Mildew Resistance Research Articles

Accurately Identifying Sound vs. Rotten Cranberries Using Convolutional Neural Network

Cranberries, native to North America, are known for their nutritional value and human health benefits. One hurdle to commercial production is losses due to fruit rot. Cranberry fruit rot results from a complex of more than ten filamentous fungi, challenging breeding for resistance. Nonetheless, our collaborative breeding program has fruit rot resistance as a significant target. This program currently relies heavily on manual sorting of sound vs. rotten cranberries. This process is labor-intensive and time-consuming, prompting the need for an automated classification (sound vs. rotten) system. Although many studies have focused on classifying different fruits and vegetables, no such approach has been developed for cranberries yet, partly because datasets are lacking for conducting the necessary image analyses. This research addresses this gap by introducing a novel image dataset comprising sound and rotten cranberries to facilitate computational analysis. In addition, we developed CARP (Cranberry Assessment for Rot Prediction), a convolutional neural network (CNN)-based model to distinguish sound cranberries from rotten ones. With an accuracy of 97.4%, a sensitivity of 97.2%, and a specificity of 97.2% on the training dataset and 94.8%, 95.4%, and 92.7% on the independent dataset, respectively, our proposed CNN model shows its effectiveness in accurately differentiating between sound and rotten cranberries.

Targeting Candida albicans O-acetyl-L-homoserine sulfhydrylase (Met15p) in antifungal treatment.

Fungal infections are a serious threat to public health as they are becoming increasingly frequent. A major problem stems also from a rising fungal resistance to currently available antifungal therapies, therefore novel molecular targets are highly desirable. Exploration of enzymes participating in the biosynthesis pathways of essential amino acids such as L-methionine (L-Met) may provide new insights into pharmaceutical development. The MET15 gene from Candida albicans, encoding O-acetyl-L-homoserine sulfhydrylase (Met15p), an enzyme catalyzing the second step in that pathway, was cloned and expressed in two versions: as N and C-terminal oligo-His-tagged fusion proteins. The recombinant enzymes revealed appropriate activity, and catalyzed conversion of O-acetyl-L-homoserine and a sulfide ion to produce L-homocysteine. A new RP-HPLC-DAD method, using the enzymatic reaction product pre-column derivatization with 5,5'-dithio-bis-(2-nitrobenzoic acid) was developed and used by us to determine Met15p activity. Newly synthesized compounds as well as two commercially available exhibited a Met15p inhibitory effect which was related to antifungal activity. Fungal cells' sensitivity to inhibitors depending on the presence or absence of L-Met in the medium clearly indicated Met15p targeting. Moreover, the synergistic effect of the first methionine biosynthetic enzyme affecting inhibitor and Met15p inhibitors indicate that methionine biosynthesis pathway enzymes are promising molecular targets.

Structural variation in the pangenome of wild and domesticated barley.

Pangenomes are collections of annotated genome sequences of multiple individuals of a species1. The structural variants uncovered by these datasets are a major asset to genetic analysis in crop plants2. Here we report a pangenome of barley comprising long-read sequence assemblies of 76 wild and domesticated genomes and short-read sequence data of 1,315 genotypes. An expanded catalogue of sequence variation in the crop includes structurally complex loci that are rich in gene copy number variation. To demonstrate the utility of the pangenome, we focus on four loci involved in disease resistance, plant architecture, nutrient release and trichome development. Novel allelic variation at a powdery mildew resistance locus and population-specific copy number gains in a regulator of vegetative branching were found. Expansion of a family of starch-cleaving enzymes in elite malting barleys was linked to shifts in enzymatic activity in micro-malting trials. Deletion of an enhancer motif is likely to change the developmental trajectory of the hairy appendages on barley grains. Our findings indicate that allelic diversity at structurally complex loci may have helped crop plantsto adapt to new selective regimes in agricultural ecosystems.

Correlation and Regression Analyses of Disease and Agronomic Traits of Ethiopian Mustard (Brassica Carinata A. Braun.) Genotypes

Ethiopian mustard (<i>Brassica carinata A. Braun</i>) is an important oilseed crop with significant potential for food and energy production. The study evaluated 36 genotypes using a 6 x 6 lattice design to analyze correlations and regression among traits, aiming to understand their relationships and identify key traits for developing high-performing varieties. The analysis of variance revealed significant variation (p < 0.001) for traits including seed yield, flowering time, maturity date, disease resistance, thousand seed weight, oil content and oil yield; indicating the potential for genetic improvement. However, traits such as downy mildew resistance, leaf spot and branching showed non-significant variation, suggesting these traits may be more influenced by environmental factors than by genetic differences among the genotypes. Pearson correlation coefficients highlighted significant relationships among traits. Days to flowering (r = 0.687) and maturity (r = 0.029) positively correlated with yield, while disease traits negatively impacted seed yield. Notably, Thousand Seed Weight (r = 0.985) strongly correlated with yield, underscoring the importance of seed size. A multiple regression model explained 99.7% of the variation in seed yield, with a highly significant intercept (1863.35, p < 0.001). Key associations were found with secondary branches (12.32), oil content (-46.79) and oil yield (2.19). This study confirms the potential for improving Ethiopian mustard yield through genetic selection of key traits. It is recommended that breeding programs focus on enhancing seed size and disease resistance while considering environmental factors to maximize yield potential.

Genome‐wide association study for powdery mildew resistance in CIMMYT's spring wheat germplasm

AbstractPowdery mildew (PM), caused by Blumeria graminis f. sp. tritici (Bgt), is a foliar disease of wheat (Triticum aestivum) that adversely affects both grain yield and quality. Growing resistant cultivars offers an effective and environmentally sustainable solution to managing PM. However, relying on the same genetic source of resistance can lead to resistance breakdown as Bgt isolates rapidly evolve. To mitigate this, identifying novel resistance sources is crucial. In this study, 225 diverse wheat genotypes were evaluated at adult plant stage in disease nurseries over the three crop seasons (2018/2019, 2019/2020 and 2020/2021). Using disease and genotyping data from 12,160 single‐nucleotide polymorphism (SNP) markers, a genome‐wide association study (GWAS) was conducted to identify novel resistance loci. We identified 22 marker loci significantly (at p < 0.005) associated with PM resistance, distributed across 14 wheat chromosomes (1A, 1B, 1D, 2A, 2B, 2D, 3A, 3B, 4A, 4B, 5D, 6A, 7A and 7B). Of these, seven loci overlap with previously identified regions, while the remaining 15 loci represent novel regions reported for the first time in this study. The identified SNP markers have significant potential for wheat breeding programmes, as they can accelerate the development of PM‐resistant cultivars through marker‐assisted selection.

Repurposing of Statins Against Superficial Fungal Infections

In a few decades fungal infections will become a major worldwide health concern. Research reveal that the fungal strain becomes resistant to current medications in cases of HIV infections, corona infections and environmental factors particularly in people with impaired immune systems. The amount of organ transplants and medication used for therapy all have contributed to an increase in the immunocompromised population. The fungal infections are becoming a more significant cause of mortality and morbidity. An estimated 1.5 million fatal consequences are caused by fungal pathogens annually. In a few decades, fungal infections will become a major worldwide health concern, so that unprecedented rates of fungal resistance to currently available antifungal medicines has been observed.The drug repurposing approaches lowers costs and time by investigating previously approved medicines with known safety and pharmacokinetics toxicity profile for novel therapeutic effects.The HMG – CoA reductase inhibitors drugs statins shows antifungal properties against tinea spp. group of common fungus that causes superficial infections. We have evaluated statins for their antifungal potential by insilico studies & Invitro studies & validate results with standard drugs itraconazole & ketoconazole.The docking studies shows highest binding energy shown by atorvastatin among all statin were used for docking studies pravastatin , atorvastatin, simavastatin ,fluvastatin & rosuvastatin . against fungal protein (PDB ID:5V5Z) & human protein (PDB ID: 3LD6) was found to be -13.52 &13.4 kcal/mole .The invitro studies shows MIC values for atorvastatin against Trichophyton rubrum , Microsporum canis & Epidermatophyton flocossum fungal strains found between 125 μg/ml to 150 125 μg/ml where as for standard drugs was found between 12.5 μg/ml to 25 μg/ml. Following insilico & invitro research atorvastatin determined and may be used for the treatment of fungal infections.

A newly identified photosystem II Subunit P gene TaPsbP4A-1 in Triticeae species negatively regulates wheat powdery mildew resistance

The photosystem II (PSII) Subunit P (PsbP) protein is a component of its oxygen-evolving complex, which can oxidize water to produce oxygen using light energy and is critical to the core components and stability of PSII. Using the whole-genome information, the PsbP genes of 10 plant species were comprehensively identified. The expression patterns of wheat PsbPs under Blumeria graminis f. sp. tritici (Bgt) infection were assessed using qRT-PCR, and the functions of TaPsbPs in wheat powdery mildew resistance were studied using barley stripe mosaic virus-induced gene silencing. In total, 122 PsbP genes were divided into 8 classes with similar gene structures. No tandem repeat events were identified in wheat PsbP, suggesting that the PsbP genes in common wheat were donated by its diploid progenitor species. The expression levels of TaPsbP2A-1, TaPsbP3A-1, TaPsbP4A-1, TaPsbP4A-2, and TaPsbP7A-2 were induced by Bgt. The silencing of TaPsbP4A-1 increased the resistance of common wheat ‘Bainong AK58’ to Bgt. This study provides valuable information for functional and evolutionary research on the PsbP gene family.

Sugar beet root susceptibility to storage rots and downregulation of plant defense genes increases with time in storage

Storage rots are a significant cause of postharvest losses for the sugar beet crop, however, intrinsic physiological and genetic factors that determine the susceptibility of roots to pathogen infection and disease development are unknown. Research, therefore, was carried out to evaluate the disease development in sugar beet roots caused by two common storage pathogens as a function of storage duration and storage temperature, and to identify changes in the expression of defense genes that may be influencing the root susceptibility to disease. To evaluate root susceptibility to disease, freshly harvested roots were inoculated with Botrytis cinerea or Penicillium vulpinum on the day of harvest or after 12, 40, or 120 d storage at 5 or 12 °C and the weight of rotted tissue present in the roots after incubation for 35 d after inoculation were determined. Disease susceptibility and progression to B. cinerea and P. vulpinum increased with storage duration with elevations in susceptibility occurring more rapidly to B. cinerea than P. vulpinum. Also, B. cinerea was more aggressive than P. vulpinum and caused greater rotting and tissue damage in postharvest sugar beet roots. Storage temperature had minimal effect on root susceptibility to these rot-causing pathogens. Changes in defense gene expression were determined by sequencing mRNA isolated from uninoculated roots that were similarly stored for 12, 40 or 120 d at 5 or 12 °C. As susceptibility to rot increased during storage, concurrent changes in defense-related gene expression were identified, including the differential expression of 425 pathogen receptor and 275 phytohormone signal transduction pathway-related genes. Furthermore, plant resistance and hormonal signaling genes that were significantly altered in expression coincident with the change in root susceptibility to storage rots were identified. Further investigation into the function of these genes may ultimately elucidate methods by which storage rot resistance in sugar beet roots may be improved in the future.

Preparation of tannic acid-based recyclable adhesive with high adhesion property, low curing temperature, and environmental tolerance

Tannin-based adhesives have demonstrated promise in decreasing dependence on petrochemical resources linked to formaldehyde-based resins. However, current tannin-based adhesives face challenges due to the incorporation of expensive or toxic reagents such as isocyanate, epoxy, and formaldehyde, as well as the inability to be recycled. This study presents a simple and eco-friendly approach for producing a tannic acid-based recyclable adhesive (TA-BVB) by employing tannic acid and 1,4-butanediol divinyl ether through acetal reactions. The resulting adhesive can be cured at a low temperature of 70℃ and demonstrated high bonding strength on wood and aluminum sheets, measuring 4.45 MPa and 5.44 MPa, respectively. Notably, the adhesive maintained its adhesion strength even under harsh conditions, including high temperatures (100℃), liquid nitrogen (-196℃), and exposure to various solvents. Moreover, the adhesive showcased excellent reusability, retaining over 100 % and 86 % of bonding strength after the first and second rounds of hot pressing, respectively. This adhesive can be repaired using infrared laser irradiation and displayed remarkable mold resistance. This research underscores the potential of tannic acid in developing environmentally friendly, high-performance, recyclable adhesives with versatile applications.

Combating Fungal Infections and Resistance with a Dual-Mechanism Luminogen to Disrupt Membrane Integrity and Induce DNA Damage.

Antifungal drug resistance is a critical concern, demanding innovative therapeutic solutions. The dual-targeting mechanism of action (MoA), as an effective strategy to reduce drug resistance, has been validated in the design of antibacterial agents. However, the structural similarities between mammalian and fungal cells complicate the development of such a strategy for antifungal agents as the selectivity can be compromised. Herein, we introduce a dual-targeting strategy addressing fungal infections by selectively introducing DNA binding molecules into fungal nuclei. We incorporate rigid hydrophobic units into a DNA-binding domain to fabricate antifungal luminogens of TPY and TPZ, which exhibit enhanced membrane penetration and DNA-binding capabilities. These compounds exhibit dual-targeting MoA by depolarizing fungal membranes and inducing DNA damage, amplifying their potency against fungal pathogens with undetectable drug resistance. TPY and TPZ demonstrated robust antifungal activity in vitro and exhibited ideal therapeutic efficacy in a murine model of C. albicans-induced vaginitis. This multifaceted approach holds promise for overcoming drug resistance and advancing antifungal therapy.

Quantitative Trait Loci Mapping for Powdery Mildew Resistance in Wheat Genetic Population

Background/Objectives: Powdery mildew is a prevalent wheat disease that affects yield and quality. The characterization and fine mapping of genes associated with powdery mildew resistance can benefit marker-assisted breeding. Methods: In this study, quantitative trait loci (QTL) associated with powdery mildew were mapped using a high-density 35K DArT genetic linkage map developed from a population of double haploid lines (DHs) created by crossing “Jinmai 33 (a highly resistance line) with Yannong 19 (a highly susceptible line)”. Results: Three stable QTLs for powdery mildew were identified on chromosomes 1B, 2B, and 6A combined with the composite interval graphing method and multiple interval mapping, explaining phenotypic variations (PVE) that range from 4.98% to 13.25%. Notably, Qpm.sxn-1B and Qpm.sxn-2B were identified across three environments, with the PVE ranging from 9.37% to 13.25% and from 4.98% to 5.23%, respectively. The synergistic effects of these QTLs were contributed by the parental line “Jinmai 33”. Qpm.sxn-1B was the major stable QTL, and Qpm.sxn-2B was close to Pm51. Furthermore, Qpm.sxn-6A was identified in two environments, accounting for PVE values of 7.13% and 7.65%, respectively, with the resistance effects originating from the male parent. Remarkably, this locus has not been reported previously, indicating that Qpm.sxn-6A represents a newly dis-covered QTL governing powdery mildew genes. Conclusions: Five molecular markers available for mark-er-assisted selection were selected for tracking Qpm.sxn-1B and Qpm.sxn-2B in the program. The identification of this novel newly discovered QTL and markers reported in this study will be useful for marker-assisted selection of powdery mildew resistance.

Phased T2T genome assemblies facilitate the mining of disease-resistance genes in Vitis davidii

Abstract Grape is an important fruit crop, and its production faces significant threat from diseases, resulting in substantial economic loss. Wild grape relatives are valuable resources for the restoration of disease-resistance loci. However, available resistance loci in wild grape genomes remain largely unexplored. In this study, we assembled two phased genomes, including a high resistant Chinese wild grape, Vitis davidii Föex, and a susceptible cultivar, V. vinifera L. cv. “Manicure Finger”. We detected a total of 36,688 structural variations (SVs), with the genes associated with heterozygous SVs showing an enrichment in allele-specific expression (ASE). Furthermore, we identified eight subgroups of R genes and found that 74.2% of R genes overlap with transposable elements (TEs). Among R genes, NBS-type genes exhibit higher expression profiles in the wild grape genome compared with those in the grape cultivar. Additionally, five specific NBS-type R gene clusters were identified in the wild grape genome that are absent in the cultivar. Through genetic mapping, we identified four quantitative trait loci (QTLs) associated with grape white rot resistance based on the Vitis davidii genome, within which six NBS-type R genes exhibit differential expression between wild and cultivated grapes. Overall, our study revealed the landscape of resistance genes in grape genomes, providing valuable genetic resources for further breeding programs.

Transcription-Aided Selection (TAS) for Crop Disease Resistance: Strategy and Evidence

A transcription-aided selection (TAS) strategy is proposed in this paper, which utilizes the positive regulatory roles of genes involved in the plant immunity pathways to screen crops with high disease resistance. Increased evidence has demonstrated that upon pathogen attack, the expression of diverse genes involved in salicylic acid (SA)-mediated SAR are differentially expressed and transcriptionally regulated. The paper discusses the molecular mechanisms of the SA signaling pathway, which plays a central role in plant immunity, and identifies differentially expressed genes (DEGs) that could be targeted for transcriptional detection. We have conducted a series of experiments to test the TAS strategy and found that the level of GmSAGT1 expression is highly correlated with soybean downy mildew (SDM) resistance with a correlation coefficient R2 = 0.7981. Using RT-PCR, we screened 2501 soybean germplasms and selected 26 collections with higher levels of both GmSAGT1 and GmPR1 (Pathogenesis-related proteins1) gene expression. Twenty-three out of the twenty-six lines were inoculated with Peronospora manshurica (Pm) in a greenhouse. Eight showed HR (highly resistant), four were R (resistant), five were MR (moderately resistant), three were S (susceptible), and three were HS (highly susceptible). The correlation coefficient R2 between the TAS result and Pm inoculation results was 0.7035, indicating a satisfactory consistency. The authors anticipate that TAS provides an effective strategy for screening crops with broad-spectrum and long-lasting resistance.

Applications of Nanotechnology in Combating Fungal Diseases in Humans: An Updated Review

In recent years, fungal infections caused by filamentous fungi have posed a serious threat to public health worldwide. Fungi such as Aspergillus, Coccidioides, and Mucorales (the most common filamentous fungi), as well as Candida auris (a non-filamentous fungus), can cause infections in humans. It can cause serious life-threatening diseases in individuals with weakened immune systems, patients infected with HIV/AIDS, uncontrolled diabetes, blood disorders, organ transplants, and chemotherapy. In this review, we describe the available nan formulations (metallic and polymeric nanoparticles) that have been developed to enhance efficacy and reduce the number of adverse effects following the administration of conventional antifungals. The burden posed by fungal infections on human health is increasing worldwide. Fungi such as Aspergillus, Candida, and Cryptococcus are among the most common pathogens responsible for human diseases, accounting for over 90% of infection-related deaths. Moreover, effective antifungal treatments are not available, primarily due to host toxicity, pathogen resistance, and immunodeficiency. In recent years, nanomaterials have proven to be not only more efficient antifungal therapeutic agents but also capable of overcoming fungal drug resistance".

Response to oxalic acid: an important supplement screening against stem rot resistance in groundnut (Arachis hypogaea L.)

BackgroundStem rot, caused by the soil-borne pathogen Sclerotium rolfsii, pose a serious challenge in the groundnut (Arachis hypogaea L) cultivation. Although this disease is widespread globally but had most adverse impact in groundnut growing regions of United States, India, and Australia. The pathogen primarily targets the crown region of the plant, resulting in systemic collapse and potentially leading to yield losses up to 80%. Effective genetic control measures are essential to mitigate the impact of this disease on groundnut production. Realizing the time and resource-consuming complex field-based phenotyping, the availability of easy and repeatable phenotyping methods may fasten the process of donor and gene discovery efforts.ResultsMulti-season phenotyping was performed for stem rot on 184 minicore germplasm accessions, including checks, under two conditions: sick field screening and response to oxalic acid assay. This study demonstrated medium to high heritability (52–63% broad-sense heritability) and significant environmental influence (36%). The response to the oxalic acid assay showed a high proportion of similarity (approximately 80%) with the percent mortality observed in the sick field indicating an easy way of performing precise phenotyping. Notably, seven genotypes—ICG163, ICG721, ICG10479, ICG875, ICG11457, ICG111, and ICG2857—exhibited stable resistance, with less than 30% mortality against stem rot disease. Among these, ICG163, ICG875, and ICG111 displayed low mortality and consistent stability across multiple seasons in both the sick field and controlled conditions of the oxalic acid assay.ConclusionsThe oxalic acid assay developed in this study effectively complements field phenotyping, as a reliable method for assessing stem rot resistance. Seven resistant genotypes identified through this assay can be utilized for the introgression of stem rot resistance into elite genotypes. Given the significant influence of the environment on stem rot resistance, it is essential to implement multi-season phenotyping to obtain precise results. Furthermore, the response to oxalic acid serves as a valuable supplement to traditional field phenotyping, since maintaining uniform disease pressure during field screenings is often challenging.

Identification of powdery mildew resistance quantitative trait loci in melon and development of resistant near-isogenic lines through marker-assisted backcrossing

BackgroundMelon (Cucumis melo L.), an important cucurbit crop, faces production limitations due to powdery mildew (PM). Developing resistant varieties offers a sustainable, genetics-based alternative to chemical treatments. Therefore, identifying PM resistance quantitative trait loci (QTL) and creating trait-associated markers are essential for efficient melon PM resistance improvement through marker-assisted backcrossing (MABC).ResultsThree F2 populations, A6, B2, and C4, were generated for QTL mapping of PM resistance. Major QTL were identified on chromosome 2 in A6, chromosome 5 in B2, and chromosomes 5 and 12 in C4. A series of TaqMan® assays targeting regions on chromosomes 2, 5, and 12 were developed and validated for foreground and recombinant selection, complemented by the double digest restriction-site associated DNA genotyping system to evaluate the recurrent parent genome recovery. Three MABC programs using resistant donor parents from A6 and C4 crossed with elite susceptible recurrent parents with green and orange fruit flesh were implemented. After two to three cycles of MABC, individual QTL was successfully introgressed into elite genetic backgrounds, giving six PM resistance lines in each green- and orange-fleshed background. PM inoculation on the twelve near-isogenic lines confirmed their resistance to PM.ConclusionsWe have identified major PM resistance QTL for melon on chromosomes 2, 5, and 12 and have introgressed individual QTL to elite genetic backgrounds using MABC in three and a half years. This study demonstrates the power of combining high-throughput genotyping with breeding efforts and showcases the efficiency of molecular breeding.

Facile preparation of bamboo with improved hydrophobicity, dimensional stability and mold resistance by paraffin/tung oil modification

Facile preparation of bamboo with improved hydrophobicity, dimensional stability and mold resistance by paraffin/tung oil modification

Population structure and markers analysis associated with powdery mildew resistance in pumpkin, Cucurbita pepo L

Pumpkin (Cucurbita pepo L.) is an economically important vegetable and summer crop. The seeds have high nutritional value due to their edible oil and protein content with a high medicinal value. Pumpkin is attacked by several fungal diseases; one of which is powdery mildew (PM) caused by Podosphaera xanthii race-0. PM causes severe disease on pumpkin leading to major yield losses globally. In this study, we analyzed the genetic diversity and population structure of fourteen local pumpkin cultivars, all under Cucurbita pepo L. based on dominance in the region using 15 Inter-Simple-Sequence-Repeats-(ISSR) primer-pairs in association with resistance against PM as well as regulating the expression of three resistant marker genes i.e. SGT1, bHLH and PSK via qRT-PCR at three stages with 10 days' interval post-inoculation-stages-(SPI) with the powdery mildew agent, P. xanthii race-0. The results showed that ISSR markers demonstrated 13 primers out of 15 primers generated 169 distinct amplified bands, out of which 143 bands showed polymorphism. The mean polymorphism information content (PIC), marker index (MI), effective-number of alleles (I), expected heterozygosity (H), and Nei's gene diversity parameters were 0.354, 3.344, 0.334, 0.205 and 0.200, respectively. According to PIC, MI, I, H, and Nei indices evaluation, ISSR10 primer had the best performance in genetic diversity of the related pumpkin population. NTSYS pc 2.02e software and several similarity coefficients (r = 0.964), placed the related genotypes into five distinct groups. Of which, ‘Maragheh1′ and ‘Shahreza’ as resistant ones with 9.4 % and 6.1 % disease severity (DS), and ‘Gorgan’, ‘Urmia1′ and 3 and ‘Maragheh3’ with 79.6–84.8 % DS, as susceptible ones into two distinct groups, respectively. Further, the marker genes SGT1, bHLH and PSK expression level changes showed that the effect of variable factors including different genotypes (susceptible and resistant), disease-causing fungus, SPI, and the mutual effect of these factors is significant with the highest increase in resistant genotypes. Considering the relative compatibility in the classification of pumpkin genotypes in the dendrograms of DS and ISSR markers, it can be expected that increasing the number of markers in evaluating the genetic diversity of these genotypes makes it possible to differentiate pumpkin genotypes resistant and susceptible to PM disease based on the degree of disease resistance. The markers associated with resistance are recommended for use in marker assisted breeding.

Dynamic covalent bonds enabled recyclable chitosan oligosaccharide-based wood adhesive with high adhesion and anti-mildew performances

Biomass wood adhesives have emerged as a promising alternative to traditional synthetic resins due to their ability to address issues related to formaldehyde pollution and reliance on petrochemical resources. However, these adhesives are generally not recyclable and require high curing temperatures. Herein, a novel eco-friendly, strong, and recyclable chitosan oligosaccharide (CS)-based wood adhesive named CS-PB was developed using CS, lignin-derived 3,4-dihydroxybenzaldehyde, and 1,4-phenylenediboronic acid. The cohesive strength and recyclability of the adhesive were significantly enhanced by the dynamic borate ester and imine networks formed through catalyst-free covalent cross-linking. The adhesive exhibited a maximum bonding strength of 5.60 MPa, surpassing many synthetic and biomass adhesives. Moreover, the recycled adhesive retained 88 % of its original strength. Even under extreme conditions such as 100 °C, −196 °C the CS-PB adhesive can still maintain high bonding strength. Notably, the CS-PB adhesive demonstrated low-temperature curing properties, achieving a high bonding strength of 5.21 MPa when cured at 90 °C, since imine bonds can be formed under mild conditions. Furthermore, the adhesive displayed excellent mildew resistance attributed to the synergistic effects of amino, boronic acid, and benzene rings. The proposed straightforward design strategy provides valuable insights for constructing high-strength and recyclable biomass adhesives.

Study on the water and mold resistance of ZnO/polyurethane superhydrophobic coating on circuit boards

In this work, superhydrophobic coatings were prepared on circuit boards based on the susceptibility of circuit boards to harsh environments such as humidity and mold adhesion, leading to reduced service life. Firstly, cetyltrimethoxysilane and γaminopropyltriethoxysilane were used to modify zinc oxide nanoparticles with different particle sizes. Then polyurethane and modified nanoparticles were successively sprayed on the circuit boards with a spraying process, and the superhydrophobic coatings were finally produced. The impact of the zinc oxide mass ratio with different particle sizes, silane coupling agent content, and surface modifier content on the hydrophobicity of the coatings were investigated. The results show that when the mass ratio of zinc oxide (30nm) to zinc oxide (90nm) is 1:1, the silane coupling agent content is 12‰. The surface modifier content is 12‰, the hydrophobicity of the coating is the best, and its CA can be up to 169.5°, and its SA can be up to 2.8°. It exhibits good protection of circuit boards in the tests of adhesion, acid, and alkali corrosion resistance, self-cleaning performance, and anti-mold performance. Performance, so that the coating is in the future field of electronic equipment applications.