Search Results (57)

Cement-based materials are essential in modern construction, valued for their versatility and performance. Rheological properties, including yield stress, plastic viscosity, and thixotropy, play indispensable roles in optimizing the workability, stability, and overall performance of cement composites. This review explores the effects of supplementary cementitious materials (SCMs), chemical admixtures, nanomaterials, and internal curing agents on modulating rheological properties. Specifically, SCMs, including fly ash (FA), ground granulated blast furnace slag (GGBFS), and silica fume (SF), generally improve the rheology of concrete while reducing the cement content and CO₂ emissions. Regarding chemical admixtures, like superplasticizers (SPs), viscosity-modifying agents (VMAs), setting-time control agents, and superabsorbent polymers (SAPs), they further optimize flow and cohesion, addressing issues such as segregation and early-age shrinkage. Nanomaterials, including nano-silica (NS) and graphene oxide (GO), can enhance viscosity and mechanical properties at the microstructural level. By integrating these materials above, it can tailor concrete for specific applications, thereby improving both performance and sustainability. This review presents a comprehensive synthesis of recent literature, utilizing both qualitative and quantitative methods to assess the impacts of various additives on the rheological properties of cement-based materials. It underscores the pivotal roles of rheological properties in optimizing the workability, stability, and overall performance of cement composites. The review further explores the influences of SCMs, chemical admixtures, nanomaterials, and internal curing agents on rheological modulation. Through the strategic integration of these materials, it is possible to enhance both the performance and sustainability of cement composites, ultimately reducing carbon emissions and advancing the development of eco-friendly construction materials. Full article

This study evaluates the influence of multiwall carbon nanotubes (MWCNTs), reduced graphene oxide (rGO), and magnesium oxide (MgO) on the thermal conductivity of alkali-activated engineered composites (AAECs). Thirty-two ambient-cured AAECs consisting of two types of powdered-form reagents/activators (type 1—calcium hydroxide: sodium meta silicate = 1:2.5; type 2—calcium hydroxide: sodium sulfate 2.5:1), two dosages of MgO (0 and 0.5%) of MgO, three percentages (0, 0.3%, and 0.6%) of MWCNTs/rGO, and binary (45% ground granulated blast furnace slag ‘GGBFS’ and 55% Class C fly ash ‘FA-C’) and ternary combinations (40% GGBFS, 25% FA-C and 35% class F fly ash ‘FA-F’) of industrial-waste-based source materials, silica sand, and polyvinyl alcohol (PVA) fiber were developed using the ‘one-part dry mix’ technique. Problems associated with the dispersion and agglomeration of nanomaterials during production were avoided through the use of defined ultra-sonication with a high-shear mixing protocol. The impact of the combination of source materials, activators, and MgO/MWCNT/rGO dosages and their combinations on the thermal properties of AAECs is evaluated and discussed based on temperature–time history and thermal conductivity/diffusivity properties along with micro-structural characteristics. It was found that the change in temperature of the AAECs decreased during testing with the addition of MWCNTs/rGO/MgO. The thermal conductivity and diffusivity of AAECs increased with the increase in MWCNT/rGO/MgO contents due to the formation of additional crystalline reaction products, improved matrix connectivity, and high conductivity of nanomaterials. MWCNT AAECs showed the highest thermal conductivity of 0.91–1.26 W/mK with 49% enhancement compared to control AAECs followed by rGO AAECs. The study confirmed the viability of producing MgO/MWCNT/rGO-incorporated AAECs with enhanced thermal properties. Full article

Penicillium griseofulvum CF3 is a fungus isolated from healthy strawberry soil, with the potential to promote the growth of plants and enhance their resistance to diseases. However, the genome sequence of P. griseofulvum CF3 remains unclear. Therefore, we performed the whole-genome CCS sequencing of P. griseofulvum CF3 using the PacBio Sequel II platform. The assembled genome comprised 104 contigs, with a total length of 37,564,657 bp, encoding 13,252 protein-coding genes. Comprehensive functional annotation was performed using various BLAST databases, including the non-redundant (Nr) protein sequence database, Gene Ontology (GO), the Kyoto Encyclopedia of Genes and Genomes (KEGG), EuKaryotic Orthologous Groups (KOG), and the Carbohydrate-Active enZymes (CAZy) database, to identify and predict protein-coding genes, tRNAs, and rRNAs. The Antibiotics and Secondary Metabolites Analysis Shell (Antismash) analysis identified 50 biosynthetic gene clusters involved in secondary metabolite production within the P. griseofulvum CF3 genome. The whole-genome sequencing of P. griseofulvum CF3 helps us to understand its potential mechanisms in promoting plant growth and enhancing disease resistance, paving the way for the application of the CF3 strain in sustainable crop production. Full article

Thirty-two ambient cured alkali-activated engineered composites (AAECs) were developed by incorporating MgO, multi-walled carbon nanotubes (MWCNTs), reduced graphene oxide (rGO), and polyvinyl alcohol (PVA) fiber with a one-part dry mix technique using powder-based activators/reagents. The effects of material variables, namely binary or ternary combination source materials (fly ash C or F and ground granulated blast furnace slag ‘GGBFS’), two types of reagents with varying chemical ratios and dosages of additives (from 0 to 5% MgO and from 0 to 6% MWCNT/rGO), on the physical (slump flow, flow time, flow velocity, and density), hardness (compressive strength from 0 to 180 days and 28-day ultrasonic pulse velocity ‘UPV’), and micro-structural (SEM/EDS, XRD and FTIR) properties were evaluated. All these variables, individually or combined, influenced the properties and microstructural aspects of AAECs. Problems associated with the dispersion and agglomeration of nanomaterials, which could disrupt the microstructure and weaken its mechanical/physical properties, were avoided through the use of defined ultra-sonication with a high-shear mixing protocol. All AAECs achieved a 28-day compressive strength ranging from 26.0 MPa to 48.5 MPa and a slump flow > 800 mm, satisfying the criteria for flowable structural concrete. The addition of 5% MgO and up to 0.3% MWCNT/rGO increased the compressive strength/UPV of AAECs with MgO-MWCNT or rGO combination provided an improved strength at a higher dosage of 0.6%. A linear correlation between compressive strength and UPV was derived. As per SEM/EDS and XRD analyses, besides common C-A-S-H/N-C-A-S-H or C-A-S-H/C-S-H gels, the addition of MgO led to the formation of magnesium-aluminum hydrotalcite (Ht) and M-S-H (demonstrating self-healing potential), while the incorporation of rGO produced zeolites which densified the matrix and increased the compressive strength/UPV of the AAECs. Fourier transform infrared spectrometer (FTIR) analysis also suggested the formation of an aluminosilicate network in the AAECs, indicating a more stable structure. The increased UPV of MWCNT/rGO-incorporated AAECs indicated their better conductivity and ability of self-sensing. The developed AAECs, incorporating carbon-nano materials and MgO additive, have satisfactory properties with self-healing/-sensing potentials. Full article

Background/Objectives: AML is an aggressive malignant disease characterized by aberrant proliferation and accumulation of immature blast cells in the patient’s bone marrow. Chemotherapeutic treatment can effectively induce remission and re-establish functional hematopoiesis. However, many patients experience chemoresistance-associated relapse and disease progression with a poor prognosis. The identification of molecular determinants of chemoresistance that could serve as potential targets for the therapeutic restoration of chemosensitivity has proven to be challenging. Methods: To address this, we have analyzed longitudinal changes in the expression of microRNAs during disease progression in a small set of four AML patients, combined with gene ontology (GO) pathway analysis and evaluation of gene expression data in patient databases. Results: MicroRNA profiling of bone marrow samples at diagnosis and after relapse revealed significant differential expression of a large number of microRNAs between the two time points. Subsequent GO pathway analysis identified 11 signal transduction pathways likely to be affected by the differential miRNA signatures. Exemplary validation of the FoxO signaling pathway by gene expression analysis confirmed significant upregulation of FOXO1 and the target genes GADD45 and SOD2. Conclusions: Here, we show how a microRNA-based pathway prediction strategy can be used to identify differentially regulated signaling pathways that represent potential targets for therapeutic intervention. Full article

Magnaporthe oryzae causes devastating rice blast disease, significantly impacting rice production in many countries. Among the many known resistance (R) genes, Piz-t confers broad-spectrum resistance to M. oryzae isolates and encodes a nucleotide-binding site leucine-rich repeat receptor (NLR). Although Piz-t-interacting proteins and those in the signal transduction pathway have been identified over the last decade, the Piz-t-mediated resistance has not been fully understood at the transcriptomic and metabolomic levels. In this study, we performed transcriptomic and metabolomic analyses in the Piz-t plants after inoculation with M. oryzae. The transcriptomic analysis identified a total of 15,571 differentially expressed genes (DEGs) from infected Piz-t and wild-type plants, with 2791 being Piz-t-specific. K-means clustering, GO term analysis, and KEGG enrichment pathway analyses of the total DEGs identified five groups of DEGs with distinct gene expression patterns at different time points post inoculation. GO term analysis of the 2791 Piz-t-specific DEGs revealed that pathways related to DNA organization, gene expression regulation, and cell division were highly enriched in the group, especially at early infection stages. The gene expression patterns in the transcriptomic datasets were well correlated with the metabolomic profiling. Broad-spectrum “pathway-level” metabolomic analyses indicated that terpenoid, phenylpropanoid, flavonoid, fatty acid, amino acid, glycolysis/TCA, and phenylalanine pathways were altered in the Piz-t plants after M. oryzae infection. This study offers new insights into the molecular dynamics of transcripts and metabolites in R-gene-mediated resistance against M. oryzae and provides candidates for enhancing rice blast resistance through the engineering of metabolic pathways. Full article

Euspira gilva, a member of the family Naticidae, is predominantly found in intertidal soft mud, sandy soil, and sandy seabeds along the coast of China, where it is valued for its nutritional richness and significant economic value. This study presents a comprehensive transcriptome sequencing and analysis of E. gilva specimens from the Lianyungang area, yielding 3385 high-quality isoform sequences and 3310 non-redundant transcripts. Annotation against various databases, including NR, Swiss-Prot, KEGG, KOG, eggNOG, GO, and Pfam, successfully annotated a significant number of transcripts. A total of 7929 simple sequence repeat (SSR) loci were identified, with single nucleotide repeats predominating at 85.0%. Predictive analysis of coding DNA sequences (CDS) resulted in 1340 BLAST comparisons, while ESTScan predicted 840. Further, 530 long non-coding RNAs (lncRNAs) were identified through the application of the CPC2, CNCI, Pfam, and PLEK algorithms. The highest overall sequence similarity in the NR database was observed with Pomacea canaliculata, a freshwater species, but with a similarity of only 36.6%, indicating a unique genetic makeup of E. gilva. The KEGG database annotation revealed a predominance of signal transduction pathways, particularly the PI3K-Akt signaling pathway, with 29 non-redundant transcripts encoding key genes such as IGH (immunoglobulin heavy chain), PCK (phosphoenolpyruvate carboxykinase), COL2A (collagen, type II, alpha), ITGB1 (integrin beta 1), and GNG7 (guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-7). These genes play crucial roles in cellular processes, including cell growth, transcription, translation, proliferation, movement, and glycogen metabolism. The findings of this research elucidate the full-length transcriptome profile of E. gilva, thereby establishing a foundational dataset and providing valuable insights for the species’ aquaculture, health management, conservation efforts, and future molecular biological investigations. Full article

Sacha Inchi (Plukenetia volubilis) oil press-cake (SIPC) represents a new source of proteins of high biological value, with promissory food applications. However, knowledge of these proteins remains limited. In this study, a Sacha Inchi protein concentrate (SPC) was extracted from the SIPC, and proteomic analysis was performed to identify the major alkaline-soluble proteins. The electrophoretic profile highlighted the efficacy of alkaline pH and moderate temperature to extract the major proteins, from which a group of proteins, not previously reported, were registered. LC-MS/MS analyses produced abundant high-quality fragmentation spectra. Utilizing the Euphorbiaceae database (DB), 226 proteins were identified, with numerous well-assigned spectra remaining unidentified. PEAKS Studio v11.5 software generated 1819 high-quality de novo peptides. Data are available via ProteomeXchange with identifier PXD052665. Gene ontology (GO) classification allowed the identification of sequenced proteins associated with biological processes, molecular functions, and cellular components in the seed. Consequently, the principal alkali-soluble proteins from SPC were characterized through derived functional analysis, covering 24 seed-storage-, 27 defense-, and 12 carbohydrate- and lipid-metabolism-related proteins, crucial for human nutrition due to their sulfur-containing amino acids, antioxidant properties, and oil yields, respectively. This research makes a significant contribution to the current understanding of the Sacha Inchi proteome and offers valuable insights for its potential applications in the food industry. Full article

Abiotic stresses such as nitrogen deficiency, drought, and salinity significantly impact coconut production, yet the molecular mechanisms underlying coconut’s response to these stresses are poorly understood. MYB proteins, a large and diverse family of transcription factors (TF), play crucial roles in plant responses to various abiotic stresses, but their genome-wide characterization and functional roles in coconut have not been comprehensively explored. This study identified 214 CnMYB genes (39 1R–MYB, 171 R2R3–MYB, 2 3R–MYB, and 2 4R–MYB) in the coconut genome. Phylogenetic analysis revealed that these genes are unevenly distributed across the 16 chromosomes, with conserved consensus sequences, motifs, and gene structures within the same subgroups. Synteny analysis indicated that segmental duplication primarily drove CnMYB evolution in coconut, with low nonsynonymous/synonymous ratios suggesting strong purifying selection. The gene ontology (GO) annotation of protein sequences provided insights into the biological functions of the CnMYB gene family. CnMYB47/70/83/119/186 and CnMYB2/45/85/158/195 were identified as homologous genes linked to nitrogen deficiency, drought, and salinity stress through BLAST, highlighting the key role of CnMYB genes in abiotic stress tolerance. Quantitative analysis of PCR showed 10 CnMYB genes in leaves and petioles and found that the expression of CnMYB45/47/70/83/85/119/186 was higher in 3-month-old than one-year-old coconut, whereas CnMYB2/158/195 was higher in one-year-old coconut. Moreover, the expression of CnMYB70, CnMYB2, and CnMYB2/158 was high under nitrogen deficiency, drought, and salinity stress, respectively. The predicted secondary and tertiary structures of three key CnMYB proteins involved in abiotic stress revealed distinct inter-proteomic features. The predicted interaction between CnMYB2/158 and Hsp70 supports its role in coconut’s drought and salinity stress responses. These results expand our understanding of the relationships between the evolution and function of MYB genes, and provide valuable insights into the MYB gene family’s role in abiotic stress in coconut. Full article

Talaromyces sp. DC2 is an endophytic fungus that was isolated from the stem of Catharanthus roseus (L.) G. Don in Hanoi, Vietnam and is capable of producing vinca alkaloids. This study utilizes the PacBio Sequel technology to completely sequence the whole genome of Talaromyces sp. DC2The genome study revealed that DC2 contains a total of 34.58 Mb spanned by 156 contigs, with a GC content of 46.5%. The identification and prediction of functional protein-coding genes, tRNA, and rRNA were comprehensively predicted and highly annotated using various BLAST databases, including non-redundant (Nr) protein sequence, Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), Clusters of Orthologous Groups (COG), and Carbohydrate-Active Enzymes (CAZy) databases. The genome of DC2 has a total of 149, 227, 65, 153, 53, and 6 genes responsible for cellulose, hemicellulose, lignin, pectin, chitin, starch, and inulin degradation, respectively. The Antibiotics and Secondary Metabolites Analysis Shell (AntiSMASH) analyses revealed that strain DC2 possesses 20 biosynthetic gene clusters responsible for producing secondary metabolites. The strain DC2 has also been found to harbor the DDC gene encoding aromatic L-amino acid decarboxylase enzyme. Conclusively, this study has provided a comprehensive understanding of the processes involved in secondary metabolites and the ability of the Talaromyces sp. DC2 strain to degrade plant cell walls. Full article

Magnaporthe oryzae is a fungal pathogen that causes rice blast. Plant metabolites such as plant hormones and phytoalexin can promote or inhibit the rice blast infection. To study the effect of plant metabolites on M. oryzae, we selected salicylic acid (SA), abscisic acid (ABA), and a phytoalexin sakuranetin to treat M. oryzae grown on the medium. Through the analysis of transcriptome data, 185 and 38 genes, 803 and 156 genes, and 1525 and 428 genes were up- or down-regulated after SA, ABA, or sakuranetin treatment. Among these differentially expressed genes (DEGs), most of them were annotated to the cellular process and metabolic process in the biological process category and binding and catalytic activity in the molecular function category by GO analysis. According to KEGG pathway analysis, metabolism is the pathway with the highest number of DEGs, and the main enriched pathway is carbohydrate, lipid, and amino acid metabolism. In addition, we also found two ABA-induced up-regulated genes that may contribute to M. oryzae infection from the transcriptome data. We verified their expressions in M. oryzae that infected rice. Full article

A total of 81,868 All-Unigenes were sequenced and assembled by the transcriptome in the dorsal skin, the lateral skin, and the peritoneal wall layer of Triplophysa stenura with a total assembly length of 123,827,585 bp, and 68,750 unigenes were annotated to seven functional databases. A total of 588 DEGs were screened between the dorsal and lateral skin, 17,097 DEGs were screened between the dorsal skin and the peritoneal wall layer, and 16,598 DEGs were screened between the lateral skin and the peritoneal wall layer. Most of DEGs in three tissues were annotated to GO terms related to cellular structures, binding, cellular processes, and catalytic activity. They were also annotated to KEGG pathways such as the MAPK signaling pathway, PI3K-Akt signaling pathway, Wnt signaling pathway, melanogenesis, tyrosine metabolism, and cell cycle. A total of twenty-three DEGs were found to be enriched in the melanin synthesis pathway by a local Blast comparison, of which nine DEGs were significantly upregulated in the peritoneal wall layer and six DEGs were significantly upregulated in the dorsal and lateral skin. The results suggest that these genes may be associated with the molecular mechanism of melanin synthesis in T. stenura, and the differential regulation of genes may be related to the differences in UVR intensity and tissue sites of melanin synthesis. Further investigation is needed on how these genes specifically regulate melanin synthesis. Full article

Tea is an important cash crop worldwide, and its nutritional value has led to its high economic benefits. Tea anthracnose is a common disease of tea plants that seriously affects food safety and yield and has a far-reaching impact on the sustainable development of the tea industry. In this study, phenotypic analysis and pathogenicity analysis were performed on knockout and complement strains of HTF2—the transcriptional regulator of tea anthracnose homeobox—and the pathogenic mechanism of these strains was explored via RNA-seq. The MoHox1 gene sequence of the rice blast fungus was indexed, and the anthracnose genome was searched for CfHTF2. Evolutionary analysis recently reported the affinity of HTF2 for C. fructicola and C. higginsianum. The loss of CfHTF2 slowed the vegetative growth and spore-producing capacity of C. fructicola and weakened its resistance and pathogenesis to adverse conditions. The transcriptome sequencing of wild-type N425 and CfHTF2 deletion mutants was performed, and a total of 3144 differentially expressed genes (DEGs) were obtained, 1594 of which were upregulated and 1550 of which were downregulated. GO and KEGG enrichment analyses of DEGs mainly focused on signaling pathways such as the biosynthesis of secondary metabolites. In conclusion, this study lays a foundation for further study of the pathogenic mechanism of tea anthracnose and provides a molecular basis for the analysis of the pathogenic molecular mechanism of CfHTF2. Full article

The necessity to understand plant adaptations to environmental stressors is underscored by the role of polyploidy in species evolution. This study focuses on the superior stress resistance exhibited by autotetraploid rice, which arises from chromosome doubling, in comparison to its diploid donor. We provide a quantitative analysis that highlights the differing susceptibilities of diploid (GFD-2X) and autotetraploid (GFD-4X) rice to rice blast disease, with GFD-2X being significantly more susceptible. Our investigation centers on transcription factors (TFs), which are crucial in regulating biological stress responses, by analyzing their expression in the face of a pathogen attack. This study uncovers variations in the number and expression timing of differentially expressed TF genes, providing a quantitative view of GFD-4X’s resistance. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses confirm the role of specific pathways, including “response to stimulus” and the “MAPK signaling pathway,” in resistance mechanisms. An extensive analysis of protein–protein interaction networks further clarifies the complex role of TFs during stress responses. The rationale for our experimental approach is rooted in the imperative to decipher the molecular basis of disease resistance across different ploidies, which has implications for crop enhancement. The conclusion from our research is that autotetraploid rice has a unique and more effective defense response regulation system, facilitated by transcription factors, when faced with rice blast disease. This finding provides a foundation for future genetic strategies aimed at improving crop resistance. Full article

Parasitic nematodes and their products are promising candidates for therapeutics against inflammatory bowel diseases (IBD). Two species of nematodes, the hookworm Necator americanus and the whipworm Trichuis suis, are being used in clinical treatment trials of IBD referred to as “helminth therapy”. Heligmosomoides polygyrus is a well-known model for human hookworm infections. Excretory–secretory (ES) products of H. polygyrus L4 stage that developed during colitis show a different immunomodulatory effect compared to the ES of H. polgyrus from healthy mice. The aim of the study was to evaluate excretory–secretory proteins produced by H. polygyrus L4 stage males and females that developed in the colitic milieu. Mass spectrometry was used to identify proteins. Blast2GO was used to investigate the functions of the discovered proteins. A total of 387 proteins were identified in the ES of H. polygyrus L4 males (HpC males), and 330 proteins were identified in the ES of L4 females that developed in the colitic milieu (HpC females). In contrast, only 200 proteins were identified in the ES of L4 males (Hp males) and 218 in the ES of L4 females (Hp females) that developed in control conditions. Most of the proteins (123) were detected in all groups. Unique proteins identified in the ES of HpC females included annexin, lysozyme-2, apyrase, and galectin. Venom allergen/Ancylostoma-secreted protein-like, transthyretin-like family proteins, and galectins were found in the secretome of HpC males but not in the secretome of control males. These molecules may be responsible for the therapeutic effects of nematodes in DSS-induced colitis. Full article