Mechanism Of Shell Formation Research Articles

Concurrent processes in the time-resolved solvation and Coulomb ejection of sodium ions in helium nanodroplets

Recent pump-probe experiments [Albrechtsen et al., Nature 623, 319 (2023)] have explored the gradual solvation of sodium cations in contact with helium nanodroplets, using a fully solvated xenon atom as a probe exerting a repulsive interaction after its own ionization. In this communication, we computationally examine by means of atomistic ring-polymer molecular dynamics the mechanisms of successive ionizations, shell formation, and Coulomb ejection that all take place within tens of picoseconds and show that their interplay subtly depends on the time delay between the two ionizations but also on the droplet size. The possibility of forming solvated Na+Xe non-covalent complexes under a few tens of picoseconds in such experiments is ruled out based on fragment distributions.

The shell formation mechanism of Turbo argyrostomus based on ultrastructure and transcriptome analysis

The gold inner shell of Turbo argyrostomus is an important morphological classification characteristic in Gastropoda. However, the gene sets responsible for shell formation in gastropods remain poorly explored. In this study, we investigated the microstructure using scanning electron microscopy (SEM), hematoxylin-eosin (HE) and Alcian blue staining-periodic acid-Schiff (AB-PAS) staining. The SEM results illustrated that the T. argyrostomus shell exhibited a special “sandwich” microstructure. The results of histological observation demonstrated two major cell types: adipocytes and mucin cells. A total of 318 differentially expressed genes were identified between edge mantle and central mantle, among which whey acidic protein, N66, and nacre-like proteins, and Lam G and EGF domains may be related to shell microstructure. 22.39% − 25.20% of the mucin genes had biomineralization related domains, which supported for the relationship between mucins and shell formation. Moreover, this study revealed energy distribution differences between the edge mantle and central mantle. These results provide insights for further understanding of the biomineralization mechanism in Gastropoda.

Laser synthesis of nanoparticles in organic solvents - products, reactions, and perspectives.

Laser synthesis and processing of colloids (LSPC) is an established method for producing functional and durable nanomaterials and catalysts in virtually any liquid of choice. While the redox reactions during laser synthesis in water are fairly well understood, the corresponding reactions in organic liquids remain elusive, particularly because of the much greater complexity of carbon chemistry. To this end, this article first reviews the knowledge base of chemical reactions during LSPC and then deduces identifiable reaction pathways and mechanisms. This review also includes findings that are specific to the LSPC method variants laser ablation (LAL), fragmentation (LFL), melting (LML), and reduction (LRL) in organic liquids. A particular focus will be set on permanent gases, liquid hydrocarbons, and solid, carbonaceous species generated, including the formation of doped, compounded, and encapsulated nanoparticles. It will be shown how the choice of solvent, synthesis method, and laser parameters influence the nanostructure formation as well as the amount and chain length of the generated polyyne by-products. Finally, theoretical approaches to address the mechanisms of organic liquid decomposition and carbon shell formation are highlighted and discussed regarding current challenges and future perspectives of LSPC using organic liquids instead of water.

Origin and Formation Mechanism of Carbon Shell-Encapsulated Metal Nanoparticles for Powerful Fuel Cell Durability

Proton exchange membrane fuel cells (PEMFCs) face technical issues of performance degradation due to catalyst dissolution and agglomeration in real-world operations. To address these challenges, intensive research has been recently conducted to introduce additional structural units on the catalyst surface. Among various concepts for surface modification, carbon shell encapsulation is known to be a promising strategy since the carbon shell can act as a protective layer for metal nanoparticles. As an interesting approach to form carbon shells on catalyst surfaces, the precursor ligand-induced formation is preferred due to its facile synthesis and tunable control over the carbon shell porosity. However, the origin of the carbon source and the carbon shell formation mechanism have not been studied in depth yet. Herein, this study aims to investigate carbon sources through the use of different precursors and the introduction of new methodologies related to the ligand exchange phenomenon. Subsequently, we provide new insights into the carbon shell formation mechanism using X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). Finally, the thermal stability and electrochemical durability of carbon shells are thoroughly investigated through in situ transmission electron microscopy (in situ TEM) and accelerated durability tests.

Novel core–shell structure of Ni3S2@LiMoNiOx(OH)y nanorod arrays toward efficient high-current–density hydrogen evolution reaction

A cost-effective, high-performance, and stable electrocatalyst at high current density is critical to an industrial hydrogen production system. Herein, the surface engineering was used to synthesize core–shell structured Ni3S2@LiMoNiOx(OH)y nanorod arrays on nickel foam by a single-step hydrothermal process. Systematic investigations confirm that the simultaneous incorporation of Li and Mo can change the morphology of pristine Ni3S2 from granules to nanorod, which facilitates electron and mass transport for electrochemical tests and provides more accessible active sites. Impressively, Ni3S2@LiMoNiOx(OH)y exhibits excellent catalytic activity for hydrogen evolution reaction (HER) with low overpotentials of −57 mV and −365 mV to achieve current densities of −10 mA/cm2 and −1000 mA/cm2, respectively. Additionally, the core–shell Ni3S2@LiMoNiOx(OH)y nanorods demonstrate a fast release of generated-H2 bubbles to favor for more than 100 h stability at a high current density of −1000 mA/cm2. The core–shell formation mechanism and the kinetic mechanism of excellent HER performance is elucidated.

Characterization of the shell proteins in two freshwater snails Pomacea canaliculata and Cipangopaludina chinensis

Uncovering the molecular mechanism of shell formation not only reveals the evolution of molluscs but also lay a foundation for shell-inspired biomaterial synthesis. Shell proteins are the key macromolecules of the organic matrices that guide the calcium carbonate deposition during shell mineralization and have thus been intensively studied. However, previous studies on shell biomineralization have mainly focused on marine species. In this study, we compared the microstructure and shell proteins in the apple snail Pomacea canaliculata which is an alien species that has invaded Asia, and a freshwater snail Cipangopaludina chinensis which is native to China. The results showed that although the shell microstructures were similar in these two snails, the shell matrix in C. chinensis contained more polysaccharides. Moreover, the compositions of shell proteins were quite different. While the shared 12 shell proteins (including PcSP6/CcSP9, Calmodulin-A, and proline-rich protein) were supposed to play key roles in shell formation, the differential proteins were mainly immune components. The presence of chitin in both shell matrices and the chitin-binding domains containing PcSP6/CcSP9 underpinned the relevance of chitin as a major fraction in gastropods. Interestingly, carbonic anhydrase was absent in both snail shells, suggesting that freshwater gastropods might have unique pathways to regulate the calcification process. Our study suggested that shell mineralization might be very different in freshwater and marine molluscs, and therefore, the field should pay more attention to the freshwater species to achieve a more comprehensive insight into biomineralization.

Silver Nanoshells with Optimized Infrared Optical Response: Synthesis for Thin-Shell Formation, and Optical/Thermal Properties after Embedding in Polymeric Films.

We describe a new approach to making ultrathin Ag nanoshells with a higher level of extinction in the infrared than in the visible. The combination of near-infrared active ultrathin nanoshells with their isotropic optical properties is of interest for energy-saving applications. For such applications, the morphology must be precisely controlled, since the optical response is sensitive to nanometer-scale variations. To achieve this precision, we use a multi-step, reproducible, colloidal chemical synthesis. It includes the reduction of Tollens' reactant onto Sn2+-sensitized silica particles, followed by silver-nitrate reduction by formaldehyde and ammonia. The smooth shells are about 10 nm thick, on average, and have different morphologies: continuous, percolated, and patchy, depending on the quantity of the silver nitrate used. The shell-formation mechanism, studied by optical spectroscopy and high-resolution microscopy, seems to consist of two steps: the formation of very thin and flat patches, followed by their guided regrowth around the silica particle, which is favored by a high reaction rate. The optical and thermal properties of the core-shell particles, embedded in a transparent poly(vinylpyrrolidone) film on a glass substrate, were also investigated. We found that the Ag-nanoshell films can convert 30% of the power of incident near-infrared light into heat, making them very suitable in window glazing for radiative screening from solar light.

Full-length transcriptome analysis provides insights into larval shell formation in Mulinia lateralis

Mollusca is the second largest animal phylum and represents one of the most evolutionarily successful animal groups. Mulinia lateralis, a small bivalve, is a promising model organism to facilitate studies of mollusc development. However, because of the lack of published genomic and transcriptomic resources, integrated research on the formation of larval shells in this species, which is a representative developmental process of molluscs and of great importance for larva survival, is hindered. In this study, the blastula, gastrula, trochophore larva, and D-shaped larva of M. lateralis were utilized for generating a comprehensive full-length transcriptome through Pacific BioSciences (PacBio) isoform sequencing (Iso-seq) and Illumina RNA-Seq. A total of 238,919 full-length transcripts with an average length of 3,267 bp and 121,424 annotated genes were obtained. Illumina RNA-Seq data analysis showed that 4,512, 10,637, and 17,829 differentially expressed genes (DEGs) were obtained between the two adjacent developmental stages. Functional annotation and enrichment analysis revealed the specific function of genes in shell biomineralization during different developmental stages. Twelve genes that may be involved in the formation of the larval shell of M. lateralis were identified, including insoluble shell matrix protein-encoding gene 1 (ISMP1), ISMP2, ISMP5, chitin synthase, tyrosinase, chitin-binding protein, collagen and pu14 involved in shell matrix deposition, and carbonic anhydrase, solute carrier family 4 member 8 (slc4a8), EF-hand, and a calmodulin coding gene C-2442 participated in ion transportation. In addition, calcium ion binding function, calcium signaling pathway, and endocrine and other factor-regulated calcium reabsorption pathways were significantly enriched. Weighted gene correlation network analysis (WGCNA) identified two modules related to biomineralization and larval shell formation, and slc4a8 and ring finger protein 41 (rnf41) were key hub genes that may be involved in this process. Moreover, it could be implied that the process of ion transport occurs earlier than the deposition of the shell matrix. This work provided a clear view of the transcriptome for M. lateralis and will be valuable in elucidating the mechanisms of larval shell formation as well as other developmental processes in molluscs.

Near Infrared Reflection and Hydrophobic Properties of Composite Coatings Prepared from Hollow Glass Microspheres Coated with Needle-Shaped Rutile Shell

Infrared thermal reflective coating is an effective material to reduce building energy consumption and carbon emission. In this work, needle-shaped-rutile-shell-coated hollow glass microbeads (HGM) were prepared by surface modification of HGM and thermohydrolysis of TiCl4, and the possible shell formation mechanism was also proposed. The near infrared (NIR) reflectance of the coated HGM reached 93.3%, which could be further increased to 97.3% after the rutile shell crystallinity was improved by heat treatment. Furthermore, HGM/styrene-acrylic composite reflective coating was prepared on the surface of gypsum board by facile blending and coating methods, and the thermal insulation performance was measured by an indigenously designed experimental heat set-up. The results show that the composite coating prepared by HGM coated with rutile shell shows better NIR reflectance and thermal insulation performance than that prepared by pure organic coating and uncoated HGM. Meanwhile, it also shows better surface hydrophobicity, which is conducive to long-term and stable infrared reflection performance.

Development of core-shell type microencapsulated phase change material with Zn-30 mass% Al alloy and its shell formation mechanism

Latent heat storage (LHS) technology is promising because it can store and release heat at a constant temperature utilizing phase change material (PCM) and is a superior alternative for sensible heat storage (SHS) technology. In this study, we report an improved preparation method for microencapsulated PCM (MEPCM) with Zn–30 mass% Al (melting temperature: 440–512 °C) as the PCM. Conventional MEPCM preparation involves boehmite treatment for 3 h in boiling water to form AlOOH shells on Zn–30 mass% Al alloy particles (average diameter: 35.7 μm) and heat-oxidation treatment to form an oxide shell in oxygen atmosphere at 800 °C. In this study, Al(OH)3 is added to the treatment solution before boehmite treatment; furthermore, precipitation treatment at 75 °C for 16 h is investigated. After heat-oxidation treatment, different Al and Zn oxide shells are formed on the surface of the alloy particles depending on the Al(OH)3 quantity added before boehmite treatment and precipitation treatment. The prepared MEPCM has a heat storage density of 0.48 GJ m−3 and excellent cyclic durability of >100 melting and solidification cycles. In addition to this, investigations related to the fabrication of composite PCM by mixing it with a glass frit was carried out for improving the durability of the MEPCM. Therefore, this material can be utilized in future medium-to-high temperature heat applications such as transportation, chemical processes, and renewable energy.

Optimized Preparation of a Low-Working-Temperature Gallium Metal-Based Microencapsulated Phase Change Material

Gallium has been considered for application in the thermal management of electronic equipment because of its high heat transfer ability and heat storage density. To address the issues of metal corrosion and leakage, a microencapsulation method, through which a stable corrosion-resistant ceramic shell can be formed from the liquid metal, is proposed. In this study, an optimized fabrication method for a microencapsulated phase change material (MEPCM) consisting of liquid-state Ga droplets, possessing high durability and heat storage density, is presented. A fabrication route comprising particle formation, hydrothermal treatment, and calcination is proposed. In particular, the thickness and crystal size of the GaOOH shell are controlled by changing the pH during hydrothermal treatment to produce a highly durable shell. The morphology and microstructure, phase composition, heat storage capacity, and durability of the prepared Ga-MEPCM are investigated. In addition, treatment conditions and the shell formation mechanism are analyzed. The results show that pH 9 is the most suitable shell-forming condition, at which the thickest Ga2O3 shell with the smallest crystal size can be produced, which is beneficial for ensuring durability. The MEPCM achieved 200 cycles without leakage and 300 cycles without shape deformation with a high heat storage density of 369.4 J·cm–3.

Hic12, a novel acidic matrix protein promotes the transformation of calcite into vaterite in Hyriopsis cumingii

Shell acidic matrix proteins are widely considered to be essential for shell formation given their low affinity and high loading for calcium ion. In the present study, a novel matrix protein, hic12, was isolated from the mantle of Hyriopsis cumingii. High expression in tissue and positive signals with in situ hybridization were detected in the mantle center and mantle pallium, indicating that hic12 mainly participated in the biomineralization of the shell nacreous layer. The expression pattern of hic12 in the pearl sac during early pearl formation indicated that it was involved in pearl biomineralization. Moreover, the recombinant protein, rGST-Hic12, was successfully expressed and purified. The addition of rGST-Hic12 could accelerate the calcium carbonate deposition rate, change the morphology of crystals, and promote the conversion of calcite to vaterite. These results may provide new insights into the molecular mechanisms of aragonite mollusk shell formation.

Transcriptome analysis of the bivalve Placuna placenta mantle reveals potential biomineralization-related genes

The shells of window pane oyster Placuna placenta are very thin and exhibit excellent optical transparency and mechanical robustness. However, little is known about the biomineralization-related proteins of the shells of P. placenta. In this work, we report the comprehensive transcriptome of the mantle tissue of P. placenta for the first time. The unigenes of the mantle tissue of P. placenta were annotated by using the public databases such as nr, GO, KOG, KEGG, and Pfam. 24,343 unigenes were annotated according to Pfam database, accounting for 21.48% of the total unigenes. We find that half of the annotated unigenes of the mantle tissue of P. placenta are consistent to the annotated unigenes from pacific oyster Crassostrea gigas according to nr database. The unigene sequence analysis from the mantle tissue of P. placenta indicates that 465,392 potential single nucleotide polymorphisms (SNPs) and 62,103 potential indel markers were identified from 60,371 unigenes. 178 unigenes of the mantle tissue of P. placenta are found to be homologous to those reported proteins related to the biomineralization process of molluscan shells, while 18 of them are highly expressed unigenes in the mantle tissue. It is proposed that four unigenes with the highest expression levels in the mantle tissue are very often related to the biomineralization process, while another three unigenes are potentially related to the biomineralization process according to the Quantitative Real-Time Polymerase Chain Reaction (qRT-PCR) analysis. In summary, the transcriptome analysis of the mantle tissue of P. Placenta shows the potential biomineralization-related proteins and this work may shed light for the shell formation mechanism of bivalves.

Microencapsulation of high temperature metallic phase change materials with SiCN shell

Metallic phase change materials (PCMs) have the advantages of large phase change latent heat, high heat storage density and broad application prospects in various high temperature industrial waste heat recovery and utilization. However, due to the strong corrosion of molten metal at high temperature, appropriate packaging technology is the prerequisite for the promotion and application of metallic PCMs. In this research, a high temperature PCM microencapsulating technology with SiCN shell and a new microencapsulation method was proposed. The high temperature microencapsulated phase change materials (MEPCMs) with the core–shell mass ratios of 5:1, 4:1 and 3:1 were prepared by “solvent evaporation-heating curing” method, using SiCN cured by organic polysilazane (OPSZ) as heat resistant shell material and Al-Si particles as core PCMs. The mechanisms of shell formation and coating of OPSZ were studied experimentally, as well as the material properties and thermal performance of MEPCMs. With the increase of temperature, OPSZ gradually formed a dense SiCN shell on the surface of Al-Si particles. The experimental results showed that MEPCMs with the core–shell mass ratio of 4:1 had a high phase change temperature (571.9 °C-573.7 °C) and good heat storage capability (281.2 J/g-282.9 J/g). SiCN shell was conducive to maintain a complete core–shell structure, and exhibited excellent thermal resistance and oxidation resistance to protect inner core materials during thermal cycles. Therefore, the prepared microcapsule was a potential heat storage material, which provided a new idea for developing microencapsulation method of high temperature PCMs.

Development of a versatile microencapsulation technique for aqueous phases using inverse emulsion

The development of microencapsulation techniques that can microencapsulate a wide variety of aqueous phases with different functions can greatly promote the advancement of microcapsule-based functional materials. Herein, a novel microencapsulation technique to microencapsulate aqueous phases with different functions was successfully established based on the inverse emulsion. Using pure water as the targeting core, the shell formation mechanism was carefully studied for this microencapsulation technique. Different cross-linkers, including glycerol, poly(vinyl alcohol) (PVA), and polyethyleneimine (PEI) with multiple reactive hydrogen atoms, were adopted to adjust the microcapsule quality. It finds that the microcapsules have relatively low quality when no cross-linker was used, and that they became robust when cross-linked agents were adopted. Importantly, the higher the functionality of the cross-linker, the better the impermeability of the microcapsules shell to retain the core content. This technique was applied to microencapsulate common compounds of different nature in the laboratory, including water-soluble organics, water-soluble inorganics, and water-based dispersions, to demonstrate its versatility. It shows that the technique can microencapsulate a wide variety of water-soluble/dispersible substances except for the inorganic strong acid. The established technique opens a window to fabricate high-quality microcapsules containing aqueous phases with diversified functions, promoting the development of microcapsule-based functional materials.

Unraveling the shell growth pathways of Pd-Pt core-shell nanocubes at atomic level by in situ liquid cell electron microscopy

Understanding the formation of core-shell nanomaterials is decisive for controlling their growth, structure, and morphology, which is particularly important in catalysis. As a promising material for photo catalysis application, Pd-Pt core-shell nanoparticles (NPs) have been in the spotlight for many years owing to their catalytic performance typically superior to that of pure Pt nanoparticles. The generation of ultra-thin Pt skins of only a few atomic layers on Pd nanoparticles has turned out to be extremely difficult because Pt tends to form islands during deposition instead of a continuous shell. Therefore, understanding the atomic mechanisms of shell formation is critical for atomic-scale design and control of the platinum shell. Here, by using in situ graphene-based liquid cell scanning transmission electron microscopy (STEM), the growth mechanisms of the Pt shell on Pd nanocubes (NCs) are studied in aqueous solution at the atomic level. Pd-Pt core-shell NPs are formed via two distinct mechanisms: (i) at low concentration of Pt atoms, an ultra-thin skin of only a few atomic layers is formed via atom-by-atom deposition and (ii) at higher concentration of Pt atoms, inhomogeneous islands and thick shells are formed via attachment of Pt clusters. Our study provides a route to control core-shell growth and helps us to understand the exact atomic mechanisms of Pt shell growth on Pd seeds.

Genome-wide identification and characterization of Pif genes in the Yesso scallop (Patinopecten yessoensis), and their expression patterns in response to Polydora shell infestation

Pif is an acid matrix protein that is known to be a key macromolecule in the shell nacre formation of molluscs. However, the investigation into the Pif gene at the whole genome level has seldom been carried out, limiting the systematic understanding of its evolution and function. The Yesso scallop (Patinopecten yessoensis), an ancient bivalve with important economic value and evolutionary status, has suffered severe shell infestation by Polydora that badly damaged shell structures. In this study, a total of eight Pif homologous genes (PyPif1–7 and PyBMSP) were identified in the whole genome of the Yesso scallop with diverse gene structures. Two conserved functional domains, VWA and chitin-binding domains, were detected in all PyPif proteins, although with variation in number of copies. Phylogenetic analysis of the Pifs among different molluscan species suggested the molecular evolution of Pif genes was consistent with taxonomic relationships. High sequence divergence of Pif proteins existed among the different species, but a high level of similarity was found in BMSPs, which own four VWA domains. High expression levels of PyBMSP in the central mantles of the healthy and Polydora shell infested Yesso scallops indicated its important role in shell formation. The other PyPifs (PyPif2, PyPif3, PyPif4, PyPif5, PyPif6) may function when the shell is injured, as significantly increased expression levels of these genes were found in the edge mantles of the infested scallops. In addition, haemocytes may also participate in shell repair by up-regulating the expression of PyPifs. This study provides new insights into the evolution and expression patterns of Pif genes in molluscs, which are valuable for elucidating the mechanism of shell repair and formation.

The 'Shellome' of the Crocus Clam Tridacna crocea Emphasizes Essential Components of Mollusk Shell Biomineralization.

Molluscan shells are among the most fascinating research objects because of their diverse morphologies and textures. The formation of these delicate biomineralized structures is a matrix-mediated process. A question that arises is what are the essential components required to build these exoskeletons. In order to understand the molecular mechanisms of molluscan shell formation, it is crucial to identify organic macromolecules in different shells from diverse taxa. In the case of bivalves, however, taxon sampling in previous shell proteomics studies are focused predominantly on representatives of the class Pteriomorphia such as pearl oysters, edible oysters and mussels. In this study, we have characterized the shell organic matrix from the crocus clam, Tridacna crocea, (Heterodonta) using various biochemical techniques, including SDS-PAGE, FT-IR, monosaccharide analysis, and enzyme-linked lectin assay (ELLA). Furthermore, we have identified a number of shell matrix proteins (SMPs) using a comprehensive proteomics approach combined to RNA-seq. The biochemical studies confirmed the presence of proteins, polysaccharides, and sulfates in the T. crocea shell organic matrix. Proteomics analysis revealed that the majority of the T. crocea SMPs are novel and dissimilar to known SMPs identified from the other bivalve species. Meanwhile, the SMP repertoire of the crocus clam also includes proteins with conserved functional domains such as chitin-binding domain, VWA domain, and protease inhibitor domain. We also identified BMSP (Blue Mussel Shell Protein, originally reported from Mytilus), which is widely distributed among molluscan shell matrix proteins. Tridacna SMPs also include low-complexity regions (LCRs) that are absent in the other molluscan genomes, indicating that these genes may have evolved in specific lineage. These results highlight the diversity of the organic molecules – in particular proteins – that are essential for molluscan shell formation.

The mantle exosome proteins of Hyriopsis cumingii participate in shell and nacre color formation

Pearl color is closely related to the nacre color of shell in Hyriopsis cumingii, and pearl color has a huge impact on its price. The nacre is an important part of the shell, and studies have suggested that mantle exosomes participated in shell formation. Exosomes contain many different proteins that are involved in different biological processes. In this study, exosomes were extracted from mantles of mussels with different nacre color. TMT quantitative proteome sequencing analysis was performed on purple and white mussel mantle exosomes, and 4861 proteins were obtained. Based on the standard of (|log2 (Fold change)| ≥ 1.2 or ≤ 0.83 and p-value ≤ 0.05), a total of 758 differentially expressed proteins were found. Some proteins involved in shell and nacre color formation were predicted with the proteins annotate, GO classification system. Moreover, 14 differentially expressed proteins (including eight up-regulated proteins and six down-regulated proteins) were validated using parallel reaction monitoring (PRM) assays. Overall, this information will be useful to improve our understanding of the molecular mechanisms of shell and nacre color formation in H. cumingii.

Novel globular C1q domain-containing protein (PmC1qDC-1) participates in shell formation and responses to pathogen-associated molecular patterns stimulation in Pinctada fucata martensii

The C1q protein, which contains the globular C1q (gC1q) domain, is involved in the innate immune response, and is found abundantly in the shell, and it participates in the shell formation. In this study, a novel gC1q domain-containing gene was identified from Pinctada fucata martensii (P. f. martensii) and designated as PmC1qDC-1. The full-length sequence of PmC1qDC-1 was 902 bp with a 534 bp open reading frame (ORF), encoding a polypeptide of 177 amino acids. Quantitative real-time PCR (qRT-PCR) result showed that PmC1qDC-1 was widely expressed in all tested tissues, including shell formation-associated tissue and immune-related tissue. PmC1qDC-1 expression was significantly high in the blastula and gastrula and especially among the juvenile stage, which is the most important stage of dissoconch shell formation. PmC1qDC-1 expression was located in the outer epithelial cells of mantle pallial and mantle edge and irregular crystal tablets were observed in the nacre upon knockdown of PmC1qDC-1 expression at mantle pallial. Moreover, the recombined protein PmC1qDC-1 increased the rate of calcium carbonate precipitation. Besides, PmC1qDC-1 expression was significantly up-regulated in the mantle pallial at 6 h and was significantly up-regulated in the mantle edge at 12 h and 24 h after shell notching. The expression level of PmC1qDC-1 in mantle edge was significantly up-regulated at 48 h after LPS stimulation and was significantly up-regulated at 12 h, 24 h and 48 h after poly I:C stimulation. Moreover, PmC1qDC-1 expression was significantly up-regulated in hemocytes at 6 h after lipopolysaccharide (LPS) and poly I:C challenge. These findings suggest that PmC1qDC-1 plays a crucial role both in the shell formation and the innate immune response in pearl oysters, providing new clues for understanding the shell formation and defense mechanism in mollusk.