Fouling-Resistant Behavior of Silver Nanoparticle-Modified Surfaces against the Bioadhesion of Microalgae

Unwanted adhesion of microalgae on submerged surfaces is a ubiquitous problem across many maritime operations. We explored the strategy of developing a silver nanoparticle (AgNP) coating for antifouling applications in marine and freshwater environments. In situ growth of AgNPs was achieved by a polydopamine (PDA)-based method. A range of most used industrial materials, including glass, polystyrene, stainless steel, paint surface, and even cobblestone, were employed, on which AgNP coatings were built and characterized. We described the fouling-resistant behavior of these AgNP-modified surfaces against two typical fouling organisms: a marine microalga Dunaliella tertiolecta and a freshwater green alga community. The PDA-mediated AgNP deposition strategy was demonstrated applicable for all the above materials; the resulting AgNP coatings showed a significant surface inhibitory effect against the adhesion of microalgae by above 85% in both seawater and freshwater environments. We observed that contact killing was the predominant antifouling mechanism of AgNP-modified surfaces, and the viability of the microalgae cells in bulk media would not be affected. In addition, silver loss from PDA-mediated AgNPs was relatively slow; it could allow the coating to persist for long-term usage. This study showed the potential of preparing environmentally friendly surfaces that can effectively manage biofouling through the direct deposition of AgNP coatings

Optical Activity and Excitonic Characteristics of Chiral CdSe Quantum Dots

Introduction of chirality to colloidal semiconductor quantum dots (QDs) triggers a chiroptical effect. However, there remains a knowledge gap in the mechanism of chirality transfer and amplification from molecules to QDs. By time-dependent density functional theory calculations combined with a correlated electron–hole picture, we explored the chiroptical activity of CdSe QDs decorated with different chiral monocarboxylic acids from an excitonic perspective. Our calculations showed strong circular dichroism (CD) signals in the visible region for the chiral CdSe QDs. The excitonic states with large CD originate from QDs, while the chiral molecules break the orthogonality between electric and magnetic transition dipoles, which synergistically facilitates the prominent dissymmetric effect. The considered monocarboxylic acid chiral molecules all favor the bidentate adsorption configuration of the carboxyl group on the CdSe surface, endowing an identical CD signature but distinct excitonic characteristics. These findings are crucial for the regulation of chirality and excitons in semiconductor QDs to develop excitonic devices

Optical Activity and Excitonic Characteristics of Chiral CdSe Quantum Dots

Introduction of chirality to colloidal semiconductor quantum dots (QDs) triggers a chiroptical effect. However, there remains a knowledge gap in the mechanism of chirality transfer and amplification from molecules to QDs. By time-dependent density functional theory calculations combined with a correlated electron–hole picture, we explored the chiroptical activity of CdSe QDs decorated with different chiral monocarboxylic acids from an excitonic perspective. Our calculations showed strong circular dichroism (CD) signals in the visible region for the chiral CdSe QDs. The excitonic states with large CD originate from QDs, while the chiral molecules break the orthogonality between electric and magnetic transition dipoles, which synergistically facilitates the prominent dissymmetric effect. The considered monocarboxylic acid chiral molecules all favor the bidentate adsorption configuration of the carboxyl group on the CdSe surface, endowing an identical CD signature but distinct excitonic characteristics. These findings are crucial for the regulation of chirality and excitons in semiconductor QDs to develop excitonic devices

An Efficient, Recyclable, and Stable Immobilized Biocatalyst Based on Bioinspired Microcapsules-in-Hydrogel Scaffolds

Design and preparation of high-performance immobilized biocatalysts with exquisite structures and elucidation of their profound structure-performance relationship are highly desired for green and sustainable biotransformation processes. Learning from nature has been recognized as a shortcut to achieve such an impressive goal. Loose connective tissue, which is composed of hierarchically organized cells by extracellular matrix (ECM) and is recognized as an efficient catalytic system to ensure the ordered proceeding of metabolism, may offer an ideal prototype for preparing immobilized biocatalysts with high catalytic activity, recyclability, and stability. Inspired by the hierarchical structure of loose connective tissue, we prepared an immobilized biocatalyst enabled by microcapsules-in-hydrogel (MCH) scaffolds via biomimetic mineralization in agarose hydrogel. In brief, the in situ synthesized hybrid microcapsules encapsulated with glucose oxidase (GOD) are hierarchically organized by the fibrous framework of agarose hydrogel, where the fibers are intercalated into the capsule wall. The as-prepared immobilized biocatalyst shows structure-dependent catalytic performance. The porous hydrogel permits free diffusion of glucose molecules (diffusion coefficient: ∼6 × 10^–6 cm² s^–1, close to that in water) and retains the enzyme activity as much as possible after immobilization (initial reaction rate: 1.5 × 10^–2 mM min^–1). The monolithic macroscale of agarose hydrogel facilitates the easy recycling of the immobilized biocatalyst (only by using tweezers), which contributes to the nonactivity decline during the recycling test. The fiber-intercalating structure elevates the mechanical stability of the in situ synthesized hybrid microcapsules, which inhibits the leaching and enhances the stability of the encapsulated GOD, achieving immobilization efficiency of ∼95%. This study will, therefore, provide a generic method for the hierarchical organization of (bio)­active materials and the rational design of novel (bio)­catalysts

DataSheet_1_Comparative transcriptome analysis of T lymphocyte subpopulations and identification of critical regulators defining porcine thymocyte identity.zip

IntroductionThe development and migration of T cells in the thymus and peripheral tissues are crucial for maintaining adaptive immunity in mammals. However, the regulatory mechanisms underlying T cell development and thymocyte identity formation in pigs remain largely underexplored. MethodHere, by integrating bulk and single-cell RNA-sequencing data, we investigated regulatory signatures of porcine thymus and lymph node T cells. ResultsThe comparison of T cell subpopulations derived from porcine thymus and lymph nodes revealed that their transcriptomic differences were influenced more by tissue origin than by T cell phenotypes, and that lymph node cells exhibited greater transcriptional diversity than thymocytes. Through weighted gene co-expression network analysis (WGCNA), we identified the key modules and candidate hub genes regulating the heterogeneity of T cell subpopulations. Further, we integrated the porcine thymocyte dataset with peripheral blood mononuclear cell (PBMC) dataset to systematically compare transcriptomic differences between T cell types from different tissues. Based on single-cell datasets, we further identified the key transcription factors (TFs) responsible for maintaining porcine thymocyte identity and unveiled that these TFs coordinately regulated the entire T cell development process. Finally, we performed GWAS of cell type-specific differentially expressed genes (DEGs) and 30 complex traits, and found that the DEGs in thymus-related and peripheral blood-related cell types, especially CD4_SP cluster and CD8-related cluster, were significantly associated with pig productive and reproductive traits. DiscussionOur findings provide an insight into T cell development and lay a foundation for further exploring the porcine immune system and genetic mechanisms underlying complex traits in pigs.</p

Conferring Natural-Derived Porous Microspheres with Surface Multifunctionality through Facile Coordination-Enabled Self-Assembly Process

In this study, multifunctional chitin microspheres are synthesized and utilized as a platform for multiple potential applications in enzyme immobilization, catalytic reduction and adsorption. Porous chitin microspheres with an average diameter of 111.5 μm and a porous architecture are fabricated through a thermally induced phase separation method. Then, the porous chitin microspheres are conferred with surface multifunctionality through facile coordination-enabled self-assembly of tannic acid (TA) and titanium (Ti^IV) bis­(ammonium lactate)­dihydroxide (Ti–BALDH). The multipoint hydrogen bonds between TA and chitin microspheres confer the TA–Ti^IV coating with high adhesion capability to adhere firmly to the surface of the chitin microspheres. In view of the biocompatibility, porosity and surface activity, the multifunctional chitin microspheres are used as carriers for enzyme immobilization. The enzyme-conjugated multifunctional porous microspheres exhibit high catalytic performance (102.8 U·mg^–1 yeast alcohol dehydrogenase). Besides, the multifunctional chitin microspheres also find potential applications in the catalytic reduction (e.g., reduction of silver ions to silver nanoparticles) and efficient adsorption of heavy metal ions (e.g., Pb²⁺) taking advantages of their porosity, reducing capability and chelation property

Enhancing Catalytic Activity and Stability of Yeast Alcohol Dehydrogenase by Encapsulation in Chitosan-Calcium Phosphate Hybrid Beads

A kind of calcium phosphate-mineralized chitosan beads (chitosan–CaP) was prepared via a one-pot method by adding droplets of Ca²⁺-containing chitosan aqueous solution into phosphate-containing sodium tripolyphosphate aqueous solution. The chitosan beads formed immediately coupled with in situ precipitation of calcium phosphate on the surface. The antiswelling properties of hybrid beads were greatly improved with the swelling degree as low as 5%. The morphology of the resultant chitosan–CaP hybrid beads was observed by scanning electron microscopy (SEM). Yeast alcohol dehydrogenase (YADH) was encapsulated in the hybrid beads with an about 40% lower enzyme leakage compared with that in the pure chitosan beads. The optimal temperature and pH value for enzymatic conversion catalyzed by YADH immobilized in the chitosan–CaP beads were 30 °C and 7.0, respectively, which were identical to those for free YADH. The immobilized YADH displayed obviously higher thermal stability, pH stability, recycling stability, and storage stability than the free YADH counterpart