bioRxiv Science⌕ Search

bioRxiv · 10.64898/2026.06.26.734652

Isolation of bioconcrete-producing bacteria for urea-free marine applications

Abstract

Concrete repair and replacement have significant environmental and economic costs. Bacteria can form bioconcrete via microbially-induced carbonate precipitation (MICP). Bioconcrete-forming bacteria can be incorporated into concrete at mixing and heal cracks where and when they occur. Bioconcrete formation is a byproduct of alterations to the local environment occurring during normal metabolic activities of bacteria. Bacteria thus "make" bioconcrete by different metabolic mechanisms, and the environment plays a substantial role in the yield and physical properties of bioconcrete produced by a given bacterium. The ureolytic bacterium Sporosarcina pasteurii is a commonly used organism for MICP, but it requires urea supplementation and generates nitrogenous waste. The marine environment is understudied for bioconcrete applications, yet self-healing structures are needed in this environment, wherein urea and nitrogenous waste would be detrimental to native biota. Here, we assessed S. pasteurii bioconcrete production under marine-like media conditions with urea and calcium supplementation. S. pasteurii generated higher bioconcrete yields in these media compared to standard medium. We then designed an enrichment protocol to isolate and characterize non-urea-requiring bioconcrete-forming bacteria from Atlantic seawater. We identified isolates from the Sulflitobacter, Marinobacter, and Bacillus genera, two of which yielded higher bioconcrete in seawater-mimicking media compared to model non-ureolytic bacteria. Scanning electron microscopy/energy dispersive spectroscopy and Fourier transform infrared spectroscopy revealed distinct chemical and structural features of bioconcrete produced by bacteria in seawater-mimicking medium. Overall, our work establishes a pipeline for the isolation and characterization of novel bioconcrete-forming bacteria from marine samples, with application to marine self-healing materials. ImportanceBacteria can stimulate the formation of calcium carbonate, referred to as bioconcrete, around their cells. Bioconcrete can be applied towards the sustainable healing of cracks in concrete structures. However, the specific chemical composition of the concrete and the environment the concrete is placed in limit the usefulness and applicability of individual bacterial species towards bioconcrete formation. Here, we focused on the marine environment, which has been less studied in the bioconcrete field relative to the terrestrial environment. We used marine-mimicking growth media to evaluate bioconcrete formation by model bacteria previously used by bioconcrete researchers as well as to isolate novel bioconcrete-forming bacteria from Atlantic seawater. Further, we used analytical chemistry and microscopy techniques to characterize the similarities and differences among the bioconcrete produced by the bacteria. Overall, we provide a framework for the isolation and characterization of bioconcrete-forming bacteria for application to sustainable infrastructure in the marine environment.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Bracewell, J., Nishat, F., Ashraf, W., Palmer, K.. 2026-06-27. Isolation of bioconcrete-producing bacteria for urea-free marine applications. https://doi.org/10.64898/2026.06.26.734652

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Matrix-controlled emergence of biofilm architecture shapes antimicrobial survival

Biofilms are structured microbial communities whose extracellular matrix is widely regarded as a basis of their protection against antimicrobial compounds. Yet how matrix production by individual bacteria gives rise to collective architecture and antimicrobial protection remains poorly understood. Here, we systematically varied expression of the master biofilm regulator csgD in Salmonella enterica and found that increasing matrix production reorganizes biofilms from dense, isotropic packings into sparse, nematically aligned communities by altering cell-cell interactions. By combining experimentally measured biofilm architectures with reaction-diffusion modeling, we show that these structural changes produce distinct patterns of antimicrobial killing, ranging from preferential killing near the liquid-biofilm interface to more uniform killing throughout the community. Consequently, increasing matrix production unexpectedly reduces antimicrobial survival by shifting the biofilm into different transport regimes, while strain-specific physiological differences further modulate antimicrobial depletion. Rather than acting as a passive barrier, EPS therefore shapes antimicrobial susceptibility by reorganizing biofilm architecture and its transport properties. EPS thus provides a physical link between molecular regulation, collective architecture and antimicrobial survival, providing a quantitative framework for understanding how cellular matrix production generates emergent biofilm function.

microbiology↗

Mapping virulence-associated protein interaction networks reveals regulators of thermotolerance in Cryptococcus neoformans

Protein-protein interactions (PPIs) influence critical biological processes in pathogenic microorganisms, such as the human fungal pathogen, Cryptococcus neoformans. Fungal thermotolerance and stress response pathways are key virulence determinants that directly impact pathogen adaptation and survival and the infection process. To establish a comprehensive baseline of PPIs in C. neoformans and explore these interactions to infer functional roles for uncharacterized proteins, we applied size exclusion chromatography coupled with mass spectrometry to the secreted and cellular proteomes of the fungi. As a result, 216 and 1699 unique proteins were identified across 24 secretome and proteome fractions, respectively. The predicted secretome networks included expected proteins associated with vesicles and virulence, indicating a role in extracellular defense. Whereas the cryptococcal proteome highlighted interactions among proteins with defined roles in fungal virulence for protein stability and thermotolerance, including two previously uncharacterized proteins, CNAG_00287 and CNAG_05199, putatively involved in complex formation with heat-shock proteins (HSP). Based on sequence and structure homology, we propose that CNAG_00287 is a tetratricopeptide repeat-containing co-chaperone that modulates Hsp 70 activity and CNAG_05199 functions as a Hsp70. We validated the thermotolerance role of CNAG_00287 in heat-related stress, as its absence significantly impaired fungal growth in nutrient-limited media at 37 {degrees}C. Together, this work resolves virulence-associated PPIs within C. neoformans and reveals new molecular regulators of thermotolerance that underpin fungal pathogenicity.

microbiology↗

Environmental filtering and host identity collectively shape root-associated microbiomes of Ericaceae and ectomycorrhizal plants in fumarole fields

Background Symbiosis with microbes is a key strategy that has enabled plants to colonize extreme environments. Since the benefits conferred by root-associated microbes depend on both environmental conditions and host-microbe combinations, plant adaptation to harsh environments is closely linked to the assembly of root microbial communities. Understanding how environmental and host filtering jointly shape these communities is therefore fundamental to elucidating the mechanisms underlying plant adaptation to extreme environments. Results In this study, we investigated the differentiation of root-associated prokaryotic and fungal communities and individual operational taxonomic units (OTUs) across two contrasting habitats surrounding fumaroles, solfatara-field and forest-edge habitats, and six dominant Ericaceae and ectomycorrhizal plant taxa. Prokaryotic and fungal OTUs rarely exhibited strong preferences for both habitat and host identity. Instead, many of prokaryotic and fungal OTUs specialized to one of these niches, collectively generating root microbial communities differentiated by both factors. Nonetheless, striking specializations in habitat and host niches were observed in the fungal family Hyaloscyphaceae (Helotiales). To gain insight into the evolutionary basis of microbial specialization, we examined phylogenetic signals in preference phenotypes. The resulting weak phylogenetic signals in these preference phenotypes further suggest that this fungal clade has undergone substantial ecological divergence. Conclusion Overall, our findings indicate that root-associated microbial communities in extreme environments are assembled through the accumulation of microbial taxa specialized to either habitat or host, and that strong ecological specialization in fungi can arise with little phylogenetic constraint.

microbiology↗