Biomineralization Process Research Articles

Assessment of the mechanical and durability characteristics of bio-mineralized Bacillus subtilis self-healing concrete blended with hydrated lime and brick powder

Cement is the main constituent of the concrete structure. Using rejected brick as pozzolana in replacement of cement reduced the utilization of natural resources, conserved the environment, and controlled waste disposal. Hydrated lime has been utilized as a chemical additive to improve the pozzolanic reaction of finely ground waste brick particles. This research investigates the process of biomineralization to enhance the strength and durability characteristics of bacterial concrete incorporating hydrated lime and brick powder (HBr). In this context, cement was partially replaced with HBr in different proportions 10%, 20%, and 30% by weight. Furthermore, the HBr mixtures were meticulously prepared with and without the incorporation of Bacillus subtilis. Tests for strength and durability were performed at the age of 28 and 56 days of concrete. The self-healing proficiency of the bacterial concrete was evaluated through compressive strength, water permeability, and chloride penetration, while the microstructure analysis was conducted using field emission scanning electron microscopy (FESEM) and energy dispersive spectroscopy (EDS). The results show that at the age of 56 days, CaCO3 precipitation caused by Bacillus subtilis increases the compressive strength of BHBr10 by 19.07%. The durability properties in terms of chloride ion penetrability and water permeability exhibited substantial improvements of 40.03% and 61.9% respectively. Additionally, the FESEM micrographs along with the EDS analysis corroborated the presence of CaCO3 precipitation crystals.

Comparative transcriptome analysis reveals deep molecular landscapes in stony coral Montipora clade.

Introduction: Coral reefs, among the most invaluable ecosystems in the world, face escalating threats from climate change and anthropogenic activities. To decipher the genetic underpinnings of coral adaptation and resilience, we undertook comprehensive transcriptome profiling of two emblematic coral species, Montipora foliosa and Montipora capricornis, leveraging PacBio Iso-Seq technology. These species were strategically selected for their ecological significance and their taxonomic proximity within the Anthozoa class. Methods: Our study encompassed the generation of pristine transcriptomes, followed by thorough functional annotation via diverse databases. Subsequently, we quantified transcript abundance and scrutinized gene expression patterns, revealing notable distinctions between the two species. Results: Intriguingly, shared orthologous genes were identified across a spectrum of coral species, highlighting a substantial genetic conservation within scleractinian corals. Importantly, a subset of genes, integral to biomineralization processes, emerged as exclusive to scleractinian corals, shedding light on their intricate evolutionary history. Furthermore, we discerned pronounced upregulation of genes linked to immunity, stress response, and oxidative-reduction processes in M. foliosa relative to M. capricornis. These findings hint at the presence of more robust mechanisms in M. foliosa for maintaining internal equilibrium and effectively navigating external challenges, underpinning its potential ecological advantage. Beyond elucidating genetic adaptation in corals, our research underscores the urgency of preserving genetic diversity within coral populations. Discussion: These insights hold promise for informed conservation strategies aimed at safeguarding these imperiled ecosystems, bearing ecological and economic significance. In synthesis, our study seamlessly integrates genomic inquiry with ecological relevance, bridging the gap between molecular insights and the imperative to conserve coral reefs in the face of mounting threats.

Influence of Intramineral Proteins on the Growth of Carbonate Crystals Using as a Scaffold Membranes of Ratite Birds and Crocodiles Eggshells.

The lack of information on structural basis where proteins are involved, as well as the biomineralization processes of different systems such as bones, diatom frustules, and eggshells, have intrigued scientists from different fields for decades. This scientific curiosity has led to the use of methodologies that help understand the mechanism involved in the formation of these complex structures. Therefore, this work focuses on the use of eggshell membranes from different species of ratites (emu and ostrich) and reptiles (two species of crocodiles) as a model to differentiate biocalcification and biosilicification by introducing calcium phosphate or silica inside the membrane fiber mantles. We performed this to obtain information about the process of eggshell formation as well as the changes that occur in the membrane during crystal formation. In order to identify and understand the early processes leading to the formation of the microstructures present in the eggshell, we decided to carry out the synthesis of silica-carbonate of calcium, barium, and strontium called biomorph in the presence of intramineral proteins. This was carried out to evaluate the influence of these proteins on the formation of specific structures. We found that the proteins on untreated membranes, present a structural growth similar to those observed in the inner part of the eggshell, while in treated membranes, the structures formed present a high similarity with those observed in the outer and intermediate part of the eggshell. Finally, a topographic and molecular analysis of the biomorphs and membranes was performed by scanning electron microscopy (SEM), Raman and Fourier-transform Infrared (FTIR) spectroscopies.

Investigation on the Microstructural Diversity of a Three-Dimensional Porous Hydroxyapatite/Wollastonite Skeleton via Biomineralization in Simulated Body Fluids

The occurrence of fractures has emerged as one of the most prevalent injuries in the human body. In bone reconstruction surgery, after the implantation of porous hydroxyapatite materials, there is an initial infiltration of body fluids into the porous implant, followed by biomineralization-mediated apatite crystal formation and the subsequent ingrowth of bone cells. Despite extensive research efforts in this field, previous investigations have primarily focused on the formation of apatite crystals on exposed surfaces, with limited literature available regarding the formation of apatite crystals within the internal microstructures of bone implants. Herein, we demonstrate the occurrence of dynamic biomineralization within a three-dimensional porous hydroxyapatite/wollastonite (HA/WS) skeleton, leading to the abundant formation of nano-sized apatite crystals across diverse internal environments. Our findings reveal that these apatite nanocrystals demonstrate distinct rates of nucleation, packing densities, and crystal forms in comparison to those formed on the surface. Therefore, the objective of this study was to elucidate the temporal evolution of biomineralization processes by investigating the microstructures of nanocrystals on the internal surfaces of HA/WS three-dimensional porous materials at distinct stages of biomineralization and subsequently explore the biological activity exhibited by HA/WS when combined with cell investigation into apatite crystal biomineralization mechanisms at the nanoscale, aiming to comprehend natural bone formation processes and develop efficacious biomimetic implants for tissue engineering applications. The simultaneous examination of bone cell attachment and its interaction with ongoing internal nanocrystal formation will provide valuable insights for designing optimal scaffolds conducive to bone cell growth, which is imperative in tissue engineering endeavors.

Biodegradable nanotherapeutic with simultaneously GSH depletion and H2O2 supplying for enhanced synergistic chemotherapy/chemodynamic therapy

Chemodynamic therapy (CDT) has been exploited as an emerging therapeutic modality for cancer treatment. However, insufficient intracellular H2O2 levels and ultrahigh glutathione (GSH) in the tumor microenvironment (TME) severely restrict CDT efficacy. To address these concerns, in this work, a self-reinforcing biodegradable nanotherapeutic was developed to modulate the TME to amplify CDT. The nanotherapeutic (GOD-FeCaP@TPZ, abbreviated GFCT) was fabricated through a mild one-step biomineralization process using the enzyme catalyst glucose oxidase (GOD) as a template to form biodegradable iron-doped calcium phosphate nanoparticles, followed by the loading of the prodrug tirapazamine (TPZ). When GFCT decomposes and releases Fe3+ in the acidic TME, the delivered GOD can effectively catalyze the oxidization of glucose to enhance the subsequent Fenton-like reaction by promoting intracellular acidity (via the production of gluconic acid) and improving the generation of H2O2. Moreover, the released iron constantly depletes GSH by self-cyclic valence alterations in Fe(III) and Fe(II) and then triggers H2O2 to produce •OH through an Fe(II)-mediated Fenton-like reaction. Moreover, the elevated level of hypoxia induced by GOD-mediated glucose oxidization can activate the prodrug TPZ for effective chemotherapy, thus achieving remarkable synergistic therapeutic outcomes. This work provides another paradigm to augment antitumor efficacy via modulation of the TME.

The Biomineralization Conundrum of Calcified Extraradicular Deposits on the Apical Root Surface of Teeth: A Case Report

Background: Calcified extraradicular deposits on the apical root surface of teeth (CEDARST) are rarely seen in the dental field, compared with dental calculus deposits, which are very frequent. However, the exact biomineralization process of this entity has remained unclear until now. Objective: To report a case of an exuberant calcified extraradicular deposit on the apical root surface of an anterior tooth with apical periodontitis and propose for the first time some potential mechanisms involved in this pathological mineralization, and thereby suggest directions for future research. Case Presentation: In brief, a root-canal-treated canine displaying a radiographic periapical radiolucency was treated, and the sinus tract persisted despite root canal retreatment in which high endodontic standards were maintained. Endodontic surgery was performed, and the curettage of the pathologic tissue revealed an exuberant calculus-like material attached to the outer root surface, around the exit of the apical foramen. Two-year follow-up radiography revealed complete bone healing, and the patient´s tooth was asymptomatic and functional. Conclusion: The development of CEDARST seems to depend on a fine synergic control exerted by specific microorganisms (mainly bacteria) on this pathological mineralization, as well as on the local chemical microenvironment of the apical lesion of the affected tooth. Microbial implications and inhibitors of mineralization seem to play a dominant role in CEDARST biomineralization.

Polycarboxy/Sulfo Betaine-Calcium Phosphate Hybrid Materials with a Remineralization Potential.

Biomacromolecules control mineral formation during the biomineralization process, but the effects of the organic components' functionality on the type of mineral phase is still unclear. The biomimetic precipitation of calcium phosphates in a physiological medium containing either polycarboxybetaine (PCB) or polysulfobetaine (PSB) was investigated in this study. Amorphous calcium phosphate (ACP) or a mixture of octacalcium phosphate (OCP) and dicalcium phosphate dihydrate (DCPD) in different ratios were identified depending on the sequence of initial solution mixing and on the type of the negative functional group of the polymer used. The more acidic character of the sulfo group in PSB than the carboxy one in PCB determines the dominance of the acidic solid phases, namely, an acidic amorphous phase or DCPD. In the presence of PCB, the formation of ACP with acicular particles arranged in bundles with the same orientation was observed. A preliminary study on the remineralization potential of the hybrid material with the participation of PSB and a mixture of OCP and DCPD did not show an increase in enamel density, contrary to the materials based on PCB and ACP. Moreover, the latter showed the creation of a newly formed crystal layer similar to that of the underlying enamel. This defines PCB/ACP as a promising material for enamel remineralization.

Newly-development of synthetic MnCO3 and MnO2 precipitate through biologically-induced mineralization for effective adsorption of As(V) in aqueous solution

As(V) is becoming one of the dangerous and toxic chemicals causing the global issue of water pollution. Among several synthesis processes of adsorbent, biomineralization method has shown good potential. This study presented the biologically-induced synthetic Manganese Carbonate Precipitate (BISMCP) through biologically-induced mineralization method and formation change of BISMCP material after calcination process which is becoming MDSMCP. Herein, the potential ability of BISMCP and MDSMCP was performed for removal of As(V) in an aqueous solution. Characterization results showed both materials were successfully synthesized by the biomineralization process. TGA analysis showed the phase transition from MnCO3 to MnO2 significantly at 200–450 ºC. The BET surface area of the as-prepared nanocomposites was found to be 109.006 m2/g (BISMCP) and 91.672 m2/g (MDS-300). EDX analysis showed the elements in the crystal BISMCP and MDSMCP were Mn, C, and O. XRD result of BISMCP and MDSMCP determined the crystal structure, which are close to rhodochrosite (MnCO3) and pyrolusite (MnO2), respectively. Effects of pH, contact time, and varying pollutant concentration were studied in detail. The pHPZC value of BISMCP and MDS-300 was 5.5 and 1.50, respectively. According effect of pH, BISMCP and MDS-300 had better adsorption capacity at pH 6 and 2, respectively. The kinetic study for BISMCP and MDS-300 indicated that well fitted with pseudo-second-order (PSO). The experimental equilibrium data followed the Langmuir isotherm model with a maximum monolayer adsorption capacity of 119.331 mg/g (BISMCP) and 112.107 mg/g (MDS-300). This study implies that BISMCP and MDS-300 are potentially useful adsorbents for the adsorption of As(V).

Quaternary ZrCuCa-based thin films metallic glasses deposited by cathodic arc deposition

The current study’s aim is to obtain quaternary ZrCuCa based thin films using a physical vapor deposition method (PVD) - cathodic arc approach – in order to improve the surface properties of 316L stainless steel and Ti6Al4V implantable materials. The developed ZrCuCa-based layers could be potential candidates in the medical industry if they are able to combine their exceptional mechanical properties with the corrosion resistance of amorphous metallic glasses. Furthermore, addition of Mo, Mg, Si, and Sr was taken into consideration for the ZrCuCa structure and the resulted quaternary systems were analysed in detail, through electrochemical tests and bioactivity assay, which were carried out in synthetic body fluid (SBF) at human body temperature (37 °C). Surface morphology and roughness of the specimens before and after the tests were also evaluated. The results showed that regardless the substrate type, the roughness of the surface has increased for all coatings from 19 nm for 316L, and 50 nm for Ti6Al4V, to 2000 nm). The adhesion of obtained coatings was reached from 8 N to 18, the coatings on Ti6Al4V alloy was found to be from 12 N to 18 N, while on 316L steel was from 8 N to 15 N, indicating that the coatings deposited on Ti alloy have a better adhesion. The corrosion current density parameter for ZrCuCaMo and ZrCuCaMg sjowe the lowest value (316L: 21.99 µA/cm2 and 11.37 µA/cm2; Ti6Al4V: 1.62 µA/cm2 and 13.37 µA/cm2), indicating the best corrosion resistance. The mass evolution of the coatings deposited on 316L was ranged from the −0.47 mg to 1.37 mg, while for those deposited on Ti6Al4V, the values were ranged from −0.08 mg to 2.66 mg, indicating a degradation and biomineralization process, respectively. In conclusion, the electrochemical studies and bioactivity experiments demonstrated that the suggested coatings improve the substrate’s behaviour in simulated conditions, highlighting their potential as biomaterials.

Physical Phenomena Governing Mineral Morphogenesis in Molluscan Nacre.

Mollusks, as well as many other living organisms, have the ability to shape mineral crystals into unconventional morphologies and to assemble them into complex functional mineral-organic structures, an observation that inspired tremendous research efforts in scientific and technological domains. Despite these, a biochemical toolkit that accounts for the formation of the vast variety of the observed mineral morphologies cannot be identified yet. Herein, phase-field modeling of molluscan nacre formation, an intensively studied biomineralization process, is used to identify key physical parameters that govern mineral morphogenesis. Manipulating such parameters, various nacre properties ranging from the morphology of a single mineral building block to that of the entire nacreous assembly are reproduced. The results support the hypothesis that the control over mineral morphogenesis in mineralized tissues happens via regulating the physico-chemical environment, in which biomineralization occurs: the organic content manipulates the geometric and thermodynamic boundary conditions, which in turn, determine the process of growth and the form of the biomineral phase. The approach developed here has the potential of providing explicit guidelines for the morphogenetic control of synthetically formed composite materials.

Assessment of microstructure, biocompatibility and in-vitro biodegradation of a biomedical Mg-Hydroxyapatite composite for bone tissue engineering

In the present study, an Mg-based biomedical composite is fabricated by addition of Hydroxyapatite bioactive nanoparticles into a substrate of bioabsorbable WE43 Mg alloy using multi pass friction stir processing (FSP). The findings indicate that applying 6 passes of FSP leads to a decrease of grain size by over 93%, crushing and redistribution of secondary phase particles within the Mg matrix, improved homogeneity of Hydroxyapatite bioactive particles and a reduction in their agglomeration. In vitro Biodegradation tests prove that as the number of FSP passes increases, the weight loss of fabricated bio-composites and biodegradation rate in simulated body fluid (SBF) decrease. Bioactivity of Mg-based bio-composites is assessed by in vitro immersion in SBF for 28 days. Biomineralization process shows that all fabricated Mg-Hydroxyapatite bio-composites exhibit bone-like apatite forming ability, and cauliflower-shaped Hydroxyapatite crystals form on their surface. Moreover, increasing the uniformity of Hydroxyapatite particles stimulates formation of cauliflower-shaped Hydroxyapatite denser crystals, which improves biocompatibility of bio-composites. Biocompatibility of fabricated bio-composites is also evaluated by MTT assay and DAPI staining. Mg-HA-6P demonstrates the highest number of healthy flattened spindle shaped L-929 fibroblast cells with 83.36% cell viability after 5 days of incubation compared to other samples. Increasing number of FSP passes causes high bioactivity, low biodegradation rate and homogeneous distribution of Hydroxyapatite particles, which in turn improve the viability of L-929 fibroblast cells. Furthermore, with the addition of Hydroxyapatite particles and an increase in the number of FSP passes, the yield strength values of the samples increase, reaching 212 MPa and 226 MPa for the Mg–6P and Mg–6P-HA samples, respectively.

Heterogeneity of otolith chemical composition from two-dimensional mapping: Relationship with biomineralization mechanisms and implications for microchemistry analyses.

Although otoliths are widely used as archives to infer life-history traits and habitat use in fishes, their biomineralization process remains poorly understood. This lack of knowledge is problematic as it can lead to misinterpretation of the different types of signals (e.g., optical or chemical) that provide basic data for research in fish ecology, fisheries management, and species conservation. Otolith calcification relies on a complex system involving a pericrystalline fluid, the endolymph, whose organic and inorganic compositions are spatially heterogeneous for some constituents. This property stems from the particular structure of the calcifying saccular epithelium. In this study, we explored the spatial heterogeneity of elemental incorporation in otoliths for two species of high economic interest, European hake Merluccius merluccius (L. 1758) and European sea bass Dicentrarchus labrax (L. 1758). Two-dimensional mappings of chemical elements were obtained using UV high-repetition-rate femtosecond laser ablation (fs-LA) system coupled to a high-resolution inductively coupled plasma sector field mass spectrometer analyses on transverse sections of sagittae. Results highlighted a clear asymmetry between proximal (sulcus) and distal (antisulcus) concentrations for elements such as magnesium (Mg), phosphorus (P), manganese (Mn), and potassium (K) with concentration gradient directions that varied depending on the element. Strontium (Sr) and barium (Ba) did not show a proximo-distal gradient. These results are discussed in light of current knowledge on the endolymph composition and the mechanisms that lead to its compartmentalization, highlighting the need for further research on otolith biomineralization. Operational implications for studies based on otolith chemical composition are also discussed with emphasis on advice for sampling strategies to avoid analytical biases and the need for in-depth analyses of analytical settings before comparing otolith signatures between species or geographical areas.

The biocide triclosan as a potential developmental disruptor in Mytilus early larvae

The broadly utilized biocide triclosan (TCS) is continuously discharged in water compartments worldwide, where it is detected at concentrations of ng-µg/L. Given its lipophilicity and bioaccumulation, TCS is considered potentially harmful to human and environmental health and also as a potential endocrine disruptor (ED) in different species. In aquatic organisms, TCS can induce a variety of effects: however, little information is available on its possible impact on invertebrate development. Early larval stages of the marine bivalve Mytilus galloprovincialis have been shown to be sensitive to environmental concentrations of a number of emerging contaminants, including EDs. In this work, the effects of TCS were first evaluated in the 48 h larval assay in a wide concentration range (0.001–1,000 μg/L). TCS significantly affected normal development of D-veligers (LOEC = 0.1 μg/L; EC50 = 236.1 μg/L). At selected concentrations, the mechanism of action of TCS was investigated. TCS modulated transcription of different genes involved in shell mineralization, endocrine signaling, ceramide metabolism, and biotransformation, depending on larval stage (24 and 48 h post-fertilization-hpf) and concentration (1 and 10 μg/L). At 48 hpf and 10 μg/L TCS, calcein staining revealed alterations in CaCO3 deposition, and polarized light microscopy showed the absence of shell birefringence due to the mineralized phase. Observations by scanning electron microscopy highlighted a variety of defects in shell formation from concentrations as low as 0.1 μg/L. The results indicate that TCS, at environmental exposure levels, can act as a developmental disruptor in early mussel larvae mainly by interfering with the processes of biomineralization.

The regulatory effect of NF-κB signaling pathway on biomineralization and shell regeneration in pearl oyster, Pinctada fucata

Pinctada fucata is an important pearl production shellfish in aquaculture. The formation of shells and pearls is a hot research topic in biomineralization, and matrix proteins secreted by the mantle tissues play the key role in this process. However, upstream regulatory mechanisms of transcription factors on the matrix protein genes remain unclear. Previous studies have shown that NF-κB signaling pathway regulated biomineralization process through expression regulation of specific matrix proteins, including Nacrein, Prismalin-14 and MSI60. In this study, we systematically investigated the regulatory effect of the NF-κB signaling pathway key factor Pf-Rel and inhibitory protein poI-κB on the biomineralization and shell regeneration process. We applied RNA interference and antibody injection assays to study in vivo function of transcription factor Pf-Rel and characterized shell morphology changes using scanning electron microscopy and Raman spectroscopy. We found that transcription factor Pf-Rel plays a positive regulatory role in the growth regulation of the prismatic and nacreous layers, while the function of inhibitory protein poI-κB is to prevent excessive growth and accumulation of both layers. RNA-seq was conducted based on RNA interference animal model to identify potential regulatory genes by transcription factor Pf-Rel. Shell damage repair experiments were performed to simulate shell regeneration process, and observations of newly formed shells revealed that NF-κB signaling pathway had different functions at different times. This study provides us with a more macroscopic perspective based on transcription factors to investigate biomineralization and shell regeneration.

Microbial-assisted synthesis of Schwertmannite@g-C3N4 composite for bisphenol AF degradation through visible light-driven peroxymonosulfate activation

Iron-based materials are considered as excellent environmental catalysts due to the characteristics of abundant reserves, low biological toxicities, and rich chemical states for redox reactions. The sea urchin-like microscopic morphology of biosynthesized schwertmannite (Sch) with abundant surface active sites is beneficial to the environmental catalytic process. In this study, flake-type graphitic carbon nitride (g-C3N4) was introduced into the mineralization process of Acidithiobacillus ferrooxidans (A. ferrooxidans) as the additive to regulate the biomineralization process and directly control the morphology and structure of iron-based minerals. Schwertmannite@g-C3N4 composites (Sch-CN) with a desired structure of sea urchin-like well-dispersed biosynthesized Sch loaded on flaky g-C3N4 were successfully prepared by A. ferrooxidans-induced biomineralization process. A Light/Peroxymonosulfate/Sch-CN catalytic system was constructed to degrade the model organic pollutant bisphenol AF (BPAF). The system combined two advanced oxidation systems of photocatalysis and peroxymonosulfate (PMS) activation, showing excellent catalytic degradation ability and wide pH adaptability. In addition, the system was also applicable to the catalytic degradation of other bisphenol pollutants. The mechanism was deduced by the results of quenching experiments and electron paramagnetic resonance (EPR) measurements. Several degradation intermediate products were identified and the probable degradation pathways of BPAF were proposed. The toxicity activities of BPAF solution towards Raphidocelis subcapitata were largely reduced after treatment by the photochemical process. Overall, the Light/PMS/Sch-CN system has great potential in treating bisphenol wastewater.

Osteoporosis and vascular calcifications.

In post-menopausal women, aged individuals, and patients with diabetes mellitus or chronic renal disease, bone mineral density (BMD) decreases while the vasculature accumulates arterial calcifications (ACs). AC can be found in the tunica intima and/or in the tunica media. Prospective studies have shown that patients with initially low BMD and/or the presence of fragility fractures have at follow-up a significantly increased risk for coronary and cerebrovascular events and for overall cardiovascular mortality. Similarly, patients presenting with abdominal aorta calcifications (an easily quantifiable marker of vascular pathology) show a significant decrease in the BMD (and an increase in the fragility) of bones irrigated by branches of the abdominal aorta, such as the hip and lumbar spine. AC induction is an ectopic tissue biomineralization process promoted by osteogenic transdifferentiation of vascular smooth muscle cells as well as by local and systemic secreted factors. In many cases, the same regulatory molecules modulate bone metabolism but in reverse. Investigation of animal and in vitro models has identified several potential mechanisms for this reciprocal bone-vascular regulation, such as vitamin K and D sufficiency, advanced glycation end-products-RAGE interaction, osteoprotegerin/RANKL/RANK, Fetuin A, oestrogen deficiency and phytooestrogen supplementation, microbiota and its relation to diet, among others. Complete elucidation of these potential mechanisms, as well as their clinical validation via controlled studies, will provide a basis for pharmacological intervention that could simultaneously promote bone and vascular health.

Effect of Ureolytic Bacteria on Compressibility of the Soils with Variable Gradation

Abstract The aim of this study is to present the effect of treatment with ureolytic bacteria (Sporosarcina pasteurii) on the compressibility parameters of mineral and anthropogenic soils. In the presence of the urease enzyme, secreted by a strain of Sporosarcina pasteurii bacteria, urea hydrolysis occurs, allowing CaCO3 to be precipitated. The literature suggests applying the Microbially Induced Calcite Precipitation (MICP) method to non-cohesive soils. In order to determine whether the biomineralization process occurs in other soil types, cohesive and anthropogenic soils were tested in the laboratory. Compressibility tests were carried out in the laboratory on MICP-treated and untreated soils as reference samples. The process of biocementation in the soil is made possible by the introduction of bacteria into the soil and subsequent activation by a cementation solution (consisting of urea and calcium ions Ca2+). This paper presents the methodology for introducing bacteria into the soil, as well as the effect of the biomineralization process on the deformation parameters of the tested materials.

Effect of amino acids on biomineralization of lead ions by Aspergillus niger.

This study investigates the biomineralization of lead ions by Aspergillus niger from aqueous environments, focusing on the dynamic effects of fungal metabolism and biological components. Three biomolecules (glutamate, methionine, and lysine) were used to induce lead oxalate mineralization under lead stress. Comparative experiments were conducted to analyze the growth characteristics and Pb (II) removal ability of A.niger, as well as the morphological and structural properties of the resulting lead oxalate minerals using inductively coupled plasma atomic emission spectroscopy, X-ray powder diffraction, and scanning electron microscopy-energy dispersive spectroscopy techniques. The findings reveal that A. niger plays a crucial role in controlling the mineralization process of Pb (II), with biomineralization experiments demonstrating the specific morphogenesis of lead oxalate over time. Additionally, the inclusion of the three biomolecules in the system indirectly influenced the rate of Pb (II) removal and mineral morphology. These results contribute to a better understanding of A. niger-mediated biomineralization process of lead oxalate and suggest its potential application in the removal of Pb (II) from aqueous environments, particularly in combination with amino acids for enhanced immobilization and mineral recovery. PRACTITIONER POINTS: Fungal activity and amino acids play a crucial role in shaping lead oxalate crystals during water treatment processes. Specific amino acids can effectively delay lead oxalate recrystallization, enhancing the stability and removal efficiency of the crystals. Biomineralization mediated by fungi offers a promising and eco-friendly approach for lead removal and recovery in wastewater treatment. Exploring the influence of organic additives and fungal metabolism on crystal growth provides valuable insights for developing efficient remediation strategies. Further research on the utilization of fungi and amino acids can help with innovative and sustainable wastewater treatment technologies.

Biomineralization of mantis shrimp dactyl club following molting: Apatite formation and brominated organic components

The stomatopod Odontodactylus scyllarus uses weaponized club-like appendages to attack its prey. These clubs are made of apatite, chitin, amorphous calcium carbonate, and amorphous calcium phosphate organized in a highly hierarchical structure with multiple regions and layers. We follow the development of the biomineralized club as a function of time using clubs harvested at specific times since molting. The clubs are investigated using a broad suite of techniques to unravel the biomineralization history of the clubs. Nano focus synchrotron x-ray diffraction and x-ray fluorescence experiments reveal that the club structure is more organized with more sub-regions than previously thought. The recently discovered impact surface has crystallites in a different size and orientation than those in the impact region. The crystal unit cell parameters vary to a large degree across individual samples, which indicates a spatial variation in the degree of chemical substitution. Energy dispersive spectroscopy and Raman spectroscopy show that this variation cannot be explained by carbonation and fluoridation of the lattice alone. X-ray fluorescence and mass spectroscopy show that the impact surface is coated with a thin membrane rich in bromine that forms at very initial stages of club formation. Proteomic studies show that a fraction of the club mineralization protein-1 has brominated tyrosine suggesting that bromination of club proteins at the club surface is an integral component of the club design. Taken together, the data unravel the spatio-temporal changes in biomineral structure during club formation. Statement of significanceMantis shrimp hunt using club-like appendages that contain apatite, chitin, amorphous calcium carbonate, and amorphous calcium phosphate ordered in a highly hierarchical structure. To understand the formation process of the club we analyze clubs harvested at specific times since molting thereby constructing a club formation map. By combining several methods ranging from position resolved synchrotron X-ray diffraction to proteomics, we reveal that clubs form from an organic membrane with brominated protein and that crystalline apatite phases are present from the very onset of club formation and grow in relative importance over time. This reveals a complex biomineralization process leading to these fascinating biomineralized tools.

Biomimetic mineralization by confined diffusion with viscous hyaluronan network: Assembly of hierarchical flower-like supraparticles

Biomolecules-mediated biomimetic mineralization has been extensively investigated and applied to fabricate nano-assemblies with unique hierarchical architectures and salient properties. The confined-source ion diffusion plays a key role in the biomineralization process, but little investigative efforts have focused on it. Here, we developed a simple method to mimic the in vivo condition by a confined diffusion method, and hydroxyapatite nanoflower assemblies (HNAs) with exquisite hierarchical architectures were obtained. The HNAs were assembled from needle-like hybrid nanocrystals of hydroxyapatite and hyaluronan. The results revealed that the strong interactions between ions and hyaluronan led to the nucleation of hydroxyapatite and the following aggregation. The combination of the external diffusion field and the internal multiple interactions induced the self-assembling processes. Additionally, HNAs with colloid stability and excellent biocompatibility were proved to be a promising cargo carrier for intranuclear delivery. This work presents a novel biomimetic mineralization strategy based on confined diffusion system for fabricating delicate hydroxyapatite, which offers a new perspective for the development of biomimetic strategies.