The objective of the current study was to develop an efficient and reproducible protocol for plant regeneration using nodal (1.0-1.5 cm) explants excised from a field grown mature plant of Cassia occidentalis L. The highest shoot regeneration frequency (80 %) with a maximum number of shoots (11.66) and shoot length (3.83 cm) after eight weeks of culture were observed on a Murashige and Skoog (MS) medium amended with 5.0 μM 6-benzyladenine, 100 μM citric acid, and 1.0 μM α-naphthalene acetic acid. A half-strength MS medium supplemented with 1.5 μM indole-3-butyric acid proved best for the induction of maximum roots (8.33) per shoot. Plantlets with well-developed shoots and roots were successfully acclimatized in plastic pots containing sterile Soilrite under two irradiances of 50 and 300 μmol m^-2 s^-1 (LI and HI, respectively) in a culture room, and after transfer to the field, the survival rate was 70 %. A significant increase in chlorophyll, carotenoid, and malondialdehyde content was found during acclimatization under both the irradiances but higher under HI. Similarly, the activities of superoxide dismutase, catalase, glutathione reductase, and ascorbate peroxidase increased more under HI. Plantlets acclimatized under HI exhibited a better growth than those under LI.

Hydroponics experiments were conducted to study the effects of sodium nitroprusside (SNP, a donor of NO) on lead toxicity in ryegrass (Lolium perenne L.) seedlings. When the ryegrass seedlings were grown in a nutrient solution containing 500 μM Pb²⁺ for two weeks, the plant biomass as well as net photosynthetic rate, transpiration rate, chlorophyll and carotenoid content of leaves decreased. The Pb stress also induced the production of superoxide anion (O₂ ^.-) and hydrogen peroxide (H₂O₂), leading to malondialdehyde (MDA) accumulation. Furthermore, the activities of superoxide dismutase (SOD), peroxidase (POD), and ascorbate peroxidase (APX) decreased in the Pb-treated seedlings, but the catalase (CAT) activity increased. Additionally, the content of Cu in shoots and the content of K, Mg, Fe, and Zn in both shoots and roots decreased, but the content of Ca in shoots and roots increased under the Pb stress. Moreover, Pb accumulated mostly in roots, whereas a small quantity was translocated to shoots. However, the addition of 50, 100, and 200 μM SNP into the solution containing Pb increased the chlorophyll content and net photosynthetic rate, reduced Pb-induced oxidative damages, improved antioxidant enzyme activities, and inhibited translocation of Pb from roots to shoots. In particular, 100 μM SNP had the best effect on promoting growth of the ryegrass seedlings under the Pb toxicity. However, the application of 400 μM SNP had no obvious alleviating effect on Pb toxicity in the ryegrass seedlings.

Pogostemon cablin (Blanco) Benth is a medicinal plant rich in terpenoids and flavonoids. Currently, the molecular mechanism of flavonoid biosynthesis in P. cablin remains unclear. In this study, three copies of the phenylalanine ammonia lyase (PAL) gene designated as PcPAL1 - PcPAL3, one copy of the chalcone synthase (CHS) gene referred to as PcCHS, and four copies of the CHS-like gene referred to as PcCHSL1 - PcCHSL4 were isolated from P. cablin. PcPAL1, PcPAL2, and PcPAL3 comprised 2 136, 2 136, and 2 148 bp full-length open reading frames (ORFs) encoding 711, 711, and 715 amino acids, respectively. PcCHS, PcCHSL1, PcCHSL2, PcCHSL3, and PcCHSL4 contained 1 173, 1 176, 1 179, 1 173, and 1 170 bp ORFs encoding 390, 391, 392, 390, and 389 amino acids, respectively. A phylogenetic analysis indicates that PcPAL2 was closer to PcPAL3 than PcPAL1, and that PcCHS was clustered with other plant CHS genes but independently to the PcCHSLs subgroup. A sequence analysis shows that PcCHSLs diverged in functional residues when compared to plant CHSs including PcCHS, suggesting that PcCHSLs may be divergent in tertiary structures. A quantitative reverse-transcription polymerase chain reaction analysis indicates that the expression profiles of PcPALs, PcCHS, and PcCHSLs in leaves and stems differed among four cultivars. Our results suggest that divergence in sequence and expression profiles of the tested genes may contribute to the diversity in flavonoids among the four cultivars.

We previously reported that LeMYB1 might be a crucial transcription factor in regulating shikonin formation in Lithospermum erythrorhizon. In this study, by overexpressing LeMYB1 under the control of CaMV35S promoter in L. erythrorhizon hairy roots, we further clarified the role of LeMYB1 in the shikonin formation and its regulation. The LeMYB1-overexpressing transgenic hairy roots were successfully induced by infecting seedling nodes with Agrobacterium rhizogenes strain ATCC15834 that carried the pBI121-LeMYB1 vector. The LeMYB1 transcripts were significantly up-regulated in the transgenic hairy root lines compared with the wild type lines, and the total content of shikonin and its derivatives was dramatically enhanced by the LeMYB1 overexpression. Real-time PCR results reveal that the enhanced shikonin biosynthesis in the overexpressing lines were mainly caused by a highly up-regulated expression of genes coding key enzymes (PAL, HMGR, and PGT) and key regulators (LeDI-2 and LePS-2) involved in the shikonin biosynthesis. Overall, our results suggest that LeMYB1 plays a positive role in regulating the shikonin biosynthesis in L. erythrorhizon.

The effect of a rare earth element europium (Eu) on the long-distance transport of a plant defence compound quercetin (Q) was investigated. The complex Q/Eu³⁺ was synthesized in a HEPES buffer and tested for its transport ability through Arabidopsis thaliana and its ability to interact with target molecules in plant cells. Our results show that complexation with Eu³⁺ enhanced the transport of Q through Arabidopsis roots. During the transport, the complex degraded and released a free Q to tissues where Q was originally not available. Thus, the plant became better supplied with the defensive compound Q. The obtained spectrophotometric data imply that one of the reasons for the Q/Eu³⁺ degradation was the interaction of the complex with double stranded RNAs (dsRNAs) present in Arabidopsis. Since dsRNAs are replicative forms of plant RNA viruses, the ability of Q/Eu³⁺ to release a free Q in their presence suggests further investigation of this complex as a potential antiviral agent.

Whereas microsatellite markers are well described, there are few studies investigating minisatellites. Therefore, this study aimed to identify, characterize, and validate minisatellite loci for papaya (Carica papaya L.). The entire papaya genome, which covers 330 Mb, was used to mine minisatellites with motifs ranging from 6 to 500 bp, and at least six replicates and 82 loci were validated in a set of 24 accessions. A total of 1 730 minisatellite loci were identified, located in 695 sequences, with an average of one minisatellite every 156 kb. Variation in GC content ranged from 0.00 to 83.84 % with an average of 28.84 % indicating that these papaya minisatellites are AT rich. Motifs of up to 20 bases represented 71.45 % of the markers. In addition, the observed variation in the number of motif repeats was from 6 to 186 with an average of 9.27 per minisatellite. Independent of the classification, the frequency of minisatellites decreased with an increase in the number of repeating units. Among the validated loci, 48.78 % were found to be polymorphic, and the number of alleles (N_A) ranged from two to seven with a mean of 3.10. The average polymorphic information content (PIC), expected heterozygosity (He), and observed heterozygosity (Ho) were 0.38, 0.43, and 0.11, respectively. According to genetic diversity parameters, such as NA, He, and PIC, no significant correlations were found among the size of motifs, the number of repeats, and the GC content of these minisatellites. This study clearly demonstrates the polymorphism of minisatellites and their potential use in detection of intraspecific genetic variations in C. papaya. The results will be useful when managing genetic resources and plant breeding.

A wheat stay-green mutant, named tasg1, was generated using the mutagen ethyl methane sulphonate applied to wheat (Triticum aestivum L.) cv. HS2. A drought stress was imposed by controlling irrigation and sheltering plants from rain. The antioxidant defence was characterized in the flag leaves of the tasg1 and wild-type (WT). Compared with WT, tasg1 had higher reduced ascorbate/oxidized ascorbate ratio, reduced glutathione/oxidized glutathione ratio, and antioxidant enzyme activities during senescence under both normal and drought stress conditions. The DHAR gene expression remained higher in tasg1 than in WT during the drought stress and tasg1 had a higher antioxidant defence competence which may contribute towards the delayed leaf senescence. The different transcriptional responses of some wheat senescence-associated genes to the drought stress between tasg1 and WT were observed. These results suggest that the competent antioxidative capacity might play an important role in the enhanced drought tolerance in tasg1.

Natural accessions of Arabidopsis thaliana exhibit a clinal variation in freezing tolerance following temperature changes across the natural habitat. Here we performed molecular evolution and population genetic analyses of homologous INDUCER OF CBF EXPRESSION1 (ICE1) and ICE2 genes, the master regulators of plant cold response. A study of ICE genes polymorphism was performed using 60 A. thaliana ecotypes grouped according to their geographic origin. The genetic diversity of ICE2 was characterized by a high number of haplotypes and an overall high diversity. The levels of nonsynonymous nucleotide polymorphism increased from a northern group southward. On the contrary, the ICE1 gene sequence was less diverse and there was no clinal variation in the sequence polymorphism. Thus, different selection forces acting on the ICE2 gene might be one of the reasons of clinal variation in freezing tolerance. This clinal variation also indicates that ICE2 is more important for a cold response than ICE1. The study of the ratio of numbers of nonsynonymous to synonymous substitutions (K_a/K_s) between A. thaliana paralogs shows that the sequence diversification and emergence of two new ICE2-specific motifs could contribute to the functional diversification of the duplicates. The K_a/K_s for ICE2 of A. thaliana and A. lyrata orthologs was an order of magnitude greater than that for the ICE1 orthologs, which suggests that the protein sequence of ICE2, an early duplicate, evolved under a weaker selective constraint. A relaxed selection on ICE2 in southern populations and more stringent in northern populations also confirmed its role in a cold resistance. The selection pressure on ICE1 might be caused by its role in the control of more essential than cold response functions.

Understanding the basis of the genetic variations responsible for the complex traits found in Eucalyptus cladocalyx under arid environmental conditions is crucial for designing genetic architecture studies. Forty-five half-sib families from Australia were used to identify inter-simple sequence repeat (ISSR) markers that are associated with growth (height, diameter at breast height, and stem straightness), flowering traits (flowering intensity, flowering precocity, reproductive capacity, and late flowering) and tree survival under arid conditions in southern Atacama Desert, Chile. Each DNA pellet consisted of a pool of five trees from each family. ISSR markers were associated with all the traits studied and accounted for 9.8 to 23.4 % of the phenotypic variation. Several loci were associated with more than one trait. For example, UBC_{810(450-500 bp)}, ISO_{1(600-610 bp)}, and TGT_{9(780-800 bp)} were associated with three of the traits studied. These identified genomic regions may contribute to the increase of the efficiency of the conventional tree breeding program for E. cladocalyx.

The present work examined seven Hypericum species (H. perforatum, H. humifusum, H. kalmianum, H. annulatum, H. tomentosum, H. pulchrum, and H. rumeliacum) produced in vitro and regenerated after cryopreservation. The aim of the study was to assess, by means of light microscopy (LM) and transmission electron microscopy (TEM), the effect of freezing temperature on leaf histological organization and mesophyll chloroplast ultrastructure. Histological analysis showed a negative effect of ultralow temperatures on leaf tissue structure in H. pulchrum and a positive effect in H. perforatum. The TEM analysis showed that chloroplasts from ultralow temperature treated H. annulatum, H. tomentosum, and H. rumeliacum had a typically structured internal membrane system without destruction of thylakoid membranes, however, those of H. humifusum had very high grana, and in H. perforatum, chloroplast thylakoid destruction occurred. The chloroplast internal membrane system of in vitro cultured control plants and in vitro cultured cryopreserved plants of H. kalmianum and H. pulchrum had a specific spatial orientation without any destruction of the membranes. The results show a specific response of each species to these experimental conditions.

Chloride channels (CLCs) play pivotal roles in plant development and anion transport. However, little research has been conducted about the CLC in fruit-bearing plants. Here we provide an insight into the evolution and expression patterns of CLC gene family members in various tissues of trifoliate orange [Poncirus trifoliata (L.) Raf.] and their responses to several treatments. Genome-wide analysis identified six PtrCLC genes. The predicted proteins had similar numbers of amino acids, but shared a low sequence identity. Phylogenetic analysis revealed that PtrCLC were classified into two separate subgroups, and PtrCLC4 and PtrCLC6 in subgroup II were more closely related to bacterial CLCs. Sequence comparison with EcCLCA from Escherichia coli reveals that PtrCLC showed amino acid divergence in anion selectivity of CLC proteins. Real time qPCR analysis shows that PtrCLC genes, particularly PtrCLC6, preferentially expressed in leaves. Nitrogen deficiency irreversibly inhibited expression of PtrCLC genes except for PtrCLC1. In contrast, NaCl stress profoundly induced expression of PtrCLC genes, particularly PtrCLC2 and PtrCLC4, both of which were also upregulated by ABA treatment. The results presented here provide a solid foundation for a future functional research on citrus CLC genes.

The aim of this work was to elucidate the molecular and biochemical mechanisms that control L-ascorbic acid (AsA) content variation in Myrciaria dubia. The AsA was quantified by high-performance liquid chromatography, gene expression by real-time quantitative PCR, and enzyme activities by spectrophotometric methods from leaves and immature fruits of two genotypes (Md-60,06 and Md-02,04) with pronounced (about 2 times) differences in the AsA content. In either genotype, the fruit peel had ∼ 1.5 times more AsA than the fruit pulp and ∼ 15.0 times more than the leaf. All tissues examined demonstrated the capability for AsA biosynthesis through the D-mannose/L-galactose pathway because mRNAs of the six key genes [GDP-D-mannose pyrophosphorylase (GMP), GDP-D-mannose-3',5'-epimerase (GME), GDP-L-galactose phosphorylase (GGP), L-galactose-1-phosphate phosphatase (GPP), L-galactose dehydrogenase (GDH), and L-galactono-1-4-lactone dehydrogenase (GLDH)] and catalytic activities of the corresponding enzymes (GMP, GDH, and GLDH) were detected. The differential expressions of genes and enzyme activities mostly correlated with the respective AsA content. Thus, the expression of several genes of the D-mannose/L-galactose pathway determined the AsA content variation in tissues of M. dubia.

A new member of the APETALA2/ethylene responsive element binding protein (AP2/EREBP) transcription factor family, HhDREB2, was isolated from Halimodendron halodendron. Based on the similarity of the AP2/ERF domain, HhDREB2 was classified into A-5 group of the DREB subfamily. The expression of HhDREB2 gene was induced by drought, high salinity, and low temperature, but not by exogenous plant hormones. Trans-activity assay demonstrated that HhDREB2 gene encodes a transcription activator. Furthermore, over-expression of HhDREB2 gene under the stress-inducible rd29A promotor in Arabidopsis resulted in enhanced tolerance to salt and drought stresses. The overall results reveal that HhDREB2 functioned as important transcription factor in regulation of stress-responsive signaling in plants and may be used for improving plant tolerance to abiotic stresses.

An essential step in the carotenoid biosynthesis pathway is the formation of phytoene by phytoene synthase (PSY). In this study, three new genes coding PSYs (CpPSYA, CpPSYB, and CpPSYC) were cloned from Cucurbita pepo and their expression patterns analysed in three cultivars of summer squash which had a different carotenoid content. The gene sequences had a high similarity with those from other plant species, and their predicted proteins were significantly different from each other. A phylogenetic analysis indicates that CpPSYA and CpPSYB shared a high homology and were also homologous with PSYs from others cucurbits, whereas CpPSYC was more closely related to orthologues from strawberry and carrot. An expression analysis revealed that CpPSYA had a higher expression in flowers compared to leaves and showed a differential expression during fruit development. The amount of CpPSYA transcript was higher in fruits with a higher carotenoid content than in those with a lower carotenoid content. However, CpPSYB and CpPSYC showed a relatively high expression in leaves, and their expression in fruits varied among the different cultivars and fruit tissues. These results suggest that the CpPSY genes were under different regulatory mechanisms and they may have different roles in C. pepo.

The effects of foliar application of 24-epibrassinolide (EBR) on chlorophyll content, oxidative damage, and antioxidant capacity in eggplant (Solanum melongena L.) seedlings during a short-term chilling stress and subsequent recovery were investigated. The eggplant seedlings pretreated with 0.1 μM EBR were exposed to 5 °C for 12 h in the dark and then recovered under a normal temperature for another 12 h. The results show that EBR alleviated a chilling-induced oxidative stress reflected by a decrease in malondialdehyde and H₂O₂ content, O₂ ^.- production rate, and an increase in chlorophyll content and activities of superoxide dismutase, guaicol peroxidase, and catalase. The EBR pretreatment also promoted activities of ascorbate peroxidase, glutathione reductase, dehydroascorbate reductase, as well as the accumulation of ascorbic acid (AsA) and glutathione (GSH) involved in the AsA-GSH cycle. Moreover, after the12 h recovery, EBR plus chilling treated leaves showed no significant changes in content of MDA and chlorophyll a, lower reactive oxygen species (ROS) content, and greater activities of AsA-GSH cycle enzymes than in seedlings only chilled. The results suggest that EBR alleviated an oxidative damage caused by the dark chilling stress and accelerated a recovery rate mainly through increasing the ROS scavenging system including the AsA-GSH cycle.

The effects of AT3-gene silencing on the expression of genes involved in capsaicinoid biosynthesis was investigated in chili pepper (Capsicum annuum L.) cv. Tampiqueño 74 fruits. Seeds were germinated and seedlings were grown in a greenhouse until they produced fruits. Capsaicinoids (capsaicin and dihydrocapsaicin) content and AT3 gene expression were determined in placenta tissue from fruits at 10, 20, 30, 40, 50, and 60 days post-anthesis (DPA). Capsaicin was more abundant than dihydrocapsaicin and both exhibited a similar accumulation pattern at different developmental stages starting at 20 DPA, reaching maximum values at 30-40 DPA before decreasing. The AT3 gene expression, as measured by quantitative RT-PCR, was positively correlated with capsaicinoid accumulation; AT3 transcripts were detected at 20 DPA, achieved a maximum at 30-40 DPA and then decreased. The Tampiqueño 74 seedlings were infected with Agrobacterium tumefaciens bearing a pTRV2-AT3 construct to induce virus-mediated silencing. Fruits were harvested at 40 DPA, and capsaicinoid content and AT3 gene expression were carried out in placenta tissue. A reduction of 81.1 % in AT3 expression and also in capsaicin (89.6 %) and dihydrocapsaicin (87.7 %) content was recorded in the AT3-gene silenced chili pepper plants. Furthermore, fruits from the AT3-silenced plants compared to the non-infected control plants showed a statistically significant reduction in the expression of genes involved in capsaicinoid biosynthesis [pAmt (89.4 %), BCAT (68.8 %), Kas (90.4 %) and Acl (58.6 %)]. These data indicate that AT3 silencing had a negative effect on the transcription of genes involved mainly in the branched-chain fatty acid pathway of capsaicinoid biosynthesis.

An excess of aluminum (Al) is a major factor limiting crop production in acidic soils. Secretion of organic acids (OAs) from the root apex of diverse plant species or genotypes via activation of anion channels has been recognized as the most important mechanism of Al exclusion. Citric, oxalic, and malic acids are the most effective OAs in detoxifying Al. In this review, we summarize biochemical properties of OAs secreted by plants. We also highlight the molecular mechanisms of Al signal perception, Al transport, signal regulators associated with OAs secretion, as well as interactions between Al and hormone signaling pathways. Based on a comprehensive understanding of the relationship between signal modulators and regulation of expression of relevant genes, a signal transduction model for Al-induced OAs secretion is proposed.

Roles for nitric oxide (NO) and reactive oxygen species (ROS) during pollen-tube growth have been well established in angiosperms, but there remains lack of information regarding their potential signalling roles in pollen tubes in gymnosperms. Here, the pollen-tube elongation of Arizona cypress (Cupressus arizonica Greene) was investigated. Nitric oxide, ROS, and actin were detected using their respective fluorescent probes. Both NO and ROS were observed in the nuclei of generative cells and pollen-tube cells, and in the cytoplasm in the tip region. An intracellular NO content in the pollen cells was lowered using an NO scavenger or an NO-synthase inhibitor. Similarly, an endogenous ROS content in the pollen cells was lowered using an NAD(P)H oxidase inhibitor. These treatments reduced pollen germination and pollen-tube growth, and induced severe morphological abnormalities. Inhibition of NO and ROS accumulation also severely disrupted the actin cytoskeleton in the pollen tubes. These data indicate that NO and ROS had signalling roles in pollen germination and pollen-tube formation in cypress.

The present study exemplifies morphogenic roles played by copper and zinc during micropropagation of Rauvolfia serpentina, an important medicinal shrub. Incorporation of 20 μM CuSO₄ or 25 μM ZnSO₄ to a Murashige and Skoog (MS) medium with optimized concentrations of auxins and cytokinins induced a maximum number of shoots per explant (40.67 ± 1.76 and 45.47 ± 0.24, respectively). However, higher concentrations of both the micronutrients negatively affected the morphogenic potential. The pigment content of the regenerants increased up to the optimal concentrations of both metals and thereafter decreased, whereas the maximum proline content was at the highest concentrations used. In vitro rooting of healthy shoots was accomplished using 0.5 μM IBA in a half strength liquid MS medium with 8.20 ± 0.37 roots, and root length of 5.50 ± 0.14 cm per microshoot. The plants survived a hardening procedure and were successfully acclimatized to field conditions with 95 % survival.

The interactive effects of salicylic acid (SA) and nitric oxide (NO) on alleviating cadmium (Cd) toxicity in peanut (Arachis hypogaea L.) were studied. Seedlings of two cultivars (Huayu 22 - a big seed type, and Xiaobaisha - a small seed type) were treated with 200 μM CdCl₂ without or with 0.1 mM SA or 0.25 mM sodium nitroprusside (SNP, an NO donor). Results show that the Cd exposure depressed the plant growth of both the cultivars but more of Huayu 22 than of Xiaobaisha. Exogenous SA and NO alleviated Cd toxicity in both the peanut cultivars: they improved growth, chlorophyll content, photosynthesis, and mineral nutrition. Furthermore, exogenous SA or NO decreased oxidative stress by increasing activities of antioxidant enzymes and content of non-enzymatic antioxidants. Besides, in roots and leaves of both the cultivars, exogenous SA and NO increased Cd accumulation in the cell wall and decreased Cd distribution to organelles. In particular, the effect of SA+SNP was most obvious.

Previously, the ascorbate peroxidase (APX1) activity and gene expression in Chinese cabbage (Brassica campestris, Bc) heat-tolerant cv. ASVEG2 were found to be significantly higher than in heat-sensitive cv. RN720 under a heat stress. Furthermore, BcAPX2 and BcAPX3, isoforms of BcAPX1, were cloned in this study. Our objective was to transfer BcAPX cDNA under the control of the ubiquitin promoter to Arabidopsis via Agrobacterium tumefaciens strain GV3101. We found that BcAPX genes were overexpressed in transgenic Arabidopsis, and the expression of APX, and the APX activity in transgenic lines were higher than in non-transgenic (NT) plants under high temperatures. The chlorophyll content and the germination rate were significantly higher, and the malondialdehyde content was lower in BcAPX1-3, 2-1, and 3-5 lines subjected to the heat-stress treatment than those in the NT plants. Compared to the NT plants, a lower heat-induced H₂O₂ accumulation was detected by diaminobenzidine staining in leaves of the transgenic lines with a high APX activity indicating that the overexpression of BcAPX in Arabidopsis could enhance heat tolerance by eliminating H₂O₂.

Gibberellic acid (GA₃) is widely used at different stages of berry development, and to understand the molecular mechanism of its action requires identification of stable reference genes. We sprayed grapevine (Vitis vinifera L.) cv. Thompson Seedless with GA₃ at rachis stage for rachis elongation, at flower cluster stage for flower thinning, and at 3-4 mm berry stage for berry elongation. Tissue samples were collected at different time points after GA₃ application. The expression of 10 candidate reference genes was analyzed using 4 different algorithms to assess their suitability for real time-PCR data normalization. Based on the overall ranking, PP2A, Sutra, and SAND were identified as the most stably expressed genes across all samples. With regard to different stages, tubulin, EF1α, and UBC were the most stable genes during rachis elongation; PP2A, SAND, and Sutra were the most suitable at the flower cluster and berry stages. The expression of GA signaling gene SPINDLY (VvSpy) was analyzed to validate the stable reference genes. After the GA₃ application, the expression of VvSpy was reduced at the rachis stage but did not change at the flower cluster and berry stages. The expression profile of VvSpy was comparable when two or three reference genes were used for data normalization.

Little is known about Ni storage in seeds of hyperaccumulating plants and its possible role in the first stages of plant development. The aim of this study was to determine Ni distribution in seeds and seedlings during germination and to test its role during germination with and without an external Ni supply. Field-harvested seeds from the South African Ni-hyperaccumulator Berkheya coddii Roessler were germinated either in Ni-free deionised water or in ultramafic soil. Sections of seeds and seedlings were analyzed using micro-proton induced X-ray emission (micro-PIXE) in order to localise Ni and other elements. Results show that high amounts of Ni were stored within the seeds. In germinating seeds, Ni was located in different parts: the lower epidermis, margins of cotyledons, and the pericarp in the micropylar area. The Ni and Ca were not mobilised during germination sensu stricto. Emergence of the first leaf seemed to trigger the translocation of Ni and Ca within the seedling. Besides, no effect of Ni supply from soil on its redistribution could be established for the germination stage.

Hydrogen peroxide is an effective abiotic elicitor that can induce secondary metabolite biosynthesis in plants. We show that in cell suspension culture of a salt-tolerant medicinal plant Cistanche salsa, the production of bioactive components phenylethanoid glycosides (PeGs) was increased after an H₂O₂ treatment. To identify genes related to PeGs biosynthesis affected by H₂O₂, we constructed a suppression subtractive hybridization library of H₂O₂ responsive genes using a C. salsa cell line and identified 105 expressed sequence tags (ESTs) and 85 genes. EST library functional annotation and gene ontology analyses showed genes related to various stress responses, biosynthesis of secondary metabolites, and transcriptional regulation. Among them we identified two genes related to the PeGs biosynthesis pathway (4-coumarate coenzyme A ligase and cinnamate 4-hydroxylase), and two WRKY type transcription factors. The expressions of selected genes after the H₂O₂ treatment were analyzed by RT-qPCR. An early increased transcription of PeG biosynthesis pathway genes after the treatment revealed that H₂O₂ induced PeGs biosynthesis via up-regulation of its key genes.

To elucidate a physiological mechanism of heat stress mitigation by exogenous glucose, seedlings of Cucumis sativus cv. Jinchun No. 4 were pretreated with glucose and then exposed to normal (25/18 °C) and elevated (42/38 °C) temperatures. We investigated whether glucose can protect cucumber plantlets and chloroplast ultrastructure from heat and whether this protection is associated with antioxidant enzymes, proline, and soluble sugars. Heat inhibited plant growth, disorganized membranes of 86.33 % of chloroplasts, and elevated the content of malondialdehyde (MDA), superoxide radical (O₂ ^.-), and hydrogen peroxide (H₂O₂). An optimum concentration of glucose was 30 mM as it significantly alleviated plant growth inhibition and obviously reduced the content of MDA, O₂ ^.-, and H₂O₂ under the heat stress. The pretreatment with 30 mM glucose mitigated heat-induced damage of chloroplast ultrastructure and changes in leaf morphology more than 30 mM mannitol suggesting that glucose did not act only as osmolyte. Moreover, the glucose pretreatment increased activities of some antioxidant enzymes and enhanced the content of proline and soluble sugars under the heat stress, as well as the transcriptions of Cu/Zn-superoxide dismutase, Mn-superoxide dismutase, catalase, and glutathione reductase genes. We conclude that the pretreatment with 30 mM glucose protected chloroplast ultrastructure and enhanced heat tolerance of the seedlings by the increased activites of antioxidants and the content of proline and soluble sugars, and repressed accumulation of reactive oxygen species.

The dehydration responsive element binding (DREB) transcription factor (TF) family comprises unique and important proteins involved in abiotic stress responses and tolerance in plants. Although DREB TFs have been well identified and characterized in a few model plants, there is no detailed information available for mulberry. In this study, 110 AP2/ERF family genes were identified based on a genome-wide analysis of the Morus genome database. Among them, 30 Morus notabilis DREB family genes (MnDREBs) were identified. A comparative analysis with DREB gene families from other plants suggests that MnDREBs could be divided into six subgroups (A-1 to A-6) and could have similar functions in response to abiotic stresses since they have similar conserved domains/motifs within each subgroup. The expression patterns of MnDREBs were analyzed using transcriptome data of different organs from M. notabilis and the quantitative real-time polymerase chain reaction. The expression of most MnDREBs was detected in different organs and induced by various abiotic stresses, which suggest their vital roles in abiotic stress tolerance.

The issue of finding plants suitable for phytoremediation of inorganic contaminants can be addressed through the preparation of genetically modified plants with an increased metal accumulation potential. A HisCUP gene, which encodes for a yeast metallothionein fused with a polyhistidine tail (His), was chosen for preparation of two plant vectors. These two plant vectors were constructed and a HisCUP gene expression was subsequently investigated. We firstly prepared a vector pNOV2819/RbcS/HisCUP which enabled selection on a mannose medium and contained the HisCUP gene under an inducible Rubisco promoter. Secondly, we designed a vector pGreen0029/35S/HisCUP which enabled selection of plants on a medium with kanamycin and carried the HisCUP gene under a constitutive CaMV 35S promoter. The transient expression of the HisCUP gene in tobacco plants was confirmed at RNA and protein levels for both constructs. The relative expression of the HisCUP gene was determined by semi-quantitative real-time PCR; a higher expression was detected for the vector pNOV2819/RbcS/HisCUP.

Growth, photosynthetic characteristics, chlorophyll (Chl) fluorescence parameters, and peroxidation of membrane lipids of Cryptotaenia japonica were studied under differing irradiances (15, 35, 60, and 100 % of full irradiance). At full irradiance, C. japonica exhibited a typical decline in net photosynthetic rate (P_N) at midday, which was not observed in the other irradiance treatments. This indicates a possible photoinhibition for C. japonica at the high irradiance. Diurnal patterns of stomatal conductance (g_s) were remarkably similar to those of P_N in each irradiance treatment, and the intercellular CO₂ concentration (c_i) had the opposite trend. C. japonica growing under 60 % of the full irradiance exhibited the highest plant height, stem diameter, leaf area, and biomass. The initial fluorescence (F₀) value was lowest at 60 % of the full irradiance. Maximal fluorescence (F_m), potential activity of photosystem II (PS II) (F_v/F₀), and maximal photochemical efficiency of PS II (F_v/F_m) values were highest at 60 % of full irradiance and lowest at 15 % of the full irradiance. The malondialdehyde (MDA) content in 15 % and 100 % of the full irradiance were higher than under the other irradiances. During the treatment, catalase, peroxidase, and superoxide dismutase activities firstly increased and then declined under 15 % and 100 % of the full irradiance and were steadily low under 60 % of the full irradiance, indicating a low production of reactive oxygen species. Therefore, C. japonica thrived best under 60 % of the full irradiance.

Iron deficiency chlorosis occurs frequently in calcareous soils. The transformation of plants with ferric chelate reductase genes (FROs) provides a potential strategy to alleviate plant chlorosis under iron deficiency. A CjFRO2 gene isolated from Citrus junos Sieb. ex Tanaka was introduced into Poncirus trifoliata (L.) Raf via Agrobacterium-mediated transformation. The transgene integration and expression were confirmed by PCR, Southern blot, and real-time PCR analyses. Hydroponic- and soil-grown transgenic plants were tested for their tolerance to iron deficiency. Compared with nontransgenic (NT) P. trifoliata plants, a rhizosphere acidification capacity in the transgenic lines increased, and a ferric chelate reductase activity in roots was up to 3.39- and 2.93-fold higher in a hydroponic solution and soil, respectively. A transgenic line TO-8, which reacted similarly in hydroponics and soil, appeared tolerant to the iron deficiency. Its leaf chlorophyll and ferrous ion content was significantly higher than in NT. These results indicate that tolerance to the iron deficiency in P. trifoliata could be improved through the genetic engineering.

We investigated the effect of sulfur (S) supply on growth, oxidative stress, and iron uptake and transport in rice (Oryza sativa L.) seedlings using a hydroponic culture with four S concentrations (0, 1.75, 3.5, and 7.0 mM). The length and fresh mass of seedlings were enhanced with the increased S concentration. In addition, the content of thiobarbituric acid reactive substances (TBARS) in rice leaves was the highest when no S was added to the nutrition solution and gradually declined with the increasing S supply. The higher S nutrition reduced the amount of Fe plaque on rice roots and increased Fe content in roots and leaves. The content of nicotianamine was significantly higher in rice roots under the S deficiency, whereas the reverse trend was observed in rice shoots. Taken together, the sufficient S nutrition promoted growth of rice, reduced oxidative stress, and ensured normal Fe uptake and distribution.