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The direct methanol fuel cell (DMFC) is an efficient and non-polluting green energy conversion device. However, the electrocatalysts for the anodic methanol oxidation reaction (MOR) in DMFC are often precious metal catalysts, which suffer from high cost, poor stability, and easy deactivation. In this work, two isostructural metal-organic frameworks (MOFs) [M 3 (μ 3 -OH)(TATB)(Nic) 2 (H 2 O) 2 (DMA)] (M = Co, Ni) were successfully synthesized under solvothermal conditions. Both frameworks possess a unique trinuclear cluster [M 3 (μ 3 -OH)(COO) 5 ] secondary building unit (SBU) and a rare binodal (3,7)-connected network. Due to the high density of metal sites and prominent pore system within CTGU-36-Ni, it can serve as an effective molecular electrocatalyst for MOR, while CTGU-36-Co is an inert material. Further experimental results showed that the introduction of conductive substances could lead to a significant increase in the MOR area activity of CTGU-36-Ni. This work not only provides a non-noble metal molecular MOR electrocatalyst but also opens a new vision for the design and application of crystalline materials in various energy conversion processes. Two isostructural metal-organic frameworks (MOFs) with atypical trinuclear cluster have been constructed successfully, which exhibit good electrocatalytic properties toward methanol oxidation reaction as molecular electrocatalysts or after the addition of conductive carbon mediums. [Display omitted] • Two isostructural MOFs with atypical trinuclear cluster have been constructed. • CTGU-36-Ni and its composites exhibit remarkable electrocatalytic activity for MOR. • This work provides a molecular MOR catalyst and a new vision for the application of MOFs. [ABSTRACT FROM AUTHOR]

[Display omitted] A critical challenge in the enzymatic conversion of acylglycerols is the limited exposure of the enzyme dissolved in the aqueous solution to the hydrophobic substrate in the oil phase. Positioning the enzyme in a microenvironment with balanced hydrophobicity and hydrophilicity in Pickering emulsion will facilitate the acylglycerol-catalyzing reactions at the interface between the oil and liquid phases. In this work, to overcome the challenge of biphasic catalysis, we report a method to immobilize enzymes in polyethylene glycol (PEG)-based hydrogel microparticles (HMPs) at the interface between the oil and water phases in Pickering emulsion to promote the enzymatic conversion of acylglycerols. 3 wt% of HMPs can stabilize the oil-in-water Pickering emulsion for at least 14 days and increase the viscosity of emulsions. Lipase-HMP conjugates showed significantly higher hydrolytic activity in Pickering emulsion; HMP-immobilized lipase SMG1 showed an activity about three times that of free lipase SMG1. Co-immobilization of a lipase and a fatty acid photodecarboxylase from Chlorella variabilis (CvFAP) in Pickering emulsion enables light-driven cascade conversion of triacylglycerols to hydrocarbons, transforming waste oil to renewable biofuels in a green and sustainable approach. HMPs stabilize the Pickering emulsion and promote interfacial biocatalysis in converting acylglycerols to renewable biofuels. [ABSTRACT FROM AUTHOR]

Our recent multi-omics studies have revealed rich sources of novel bioactive proteins and polypeptides from marine organisms including cnidarians. In the present study, we initially conducted a transcriptomic analysis to review the composition profile of polypeptides from Zoanthus sociatus. Then, a newly discovered NPY-like polypeptide-ZoaNPY was selected for further in silico structural, binding and virtually pharmacological studies. To evaluate the pro-angiogenic effects of ZoaNPY, we employed an in vitro HUVECs model and an in vivo zebrafish model. Our results indicate that ZoaNPY, at 1–100 pmol, enhances cell survival, migration and tube formation in the endothelial cells. Besides, treatment with ZoaNPY could restore a chemically-induced vascular insufficiency in zebrafish embryos. Western blot results demonstrated the application of ZoaNPY could increase the phosphorylation of proteins related to angiogenesis signaling including PKC, PLC, FAK, Src, Akt, mTOR, MEK, and ERK1/2. Furthermore, through molecular docking and surface plasmon resonance (SPR) verification, ZoaNPY was shown to directly and physically interact with NPY Y2 receptor. In view of this, all evidence showed that the pro-angiogenic effects of ZoaNPY involve the activation of NPY Y2 receptor, thereby activating the Akt/mTOR, PLC/PKC, ERK/MEK and Src- FAK-dependent signaling pathways. Furthermore, in an excision wound model, the treatment with ZoaNPY was shown to accelerate the wound healing process in mice. Our findings provide new insights into the discovery and development of novel pro-angiogenic drugs derived from NPY-like polypeptides in the future. [Display omitted] [ABSTRACT FROM AUTHOR]