Integrated Transcriptomic and Metabolomics Analyses Reveal Molecular Responses to Cold Stress in Coconut (Cocos nucifera L.) Seedlings.

Coconut is an important tropical and subtropical fruit and oil crop severely affected by cold temperature, limiting its distribution and application. Thus, studying its low-temperature reaction mechanism is required to expand its cultivation range. We used growth morphology and physiological analyses to characterize the response of coconuts to 10, 20, and 30 d of low temperatures, combined with transcriptome and metabolome analysis. Low-temperature treatment significantly reduced the plant height and dry weight of coconut seedlings. The contents of soil and plant analyzer development (SPAD), soluble sugar (SS), soluble protein (SP), proline (Pro), and malondialdehyde (MDA) in leaves were significantly increased, along with the activities of superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT), and the endogenous hormones abscisic acid (ABA), auxin (IAA), zeatin (ZR), and gibberellin (GA) contents. A large number of differentially expressed genes (DEGs) (9968) were detected under low-temperature conditions. Most DEGs were involved in mitogen-activated protein kinase (MAPK) signaling pathway-plant, plant hormone signal transduction, plant-pathogen interaction, biosynthesis of amino acids, amino sugar and nucleotide sugar metabolism, carbon metabolism, starch and sucrose metabolism, purine metabolism, and phenylpropanoid biosynthesis pathways. Transcription factors (TFs), including WRKY, AP2/ERF, HSF, bZIP, MYB, and bHLH families, were induced to significantly differentially express under cold stress. In addition, most genes associated with major cold-tolerance pathways, such as the ICE-CBF-COR, MAPK signaling, and endogenous hormones and their signaling pathways, were significantly up-regulated. Under low temperatures, a total of 205 differentially accumulated metabolites (DAMs) were enriched; 206 DAMs were in positive-ion mode and 97 in negative-ion mode, mainly including phenylpropanoids and polyketides, lipids and lipid-like molecules, benzenoids, organoheterocyclic compounds, organic oxygen compounds, organic acids and derivatives, nucleosides, nucleotides, and analogues. Comprehensive metabolome and transcriptome analysis revealed that the related genes and metabolites were mainly enriched in amino acid, flavonoid, carbohydrate, lipid, and nucleotide metabolism pathways under cold stress. Together, the results of this study provide important insights into the response of coconuts to cold stress, which will reveal the underlying molecular mechanisms and help in coconut screening and breeding.

HQG-Net: Unpaired Medical Image Enhancement With High-Quality Guidance.

Unpaired medical image enhancement (UMIE) aims to transform a low-quality (LQ) medical image into a high-quality (HQ) one without relying on paired images for training. While most existing approaches are based on Pix2Pix/CycleGAN and are effective to some extent, they fail to explicitly use HQ information to guide the enhancement process, which can lead to undesired artifacts and structural distortions. In this article, we propose a novel UMIE approach that avoids the above limitation of existing methods by directly encoding HQ cues into the LQ enhancement process in a variational fashion and thus model the UMIE task under the joint distribution between the LQ and HQ domains. Specifically, we extract features from an HQ image and explicitly insert the features, which are expected to encode HQ cues, into the enhancement network to guide the LQ enhancement with the variational normalization module. We train the enhancement network adversarially with a discriminator to ensure the generated HQ image falls into the HQ domain. We further propose a content-aware loss to guide the enhancement process with wavelet-based pixel-level and multiencoder-based feature-level constraints. Additionally, as a key motivation for performing image enhancement is to make the enhanced images serve better for downstream tasks, we propose a bi-level learning scheme to optimize the UMIE task and downstream tasks cooperatively, helping generate HQ images both visually appealing and favorable for downstream tasks. Experiments on three medical datasets verify that our method outperforms existing techniques in terms of both enhancement quality and downstream task performance. The code and the newly collected datasets are publicly available at https://github.com/ChunmingHe/HQG-Net.

Suppressing Methane Production to Boost High-Purity Hydrogen Production in Microbial Electrolysis Cells.

Hydrogen gas (H2) is an attractive fuel carrier due to its high specific enthalpy; moreover, it is a clean source of energy because in the combustion reaction with oxygen (O2) it produces water as the only byproduct. The microbial electrolysis cell (MEC) is a promising technology for producing H2 from simple or complex organics present in wastewater and solid wastes. Methanogens and non-archaeal methane (CH4)-producing microorganisms (NAMPMs) often grow in the MECs and lead to rapid conversion of produced H2 to CH4. Moreover, non-archaeal methane production (NAMP) catalyzed by nitrogenase of photosynthetic bacteria was always overlooked. Thus, suppression of CH4 production is required to enhance H2 yield and production rate. This review comprehensively addresses the principles and current state-of-the-art technologies for suppressing methanogenesis and NAMP in MECs. Noteworthy, specific strategies aimed at the inhibition of methanogenic enzymes and nitrogenase could be a more direct approach than physical and chemical strategies for repressing the growth of methanogenic archaea. In-depth studies on the multiomics of CH4 metabolism can possibly provide insights into sustainable and efficient approaches for suppressing metabolic pathways of methanogenesis and NAMP. The main objective of this review is to highlight key concepts, directions, and challenges related to boosting H2 generation by suppressing CH4 production in MECs. Finally, perspectives are briefly outlined to guide and advance the future direction of MECs for production of high-purity H2 based on genetic and metabolic engineering and on the interspecific interactions.

Interface engineering strategy of a Ti4O7 ceramic membrane via graphene oxide nanoparticles toward efficient electrooxidation of 1,4-dioxane.

Although Ti4O7 ceramic membrane has been recognized as one of the most promising anode materials for electrochemical advanced oxidation process (EAOP), it suffers from relatively low hydroxyl radical (•OH) production rate and high charge-transfer resistance that restricted its oxidation performance of organic pollutants. Herein, we reported an effective interface engineering strategy to develop a Ti4O7 reactive electrochemical membrane (REM) doped by graphene oxide nanoparticles (GONs), GONs@Ti4O7 REM, via strong GONs-O-Ti bonds. Results showed that 1% (wt%) GON doping on Ti4O7 REM significantly reduced the charge-transfer resistance from 73.87 to 8.42 Ω compared with the pristine Ti4O7 REM, and yielded •OH at 2.5-2.8 times higher rate. The 1,4-dioxane (1,4-D) oxidation rate in batch experiments by 1%GONs@Ti4O7 REM was 1.49×10-2 min-1, 2 times higher than that of the pristine Ti4O7 REM (7.51×10-3 min-1) and similar to that of BDD (1.79×10-2 min-1). The 1%GONs@Ti4O7 REM exhibited high stability after a polarization test of 90 h at 80 mA/cm2, and within 15 consecutive cycles, its oxidation performance was stable (95.1-99.2%) with about 1% of GONs lost on the REM. In addition, REM process can efficiently degrade refractory organic matters in the groundwater and landfill leachate, the total organic carbon was removed by 54.5% with a single-pass REM. A normalized electric energy consumption per log removal of 1,4-D (EE/O) was observed at only 0.2-0.6 kWh/m3. Our results suggested that chemical-bonded interface engineering strategy using GONs can facilitate the EAOP performance of Ti4O7 ceramic membrane with outstanding reactivity and stability.

Peroxymonosulfate activation by oxygen vacancies-enriched MXene nano-Co3O4 co-catalyst for efficient degradation of refractory organic matter: Efficiency, mechanism, and stability.

Cobalt-based catalysts have been widely explored in the degradation of organic pollutants based on peroxymonosulfate (PMS) activation. Herein, we report an MXene nano-Co3O4 co-catalyst enriched with oxygen vacancies (Ov) and steadily fixed in nickel foam (NF) plates, which is used as an efficient and stable PMS activator for the removal of 1,4-dioxane (1,4-D). Ti originating from MXene was doped into the Co3O4 crystal, generating large amounts of Ov, which could provide more active sites to enhance PMS activation and facilitate the transformation of Co2+ and Co3+, causing a high stability. As a result, the 1,4-D removal efficiency of the NF/MXene-Co3O4/PMS system (kapp: 2.41 min-1) was about four times higher than that of the NF/Co3O4/PMS system (kapp: 0.62 min-1). In addition, singlet oxygen was the predominant reactive oxygen species. Notably, the 1,4-D removal of the NF/MXene-Co3O4/PMS system was over 95% after 20 h operation in the single-pass filtration mode with only 3.72% accumulative Co leaching, showing excellent stability and reusability of NF/MXene-Co3O4. This work provides a defect engineering strategy to design a robust and stable catalytic system for water treatment, which expands the application of MXene in the field of environmental remediation.

Aza-Based Donor-Acceptor Conjugated Polymer Nanoparticles for Near-Infrared Modulated Photothermal Conversion.

It is highly desired that synthesis of photothermal agents with near-infrared (NIR) absorption, excellent photostability, and high photothermal conversion efficiency are essential for potential applications. In this work, three (D-A) conjugated polymers (PBABDF-BDTT, PBABDF-BT, and PBABDF-TVT) based on aza-heterocycle, bis(2-oxo-7-azaindolin-3-ylidene)benzodifurandione (BABDF) as the strong acceptor, and benzodithiophene-thiophene (BDTT), bithiophene (BT), and thiophene-vinylene-thiophene (TVT) as the donors, were designed and synthesized. The conjugated polymers showed significant absorption in the NIR region and a maximum absorption peak at 808 nm by adjusting the donor and acceptor units. Their photothermal properties were also investigated by using poly(ethylene glycol)-block-poly(hexyl ethylene phosphate) (mPEG-b-PHEP) to stabilize the conjugated polymers. Photoexcited conjugated polymer (PBABDF-TVT) nanoparticles underwent non-radiative decay when subjected to single-wavelength NIR light irradiation, leading to an excellent photothermal conversion efficiency of 40.7%. This work indicated the aza-heterocycle BABDF can be a useful building block for constructing D-A conjugated polymer with high conversion efficiency.

Biocompatible HA@Fe3 O4 @N-CDs hybrids for detecting and absorbing lead ion.

The trinary hydroxyapatite@Fe3 O4 @N-doped carbon dots (HA@Fe3 O4 @N-CDs) hybrids were prepared by one-pot hydrothermal approach and utilized to detect and remove lead ion from aqueous solution. The structures and morphologies of as-obtained nanorod-like HA@Fe3 O4 @N-CDs hybrids were characterized by X-ray diffraction, scanning electron microscopy, and X-ray photoelectron spectroscopy measurements. These HA@Fe3 O4 @N-CDs hybrids possess good magnetism by magnetic hysteresis test and multi-colored fluorescence by the CLSM measurement. Furthermore, the as-obtained hybrids display excellent biocompatibility by MTT assay. Importantly, the trinary magnetic HA@Fe3 O4 @N-CDs hybrids as a green detector and adsorbent of Pb2+ were investigated. The influence of the different pH, the concentration of heavy metal, and the maximum adsorption capacity on removal efficiency was measured in detail. The maximum Pb2+ adsorption capacity on HA@Fe3 O4 @N-CDs hybrids is 450 mg/g. The kinetic mechanism was a pseudo-second order model, and the isotherm data was fitted well by the Langmuir isotherm and Freundlich model. Hence, the nanorod-like HA@Fe3 O4 @N-CDs hybrids could be a multifunctional material with significant potential applications in heavy metal detection and adsorption, bone tissue regeneration, magnetic therapy, and biomedicine. © 2019 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2019.

Fluorescent CDs@PCL hybrids via tartaric acid, CDs-cocatalyzed polymerization.

In this paper, the environment-friendly, water-soluble carbon dots (CDs) with stable photoluminescence (PL) have been prepared via the one-step pyrolysis of lotus leaf. Then the as-prepared CDs containing abundant hydroxylic and carboxylic groups were employed as cocatalyst with tartaric acid (TA) in ring-opening polymerization (ROP) of ε-caprolactone (ε-CL). The low-toxic organic acid TA, as main catalyst, was used to catalyze the ROP of ε-CL efficiently. The fluorescent CDs@PCL hybrids were obviously hydrophobic and they exhibited an excellent biocompatibility, and biodegradability due to the existence of PCL. Therefore the hydrophobic, biodegradable and multi-color fluorescent CDs@PCL hybrids may have potential applications in biomedicine, photocatalyst, bioimaging, and environmental analysis. Furthermore the application of CDs in catalyzing and initiating polymerization reaction will exemplify the versatility of CDs in the most unexpected fields.

A bis(2-oxoindolin-3-ylidene)-benzodifuran-dione containing copolymer for high-mobility ambipolar transistors.

A bis(2-oxoindolin-3-ylidene)-benzodifuran-dione (BIBDF)-based low band gap polymer (PBIBDF-BT), containing a solubilizing alkyl chain bithiophene unit as a donor, has been synthesized. The polymer with a low-lying LUMO/HOMO energy level (-4.03/-5.55 eV) exhibits efficient ambipolar charge transport. The electron and hole mobilities are as high as 1.08 and 0.30 cm(2) V(-1) s(-1), respectively.