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Genetic optimisation of bacteria-induced calcite precipitation in Bacillus subtilis

BACKGROUND: Microbially induced calcite precipitation (MICP) is an ancient property of bacteria, which has recently gained considerable attention for biotechnological applications. It occurs as a by-product of bacterial metabolism and involves a combination of chemical changes in the extracellular e...

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Autores principales: Hoffmann, Timothy D., Paine, Kevin, Gebhard, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8600894/
https://www.ncbi.nlm.nih.gov/pubmed/34794448
http://dx.doi.org/10.1186/s12934-021-01704-1
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author Hoffmann, Timothy D.
Paine, Kevin
Gebhard, Susanne
author_facet Hoffmann, Timothy D.
Paine, Kevin
Gebhard, Susanne
author_sort Hoffmann, Timothy D.
collection PubMed
description BACKGROUND: Microbially induced calcite precipitation (MICP) is an ancient property of bacteria, which has recently gained considerable attention for biotechnological applications. It occurs as a by-product of bacterial metabolism and involves a combination of chemical changes in the extracellular environment, e.g. pH increase, and presence of nucleation sites on the cell surface or extracellular substances produced by the bacteria. However, the molecular mechanisms underpinning MICP and the interplay between the contributing factors remain poorly understood, thus placing barriers to the full biotechnological and synthetic biology exploitation of bacterial biomineralisation. RESULTS: In this study, we adopted a bottom-up approach of systematically engineering Bacillus subtilis, which has no detectable intrinsic MICP activity, for biomineralisation. We showed that heterologous production of urease can induce MICP by local increases in extracellular pH, and this can be enhanced by co-expression of urease accessory genes for urea and nickel uptake, depending on environmental conditions. MICP can be strongly enhanced by biofilm-promoting conditions, which appeared to be mainly driven by production of exopolysaccharide, while the protein component of the biofilm matrix was dispensable. Attempts to modulate the cell surface charge of B. subtilis had surprisingly minor effects, and our results suggest this organism may intrinsically have a very negative cell surface, potentially predisposing it for MICP activity. CONCLUSIONS: Our findings give insights into the molecular mechanisms driving MICP in an application-relevant chassis organism and the genetic elements that can be used to engineer de novo or enhanced biomineralisation. This study also highlights mutual influences between the genetic drivers and the chemical composition of the surrounding environment in determining the speed, spatial distribution and resulting mineral crystals of MICP. Taken together, these data pave the way for future rational design of synthetic precipitator strains optimised for specific applications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-021-01704-1.
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spelling pubmed-86008942021-11-19 Genetic optimisation of bacteria-induced calcite precipitation in Bacillus subtilis Hoffmann, Timothy D. Paine, Kevin Gebhard, Susanne Microb Cell Fact Research BACKGROUND: Microbially induced calcite precipitation (MICP) is an ancient property of bacteria, which has recently gained considerable attention for biotechnological applications. It occurs as a by-product of bacterial metabolism and involves a combination of chemical changes in the extracellular environment, e.g. pH increase, and presence of nucleation sites on the cell surface or extracellular substances produced by the bacteria. However, the molecular mechanisms underpinning MICP and the interplay between the contributing factors remain poorly understood, thus placing barriers to the full biotechnological and synthetic biology exploitation of bacterial biomineralisation. RESULTS: In this study, we adopted a bottom-up approach of systematically engineering Bacillus subtilis, which has no detectable intrinsic MICP activity, for biomineralisation. We showed that heterologous production of urease can induce MICP by local increases in extracellular pH, and this can be enhanced by co-expression of urease accessory genes for urea and nickel uptake, depending on environmental conditions. MICP can be strongly enhanced by biofilm-promoting conditions, which appeared to be mainly driven by production of exopolysaccharide, while the protein component of the biofilm matrix was dispensable. Attempts to modulate the cell surface charge of B. subtilis had surprisingly minor effects, and our results suggest this organism may intrinsically have a very negative cell surface, potentially predisposing it for MICP activity. CONCLUSIONS: Our findings give insights into the molecular mechanisms driving MICP in an application-relevant chassis organism and the genetic elements that can be used to engineer de novo or enhanced biomineralisation. This study also highlights mutual influences between the genetic drivers and the chemical composition of the surrounding environment in determining the speed, spatial distribution and resulting mineral crystals of MICP. Taken together, these data pave the way for future rational design of synthetic precipitator strains optimised for specific applications. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12934-021-01704-1. BioMed Central 2021-11-18 /pmc/articles/PMC8600894/ /pubmed/34794448 http://dx.doi.org/10.1186/s12934-021-01704-1 Text en © The Author(s) 2021 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
Hoffmann, Timothy D.
Paine, Kevin
Gebhard, Susanne
Genetic optimisation of bacteria-induced calcite precipitation in Bacillus subtilis
title Genetic optimisation of bacteria-induced calcite precipitation in Bacillus subtilis
title_full Genetic optimisation of bacteria-induced calcite precipitation in Bacillus subtilis
title_fullStr Genetic optimisation of bacteria-induced calcite precipitation in Bacillus subtilis
title_full_unstemmed Genetic optimisation of bacteria-induced calcite precipitation in Bacillus subtilis
title_short Genetic optimisation of bacteria-induced calcite precipitation in Bacillus subtilis
title_sort genetic optimisation of bacteria-induced calcite precipitation in bacillus subtilis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8600894/
https://www.ncbi.nlm.nih.gov/pubmed/34794448
http://dx.doi.org/10.1186/s12934-021-01704-1
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