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Cellulose-mediated floc formation by the activated sludge bacterium Shinella zoogloeoides ATCC 19623
BACKGROUND: Bacterial floc formation plays a central role in the activated sludge (AS) process. The formation of AS flocs has long been known to require exopolysaccharide biosynthesis. We had demonstrated that both expolysaccharides and PEP-CTERM (a short C-terminal domain includes a near-invariant...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012009/ https://www.ncbi.nlm.nih.gov/pubmed/35421928 http://dx.doi.org/10.1186/s12866-022-02516-y |
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author | Gao, Na Dai, Jingcheng Liu, Yaqi Li, Shuyang Wang, Jing Lu, Wenxuan Qiu, Dongru |
author_facet | Gao, Na Dai, Jingcheng Liu, Yaqi Li, Shuyang Wang, Jing Lu, Wenxuan Qiu, Dongru |
author_sort | Gao, Na |
collection | PubMed |
description | BACKGROUND: Bacterial floc formation plays a central role in the activated sludge (AS) process. The formation of AS flocs has long been known to require exopolysaccharide biosynthesis. We had demonstrated that both expolysaccharides and PEP-CTERM (a short C-terminal domain includes a near-invariant motif Pro-Glu-Pro (PEP)) proteins were required for floc-forming in Zoogloea resiniphila MMB, a dominant AS bacterium. However, the PEP-CTERM proteins are not encoded in the genome of AS bacterium Shinella zoogloeoides ATCC 19623 (formerly known as Zoogloea ramigera I-16-M) and other sequenced AS bacteria strains. The mechanism underlying floc formation of Shinella and related AS bacteria remained largely unclear. RESULTS: In this study, we have sequenced and annotated the complete genome of S. zoogloeoides ATCC 19623 (aka I-16-M), previously isolated in USA and treated as the neotype for the AS floc-forming bacterium Zoogloea ramigera I-16-M, and another AS strain XJ20 isolated in China. Mariner transposon mutagenesis had been conducted to isolate floc-forming-deficient mutants in the strain ATCC 19623 as previously performed by using Tn5 transposon three decades ago. The transposon insertional sites of multiple mutants were mapped to the gene cluster for bacterial cellulose synthesis (bcs) and secretion, and the role played by these genes in floc-formation had been further confirmed by genetic complementation. Interestingly, the restriction map of this bcs locus-flanking region was highly similar to that of the previously identified DNA fragment required for floc-formation in 1980s. Cellulase treatment abolished the floc-forming phenotype of S. zoogloeoides ATCC 19623 but not that of Z. resiniphila MMB strain. The FTIR spectral analyses revealed that the samples extracted from S. zoogloeoides ATCC 19623 were cellulose polymer. CONCLUSION: Our results indicated that we have largely reproduced and completed the unfinished pioneering work on AS floc-formation mechanism, demonstrating that the floc-formation and flocculating capability of Shinella were mediated by extracellular cellulose polymers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-022-02516-y. |
format | Online Article Text |
id | pubmed-9012009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90120092022-04-16 Cellulose-mediated floc formation by the activated sludge bacterium Shinella zoogloeoides ATCC 19623 Gao, Na Dai, Jingcheng Liu, Yaqi Li, Shuyang Wang, Jing Lu, Wenxuan Qiu, Dongru BMC Microbiol Research BACKGROUND: Bacterial floc formation plays a central role in the activated sludge (AS) process. The formation of AS flocs has long been known to require exopolysaccharide biosynthesis. We had demonstrated that both expolysaccharides and PEP-CTERM (a short C-terminal domain includes a near-invariant motif Pro-Glu-Pro (PEP)) proteins were required for floc-forming in Zoogloea resiniphila MMB, a dominant AS bacterium. However, the PEP-CTERM proteins are not encoded in the genome of AS bacterium Shinella zoogloeoides ATCC 19623 (formerly known as Zoogloea ramigera I-16-M) and other sequenced AS bacteria strains. The mechanism underlying floc formation of Shinella and related AS bacteria remained largely unclear. RESULTS: In this study, we have sequenced and annotated the complete genome of S. zoogloeoides ATCC 19623 (aka I-16-M), previously isolated in USA and treated as the neotype for the AS floc-forming bacterium Zoogloea ramigera I-16-M, and another AS strain XJ20 isolated in China. Mariner transposon mutagenesis had been conducted to isolate floc-forming-deficient mutants in the strain ATCC 19623 as previously performed by using Tn5 transposon three decades ago. The transposon insertional sites of multiple mutants were mapped to the gene cluster for bacterial cellulose synthesis (bcs) and secretion, and the role played by these genes in floc-formation had been further confirmed by genetic complementation. Interestingly, the restriction map of this bcs locus-flanking region was highly similar to that of the previously identified DNA fragment required for floc-formation in 1980s. Cellulase treatment abolished the floc-forming phenotype of S. zoogloeoides ATCC 19623 but not that of Z. resiniphila MMB strain. The FTIR spectral analyses revealed that the samples extracted from S. zoogloeoides ATCC 19623 were cellulose polymer. CONCLUSION: Our results indicated that we have largely reproduced and completed the unfinished pioneering work on AS floc-formation mechanism, demonstrating that the floc-formation and flocculating capability of Shinella were mediated by extracellular cellulose polymers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-022-02516-y. BioMed Central 2022-04-15 /pmc/articles/PMC9012009/ /pubmed/35421928 http://dx.doi.org/10.1186/s12866-022-02516-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Gao, Na Dai, Jingcheng Liu, Yaqi Li, Shuyang Wang, Jing Lu, Wenxuan Qiu, Dongru Cellulose-mediated floc formation by the activated sludge bacterium Shinella zoogloeoides ATCC 19623 |
title | Cellulose-mediated floc formation by the activated sludge bacterium Shinella zoogloeoides ATCC 19623 |
title_full | Cellulose-mediated floc formation by the activated sludge bacterium Shinella zoogloeoides ATCC 19623 |
title_fullStr | Cellulose-mediated floc formation by the activated sludge bacterium Shinella zoogloeoides ATCC 19623 |
title_full_unstemmed | Cellulose-mediated floc formation by the activated sludge bacterium Shinella zoogloeoides ATCC 19623 |
title_short | Cellulose-mediated floc formation by the activated sludge bacterium Shinella zoogloeoides ATCC 19623 |
title_sort | cellulose-mediated floc formation by the activated sludge bacterium shinella zoogloeoides atcc 19623 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012009/ https://www.ncbi.nlm.nih.gov/pubmed/35421928 http://dx.doi.org/10.1186/s12866-022-02516-y |
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