Establishment of plastic-associated microbial community from superworm gut microbiome
Gut microbial communities of plastic-munching worms provide novel insights for the development of plastic-processing biotechnologies. Considering the complexity of worm maintenance and the gut microbial communities, it is challenging to apply the worms directly in plastic processing. Harnessing the...
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sg-ntu-dr.10356-1731562024-01-19T15:33:37Z Establishment of plastic-associated microbial community from superworm gut microbiome Liu, Yinan Bairoliya, Sakcham Zaiden, Norazean Cao, Bin School of Civil and Environmental Engineering Singapore Centre for Environmental Life Sciences and Engineering (SCELSE) Engineering::Environmental engineering Plastic-Microbe Interaction Biofilm Gut microbial communities of plastic-munching worms provide novel insights for the development of plastic-processing biotechnologies. Considering the complexity of worm maintenance and the gut microbial communities, it is challenging to apply the worms directly in plastic processing. Harnessing the power of microbial communities derived from the worm gut microbiomes in vitro may enable a promising bioprocess for plastic degradation. Here, we established stable and reproducible plastic-associated biofilm communities derived from the gut microbiome of a superworm, Zophobas atratus, through a two-stage enrichment process: feeding with plastics (HDPE, PP, and PS) and in vitro incubation of gut microbiomes obtained from the plastic-fed worms. Plastic feeding exhibited marginal influence on bacterial diversity but substantially changed the relative abundance of different bacterial groups, and intriguingly, enriched potential plastic degraders. More prominent shifts of microbial communities were observed during the in vitro incubation of the gut microbiomes. Taxa containing plastic-degrading strains were further enriched, while other taxa represented by lactic acid bacteria were depleted. Additionally, the plastic characterization confirmed the degradation of the incubated plastics by the plastic-associated microbial communities. Community functional inference for both gene abundance and community phenotype suggested that the in vitro incubation enhanced plastic-degrading potential. Deterministic ecological effects, in particular, selection processes, were identified as the main driving force of the observed community shifts. Our findings provide novel insights into plastic-munching-worm-inspired bioprocessing of plastic wastes. Ministry of Education (MOE) Nanyang Technological University National Research Foundation (NRF) Published version This research was supported by the Accelerating Creativity and Excellence (ACE) grant (Award no.: NTU-ACE2021-01 to B.C.), Nanyang Technological University, Singapore, and by the NRF and Ministry of Education Singapore under its Research Centre of Excellence Programme, Singapore Centre for Environmental Life Sciences Engineering (M4330005.C70 to B.C.), Nanyang Technological University, Singapore. 2024-01-15T08:24:38Z 2024-01-15T08:24:38Z 2024 Journal Article Liu, Y., Bairoliya, S., Zaiden, N. & Cao, B. (2024). Establishment of plastic-associated microbial community from superworm gut microbiome. Environment International, 183, 108349-. https://dx.doi.org/10.1016/j.envint.2023.108349 0160-4120 https://hdl.handle.net/10356/173156 10.1016/j.envint.2023.108349 38039945 2-s2.0-85178150257 183 108349 en NTU-ACE2021-01 M4330005.C70 Environment International © 2023 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/bync-nd/4.0/). application/pdf |
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Engineering::Environmental engineering Plastic-Microbe Interaction Biofilm Liu, Yinan Bairoliya, Sakcham Zaiden, Norazean Cao, Bin Establishment of plastic-associated microbial community from superworm gut microbiome |
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Gut microbial communities of plastic-munching worms provide novel insights for the development of plastic-processing biotechnologies. Considering the complexity of worm maintenance and the gut microbial communities, it is challenging to apply the worms directly in plastic processing. Harnessing the power of microbial communities derived from the worm gut microbiomes in vitro may enable a promising bioprocess for plastic degradation. Here, we established stable and reproducible plastic-associated biofilm communities derived from the gut microbiome of a superworm, Zophobas atratus, through a two-stage enrichment process: feeding with plastics (HDPE, PP, and PS) and in vitro incubation of gut microbiomes obtained from the plastic-fed worms. Plastic feeding exhibited marginal influence on bacterial diversity but substantially changed the relative abundance of different bacterial groups, and intriguingly, enriched potential plastic degraders. More prominent shifts of microbial communities were observed during the in vitro incubation of the gut microbiomes. Taxa containing plastic-degrading strains were further enriched, while other taxa represented by lactic acid bacteria were depleted. Additionally, the plastic characterization confirmed the degradation of the incubated plastics by the plastic-associated microbial communities. Community functional inference for both gene abundance and community phenotype suggested that the in vitro incubation enhanced plastic-degrading potential. Deterministic ecological effects, in particular, selection processes, were identified as the main driving force of the observed community shifts. Our findings provide novel insights into plastic-munching-worm-inspired bioprocessing of plastic wastes. |
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School of Civil and Environmental Engineering |
author_facet |
School of Civil and Environmental Engineering Liu, Yinan Bairoliya, Sakcham Zaiden, Norazean Cao, Bin |
format |
Article |
author |
Liu, Yinan Bairoliya, Sakcham Zaiden, Norazean Cao, Bin |
author_sort |
Liu, Yinan |
title |
Establishment of plastic-associated microbial community from superworm gut microbiome |
title_short |
Establishment of plastic-associated microbial community from superworm gut microbiome |
title_full |
Establishment of plastic-associated microbial community from superworm gut microbiome |
title_fullStr |
Establishment of plastic-associated microbial community from superworm gut microbiome |
title_full_unstemmed |
Establishment of plastic-associated microbial community from superworm gut microbiome |
title_sort |
establishment of plastic-associated microbial community from superworm gut microbiome |
publishDate |
2024 |
url |
https://hdl.handle.net/10356/173156 |
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1789482913680588800 |