Journal
CHEMOSPHERE
Volume 301, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2022.134723
Keywords
Microbial community; Microbial interactions; Biodegradation; Ancylobacter polymorphus; Co-occurrence analysis; Multi omics
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This study used metagenomic, metatranscriptomic, and co-occurrence network analyses to investigate the microbial cooperation in the biodegradation of 1,4-dioxane. The results revealed that Ancylobacter polymorphus ZM13 played a key role in the degradation process and cooperated with other bacterial genera. The presence of 1,4-dioxane also facilitated the shift in biodiversity and function of the microbial consortium, with the cooperators providing nutrients and relieving environmental stresses. These findings contribute to our understanding of microbial interactions during 1,4-dioxane degradation and have implications for constructing efficient synthetic consortia for remediation.
1,4-Dioxane is an emerging wastewater contaminant with probable human carcinogenicity. Our current understanding of microbial interactions during 1,4-dioxane biodegradation process in mixed cultures is limited. Here, we applied metagenomic, metatranscriptomic and co-occurrence network analyses to unraveling the microbial cooperation between degrader and non-degraders in an efficient 1,4-dioxane-degrading microbial consortium CH1. A 1,4-dioxane-degrading bacterium, Ancylobacter polymorphus ZM13, was isolated from CH1 and had a potential of being one of the important degraders due to its high relative abundance, highly expressed monooxygenase genes tmoABCDEF and high betweenness centrality of networks. The strain ZM13 cooperated obviously with 6 bacterial genera in the network, among which Xanthobacter and Mesorhizobium could be involved in the intermediates metabolism with responsible genes encoding alcohol dehydrogenase (adh), aldehyde dehydrogenase (aldh), glycolate oxidase (glcDEF), glyoxylate carboligase (gcl), malate synthase (glcB) and 2isopropylmalate synthase (leuA) differentially high-expressed. Also, 1,4-dioxane facilitated the shift of biodiversity and function of CH1, and those cooperators cooperated with ZM13 in the way of providing amino acids or fatty acids, as well as relieving environmental stresses to promote biodegradation. These results provide new insights into our understandings of the microbial interactions during 1,4-dioxane degradation, and have important implications for predicting microbial cooperation and constructing efficient and stable synthetic 1,4dioxane-degrading consortia for practical remediation.
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