Columnar apple is a valuable resource for genetic improvement of cultivated apples due to its special tree architecture. Strigolactones (SLs) are a novel class of plant hormones controlling shoot branching. The content of SLs is higher in columnar apple than in standard apples. In this study, the members of major gene families involved in SLs biosynthesis and signaling were identified from apple genomic sequences and their expression profiles were characterized in columnar and standard apples using reverse transcription quantitative polymerase chain reactions. In comparison with standard apple, the higher expressions of MORE AXILLARY GROWTH genes MdMAX3-1 and MdMAX4-4 were detected in both buds and shoots of columnar apple but the expression of DWARF gene MdD53-4 showed a lower expression in columnar apple. Overexpression of Columnar gene MdCo31 in tobacco increased SLs content and weakened the inhibition of SLs signal transduction by increasing expression of MAX3 and down-regulating the transcription of D53. Thus MdCo31 could be a strong candidate gene for the control of columnar habit.

To clarify the effects of the introduction of Festuca pratensis-derived genomic regions in a tetraploid Lolium perenne genomic background, we analyzed quantitative trait loci (QTLs) for winter hardiness and eight other agronomic traits using two mapping populations generated by sequential backcrosses of two different amphiploid F. pratensis × L. perenne hybrids to tetraploid L. perenne. We constructed two interspecific linkage maps: FLBC2A (143 DNA markers, 301.2 cM total) and FLBC2C (126 markers, 256.2 cM), based on F. pratensis-derived alleles, with 72 markers in common. Interval mapping detected QTLs for seven traits in FLBC2A and for six traits in FLBC2C. In both populations, QTLs for winter hardiness with a positive effect of the F. pratensis allele were detected around common markers on linkage group (LG) 1. In FLBC2A, other additional QTLs for winter hardiness with a positive effect of the F. pratensis allele were detected on LG4 and LG5, and one with a negative effect was detected on LG2. In both populations, a QTL for heading date was detected on LG7. Quantitative trait loci for vigor after planting and stubble width were detected on different LGs between populations. Quantitative trait loci for dry matter yield before winter, plant growth habit, inflorescence length, number of spikelets per inflorescence, and leaf width were detected in only one population. Population-dependent QTLs thought to be involved in intraspecific variation in addition to interspecific one. On the other hand, QTLs found in the two different populations could lead to the development of versatile markers for Festulolium breeding.

The calcineurin B-like protein (CBL)-interacting protein kinase (CIPK) complex is an essential calcium sensor and contributes to biotic and abiotic stress responses. However, citrus CBL and CIPK gene family members and their underlying roles during drought and arbuscular mycorrhizal fungi (AMF) colonization remain relatively unknown. In the present study, CBLs and CIPKs were characterized in Citrus sinensis by analyzing the presence of specific domains such as the elongation factor (EF)-hand motif in CBLs, and a protein kinase and an Asn-Ala-Phe domain in CIPKs. After mining the C. sinensis genome, we identified 8 CsCBLs and 17 CsCIPKs. Among these genes, three CsCBLs and nine CsCIPKs showed syntenic relationships with the Arabidopsis thaliana homologs AtCBLs and AtCIPKs, respectively. According to gene expression and cis-acting element analysis, all 8 CsCBLs and 16 CsCIPKs were expressed in the roots, where the regulation of expression was not consistent with their promoter cis-elements. Drought treatment remarkably downregulated the expression of CsCBL8 and upregulated CsCBL7, CsCIPK4, and CsCIPK7 expressions. The AMF colonization induced CsCBL4, 5, 6, and 7 as well as CsCIPK2, 4, 10, 11, 13, 14, and 16 expressions and repressed CsCBL1, 2, 3, and 8 and CsCIPK1, 3, 6, 8, 9, and 12 expressions. Based on the expression data and co-expression analysis, CsCBL1-CsCIPK1, CsCBL1-CsCIPK3, CsCBL1-CsCIPK6, and CsCBL1-CsCIPK9 showed the significant positive correlations to drought and AMF responses.

Tissue culture of hazelnut (Corylus avellana L.) represented the promising strategy for production of its valuable compound, paclitaxel, but one of the most important problems is initial callus browning in its callus culture. To obtain healthy callus cells of C. avellana, three different culture media, Murashige and Skoog (MS), Nas and Read (NRM), and Driver and Koniuki (DKW), in combination with 500 mg dm^-3 citric acid, 500 mg dm^-3 acetic acid, and 500 mg dm^-3 polyvinylpyrrolidone (PVP) were applied. These cultures were passed two sub-cultures in the same media. Also, a novel modified sub-culture system was designed and compared to routine techniques. The sub-culture system was changed as following: the induced calli were transferred to a liquid media with the same composition and after developing the cell suspension, the cells were immobilized on a solid medium. In the first experiment, it was demonstrated that the medium compositions had an effect on the growth rate and callus browning reduction although they could not eliminate the browning. The results have shown that the highest growth indices were related to NRM with 500 mg dm^-3 acetic acid + 500 mg dm^-3 citric acid and to NRM with 500 mg dm^-3 PVP in the first culture. These media had the least amount of browning (9.15 %). In the two next sub-cultures, NRM without additives had the maximum growth rate and the lowest browning was observed on the same media as in the first subculture (13.3 %). The technique of modified sub-cultures increases growth rate ten times in comparison with routine cultivation method.

Silicon has been widely reported to have a beneficial effect on improving plant tolerance to biotic and abiotic stresses. However, the mechanisms of Si in mediating responses to simultaneous salt and drought stresses are still poorly understood. Glycyrrhiza uralensis Fisch. is classified as a non-Si accumulator and suffered from salt and drought stresses. In this study, we investigated the long-term application of Si on Si content in G. uralensis roots, stems and leaves, leaf anatomy, ultrastructure, chlorophyll (Chl) content, gas exchange characteristics, relative water content, and growth of two-year-old plants under different salt and drought stresses. Silicon application resulted in a higher Si uptake in G. uralensis roots and more Si accumulation in leaves (especially deposition of Si on cell walls), and Si counteracted the adverse effects induced by salt and drought stresses on the leaf anatomy and ultrastructure. In plants treated with Si, a higher chlorophyll content, net photosynthetic rate and relative water content led to a higher growth rate and dry mass under salt and drought stresses compared with corresponding non-Si treated plants.

Small RNAs (sRNAs) are essential components of gene-regulatory networks, which guide plant development and tune it to environmental challenges. Though the past years have witnessed evidences on sRNA importance for stress response, there is scarce data on their involvement in resurrection plant survival under severe drought. Haberlea rhodopensis (hrh) is an angiosperm resurrection species, whose vegetative tissues can tolerate desiccation and recover upon rehydration. In this study, high-throughput sequencing sRNAs indicated a higher complexity of the sRNA population, especially of a 24 nt sRNA category, in the desiccated vegetative tissue of H. rhodopensis compared to unstressed tissues. The cross-species discovery was performed to predict 77 mature microRNAs (miRNAs), most of which were assigned to 23 high-confidence conserved miRNA families in the leaf tissue. Several members of the miR156/157, miR166, and miR399 families were found to be desiccation-responsive. The miR156/157 family members were found up-regulated upon dehydration and down-regulated upon rehydration, while the miR166 and miR399 family members followed an opposite trend of expression. A probable miR156/157 target, orthologous to the SQUAMOSA promoter binding protein-like, was reconstructed in H. rhodopensis based on genomic data available for this species and the closely related Boea hygrometrica. Reverse transcription quantittative PCR analysis confirmed the expression profile of hrh-miR156a-5p and hrh-miR157-5p established by sRNA sequencing and revealed an inverse expression pattern between these miRNAs and their targets in the desiccated tissue. Our study suggests that the miR156/157 and miR399 families are essential for plant survival under severe drought due to their ability to control plant development and growth by modulating transcription factor expression.

The miR399 is a conserved microRNA (miRNA) family, and it has been characterized as an essential regulator of phosphorus transport in plants. However, the biological function of miR399 in Cunninghamia lanceolata is still largely unclear. In this study, the comparison of mature miR399 sequence revealed a high similarity between Arabidopsis thaliana and C. lanceolate, and the pre-miR399 was capable of forming a typical stem-loop hairpin structure. A gene PHOSPHATE 2 (PHO2) was identified as a target of cln-miR399 using 5' rapid amplification of cDNA ends. Furthermore, the relationship between cln-miR399 and PHO2 was further confirmed through a transient co-expression of both genes in Nicotiana benthamiana. To examine the function of miR399 in Arabidopsis, miR399-overexpressing transgenic Arabidopsis thaliana was acquired using Agrobacterium-mediated approach. Real-time PCR showed that the amount of cln-MIR399 transcripts was higher in miR399-overexpressing plants than in wild-type plants, which was accompanied with down-regulation of expression of its target gene AtPHO2. The P content was 1.40 to 1.56-fold higher in the leaves of three transgenic lines than in wild type plants. However, the P content in the roots of the three transgenic lines was 24.5 - 37.2 % less than that in wild type plants. Moreover, the transcriptions of three phosphate transporter genes (PHT1, PHT2, and PHT3) were up-regulated in roots of miR399-overexpressing Arabidopsis plants. Interestingly, the transgenic lines exhibited retarded growth under normal P conditions compared with the wild type. Our findings demonstrate that cln-miR399 may play crucial roles in P transport and plant growth via regulation of its target gene PHO2.

Cadmium (Cd) is a highly toxic and widespread soil pollutant, which negatively affects various aspects of plant growth and physiology. Here, the role of photosynthesis in response to Cd was investigated in the Cd-tolerant pea (Pisum sativum L.) mutant SGECd^t. The wild type SGE and the mutant SGECd^t were grown in a hydroponic solution supplemented with 1, 3, or 4 µM CdCl₂ for 12 d. Root and shoot biomasses of the Cd-treated SGECd^t were significantly higher than of SGE. Cadmium had little effect on the quantum yield of photosystem II (φPSII) and chlorophyll content of intact leaves of both pea genotypes. However, when leaf slices were taken from Cd-exposed plants and incubated with high Cd concentrations, the SGECd^t mutant showed 1.5 - 2 times higher φPSII values than SGE, with genotypic differences maximal at 0.1 and 1 mM CdCl₂. In contrast, when leaf slices were taken from plants previously unexposed to Cd, both pea genotypes exhibited similar φPSII values. Cadmium content in leaves and mesophyll protoplasts of Cd-treated SGECd^t were about 2 - 3 times higher than in SGE ones. The mutant leaves and mesophyll protoplasts had also higher Ca, Mg, Mn, and Zn content. Thus, SGECd^t acclimated to Cd during growth in the Cd-supplemented nutrient solution by developing a molecular mechanism related to photosynthetic integrity. A higher foliar nutrient content likely allows enhanced photosynthesis by counteracting the damage of leaves caused by Cd.

The WRKY belongs to an important plant specific transcription factor families which are involved in response to various environmental stresses, as well as in growth and developmental processes. In the present report, a genome-wide identification and characterization of WRKY gene family in barley led to revision of HvWRKYs to 93 members. The phylogenetic tree was also reconstructed based on the full-length WRKY protein sequences in barley and Arabidopsis. HvWRKYs were classified into three major groups (I, II, and III) and group II was further divided to 5 subgroups (a to e). HvWRKYs were named after this classification. Interestingly, some specific motifs were discovered in subgroups IIa, IIb, and III. Analyzing the available microarray data revealed eight candidate WRKY genes which were up-regulated under drought and salinity stresses compared to the optimum conditions at seedling stage in barley. Expression profiles of these WRKY genes were validated by quantitative real-time PCR. All the investigated candidate genes (HvWRKY_IIc2, HvWRKY_III11, HvWRKY_IIb2, HvWRKY_IId4, HvWRKY_III23, HvWRKY_IIa5 and HvWRKY_IIc19) except for HvWRKY_I8 were significantly up-regulated by drought stress at the seedling stage in drought-tolerant genotype, indicating their role in drought tolerance. We hope the presented information would be helpful toward achieving drought tolerant cultivars through genetic engineering or molecular breeding.

To further elucidate the molecular mechanism of the germination in common wheat, a differential proteomic analysis was completed between the F₁ hybrid RS5322 and its parental lines (RS53 and SN22) using isobaric tags for relative and absolute quantitation (iTRAQ) based strategy. Rapid grain germination and superior young seedling growth were observed in the F₁ hybrid line. A total of 807 differentially abundant proteins (DAPs) were identified by iTRAQ analysis of grains at 48 h after imbibition in distilled water. Bioinformatics analysis shows that 638 DAPs were annotated in 38 Gene Ontology functional groups, 764 DAPs were classified into 23 clusters of orthologous groups of protein categories, and 538 DAPs were enriched in 65 Kyoto encyclopedia of genes and genomes pathways. Real time quantitative PCR of 12 genes encoding different important proteins showed certain transcriptional and translational expression similarities during grain development. In the F₁ hybrid, the DAPs were particularly those involved in starch and sugar metabolism, protein metabolism, protein modification, and ubiquitin proteasome system (UPS). It was speculated that UPS might be responsible for a high germination ability in the F₁ hybrid by regulating storage substance metabolism. The DAPs identified in this study provide a scope for improving the grain germination trait in agricultural crops.

Uridine diphosphate glucose dehydrogenase (UGDH) is a key enzyme in the hemicellulose and pectin biosynthesis pathway and participates in the regulation of growth and development in plants. In this study, we isolated a BpUGDH gene from paper mulberry (Broussonetia kazinoki × Broussonetia papyifera) and analyzed its function and expression characteristics. The results show that the BpUGDH was expressed in all organs of paper mulberry with a higher expression in stems than in leaves and roots. A pBpUGDH::GUS gene construct was highly expressed in transgenic Arabidopsis thaliana seedlings, and its expression was induced by a low temperature, methyl jasmonate, gibberellin A₃, ethylene, and auxin. The overexpression of BpUGDH increased the soluble sugar content, promoted the accumulation of hemicellulose, and enhanced the vegetative growth of transgenic plants. These results provide a basis for regulating the growth and adaptability of paper mulberry and improving its utilization value via genetic modification of the BpUGDH gene.

Imidazolinone herbicides combined with imidazolinone resistant (IMI-R) crops provide a tool for solving the important problem of the occurrence of weeds during the early growth stages of sunflower. These herbicides inhibit the synthesis of branched chain amino acids by interrupting the key enzyme acetohydroxyacid synthase (AHAS). We studied the imazamox detoxification in an IMI-R sunflower hybrid together with plant growth and photosynthetic performance. Inhibition of photosynthesis and growth were observed as initial effects of imazamox application. A slight decrease in AHAS activity was also noticed. These effects disappeared within two weeks after application. A fast and well-functioning detoxification mechanism for the herbicide, of which the content decreased for about 90 % at 14 d after application, seems to be responsible for this. The activity of the xenobiotic detoxifying enzyme glutathione S-transferases (GSTs) significantly increased after imazamox application. Our results suggest that the metabolite glutathione serves as an auxiliary tool for imazamox detoxification through conjugation reactions realized by the GSTs, thereby taking part in the non-target mechanisms of resistance in IMI-R sunflower hybrids.

It is well known that phloem is essential for transporting proteins as long-distance signals. In this study, a proteomic approach was carried out to identify proteins accumulated in phloem exudates at the pre-floral induction (PFId) stage, at the floral induction (FId) stage, and at the floral initiation (FIn) stage. As a result, 45 phloem exudate proteins were detected. Six proteins were found at all three stages. Sixteen proteins were specific to the PFId stage, 14 proteins were specific to the FId and FIn stages. From the enriched gene ontology (GO)-terms related to transport, signaling, hormone, and development, 12 transport-related, 5 signaling-related, 10 hormone-related, and 9 development-related proteins were identified. It was found that arginine glycine glycine repeats nuclear RNA binding protein A (RGGA) was specific to the FId stage whereas heat shock protein 90-7, plasma membrane intrinsic protein 1-4, and the homolog protein encoded by At4g27190 were specific to the FIn stage. The relative abundances of sporulation protein F10D13.7 and ATP-dependent binding casette transporter G family member 37 were higher at the FId stage than at the PFId stage, and that of enolase 2 was higher at the FIn stage than at the PFId stage, suggesting that these phloem exudate proteins might act as long-distance signals involved in the transition from vegetative growth to reproductive growth in litchi. This study contributes to the comparative proteomic analysis of plant phloem sap, which will provide insights into proteins involved in floral induction as well as inter-organ communication during development in litchi.

Chilling stress is a major abiotic factor that limits the growth and productivity of melon (Cucumis melo L.). The application of nitric oxide (NO) can enhance plant tolerance to chilling stress; however, the underlying molecular mechanisms for this process remain poorly understood. In this study, RNA sequencing was performed on melon seedlings exposed to control conditions, chilling stress, or chilling stress in the presence of NO donor sodium nitroprusside (SNP), to identify NO-mediated transcript changes in response to chilling stress. The results identified 488, 1 012, and 1 589 differentially expressed genes (DEGs) between plants in optimum conditions (CK) and chilling stress (CS) groups, plants in the CS and chilling stress + SNP (CN) groups, and those in CK and CN groups, respectively. Through gene ontology (GO) database and Kyoto encyclopedia of genes and genomes (KEGG) enrichment analyses, the DEGs were classified as predominantly involved in saccharide metabolism, biosynthesis of other secondary metabolites, lipid metabolism, amino-acid metabolism, and signal transduction pathways. In addition, 39 genes related to sugar metabolism including those encoding UDP-glucuronate-4-epimerase, β-glucosidase, glucuronosyltransferase, α-1,4-galacturonosyl transferase, and hexokinase, were upregulated in the CK vs. CS comparison, and genes encoding fructose-bisphosphate aldolase and glucan-endo-1,3-β-glucosidase were upregulated in the CS vs. CN, and CK vs. CN comparisons. A gene encoding an EREBP-like factor was upregulated in the CK vs. CS, CS vs. CN, and CK vs. CN comparisons. The expression profiles of 10 selected genes were analyzed using real-time quantitative PCR, and the candidate gene expression patterns were consistent with the DEG classification from RNA-seq. Overall, the data provide insight into the transcriptional regulation by exogenous NO in the response of melon seedlings to chilling stress. The data from this study are relevant for further research on the molecular mechanisms that underlie chilling resistance in melon plants.

Effect of gibberellic acid (GA₃) combined with saponin on shoot elongation of Asparagus officinalis was evaluated in tissue culture. Addition of saponin to GA₃ supplemented Murashige and Skoog (MS) basal medium showed a dose depended effect on shoot length of Asparagus officinalis. However, increasing concentration of saponin above 3.0 mg dm^-3 decreased shoot length and showed yellowing and thinning of shoots. Saponin (3.0 mg dm^-3) + GA₃ (0.2 mg dm^-3) mixture treated by variable duration of sonication (0, 1, 3, 5, 7, 9, 11, 13 and 15 min) were evaluated for shoot elongation on MS basal medium. The highest shoot lengths (14.4 ± 0.3 and 15.1 ± 0.1 cm) were found after 5 and 7 min sonication.

The growth of the Cd-hyperaccumulator Solanum nigrum L. and its physiological responses to a short-term (7 d) Cd stress and to exogenous methyl jasmonate (MeJA) were investigated. Compared with the leaves of S. nigrum, the roots were more liable to Cd and showed a significantly decreased dry mass and increased malondialdehyde content. Cd accumulation in the shoots and roots of S. nigrum were proportional to the Cd concentration in the hydroponic solution. The application of a low concentration of MeJA (0.01 μM) significantly reduced the translocation/accumulation of Cd in both the shoots and roots compared with a 40 mg dm^-3 Cd treatment only. Moreover, 40 mg dm^-3 Cd significantly decreased the activity of leaf superoxide dismutase, but 0.01 μM MeJA restored it. MeJA also enhanced the activity of catalase in the leaves but showed no significant effect on peroxidase activity. The content of both endogenous jasmonic acid (JA) and MeJA in the leaves of S. nigrum increased with the increase of exogenous MeJA concentration.

Effects of salinity (0, 50, 100 and 250 mM NaCl) on growth, root:shoot dry mass ratio, osmotic potential (ψ_x), electrolyte leakage and contents of Na⁺ and K⁺, polyamines and abscisic acid (ABA) were studied in the grape rootstocks Dogridge, 1613, St. George and Salt Creek. In control rootstocks, the root length was highest in Dogridge and contents of K⁺ and ABA in Salt Creek. Salinity treatments increased root Na⁺ and decreased K⁺ content and St. George exhibited highest Na⁺ content and Na⁺:K⁺ ratio. The root:shoot dry mass ratio in all rootstocks increased upto 100 mM NaCl. With increasing NaCl concentration, putrescine, spermine and spermidine contents showed consistent increase and putrescine increase was highest in St. George and spermidine and spermine in the Dogridge and Salt Creek. Under salinity, the ABA content increased in all the rootstocks but more in Salt Creek and Dogridge than in St. George.

The aim of this study was to investigate the effects of salinity on germination, seedling growth, free polyamines (putrescine, spermidine, and spermine), and ethylene metabolism of two species (Atriplex prostrata Bouchér and Plantago coronopus L.) with different salt sensitivities. Seeds collected from Barranco Hondo (salt marshes, Jaén, southern Spain) were germinated at 0, 50, 100, and 200 mM NaCl in a growth chamber. The germination of P. coronopus seeds decreased considerably with an increasing NaCl concentration, however, seeds of A. prostrata showed high germination percentages (84, 87, and 80 %) at 0 (control), 50, and 100 mM NaCl, respectively, and only at 200 mM NaCl, the germination was reduced to 25 %. In the early phase of vegetative growth (8-d-old seedlings), the fresh mass increased in A. prostrata at 50 and 100 mM NaCl but the fresh mass of P. coronopus showed no significant differences. With respect to polyamines, there was a decrease of the putrescine and spermidine content at all the NaCl treatments, however, the spermine content increased and was much higher in P. coronopus than in A. prostrata. The ethylene, 1-aminocyclopropane-1-carboxylic acid content, and the 1-amino-cyclopropane-1-carboxylic acid synthase activity increased with the increasing NaCl concentration in A. prostrata, and only the ethylene content in P. coronopus. These results indicate that P. coronopus increased the free spermine content, whereas A. prostrata increased the ethylene biosynthetic pathway in order to survive in the saline conditions.

The effects of cadmium and zinc on growth and mineral distribution in Populus tremula × P. alba genotype 717-1B4 were investigated. Exposure to 360 mg(Cd) kg^-1(soil) resulted in accumulation of Cd in all organs and inhibition of primary and secondary growth as well as of the net photosynthetic rate. No growth inhibition occurred under zinc exposure. Cd was mainly stored in the woody parts of stem, whereas zinc was preferentially localized in the leaves. Cd treatment also altered distribution of Zn²⁺, Ca²⁺, Mg²⁺, K⁺, and Fe²⁺ in different organs.

The present study investigated differences in cadmium resistance of two wheat (Triticum aestivum L.) cultivars. The cvs. RAJ 4161 (Cd resistant) and PBW 343 (Cd sensitive) were treated with 200 mg(Cd) kg^-1(soil) for 3, 5, 7, and 10 d. The effect of the Cd stress was estimated by measuring growth parameters, accumulation of cadmium, sulphur, and glutathione (GSH), and by expression of some defence genes [phytochelatin synthase (PCS), glutathione reductase (GR), and ascorbate peroxidase (APX)]. The Cd treatment resulted in a significant reduction in plant growth and in an increase in the accumulation of S and GSH. Further, the expressions of PCS, GR, and APX were also mostly enhanced. The PCS was upregulated significantly in roots of RAJ 4161 (0.6-fold) and downregulated (0.9-fold) in PBW 343 on day 3 of the Cd treatment. In RAJ 4161, the expressions of APX and GR recorded a maximum increase of 2.1- and 2.4-fold in roots and leaves, respectively, after 10 d of the stress. The results show that a different ability of RAJ 4161 and PBW 343 to modulate mRNA expression after the Cd treatment was related to their Cd tolerance.

The primary objective of this work was to investigate the role of polyamines (PAs) on root formation and growth in two sweet orange (Citrus sinensis L. Osb.) cultivars Pineapple and Pêra. Adventitious shoots (30-d-old) derived from epicotyl explants were transferred to root induction medium containing Murashige and Skoog salts at different strengths and supplemented with different concentrations and combinations of auxins. Root formation and development decreased in both sweet orange cultivars concomitant with the reduction of medium strength. The α-naphtaleneacetic acid was important during the root differentiation phase, but its combination with indole-3-butyric acid was essential for root elongation. The addition of PAs significantly improved root formation and/or growth, depending on their concentration, whereas the presence of inhibitor of PAs biosynthesis α-difluoromethylornithine (DFMO) inhibited these processes. The rooting impairment caused by DFMO was partially reversed by the supplementation of putrescine. Aminoethoxyvinylglycine AVG and AgNO₃ also inhibited in vitro rooting in both sweet orange cultivars, indicating that ethylene was likewise important for rhizogenesis in sweet orange.

The study was conducted in mango to understand the relationship of various metabolites with flower sex ratio (hermaphrodite/male) and fruit set using stem girdling technique. Girdling one year old branches was carried out in two cultivars, Mangifera indica 'Alphonso' and 'Totapuri' to retain 50, 100 and 150 leaves to vary the content of hormones, sugars, total carbohydrates, and amino acids. The increased leaf number was found to increase the total carbohydrates, glucose, fructose, and other sugars. Girdling also significantly increased the concentration of abscisic acid (ABA), salicylic acid (SA), jasmonic acid (JA), indole acetic acid, indole butyric acid but decreased gibberellins and cytokinins. Amino acids also increased in the girdled branches. Girdling improved the flower sex ratio as well as fruit set more efficiently in 'Alphonso' than in 'Totapuri'. Results indicate that the increase in production of hermaphrodite flowers may be more related to the higher production of growth inhibitors, like ABA, SA, and JA along with increased concentration of sugars. Increased auxin concentration also might play an important role in increasing the fruit set.

The aim of the study was to examine the effect of exogenous 24-epibrassinolide on its uptake and content of endogenous brassinosteroids in wheat seedlings. 24-Epibrassinolide was applied at two concentrations (0.1 and 2.0 μM) and in three different methods: by soaking seeds, by drenching and by spraying plants. Brassinosteroids were determined by high-performance liquid chromatography combined with electrospray mass spectrometry. Three important brassinosteroids, 24-epibrassinolide, brassinolide and castasterone, were detected in the wheat leaves, but their contents varied with leaf insertion and plant age. Increased 24-epibrassinolide content in the leaf tissue was found when this hormone was applied by soaking or drenching. Additionally the seed treatment influenced brassinosteroid balance in seedlings. The growth response of wheat seedlings treated with 24-epibrassinolide has been also investigated.

This study was carried out to better understand the role of 24-epibrassinolide (EBR) in thermotolerance of melon (Cucumis melo L.). The melon seedlings were pretreated with various concentrations of EBR (0, 0.05, 0.1, 0.5, 1.0, and 1.5 mg dm^-3) as foliar spray and then exposed to a high temperature (HT) stress. Exogenous EBR (0.5-1.5 mg dm^-3) alleviated HT-caused growth suppression. In parallel, 1.0 mg dm^-3 EBR attenuated the decrease in chlorophyll content, net photosynthetic rate, stomatal conductance, maximum quantum efficiency of photosystem (PS) II, quantum yield of PS II, and photochemical quenching of chlorophyll a fluorescence in HT-stressed plants, and inhibited transpiration rate and non-photochemical quenching. Furthermore, exogenous EBR also significantly reduced the content of malondialdehyde (MDA) and increased the content of soluble proteins and free proline, and activities of antioxidant enzymes including superoxide dismutase, guaiacol peroxidase, catalase, and ascorbate peroxidase under the HT stress. The results show that protective effects of EBR against the HT stress in the melon seedlings were most likely mediated through the improvement of photosynthesis and the stimulation of antioxidant capacity.

Fructose-1,6-bisphosphate aldolase (FBA), an essential enzyme involved in the glycolytic pathway, gluconeogenesis, and the Calvin cycle, plays significant roles in the regulation of plant growth, development, and stress responses. In this study, a novel gene, AhFBA (GenBank accession number KF470788), containing a 1077-bp open reading frame and encoding a protein of 358 amino acids, was isolated from Arachis hypogaea L. Bioinformatic analysis revealed that AhFBA belonged to class-I aldolases and preferentially localized in the cytoplasm. Real-time quantitative PCR analysis indicated that AhFBA had a higher expression in young fruits than in leaves and stems, and NaCl could trigger the highest expression of AhFBA in roots and leaves after 3-h and 6-h treatments. The salinity tolerance and survival of Escherichia coli transformed with AhFBA were notably enhanced compared with the control. Transgenic tobacco (Nicotiana tabacum L.) overexpressing the AhFBA gene exhibited a lower hydrogen peroxide content, electrolyte leakage, and malondialdehyde content and a higher photosynthetic efficiency, net photosynthetic rate, relative water content, and sucrose and proline content compared with control plants. Taken together, the results demonstrate that AhFBA functioned as a positive factor enhancing the tolerance of E. coli and N. tabacum to salinity stress, possibly by maintaining the osmotic balance and scavenging hydrogen peroxide.

Drought is a major factor decreasing the growth, development, and productivity of rice in about one-third of the world area. The characterization of genes imparting tolerance to drought in rice, is an attractive strategy for genetic engineering to improve drought tolerance. It is demonstrated that ectopic overexpression of Brachypodium distachyon RING-H₂ finger gene (designated as BdRHP1) enhances drought tolerance in rice at both the vegetative and reproductive stages. When subjected to drought, positive transgenic lines showed delayed wilting, and improved recovery after rewatering. However, the transgenic plants exhibited more significant germination delay and shoot and root growth arrest than WT under 5 μM abscisic acid (ABA) treatment. When they were subjected to drought at the reproductive stage, the transgenic plants lost water more slowly compared to WT and they had higher leaf relative water content. After 28 d of slow progressive soil drying, transgenic plants recovered better after rewatering and flowered earlier than WT plants. The yield of water-stressed transgenic plants was higher than that of WT plants. Together, the data suggest that BdRHP1 has a specific function in positive modulation of improving drought tolerance in rice.

Apyrases belong to the ATPase family of enzymes that hydrolyze phosphoanhydride bonds of nucleoside tri- and di-phosphates. These enzymes differ markedly from other phosphohydrolases due to their high specific activity, broad divalent cation requirement, broad nucleotide substrate specificity, and insensitivity to various inhibitors. In the past 30 years, apyrases have been frequently studied in mammals. In comparison, research of apyrases in plants has received little attention, despite the growth of plants being closely related to the apyrases. In this review, we summarize the research of the apyrases in Arabidopsis thaliana and point to the possible future directions of research. Apyrases have seven members found in Arabidopsis thaliana, each with different properties and functions. Currently, the characterization and functions of AtAPY1 and AtAPY2 have been reported, though, to the best of our knowledge, the other apyrase members (AtAPY3 to 7) have not yet been sufficiently described. In this review, we also summarize the progress being made and the difficulties encountered in apyrase research in Arabidopsis thaliana.

Drought is one of the major environmental stresses limiting crop production worldwide because both the duration and the severity of the stress are critical. Plants display a variety of physiological and biochemical stress responses towards prevailing drought stress thus making it a complex phenomenon. To address the modulation of stress responses, we used Glycine max cv. MG/BR 46 Conquista (non-transgenic) and cv. BRS Valiosa (transgenic) to analyze the effects of  progressive drought stress during two stages of soybean development (V2 and V4) on physiological and biochemical parameters. Three minimum soil water potentials (Ψs) were established: -0.03 MPa (well-watered), -0.07 MPa (a moderate stress), and -0.5 MPa (a severe stress). Gas-exchange measurements, lipid peroxidation, H₂O₂ and proline content, and antioxidant enzyme activities were analyzed in the leaves of both cultivars in the different water management levels. The results show a decrease in plant growth and gas-exchange parameters in both genotypes during progressive drought stress; the effects were more pronounced in MG/BR 46 Conquista. Proline content was less affected in BRS Valiosa. Malondialdehyde and H₂O₂ content increased during the drought stress but less in transgenic plants. Superoxide dismutase, catalase, and ascorbate peroxidase activities increased in BRS Valiosa at the V4 stage, whereas MG/B R 46 Conquista did not overcome stress conditions at this period. The overall results suggest that BRS Valiosa (transgenic) soybean cultivar exhibited later stress responses, which could enhance its survival during long periods of water deficit.

Waterlogging, a major environmental stress, impairs plant growth and development and induces synthesis of different proteins. To understand the molecular mechanisms coupled with morpho-physiological alterations underlying waterlogging tolerance, the LTQ-FTICR MS/MS technique was employed to map the proteomes of leaves of sesame grown under control and waterlogged conditions. The waterlogging treatment caused dramatic alterations in morphological and biochemical properties of the leaves of sesame. For proteome analysis, more than 75 reproducible protein spots were identified on 2-DE gels wherein 51 protein spots (≥ 1.5-fold change) were used for analysis by mass spectrometry. Among 51 differentially abundant proteins, 20 were specific to the 10-leaf stage and 31 were specific to the flowering stage. Most of the differentially abundant proteins were involved in group metabolism, and energy and stress defense. Oxygen-evolving enhancer protein 1, ATP synthase subunit, heat shock proteins, glutamine synthetase, glyceraldehyde-3-phosphate dehydrogenase, and superoxide dismutase were upregulated under waterlogging. However, the photosynthesis- and protein biosynthesis-related proteins (e.g., ribulose-1,5-bisphosphate carboxylase/oxygenase activase, and S-adenosylmethionine synthase 1) were down-regulated under waterlogging. The protein interaction network indicates that energy metabolism- and stress- and defense-related proteins were involved in the protein-protein interaction network, which could form an indispensable network in sesame leaves. To this end, physiological results highlighted the impairment of photosyntheis, which is consistent with results obtained at the proteome level. The upregulation of metabolism-, energy-, and stress defense-related proteins in response to waterlogging stress may provide new insights into the complex mechanisms underlying waterlogging tolerance in sesame.

The increasing world population and limited amount of land area appropriate for intensive agriculture necessitate high-yield cultivars. The focus is on the enrichment of existing crops deficient in nutrients, which is also called biofortification. Microelements, vitamins, and fatty acids belong to most important traits being subjected to biofortification. Biofortification strategies can be divided on fertilization-based strategy, which is characterized by direct application of nutrients or plant growth promoting substances on plants, and biotechnological strategy, which involves molecular biology techniques in order to enhance transport, production, and accumulation of nutrients. Recent advances in plant biotechnology, such as genome-editing, clustered regularly interspaced short palindromic repeats (CRISPR)-associated 9, and transcription activator-like effector nuclease, as well as an extensive study of genetic diversity, are acceptable approaches to the development of biofortified crops.