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Engineering living building materials for enhanced bacterial viability and mechanical properties.

ABSTRACT: Living building materials (LBMs) utilize microorganisms to produce construction materials that exhibit mechanical and biological properties. A hydrogel-based LBM containing bacteria capable of microbially induced calcium carbonate precipitation (MICP) was recently developed. Here, LBM design factors, i.e., gel/sand ratio, inclusion of trehalose, and MICP pathways, are evaluated. The results show that non-saturated LBM (gel/sand = 0.13) and gel-saturated LBM (gel/sand = 0.30) underwent distinct failure modes. The inclusion of trehalose maintains bacterial viability under ambient conditions with low relative humidity, without affecting mechanical properties of the LBM. Comparison of biotic and abiotic LBM shows that MICP efficiency in this material is subject to the pathway selected: the LBM with heterotrophic ureolytic Escherichia coli demonstrated the most mechanical enhancement from the abiotic controls, compared with either ureolytic or CO₂-concentrating mechanisms from Synechococcus. The study shows that tailoring of LBM properties can be accomplished in a manner that considers both LBM microstructure and MICP pathways.

SUBMITTER: Qiu J

PROVIDER: S-EPMC7868992 | biostudies-literature | 2021 Feb

REPOSITORIES: biostudies-literature

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Engineering living building materials for enhanced bacterial viability and mechanical properties.

Qiu Jishen J Cook Sherri S Srubar Wil V WV Hubler Mija H MH Artier Juliana J Cameron Jeffrey C JC

iScience 20210121 2

Living building materials (LBMs) utilize microorganisms to produce construction materials that exhibit mechanical and biological properties. A hydrogel-based LBM containing bacteria capable of microbially induced calcium carbonate precipitation (MICP) was recently developed. Here, LBM design factors, i.e., gel/sand ratio, inclusion of trehalose, and MICP pathways, are evaluated. The results show that non-saturated LBM (gel/sand = 0.13) and gel-saturated LBM (gel/sand = 0.30) underwent distinct f ...[more]

PMID: 33598643

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Project description:Natural materials, such as bone, integrate living cells composed of organic molecules together with inorganic components. This enables combinations of functionalities, such as mechanical strength and the ability to regenerate and remodel, which are not present in existing synthetic materials. Taking a cue from nature, we propose that engineered 'living functional materials' and 'living materials synthesis platforms' that incorporate both living systems and inorganic components could transform the performance and the manufacturing of materials. As a proof-of-concept, we recently demonstrated that synthetic gene circuits in Escherichia coli enabled biofilms to be both a functional material in its own right and a materials-synthesis platform. To demonstrate the former, we engineered E. coli biofilms into a chemical-inducer-responsive electrical switch. To demonstrate the latter, we engineered E. coli biofilms to dynamically organize biotic-abiotic materials across multiple length scales, template gold nanorods, gold nanowires, and metal/semiconductor heterostructures, and synthesize semiconductor nanoparticles (Chen, A. Y. et al. (2014) Synthesis and patterning of tunable multiscale materials with engineered cells. Nat. Mater. 13, 515-523.). Thus, tools from synthetic biology, such as those for artificial gene regulation, can be used to engineer the spatiotemporal characteristics of living systems and to interface living systems with inorganic materials. Such hybrids can possess novel properties enabled by living cells while retaining desirable functionalities of inorganic systems. These systems, as living functional materials and as living materials foundries, would provide a radically different paradigm of materials performance and synthesis-materials possessing multifunctional, self-healing, adaptable, and evolvable properties that are created and organized in a distributed, bottom-up, autonomously assembled, and environmentally sustainable manner.

Project description:Background: Microtissues constructed with hydrogels promote cell expansion and specific differentiation by mimicking the microarchitecture of native tissues. However, the suboptimal mechanical property and osteogenic activity of microtissues fabricated by natural polymers need further improvement for bone reconstruction application. Core-shell designed structures are composed of an inner core part and an outer part shell, combining the characteristics of different materials, which improve the mechanical property of microtissues. Methods: A micro-stencil array chip was used to fabricate an open porous core-shell micro-scaffold consisting of gelatin as shell and demineralized bone matrix particles modified with bone morphogenetic protein-2 (BMP-2) as core. Single gelatin micro-scaffold was fabricated as a control. Rat bone marrow mesenchymal stem cells (BMSCs) were seeded on the micro-scaffolds, after which they were dynamic cultured and osteo-induced in mini-capsule bioreactors to fabricate microtissues. The physical characteristics, biocompatibility, osteo-inducing and controlled release ability of the core-shell microtissue were evaluated in vitro respectively. Then microtissues were tested in vivo via ectopic implantation and orthotopic bone implantation in rat model. Results: The Young's modulus of core-shell micro-scaffold was nearly triple that of gelatin micro-scaffold, which means the core-shell micro-scaffolds have better mechanical property. BMSCs rapidly proliferated and retained the highest viability on core-shell microtissues. The improved osteogenic potential of core-shell microtissues was evidenced by the increased calcification based on von kossa staining and osteo-relative gene expression. At 3months after transplantation, core-shell microtissue group formed the highest number of mineralized tissues in rat ectopic subcutaneous model, and displayed the largest amount of new bony tissue deposition in rat orthotopic cranial defect. Conclusion: The novel core-shell microtissue construction strategy developed may become a promising cell delivery platform for bone regeneration.

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Engineering living building materials for enhanced bacterial viability and mechanical properties.

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Engineering living building materials for enhanced bacterial viability and mechanical properties.

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