ABA Metabolites Research Articles

Exogenous Melatonin Alters Stomatal Regulation in Tomato Seedlings Subjected to Combined Heat and Drought Stress through Mechanisms Distinct from ABA Signaling

The understanding of stomatal regulation in climate stress is essential for ensuring resilient crops. The investigation of the stomatal regulation in combined heat and drought stress aimed to link effects of exogenous melatonin on stomatal conductance (gs) and its mechanistic interactions with ABA or ROS signaling. Melatonin-treated and non-treated tomato seedlings were subjected to moderate and severe levels of heat (38°C for one or three days) and drought stress (soil relative water content of 50% or 20%) applied individually and in combination. We measured gs, stomatal anatomy, ABA metabolites and enzymatic ROS scavengers. The stomata in combined stress responded predominantly to heat at soil relative water content (SRWC) = 50% and to drought stress at SRWC = 20%. Drought stress increased ABA levels at severe stress, whereas heat stress caused an accumulation of the conjugated form, ABA glucose ester, at both moderate and severe stress. The melatonin treatment affected gs and the activity of ROS scavenging enzymes but had no effect on ABA levels. The ABA metabolism and conjugation of ABA might play a role in stomatal opening toward high temperatures. We provide evidence that melatonin increases gs in combined heat and drought stress, but the effect is not mediated through ABA signaling.

Involvement of the miR156/SPL module in flooding response in Medicago sativa

The highly conserved plant microRNA, miR156, affects plant development, metabolite composition, and stress response. Our previous research revealed the role of miR156 in abiotic stress response in Medicago sativa exerted by downregulating SQUAMOSA-PROMOTER BINDING PROTEIN-LIKE transcription factors. Here we investigated the involvement and possible mechanism of action of the miR156/SPL module in flooding tolerance in alfalfa. For that, we used miR156 overexpressing, SPL13RNAi, flood-tolerant (AAC-Trueman) and -sensitive (AC-Caribou) alfalfa cultivars exposed to flooding. We also used Arabidopsis ABA insensitive (abi1-2, abi5-8) mutants and transgenic lines with either overexpressed (KIN10-OX1, KIN10-OX2) or silenced (KIN10RNAi-1, KIN10RNAi-2) catalytic subunit of SnRK1 to investigate a possible role of ABA and SnRK1 in regulating miR156 expression under flooding. Physiological analysis, hormone profiling and global transcriptome changes revealed a role for miR156/SPL module in flooding tolerance. We also identified nine novel alfalfa SPLs (SPL1, SPL1a, SPL2a, SPL7, SPL7a, SPL8, SPL13a, SPL14, SPL16) responsive to flooding. Our results also showed a possible ABA-dependent SnRK1 upregulation to enhance miR156 expression, resulting in downregulation of SPL4, SPL7a, SPL8, SPL9, SPL13, and SPL13a. We conclude that these effects induce flooding adaptive responses in alfalfa and modulate stress physiology by affecting the transcriptome, ABA metabolites and secondary metabolism.

Preparation of alginate oligosaccharides and their biological activities in plants: A review

Alginate oligosaccharide (AOS) is the degradation product of alginates extracted from brown algae. As a multifunctional oligomer, it has attracted widespread attention in plant research. Different methods of preparation generate AOS possessing diverse structural properties, and result in differences in AOS activity. In this review, the methods of preparation and characterization of AOS are briefly summarized, followed by a systematic introduction to the activity and mechanisms of AOS in plants. AOS can act as a growth promoter at different growth stages of plants. AOS also enhances resistance to pathogens, drought, salt, heavy metals and other stressors by triggering plant immunity, exerting bioactivity just like a pathogen-associated molecular pattern. In addition, AOS can regulate ABA biosynthesis and metabolite to preserve fruit quality and enhance shelf life. This review provides a comprehensive summary of the biological activity of AOS in plants, which will support research and the application of AOS treatments for plants in the future.

Endogenous gibberellins and abscisic acid-metabolites: their role for during flower bud abscission and embryo development in pistachio

This study was carried out to determine the effect of different growth periods and possible role of gibberellins GAs and abscisic acid ABA metabolites the alternate bearing of the pistachio Pistacia vera L. . For this purpose, the levels of GAs and ABA in the panicles and nuts of the trees during flower bud abscission and embryo development were analyzed in the crop on year. The results showed significant differences and changes in ABA and GAs among the tissues and periods investigated. Dihydrophaseic acid DPA and GA19 were the dominant ABA and GAs in the pistachio concentrates analyzed in this work, respectively. The nut samples had higher values for almost all ABA metabolites and GAs than panicles. The ABA content of the panicles and nuts increased rapidly during flower development 35 DAFB prior to flower bud abscission while the initial decrease in the ABA content remained constant at a relatively low level at the end of June intense flower bud abscission , with the minimum levels being obtained during embryo development stage 65 DAFB . However, day 65 after full flowering, GA19 and GA44 were found to have increased. The plant growth regulator profiles of the pistachio showed delayed spikes in GA and ABA groups indicating that there is a hormone requirement during flower bud abscission and embryo development in pistachio. As a results, GA and ABA metabolites produced in different organs play an important role in the control of pistachios during embryo development and

Comparison of phytohormone levels and transcript profiles during seasonal dormancy transitions in underground adventitious buds of leafy spurge.

Leafy spurge (Euphorbia esula L.) is an herbaceous perennial weed that maintains its perennial growth habit through generation of underground adventitious buds (UABs) on the crown and lateral roots. These UABs undergo seasonal phases of dormancy under natural conditions, namely para-, endo-, and ecodormancy in summer, fall, and winter, respectively. These dormancy phases can also be induced in growth chambers by manipulating photoperiod and temperature. In this study, UABs induced into the three phases of dormancy under controlled conditions were used to compare changes in phytohormone and transcriptome profiles. Results indicated that relatively high levels of ABA, the ABA metabolite PA, and IAA were found in paradormant buds. When UABs transitioned from para- to endodormancy, ABA and PA levels decreased, whereas IAA levels were maintained. Additionally, transcript profiles associated with regulation of soluble sugars and ethylene activities were also increased during para- to endodormancy transition, which may play some role in maintaining endodormancy status. When crown buds transitioned from endo- to ecodormancy, the ABA metabolites PA and DPA decreased significantly along with the down-regulation of ABA biosynthesis genes, ABA2 and NCED3. IAA levels were also significantly lower in ecodormant buds than that of endodormant buds. We hypothesize that extended cold treatment may trigger physiological stress in endodormant buds, and that these stress-associated signals induced the endo- to ecodormancy transition and growth competence. The up-regulation of NAD/NADH phosphorylation and dephosphorylation pathway, and MAF3-like and GRFs genes, may be considered as markers of growth competency.

Root biomass in the upper layer of the soil profile is related to the stomatal response of wheat as the soil dries.

Terminal drought is a common abiotic stress affecting wheat yield in Mediterranean-type environments. As terminal drought develops, top layers of the soil profile dry, exposing the upper part of the root system to soil water deficit while deeper roots can still access soil water. Since open stomata rapidly exhausts available soil water, reducing stomatal conductance to prolong availability of soil water during grain filling may improve wheat yields in water-limited environments. It was hypothesised that genotypes with more root biomass in the drying upper layer of the soil profile accumulate more abscisic acid in the leaf and initiate stomatal closure to regulate water use under terminal drought. The wheat cultivar Drysdale and the breeding line IGW-3262 were grown in pots horizontally split into two segments by a wax-coated layer that hydraulically isolated the top and bottom segments, but allowed roots to grow into the bottom segment. Terminal drought was induced from anthesis by withholding water from (i) the top segment only (DW) and (ii) the top and bottom segments (DD) while both segments in well-watered pots (WW) were maintained at 90% pot soil water capacity. Drysdale, initiated stomatal closure earlier than IGW-3262, possibly due to higher signal strength generated in its relatively larger proportion of roots in the drying top segment. The relationship between leaf ABA and stomatal conductance was strong in Drysdale but weak in IGW-3262. Analysis of ABA metabolites suggests possible differences in ABA metabolism between these two genotypes. A higher capability of deeper roots to extract available water is also important in reducing the gap between actual and potential yield.

Controlling sprouting in potato tubers using ultraviolet-C irradiance

Legislation limiting the use of chlorpropham (CIPC), the major potato sprout suppressant, has led to a need for new technologies to extend storage life of tubers. Ultra violet C (UV-C) has been used postharvest to reduce disease incidence on many crops, yet its use and efficacy as a sprout suppressant has not been investigated. The aim of this project was to identify the optimum dose and treatment timing of UV-C treatment on potato tubers as an alternative method of sprout suppression to reduce the dependence on chemical sprout suppressants. Up to six potato cultivars over two seasons were treated with varying doses of UV-C ranging from 0 to 30kJm−2 either at harvest or at first indication of dormancy break. The tubers were stored at 9°C and sprout growth and incidence assessed. Treatment with moderate UV-C doses (5–20kJm−2) suppressed sprout length and sprout incidence in a range of cultivars. Periderm DNA damage and programmed cell death were not detected in response to any of the UV-C doses. The inactive ABA metabolite, ABA-GE, increased in response to 10 or 20kJm−2 within 72h of treatment. Multivariate analysis showed a negative relationship between ABA metabolites and sprout growth/incidence during storage. This study found that UV-C reduced sprout growth in potato with no deleterious effects on tuber quality. This suggests potential for further development as an alternative or supplement to conventional sprout suppressant technologies.

High-level expression of sugar inducible gene2 (HSI2) is a negative regulator of drought stress tolerance in Arabidopsis

BackgroundHIGH-LEVEL EXPRESSION OF SUGAR INDUCIBLE GENE2 (HSI2), also known as VAL1, is a B3 domain transcriptional repressor that acts redundantly with its closest relative, HSI2-LIKE1 (HSL1), to suppress the seed maturation program following germination. Mutant hsi2 hsl1 seedlings are arrested early in development and differentially express a number of abiotic stress-related genes. To test the potential requirement for HSI2 during abiotic stress, hsi2 single mutants and plants overexpressing HSI2 were subjected to simulated drought stress by withholding watering, and characterized through physiological, metabolic and gene expression studies.ResultsThe hsi2 mutants demonstrated reduced wilting and maintained higher relative water content than wild-type after withholding watering, while the overexpressing lines displayed the opposite phenotype. The hsi2 mutant displayed lower constitutive and ABA-induced stomatal conductance than wild-type and accumulated lower levels of ABA metabolites and several osmolytes and osmoprotectants following water withdrawal. Microarray comparisons between wild-type and the hsi2 mutant revealed that steady-state levels of numerous stress-induced genes were up-regulated in the mutant in the absence of stress but down-regulated at visible wilting. Plants with altered levels of HSI2 responded to exogenous application of ABA and a long-lived ABA analog, but the hsi2 mutant did not show altered expression of several ABA-responsive or ABA signalling genes 4 hr after application.ConclusionsThese results implicate HSI2 as a negative regulator of drought stress response in Arabidopsis, acting, at least in part, by regulating transpirational water loss. Metabolic and global transcript profiling comparisons of the hsi2 mutant and wild-type plants do not support a model whereby the greater drought tolerance observed in the hsi2 mutant is conferred by the accumulation of known osmolytes and osmoprotectants. Instead, data are consistent with mutants experiencing a relatively milder dehydration stress following water withdrawal.

DOES ABA PLAY A ROLE IN SEED GERMINATION

The possible role of ABA in induction and maintenance of dormancy, and in seed maturation and germination is discussed. The physiological activities of ABA metabolites are also assessed. It is not clear at present whether ABA plays a role in the induction of dormancy. Reduction in ABA content is not sufficient to break dormancy and it has not yet been demonstrated that a reduction is even necessary. There is considerable evidence that ABA levels rise and then fall during maturation of non-dormant seeds. It has been suggested that ABA prevents precocious germination, but more evidence is necessary to support this hypothesis and to determine the mechanism by which ABA might effect this. Although most of the known ABA metabolites have reduced ABA physiological activities, phaseic acid has been found active in several bioassays.

Wounding of potato tubers induces increases in ABA biosynthesis and catabolism and alters expression of ABA metabolic genes

The effects of physical wounding on ABA biosynthesis and catabolism and expression of genes encoding key ABA metabolic enzymes were determined in potato tubers. An increase in ABA and ABA metabolite content was observed 48h after wounding and remained elevated through 96h. Wounding induced dramatic increases in the expression of the ABA metabolic genes encoding zeaxanthin epoxidase (ZEP), 9-cis-epoxycarotenoid dioxygenase (NCED), and ABA-8′-hydroxylase. Although the patterns of wound-induced expression of individual genes varied, increased gene expression was observed within 3h of wounding and remained elevated through 96h. An apparent correlation between expression of the gene encoding ZEP and the increase in ABA content suggested that the wound-induced increase in ABA biosynthesis was regulated by both substrate availability and increased NCED activity. Suppression of wound-induced jasmonic acid accumulation by rinsing the wounded tissue with water did not inhibit the subsequent increase in ABA content. Exogenous ethylene completely suppressed the wound-induced increase in ABA content and dramatically reduced wound-induced up-regulation of ABA metabolic genes. This study is the first to identify the molecular bases for increased ABA accumulation following physical trauma in potato tubers and highlights the complex physiological interactions between various wound-induced hormones.

Comprehensive Hormone Profiling in Developing Arabidopsis Seeds: Examination of the Site of ABA Biosynthesis, ABA Transport and Hormone Interactions

ABA plays important roles in many aspects of seed development, including accumulation of storage compounds, acquisition of desiccation tolerance, induction of seed dormancy and suppression of precocious germination. Quantification of ABA in the F(1) and F(2) populations originated from crosses between the wild type and an ABA-deficient mutant aba2-2 demonstrated that ABA was synthesized in both maternal and zygotic tissues during seed development. In the absence of zygotic ABA, ABA synthesized in maternal tissues was translocated into the embryos and partially induced seed dormancy. We also analyzed the levels of ABA metabolites, gibberellins, IAA, cytokinins, jasmonates and salicylic acid (SA) in the developing seeds of the wild type and aba2-2. ABA metabolites accumulated differentially in the silique and seed tissues during development. Endogenous levels of SA were elevated in aba2-2 in the later developmental stages, whereas that of IAA was reduced compared with the wild type. These data suggest that ABA metabolism depends on developmental stages and tissues, and that ABA interacts with other hormones to regulate seed developmental processes.

ABA metabolites induce group 3 LEA mRNA and inhibit germination in wheat

In plants, metabolism of the plant hormone (+)‐S‐abscisic acid (ABA) occurs by oxidation at the 8′‐carbon on the ABA ring, producing (+)‐8′‐hydroxy‐ABA (8′OH‐ABA), which undergoes ring closure to phaseic acid (PA), or at the 7′‐carbon producing 7′‐hydroxy‐ABA (7′OH‐ABA). New methods for synthesixing and stabilizing 8′OH‐ABA have enabled us for the first time to compare the biological activities of the ABA metabolites. 8′OH‐ABA. PA and 7′OH‐ABA. Activities were determined in wheat (Triticum aestivum, cvs Brevor and Clarks Cream) using optically pure natural enantiomers of ABA. 8′OH‐ABA, PA, and 7′OH‐ABA. Comparison of wheat embryo germination inhibitory activity showed that only the metabolite 7′OH‐ABA had significant activity (10 to 40% of effective ABA activity) as a germination inhibitor of wheat embryos. The metabolites had differential effects on ABA‐responsive gene expression. Both 8′OH‐ABA and PA were effective inducers of an ABA‐responsive LEA (late embryogenesis abundant) gene, wheat group 3 LEA, in seedling roots, suggesting that ABA metabolites can maintain and prolong LEA gene expression. The metabolites had only a slight effect on accumulation of an ABA‐responsive protein kinase (PKABA1) mRNA or pMA1951. These results are consistent with the idea that there are several control points in the ABA metabolic pathway and indicate that assessment of ABA signalling responses should include consideration of the biological activities of ABA metabolites.

ABA metabolites induce group 3 LEA mRNA and inhibit germination in wheat

ABA metabolites induce group 3 LEA mRNA and inhibit germination in wheat

Role and metabolism of abscisic acid in potato tuber dormancy and sprouting

Tubers cv. Monalisa were analysed to determine the content of abscisic acid (c-t-(+)ABA) and related metabolites in three tuber parts (eyes, sub-eye tissues and pith). Analyses were performed from the last period of tuber growth until sprouting under two different storage temperatures (3 °C and 23 °C). ABA content rises in eyes and sub-eye tissues as sprouting approaches, regardless of storage temperature. Dihydrophaseic acid is the main ABA metabolite while phaseic acid was not detected, probably because of its further metabolization to DPA. ABA-glucose ester concentrations are generally low in all tissues except in eyes before harvest. The results are discussed in relation to the current hypotheses on the role of ABA in the control of potato tuber dormancy.

Induction of Lipid and Oleosin Biosynthesis by (+)-Abscisic Acid and Its Metabolites in Microspore-Derived Embryos of Brassica napus L.cv Reston (Biological Responses in the Presence of 8[prime]-Hydroxyabscisic Acid).

Microspore-derived (MD) embryos of Brassica napus L. cv Reston were used to test the effects of (+)-abscisic acid ([(+)-ABA]) and its metabolites, 8[prime]-hydroxyabscisic acid (8[prime]-OH ABA) and (-)-phaseic acid (PA), on the accumulation of very long-chain monounsaturated fatty acids (VLCMFAs) and induction of genes encoding a 19-kD oleosin protein and a [delta]15 desaturase during embryogenesis. Developing early to mid-cotyledonary MD embryos at 16 to 19 d in culture were treated with 10 [mu]M hormone/metabolite for 4 d. At various times during incubation, embryos and medium were analyzed to determine levels of hormone/metabolite, VLCMFAs, and oleosin or [delta]15 desaturase transcripts. The VLCMFAs, 20:1 and 22:1, primarily in triacylglycerols, increased by 200% after 72 h in the presence of (+)-ABA and 8[prime]-OH ABA relative to the control. In contrast, treatment with PA for 72 h had little effect (20% increase) on the level of VLCMFAs. The first 24 to 72 h of (+)-ABA treatment were critical in the induction of VLCMFA biosynthesis, with 8[prime]-OH ABA lagging slightly behind (+)-ABA in promoting this response. The accumulation of VLCMFAs was positively correlated with an increase in elongase activity. (+)-ABA and its 8[prime]-OH ABA metabolite induced the accumulation of a 19-kD oleosin transcript within 2 to 4 h in culture. In addition, both (+)-ABA and 8[prime]-OH ABA induced the same level of [delta]15 desaturase transcript by 8 h. PA had no effect on the induction of either oleosin or [delta]15 desaturase transcripts. To our knowledge, this is the first report of the biological activity of 8[prime]-OH ABA and of stimulatory effects of (+)-ABA and 8[prime]-OH ABA on lipid and oleosin biosynthesis.

ABA Metabolite Levels in Developing Embryo of "Sechium Edule" Sw.

ABA Metabolite Levels in Developing Embryo of "Sechium Edule" Sw.

Uptake and metabolism of 2-[14C]abscisic acid in lettuce fruits var. Great Lakes

There are two phases of 2-[(14)C]ABA uptake in lettuce fruits. Although the first phase appears to relate to the imbibition of water, uptake continues for three hours following complete imbibition. The second phase corresponds with the commencement of radicle extension.Exogenously applied radioactive ABA is metabolised to form an unidentified substance which has chromatographic properties different to previously described ABA metabolites. When ABA is present in the bathing solution, the quantity of metabolite never significantly exceeds that of labelled ABA in the tissues.