mee M. T., Collins J. J., Church G. M., Wang H. H. (2014). Syntrophic exchange in synthetic microbial communities. Proceedings of the National Academy of Sciences, 111 (20), E2149– 56. 10.1073/pnas.1405641111 PMC4034247 24778240 · DOI
  107. Mikesell M. D., Boyd S. A. (1988). Enhancement of pentachlorophenol degradation in soil through induced anaerobiosis and bioaugmentation with anaerobic sewage sludge. Environmental Science & Technology, 22 (12), 1411– 1414. 10.1021/es00177a003 22200465 · DOI
  108. Mills S., Trego A. C., Prevedello M., De Vrieze J., O'Flaherty V., Lens P. N. L., Collins G. (2024). Unifying concepts in methanogenic, aerobic, and anammox sludge granulation. Environmental Science and Ecotechnology, 17, 100310. 10.1016/j.ese.2023.100310 37705860 PMC10495608 · DOI
  109. Naresh Kumar M., Ravikumar R., Thenmozhi S., Ranjith Kumar M., Kirupa Shankar M. (2019). Choice of pretreatment technology for sustainable production of bioethanol from lignocellulosic biomass: Bottle necks and recommendations. Waste and Biomass Valorization, 10 (6), 1693– 1709. 10.1007/s12649-017-0177-6 · DOI
  110. Okurowska K., Karunakaran E., Al-Farttoosy A., Couto N., Pandhal J. (2021). Adapting the algal microbiome for growth on domestic landfill leachate. Bioresource Technology, 319, 124246. 10.1016/j.biortech.2020.124246 33254468 · DOI
  111. Pagliano G., Gugliucci W., Torrieri E., Piccolo A., Cangemi S., Di Giuseppe F. A., Robertiello A., Faraco V., Pepe O., Ventorino V. (2020). Polyhydroxyalkanoates (PHAs) from dairy wastewater effluent: Bacterial accumulation, structural characterization and physical properties. Chemical and Biological Technologies in Agriculture, 7 (1), 29. 10.1186/s40538-020-00197-1 · DOI
  112. Parvin F., Tareq S. M. (2021). Impact of landfill leachate contamination on surface and groundwater of Bangladesh: A systematic review and possible public health risks assessment. Applied Water Science, 11 (6), 100. 10.1007/s13201-021-01431-3 34094797 PMC8164486 · DOI
  113. Passi A., Tibocha-Bonilla J. D., Kumar M., Tec-Campos D., Zengler K., Zuniga C. (2021). Genome-scale metabolic modeling enables In-depth understanding of big data. Metabolites, 12 (1), 14. 10.3390/metabo12010014 35050136 PMC8778254 · DOI
  114. Phua Z., Giannis A., Dong Z.-L., Lisak G., Ng W. J. (2019). Characteristics of incineration ash for sustainable treatment and reutilization. Environmental Science and Pollution Research, 26 (17), 16974– 16997. 10.1007/s11356-019-05217-8 31041714 · DOI
  115. Poulsen J. S., Macêdo W. V., Bonde T., Nielsen J. L. (2023). Energetically exploiting lignocellulose-rich residues in anaerobic digestion technologies: From bioreactors to proteogenomics. Biotechnology for Biofuels and Bioproducts, 16 (1), 183. 10.1186/s13068-023-02432-x 38017526 PMC10685487 · DOI
  116. Probst D., Manica M., Nana Teukam Y. G., Castrogiovanni A., Paratore F., Laino T. (2022). Biocatalysed synthesis planning using data-driven learning. Nature Communications, 13 (1), 964. 10.1038/s41467-022-28536-w PMC8857209 35181654 · DOI
  117. Qin R., Zhu Y., Ai M., Jia X. (2022). Reconstruction and optimization of a Pseudomonas putida-Escherichia coli microbial consortium for mcl-PHA production from lignocellulosic biomass. Frontiers in Bioengineering and Biotechnology, 10, 1023325. 10.3389/fbioe.2022.1023325 36338139 PMC9626825 · DOI
  118. Ravikrishnan A., Blank L. M., Srivastava S., Raman K. (2020). Investigating metabolic interactions in a microbial co-culture through integrated modelling and experiments. Computational and Structural Biotechnology Journal, 18, 1249– 1258. 10.1016/j.csbj.2020.03.019 32551031 PMC7286961 · DOI
  119. Ravikrishnan A., Nasre M., Raman K. (2018). Enumerating all possible biosynthetic pathways in metabolic networks. Scientific Reports, 8 (1), 9932. 10.1038/s41598-018-28007-7 29967471 PMC6028704 · DOI
  120. Reddy M. V., Hayashi S., Choi D., Cho H., Chang Y.-C. (2018). Short chain and medium chain fatty acids production using food waste under non-augmented and bio-augmented conditions. Journal of Cleaner Production, 176, 645– 653. 10.1016/j.jclepro.2017.12.166 · DOI
  121. Rhee S. K., Pack M. Y. (1980). Effect of environmental pH on fermentation balance of Lactobacillus bulgaricus. Journal of Bacteriology, 144 (1), 217– 221. 10.1128/jb.144.1.217-221.1980 7419489 PMC294626 · DOI
  122. Roell G. W., Zha J., Carr R. R., Koffas M. A., Fong S. S., Tang Y. J. (2019). Engineering microbial consortia by division of labor. Microbial Cell Factories, 18 (1), 35. 10.1186/s12934-019-1083-3 30736778 PMC6368712 · DOI
  123. Rubin B. E., Diamond S., Cress B. F., Crits-Christoph A., Lou Y. C., Borges A. L., Shivram H., He C., Xu M., Zhou Z., Smith S. J., Rovinsky R., Smock D. C. J., Tang K., Owens T. K., Krishnappa N., Sachdeva R., Barrangou R., Deutschbauer A. M., Doudna J. A. (2021). Species- and site-specific genome editing in complex bacterial communities. Nature Microbiology, 7 (1), 34– 47. 10.1038/s41564-021-01014-7 PMC9261505 34873292 · DOI
  124. Sahil S., Karvembu P., Kaur R., Katyal P., Phutela U. G. (2023). Enhanced biogas production from rice straw through pretreatment with cellulase producing microbial consortium. Energy Nexus, 12, 100246. 10.1016/j.nexus.2023.100246 · DOI
  125. Sanchez-Gorostiaga A., Bajić D., Osborne M. L., Poyatos J. F., Sanchez A. (2019). High-order interactions distort the functional landscape of microbial consortia. PLoS Biology, 17 (12), e3000550. 10.1371/journal.pbio.3000550 31830028 PMC6932822 · DOI
  126. Sauer M., Marx H. (2023). Co-cultures and synthetic microbial communities for green chemical production. Current Opinion in Green and Sustainable Chemistry, 42, 100842. 10.1016/j.cogsc.2023.100842 · DOI
  127. Schwander T., Schada Von Borzyskowski L., Burgener S., Cortina N. S., Erb T. J. (2016). A synthetic pathway for the fixation of carbon dioxide in vitro. Science, 354 (6314), 900– 904. 10.1126/science.aah5237 27856910 PMC5892708 · DOI
  128. Scott W. T., Benito-Vaquerizo S., Zimmermann J., Bajić D., Heinken A., Suarez-Diez M., Schaap P. J. (2023). A structured evaluation of genome-scale constraint-based modeling tools for microbial consortia. PLOS Computational Biology, 19 (8), e1011363. 10.1371/journal.pcbi.1011363 37578975 PMC10449394 · DOI
  129. Seaver S. M. D., Liu F., Zhang Q., Jeffryes J., Faria J. P., Edirisinghe J. N., Mundy M., Chia N., Noor E., Beber M. E., Best A. A., DeJongh M., Kimbrel J. A., D'haeseleer P., McCorkle S. R., Bolton J. R., Pearson E., Canon S., Wood-Charlson E. M., Henry C. S. (2021). The ModelSEED Biochemistry Database for the integration of metabolic annotations and the reconstruction, comparison and analysis of metabolic models for plants, fungi and microbes. Nucleic Acids Research, 49 (D1), D575– D588. 10.1093/nar/gkaa746 32986834 PMC7778927 · DOI
  130. Seviour T., Pijuan M., Nicholson T., Keller J., Yuan Z. (2009). Understanding the properties of aerobic sludge granules as hydrogels. Biotechnology and Bioengineering, 102 (5), 1483– 1493. 10.1002/bit.22164 18988268 · DOI
  131. Shahab R. L., Brethauer S., Davey M. P., Smith A. G., Vignolini S., Luterbacher J. S., Studer M. H. (2020a). A heterogeneous microbial consortium producing short-chain fatty acids from lignocellulose. Science, 369 (6507), eabb1214. 10.1126/science.abb1214 32855308 · DOI
  132. Shahab R. L., Brethauer S., Luterbacher J. S., Studer M. H. (2020b). Engineering of ecological niches to create stable artificial consortia for complex biotransformations. Current Opinion in Biotechnology, 62, 129– 136. 10.1016/j.copbio.2019.09.008 31671322 · DOI
  133. Shahab R. L., Luterbacher J. S., Brethauer S., Studer M. H. (2018). Consolidated bioprocessing of lignocellulosic biomass to lactic acid by a synthetic fungal-bacterial consortium. Biotechnology and Bioengineering, 115 (5), 1207– 1215. 10.1002/bit.26541 29315476 · DOI
  134. Shan X., Guo H., Ma F., Shan Z. (2023). Enhanced treatment of synthetic wastewater by bioaugmentation with a constructed consortium. Chemosphere, 338, 139520. 10.1016/j.chemosphere.2023.139520 37454986 · DOI
  135. Shrestha S., Colcord B., Fonoll X., Raskin L. (2022). Fate of influent microbial populations during medium chain carboxylic acid recovery from brewery and pre-fermented food waste streams. Environmental Science: Water Research & Technology, 8 (2), 257– 269. 10.1039/D1EW00656H · DOI
  136. Shrestha S., Goswami S., Banerjee D., Garcia V., Zhou E., Olmsted C. N., Majumder E. L. -W., Kumar D., Awasthi D., Mukhopadhyay A., Singer S. W., Gladden J. M., Simmons B. A., Choudhary H. (2024). Perspective on lignin conversion strategies that enable next generation biorefineries. Chemsuschem, e202301460. 10.1002/cssc.202301460 38669480 · DOI
  137. Shrestha S., Xue S., Raskin L. (2023). Competitive reactions during ethanol chain elongation were temporarily suppressed by increasing hydrogen partial pressure through methanogenesis inhibition. Environmental Science & Technology, 57 (8), 3369– 3379. 10.1021/acs.est.2c09014 36790331 PMC9979639 · DOI
  138. Singh A. H., Kaufmann-Malaga B. B., Lerman J. A., Dougherty D. P., Zhang Y., Kilbo A. L., Wilson E. H., Ng C. Y., Erbilgin O., Curran K. A., Reeves C. D., Hung J. E., Mantovani S., King Z. A., Ayson M. J., Denery J. R., Lu C.-W., Norton P., Tran C., Meadows A. L. (2023). An Automated Scientist to Design and Optimize Microbial Strains for the Industrial Production of Small Molecules [Preprint]. Synthetic Biology. 10.1101/2023.01.03.521657 · DOI
  139. Song H.-S., Renslow R. S., Fredrickson J. K., Lindemann S. R. (2015). Integrating ecological and engineering concepts of resilience in microbial communities. Frontiers in Microbiology, 6, 1298. 10.3389/fmicb.2015.01298 26648912 PMC4664643 · DOI · Paper page
  140. Soyer O. S. (Ed.). (2012). Evolutionary Systems Biology (Vol. 751). Springer: New York, NY. 10.1007/978-1-4614-3567-9 · DOI
  141. Tang J., Wang X. C., Hu Y., Zhang Y., Li Y. (2017). Effect of pH on lactic acid production from acidogenic fermentation of food waste with different types of inocula. Bioresource Technology, 224, 544– 552. 10.1016/j.biortech.2016.11.111 27939870 · DOI
  142. Tayou L. N., Lauri R., Incocciati E., Pietrangeli B., Majone M., Micolucci F., Gottardo M., Valentino F. (2022). Acidogenic fermentation of food waste and sewage sludge mixture: Effect of operating parameters on process performance and safety aspects. Process Safety and Environmental Protection, 163, 158– 166. 10.1016/j.psep.2022.05.011 · DOI
  143. Tsoi R., Wu F., Zhang C., Bewick S., Karig D., You L. (2018). Metabolic division of labor in microbial systems. Proceedings of the National Academy of Sciences, 115 (10), 2526– 2531. 10.1073/pnas.1716888115 PMC5877992 29463749 · DOI
  144. Valentino F., Gottardo M., Micolucci F., Pavan P., Bolzonella D., Rossetti S., Majone M. (2018). Organic fraction of municipal solid waste recovery by conversion into added-value polyhydroxyalkanoates and biogas. ACS Sustainable Chemistry & Engineering, 6 (12), 16375– 16385. 10.1021/acssuschemeng.8b03454 · DOI
  145. VanArsdale E., Pitzer J., Wang S., Stephens K., Chen C., Payne G. F., Bentley W. E. (2022). Electrogenetic signal transmission and propagation in coculture to guide production of a small molecule, tyrosine. ACS Synthetic Biology, 11 (2), 877– 887. 10.1021/acssynbio.1c00522 35113532 PMC9026653 · DOI
  146. Venkateswar Reddy M., Venkata Mohan S. (2012). Influence of aerobic and anoxic microenvironments on polyhydroxyalkanoates (PHA) production from food waste and acidogenic effluents using aerobic consortia. Bioresource Technology, 103 (1), 313– 321. 10.1016/j.biortech.2011.09.040 22055090 · DOI
  147. Wang D., Hunt K. A., Candry P., Tao X., Wofford N. Q., Zhou J., McInerney M. J., Stahl D. A., Tanner R. S., Zhou A., Winkler M., Pan C. (2023b). Cross-feedings, competition, and positive and negative synergies in a four-species synthetic community for anaerobic degradation of cellulose to methane. mBio, 14 (2), e03189– 22. 10.1128/mbio.03189-22 36847519 PMC10128006 · DOI
  148. Wang H., Marcišauskas S., Sánchez B. J., Domenzain I., Hermansson D., Agren R., Nielsen J., Kerkhoven E. J. (2018). RAVEN 2.0: A versatile toolbox for metabolic network reconstruction and a case study on Streptomyces coelicolor. PLOS Computational Biology, 14 (10), e1006541. 10.1371/journal.pcbi.1006541 30335785 PMC6207324 · DOI · Paper page
  149. Wang K., Yin J., Shen D., Li N. (2014). Anaerobic digestion of food waste for volatile fatty acids (VFAs) production with different types of inoculum: Effect of pH. Bioresource Technology, 161, 395– 401. 10.1016/j.biortech.2014.03.088 24727700 · DOI
  150. Wang Y., He Y., Zheng K., Wei W., Ngo H. H., Guo W., Ni B.-J., Zhu T., Horn H., Liu Y. (2023a). Ferric oxide stimulates medium-chain carboxylic acids synthesis from waste activated sludge via ethanol-driven chain elongation: Mechanisms and implications. Journal of Cleaner Production, 389, 136044. 10.1016/j.jclepro.2023.136044 · DOI
  151. Wang Y., Wilhelm R. C., Swenson T. L., Silver A., Andeer P. F., Golini A., Kosina S. M., Bowen B. P., Buckley D. H., Northen T. R. (2022). Substrate utilization and competitive interactions among soil bacteria vary with life-history strategies. Frontiers in Microbiology, 13, 914472. 10.3389/fmicb.2022.914472 35756023 PMC9225577 · DOI
  152. Weisenberger M. S., Deans T. L. (2018). Bottom-up approaches in synthetic biology and biomaterials for tissue engineering applications. Journal of Industrial Microbiology and Biotechnology, 45 (7), 599– 614. 10.1007/s10295-018-2027-3 29552703 PMC6041164 · DOI
  153. Wen Z., Minton N. P., Zhang Y., Li Q., Liu J., Jiang Y., Yang S. (2017). Enhanced solvent production by metabolic engineering of a twin-clostridial consortium. Metabolic Engineering, 39, 38– 48. 10.1016/j.ymben.2016.10.013 27794465 · DOI
  154. Werner J. J., Knights D., Garcia M. L., Scalfone N. B., Smith S., Yarasheski K., Cummings T. A., Beers A. R., Knight R., Angenent L. T. (2011). Bacterial community structures are unique and resilient in full-scale bioenergy systems. Proceedings of the National Academy of Sciences, 108 (10), 4158– 4163. 10.1073/pnas.1015676108 PMC3053989 21368115 · DOI
  155. Wongfaed N., O-Thong S., Sittijunda S., Reungsang A. (2023). Taxonomic and enzymatic basis of the cellulolytic microbial consortium KKU-MC1 and its application in enhancing biomethane production. Scientific Reports, 13 (1), 2968. 10.1038/s41598-023-29895-0 36804594 PMC9941523 · DOI
  156. Yuan X., Cao Y., Li J., Wen B., Zhu W., Wang X., Cui Z. (2012). Effect of pretreatment by a microbial consortium on methane production of waste paper and cardboard. Bioresource Technology, 118, 281– 288. 10.1016/j.biortech.2012.05.058 22705535 · DOI
  157. Zampieri G., Campanaro S., Angione C., Treu L. (2023). Metatranscriptomics-guided genome-scale metabolic modeling of microbial communities. Cell Reports Methods, 3 (1), 100383. 10.1016/j.crmeth.2022.100383 36814842 PMC9939383 · DOI
  158. Zelezniak A., Andrejev S., Ponomarova O., Mende D. R., Bork P., Patil K. R. (2015). Metabolic dependencies drive species co-occurrence in diverse microbial communities. Proceedings of the National Academy of Sciences, 112 (20), 6449– 6454. 10.1073/pnas.1421834112 PMC4443341 25941371 · DOI · Paper page
  159. Zhang M., Han F., Li Y., Liu Z., Chen H., Li Z., Li Q., Zhou W. (2021). Nitrogen recovery by a halophilic ammonium-assimilating microbiome: A new strategy for saline wastewater treatment. Water Research, 207, 117832. 10.1016/j.watres.2021.117832 34781183 · DOI
  160. Zhou J.-J., Shen J.-T., Jiang L.-L., Sun Y.-Q., Mu Y., Xiu Z.-L. (2017). Selection and characterization of an anaerobic microbial consortium with high adaptation to crude glycerol for 1,3-propanediol production. Applied Microbiology and Biotechnology, 101 (15), 5985– 5996. 10.1007/s00253-017-8311-8 28512675 · DOI
  161. Zhou K., Qiao K., Edgar S., Stephanopoulos G. (2015). Distributing a metabolic pathway among a microbial consortium enhances production of natural products. Nature Biotechnology, 33 (4), 377– 383. 10.1038/nbt.3095 PMC4867547 25558867 · DOI
  162. Zhou S.-P., Ke X., Jin L.-Q., Xue Y.-P., Zheng Y.-G. (2024). Sustainable management and valorization of biomass wastes using synthetic microbial consortia. Bioresource Technology, 395, 130391. 10.1016/j.biortech.2024.130391 38307483 · DOI
  163. Zimmermann J., Kaleta C., Waschina S. (2021). gapseq: Informed prediction of bacterial metabolic pathways and reconstruction of accurate metabolic models. Genome Biology, 22 (1), 81. 10.1186/s13059-021-02295-1 33691770 PMC7949252 · DOI
  164. Zomorrodi A. R., Islam M. M., Maranas C. D. (2014). d-OptCom: Dynamic multi-level and multi-objective metabolic modeling of microbial communities. ACS Synthetic Biology, 3 (4), 247– 257. 10.1021/sb4001307 24742179 · DOI
  165. Zomorrodi A. R., Maranas C. D. (2012). OptCom: A multi-level optimization framework for the metabolic modeling and analysis of microbial communities. PLoS Computational Biology, 8 (2), e1002363. 10.1371/journal.pcbi.1002363 22319433 PMC3271020 · DOI
  166. Zou L., Ouyang S., Hu Y., Zheng Z., Ouyang J. (2021). Efficient lactic acid production from dilute acid-pretreated lignocellulosic biomass by a synthetic consortium of engineered Pseudomonas putida and Bacillus coagulans. Biotechnology for Biofuels, 14 (1), 227. 10.1186/s13068-021-02078-7 34838093 PMC8627035 · DOI
  167. Zuñiga C., Li T., Guarnieri M. T., Jenkins J. P., Li C.-T., Bingol K., Kim Y.-M., Betenbaugh M. J., Zengler K. (2020). Synthetic microbial communities of heterotrophs and phototrophs facilitate sustainable growth. Nature Communications, 11 (1), 3803. 10.1038/s41467-020-17612-8 PMC7393147 32732991 · DOI
  168. Zuniga C., Tibocha-Bonilla J. D., Betenbaugh M. J. (2021). Kinetic, metabolic, and statistical analytics: Addressing metabolic transport limitations among organelles and microbial communities. Current Opinion in Biotechnology, 71, 91– 97. 10.1016/j.copbio.2021.06.024 34293631 · DOI

Authors
Lyu, X., Nuhu, M., Candry, P., Wolfanger, J., Betenbaugh, M., Saldivar, A., Zuniga, C., Wang, Y., & Shrestha, S.
Affiliations
  • Johns Hopkins University (US)
  • Wageningen University & Research (NL)
  • San Diego State University (US)
  • Department of Biology, San Diego State University , San Diego, CA 92182-4614,
  • Texas A&M University (US)
Corresponding author
Shrestha, Shilva
Venue
Journal of Industrial Microbiology and Biotechnology
Published
2024
Volume
51
ISSN
  • 1367-5435 (ISSN-L)
  • 1476-5535
OpenAlex
W4400612253
Cited by
53
References
5
Citations by year
2026: 38 · 2025: 14 · 2024: 1
FWCI
2.08
Type
journal article
Language
en
Open access
Locations
  • Journal of Industrial Microbiology & Biotechnology (publishedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • eScholarship (California Digital Library) (submittedVersion, cc-by-nc-nd)
  • Socio-Environmental Systems Modeling (submittedVersion, cc-by-nc-nd)
Funders
Johns Hopkins University
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Microbial Metabolic Engineering and Bioproduction
  • Physical Sciences › Environmental Science › Pollution › Microbial bioremediation and biosurfactants
  • Physical Sciences › Environmental Science › Environmental Engineering › Microbial Fuel Cells and Bioremediation
Keywords
microbiome engineering, microbial consortia, waste valorization, synthetic microbial consortia, metabolic engineering, metabolic modeling, ecological engineering, circular economy, resource recovery
MeSH terms
Bacteria, Biotechnology, Biomass, Metabolic Networks and Pathways, Microbial Consortia, Metabolic Engineering, Microbiota

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review