Search

Peanut (Arachis hypogaea L.) holds significant commercial and dietary importance as a major source of edible oil and protein in Turkey. Stem, collar or root rot, caused by several fungal disease agent, are serious soil-borne diseases of peanut. Accurate and precise identification of the disease agent provides fundamental and precise information for integrated plant management. During the period from June to September 2021, symptoms consistent with collar rot disease, including dark-brown stem rot, chlorotic leaves, wilting, and eventual whole plant death, were observed on peanut plants cultivated in the different districts of Osmaniye Province of Turkey. The disease incidence ranged from 8.0 to 45.0% in the inspected fields with an average of 3.4% overall. Twenty-four single-spore representative isolates were obtained from surface-disinfected symptomatic tissues. Morphological characteristics of fungal mycelium, conidial and pycnidial structures on potato sucrose agar (PSA) and water agar (WA) closely resembled those described for Lasiodiplodia spp. All isolates caused typical collar rot symptoms upon artificial inoculation of peanut seedlings. Morphological identification of Lasiodiplodia spp. isolates was corroborated by MALDI-TOF and molecular analyses utilizing sequences from the internal transcribed spacer (ITS), β-tubulin 2 (tub2) and translation elongation factor-1 alpha (TEF1-α) loci. Phylogenetic analysis confirmed that the representative fungal isolates (MKUBK-B1 and MKUBK-K22) belong to Lasiodiplodia pseudotheobromae. To the best of our knowledge, this is the first report of L. pseudotheobromae infecting peanut plants in Turkey. This work is expected to contribute to previously limited knowledge regarding the host range, incidence and prevalence of L. pseudotheobromae as a soilborne pathogen of peanuts. Due to the potential destructiveness and broad host range of this pathogen, it is essential to develop new strategies to establish more reliable, environmentally sustainable, and cost-effective management approaches for this disease. [ABSTRACT FROM AUTHOR]

Copyright of Revista Brasileira de Engenharia Agricola e Ambiental - Agriambi is the property of Revista Brasileira de Engenharia Agricola e Ambiental and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Peanuts (Arachis hypogaea) are of significant agricultural importance due to their versatile uses, providing a valuable source of edible oil and protein-rich food products and serving in industrial applications. Peanuts are susceptible to various diseases, one of them being net syndrome, a poorly understood threat triggered by an undefined causal agent, with symptoms including black coloring and lesions of the peanut pod that affect product quality. In this study, amplicon sequencing was harnessed to explore the fungal and bacterial populations associated with the syndrome. Using this approach, we identified a specific Fusarium sp. amplicon sequence variant that demonstrated a significant correlation with the presence of net syndrome symptoms in both young and mature peanuts. This finding was further validated by Koch's postulates testing, including isolation, cultivation, and application of this strain to corroborate its involvement in net syndrome in peanuts. Our findings contribute to a better understanding of the interactions between peanuts and their microbial communities and to identification of the previously undetermined agent involved in net syndrome and the etiology of the disease.

In the present study, the thermal conversion of Arachis hypogaea (groundnut) husk into biochar and its subsequent application in the adsorptive removal of Cr(VI) from an aqueous solution has been studied. The SEM–EDX and LIBS analyses showed that the adsorbent material incorporates both magnesium (Mg) and chromium (Cr) on its surface. The FTIR spectra revealed the involvement of several functional groups in the Cr(VI) adsorption, including –OH, Mg–O–Mg, –CH, –NH, and –COO. Specific surface area (SSA) is determined using BET (Brunauer–Emmett–Teller) analysis and the SSA of adsorbent material was 35.83 m2 g−1. Data from batch adsorption experiments demonstrated that magnesium-supported biochar increased the binding capacity of the adsorbent to the Cr(VI) ions. Adsorption experiment data at equilibrium conditions showed that the Langmuir model provided a best suited to the nMgO@GHBC than the Freundlich and Temkin models with a maximum adsorption capacity of 93.86 mg g−1. The kinetic-second-order model with the highest R2 value of 0.993 and the lowest values for root mean square error and chi-square (χ2) can reasonably explain the hexavalent chromium adsorption data. This study suggested that the mechanism of Cr(VI) adsorption onto both adsorbents might be chemisorption or ion exchange processes as adsorption data effectively fitted the PSO model. The outcomes of thermodynamic parameters like ΔG° indicated that Cr(VI) adsorption on pGHBC and nMgO@GHBC was spontaneous. Fixed-bed-column studies were conducted at different experimental conditions, such as inlet flow rate and bed height. The outcomes of the experimental data showed that the adsorption capacity of adsorbent for Cr(VI) adsorption in a fixed bed continuous flow was 50 mg g−1. The adsorbent was recycled ten times using NaOH, HNO3, H2SO4, and EDTA. The continuous adsorption and desorption of Cr ions for up to 10 cycles showed the reusability of spent biochar. [ABSTRACT FROM AUTHOR]

Insoluble phosphorous compounds solubilization by soil bacteria is of great relevance since it puts available the phosphorus to be used by plants. The production of organic acids is the main microbiological mechanism by which insoluble inorganic phosphorus compounds are solubilized. In Gram negative bacteria, gluconic acid is synthesized by the activity of the holoenzyme glucose dehydrogenase-pyrroloquinoline quinine named GDH-PQQ. The use of marker genes is a very useful tool to evaluate the persistence of the introduced bacteria and allow to follow-up the effect of biotic and abiotic factors on these beneficial microorganisms in the soil. In previous studies we detected the presence of the pqqE gene in a great percentage of both non-culturable and culturable native soil bacteria. The objective of this study was to analyze the phylogeny of the sequence of pqqE gene and its potential for the study of phosphate solubilizing bacteria from pure and mixed bacterial cultures and rhizospheric soil samples. For this, the presence of the pqqE gene in the genome of phosphate solubilizing bacteria that belong to several bacteria was determined by PCR. Also, this gene was analyzed from mixed bacterial cultures and rhizospheric soil associated to peanut plants inoculated or not with phosphate solubilizing bacteria. For this, degenerate primers designed from several bacterial genera and specific primers for the genus Pseudomonas spp., designed in this study, were used. DNA template used from simple or mixed bacterial cultures and from rhizospheric soil samples was obtained using two different DNA extraction techniques. Results indicated that pqqE gene amplification product was found in the genome of all Gram negative phosphate solubilizing bacteria analyzed. It was possible to detect this gene in the DNA obtained from mixed cultures where these bacteria grew in interaction with other microorganisms and in that obtained from rhizospheric soil samples inoculated or not with these bacteria. The phylogenetic analysis indicated that pqqE gene is a conserved gene within related genera. In conclusion, pqqE gene could be a potential marker for the study of phosphate solubilizing bacterial populations. [ABSTRACT FROM AUTHOR]

Stem rot of groundnut (Arachis hypogaea L.) caused by Scelrotium rolfsii is the main threat to groundnut production, causing significant economic losses. The present study aims to provide an overview of the potentiality of Trichoderma viride (Tv), Trichoderma harzianum (Th), Pseudomonas fluorescens (Pf), and Bacillus subtilis (Bs), applied either individually or in mixed combination, against Sclerotium rolfsii (isolate SrBKN). The treatment with T. harzianum and P. fluorescens resulted in the highest mycelial growth inhibition (79.61, 83.51, and 86.77%), followed by T. viride and P. fluorescens (75.74, 79.63, and 83.14%). Under in vitro conditions, the combination of bio-agents at 5% culture filtrate proved to be superior against the test pathogen. Seed treatment and soil application of T. harzianum and Pf at 10 (5 + 5) g kg−1 + 10 (5 + 5) kg ha−1, followed by seed treatment and soil application of T. viride and Pf at 10 (5 + 5) g kg−1 + 10 (5 + 5) kg ha−1, resulted in the lowest disease incidence (7.40 and 8.0%), highest disease control (69.37 and 66.88%), maximum dry weight (151 and 147 g plant−1), highest increase in dry weight (75.58 and 70.93), highest pod yield (2665 and 2498 kg ha−1), and highest increase in pod yield (96.38 and 84.08%) under in vivo conditions. We present an effective bio-control-based management module from the lab to the field for the successful control of groundnut stem rot caused by S. rolfsii. Based on the results, it is concluded that the dual formulation of T. harzianum and P. fluorescens, followed by T. viride and P. fluorescens, were the most effective BCAs in suppressing the S. rolfsii. Therefore, an integrated disease management module with these BCAs needs to be developed and validated with a farmers' participatory mode under field conditions. [ABSTRACT FROM AUTHOR]

Rhizobia are bacteria that symbiosis with host plant, as shown in the root nodules formation, and provide nitrogen that can be absorbed by plants in greater quantities than rhizobacteria. Available Nitrogen, which absorbed by plants, is the essential requirement for plant growth because its role in increasing yield and quality, hence it is needed in greater quantities than other nutrients. The study aimed to determine the macroscopic and microscopic diversity of rhizobia isolates from the groundnut nodules and their potential as PGPRs, and to identify 16S rRNA isolates with the best potential as PGPRs molecularly. The methods used were isolation from root nodules, screening of PGPR potential, molecular identification based on the 16S rRNA gene, and phylogenetic analysis to determine their kinship. Based on the isolation results, 17 Gram-negative isolates were obtained white to pink or orange color on AG media with various colony characteristics in terms of shape, margin, elevation, and texture. KT 20, which was selected as rhizobia isolate with the best potential as PGPR, has ammonium concentration of 23.12 ppm, synthesizes IAA with a concentration of 10.36 ppm, and phosphates solubilization activity, although its ability to synthesize proteases is low. The results of molecular identification of 16S rRNA showed that KT 20 belongs to the Rhizobium genus with a similarity of 99.48 % and bootstrap value of 96 %. [ABSTRACT FROM AUTHOR]

Peanut stem rot disease, caused by the necrotrophic soil-borne fungus Sclerotium rolfsii, has a significant negative impact on crop yields. Chemical fungicides can mitigate the loss incurred by fungus, however, their usage raises environmental and human health concern. Seaweeds extracts are getting importance as bio-stimulant for improving growth and disease resistance in different plants. In the present study, we investigated the potential of Sargassum tenerrimum extract (S-extract) in controlling stem rot disease in peanuts. The foliar application of S-extract was applied at vegetative and reproductive stages on peanut plants to study plant growth and reduction of S. rolfsii-induced disease. Plant height, number of branches and branch length increased in S-extract treated plants (S) as compared to S-extract + S. rolfsii treated plants (S + F). Similarly, the activity of anti-oxidative enzymes such as catalase (CAT), guaiacol peroxidase (GPOX), polyphenol oxidase (PPO), and superoxide dismutase (SOD) increased by application of S-extract. Pigments such as chlorophyll a, chlorophyll b, and carotenoids showed higher accumulation in S-extract treated plants. The increased membrane stability index and reduced electrolyte leakage in S and S + F plants, positively affected the health and biotic stress tolerance of the plants. S-extract reduced the reactive oxygen species (ROS) such as O2•− and H2O2. Total phenol, soluble sugars and total amino acid accumulation were higher in S and S + F plants compared to C and F at vegetative stage. The mitigation of disease can be attributed to the application of S-extract leading to the elevated activity of antioxidant enzymes and the accumulation of non-enzymatic antioxidants, osmolytes, and pigments. Therefore, S-extract represents an environmentally friendly resource that can be employed in sustainable agriculture practices to boost plant growth and enhance disease tolerance. [ABSTRACT FROM AUTHOR]

Peanut production is threatened by climate change. Damage to seedlings from low temperatures in early spring can limit yield. Plant adaptations to chilling stress remain unclear in peanut seedlings. It is essential to understand how peanut acquires chilling tolerance.We evaluated effects of chilling stress on growth and recovery of peanut seedlings. We compared and analysed biological characteristics, antioxidants, photosynthesis, biochemical and physiological responses, and nutrient absorption at varying levels of chilling.Compared with chilling‐sensitive FH18, the reduced impact of chilling stress on chilling‐tolerant NH5 was associated with reduced ROS accumulation, higher ascorbate peroxidase activity and soluble sugar content, lower soluble protein content, and smaller reductions in nutrient content during stress. After removal of chilling stress, FH18 had significant accumulation of O2•− and H2O2, which decreased photosynthesis, nutrient absorption, and transport. ROS‐scavenging reduced damage from chilling stress, allowed remobilization of nutrients, improved chilling tolerance, and restored plant functioning after chilling stress removal.These findings provide a reference for targeted research on peanut seedling tolerance to chilling and lay the foundation for bioinformatics‐based research on peanut chilling tolerance mechanisms. [ABSTRACT FROM AUTHOR]

Low plant density and weed infestation are major challenges for groundnut production in northern Ghana. A two‐year on‐farm study was conducted to determine the effect of plant density and variety on grain and fodder yields, incidence of leaf spot disease, weed species diversity and biomass. A factorial treatment combination of 6 varieties and 4 plant densities laid in strip plot design with 4 replications was used. The varieties were (early maturity type: Chinese, Yenyewoso, Samnut 23 and late maturity type: Azivivi, Manipinta, Samnut 22). The plants density included 9, 11, 15 and 22 plants/m2. The late maturity varieties recorded higher (p <.05) canopy cover, grain and fodder yields relative to that of the early maturity varieties. The late maturity varieties also recorded the least sedge weed species frequency, density and incidence of leaf spot disease compared with that of the early maturity varieties. The canopy cover, grain and fodder yields increased with increasing plant density. Broadleaf weed species frequency and density, weed biomass, richness, and diversity declined with increasing plant density. Grain yield showed negative and significant correlation with broadleaf weed species frequency, density and weed biomass. The results suggest that both early and late maturity groundnut varieties can be planted at a density of 22 plants/m2 to increase grain and fodder yields and reduce weed species richness, diversity and growth in northern Ghana and similar agro‐ecology in West Africa. [ABSTRACT FROM AUTHOR]

DBV712 250 µg (also referred to as Viaskin Peanut or peanut patch; Viaskin is a trademark of DBV Technologies) is an innovative approach to epicutaneous immunotherapy (EPIT). The patch-based technology system facilitates peanut protein (allergen) absorption into the intact non-vascularized epidermis to promote desensitization to peanut while limiting systemic allergen exposure. Efficacy and safety in children have been evaluated in four completed phase 3 studies. Overall, the results from these studies have demonstrated the peanut patch to be superior in desensitization compared with placebo and safe for daily use over multiple years. These findings, as well as supportive evidence from phase 2 studies, confirm the potential for an effective treatment of peanut allergy in children. The purpose of this review is to summarize the safety and efficacy of the peanut patch in the treatment of peanut allergy. [ABSTRACT FROM AUTHOR]

The ratio of oleic acid to linoleic acid (O/L) is crucial for determining the shelf life of peanut oil. In peanuts, the expression of the Fatty Acid Desaturase 2 (FAD2) enzyme, which converts oleic acid to linoleic acid, is regulated by two homeologous genes called AhFAD2A and AhFAD2B. It has been observed that the Indian peanut cultivar GG20 does not possess natural mutations in the AhFAD2B gene. We successfully introduced a construct called CRISPR_GG20_AhFAD2B into the de-embryonated cotyledon of the GG20 plant. The purpose of this construct was to utilize the CRISPR-Cas9 gene editing technology to modify the AhFAD2B gene. Genotyping analysis of the plants that were potentially transformed with the construct confirmed that the target-specific editing had occurred in the AhFAD2B gene. Subsequently, the edited GG20 plants were phenotypically evaluated to assess the fatty acid composition in the peanut kernels. The results showed a notable increase in the O/L ratio, which rose from 3.1 in the control to 7.3 in the edited GG20 plants. This implies that the gene editing technique successfully enhanced the oleic acid to linoleic acid ratio in the peanuts, potentially improving the shelf life of the resulting peanut oil. [ABSTRACT FROM AUTHOR]

Peanuts (Arachis hypogaea L.) are a crop from tropical and subtropical regions. Argentina is a significant producer and exporter, with the province of Córdoba concentrating ca. 84% of the peanut-cultivated area in the country. Thrips pose a threat to the crop by causing direct damage through feeding and indirect damage as vectors of orthotospovirus. Despite the importance of these insects and the crop, little is known about the diversity of thrips in the vegetation surrounding peanut crops in Córdoba province. The aim of this study was to expand knowledge on thrips diversity in the plant environment around peanut crops in fields located in Río primero, Río Segundo and General Roca counties (Córdoba, Argentina). Sampling was conducted during the 2021-2022 growing season. The adult trips were collected from spontaneous plants and crops neighboring the peanut, and they were prepared and identified using special keys. In 14 plant species, specimens of Frankliniella schultzei (Trybom), Frankliniella gemina Bagnall, Caliothrips phaseoli (Hood), Frankliniella occidentalis (Pergande), Thrips tabaci (Lindeman), Frankliniella frumenti Moulton, Arorathrips mexicanus (Crawford), and individuals from the genera Heterothrips and Hoplandrothrips were collected. Frankliniella schultzei was the most frequent and abundant species. Spontaneous plants and soybean crops contained thrips species able to transmit orthotospovirus. This study reports for the first time the presence of F. schultzei in Gomphrena pulchella, as well as the first documentation of thrips diversity and their association with spontaneous vegetation in peanut fields in the province of Córdoba.

This article discusses the use of CRISPR-Cas9 gene editing technology to silence the 2S albumin genes in peanuts, which are known to be potent allergens. The researchers successfully edited the genes using a multiplex gene editing strategy and confirmed the elimination of the allergenic proteins through protein analysis. However, further testing is needed to determine if the edited peanuts have reduced allergenicity. The study was supported by Ukko, Inc. and the data supporting the findings are available in the supplementary material of the article. [Extracted from the article]

Effect of processing on the nutritional composition of groundnut seeds were carried out using standard analytical methods. Raw, boiled and fried groundnut seeds were analyzed for proximate composition, mineral contents, and phytochemical screening. The result reported that the raw, boiled, and fried contains (5.357±0.190%, 4.545±0.050% and 3.896±0.015%, moisture contents), (2.401±0.011%, 3.225±0.004% and 2.816±0.001%, ash contents), (46.591±0.001%, 25.333±0.003% and 48.012±0.953%, crude fat), (4.126±0.887%, 15.001±0.030% and 7.692±0.002%, crude fibre), (19.520±0.040%, 21.580±0.040% and 23.540±0.000%, crude protein), (22.005±0.587%, 30.316±0.056% and 14.044±0.939%, carbohydrate) respectively. A significant difference was observed. Processing has significant effects on the mineral components of the seeds. The results revealed that raw, boiled and fried contains (56.900mg/100g, 48.400mg/100g and 35.00mg/100g Sodium), (0.215mg/100g, 0.185mg/100g and 0.540mg/100g Zinc), (65.500mg/100g, 42.700mg/100g and 25.500mg/100g Magnesium), (0.218mg/100g, 0.230mg/100g and 0.230mg/100g Iron), (0.250mg/100g, 0.110mg/100g and 0.100mg/100g Manganese). The phytochemical screening shows the presence of alkaloids, carbohydrates and proteins in all the samples and the result reveals that processing does not really have effect on phytochemical constituents. The investigation shows that fresh groundnut is a good source of mineral content, while raw and processed groundnut is a good source of some phytochemical constituents and processed groundnut is a good source of protein, fat, and carbohydrate with high nutritional value.

Abstract The effects of inhibitor concentration on the corrosion rate and inhibition efficiency of AISI 1020 steel in an acidic and alkaline environment were investigated by means of weight loss measurement at an interval of 7 days and 14 days. To carry out this investigation, the Arachis hypogaea hull was extracted and concentrated in various weight percentages. The inhibition efficiency increased with the increased concentrations of AISI 1020 steel that were immersed in acidic and alkaline solution in the absence and presence of varying inhibitor concentrations of Arachis hypogaea hull extracts. The corrosion behavior, including the corrosion rate, is meticulously characterized through the corrosion rate analysis. The results showed that there is an increase in inhibition efficiency with an increase in inhibitor concentration and that there is a decrease in inhibition efficiency with an increase in immersion time. The organic inhibitor (Arachis hypogaea hull) produced the best inhibition efficiency of 96.4% at a 30% concentration. From the result obtained, Arachis hypogaea hull extracts revealed that it is best suited for inhibition of corrosion of mild steel in both acidic and alkaline environments. The goal of this research paper is to develop a comprehensive understanding of the corrosion inhibition and adsorption mechanisms associated with the implementation of the Arachis hypogaea hull as a natural corrosion inhibitor.

The potential production and productivity of groundnuts are limited due to severe drought stress associated with climate change. The current study aimed to identify genomic regions and candidate genes associated with drought tolerance and component traits for gene introgression and to guide marker-assisted breeding of groundnut varieties. Ninety-nine genetically diverse groundnut genotypes were phenotyped under drought-stressed and non-stressed field conditions in 2018/19 and 2019/20, and using the LeasyScan platform under non-stressed conditions in 2019/20 at the International Crops Research Institute for the Semi-Arid Tropics (ICRISAT)/India. The samples were genotyped using 48 K single nucleotide polymorphisms (SNPs) markers at the University of Georgia/USA. Phenotypic data was collected on 17 agronomic traits and subjected to statistical analyses. The SNP data were computed, and population structure was inferred using a Bayesian clustering method in Structure version 2.3.4, while linkage disequilibrium was calculated using the GAPIT program in R software. Marker-trait associations were deduced using Tassel 5.2.86. Significant phenotypic variations were recorded for drought tolerance and the assessed agronomic traits. GWAS analysis using PCA+K and Q+K models identified significant SNPs associated with leaf area (1 SNP), leaf area Index (1 SNP), specific leaf area (1 SNP), leaf relative water content (43 SNPs), number of primary branches (1 SNP) and hundred seed weight (1 SNP). Forty-seven and one marker-trait associations were detected under drought-stressed and non-stressed conditions, respectively. The candidate genes and markers identified in the current study are useful for accelerated groundnut breeding targeting drought tolerance and market-preferred traits. [ABSTRACT FROM AUTHOR]

Calcium deficiency is a leading cause of reduced peanut (Arachis hypogaea) seed quality and has been linked to increased disease susceptibility, specifically to soilborne fungal pathogens. Sufficient calcium at flowering time is critical to ensure proper pod development. Calcite-dissolving bacteria (CDB) isolated from farming fields can dissolve calcite (CaCO3) on plates and increase soluble calcium levels in soil. However, the phylogenetic diversity and geographic distribution of CDB is unclear. Here, we surveyed soil samples from 15 peanut-producing fields in three regions in southern Georgia, representing distinct soil compositions. We isolated CDB through differentiating media and identified 52 CDB strains. CDB abundance was not associated with any of the soil characteristics we evaluated. Three core genera, represented by 43 strains, were found in all three regions. Paenibacillus was the most common CDB found in all regions, making up 30 of the 52 identified strains. Six genera, represented by eight strains, are unique to one region. Members of the core and unique communities showed comparable solubilization indexes on plates. We conclude that a diversified phylogenetic population of CDB is present in Georgia peanut fields. Despite the phylogenetic diversity, as a population, they exhibit comparable functions in solubilizing calcite on plates. [ABSTRACT FROM AUTHOR]

Peanut is a leguminous crop with an indeterminate growth habit that will continuously flower during the entire reproductive development stage. Flowering redundancy adversely affects the yield and quality of peanut. In this study, eight flowering and five yield-related traits were collected and comprehensively evaluated from a diverse germplasm panel consisting of 232 peanut accessions, aiming to provide a theoretical basis for improving the flowering habit and yield for future peanut breeding efforts. As a result, large phenotypic diversity was observed in 13 traits. Most of the traits suggested high heritability, except high effective flowering duration (HEFD), days to 100% flower cessation (DTC100), and yield per plant (YPP). Days to 90% flower cessation (DTC90), days to DTC100, flowering duration (FD), and low effective flowering duration (LEFD) showed significant negative correlations with 100-seed weight, 100-pod weight, YPP, average weight per pod, and shelling percentage. Principal component analysis (PCA) suggested that flowering redundancy traits as well as yield-related traits contributed more to the first three PCs when compared to other traits. This study addresses the lack of peanut flowering phenotypic and genetic diversity and lays the foundation for in-depth research on redundancy-related genes in peanut flowering. [ABSTRACT FROM AUTHOR]

Summary: As peanuts are prone to fungal attack, techniques like ozonation and heat treatment hold enormous potential. Peanut oil, being health‐healthy, was extracted from O1: control, O2: roasted (166 °C for 7 min), O3: ozonated (6 mg L−1 for 30 min), and O4: ozonated + roasted peanuts and analysed for chemical, colour, phenolic, fatty acids and rheological properties. Roasting significantly affected peroxide, iodine, acid, p‐anisidine values and stability of oils as compared to other treatments. The results indicated a decline in colour attributes of all oils except hue angle which were strongly correlated to increased levels of functional compounds expressed by third‐degree polynomial. O4 oil indicated best quality in terms of high atherogenic, thrombogenic, calculated oxidisability value and low hypocholesterolaemic: hypercholesterolaemic indices of fatty acid. Oils exhibited pseudoplasticity postulated by Ostwald‐de Waele and Herschel–Bulkley models. Arrhenius equation and oscillatory rheology predicted temperature dependency and crystal matrix behaviour. Overall, the O4 oils followed by O3 from ozonated peanuts individually and along with roasting are pivotal to cater the rising demands of oils due to their better appearance, fatty acids and rheology. [ABSTRACT FROM AUTHOR]

The effects of inhibitor concentration on the corrosion rate and inhibition efficiency of AISI 1020 steel in an acidic and alkaline environment were investigated by means of weight loss measurement at an interval of 7 days and 14 days. To carry out this investigation, the Arachis hypogaea hull was extracted and concentrated in various weight percentages. The inhibition efficiency increased with the increased concentrations of AISI 1020 steel that were immersed in acidic and alkaline solution in the absence and presence of varying inhibitor concentrations of Arachis hypogaea hull extracts. The corrosion behavior, including the corrosion rate, is meticulously characterized through the corrosion rate analysis. The results showed that there is an increase in inhibition efficiency with an increase in inhibitor concentration and that there is a decrease in inhibition efficiency with an increase in immersion time. The organic inhibitor (Arachis hypogaea hull) produced the best inhibition efficiency of 96.4% at a 30% concentration. From the result obtained, Arachis hypogaea hull extracts revealed that it is best suited for inhibition of corrosion of mild steel in both acidic and alkaline environments. The goal of this research paper is to develop a comprehensive understanding of the corrosion inhibition and adsorption mechanisms associated with the implementation of the Arachis hypogaea hull as a natural corrosion inhibitor. [ABSTRACT FROM AUTHOR]

Copyright of Journal of Food Safety & Quality is the property of Journal of Food Safety & Quality Editorial Department and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

As there was no maximum permissible limit prescription for aflatoxin B1 (AFB1) in Ethiopia, this study has been conducted to generate data on AFB1 levels in Ethiopian groundnut accessions/landraces. Besides, an attempt was made to find out if there is any relationship between AFB1 and other parameters such as altitude of cultivation, individual seed weight, kernel colonization by Aspergillus flavus, total carbohydrates, protein and total free amino acids. Out of the 28 accessions studied, merely six accessions registered ≤2 ppb AFB1 and thus, they comply with maximum permissible limit set by European Union. Altitude of cultivation had no relationship with AFB1 levels. Interestingly, total carbohydrates in the seeds as well as kernel colonization by A. flavus showed statistically significant (p

ABSTRACT The success of intercropping depends on the spatial arrangement between crops, aiming at the best use of the planting area and greater profitability for the farmer. Here, we evaluated the effect of cassava-peanut intercropping on several agronomic parameters. The research was carried out in the APTA experimental area, in the state of São Paulo, Brazil. The experimental design was randomized blocks with four treatments (peanut in monoculture - P; cassava in monoculture - C, cassava intercropped with peanuts planted between rows - CPb, and intercropping in alternating double rows - CPd) and eight replications. The variables analyzed were vegetative growth of cassava plants, soil vegetation cover and weed control, incidence of the main cassava and peanut pests, productivity, and the land equivalent ratio (LER). Only CPb inhibited cassava vegetative growth, significantly affecting its final height. Greater vegetation coverage and, consequently, lower occurrence of weeds, was obtained in CPb in addition to lower incidence of whiteflies in cassava. The intercropping system, regardless of the spatial arrangement used, increased the incidence of the lace bug in cassava and reduced the incidence of peanut pests. Crop productivity was lower in CPd due to the lower planting density of intercrops. However, both intercropping arrangements increased LER. Thus, despite the spatial arrangement of the intercropping system having implied different agronomic responses of the crops, planting peanuts between the cassava rows brought the best agronomic results.

El mercado de hongos comestibles es muy grande, siendo una alternativa alimenticia para reemplazar la carne, sumado a sus propiedades nutracéuticas y con la posibilidad de cultivarlos aprovechando desechos orgánicos de origen agrícola. Se recolectaron y prepararon semillas de almendra (Terminalia catappa) y cáscaras de achiote (Biza orellana), cacahuate (Arachis hypogaea) y arroz (Oriza sativa) e inocularon con micelio de Pleurotus pulmonarius. Se evaluaron los tiempos de crecimiento del hongo, la eficiencia biológica y relación entre minerales del sustrato y producto. En achiote y maní hubo mayor acumulación de proteína (12,4%±1,6 y 10,9%±0,6 respectivamente). La cáscara de maní fue el único sustrato donde fructificó el P. pulmonarius con relación entre la concentración de nitrógeno vs. diámetro del sombrero, del pie y longitud del pie (p

Members of bZIP gene family play crucial roles in various biological processes, including plant growth and development, stress response, and light signal transduction. Despite their significance, there is limited information on the function of the bZIP gene family in peanuts. In this investigation, we identified a total of 99 bZIP gene family members in the peanut genome, distributed across 20 chromosomes. Phylogenetic tree analysis categorized the peanut bZIP gene family into 10 groups, with groups I, D, A and S being the most widely distributed. Transcriptome analysis of peanut pods revealed that 10 bZIP family genes exhibited significant induction in response to light, suggesting their potential involvement in light signal transduction in peanuts. Within the peanut bZIP family, group H comprises six genes AhbZIP13, AhbZIP63, AhbZIP39, AhbZIP44, AhbZIP91 and AhbZIP96. Particularly, the expression of the AhbZIP63 (AhHYH) gene significantly increased under light induction, indicating a pivotal role in light signal transduction. DAP-seq analysis of AhbZIP63 (AhHYH) demonstrated its direct regulation of genes associated with UV response and cellular response to nutrient levels.

Abstract Background Calmodulins (CaMs)/CaM-like proteins (CMLs) are crucial Ca2+-binding sensors that can decode and transduce Ca2+ signals during plant development and in response to various stimuli. The CaM/CML gene family has been characterized in many plant species, but this family has not yet been characterized and analyzed in peanut, especially for its functions in response to Ralstonia solanacearum. In this study, we performed a genome-wide analysis to analyze the CaM/CML genes and their functions in resistance to R. solanacearum. Results Here, 67, 72, and 214 CaM/CML genes were identified from Arachis duranensis, Arachis ipaensis, and Arachis hypogaea, respectively. The genes were divided into nine subgroups (Groups I-IX) with relatively conserved exon‒intron structures and motif compositions. Gene duplication, which included whole-genome duplication, tandem repeats, scattered repeats, and unconnected repeats, produced approximately 81 pairs of homologous genes in the AhCaM/CML gene family. Allopolyploidization was the main reason for the greater number of AhCaM/CML members. The nonsynonymous (Ka) versus synonymous (Ks) substitution rates (less than 1.0) suggested that all homologous pairs underwent intensive purifying selection pressure during evolution. AhCML69 was constitutively expressed in different tissues of peanut plants and was involved in the response to R. solanacearum infection. The AhCML69 protein was localized in the cytoplasm and nucleus. Transient overexpression of AhCML69 in tobacco leaves increased resistance to R. solanacearum infection and induced the expression of defense-related genes, suggesting that AhCML69 is a positive regulator of disease resistance. Conclusions This study provides the first comprehensive analysis of the AhCaM/CML gene family and potential genetic resources for the molecular design and breeding of peanut bacterial wilt resistance.

Background: Calmodulins (CaMs)/CaM-like proteins (CMLs) are crucial Ca2+-binding sensors that can decode and transduce Ca2+ signals during plant development and in response to various stimuli. The CaM/CML gene family has been characterized in many plant species, but this family has not yet been characterized and analyzed in peanut, especially for its functions in response to Ralstonia solanacearum. In this study, we performed a genome-wide analysis to analyze the CaM/CML genes and their functions in resistance to R. solanacearum. Results: Here, 67, 72, and 214 CaM/CML genes were identified from Arachis duranensis, Arachis ipaensis, and Arachis hypogaea, respectively. The genes were divided into nine subgroups (Groups I-IX) with relatively conserved exon‒intron structures and motif compositions. Gene duplication, which included whole-genome duplication, tandem repeats, scattered repeats, and unconnected repeats, produced approximately 81 pairs of homologous genes in the AhCaM/CML gene family. Allopolyploidization was the main reason for the greater number of AhCaM/CML members. The nonsynonymous (Ka) versus synonymous (Ks) substitution rates (less than 1.0) suggested that all homologous pairs underwent intensive purifying selection pressure during evolution. AhCML69 was constitutively expressed in different tissues of peanut plants and was involved in the response to R. solanacearum infection. The AhCML69 protein was localized in the cytoplasm and nucleus. Transient overexpression of AhCML69 in tobacco leaves increased resistance to R. solanacearum infection and induced the expression of defense-related genes, suggesting that AhCML69 is a positive regulator of disease resistance. Conclusions: This study provides the first comprehensive analysis of the AhCaM/CML gene family and potential genetic resources for the molecular design and breeding of peanut bacterial wilt resistance. [ABSTRACT FROM AUTHOR]

The development of dicamba and 2,4-D resistant crops may result in the widespread use of these herbicides in agricultural areas, potentially affecting nearby susceptible crops. This study aimed to evaluate the sensitivity of bean, peanut, and cotton to different doses of Dicamba and 2,4-D. To do so, separate experiments were conducted for each crop and herbicide in a greenhouse, using a completely randomized design with four replications. Both herbicides were applied at different doses to plants with the second pair of true leaves. Phytotoxicity and dry biomass were evaluated. For cotton, 2,4-D showed high phytotoxicity at doses of up to 83.75 g ai ha-1, with a reduction in suppressive effect observed at 20.93 g ai ha-1. Dicamba exhibited a pronounced reduction in crop biomass up to a dose of 70 g ai ha-1, with 94 % phytotoxicity. For beans, the evolution of symptoms using 2,4-D occurred more slowly, but the highest doses resulted in phytotoxicity of up to 95 % and a 30 % reduction in biomass at 167.5 g ai ha-1, indicating a significant impact on the crop. Dicamba also had a high negative impact, with a 100 % reduction in biomass at 70 g ai ha-1. The peanut crop was more tolerant to herbicides, with 2,4-D doses of 670, 335, and 167.5 g ai ha-1 resulting in phytotoxicities of 69.5, 37.49, and 14.37 %, respectively. Dicamba significantly reduced dry biomass at doses of up to 70 g ai ha-1. The results show that, despite the differences in sensitivity of cotton, bean, and peanut to 2,4-D and Dicamba, even low doses of these herbicides applied early in development had a significant negative impact on these crops. [ABSTRACT FROM AUTHOR]

Peanut smut (causal agent Thecaphora frezzii) and seasonal drought are the two main factors reducing peanut yields in Argentina. There are no previous studies about the effect of drought on peanut smut occurrence. We evaluated the effect of soil water limitation on smut symptoms in greenhouse and field assays. Additionally, we analysed the biochemical responses of plants to the combined stress caused by water limitation and smut infection in greenhouse experiments. We found that a moderate water deficit (30% of soil water‐holding capacity) increased smut symptoms and differentially increased proline and reduced chlorophylls in the host. Subsequently, we studied the correlation between field precipitation data and smut damage from 2015 to 2020 in naturally infected fields with a high T. frezzii spore load in the soils. Strong correlations between precipitation and severely affected pods, severity disease index and incidence were found from January to March (susceptibility window for T. frezzii infections). We suggest a strategy of irrigation in a specific time frame to mitigate smut damage when there is a water deficit in the growing season. [ABSTRACT FROM AUTHOR]

The quantity and quality of spray deposition are fundamental for improving pesticide performance in plant pests. This study evaluated how spray droplet size (1) and spray nozzle type (2) affect the quantity and quality of spray deposition on peanut plants at the vegetative and reproductive growth stages. Two greenhouse experiments were performed on peanut plants at the V1 and R1 growth stages. Experiment 1 treatments included three droplet sizes: medium (flat fan XR 11002), very coarse (TT 11002), and extremely coarse (AIXR 11002). Experiment 2 treatments were five spray nozzles: hollow cone (TXA 8002 VK), twin flat fan (TTJ60 11002), air induction flat fan (AIXR 110025), drift guard twin flat fan (DGTJ60 11002), and extended range flat fan (XR 11003). Spray deposition values were determined using a solution of brilliant blue dye sprayed by a CO2-pressurized backpack sprayer. The medium droplet size provided higher spray deposition on peanut plants at the V1 and R1 growth stages. Increasing the droplet size from medium to extremely coarse reduces spray deposition at the V1 growth stage. Spray deposition uniformity increased as droplet size increased at the V1 growth stage. The spray uniformity decreased at the R1 growth stage as the droplet size increased. The flat fan XR 11003 (medium droplet) and hollow cone nozzle TXA 8002 VK (fine droplet) provided a higher spray deposition on peanut plants at both growth stages. The spray nozzles that provide a higher spray deposition did not perform well on spray uniformity. [ABSTRACT FROM AUTHOR]

The ferric chelate reductase (FRO) family plays a vital role in metal ion homeostasis in a variety of locations in the plants. However, little is known about this family in peanut (Arachis hypogaea). This study aimed to identify FRO genes from the genomes of peanut and the two diploid progenitors (A. duranensis and A. ipaensis) and to analyze their gene/protein structures and evolution. In addition, transcriptional responses of AhFRO genes to Fe deficiency and/or Cu exposure were investigated in two peanut cultivars with different Fe deficiency tolerance (Silihong and Fenghua 1). A total of nine, four, and three FRO genes were identified in peanut, A. duranensis, and A. ipaensis, respectively, which were divided into three groups. Most AhFRO genes underwent WGD/segmental duplication, leading to the expansion of the AhFRO gene family. In general, clustered members share similar gene/protein structures. However, significant divergences occurred in AhFRO2 genes. Three out of five AhFRO2 genes were lowly expressed in all tissues under normal conditions, which may be beneficial for avoiding gene loss. Transcription analysis revealed that AhFRO2 and AhFRO7 genes might be involved in the reduction of Fe/Cu in plasma membranes and plastids, respectively. AhFRO8 genes appear to confer Fe reduction in the mitochondria. Moreover, Fe deficiency induced an increase of Cu accumulation in peanut plants in which AhFRO2.2/2.4/2.5 and FRO7.1/7.2 might be involved. Our findings provided new clues for further understanding the roles of AhFRO genes in the Fe/Cu interaction in peanut. [ABSTRACT FROM AUTHOR]

Pentatricopeptide repeat (PPR) proteins, with tandem 30–40 amino acids, were characterized as one kind of nucleus coding protein. They have been demonstrated to play important roles in RNA editing, plant growth and development, and plant immunity. Although the PPR gene family has been characterized in some plant species, less is known about this family in peanut, especially their functions in response to Ralstonia solanacearum. In this study, we performed a genome-wide analysis to identify PPR genes and their functions in resistance to R. solanacearum. Here, 389, 481, and 1079 PPR genes were identified from Arachis duranensis, Arachis ipaensis, and Arachis hypogaea, respectively. Allopolyploidization was the main reason for the increased number of the AhPPR members. Gene duplication brought about 367 pairs of homologous genes of PPRs in A. hypogaea. Whole-genome replication, tandem repeats, scattered repeats, and unconnected repeats constituted the replication types. The substitution rates of nonsynonymous (Ka) versus synonymous (Ks) of all homologous pairs were less than 1.0, suggesting that the homologous AhPPRs underwent intense purifying selection pressure and remained conserved in both structure and function. RNA-seq and RT-qPCR analyses showed that AhPPR598 gene was highly expressed in the aerial part of peanut and involved in response to R. solanacearum. The transient expression of AhPPR598 in Nicotiana benthamiana induced the HR-mediated cell death, up-regulated expression of resistant marker genes, and enhanced the resistance to R. solanacearum, suggesting AhPPR598 was a positive regulator of immunity by regulating the JA and SA pathways. These results provide a new understanding of the origin, distribution, and evolution of the AhPPR gene family and potential gene resources for peanut-resistant breeding. [ABSTRACT FROM AUTHOR]

A large seed mutant, TG 89 having a 76.7% increment in hundred kernel weight in comparison to its parent TG 26, was isolated from an electron beam-induced mutagenized population. Studies based on environmental scanning electron microscopy of both parent and mutant revealed that the mutant seed cotyledon had significantly bigger cell size than parent. A mapping population with 122 F2 plants derived from the mutant and a distant normal seed genotype (ICGV 15007) was utilized to map the QTL associated with higher HKW. Bulk segregant analysis revealed putative association of three markers with this mutant large seed trait. Further, genotyping of F2 individuals with polymorphic markers detected 14 linkage groups with a map distance of 1053 cM. QTL analysis revealed a significant additive major QTL for the mutant large seed trait on linkage group A05 explaining 12.7% phenotypic variation for the seed size. This QTL was located between flanking markers AhTE333 and AhTE810 having a map interval of 4.7 cM which corresponds to 90.65 to 107.24 Mbp in A05 chromosome, respectively. Within this genomic fragment, an ortholog of the BIG SEEDS 1 gene was found at 102,476,137 bp. Real-time PCR revealed down-regulation of this BIG SEEDS 1 gene in the mutant indicating a loss of function mutation giving rise to a large seed phenotype. This QTL was validated in 11 advanced breeding lines having large seed size from this mutant but with varied genetic backgrounds. This validation showcased a highly promising selection accuracy of 90.9% for the marker-assisted selection. [ABSTRACT FROM AUTHOR]

This study reports the utilization of raw agricultural biowaste groundnut shell (GS) as a potential immobilization matrix for an isolated bacterial consortium as a sustainable means to remove 4-nitrophenol (4-NP). Optimization of five parameters such as immobilization matrix size, matrix dosage, pH, temperature, and agitation and their three levels was done through Taguchi Orthogonal Array approach by Qualitek-4 software. Taguchi methodology indicated the optimum reaction conditions to be (in order of their significance) agitation speed (100 rpm), immobilization matrix dosage (4 g), matrix size (800 µm), pH (9), and temperature (32 °C), resulting in an overall enhancement of 57.30% 4-NP removal efficiency under the optimized conditions. GS-immobilized cells exhibited an improved substrate removal efficiency and high substrate tolerance over free cells, indicating the synergistic effects of adsorption and biodegradation on the removal process. The GS immobilized cells could remove 1000 mg l−1 of 4-NP as opposed to only 700 mg l−1 by the free cells. Biodegradation kinetics were analyzed using various substrate inhibition models, and Haldane model fitted the experimental data reasonably well. GS immobilized cells retained a stable activity of 85.5 ± 3.48% for 45 days when stored at 4 °C and could be efficiently reused for 4 consecutive cycles. Thus, utilizing untreated agricultural wastes like GS will be a cost-effective alternative to conventional immobilization matrices in small-scale industries and can be a step towards sustainable agro-waste management and contaminated wastewater treatment. [ABSTRACT FROM AUTHOR]

The heavy metal ATPase (HMA) family belongs to the P-type ATPase superfamily and plays an essential role in the regulation of metal homeostasis in plants. However, the gene family has not been fully investigated in peanut. Here, a genome-wide identification and bioinformatics analysis was performed on AhHMA genes in peanut, and the expression of 12 AhHMA genes in response to Cu, Zn, and Cd was evaluated in two peanut cultivars (Silihong and Fenghua 1) differing in Cd accumulation. A total of 21 AhHMA genes were identified in the peanut genome, including ten paralogous gene pairs derived from whole-genome duplication, and an additional gene resulting from tandem duplication. AhHMA proteins could be divided into six groups (I–VI), belonging to two clades (Zn/Co/Cd/Pb-ATPases and Cu/Ag-ATPases). Most AhHMA proteins within the same clade or group generally have a similar structure. However, significant divergence exists in the exon/intron organization even between duplicated gene pairs. RNA-seq data showed that most AhHMA genes are preferentially expressed in roots, shoots, and reproductive tissues. qRT-PCR results revealed that AhHMA1.1/1.2, AhHMA3.1/3.2, AhHMA7.1/7.4, and AhHMA8.1 might be involved in Zn transport in peanut plants, while AhHMA3.2 and AhHMA7.5 might be involved in Cd transport. Our findings provide clues to further characterize the functions of AhHMA genes in metal uptake and translocation in peanut plants. [ABSTRACT FROM AUTHOR]

Copyright of Revista Colombiana de Biotecnología is the property of Universidad Nacional de Colombia and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Sclerotium rolfsii is a necrotrophic fungus that causes devastating stem rot disease on peanuts under high temperature and humidity conditions. Developing more resistant stem rot varieties is a better disease management strategy from an economic and environmental point of view. In this study, 105 peanut accessions from the USDA mini-core collection were screened for resistance against stem rot under growth chamber and greenhouse conditions at the New Mexico State University Agricultural Science Center in Clovis, NM, USA. The accessions were inoculated with a virulent isolate of S. rolfsii, and disease development was monitored and scored at 5, 7, 9, 11, and 17-days post-inoculation (DPI). Mean disease score, lesion length and broad sense heritability were calculated, and cluster analysis was performed. Though the accessions were not significantly different for the mean disease parameters, numerical differences were observed in disease score and lesion length among the accessions at 17-DPI. Eleven accessions showed moderate resistance and performed better than stem rot resistant commercial cultivar, 'G03L', and ninety-four accessions were susceptible based on mean disease scores under both growing conditions. Low broad-sense heritability for disease score (0.05 to 0.06) and lesion length (0.03 to 0.06) under different environments indicates that most of the variance for these traits is due to environmental effects, and that stem rot resistance can be a complex trait. The identified resistant accessions can be used for genotyping and finding major QTLs through genome-wide association mapping to dissect genetic basis of stem rot resistance in peanuts. This information would be helpful to the peanut breeding program to develop more resistant varieties. [ABSTRACT FROM AUTHOR]

Stilbenes, including resveratrol, are prominent bioactive compounds in peanuts widely recognized for their health benefits. However, limited research has focused on the production of resveratrol and its derivatives piceatannol and piceid from Arachis hypogaea. This research aims to study the production of these stilbenes using in vitro systems. Callus cultures have been established but only limited amounts of stilbenes were produced. Biotic elicitors, namely fungal culture filtrate (CF), mycelial extract (ME) and volatiles (VOCs) derived from three fungi (Serendipita indica , Fusarium solani and Alternaria alternata) were investigated in callus cultures. Based on Principal Components Analysis, 5 % v/v CF from A. alternata resulted in a significant increase in piceid production after 8 h. Similarly, 5 % v/v CF from S. indica after 16 h exhibited a notable enhancement in resveratrol and piceatannol levels. Enzyme activity of PAL and TAL was also promoted. Subsequent investigations involved establishing a cell suspension culture using CF from A. alternata and S. indica. In contrast to the callus culture, the levels of resveratrol remained comparatively lower. These results point towards a new method for piceid production using callus culture of peanuts, as well as a potential opportunity to obtain resveratrol and piceatannol via fungal elicitation. [Display omitted] • Piceid was produced in peanut callus culture without the need for elicitation. • Culture filtrate from Alternaria alternata increased piceid production. • Culture filtrate from Serendipita indica resulted in a higher amount of resveratrol and piceatannol. • Culture filtrate from Serendipita indica successfully led to extracellular resveratrol production in peanut cell suspension. • Callus culture has proved to be a more favorable biotechnological approach to the production of natural stilbenes than cell suspensions. [ABSTRACT FROM AUTHOR]

Malate dehydrogenase (MDH) is one kind of oxidation–reduction enzyme that catalyzes the reversible conversion of oxaloacetic acid to malic acid. It has vital functions in plant development, photosynthesis, abiotic stress responses, and so on. However, there are no reports on the genome-wide identification and gene expression of the MDH gene family in Arachis hypogaea. In this study, the MDH gene family of A. hypogaea was comprehensively analyzed for the first time, and 15 AhMDH sequences were identified. According to the phylogenetic tree analysis, AhMDHs are mainly separated into three subfamilies with similar gene structures. Based on previously reported transcriptome sequencing results, the AhMDH expression quantity of roots and leaves exposed to manganese (Mn) toxicity were explored in A. hypogaea. Results revealed that many AhMDHs were upregulated when exposed to Mn toxicity, suggesting that those AhMDHs might play an important regulatory role in A. hypogaea's response to Mn toxicity stress. This study lays foundations for the functional study of AhMDHs and further reveals the mechanism of the A. hypogaea signaling pathway responding to high Mn stress. [ABSTRACT FROM AUTHOR]

Late leaf spot (LLS) caused by the Ascomycete Nothopassalora personata (N.p.) (Syn. Cercosporidium personatum) is the main foliar disease of peanuts in Argentina and in peanut producing areas of the world, causing up to 70% yield losses. The extremely slow growth of this fungus in culture, that takes around one month to form a 1 cm colony (0.45 mm/day), and the lack of adequate young tissues from where to extract nucleic acids, have hindered genetic studies of this pathogen. Here, we report the first genome sequence of a N. personata isolate from South America, as well as genetic variants on its conserved genes, and the complete sequence of its mating-type locus MAT1-2 idiomorph. The N. personata isolate IPAVE 0302 was obtained from peanut leaves in Córdoba, Argentina. The whole genome sequencing of IPAVE 0302 was performed as paired end 150 bp NovaSeq 6000 and de novo assembled. Clean reads were mapped to the reference genome for this species NRRL 64463 and the genetic variants on highly conserved genes and throughout the genome were analyzed. Sequencing data were submitted to NCBI GenBank Bioproject PRJNA948451, accession number SRR23957761. Additional Fasta files are available from Harvard Dataverse (https://doi.org/10.7910/DVN/9AGPMG and https://doi.org/10.7910/DVN/YDO3V6). The data reported here will be the basis for the analysis of genetic diversity of the LLS pathogen of peanut in Argentina, information that is critical to make decisions on management strategies.

Abstract Background Puccinia arachidis fungus causes rust disease in the peanut plants (Arachis hypogaea L.), which leads to high yield loss. Metabolomic profiling of Arachis hypogaea was performed to identify the pathogen-induced production of metabolites involved in the defense mechanism of peanut plants. In this study, two peanut genotypes, one susceptible (JL-24) and one resistant (GPBD-4) were inoculated with Puccinia arachidis fungal pathogen. The metabolic response was assessed at the control stage (0 day without inoculation), 2 DAI (Day after inoculation), 4 DAI and 6 DAI by Gas Chromatography-Mass Spectrometry (GC-MS). Results About 61 metabolites were identified by NIST library, comprising sugars, phenols, fatty acids, carboxylic acids and sugar alcohols. Sugars and fatty acids were predominant in leaf extracts compared to other metabolites. Concentration of different metabolites such as salicylic acid, mannitol, flavonoid, 9,12-octadecadienoic acid, linolenic acid and glucopyranoside were higher in resistant genotype than in susceptible genotype during infection. Systemic acquired resistance (SAR) and hypersensitive reaction (HR) components such as oxalic acid was elevated in resistant genotype during pathogen infection. Partial least square-discriminant analysis (PLS-DA) was applied to GC-MS data for revealing metabolites profile between resistant and susceptible genotype during infection. Conclusion The phenol content and oxidative enzyme activity i.e. catalase, peroxidase and polyphenol oxidase were found to be very high at 4 DAI in resistant genotype (p-value

High yield is a major objective for peanut (Arachis hypogaea L.) breeding worldwide. However, fewer yield-related quantitative trait loci (QTL) have been reported in peanut than in other staple food crops such as rice (Oryza sativa), wheat (Triticum aestivum), and maize (Zea mays). This study aimed to identify stable major-effect QTL associated with pod yield per plant, hundred-pod weight for double-seeded pods, hundred-seed weight, shelling percentage, and pod number per plant, allowing us to predict candidate genes by means of transcriptome and genome sequencing. To this end, we used a population of recombinant inbred lines comprising 192 F9:11 families derived from a JH6 × KX01-6 cross to construct a high-resolution genetic map (1705.7 cM) consisting of 2273 polymorphic SNPs, with 0.75 cM (on average) between adjacent SNPs. We identified two high-confidence, yield-related QTL, qHYF_A08 and qHYF_B06, explaining 5.78%–31.40% of phenotypic variation and with LOD values of 5.10–24.48, in six environments. qHYF_A08 mainly explained the variation in shelling percentage, whereas qHYF_B06 explained variation in hundred-pod weight and hundred-seed weight and accounted for 8.77%–31.40% of the variation in effective pod number per plant, pod number per plant, and shelling percentage. We narrowed down qHYF_B06 to an 890-kb interval using an advanced mapping population. Transcriptome and genome analyses revealed that only Arahy.129FS0 and Arahy.3R9A5K in the candidate mapping interval were differentially expressed between JH6 and KX01-6, with substantial structural variations in their promoter and coding regions. Genotypes of 208 peanut accessions determined using a diagnostic CAPS marker suggested that the two haplotypes of Arahy.3R9A5K were highly associated with hundred-seed weight and hundred-pod weight; this diagnostic CAPs marker could therefore be useful for selecting high-yielding lines during peanut breeding. Overall, our results provide valuable information for cloning alleles with favorable effects on peanut yield.

Stem rot of groundnut (Arachis hypogaea L.) caused by Scelrotium rolfsii is the main threat to groundnut production, causing significant economic losses. The present study aims to provide an overview of the potentiality of Trichoderma viride (Tv), Trichoderma harzianum (Th), Pseudomonas fluorescens (Pf), and Bacillus subtilis (Bs), applied either individually or in mixed combination, against Sclerotium rolfsii (isolate SrBKN). The treatment with T. harzianum and P. fluorescens resulted in the highest mycelial growth inhibition (79.61, 83.51, and 86.77%), followed by T. viride and P. fluorescens (75.74, 79.63, and 83.14%). Under in vitro conditions, the combination of bio-agents at 5% culture filtrate proved to be superior against the test pathogen. Seed treatment and soil application of T. harzianum and Pf at 10 (5 + 5) g kg−1 + 10 (5 + 5) kg ha−1, followed by seed treatment and soil application of T. viride and Pf at 10 (5 + 5) g kg−1 + 10 (5 + 5) kg ha−1, resulted in the lowest disease incidence (7.40 and 8.0%), highest disease control (69.37 and 66.88%), maximum dry weight (151 and 147 g plant−1), highest increase in dry weight (75.58 and 70.93), highest pod yield (2665 and 2498 kg ha−1), and highest increase in pod yield (96.38 and 84.08%) under in vivo conditions. We present an effective bio-control-based management module from the lab to the field for the successful control of groundnut stem rot caused by S. rolfsii. Based on the results, it is concluded that the dual formulation of T. harzianum and P. fluorescens, followed by T. viride and P. fluorescens, were the most effective BCAs in suppressing the S. rolfsii. Therefore, an integrated disease management module with these BCAs needs to be developed and validated with a farmers’ participatory mode under field conditions.