Cell Wall Degradation Research Articles

Genomic Sequencing and Functional Analysis of the Ex-Type Strain of Malbranchea zuffiana.

Malbranchea is a genus within the order Onygenales (phylum Ascomycota) that includes predominantly saprobic cosmopolitan species. Despite its ability to produce diverse secondary metabolites, no genomic data for Malbranchea spp. are currently available in databases. Therefore, in this study, we obtained, assembled, and annotated the genomic sequence of the ex-type strain of Malbranchea zuffiana (CBS 219.58). For the genomic sequencing, we employed both the Illumina and PacBio platforms, followed by hybrid assembly using MaSuRCA. Quality assessment of the assembly was performed using QUAST and BUSCO tools. Annotation was conducted using BRAKER2, and functional annotation was completed with InterProScan. The resulting genome was of high quality, with a size of 26.46 Mbp distributed across 38 contigs and a BUSCO completion rate of 95.7%, indicating excellent contiguity and assembly completeness. A total of 8248 protein-encoding genes were predicted, with functional annotations assigned to 73.9% of them. Moreover, 82 genes displayed homology with entries in the Pathogen Host Interactions (PHI) database, while 494 genes exhibited similarity to entries in the Carbohydrate-Active Enzymes (CAZymes) database. Furthermore, 30 biosynthetic gene clusters (BGCs) were identified, suggesting significant potential for the biosynthesis of diverse secondary metabolites. Comparative functional analysis with closely related species unveiled a considerable abundance of domains linked to enzymes involved in keratin degradation, alongside a restricted number of domains associated with enzymes engaged in plant cell wall degradation in all studied species of the Onygenales. This genome-based elucidation not only enhances our comprehension of the biological characteristics of M. zuffiana but also furnishes valuable insights for subsequent investigations concerning Malbranchea species and the order Onygenales.

Varying concentrations of ethephon induce antioxidant defences and cell wall degradation to regulate storage quality of fresh-cut lotus root

This study examined the impact of varying concentrations of ethephon (ET) immersion on the storage quality of fresh-cut lotus root. Compared to the 0.1%, the 0.8% and 1.6% ET groups inhibited phenolic oxidation and showed stronger antioxidant and reactive oxygen species balancing capacity during early storage, which led to better browning inhibition. During the early storage period, varying concentrations of ET treatments were inversely associated with microbial growth, and Pseudomonas as the major microorganism was significantly inhibited. During the post-storage period, the ET group exacerbated cell wall metabolism, contributed to the softening of lotus root slices. Additionally, ET stimulated enhanced respiration and reduced total soluble solids content as ET concentration increased. The heightened expression of NnERF in the late storage stage suggested a potential link to the regulation of root quality deterioration. Both browning inhibition and quality deterioration promotion exhibited gradient shifts in accordance with ET concentration. Combined with DNA affinity purification sequencing technology to identify the presence of motifs that bind specifically to ERF1B in lotus root, and screening for the possible target genes NnPL18 and NnACO that may be regulated by NnERF1B-like (104610030), it further suggests that NnERF1B-like (104610030) may mediate the process of lotus root flake softening and ethylene biosynthesis.

THE USE OF PURPLE EGGPLANT FRUIT CALYX STEM (Solanum melongena L.) AS AN ALTERNATIVE SOURCE OF LACTASE-PRODUCING LACTIC ACID BACTERIA

Lactose intolerance is a condition where body is unable to digest lactose due to an enzyme lactase deficiency in digestive system, leading to various health problems ranging from bloating, diarrhea, and abdominal pain to severe problems that can result in stunting in children. One attempt to prevent stunting due to lactose intolerance is administration of low-lactose dairy products, such as yogurt. The production of yogurt requires a starter known as lactic acid bacteria (LAB). Starter bacteria are often derived from yeast or commercially available bacteria, which are relatively expensive. This research aims to utilize waste products, namely the purple eggplant (Solanum melongena L.) stalks, as a new source of LAB for lactase enzyme production. Fermenting cow's milk using purple eggplant stalks results in yogurt. Inoculating this yogurt onto MRS Broth and MRS Agar media confirms the presence of LAB from the milk fermentation. To test the lactase enzyme, bacterial cell wall degradation is achieved using sonication, allowing for lactase enzyme testing. Characterization test for lactase enzyme is conducted at various temperatures and pH levels to determine the optimum conditions for the lactase enzyme. The optimum temperature for lactase enzyme is at 70°C with a specific enzyme activity of 0.0061 U/mg, optimum pH is 7 with a specific enzyme activity of 0.0044 U/mg. This study demonstrates that purple eggplant stalks can be utilized as a new source of LAB to produce lactase enzyme as an alternative starter bacterium for yogurt production, particularly for lactose intolerance therapy in the future.

Ethylene Promotes Fruit Softening of ‘Nanguo’ Pear via Cell Wall Degradation

Ethylene Promotes Fruit Softening of ‘Nanguo’ Pear via Cell Wall Degradation

Transcriptome and protein-protein interaction analysis reveals the tolerance of poplar to high boron toxicity regulated by transport and cell wall synthesis pathways

Soil contamination with high levels of boron (B) destroys the balance of the soil ecosystem, reduces crop yields and poses a potential threat to human health and safety. Hyperaccumulator plants such as poplar can be used to mitigate high B soil contamination and its negative effects. Despite having a certain level of understanding of the physiological response of poplars to high boron stress tolerance, the differences in boron accumulation efficiency among different clones and their underlying molecular mechanisms are still unclear. The effects of high B toxicity on growth, B accumulation and physiological parameters were investigated in this research to compare the high B tolerance and high B accumulation abilities of five poplar clones (717, SXY, NL895, 84 K, and T89). Then two poplar clones (SXY and T89) were selected, due to their differences in B content and accumulation under high B toxicity, for transcriptomic and protein-protein interactions (PPI) analysis. The plant biomass and root-to-shoot ratio were reduced, the leaves exhibited symptoms of chlorosis and shrinkage of high B stressed five poplar clones. Boron toxicity significantly decreased the net photosynthetic rates, disturbed the balance of redox, induced the accumulation of H2O2 and malondialdehyde (MDA), and caused the increase in free proline levels in roots and leaves. B accumulation was significantly increased in the high B treated new leaves. The SXY clones showed the highest B accumulation, making it a potential hyperaccumulator for B contaminated soils. The transcriptome analysis of SXY and T89 revealed differential expression of genes involved in cell wall organization, active transmembrane transporter activity, cell wall synthesis, and B transport. The analysis of PPI indicates that these proteins work together in group functions. We identified some key differentially expressed genes (DEGs) related to transport and cell wall degradation. Our findings suggest that poplar is a plant that can tolerate high levels of boron, and it is possible to select poplar clones that accumulate high levels of boron to reduce soil boron pollution. The potential candidate genes, involved in transport and cell wall synthesis, can be focused on to improve poplar tolerance to high B in future breeding programs.

Continuous pulsed electric field processing for intensification of aqueous extraction of protein from fresh green seaweed Ulva sp. biomass

The green marine macroalgae Ulva sp. can reach a high protein content and a high composition of essential amino acids. In this study, we have developed a novel device and investigated the parameters for a continuous Pulsed Electric Field (PEF) process, coupled with enzyme treatment followed by a spray drying, to facilitate the aqueous fractionation of Ulva protein. The process demonstrated 8.79 ± 0.58 (% w/w) protein extraction yield. Furthermore, the aqueous fractionation of protein exhibited a substantial 41.45% essential amino acid content and a branched amino acids composition of 17.58%. Additionally, it displayed an in vitro relative digestibility of 87.4 ± 1.36% compared to soy protein, along with a water holding capacity of 7.15 ± 0.17 g water/g sample and an oil holding capacity of 1.76 ± 0.11 g oil/g sample. These findings suggest that employing a continuous PEF process in conjunction with enzyme-induced cell wall degradation could position green marine macroalgae as an important potential source for food protein ingredients.

Genome sequencing of Elaeocarpus spp. stem blight pathogen Pseudocryphonectria elaeocarpicola reveals potential adaptations to colonize woody bark

BackgroundElaeocarpus spp. stem blight, caused by Pseudocryphonectria elaeocarpicola, is a destructive disease, which will significantly reduce the productivity and longevity of Elaeocarpus spp. plants, especially in the Guangdong Province of China. However, few information is available for P. elaeocarpicola. To unravel the potential adaptation mechanism of stem adaptation, the whole genome of P. elaeocarpicola was sequenced by using the DNBSEQ and PacBio platforms.ResultsP. elaeocarpicola harbors 44.49 Mb genome with 10,894 predicted coding genes. Genome analysis revealed that the P. elaeocarpicola genome encodes a plethora of pathogenicity-related genes. Analysis of carbohydrate-active enzymes (CAZymes) revealed a rich variety of enzymes participated in plant cell wall degradation, which could effectively degrade cellulose, hemicellulose and xyloglucans in the plant cell wall and promote the invasion of the host plant. There are 213 CAZyme families found in P. elaeocarpicola, among which glycoside hydrolase (GH) family has the largest number, far exceeding other tested fungi by 53%. Besides, P. elaeocarpicola has twice as many genes encoding chitin and cellulose degradation as Cryphonectria parasitica, which belong to the same family. The predicted typical secreted proteins of P. elaeocarpicola are numerous and functional, including many known virulence effector factors, indicating that P. elaeocarpicola has great potential to secrete virulence effectors to promote pathogenicity on host plants. AntiSMASH revealed that the genome encoded 61 secondary metabolic gene clusters including 86 secondary metabolic core genes which was much higher than C. parasitica (49). Among them, two gene cluster of P. elaeocarpicola, cluster12 and cluster52 showed 100% similarity with the mycotoxins synthesis clusters from Aspergillus steynii and Alternaria alternata, respectively. In addition, we annotated cytochrome P450 related enzymes, transporters, and transcription factors in P. elaeocarpicola, which are important virulence determinants of pathogenic fungi.ConclusionsTaken together, our study represents the first genome assembly for P. elaeocarpicola and reveals the key virulence factors in the pathogenic process of P. elaeocarpicola, which will promote our understanding of its pathogenic mechanism. The acquired knowledge lays a foundation for further exploration of molecular interactions with the host and provide target for management strategies in future research.

Melatonin extends shelf life in postharvest okra via delaying fruit softening and reducing weight loss.

Melatonin, a hormone present in animals and some plants, has garnered attention for its potential in preserving harvested produce. Softening due to changes in cell wall composition and wilting caused by weight loss are the major reasons for the loss of commercial value in postharvest okra. This study aimed to evaluate the impact of melatonin on the softening and weight loss of postharvest okra. The results revealed that the application of melatonin had a significant influence on the maintenance of fruit firmness by inhibiting the breakdown and dissolution of cell wall polysaccharides by suppressing the expression of specific genes responsible for cell wall degradation in okra. Conversely, melatonin treatment positively influenced the expression of genes involved in the synthesis of cell wall components. Furthermore, the treatment exhibited notable benefits in reducing weight loss in okra, which was accomplished by promoting the closure of stomata - the tiny pores on the surface of the fruit. Melatonin could serve as a novel approach to reduce water loss, delay fruit softening and extend the shelf life of okra. © 2024 Society of Chemical Industry.

The C2H2 Transcription Factor Con7 Regulates Vegetative Growth, Cell Wall Integrity, Oxidative Stress, Asexual Sporulation, Appressorium and Hyphopodium Formation, and Pathogenicity in Colletotrichum graminicola and Colletotrichum siamense.

The Colletotrichum genus is listed as one of the top 10 important plant pathogens, causing significant economic losses worldwide. The C2H2 zinc finger protein serves as a crucial transcription factor regulating growth and development in fungi. In this study, we identified two C2H2 transcription factors, CgrCon7 and CsCon7, in Colletotrichum graminicola and Colletotrichum siamense, as the orthologs of Con7p in Magnaporthe oryzae. Both CgrCon7 and CsCon7 have a typical C2H2 zinc finger domain and exhibit visible nuclear localization. Disrupting Cgrcon7 or Cscon7 led to a decreased growth rate, changes in cell wall integrity, and low tolerance to H2O2. Moreover, the deletion of Cgrcon7 or Cscon7 dramatically decreased conidial production, and their knockout mutants also lost the ability to produce appressoria and hyphopodia. Pathogenicity assays displayed that deleting Cgrcon7 or Cscon7 resulted in a complete loss of virulence. Transcriptome analysis showed that CgrCon7 and CsCon7 were involved in regulating many genes related to ROS detoxification, chitin synthesis, and cell wall degradation, etc. In conclusion, CgrCon7 and CsCon7 act as master transcription factors coordinating vegetative growth, oxidative stress response, cell wall integrity, asexual sporulation, appressorium formation, and pathogenicity in C. graminicola and C. siamense.

Identification and functional analysis of long non-coding RNA (lncRNA) and metabolites response to mowing in hulless barley (Hordeum vulgare L. var. nudum hook. f.)

BackgroundHulless barley (Hordeum vulgare L. var. nudum Hook. f.) is a significant cereal crop and a substantial source of forage for livestock. Long non-coding RNAs (lncRNAs) and metabolites play crucial roles in the nutrient accumulation and regeneration of hulless barley plants following mowing. The study aimed to identify differentially expressed lncRNAs and metabolites in hulless barley plants by analyzing transcriptomic and metabolomic datasets at 2 h, 24 h, and 72 h following mowing.ResultsThe study revealed that 190, 90, and 438 lncRNA genes were differentially expressed at the 2 h, 24 h, and 72 h time points compared to the non-mowing control. We identified 14 lncRNA genes—11 downregulated and 3 upregulated—showing consistently significant differential expression across all time points after mowing. These differentially expressed lncRNAs target genes involved in critical processes such as cytokinin signaling, cell wall degradation, storage protein accumulation, and biomass increase. In addition, we identified ten differentially expressed metabolites targeting diverse metabolic pathways, including plant hormones, alkaloids, and flavonoids, before and after mowing at various time points. Endogenous hormone analysis revealed that cytokinin most likely played a crucial role in the regeneration of hulless barley after mowing.ConclusionsThis study created a comprehensive dataset of lncRNAs, metabolites, and hormones in hulless barley after mowing, revealing valuable insights into the functional characteristics of lncRNAs, metabolites, and hormones in regulating plant regeneration. The results indicated that cytokinin plays a significant role in facilitating the regeneration process of hulless barley after mowing. This comprehensive dataset is an invaluable resource for better understanding the complex mechanisms that underlie plant regeneration, with significant implications for crop improvement.

Edible coating functionalized with ornamental plant extracts affect the postharvest quality of guava (Psidium guajava) during storage

Present study was carried out during 2021–23 at ICAR-Indian Agricultural Research Institute, New Delhi to investigate the efficacy of active edible coatings, incorporated with extracts from rose leaves and marigold petals in preserving the quality of mature green guava (Psidium guajava L.) cv. Allahabad Safeda during storage at both ambient (25±2°C) and cold (10±1°C) conditions. The coatings, particularly carboxy methyl cellulose combined with rose leaf extract (CMC+RL) demonstrated the highest effectiveness in minimizing per cent firmness reduction (PFR; 77.02% and 84.71%) compared to the control (89.95% and 89.73%) after 4 and 18 days of ambient and cold storage, respectively. Additionally, the coatings significantly influenced total soluble solids (TSS), total sugar content (TSC) and yellowness index (YI) showing potential in slowing down the fruit ripening. Moreover, the coatings demonstrated notable antioxidant activity with CMC+RL coating exhibited the highest activity. Furthermore, the coatings exhibited a substantial inhibitory effect on polygalactouronase (PG) activity, indicating a potential to mitigate cell wall degradation. Overall, the results highlight the promise of these biodegradable coatings as an alternative to synthetic preservatives in preserving postharvest quality and enhancing the shelf-life of guava fruits.

Physiological, biochemical, and global transcriptomic and metabolomic analyses of the effect of the antifungal compound isobavachalcone on Botrytis cinerea on cherry tomatoes

Botrytis cinerea is a major postharvest pathogen on cherry tomato (Solanum lycopersicum). In this study, isobavachalcone (IBC) exhibited inhibitory activity against fungus B. cinerea in vitro and in vivo. Morphological and ultrastructural observations were conducted revealing that IBC caused significant changes in B. cinerea, including rupturing of the cell membrane, loosening of the cell wall, swelling of mitochondria, and massive reductions in the number of ribosomes. Physiological and biochemical analyses confirmed that IBC increased the permeability of the cell wall and membrane which had led to decrease in mitochondrial membrane potential (MMP), while significant increase in reactive oxygen species (ROS) level. According to transcriptomic and metabolomic analysis, IBC inhibited the expression of chitin deacetylase (CDA), glucan 1,3-beta-glucosidase (EXG), and squalene monooxygenase (ERG1) genes, which may result in the degradation of cell wall and membrane components, ultimately increasing cell permeability. IBC also interfered with the expression of cytochrome P450 (CYP102A) and cytochrome-b5 reductase (CYB5R) genes, which had a negative impact on mitochondrial energy metabolism. Additionally, the structure of the ribosomal large subunit and small subunit were altered by IBC, thus, interfering with translation initiation and polypeptide extension. These results provide an effective alternative approach against B. cinerea on cherry tomato.

Influence of Ecological Zones on Immune Function and Viability in Sur Karakol Lambs: A Comparative Study of Mountainous and Desert-Steppe Regions

Background: The adaptation of Sur Karakol lambs to different ecological zones is crucial for their survival and productivity. This study explores the biochemical and immunological responses of lambs raised in the mountainous region of Samarkand and the desert-steppe region of Kashkadarya. The study aimed to evaluate the phagocytic, bactericidal, and lysozyme activities in the blood, along with immunoglobulin levels, to assess the immune status of lambs in these contrasting environments. Methods: Blood samples were collected from lambs aged 120-135 days to measure phagocytic activity, bactericidal activity, lysozyme activity, and immunoglobulin levels (IgA, IgM, IgG). Phagocytic activity was determined by the percentage of neutrophils engulfing bacteria, bactericidal activity by the ability of blood to kill bacteria, and lysozyme activity by the degradation of bacterial cell walls. Results: The study found that lambs in the desert-steppe region exhibited slightly higher phagocytic activity (46.5%-47.4%), bactericidal activity (50.9%-52.0%), and lysozyme activity (46.7%-49.6%) compared to those in the mountainous region. Immunoglobulin levels showed a typical pattern of increasing IgA and IgM with age, while IgG decreased, indicating a normal transition from maternal to self-generated immunity. Conclusion: The harsher conditions of the desert-steppe region appear to stimulate a stronger innate immune response in Sur Karakol lambs, enhancing their resilience and survival rates compared to lambs in the mountainous region. These findings suggest that environmental factors significantly influence the immune competence and overall vitality of lambs.

Cinnamic acid derivatives played a major role in the resistance of peach leaves to Xanthomonas arboricola pv. pruni infection

AbstractPeach bacterial shot hole is a common global disease of peach trees caused by the pathogen Xanthomonas arboricola pv. pruni (Xap). To preliminarily explore the resistance mechanism of peach bacterial shot hole, leaves of the resistant variety ‘Yanbao’ and the susceptible variety ‘Frederic’ were used as test materials. The contents of total phenols, total flavonoids and lignin were analysed after 1 day of inoculation treatment, and the activities of defence enzymes and cell wall degradation enzymes in the leaves were determined. Furthermore, the resistant substances were screened by combining broad‐target metabolomics technology and in vitro antibacterial activity. The results showed that the contents of total phenols, total flavonoids and lignin in peach leaves were related to resistance. The resistant varieties resisted infection by inhibiting the activities of polygalacturonase (PG) and pectin methyl trans‐eliminase (PMTE) produced by Xap in peach leaves and increasing the activities of 4‐coumarate:coenzyme A ligase (4CL), cinnamic acid‐4‐hydroxylase (C4H), phenylalanine ammonia lyase (PAL) and peroxidase (POD). A total of six resistant compounds were screened from 85 differential metabolites. The minimum inhibitory concentrations of methyl ferulate (MF), p‐coumaric acid (p‐CA) and methyl caffeate (MC) on Xap were 0.0625, 00625 and 0.125 mg/mL, respectively, while that of the positive control drug oxytetracycline (OTC) was 0.125 mg/mL. The antibacterial activities of MF and p‐CA were better than that of OTC, and MF was equivalent to OTC. In addition, homoeriodictyol, hesperetin and fraxin have certain antibacterial effects. Before inoculation treatment, the contents of MF, p‐CA and MC in ‘Yanbao’ were 1.13, 1.24 and 1.96 times higher than those in ‘Frederic’, respectively, while they were 1.29, 1.80 and 1.94 times after inoculation treatment, respectively. During the process of pathogen infection, MF and p‐CA in the leaves of resistant peach varieties played a role in inducing resistance, while MC was a component of resistance. The above three cinnamic acid derivatives play an important roles in the resistance of peach bacterial shot hole and are potential control drugs.

Drought-induced cell wall degradation in the base of pedicel is associated with accelerated cotton square shedding

Drought significantly impacts cotton square (flower buds with bracts) shedding, directly affecting yield. To address the internal physiological mechanisms of drought affecting cotton square shedding, a polyethylene glycol-simulated drought study was conducted with Dexiamian 1 and Yuzaomian 9110 to investigate cell wall degradation changes in the base of pedicel where the detachment of cotton square takes place, and its relationship with cotton square shedding. Results revealed significant decreases in cellulose, hemicellulose, and pectin contents in the base of square pedicel, leading to cell wall degradation and consequent square shedding. Furthermore, drought stress exacerbated the hydrolysis of cellulose and pectin in the base of pedicel, although not hemicellulose, resulting in more noticeable alterations in the morphology and structure of the base of pedicel, such as more significant degradation in the epidermis, cortex, and phloem. Regarding the cellulose hydrolysis, drought mainly increased the expression of genes β-glucosidase (GhBG1) and endoglucanase (GhEG1), and the activity of β-glucosidase and endoglucanase in the base of pedicel, promoting the conversion of cellulose to cellobiose, and eventually glucose. Regarding the pectin hydrolysis, drought significantly enhanced the expression of the gene pectin methylase (GhPE1), thereby accelerating pectin hydrolysis to generate polygalacturonic acid. Additionally, drought increased the expression of genes pectin lyase (GhPL1) and polygalacturonase (GhPG1), as well as the activity of pectin lyase, which further accelerated the hydrolysis of polygalacturonic acid into galacturonic acid. These findings suggest that drought mainly promotes cellulose and pectin hydrolysis in the base of pedicel, hastening cell wall degradation and final cotton square shedding.

Effects of glycine betaine on the postharvest quality and cell wall metabolism of Malus domestica fruit

ABSTRACT Quality decline resulting from senescence and fungal invasion is a crucial factor that impacts the economic value of fruit. The present study aimed to reveal the impacts of 10 mmol L−1 glycine betaine immersion for 10 min on cell wall degradation in ‘Qiujin’ apples during storage at ambient condition for 15 d. The results showed that glycine betaine exhibited higher levels of soluble solids content, flesh firmness, and water-insoluble pectin, while also delaying the increase in mass loss, total colouration difference, and water-soluble pectin content. Furthermore, glycine betaine effectively restrained the enzymatic activities and gene expressions of pectate lyase, pectin methylesterase, polygalacturonase, cellulase, β-galactosidase, and β-glucosidase, thereby inhibiting the reduction in water-insoluble pectin content and the formation of water-soluble pectin. These findings suggest that glycine betaine can preserve the postharvest quality of ‘Qiujin’ apples by suppressing the activity and gene expression of key enzymes involved in cell wall metabolism, as well as reducing respiratory rate and ethylene release. In conclusion, the utilisation of glycine betaine treatment may present an effective technique for alleviating softening in postharvest apples and can serve as a promising natural alternative to synthetic chemicals.

Role of methyl jasmonate in alleviating chilling injury in 'Xuxiang' kiwifruit: Insights from transcriptomic evidence

'Xuxiang' kiwifruit is highly susceptible to chilling injury (CI) during prolonged low-temperature storage, significantly impacting its storage quality and shelf life. Methyl jasmonate (MeJA) has emerged as a pivotal signaling molecule for alleviating CI in fruit. In this study, we conducted a comparative analysis of the changes in physiological and biochemical indicators and related differentially expressed genes (DEGs) through transcriptomics in kiwifruit treated with 10 μM MeJA during low-temperature storage. The results demonstrated that exogenous MeJA effectively alleviated the symptoms of CI in kiwifruit by suppressing the activity of membrane lipid peroxidation-related substances and enzymes, as well as regulating multiple genes associated with ethylene biosynthesis, cell wall degradation, plant hormone signal transduction, and relevant transcription factors. These genes were screened by cis-acting element analysis, and the physical and chemical properties of the proteins were predicted. Our study provides a theoretical basis for the physiological and biochemical mechanisms and related key genes of exogenous MeJA in alleviating the CI of kiwifruit.

Involvement of energy and cell wall metabolisms in chilling tolerance improved by hydrogen sulfide in cold-stored tomato fruits.

Hydrogen sulfide improved cold resistance of tomato fruits by regulating energy metabolism and delaying cell wall degradation, thereby alleviating the damage of cold storage on fruits. Postharvest cold storage in tomato fruits extended shelf life but caused the appearance of chilling injury (CI), appeared by softness and spots on the surface of the fruits. These changes were linked closely with energy and cell wall metabolisms. Hydrogen sulfide (H2S), as the gaseous fresh-keeping regulator, was used in the present study to investigate the effects of H2S on energy and cell wall metabolisms in tomato fruits during cold storage. Fruits after harvest were fumigated with different concentrations (0, 0.5, 1, 1.5mM) of sodium hydrosulfide (NaHS) solution as H2S honor for 24h and stored at 4°C for 25days. The results showed that 1 and 1.5mM NaHS solution fumigation promoted the accumulation of endogenous H2S, followed by the increase in L-cysteine desulfurase (LCD) and D-cysteine desulfurase (DCD) activities in fruits during cold storage. It was also found that 1 and 1.5mM NaHS treatments improved H+-ATPase, Ca2+-ATPase, cytochrome C oxidase (CCO), and succinic dehydrogenase (SDH) activities. Moreover, the contents of cellulose and hemicellulose were increased by 1 and 1.5mM NaHS, following down-regulated activities of cellulase (CL), pectin lyase (PL), α-mannosidase (α-man) and β-Galactosidase (β-Gal) and down-regulated expression of PL1, PL8, MAN4 and MAN7 genes. Thus, H2S alleviates CI led by cold storage in tomato fruits via regulating energy and cell wall metabolisms.

Thymol application delays the decline of fruit quality in blueberries via regulation of cell wall, energy and membrane lipid metabolism

In this study, we evaluated the potential for exogenous thymol to slow this decline by measuring the effects of thymol application on cell wall, energy, and membrane lipid metabolism. The results showed that thymol application improved the preservation of the total soluble solids, titratable acidity, decay rate, and anthocyanin content, and effectively inhibited the accumulation of O2·-, H2O2, and malondialdehyde in blueberries during storage. Thymol application also effectively maintained fruit firmness, cell wall structure, and energy levels, while delaying the degradation of membrane phospholipids and unsaturated fatty acids during the storage of post-harvest blueberries. Therefore, exogenous thymol can maintain the quality of blueberry fruits by regulating energy and membrane lipid metabolism and reducing cell wall degradation. Thus, thymol-treatment could be a suitable biocontrol agent for maintaining blueberry quality and extending blueberry fruit storage life.

Barley varieties registered in the Czech Republic after the harvest of 2023

After the 2023 harvest, four varieties of spring barley were registered in the Czech Republic. The malting quality was determined in three varieties. After four years of testing, LG Tuplak was registered. After three years of testing, the spring barley varieties LG Lokal, Sting, and the non-malting variety Ranee were registered. LG Tuplak and LG Lokal showed low activity of proteolytic and cytolytic enzymes and a low level of apparent final attenuation and thus fulfilled the conditionsfor varieties recommended for the production of beer with the protected geographical indication 'České pivo'. The spring barley variety Sting showed very good malting quality. It provided a sweet wort with a rich extract content in malt dry matter (above 83%). Proteolytic modification was optimal to higher in this variety. Cell wall degradation was at an optimal level in the Sting variety. The varieties tested gave clear to opalescent sweet wort.