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The positive response of grafting by tolerant rootstocks or scion-stock interactions on yield and fruit traits of tomatoes under saline conditions is attributed to several physiological and biochemical changes. In this study, we investigated some tolerance mechanisms by which grafting on wild rootstocks in tomatoes can prevent or minimize the effects of salt stress in plants under hydroponics conditions. Two tomato cultivars H2274 and Galaxy were grafted onto three S. pimpinellifolium, three S. habrochaites, S. lycopersicum L. × S. pimpinellifolium and S. lycopersicum L. × S. Habrochaites hybrid tomato genotypes. Plants were grown in hydroponic culture at two electrical conductivity (EC) levels (control at 1.5 dSm-1 and salt at 8.0 dSm-1). Salt stress led to a significant reduction in biomass growths of both grafted and nongrafted tomatoes. However, the plants that are least affected by salt stress are those grafted on wild tomato rootstocks. Leaf nutrient contents were significantly affected by rootstocks under both control and salt stress conditions. In this study, under saline conditions, plants grafted on wild rootstocks had higher N, P, K, Ca, Mg, S, Mn, Fe, Zn and B contents in leaf tissues and lower Na and Cl contents than ungrafted plants. Biochemical and physiological results revealed that S. pimpinellifolium and S. habrochaites have inherited salt tolerance from their genetic background. These wild tomato genotypes can be used as rootstocks in tomato breeding programs to develop salt-tolerant tomatoes or in grafting techniques under saline irrigation conditions. [ABSTRACT FROM AUTHOR]

Almost all research on natural attenuation and phytoremediation of sites contaminated with briny produced water has been conducted in temperate climates, however, there is a dearth of information on the use of tropical species for this purpose. It is within this context, that we investigated a spontaneously growing hypersaline spikerush from a contaminated site in southeast Mexico, to determine its soil salinity limits, the relationship between soil organic matter and salinity, and for preliminary documentation of floristic succession with Typha sp. for phytoremediation o f brine s pills. Soil was sampled (0 cm–20 cm) three times between 2018–2021, focusing on the end of the dry season (most critical period). The species tentatively identified as Eleocharis mutata was tolerant to soil hypersalinity (Electrical Conductivity: 125 dS/m) and appeared to generate a cyclic process of succession to recover areas with soil salinity levels higher than it could otherwise tolerate. A salinity gradient was found between the most heavily contaminated part of the site (“kill zone”, > 212 dS/m), the first Eleocharis sp. individuals (125 dS/m), slowly advancing through the main spikerush stand, and finally into a cattail stand (< 8.02 dS/m). Similarly, an inverse relationship between Soil Organic Matter content and soil salinity was observed. This is the first time this species has been identified with a brine spill, its salinity limits determined, and investigated for use in phytoremediation of this kind. [ABSTRACT FROM AUTHOR]

The rhizobacterial isolate SP-167 exhibited considerable phosphate solubilization, IAA production, exo-polysaccharides, proline, APX, and CAT at a concentration of 6% NaCl (w/v). 16S rDNA sequencing and BLAST analysis showed that isolate SP-167 was Klebsiella sp. In this study, T2 and T8 consortium was developed on the basis of the compatibility of isolate SP-167 with Kluyvera sp. and Enterobacter sp. At 6% NaCl (w/v) concentration, T2 and T8 showed increased PGP properties such as phosphate solubilization, IAA, Proline activity, CAT, POD, and EPS than isolate SP-167. The maximum increase in shoot length was recorded in T2-treated maize plants as compared to the control after 60 days in 1% NaCl stress. The N, P, and K content of leaves were significantly increased in maize plants with the inoculation of both the T2 and T8 consortium. The electrical conductivity of soil was decreased significantly in the T2 inoculated 1% NaCl (w/v) treated pot after 30, 60, and 90 days. In this study, soil enzymes DHA and PPO were significantly increased in both T2 and T8 treated combinations. The Na concentration in root and shoot were significantly decreased in T8 inoculated plant than in T2, as confirmed by the translocation factor study. [ABSTRACT FROM AUTHOR]

Abstract Realising a fully circular bioeconomy requires the valorisation of lignocellulosic biomass. Cellulose is the most attractive component of lignocellulose but depolymerisation is inefficient, expensive and resource intensive requiring substantial volumes of potable water. Seawater is an attractive prospective replacement, however seawater tolerant enzymes are required for the development of seawater-based biorefineries. Here, we report a halophilic cellobiohydrolase SMECel6A, identified and isolated from a salt marsh meta-exo-proteome dataset with high sequence divergence to previously characterised cellobiohydrolases. SMECel6A contains a glycoside hydrolase family 6 (GH6) domain and a carbohydrate binding module family 2 (CBM2) domain. Characterisation of recombinant SMECel6A revealed SMECel6A to be active upon crystalline and amorphous cellulose. Mono- and oligosaccharide product profiles revealed cellobiose as the major hydrolysis product confirming SMECel6A as a cellobiohydrolase. We show SMECel6A to be halophilic with optimal activity achieved in 0.5X seawater displaying 80.6 ± 6.93% activity in 1 × seawater. Structural predictions revealed similarity to a characterised halophilic cellobiohydrolase despite sharing only 57% sequence identity. Sequential thermocycling revealed SMECel6A had the ability to partially reversibly denature exclusively in seawater retaining significant activity. Our study confirms that salt marsh ecosystems harbour enzymes with attractive traits with biotechnological potential for implementation in ionic solution based bioprocessing systems.

Realising a fully circular bioeconomy requires the valorisation of lignocellulosic biomass. Cellulose is the most attractive component of lignocellulose but depolymerisation is inefficient, expensive and resource intensive requiring substantial volumes of potable water. Seawater is an attractive prospective replacement, however seawater tolerant enzymes are required for the development of seawater-based biorefineries. Here, we report a halophilic cellobiohydrolase SMECel6A, identified and isolated from a salt marsh meta-exo-proteome dataset with high sequence divergence to previously characterised cellobiohydrolases. SMECel6A contains a glycoside hydrolase family 6 (GH6) domain and a carbohydrate binding module family 2 (CBM2) domain. Characterisation of recombinant SMECel6A revealed SMECel6A to be active upon crystalline and amorphous cellulose. Mono- and oligosaccharide product profiles revealed cellobiose as the major hydrolysis product confirming SMECel6A as a cellobiohydrolase. We show SMECel6A to be halophilic with optimal activity achieved in 0.5X seawater displaying 80.6 ± 6.93% activity in 1 × seawater. Structural predictions revealed similarity to a characterised halophilic cellobiohydrolase despite sharing only 57% sequence identity. Sequential thermocycling revealed SMECel6A had the ability to partially reversibly denature exclusively in seawater retaining significant activity. Our study confirms that salt marsh ecosystems harbour enzymes with attractive traits with biotechnological potential for implementation in ionic solution based bioprocessing systems. [ABSTRACT FROM AUTHOR]

Among cereal crops, rice (Oryza sativa L.) is the most susceptible to salinity. Due to emerging salinity impacts on food security, different strategies have been implemented including developing salt tolerant varieties. Therefore, this study was conducted to produce salt tolerant lines of 'MARDI Siraj 297' through in vitro callus selection, enhancement of salinity tolerance through supplementation of salicylic acid (SA) (0, 0.5 and 1.0 mM) and regeneration of the selected salt tolerant callus. Embryogenic calli were induced and then treated in selection medium containing 0, 25, 50, 75, 100, 125 and 150 mM NaCl for 5 mo, followed by screening and selection of salt tolerant variants using morphology and biochemical parameters associated with salt tolerance. The salt tolerant calli showed reduced tissue necrosis and maintain their viability. Biochemical profile of these salt tolerant calli showed significantly (p < 0.05) higher content of proline (0.28 to 0.38 mg g-1), total soluble sugar (6.4 to 12.9 mg g-1), catalase activity (0.9 to 8.0 μmol min-1 mg-1 protein), ascorbate peroxidase activity (5.4 to 20.3 μmol min-1 mg-1 protein), malondialdehyde (6 to 17 μg g-1 protein) and K+/Na+ ratio (1.0 to 3.0) while reduced in protein content as compared to the non-tolerant control. These characteristics are typically associated with tolerance against salinity, therefore lines potentially tolerant to this stress have been regenerated. The selected salt tolerant calli were transferred into medium with SA to enhance their tolerance. Supplementation of 1.0 mM SA results in reduced morphological injury, higher regeneration frequency and shoot number (56% and 6 shoots, respectively) as compared to the non-SAtreated. Hence, this study demonstrates the protective effect of SA against salinity and provides a reliable protocol for establishment of salt tolerant rice lines through in vitro selection. [ABSTRACT FROM AUTHOR]

Salt stress is a significant abiotic stress that reduces crop yield and quality globally. In this study, we utilized RNA sequencing (RNA-Seq) to identify differentially expressed genes (DEGs) in response to salt stress induced by gamma-ray irradiation in a salt-tolerant soybean mutant. The total RNA library samples were obtained from the salt-sensitive soybean cultivar Kwangan and the salt-tolerant mutant KA-1285. Samples were taken at three time points (0, 24, and 72 h) from two tissues (leaves and roots) under 200 mM NaCl. A total of 967,719,358 clean reads were generated using the Illumina NovaSeq 6000 platform, and 94.48% of these reads were mapped to 56,044 gene models of the soybean reference genome (Glycine_max_Wm82.a2.v1). The DEGs with expression values were compared at each time point within each tissue between the two soybeans. As a result, 296 DEGs were identified in the leaves, while 170 DEGs were identified in the roots. In the case of the leaves, eight DEGs were related to the phenylpropanoid biosynthesis pathway; however, in the roots, Glyma.03G171700 within GmSalt3, a major QTL associated with salt tolerance in soybean plants, was differentially expressed. Overall, these differences may explain the mechanisms through which mutants exhibit enhanced tolerance to salt stress, and they may provide a basic understanding of salt tolerance in soybean plants. [ABSTRACT FROM AUTHOR]

This article evaluates the genetic variability and viability association of eight mungbean varieties under different levels of salinity stress. The study found that four elite genotypes (Utkarsh, TARM 1, Vamban, and Vishal) performed better than others under various levels of salinity. The study also examined the effects of salinity on various growth parameters of mungbean plants, finding that increasing salinity levels negatively affected plant growth and development. Additionally, the study discussed the effects of salt stress on seed weight and yield, finding that increasing salinity levels resulted in a decrease in seed weight and yield per plant. The document concludes by recommending the use of the four superior genotypes in breeding programs for salt-tolerant mungbean varieties. [Extracted from the article]

The cooperative role of vital components of the antioxidative defense pathway in addition to redox couples was studied in a growth-phase dependent manner at 20, 30, and 40 days after subculturing (DAS) in five different euryhaline microalgal strains (EMS) Scenedesmus MKB (B-S), Spirulina subsalsa (B-6), Anabaena sp. (B-7), Chlorella sp. (B-8), and Chlorosarcinopsis eremi (B-18) collected from waterlogged areas of Punjab, India and in two freshwater microalgal strains (FMS). EMS surpasses to maintain a high redox couple's ratio ascorbic acid/dehydroascorbate (AsA/DHA), and reduced glutathione/oxidized glutathione (GSH/GSSG) through a close-knit pattern of antioxidative enzymes including high specific activities of ascorbate peroxidase (APX), monodehydroascorbate reductase (MDHAR), glutathione reductase (GR), dehydroascorbate reductase (DHAR) and less specific activity of glutathione peroxidase (GPX). While FMS struggled for the same irrespective of near similar total glutathione and higher specific activity of GPX might be answerable for the lesser redox ratio than EMS. However, high specific activity of catalase (CAT) might be sought to compensate for the less increase of APX in FMS. The fact significantly less H2O2, and malondialdehyde (MDA) with DAS in EMS than in FMS and higher redox ratios exquisitely elevate their tolerance ability making EMS a captivating prospect for cultivation in waterlogged areas. Additionally, their abundance of potent antioxidants further highlights the potential of EMS as an excellent source of these beneficial compounds. [ABSTRACT FROM AUTHOR]

Salt stress is a significant abiotic stress that reduces crop yield and quality globally. In this study, we utilized RNA sequencing (RNA-Seq) to identify differentially expressed genes (DEGs) in response to salt stress induced by gamma-ray irradiation in a salt-tolerant soybean mutant. The total RNA library samples were obtained from the salt-sensitive soybean cultivar Kwangan and the salt-tolerant mutant KA-1285. Samples were taken at three time points (0, 24, and 72 h) from two tissues (leaves and roots) under 200 mM NaCl. A total of 967,719,358 clean reads were generated using the Illumina NovaSeq 6000 platform, and 94.48% of these reads were mapped to 56,044 gene models of the soybean reference genome (Glycine_max_Wm82.a2.v1). The DEGs with expression values were compared at each time point within each tissue between the two soybeans. As a result, 296 DEGs were identified in the leaves, while 170 DEGs were identified in the roots. In the case of the leaves, eight DEGs were related to the phenylpropanoid biosynthesis pathway; however, in the roots, Glyma.03G171700 within GmSalt3, a major QTL associated with salt tolerance in soybean plants, was differentially expressed. Overall, these differences may explain the mechanisms through which mutants exhibit enhanced tolerance to salt stress, and they may provide a basic understanding of salt tolerance in soybean plants.

Cultivating salt-tolerant crops is a feasible way to effectively utilize saline-alkali land and solve the problem of underutilization of saline soils. Quinoa, a protein-comprehensive cereal in the plant kingdom, is an exceptional crop in terms of salt stress tolerance level. It seems an excellent model for the exploration of salt-tolerance mechanisms and cultivation of salt-tolerant germplasms. In this study, the seeds and seedlings of the quinoa cultivar Shelly were treated with different concentrations of NaCl solution. The physiological, biochemical characteristics and agronomic traits were investigated, and the response patterns of three salt stress-responsive genes (SSRGs) in quinoa were determined by real-time PCR. The optimum level of stress tolerance of quinoa cultivar Shelly was found in the range of 250-350 mM concentration of NaCl. Salt stress significantly induced expression of superoxide dismutase (SOD), peroxidase (POD), and particularly betaine aldehyde dehydrogenase (BADH). BADH was discovered to be more sensitive to salt stress and played an important role in the salt stress tolerance of quinoa seedlings, particularly at high NaCl concentrations, as it displayed upregulation until 24 h under 100 mM salt treatment. Moreover, it showed upregulation until 12 h under 250 mM salt stress. Taken together, these results suggest that BADH played an essential role in the salt-tolerance mechanism of quinoa. Based on the expression level and prompt response induced by NaCl, we suggest that the BADH can be considered as a molecular marker for screening salt-tolerant quinoa germplasm at the early stages of crop development. Salt treatment at different plant ontogeny or at different concentrations had a significant impact on quinoa growth. Therefore, an appropriate treatment approach needs to be chosen rationally in the process of screening salt-tolerant quinoa germplasm, which is useful to the utilization of saline soils. Our study provides a fundamental information to deepen knowledge of the salt tolerance mechanism of quinoa for the development of salt-tolerant germplasm in crop breeding programs. [ABSTRACT FROM AUTHOR]

Copyright of Acta Agronomica Sinica is the property of Crop Science Society of China 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.)

An alkali and salt-tolerating strain FJAT-44876T was isolated from the bauxite residue sample. The 16S rRNA gene sequence and phylogenetic analysis suggest that strain FJAT-44876T was a member of the genus Evansella. It grew at 15–45 ℃ (optimum 20–25 ℃) and pH 6.5–11.0 (optimum pH 8.0–9.0) with 0–20% (w/v) NaCl (optimum 6–8%). The major fatty acids were anteiso-C15:0, iso-C15:0, anteiso-C17:0, iso-C17:0, and C16:0. The cell wall peptidoglycan contained meso-diaminopimelic acid and MK-7 as the menaquinone. The major polar lipids were diphosphatidylglycerol, phosphatidylmethylethanolamine, phosphatidylethanolamine, and phosphatidylglycerol. The genomic DNA G+C content was 38.2%. The average nucleotide identity values between strain FJAT-44876T and closely related members were below the cutoff level for species delineation. Thus, based on the above results, strain FJAT-44876T represents a novel species of the genus Evansella, for which the name Evansella halocellulosilytica sp. nov., is proposed. The type strain is FJAT-44876T (=CCTCC AB 2016264T = DSM 104633T). [ABSTRACT FROM AUTHOR]

Abstract Background Soil salinity has been one of the biggest hurdles in achieving better crop yield and quality. Plant growth-promoting rhizobacteria (PGPR) are the symbiotic heterogeneous bacteria that play an important role in the recycling of plant nutrients through phytostimulation and phytoremediation. In this study, bacterial isolates were isolated from salt-polluted soil of Jhajjar and Panipat districts of Haryana, India. The potential salt-tolerant bacteria were screened for their PGPR activities such as phosphate solubilization, hydrogen cyanide (HCN), indole acetic acid (IAA) and ammonia production. The molecular characterization of potent isolates with salt tolerance and PGPR activity was done by 16S rDNA sequencing. Results Eighteen soil samples from saline soils of Haryana state were screened for salt-tolerant bacteria. The bacterial isolates were analyzed for salt tolerance ranging from 2 to 10%. Thirteen isolates were found salt tolerant at varied salt concentrations. Isolates HB6P2 and HB6J2 showed maximum tolerance to salts at 10% followed by HB4A1, HB4N3 and HB8P1. All the salt-tolerant bacterial isolates showed HCN production with maximum production by HB6J2. Phosphate solubilization was demonstrated by three isolates viz., HB4N3, HB6P2 and HB6J2. IAA production was maximum in HB4A1 (15.89) and HB6P2 (14.01) and least in HB4N3 (8.91). Ammonia production was maximum in HB6P2 (12.3) and least in HB8P1 (6.2). Three isolates HB6J2, HB8P1 and HB4N3 with significant salt tolerance, and PGPR ability were identified through sequencing of amplified 16SrRNA gene and were found to be Bacillus paramycoides, Bacillus amyloliquefaciens and Bacillus pumilus, respectively. Conclusions The salt-tolerant plant growth-promoting rhizobacteria (PGPR) isolated from saline soil can be used to overcome the detrimental effects of salt stress on plants, with beneficial effects of physiological functions of plants such as growth and yield, and overcome disease resistance. Therefore, application of microbial inoculants to alleviate stresses and enhance yield in plants could be a low cost and environmental friendly option for the management of saline soil for better crop productivity.

Salinized soil is a major environmental stress affecting plant growth and development. Excessive salt in the soil inhibits the growth of most plants and even threatens their survival. Halophytes are plants that can grow and develop normally on saline-alkali soil due to salt tolerance mechanisms that emerged during evolution. For this reason, halophytes are used as pioneer plants for improving and utilizing saline land. Tamarisk, a family of woody halophytes, is highly salt tolerant and has high economic value. Understanding the mechanisms of salt tolerance in tamarisk and identifying the key genes involved are important for improving saline land and increasing the salt tolerance of crops. Here, we review recent advances in our understanding of the salt tolerance mechanisms of tamarisk and the economic and medicinal value of this halophyte. [ABSTRACT FROM AUTHOR]

Generally, the yield of most crops relies the intensity of drought and the stage of plant growth period where it occurs. Various wheat genotypes viz. IBWSN-1010, IBWSN-1025 (Salt tolerant liens), TD-1, ESW-9526 (Hybrid lines) Khirman (Commercial cultivated cultivar) and Chakwal-86 (Drought tolerant) were evaluated to examine the growth and physiological responses to drought stress. Growth and water relations were investigated in the fourth leaf over a twenty-day timescale under drought and control conditions. The results were used to evaluate whether the salt tolerant cultivars IBWSN-1010 and IBWSN-1025 are also tolerant to drought stress. In the drought treatment, the cultivars Chakwal-86 (drought tolerant), IBWSN-1010, IBWSN-1025 (salt tolerant liens) and TD-1 and ESW-9525 (Lines) had a significantly higher number of live leaves, leaf and shoot fresh and dry mass, retained higher leaf and relative water content, and had a lower leaf mortality compared to Khirman. The salt and drought tolerant cultivars all showed significantly higher leaf water potential compared to the hybrid lines and Khirman. No significant differences were observed in soil water content and potential, meaning that all cultivars depleted soil water equally. Longer leaf longevity and greater fresh mass retention show that salt tolerant cultivars are also drought tolerant. [ABSTRACT FROM AUTHOR]

This research project was undertaken to study salinity stress changes in the nutritional quality of wheat genotypes. Four wheat genotypes SARC-1, SARC-5, SARC-7, and SARC-8 were grown under nonsaline and saline (7.5 dS/m and 15 dS/m) treatments. Salinity was created artificially by the addition of NaCl in soil before filling in pots. Recommended fertilizers N (120 kg/ha), P (100 kg/ha) and K (60 kg/ha) were used in the form of Urea, diammonium phosphate (DAP) and sulphate of potash (SOP) in both saline and non-saline treatments. The grains of wheat genotypes were evaluated for nutritional quality i.e. chemical composition, mineral contents, wet and dry gluten, gliadin and glutenin, and SDS-sedimentation value. The results showed that growth parameters (biological yield, number of grains, thousand grain weight, grain yield and grain length) were affected significantly by salinity stress. Protein contents were increased with salinity, whereas other parameters (moisture, ash, fat, fiber, glutenin, and SDS-Sedimentation value) were decreased by increasing salinity stress. Similarly, Na content increased while K, Ca, P, Fe, Mg and Zn decreased significantly by increasing salinity stress. Salinity stress affect positively on protein contents in grain of all wheat genotypes. SARC-7 and SARC-5 performed better than SARC-1 and SARC-8.

In this study, in order to determine the resistance of registered lentil varieties to different salt concentrations during germination periods, this study was carried out in 2020 in University of Selçuk Faculty of Agriculture Department of Field Crops Laboratory in 4 replications according to the Randomized Plots Design. Çağıl, Çiftçi, Evirgen, Fırat-87, Kafkas, Özbek, Şakar, Şanlıbey and Tigris varieties were used as materials in the study. The effects of different salt concentrations (0 (control), 30 mM, 60 mM, 90 mM and 120 mM) on germination rate, germination speed, average germination time and sensitivity index were investigated. As a result of the study, it was determined that there were decreases in all the traits examined compared to the control application due to the increase in salt concentrations in all varieties. Especially in 90 and 120 mM NaCl applications, it was determined that the salt tolerance of the varieties decreased. Lentil varieties have been differently affected by salt applications, and the presence of genetic variation between varieties has helped us identify salt-resistant varieties. The varieties most sensitive to salinity were determined as Evirgen and Tigris. When all parameters are evaluated together, Özbek, Çağıl and Şanlıbey varieties have been determined as the best performing genotypes in terms of salt resistance. [ABSTRACT FROM AUTHOR]

Background: Soil salinity has been one of the biggest hurdles in achieving better crop yield and quality. Plant growth-promoting rhizobacteria (PGPR) are the symbiotic heterogeneous bacteria that play an important role in the recycling of plant nutrients through phytostimulation and phytoremediation. In this study, bacterial isolates were isolated from salt-polluted soil of Jhajjar and Panipat districts of Haryana, India. The potential salt-tolerant bacteria were screened for their PGPR activities such as phosphate solubilization, hydrogen cyanide (HCN), indole acetic acid (IAA) and ammonia production. The molecular characterization of potent isolates with salt tolerance and PGPR activity was done by 16S rDNA sequencing. Results: Eighteen soil samples from saline soils of Haryana state were screened for salt-tolerant bacteria. The bacterial isolates were analyzed for salt tolerance ranging from 2 to 10%. Thirteen isolates were found salt tolerant at varied salt concentrations. Isolates HB6P2 and HB6J2 showed maximum tolerance to salts at 10% followed by HB4A1, HB4N3 and HB8P1. All the salt-tolerant bacterial isolates showed HCN production with maximum production by HB6J2. Phosphate solubilization was demonstrated by three isolates viz., HB4N3, HB6P2 and HB6J2. IAA production was maximum in HB4A1 (15.89) and HB6P2 (14.01) and least in HB4N3 (8.91). Ammonia production was maximum in HB6P2 (12.3) and least in HB8P1 (6.2). Three isolates HB6J2, HB8P1 and HB4N3 with significant salt tolerance, and PGPR ability were identified through sequencing of amplified 16SrRNA gene and were found to be Bacillus paramycoides, Bacillus amyloliquefaciens and Bacillus pumilus, respectively. Conclusions: The salt-tolerant plant growth-promoting rhizobacteria (PGPR) isolated from saline soil can be used to overcome the detrimental effects of salt stress on plants, with beneficial effects of physiological functions of plants such as growth and yield, and overcome disease resistance. Therefore, application of microbial inoculants to alleviate stresses and enhance yield in plants could be a low cost and environmental friendly option for the management of saline soil for better crop productivity. [ABSTRACT FROM AUTHOR]

An endospore producing, strict aerobic, Gram-stain-positive, orange-colored colony forming bacterium designated as strain JC1013T was isolated from an orange pond near a solar saltern of Tamil Nadu, India. Phylogenetic analysis of the 16S rRNA gene sequences indicated that strain was affiliated to the family Bacillaceae of the phylum Firmicutes. Strain showed highest 16S rRNA gene sequence identity of 98.7% with Mesobacillus selenatarsenatis SF-1 T and below 98.3% with other members of the genus Mesobacillus. Strain JC1013T produced carotenoid pigments and indole compounds. Major cellular fatty acids of strain JC1013T were iso-C15:0, anteiso-C15:0, C16:0 3-OH, iso-C17:0ω10c and summed feature 4 (iso-C17:1 I/ anteisoB). Polar lipids were diphosphatidylglycerol, phosphatidylethanolamine, phosphatidylglycerol, two unidentified aminolipids and four unidentified phospholipids. Strain JC1013T constituted m-diaminopimelic acid as diagnostic cell wall amino acids. MK-7 is the predominant menaquinone of strain JC1013T. The genome size of strain JC1013T was 4.6 Mbp and its G + C content was 42.7 mol%. For the affirmation of strain's taxonomic status, a detailed phylogenomic study was done. Based on the phylogenetic analyses, low ANI (84.6%), AAI (88.5%) values, in-silico DDH (< 29%) value, morphological, physiological and chemo-taxonomical characteristics, strain JC1013T was clearly distinguished from the nearest phylogenetic neighbor, Mesobacillus selenatarsenatis SF-1T to conclude that it is a new species of the genus Mesobacillus. We propose the name as Mesobacillus aurantius with type strain JC1013T (= NBRC 114146T = KACC 21451 T). [ABSTRACT FROM AUTHOR]

Salinity stress is one of the most serious environmental issues in agricultural regions worldwide. Excess salinity inhibits root growth of various crops, and results in reductions of yield. It is of crucial to understand the molecular mechanisms mediating salinity stress responses for enhancing crops' salt tolerance. Marine red yeast Sporobolomyces pararoseus should have evolved some unique salt-tolerant mechanism, because they long-term live in high-salt ecosystems. However, little research has conducted so far by considering S. pararoseus as model microorganisms to study salt-tolerant mechanisms. Here, we successfully integrated metabolomics with transcriptomic profiles of S. pararoseus in response to salinity stress. Screening of metabolite features with untargeted metabolic profiling, we characterized 4862 compounds from the LC–MS/MS-based datasets. The integrated results showed that amino acid metabolism, carbohydrate metabolism, and lipid metabolism is significantly enriched in response to salt stress. Co-expression network analysis showed that 28 genes and 8 metabolites play an important role in the response of S. pararoseus, which provides valuable clues for subsequent validation. Together, the results provide valuable information for assessing the central metabolism of mediating salt responses in S. pararoseus and offer inventories of target genes for salt tolerance improvement via genetic engineering. [ABSTRACT FROM AUTHOR]

ABSTRACT Some plant-specific resistance genes could affect rhizosphere microorganisms by regulating the release of root exudates. In a previous study, the SST (seedling salt tolerant) gene in rice (Oryza sativa) was identified, and loss of SST function resulted in better plant adaptation to salt stress. However, whether the rice SST variation could alleviate salt stress via regulating soil metabolites and microbiota in the rhizosphere is still unknown. Here, we used transgenic plants with SST edited in the Huanghuazhan (HHZ) and Zhonghua 11 (ZH11) cultivars by the CRISPR/Cas9 system and found that loss of SST function increased the accumulation of potassium and reduced the accumulation of sodium ions in rice plants. Using 16S rRNA gene amplicon high-throughput sequencing, we found that the mutant material shifted the rhizobacterial assembly under salt-free stress. Importantly, under salt stress, the sst, HHZcas, and ZH11cas plants significantly changed the assembly of the rhizobacteria. Furthermore, the rice SST gene also affected the soil metabolites, which were closely related to the dynamics of rhizosphere microbial communities, and we further determined the relationship between the rhizosphere microbiota and soil metabolites. Overall, our results show the effects of the rice SST gene on the response to salt stress associated with the soil microbiota and metabolites in the rhizosphere. This study reveals a helpful linkage among the rice SST gene, soil metabolites, and rhizobacterial community assembly and also provides a theoretical basis for improving crop adaptation through soil microbial management practices. IMPORTANCE Soil salinization is one of the major environmental stresses limiting crop productivity. Crops in agricultural ecosystems have developed various strategies to adapt to salt stress. We used rice mutant and CRISPR-edited lines to investigate the relationships among the Squamosa promoter Binding Protein box (SBP box) family gene (SST/OsSPL10), soil metabolites, and the rhizosphere bacterial community. We found that during salt stress, there are significant differences in the rhizosphere bacterial community and soil metabolites between the plants with the SST gene and those without it. Our findings provide a useful paradigm for revealing the roles of key genes of plants in shaping rhizosphere microbiomes and their relationships with soil metabolites and offer new insights into strategies to enhance rice tolerance to high salt levels from microbial and ecological perspectives.

Salinized soil is a major environmental stress affecting plant growth and development. Excessive salt in the soil inhibits the growth of most plants and even threatens their survival. Halophytes are plants that can grow and develop normally on saline-alkali soil due to salt tolerance mechanisms that emerged during evolution. For this reason, halophytes are used as pioneer plants for improving and utilizing saline land. Tamarisk, a family of woody halophytes, is highly salt tolerant and has high economic value. Understanding the mechanisms of salt tolerance in tamarisk and identifying the key genes involved are important for improving saline land and increasing the salt tolerance of crops. Here, we review recent advances in our understanding of the salt tolerance mechanisms of tamarisk and the economic and medicinal value of this halophyte.

The wastewaters produced from dyeing process in textile industries contain xenobiotic mixed reactive dyes that have negative impact on ecosystem when discharged as untreated/partially treated. The present study aims to degrade mixed dyes (reactive red 21 (RR21) and reactive orange 16 (RO16)) present in wastewater by Pseudomonas aeruginosa 23N1. The process optimization and the effect of experimental parameters (like amount of co-substrate, pH and temperature) on process performance are investigated through response surface methodology. To understand the extent of degradation of dye compounds, metabolites extracted from treated water samples were investigated using UV–visible, FTIR and GC-MS analyses. The results reveal that the bacteria could significantly reduce ADMI value of wastewater by ~ 87% against the initial mixed dyes containing aqueous solution (50 mg/L each of RR21 and RO16 dyes). The analysis of extracted metabolites from treated water sample indicates the utilization of dye compounds as nutrient by bacteria. The bacteria might exhibit satisfactory ADMI reduction in the presence of initial ≤ 100 mg/L Cr(VI) concentration. The bio-degradation is performed under microbial fuel cell in the presence of co-substrate yeast extract and found very much promising in terms of faster ADMI reduction and energy production. The maximum output voltage generation of 790 ± 5 mV and power density 940.61 ± 5 mW/m2 are recorded during decolourization of mixed dye-laden real wastewater in a microbial fuel cell. The bacteria studied here confirm the effective bio-decolourization of real textile wastewater. [ABSTRACT FROM AUTHOR]

Copyright of Baghdad Science Journal is the property of Republic of Iraq Ministry of Higher Education & Scientific Research (MOHESR) 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.)

The effects of drought and salinity stresses on morpho-physiological characteristics of three Iris (Iris spp.) cultivars ('Purple Blue Magic', 'White Madonna' and 'Blue Deep River') were investigated. Drought stress experiment included three drought levels (60, 75, and 90% of field capacity), and the salinity stress experiment included four concentration of NaCl (0, 50, 100 and 150 mM). Different drought and salt treatments had significant effects on the morphological characteristics (leaf surface, main root diameter, number of branched roots and corm dry weight) and the physiological characteristics (Relative Water Content= RWC, Carotenoid, Lipid Peroxidation= MDA, and Electrolyte Leakage= EL) of the three iris cultivars. The best vegetative growth characteristics and physiological conditions were recorded under the control treatments [most favorable moisture conditions (90% FC) and without using salt in irrigation water] and the poorest were under the most severe stress conditions (60% FC and 150 mM NaCl in irrigation water). With increasing drought stress in 60% FC level and increasing NaCl salt treatments in 100 and 150 mM, no flower appeared in the 'Madonna' and 'Blue Magic' cultivar, respectively. In this aspect, only 'Deep River' cultivar could reach flowering phase and complete life cycle in both drought and salinity stresses. We concluded that the process of flowering in some iris cultivars were sensitive to drought stress and salinity. However, by selection, resistant or tolerant cultivars or genotypes could be identified and promoted under these abiotic stress conditions. [ABSTRACT FROM AUTHOR]

This research project was undertaken to study salinity stress changes in the nutritional quality of wheat genotypes. Four wheat genotypes SARC-1, SARC-5, SARC-7, and SARC-8 were grown under nonsaline and saline (7.5 dS/m and 15 dS/m) treatments. Salinity was created artificially by the addition of NaCl in soil before filling in pots. Recommended fertilizers N (120 kg/ha), P (100 kg/ha) and K (60 kg/ha) were used in the form of Urea, diammonium phosphate (DAP) and sulphate of potash (SOP) in both saline and non-saline treatments. The grains of wheat genotypes were evaluated for nutritional quality i.e. chemical composition, mineral contents, wet and dry gluten, gliadin and glutenin, and SDS-sedimentation value. The results showed that growth parameters (biological yield, number of grains, thousand grain weight, grain yield and grain length) were affected significantly by salinity stress. Protein contents were increased with salinity, whereas other parameters (moisture, ash, fat, fiber, glutenin, and SDS-Sedimentation value) were decreased by increasing salinity stress. Similarly, Na content increased while K, Ca, P, Fe, Mg and Zn decreased significantly by increasing salinity stress. Salinity stress affect positively on protein contents in grain of all wheat genotypes. SARC-7 and SARC-5 performed better than SARC-1 and SARC-8. [ABSTRACT FROM AUTHOR]

The purpose of this work was to assess how salt-tolerant wheat endophytic fungi promoted the growth of salt-sensitive wheat after inoculation. The endophytic fungal assemblages from salt-tolerant wheat genotypes (KRL-213, KRL-210 and KRL-19) and from salt-sensitive wheat genotype (PBW-343) were characterized, identified and determined for the current study. Of the fifty fungal isolates collected from both the salt-tolerant and the salt-sensitive wheat genotypes, 8 isolates recovered from salt-tolerant varieties were found to be resistant at high salt concentrations. These 8 isolates were characterized through several biochemical tests, such as plant growth promoting assay, extracellular enzymatic assay, carbohydrate utilization assay, antagonism versus plants pathogens and capacity to promote wheat seedlings (pot experiments). All tests revealed the positive results for 4 fungal strains (K13TR/150, K19TR/200, K-19TL/150 and K-19TL/200). These 4 fungi were identified as Aspergillus medius (K19TR/200) , Cladosporium parahalotolerant (K13TR/150) , Aspergillus versicolor (K19TL/150) and Aspergillus nishimurae (K19TL/200) through 18 S rDNA sequencing. Out of these, C. parahalotolerant and A. medius showed the synergistic effect with each other, so these 2 isolates were used in further experiments. These 2 isolates were involved in increasing the root-shoot length, proline and MDA contents. SEM and fluorescence microscopy were used to detect endophytic fungal colonization in the root of seedlings. C. parahalotolerant and A. medius heavily colonized the roots and it was noticed on the 21st day of the growth phase. These findings imply that fungal isolates have the potential to confer stress tolerance to their respective hosts and may enhance the agricultural production in the future, especially considering the changes in climate. [Display omitted] [ABSTRACT FROM AUTHOR]

Mangroves represent intricate and ever-changing ecosystems, exhibiting fluctuations in water level, salinity, and nutrient (such as NPK) availability as well as a wide array of unique bacterial communities. Microbial interactions in different components (e.g., tree roots) of the mangrove ecosystem are crucial to understand the ecosystem functioning for potential application in pollution mitigation and agricultural production. This study aimed to isolate phosphate-solubilizing bacteria (PSB) from the rhizosphere sediment of mangrove (Avicennia sp.) in terms of heavy metals (HMs) and salinity tolerance as well as plant growth promoting (PGP) traits, where the effective PSB were used on Brassica chinensis for their seed priming and growth under salinity stress. The effective two PSB isolates were identified by 16S rRNA, where JKD01 and JKD02 were closely related (99%) to Enterobacter cloacae (OQ271412) and Kocuria rhizophila (OQ271413), respectively. Both the strains exhibited phosphate solubilization, IAA, NH 3, and EPS production ability as well as HMs resistant ability where, E. cloacae (OQ271412) and K. rhizophila (OQ271413), are effectively remove the Cu from the water with 33.23% and 27.54%, respectively. The FTIR results showed functional group shifts (carboxyl, phosphate, and amino) in Cu-treated bacterial biomass and intracellular Cu presence, indicating the involvement of Cu in the bio-sorption and intracellular bioaccumulation process, respectively. The findings suggested PSB tolerance to salinity and HMs are present in mangroves, making them a valuable source for isolating effective bacteria to reduce stress in plants, lower HMs accumulation in mangroves, and aid in the bioremediation of HMs-contaminated environments. • PSB isolation: Enterobacter cloacae and Kocuria rhizophila from mangrove ecosystem. • PSBs exhibited PGP characters such as P solubilization, IAA, NH 3 , EPS. • PSBs have salinity and heavy metals resistant ability. • PSBs demonstrated effectiveness in bio-priming activity under salinity stress. • Both PSBs showed Cu removal from water by bio-sorption and accumulation. [ABSTRACT FROM AUTHOR]

Salinity is a leading threat to crop growth throughout the world. Salt stress induces altered physiological processes and several inhibitory effects on the growth of cereals, including wheat (Triticum aestivum L.). In this study, we determined the effects of salinity on five spring and five winter wheat genotypes seedlings. We evaluated the salt stress on root and shoot growth attributes, i.e., root length (RL), shoot length (SL), the relative growth rate of root length (RGR-RL), and shoot length (RGR-SL). The ionic content of the leaves was also measured. Physiological traits were also assessed, including stomatal conductance (gs), chlorophyll content index (CCI), and light-adapted leaf chlorophyll fluorescence, i.e., the quantum yield of photosystem II (Fv′/Fm′) and instantaneous chlorophyll fluorescence (Ft). Physiological and growth performance under salt stress (0, 100, and 200 mol/L) were explored at the seedling stage. The analysis showed that spring wheat accumulated low Na+ and high K+ in leaf blades compared with winter wheat. Among the genotypes, Sakha 8, S-24, W4909, and W4910 performed better and had improved physiological attributes (gs, Fv′/Fm′, and Ft) and seedling growth traits (RL, SL, RGR-SL, and RGR-RL), which were strongly linked with proper Na+ and K+ discrimination in leaves and the CCI in leaves. The identified genotypes could represent valuable resources for genetic improvement programs to provide a greater understanding of plant tolerance to salt stress.

Abstract Background Bipolaris sorokiniana is a filamentous fungus that causes spot blotch disease in cereals like wheat and has severe economic consequences. However, information on the identities and role of the cell wall-degrading enzymes (CWDE) in B. sorokiniana is very limited. Several fungi produce CWDE like glycosyl hydrolases (GHs) that help in host cell invasion. To understand the role of these CWDE in B. sorokiniana, the first step is to identify and annotate all possible genes of the GH families like GH3, GH6, GH7, GH45 and AA9 and then characterize them biochemically. Results We confirmed and annotated the homologs of GH3, GH6, GH7, GH45 and AA9 enzymes in the B. sorokiniana genome using the sequence and domain features of these families. Quantitative real-time PCR analyses of these homologs revealed that the transcripts of the BsGH7-3 (3rd homolog of the GH 7 family in B. sorokiniana) were most abundant. BsGH7-3, the gene of BsGH7-3, was thus cloned into pPICZαC Pichia pastoris vector and expressed in X33 P. pastoris host to be characterized. BsGH7-3 enzyme showed a temperature optimum of 60 °C and a pHopt of 8.1. BsGH7-3 was identified to be an endoglucanase based on its broad substrate specificity and structural comparisons with other such endoglucanases. BsGH7-3 has a very long half-life and retains 100% activity even in the presence of 4 M NaCl, 4 M KCl and 20% (v/v) ionic liquids. The enzyme activity is stimulated up to fivefold in the presence of Mn+2 and Fe+2 without any deleterious effects on enzyme thermostability. Conclusions Here we reanalysed the B. sorokiniana genome and selected one GH7 enzyme for further characterization. The present work demonstrates that BsGH7-3 is an endoglucanase with a long half-life and no loss in activity in the presence of denaturants like salt and ionic liquids, and lays the foundation towards exploring the Bipolaris genome for other cell wall-degrading enzymes.

Plants need to maintain a low Na+/K+ ratio for their survival and growth when there is high sodium concentration in soil. Under these circumstances, the high affinity K+ transporter (HKT) and its homologs are known to perform a critical role with HKT1;5 as a major player in maintaining Na+ concentration. Preferential expression of HKT1;5 in roots compared to shoots was observed in rice and rice-like genotypes from real time PCR, microarray, and RNAseq experiments and data. Its expression trend was generally higher under increasing salt stress in sensitive IR29, tolerant Pokkali, both glycophytes; as well as the distant wild rice halophyte, Porteresia coarctata, indicative of its importance during salt stress. These results were supported by a low Na+/K+ ratio in Pokkali, but a much lower one in P. coarctata. HKT1;5 has functional variability among salt sensitive and tolerant varieties and multiple sequence alignment of sequences of HKT1;5 from Oryza species and P. coarctata showed 4 major amino acid substitutions (140 P/A/T/I, 184 H/R, D332H, V395L), with similarity amongst the tolerant genotypes and the halophyte but in variance with sensitive ones. The best predicted 3D structure of HKT1;5 was generated using Ktrab potassium transporter as template. Among the four substitutions, conserved presence of aspartate (332) and valine (395) in opposite faces of the membrane along the Na+/K+ channel was observed only for the tolerant and halophytic genotypes. A model based on above, as well as molecular dynamics simulation study showed that valine is unable to generate strong hydrophobic network with its surroundings in comparison to leucine due to reduced side chain length. The resultant alteration in pore rigidity increases the likelihood of Na+ transport from xylem sap to parenchyma and further to soil. The model also proposes that the presence of aspartate at the 332 position possibly leads to frequent polar interactions with the extracellular loop polar residues which may shift the loop away from the opening of the constriction at the pore and therefore permit easy efflux of the Na+. These two substitutions of the HKT1;5 transporter probably help tolerant varieties maintain better Na+/K+ ratio for survival under salt stress.

Plants need to maintain a low Na+/K+ ratio for their survival and growth when there is high sodium concentration in soil. Under these circumstances, the high affinity K+ transporter (HKT) and its homologs are known to perform a critical role with HKT1;5 as a major player in maintaining Na+ concentration. Preferential expression of HKT1;5 in roots compared to shoots was observed in rice and rice-like genotypes from real time PCR, microarray, and RNAseq experiments and data. Its expression trend was generally higher under increasing salt stress in sensitive IR29, tolerant Pokkali, both glycophytes; as well as the distant wild rice halophyte, Porteresia coarctata , indicative of its importance during salt stress. These results were supported by a low Na+/K+ ratio in Pokkali, but a much lower one in P. coarctata. HKT1;5 has functional variability among salt sensitive and tolerant varieties and multiple sequence alignment of sequences of HKT1;5 from Oryza species and P. coarctata showed 4 major amino acid substitutions (140 P/A/T/I, 184 H/R, D332H, V395L), with similarity amongst the tolerant genotypes and the halophyte but in variance with sensitive ones. The best predicted 3D structure of HKT1;5 was generated using Ktrab potassium transporter as template. Among the four substitutions, conserved presence of aspartate (332) and valine (395) in opposite faces of the membrane along the Na+/K+ channel was observed only for the tolerant and halophytic genotypes. A model based on above, as well as molecular dynamics simulation study showed that valine is unable to generate strong hydrophobic network with its surroundings in comparison to leucine due to reduced side chain length. The resultant alteration in pore rigidity increases the likelihood of Na+ transport from xylem sap to parenchyma and further to soil. The model also proposes that the presence of aspartate at the 332 position possibly leads to frequent polar interactions with the extracellular loop polar residues which may shift the loop away from the opening of the constriction at the pore and therefore permit easy efflux of the Na+. These two substitutions of the HKT1;5 transporter probably help tolerant varieties maintain better Na+/K+ ratio for survival under salt stress. [ABSTRACT FROM AUTHOR]

Premise of research. Halophyte species grow where salt concentrations are high. Still, their germination may be affected by salts, either by creating an osmotic potential that prevents water uptake or by dissociating in ions that can cause different grades of toxicity. With the increase of salinized areas, it becomes important to understand the behavior of these species. Methodology. We studied how the germination of five halophyte species that occur along a salinity gradient in the Bahía Blanca coastal zone, Atriplex undulata , Cyclolepis genistoides , Allenrolfea patagonica , Sarcocornia perennis , and Heterostachys ritteriana , responds to variations in osmotic agents, osmotic potential, and temperature. Seeds were exposed to different osmotic potentials using NaCl (neutral salt), Na2CO3 (alkaline salt), and mannitol solutions in a germination chamber experiment. Germination was recorded during 42 d. Germination percentage, mean germination time, and synchrony were calculated. Pivotal results. Our experimental results showed that for the five halophyte species under study, germination was mostly driven by osmotic potentials and osmotic agents. At high osmotic potential, the germination response did not differ significantly from controls, except for Allenrolfea and Cyclolepis , which showed lower germination when treated with Na2CO3. Low osmotic potentials and Na2CO3 were detrimental to germination, reflected by lower germination percentages, higher mean germination times, and lower synchrony. Conclusions. In general, the response to the alkaline salt was more negative than that to the neutral salt or mannitol, regardless of the species. Each species showed a different response to the salts under study, and this response matched well with the distribution of species along the salinity gradient observed in the field. [ABSTRACT FROM AUTHOR]

Abstract In the past decades, the microbial fuel cell (MFC) technology has caught the attention of the scientific community for its potential in transforming petroleum hydrocarbon (PHC) pollutants directly into electricity through microbial catalyzed anodic. The microbe was one of the most important factors that both influence MFCs and PHC degradation. Here we aimed to identify new microbes to expand the list of microbial species which are both electrogenic and diesel hydrocarbon degrading. In this text, we depicted a strain of microbe named E2, isolated from on the anode surface of MFC, and using diesel as sole carbon source. E2 exhibited electrochemical activity in cyclic voltammetry curve, implicating that it had electrogenic ability. E2 degraded about 50% diesel (3.26 g/L) in maximum during 8 days. Pyrosequencing of 16S rRNA gene of E2 revealed E2 was a sub-strain of Vibrio. Corresponding to salt and alkali tolerant properties of vibrio , the optimal condition for E2 in degrading diesel was 3%–4% in salinity, and pH 8–9 in mineral medium. Collectively, as a member of Gammaproteobacteria class, E2 was novel marine microbe both electricity generation and diesel degradation, which may attract its future application toward artificial microbial community construction in MFC in promoting the PHC pollution removal. Graphical abstract Image 1 Highlights • E2 belonging to Vibrio. Sp. , was atypical exoelectrogen of a MFC. • E2 degraded PHCs in medium with high salinity and weak alkalinity. • The immobilization of E2 enhanced the PHC degradation efficiency. [ABSTRACT FROM AUTHOR]

To explore the effect of salt stress on photosynthetic traits and gene expression in Indian mustard, four genotypes CS 54 (national check for salinity), CS 52-SPS-1-2012 (salt tolerant mutant), CS 614-4-1-4-100-13 (salt sensitive mutant) and Pusa bold (high yielding variety) were evaluated under irrigation water salinity (ECiw 12, and 15 dS m−1). Results suggest genotype CS 52-SPS-1-2012 followed by CS 54 performed better under imposed salt stress due to differential regulation of Na+ accumulation in the roots and main stem, restriction of Na+ influx from root to shoot, maintaining higher net photosynthetic traits under saline stress compared to CS 614-4-1-4-100-13 and Pusa bold. Further, overexpression of antiporters (SOS1, SOS2, SOS3, ENH1 and NHX1) and antioxidant (APX1, APX4, DHAR1 and MDHAR) genes in salt tolerant genotypes CS 52-SPS-1-2012 and CS 54 demonstrated their significant role in imparting salt tolerance in Indian mustard. [ABSTRACT FROM AUTHOR]

An acid stable α-galactosidase was produced and purified from mannolytic fungal strain, Penicillium aculeatum APS1. Enzyme was produced using wheat bran and copra cake moistened with corn steep liquor by solid state fermentation. APS1αgal having molecular weight of 65.4 kDa was purified to electrophoretic homogeneity by three phase partitioning and gel permeation chromatography with high enzyme recovery. APS1αgal was found to be maximally active at 55 °C and pH 4.5, having high stability at acidic pH. Thermal stability and thermal inactivation kinetics of APS1αgal were also studied. APS1αgal was found to effectively hydrolyse oligosaccharides as well as polysaccharides having α-1,6 linked galactose. Abolishment of enzyme activity in N-brommosuccinimide revealed an important role of tryptophan residue in catalysis. APS1αgal had shown outstanding tolerance to NaCl and proteases. MALDI-TOF MS/MS analysis indicated that enzyme is probably a member of family GH27. Synergistic interaction between APS1αgal and β-mannanase for hydrolysis of galactomannan was very clear and maximum 2.0° of synergy was found under simultaneous mode of action. This study reports a new source of α-galactosidase with biochemical properties suitable for applications in food and feed industries. [Display omitted] • Fungal α-galactosidase was produced and purified to electrophoretic homogeneity. • APS1 α-galactosidase having molecular weight of 65.4 kDa maybelongs to GH27 family. • APS1 was found to be acid stable, salt tolerant and protease resistant. • Synergistic interaction of APS1 α-galactosidase with APS1 β-mannanase was observed. [ABSTRACT FROM AUTHOR]

A xylanase (Xyn10A) gene from the saline-alkali-tolerant microorganism Bacillus cellulosilyticus DSM 2522 was cloned and expressed in Escherichia coli BL21 (DE3). The open reading frame was composed of 1008 base pairs, and it encoded 335 amino acid residues belonging to glycosyl hydrolase family 10. The optimal temperature and pH of the purified Xyn10A were 40 °C and 8.0, respectively. The Xyn10A was sensitive to heat and showed obvious cold-adapted activity, retaining 38.3%, 55.7%, and 82.9% of the optimal activity at 4, 20, and 30 °C, respectively. Xyn10A also showed a high level of NaCl tolerance. The highest activity was observed with 1.5 M NaCl. The specific enzyme activity of Xyn10A was as much as 163.8 U/mg. Kinetic assays showed that Km, Vmax, and Kcat were 2.56 mg/mL, 202.5 μM/min/mg, and 132.6 /s, respectively. Additionally, the main hydrolysis products using birchwood xylan as substrate were xylobiose, xylotriose, and xylotetraose, as determined by thin layer chromatography analysis. As a cold-adapted and salt-tolerant enzyme, Xyn10A is an ideal candidate for further research and biotechnological applications.

The purpose of this work was to assess how salt-tolerant wheat endophytic fungi promoted the growth of salt-sensitive wheat after inoculation. The endophytic fungal assemblages from salt-tolerant wheat genotypes (KRL-213, KRL-210 and KRL-19) and from salt-sensitive wheat genotype (PBW-343) were characterized, identified and determined for the current study. Of the fifty fungal isolates collected from both the salt-tolerant and the salt-sensitive wheat genotypes, 8 isolates recovered from salt-tolerant varieties were found to be resistant at high salt concentrations. These 8 isolates were characterized through several biochemical tests, such as plant growth promoting assay, extracellular enzymatic assay, carbohydrate utilization assay, antagonism versus plants pathogens and capacity to promote wheat seedlings (pot experiments). All tests revealed the positive results for 4 fungal strains (K13TR/150, K19TR/200, K-19TL/150 and K-19TL/200). These 4 fungi were identified as Aspergillus medius (K19TR/200), Cladosporium parahalotolerant (K13TR/150), Aspergillus versicolor (K19TL/150) and Aspergillus nishimurae (K19TL/200) through 18 S rDNA sequencing. Out of these, C. parahalotolerant and A. medius showed the synergistic effect with each other, so these 2 isolates were used in further experiments. These 2 isolates were involved in increasing the root-shoot length, proline and MDA contents. SEM and fluorescence microscopy were used to detect endophytic fungal colonization in the root of seedlings. C. parahalotolerant and A. medius heavily colonized the roots and it was noticed on the 21st day of the growth phase. These findings imply that fungal isolates have the potential to confer stress tolerance to their respective hosts and may enhance the agricultural production in the future, especially considering the changes in climate., Competing Interests: Declaration of Competing Interest The authors declare that they have no conflict of interest., (Copyright © 2023 Elsevier GmbH. All rights reserved.)

Copyright of Acta Agronomica Sinica is the property of Crop Science Society of China 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.)