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To acclimate to waterlogged conditions, wetland plants form a barrier to radial oxygen loss (ROL) that can enhance oxygen transport to the root apex. We hypothesized that one or more hormones are involved in the induction of the barrier and searched for such hormones in rice. We previously identified 98 genes that were tissue-specifically upregulated during ROL barrier formation in rice. The RiceXPro database showed that most of these genes were highly enhanced by exogenous abscisic acid (ABA). We then examined the effect of ABA on ROL barrier formation by using an ABA biosynthesis inhibitor (fluridone, FLU), by applying exogenous ABA and by examining a mutant with a defective ABA biosynthesis gene (osaba1). FLU suppressed barrier formation in a stagnant solution that mimics waterlogged soil. Under aerobic conditions, rice does not naturally form a barrier, but 24 h of ABA treatment induced barrier formation. osaba1 did not form a barrier under stagnant conditions, but the application of ABA rescued the barrier. In parallel with ROL barrier formation, suberin lamellae formed in the exodermis. These findings strongly suggest that ABA is an inducer of suberin lamellae formation in the exodermis, resulting in an ROL barrier formation in rice.

Mepiquat chloride (MC) priming alleviates the effects of salt stress during seed germination in cotton (Gossypium hirsutum L.), but the mechanisms underlying its effects are unknown. We found that MC priming increases salt tolerance, as evidenced by marked increases in seed vigor and germination rates, and alleviated salt toxicity by reducing Cl− accumulation in germinating seeds. Consistently, electrophysiological experiments revealed that the seeds with MC priming displayed superior Cl− exclusion ability in the root apex. These beneficial effects of MC priming were abolished by the abscisic acid (ABA)-synthesis blocker fluridone under salt stress. MC priming induced an early response to acclimatization and stress, as indicated by rapidly increasing ABA content during initial exposure to salt stress. Transcriptome analyses revealed that MC priming induced an array of differentially expressed genes (DEGs) in germinating seeds. The most noticeable changes in germinating seeds were MC priming-induced increases in the expression of DEGs encoding components of ABA biosynthesis, ABA catabolism, and ABA signaling pathways under salt stress. MC priming also increased the expression of some DEGs encoding Cl− ion transporters (e.g. CCC, SLAC1/SLAH1/SLAH3, CLC, and ALMT9) in germinating seeds. These results indicate that MC priming-induced ABA contributes to Cl− homeostasis in tissues and acts as a positive regulator of salt tolerance via regulation of Cl− transporters (particularly CCC and SLAC1/SLAH1/SLAH3). Taken together, these findings shed light on the molecular mechanism underlying MC-mediated tolerance to salt stress during seed germination.

Cadmium (Cd) is a highly toxic heavy metal. Abscisic acid (ABA) is a regulator that has various functions in plants. To further explore the mechanism by which ABA alleviates Cd damage in plants, ABA and fluridone, which inhibits ABA biosynthesis, were separately sprayed on the leaves of Malus hupehensis Rehd. (M. hupehensis) seedlings treated with Cd. The root Cd2+ flux in vivo, the accumulation and transport of Cd2+ in roots, the cell death in roots and the transpiration rate in leaves were then analyzed. The results showed that the amount of cell death in roots gradually increased from 6 to 72 h in the Cd treatment. After spraying ABA on M. hupehensis leaves in the Cd treatment, the number of root cell deaths, the accumulation of hydrogen peroxide (H2O2) and malondialdehyde (MDA) in roots and the transpiration rate in leaves decreased significantly compared with those in the samples in the Cd-only treatment. In addition, the influx rate of Cd2+ in roots, the content of Cd in plants and the migration rate of Cd from the roots to the aerial parts were also significantly reduced. In contrast, all of these parameters increased significantly in M. hupehensis sprayed with fluridone under the Cd treatment. These results indicate that spraying ABA on leaves alleviates Cd damage in M. hupehensis roots by decreasing cell death as well as the contents of H2O2 and MDA in roots. Given that transpiration is the main driving force for the absorption and transport of inorganic salts in plants, our results showed that the alleviation of Cd damage in roots resulted from the reduced leaf transpiration rate, which decreased the influx and accumulation of Cd2+ in roots.

Drought stress is a limiting factor for wheat production and food security. Drought priming has been shown to increase drought tolerance in wheat. However, the underlying mechanisms are unknown. In the present study, the genes encoding the biosynthesis and metabolism of abscisic acid (ABA) and jasmonic acid (JA), as well as genes involved in the ABA and JA signaling pathways were up-regulated by drought priming. Endogenous concentrations of JA and ABA increased following drought priming. The interplay between JA and ABA in plant responses to drought priming was further investigated using inhibitors of ABA and JA biosynthesis. Application of fluridone (FLU) or nordihydroguaiaretic acid (NDGA) to primed plants resulted in lower chlorophyll-fluorescence parameters and activities of superoxide dismutase and glutathione reductase, and higher cell membrane damage, compared to primed plants (PD) under drought stress. NDGA + ABA, but not FLU + JA, restored priming-induced tolerance, as indicated by a finding of no significant difference from PD under drought stress. Under drought priming, NDGA induced the suppression of ABA accumulation, while FLU did not affect JA accumulation. These results were consistent with the expression of genes involved in the biosynthesis of ABA and JA. They suggest that ABA and JA are required for priming-induced drought tolerance in wheat, with JA acting upstream of ABA.

Fruit development and ripening are controlled by multiple plant hormones; for strawberries, recent evidence supports the role of abscisic acid (ABA) as a promoter of fruit ripening. Fruit softening during ripening is mainly a consequence of the solubilization and depolymerization of cell wall components mediated by the action of a complex set of enzymes and proteins. In the present work, we performed a comparative study (ABA-treatment vs. control) of the changes in the physiological properties of the cell wall-associated polysaccharide contents of strawberry fruit (Fragaria x ananassa ‘Camarosa’) via analysis of thermogravimetry (TG) combined with analysis of mRNA abundance, enzymatic activity and physiological characteristics. ‘Camarosa’ did not show a decline in the fruit firmness at 48 h post-treatment; however, we observed changes in cell wall stability based on the TG and differential thermogravimetric (DTG) analysis curves, which demonstrated the degradation of the cell wall polymers after ABA hormone treatment for 48 h, principally for hemicellulose polymers. Additionally, DTG analysis showed that dried samples derived from the treatment of the fruit with the ABA biosynthesis inhibitor fluridone maintained the same thermal stability as the control samples. Finally, the existence of a relationship between thermal stability, transcriptional analysis and enzymatic activity after hormone treatment was demonstrated, which provides the basis for a model for understanding the changes in the cell wall polymers of F. x ananassa mediated by the ABA hormone during fruit ripening.

Genetic assays to identify herbicide-resistant plants are a promising tool to reduce herbicide failures. However, the genetic basis of herbicide resistance is frequently unknown. In clonal weed species, DNA fingerprinting could be a useful tool to identify known resistant versus susceptible genets (clones) that occur in multiple locations, without an immediate need for understanding the genetic mutation(s) conferring resistance. Eurasian watermilfoil (Myriophyllum spicatum L.) and hybrids with native northern watermilfoil (Myriophyllum spicatum × Myriophyllum sibiricum Kom.) are mostly clonal invasive aquatic plants, and the same clones can be found in multiple waterbodies. Previously, a clone was confirmed as resistant to the commonly used herbicide fluridone, and a recent genetic survey in Michigan identified this genotype (MG-237) in at least seven other lakes. We hypothesized that MG-237 collected from different lakes would also exhibit fluridone resistance. However, MG-237 may have accumulated resistance mutations at different times during its spread across Michigan, resulting in fluridone-resistant and fluridone-susceptible MG-237 clones distributed in different lakes. We used a herbicide assay to test the response of several accessions, including MG-237 accessions from multiple lakes, to the Michigan operational rate of 6 µg L−1 fluridone. We found that all accessions of MG-237 exhibited resistance to 6 µg L−1 fluridone. A second genotype (MG-377) was also resistant to 6 µg L−1 fluridone. The rest of the accessions were found to be significantly injured by 6 µg L−1 fluridone. Our results suggest that 6 µg L−1 fluridone would not effectively control waterbodies dominated by MG-237 or MG-377, whereas waterbodies dominated by the other genotypes in our study would likely be controlled. Although more studies are needed to identify the variation in sensitivity of the accessions tested here and the genetic basis of fluridone resistance in Myriophyllum, our results suggest that multilocus genotype data may be an effective tool to identify and track herbicide-resistant genotypes of Myriophyllum in the short term.

In plants, glucose (Glc) plays pivotal roles in development and stress responses mainly by supplying fuel for growth and regulating expression of genes essential for crosstalk with hormonal, oxidative, and defense signaling. However, the complicated relationship between Glc and plant hormones is still not very clear. In this study, gsm3 (glucose-sensitive mutant 3), an Arabidopsis mutant with Glc-sensitive phenotype, was identified. Compared to wild type, the cotyledon expansion rate of gsm3 was significantly decreased under the condition of 4.5% Glc. Fluridone was able to rescue the Glc-induced defects of gsm3 in cotyledon expansion. AAO3 and ABI4 are key genes involved in abscisic acid (ABA) biosynthesis and signaling transduction, respectively. We found that inactivation of AAO3 or ABI4 in gsm3 background led to reduced sensitivity to Glc. These results indicated that increased ABA synthesis resulted in the sensitivity of gsm3 to Glc. Moreover, our results indicated that gsm3 mutant accumulated more ROS, which made it more sensitive to the application of exogenous H2O2. Overall, GSM3 plays an important role in Glc-ABA signaling cascade during seed germination and early seedling growth.

Copper‐based antimicrobial compounds are widely and historically used to control plant diseases, such as late blight caused by Phytophthora infestans, which seriously affects the yield and quality of potato. We previously identified that copper ion (Cu2+) acts as an extremely sensitive elicitor to induce ethylene (ET)‐dependent immunity in Arabidopsis. Here, we found that Cu2+ induces the defence response to P. infestans in potato. Cu2+ suppresses the transcription of the abscisic acid (ABA) biosynthetic genes StABA1 and StNCED1, resulting in decreased ABA content. Treatment with ABA or inhibitor fluridone made potato more susceptible or resistance to late blight, respectively. In addition, potato with knockdown of StABA1 or StNCED1 showed greater resistance to late blight, suggesting that ABA negatively regulates potato resistance to P. infestans. Cu2+ also promotes the rapid biosynthesis of ET. Potato plants treated with 1‐aminocyclopropane‐1‐carboxylate showed enhanced resistance to late blight. Repressed expression of StEIN2 or StEIN3 resulted in enhanced transcription of StABA1 and StNCED1, accumulation of ABA and susceptibility to P. infestans. Consistently, StEIN3 directly binds to the promoter regions of StABA1 and StNCED1. Overall, we concluded that Cu2+ triggers the defence response to potato late blight by activating ET biosynthesis to inhibit the biosynthesis of ABA., Cu2+‐mediated late blight resistance activates ET signalling, subsequently suppressing ABA biosynthesis. This recalls two tips when using copper‐based antimicrobial compounds: water in advance; avoid strong sunshine and drought.

Graptopetalum paraguayense E. Walther is an edible succulent plant that is native to Mexico. When leaves of G. paraguayense are detached from the mother plant, shoots and roots regenerate from the leaf base. To investigate the endogenous hormonal regulation of plant regeneration in G. paraguayense, we evaluated the effects of applying gibberellin (GA), abscisic acid (ABA), and phytohormone biosynthesis inhibitors to leaves detached from the mother plant. GA3 and paclobutrazol did not affect plant regeneration of G. paraguayense, whereas ABA treatment significantly suppressed plant regeneration. When leaves were treated with the ABA biosynthesis inhibitor fluridone at 10 μM, the frequency of shoot regeneration was more than twice that of the control on the 6th day after leaf detachment. In addition, when both fluridone and ABA were applied at the same time, the frequency of plant regeneration decreased to control levels or below. Endogenous ABA in leaves was approximately 1.3 ng gFW−1 just after leaf detachment, decreased to 0.3 ng gFW−1 by the 1st day after leaf detachment, and increased to 3.0 ng gFW−1 by the 9th day after leaf detachment. These findings indicate that ABA plays an important role in suppression of plant regeneration in G. paraguayense. Although plant regeneration during storage and transportation currently reduces the economic value of G. paraguayense, our findings may provide a method to delay unwanted plant formation at the leaf base.

Background Diflufenican resistance has been reported in wild radish populations since 1998, but the resistance mechanisms have not been investigated. Recently, we identified a wild radish population (H2/10) from the Western Australian grain belt that is resistant (R) to the phytoene desaturase (PDS)-inhibiting herbicide diflufenican. Results Dose-response results showed this R population is 4.9-fold more resistant than the susceptible (S) population based on the LD50 R/S ratio. In addition, the R population also exhibits cross-resistance to the PDS-inhibiting herbicide fluridone. The cytochrome P450 inhibitor malathion reversed diflufenican resistance and partially reversed fluridone resistance in the R population. The full coding sequences of the PDS gene were cloned from the S and R plants and there are natural variations in the PDS gene transcripts/alleles with no correlation to resistance. In addition, the R plants had a level of PDS gene expression that is not significantly different from the S plants. Conclusion These results demonstrated that diflufenican resistance in this R wild radish population is likely due to non-target-site based enhanced herbicide metabolism involving cytochrome P450s. © 2019 Society of Chemical Industry.

An improved understanding of seed quality and germination control can contribute effectively to the use and conservation of neglected native species with ecological and economic value, such as Trichocline catharinensis, an endemic Asteraceae species from southern Brazil. We investigated the effects of applying gibberellin (GA3), abscisic acid (ABA) and their biosynthesis inhibitors, paclobutrazol (PAC) and fluridone (FLU), respectively, on T. catharinensis seed germination, and on polyamine (PA) content and antioxidant enzyme activities in germinating seeds. FLU and GA3 increased seed germination speed compared to treatment with H2O only. ABA inhibited both germination speed index and percentage, while PAC severely inhibited seed germination. The stimulatory effect of GA3 and FLU was associated with increased contents of putrescine (PUT) and spermidine (SPD) relative to spermine (SPM). As a result, high ratio (PUT + SPD/SPM) as well as superoxide dismutase (SOD), catalase (CAT) and ascorbate peroxidase (APX) enzyme activities were observed when seed germination occurs. In contrast, in low or no seed germination treatment (ABA and PAC), low ratio (PUT + SPD/SPM) was observed, while the antioxidant enzymes, mainly SOD activity, tended to increase. Application of PAs at 200 μM stimulated germination through improving the speed and uniformity, and this effect was associated with antioxidant enzyme activity. Our results suggest a relationship between PA and the antioxidant system with the physiological mechanism of seed germination. These results improve the physiological knowledge of seed germination control in Asteraceae and contribute to the biological groundwork for future studies on the use and conservation of native species.

Abscisic acid (ABA) may play roles in mediating cross stress tolerance in plants. The objectives of this study were to investigate the priming effects of drought and ABA on heat tolerance and to determine how ABA may be involved in enhanced heat tolerance by drought. Focusing on the transcriptional level, two independent experiments were conducted, using a perennial grass species, tall fescue (Festuca arundinacea) and Arabidopsis. In experiment 1, tall fescue plants were exposed to mild drought by withholding irrigation for 8 days (drought priming) and foliar sprayed with ABA or an ABA-synthesis inhibitor (fluridone). After that they were subsequently subjected to heat stress (38/33°C day/night) for 25 days in growth chambers. In experiment 2, Arabidopsis Columbia ecotype (wild-type) and ABA-deficient mutant (aba3-1, CS157) were pre-treated with drought priming and then exposed to heat stress (45/40°C) for 3 days. The physiological analysis demonstrated that both drought priming and foliar application of ABA-enhanced heat tolerance in tall fescue, while drought priming had no significant effects on heat tolerance in ABA-deficient Arabidopsis plants. Application of fluridone to tall fescue and ABA-deficient mutants of Arabidopsis exhibited diminished or attenuated positive effects of drought priming on heat tolerance. ABA mediation of acquired heat tolerance by drought priming was associated with the upregulation of CDPK3, MPK3, DREB2A, AREB3, MYB2, MYC4, HsfA2, HSP18, and HSP70. Our study revealed the roles of ABA in drought priming-enhanced heat tolerance, which may involve transcriptional regulation for stress signaling, ABA responses and heat protection.

Soil drying enhances root ABA accumulation and rhizosheath formation, but whether ABA mediates rhizosheath formation is unclear. Here, we used the ABA-deficient mutant Az34 to investigate molecular and morphological changes by which ABA could affect rhizosheath formation. Mild soil drying with intermittent watering increased rhizosheath formation by promoting root and root hair elongation. Attenuated root ABA accumulation in Az34 barley constrained the promotion of root length and root hair length by drying soil, such that Az34 had a smaller rhizosheath. Pharmacological experiments of adding fluridone (an ABA biosynthesis inhibitor) and ABA to drying soil restricted and enhanced rhizosheath formation respectively in Az34 and wild-type Steptoe barley. RNA sequencing suggested that ABA accumulation mediates auxin synthesis and responses and root and root hair elongation in drying soil. In addition, adding indole-3-acetic acid (IAA) to drying soil increased rhizosheath formation by promoting root and root hair elongation in Steptoe and Az34 barley. Together, these results show that ABA accumulation induced by mild soil drying enhance barley rhizosheath formation, which may be achieved through promoting auxin response. © 2021 John Wiley & Sons Ltd.

Cadmium (Cd2 +) is among the toxic non-essential heavy metals that adversely affect plants metabolic processes and the safety of produce. However, plant hormones can improve plant’s tolerance to various stresses. This study investigated the effect of exogenous abscisic acid (ABA) on the biochemical and physiological processes and food safety of cadmium (Cd2 +)-sensitive lettuce genotype (Lüsu). Seedlings were subjected to five treatments: [(i) Control (untreated plants), (ii) 100 µM CdCl2, (iii) 100 µM CdCl2+10 µg L−1 ABA (iv) 10 µg L−1 ABA, and (v) 0.01 g L−1 ABA-inhibitor (fluridone)] for fourteen days in hydroponic system. The 100 µM CdCl2 increased the contents of hydrogen peroxide (H2O2) and malondialdehyde (MDA), decreased photosynthesis and plant biomass. Moreover, it decreased the contents of essential nutrients (except copper) in the leaves but increased the contents of toxic Cd2 + in the leaves and roots of the plants. Foliar application of fluridone (0.01 g L−1) also caused oxidative stress by increasing the contents of H2O2 and MDA. It also decreased the contents of nutrient elements in the leaves of the plants. However, exogenous ABA (10 µg L−1) mitigated the Cd2 +-induced stress, increased antioxidant enzymes activities, photosynthesis and plant biomass under CdCl2 treatment. Remarkably, exogenous ABA increased the contents of essential nutrient elements but decreased the Cd2 + content in leaves under the CdCl2 treatment. Our results have demonstrated that foliar application of ABA mitigates Cd2 + stress and increases the nutritional quality and food safety of Cd2 +-sensitive lettuce genotype under CdCl2 treatment.

Moss paraphyllia, the trichome-like or foliose structures on moss stem surfaces, are usually treated as epidermal outgrowths. However, in some taxa of the moss families Leskeaceae, Neckeraceae, and Amblystegiaceae their distribution along the stem is consistently correlated with parts of the stem surface near branch primordia. In other moss families, Climaciaceae, Hylocomiaceae, and Pseudoleskeaceae the specific paraphyllia-generating epidermal layer produces paraphyllia evenly all along the stem. These results suggest that there are at least two different types of regulation of paraphyllia development; however, both of them may be involved in the morphogenesis of paraphyllia in some families, for example in the Thuidiaceae. Exogenous abscisic acid treatment consistently increases the number of paraphyllia of the Leskea-type, and it also induces the development of proximal branch leaves that normally do not develop a lamina above the stem surface. This fact supports conclusions regarding the homology of the Leskea-type of paraphyllia with leaves.

ABA and GA metabolism during incubation rather than hormone contents in dry seeds is the key to understanding secondary dormancy and germination of Syngonanthus verticillatus seeds. The mechanism of seed dormancy cycle, although very important for preventing germination during unfavorable periods for seedling establishment, is poorly understood in tropical species. Here, we used a perennial tropical species of the Brazilian campo rupestre, Syngonanthus verticillatus (Eriocaulaceae), to investigate the involvement of ABA and GA in modulating secondary dormancy of seeds buried in situ over time and the dynamic of these hormones during the incubation of dormant and non-dormant seeds. Hormone analyses were carried out with freshly harvested seeds and on buried seeds exhumed after 3, 6 and 9 months. Dynamics of ABA and GAs in dormant and non-dormant seeds during incubation (0, 12, 24 and 36 h) under favorable conditions for germination (at 20 °C in the presence of light) were also investigated. In addition, the effects of GA4 and fluridone were evaluated for overcoming secondary dormancy. Our results showed that changes in the contents of both ABA and GA4 occurred after burial, suggesting they may be related to the modulation of secondary dormancy/germination of S. verticillatus seeds. The application of fluridone was more effective than GA4 at overcoming secondary dormancy. We conclude that during incubation, de novo ABA synthesis and its consequent maintenance at high contents regulate the inhibition of germination in dormant seeds, while GA4 synthesis and ABA catabolism modulate the germination of non-dormant seeds. ABA and GA metabolism during incubation of both dormant and non-dormant seeds rather than hormone contents of dry seeds in the field is thought to be the key to understanding secondary dormancy and germination.

Carotenoids are a group of natural tetraterpenoid pigments with essential roles in a variety of physiological processes of plants. Although carotenoid biosynthesis has been well characterized, the genetic basis of the pathway, especially in crop plants, is largely unknown. In this study, we characterized a new albino maize mutant called albino1 (alb1), which was obtained from a Mutator mutagenized population. The alb1 mutant showed defective chloroplast development and declined photosynthetic pigments, leading to a seedling-lethal phenotype. Genetic and molecular analyses indicated that ALB1 encoded a putative ζ-carotene desaturase (ZDS) involved in carotenoid biosynthesis. Measurement of carotenoids revealed that several major carotenoid compounds downstream of the ZDS were significantly reduced in alb1 mutant, indicating that ALB1 is a functional ZDS. Further transcriptome analysis revealed that several groups of nuclear genes involved in photosynthesis, such as light-harvesting complex, pigment metabolism, and chloroplast function, were significantly down-regulated in alb1 compared with wide type. Interestingly, expression of some maize plastid-localized nuclear genes, including POR, CAO, Lhcb, and RbcS, was substantially reduced in alb1 plants. Furthermore, treatment of the inhibitor fluridone significantly rescued gene transcripts of these nucleus-encoded genes in alb1 mutant, which supported the retrograde signaling of ζ-carotene/phytofluene derived molecules. These results suggested that ALB1/ZDS might function as a regulator to coordinate nuclear photosynthetic gene expression in plastid-to-nucleus retrograde signaling during development of maize plants. Together, these results have demonstrated that ALB1/ZDS is essential for carotenoids biosynthesis and plays crucial roles in chloroplast biogenesis and development in maize.

Stevia is a herbaceous plant containing non-sugar sweeteners that could be regarded as a successor to sugar for diabetics. However, there are some problems with the cultivation of stevia, especially in the greenhouse, including unbranching and low sweetening agents. To overcome this issue, an experiment was designed to increase not only the branching and leaf production but also the sweetness. Therefore, a novel strategy using abscisic acid (0, 50, 100, 150 μM), its inhibitor, i.e. fluridone (0, 50, 100, 150 μM) and decapitation of plant apical meristems was applied. Results showed that when stevia was decapitated, dormant buds responded to the application of abscisic acid and fluridone. Under these conditions, axillary buds were developed to branches. As well leaf, total dry weight, soluble sugars and steviol glycosides (SGs) were significantly increased. In addition, the interaction of abscisic acid (50 and 100 μM) and fluridone (50 μM) had the highest positive effects on plant growth and steviol glycosides production rather than their sole applications. Results also indicated that decapitation removed a terminal dominance over a limited period of time and the terminal dominance was re-established with the growth of the terminal branches, whereas the influence of 50 µM fluridone on stevia was long term and the number of shoots was greater. Since stevia is a costly sweetener, the results of this study could be used in greenhouses, where the cultivation of stevia seems to be reasonable in terms of economic aspects.

Arabidopsis ACYL-COENZYME-A-BINDING PROTEIN1 (ACBP1) plays a positive role in abscisic acid (ABA) signaling during seed dormancy and germination. As a putative component of the ABA signaling pathway, its potential role in salt and osmotic signaling was tested using ACBP1pro::GUS transgenic lines, ACBP1-overexpressors (ACBP1-OXs), the acbp1 mutant and ACBP1-complemented lines (acbp1-COM). ACBP1-OXs were more sensitive than the wild type to NaCl and mannitol during seed germination and seedling establishment, while the acbp1 mutant was less sensitive during seed germination. Germination assays were conducted using the ABA biosynthesis inhibitor, fluridone, to determine whether the ACBP1 response was ABA-related. The germination potential of Col-0, acbp1, ACBP1-OXs, and acbp1-COM recovered to a level similar to the water control when fluridone was applied to NaCl- and mannitol-treated seeds, indicating that phenotypic variation amongst these lines was related to de novo ABA biosynthesis. Furthermore, yeast two-hybrid, bimolecular complementation assays and pull-down assays showed that ACBP1 interacted with ABA-RESPONSIVE ELEMENT BINDING PROTEIN1 (AREB1) via its ankyrin repeats. The target genes of AREB1 were up-regulated in ACBP1-OXs but down-regulated in acbp1; and the localization of DsRed-AREB1 was affected in ACBP1-OX. These results indicate that ACBP1 promotes ABA signaling under salt and osmotic stress during seed to seedling transition.

Abscisic acid (ABA) and nitric oxide (NO) are both extremely important signalling molecules employed by plants to mediate plant tolerance under abiotic stresses. In the present study, the role of NO in ABA-induced photosynthesis and antioxidant system in leaves of tall fescue (Festuca arundinacea Schreb.) seedlings was investigated. Low-light (LL) stress increased intercellular CO2 concentration (Ci), as well as decreased plant height, leaf width, tiller number, biomass, chlorophyll content, net photosynthetic rate (Pn), stomatal conductance (Gs), transpiration rate (Tr), the maximum quantum yield of photosystem photochemistry (Fv/Fm), actual photochemical efficiency of photosystem II (ΦPSII), photochemical quenching (qP), the apparent electron transport rate (ETR), enzymatic activity of ribulose-1,5-bisphosphate carboxylase (Rubisco) and glyceraldehyde phosphate dehydrogenase (GADPH) and phosphoribulokinase (PRK), which were substantially alleviated by exogenous ABA application. Moreover, application of these leaves with exogenous ABA resulted in reduced LL stress induced ion leakage and reduced contents of MDA, H2O2 and superoxide radicals O 2 • - , as well as higher activities of peroxidase (POD), superoxide dismutase (SOD), catalase (CAT), and ascorbate peroxidase (APX). Expression of genes coding antioxidant enzymes increased in tall fescue in the presence of ABA under LL stress. These responses could be reversed by treatment with fluridone (the ABA biosynthesis inhibitor). The application of ABA elevated NO level, enhanced nitric oxide synthase (NOS)-like activity and up-regulated the tall fescue nitric oxide synthase-associated gene, NITRIC OXIDE ASSOCIATED 1 (FaNOA1) expression level. In addition, neither exogenous NO nor specific NO scavenger 2-(4-carboxy-2-phenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide (PTIO) or NO synthase (NOS) specific inhibitor Nω-nitro-L-arginine (LNNA) treatments had no effect on endogenous ABA concentration and ABA receptors transcript levels (FaPYR1 and FaPYL1), implying that the protective effect of ABA under LL stress might be mediated by NO. These results indicated that NO was involved in the ABA-mediated LL tolerance via regulating the antioxidant defense system and keeping a high level of photosynthetic rate in tall fescue.

ABA produced in the fig fruit triggers ethylene production in the inflorescence and induces non-climacteric ripening in the receptacle tissue., The common fig bears a unique closed inflorescence structure, the syconium, composed of small individual drupelets that develop from the ovaries, which are enclosed in a succulent receptacle of vegetative origin. The fig ripening process is traditionally classified as climacteric; however, recent studies have suggested that distinct mechanisms exist in its reproductive and non-reproductive parts. We analysed ABA and ethylene production, and expression of ABA-metabolism, ethylene-biosynthesis, MADS-box, NAC, and ethylene response-factor genes in inflorescences and receptacles of on-tree fruit treated with ABA, ethephon, fluridone, and nordihydroguaiaretic acid (NDGA). Exogenous ABA and ethephon accelerated fruit ripening and softening, whereas fluridone and NDGA had the opposite effect, delaying endogenous ABA and ethylene production compared to controls. Expression of the ABA-biosynthesis genes FcNCED2 and FcABA2, ethylene-biosynthesis genes FcACS4, FcACOL, and FcACO2, FcMADS8, 14, 15, FcNAC1, 2, 5, and FcERF9006 was up-regulated by exogenous ABA and ethephon. NDGA down-regulated FcNCED2 and FcABA2, whereas fluridone down-regulated FcABA2; both down-regulated the ethylene-related genes. These results demonstrate the key role of ABA in regulation of ripening by promoting ethylene production, as in the climacteric model plant tomato, especially in the inflorescence. However, increasing accumulation of endogenous ABA until full ripeness and significantly low expression of ethylene-biosynthesis genes in the receptacle suggests non-climacteric, ABA-dependent ripening in the vegetative-originated succulent receptacle part of the fruit.

Fomesafen provides effective control of glyphosate-resistant Palmer amaranth in cotton. However, cotton seedlings can be injured when fomesafen is applied PRE. Therefore, greenhouse and field experiments were conducted at Athens, GA, and at six locations in Alabama and Georgia in 2013 and 2016 to evaluate cotton growth and yield response to fomesafen applied PRE at 70, 140, 280, 560, 1,120, or 2,240 g ai ha-1, and in combination with pendimethalin, diuron, acetochlor, and fluridone at 1× label rates. Greenhouse bioassays indicated that fomesafen reduced cotton height and dry weight with increasing rate in Cecil sandy loam and Tifton loamy sand but not in Greenville sandy clay loam--possibly as a result of this soil's higher organic matter (OM) and clay content. Fomesafen applied at 2,240 g ai ha-1 reduced cotton stand by as much as 83% compared to the nontreated check (NTC) at all field locations except Alabama's Macon and Baldwin counties, and 1,120 g ai ha-1 reduced cotton stand only at Pulaski County, GA, by 52%. Cotton height was reduced by the two highest rates of fomesafen at all locations except Clarke County, GA, and Baldwin County, AL. Injury data indicated more visual injury followed increasing fomesafen rates, and high-rate treatments produced more injury in sandier soils. Cotton yield was unaffected by herbicide treatments at any location, except for the 1,120 g ai ha-1 rate at Pulaski County (49% yield loss compared to NTC), 2,240 g ai ha-1 at Pulaski County (72% yield loss), and Tift County (29% yield loss). These data indicated cotton yield should not be negatively affected by fomesafen applied PRE alone within label rates or in combination with pendimethalin, diuron, acetochlor, and fluridone at 1× label rates, although some visual injury, or stand or height reduction may occur early in the growing season.Nomenclature: Acetochlor; diuron; fluridone; fomesafen; glyphosate; pendimethalin; Palmer amaranth, Amaranthus palmeri S. Wats.; cotton, Gossypium hirsutum L.

Research was conducted to evaluate the sensitivity of cover crops to a low rate of soil-applied herbicides and investigate the likelihood of herbicide carryover to fall-seeded cover crops following an irrigated corn crop. In the sensitivity study, herbicides were applied at a 1/16× rate (to simulate four half-lives) 1 d after cover crop planting, whereas for the carryover study residual herbicides were applied at a 2× rate at the maximum label corn height or growth stage and cover crops sown immediately after corn harvest. In the sensitivity experiment, atrazine, diuron, fluridone, fomesafen, metribuzin, pyrithiobac, and sulfentrazone reduced emergence of the leguminous cover crops Austrian winterpea, crimson clover, and hairy vetch. However, reduced biomass production of leguminous cover crops in the spring was only observed for atrazine, fluridone, and pyrithiobac. For rapeseed, atrazine, flumioxazin, fluridone, pyrithiobac, pyroxasulfone, sulfentrazone, and tembotrione reduced emergence, but biomass production was reduced only by atrazine and fluridone. Conversely, wheat, cereal rye, barley, oats, and triticale were not affected by soil-applied herbicides. Barley was the only cereal cover crop that showed biomass reduction due to the application of flumioxazin, fluridone, mesotrione, S-metalochlor, and sulfentrazone. In the carryover study, with the exception of crimson clover, Austrian winterpea, cereal rye, hairy vetch, rapeseed, and wheat showed no negative affect on biomass production following a 2× rate of postemergence-applied residual herbicide in corn.Nomenclature: Atrazine; diuron; flumioxazin; fluridone; mesotrione; metribuzin; pyrithiobac; pyroxasulfone; S-metolachlor; sulfentrazone; tembotrione; Austrian winterpea, Lathryrus hirsutus L.; barley, Hordeum vulgare L.; cereal rye, Secale cereale L.; corn, Zea mays L.; crimson clover, Trifolium incarnatum L., hairy vetch, Vicia villosa Roth; oats, Avena sativa L.; rapeseed, Brassica napus L.; triticale, Triticale hexaploide Lart.; wheat, Triticum aestivum L.

Fluridone (FLU) is widely used as a herbicide and interferes with photosynthesis via induction of leaf bleaching. However, the mechanism of FLU-induced leaf bleaching remains elusive. In this study, the effects of FLU on the metabolism of leaf pigments, including chlorophyll and carotenoids, were investigated. Our results demonstrate that FLU induced rice leaf bleaching in a dose-dependent manner. Treatment with 5 µM FLU strongly induced leaf bleaching by decreasing pigment content, with carotenoids and chlorophyll decreased by 98 and 95%, respectively, in the second leaves of rice seedlings. Our results indicate that the transcription levels of leaf pigment biosynthetic and catabolic genes were significantly downregulated by 5 µM FLU treatment. These results suggest that FLU induces leaf bleaching by decreasing leaf pigment content via downregulation of the transcription levels of leaf pigment biosynthetic genes, and that the downregulation of transcription levels of leaf pigment catabolic genes is a result of feedback inhibition mediated by FLU-decreased leaf pigment content. In addition, to test whether FLU-induced leaf bleaching is due to FLU-induced abscisic acid (ABA) deficiency, the effect of FLU treatment on endogenous ABA content and the recovery effect of ABA on FLU-induced leaf bleaching were investigated. Application of FLU significantly decreased endogenous ABA content, but FLU-induced leaf bleaching was not rescued by ABA application, thus FLU-induced leaf bleaching is not due to FLU-induced ABA deficiency.

Strigolactones, a novel class of phytohormones, regulate plant architecture and act as rhizosphere signals. Species-specific biosynthetic pathways convert a common precursor, carlactone, to strigolactones., Strigolactones (SLs), comprising compounds with diverse but related chemical structures, are determinant signals in elicitation of germination in root parasitic Orobanchaceae and in mycorrhization in plants. Further, SLs are a novel class of plant hormones that regulate root and shoot architecture. Dissecting common and divergent biosynthetic pathways of SLs may provide avenues for modulating their production in planta. Biosynthesis of SLs in various SL-producing plant species was inhibited by fluridone, a phytoene desaturase inhibitor. The plausible biosynthetic precursors of SLs were exogenously applied to plants, and their conversion to canonical and non-canonical SLs was analysed using liquid chromatography–tandem mass spectrometry. The conversion of carlactone (CL) to carlactonoic acid (CLA) was a common reaction in all investigated plants. Sorghum converted CLA to 5-deoxystrigol (5-DS) and sorgomol, and 5-DS to sorgomol. One sorgomol-producing cotton cultivar had the same SL profile as sorghum in the feeding experiments. Another cotton cultivar converted CLA to 5-DS, strigol, and strigyl acetate. Further, 5-DS was converted to strigol and strigyl acetate. Moonseed converted CLA to strigol, but not to 5-DS. The plant did not convert 5-DS to strigol, suggesting that 5-DS is not a precursor of strigol in moonseed. Similarly, 4-deoxyorobanchol was not a precursor of orobanchol in cowpea. Further, sunflower converted CLA to methyl carlactonoate and heliolactone. These results indicated that the biosynthetic pathways of hydroxy SLs do not necessarily involve their respective deoxy SL precursors.

In tomato fruits, chlorophyll, lycopene and ß-carotene are mostly responsible for the color. During ripening of tomato fruits, the color of the pericarp changes from green to red as chlorophyll is degraded and carotenoids accumulate. These changes are associated with an increase in respiration and ethylene production. Carotenoid biosynthesis pathway in plants can be disturbed by herbicide fluridone (1-methyl-3-phenyl-5-[3-trifluoromethyl(phenyl)]- 4(1H)-pyridinone), which inhibits the activity of phytoene desaturase, an enzyme responsible for conversion of phytoene to phytofluene. Fluridone is also used as an inhibitor of biosynthesis of abscisic acid (ABA) and strigolactones, and it reduces chlorophyll production in plants. In our research we studied the effect of fluridone on some physiological parameters, such as color, firmness, ethylene production, lycopene and chlorophyll content during ripening of the tomato fruit. Tomato plants cv. Altadena (Syngenta) were cultivated in a greenhouse in controlled temperature and both immature and mature fruits were used for the experiments, performed between August and November 2016. Fluridone at concentrations of 0.1% and 1.0% in lanolin paste was applied as a 2-3 mm stripe from the top to the base of tomato fruits, and as a control a stripe of lanolin was applied in the same way on the opposite side of the fruits. Fluridone at a concentration of 1.0% greatly inhibited lycopene accumulation in the pericarp of tomato fruits from the treated side. The measurements of fruit firmness have shown no significant differences between firmness of the part of the tomato fruits treated with fluridone, and the non-treated ones. Tomato fruits treated with fluridone produced amounts of ethylene similar to those found in control tissues on the opposite side of the same fruit. Fluridone delayed chlorophyll degradation in tomato fruits. The metabolic significance of these findings is discussed with the role of carotenogenesis inhibition in tomato fruit ripening.

Genetic engineering for heat stress tolerance can promote crop growth and improve yield. One wheat (Triticum aestivum L.) line Y16 (wild type) and two transgenic plants (Y16-3 and Y16-46) that express Hpa110-42, a functional fragment of harpin protein, were used in this study to investigate their possible abiotic stress tolerance under heat stress. Results showed that enhanced thermotolerance was observed in the Y16-3 and Y16-46 lines over the control wheat under stress conditions. However, this increased stress tolerance was significantly abolished by specific inhibitors such as fluridone or sodium tungstate (i.e., arrests abscisic acid (ABA) biosynthesis) and EGTA or La3+ (i.e., arrests Ca2+ signaling pathway) under heat exposure. By contrast, high activities of antioxidant enzymes such as superoxide dismutase, catalase, and ascorbate peroxidase (but not peroxidase) and low levels of oxidative damage (thiobarbituric acid reactive substance (TBARS) and chlorophyll) were detected in transgenic wheat lines compared with the control plant under stress exposure. However, this significant difference diminished after the addition of these specific inhibitors. Furthermore, a slight increase of H2O2 was observed in the transgenic plant, instead of the control, without the addition of chemicals under heat stress. These results suggested that antioxidant enzymes, calcium, and ABA signaling pathways were involved in this Hpa110–42-mediated thermotolerance of transgenic wheat plants under stress exposure. Finally, a hypothetical model based on H2O2 signaling was proposed to illustrate the possible mechanism of this enhanced heat stress tolerance.

Auxin is an important phytohormone which mediates diverse development processes in plants. Published research has demonstrated that auxin induces seed dormancy. However, the precise mechanisms underlying the effect of auxin on seed germination need further investigation, especially the relationship between auxins and both abscisic acid (ABA) and gibberellins (GAs), the latter two phytohormones being the key regulators of seed germination. Here we report that exogenous auxin treatment represses soybean seed germination by enhancing ABA biosynthesis, while impairing GA biogenesis, and finally decreasing GA1/ABA and GA4/ABA ratios. Microscope observation showed that auxin treatment delayed rupture of the soybean seed coat and radicle protrusion. qPCR assay revealed that transcription of the genes involved in ABA biosynthetic pathway was up-regulated by application of auxin, while expression of genes involved in GA biosynthetic pathway was down-regulated. Accordingly, further phytohormone quantification shows that auxin significantly increased ABA content, whereas the active GA1 and GA4 levels were decreased, resulting insignificant decreases in the ratiosGA1/ABA and GA4/ABA.Consistent with this, ABA biosynthesis inhibitor fluridone reversed the delayed-germination phenotype associated with auxin treatment, while paclobutrazol, a GA biosynthesis inhibitor, inhibited soybean seed germination. Altogether, exogenous auxin represses soybean seed germination by mediating ABA and GA biosynthesis.

Herbicide resistance has increased the need for novel weed control strategies. Fluridone has herbicidal as well as potential germination stimulant activity. The objectives of this study were to evaluate fluridone as a fall-applied germination stimulant for weed control and to assess rotational crop tolerance. Fall-applied fluridone was compared with a nontreated control in areas established with false cleavers, volunteer canola, and wild oat at Lacombe, AB, in 2014–2015 and 2015–2016, and at St Albert, AB, in 2015–2016. In the fall, there was a trend for weed densities to be higher in fluridone treatments than in untreated controls across site-years. The stimulatory effect of fluridone on weed germination was not statistically significant in fall assessments, while the weed control effect was significant in 33% of spring assessments. While fluridone reduced weed biomass for some site-years, it also reduced canola crop emergence and biomass at St Albert in 2015–2016, and caused injury symptoms on wheat and field pea. Risk of carryover to subsequent crops outweighed the benefits of using fluridone in the fall to stimulate weed germination in this study.Nomenclature: Fluridone; false cleavers, Galium spurium L. GALSP; canola, Brassica napus L. BRSNN; wild oat, Avena fatua L. AVEFA; field pea, Pisum sativum L.; wheat, Triticum aestivum L.

There is a growing preference for using doubled haploids (DHs) in maize breeding programs because they reduce the time required to generate and evaluate new lines to 2 years or less. However, there is an urgent need for efficient techniques that accurately discriminate between haploid and diploid maize kernels. Here, we investigate the effects of several hormones and chemicals on the germination of haploid and diploid maize kernels, including auxin, cytokinin, ethylene, abscisic acid (ABA) biosynthesis inhibitor (fluridone), ABA catabolism inhibitor (diniconazole), methyl jasmonate (MeJA), and NaCl. Ethylene effectively stimulated the germination of both haploid and diploid maize kernels. The ABA biosynthesis inhibitor fluridone, the ABA catabolism inhibitor diniconazole, and MeJA selectively stimulated the germination of haploid maize kernels. By contrast, gibberellin, 1-naphthaleneacetic acid (NAA), kinetin, and NaCl inhibited the germination of both haploid and diploid maize kernels. These results indicate that the germination of haploid maize kernels is selectively stimulated by fluridone and diniconazole, and suggest that ABA-mediated germination of haploid maize kernels differs from that of diploid maize kernels and other plant seeds.

Data on ABA involvement in osmoregulation of in vitro germinating petunia (Petunia hybrida L.) male gametophyte were obtained. Two potential targets of ABA action in a pollen tube (PT) are identified. These are represented by (1) plasma membrane (PM) H+-ATPase, electrogenic proton pump participating in PM polarization, and (2) Ca-dependent K+-channels localized in the same membrane. It was established that a stimulatory effect of ABA on electrogenic activity of H+-ATPase is mediated by the increase in free Ca2+ level in the cytosol of a PT and reactive oxygen species (ROS) generation. Based on the results obtained on the role of K+ ions in the hormonal control of water transport-driving forces in a PT, the hypothesis suggesting that ABA stimulated pollen grains (PGs) germinating and PT growth by activating K+-channels was put forward. The revealed ABA-induced shift in cytoplasmic pH (pHc) is suggested to be involved in a cascade of the events of the progamic phase of fertilization, including pH-dependent K+-channels functioning. It was established that ABA abolishes the inhibitory effects of ethylene receptors blocker, 1-methylcyclopropene (1-MCP), and blockers of ACC and ABA synthesis (aminooxyacetic acid, AOA, and fluridone, respectively) on PT germination and growth, whereas ethrel blocks the inhibitory effect of fluridone on PT growth. In stigmas pretreated with ABA and AOA before pollination, this phytohormone was found to suppress inhibitory effect of AOA on ACC synthesis in the pollen-pistil system. All these findings, taken together, led us to the conclusion that ABA is involved in petunia male gametophyte osmoregulation interacting with ethylene at the level of ACC synthesis in the progamic phase of fertilization.

Seeds of Bunium persicum (Boiss.) B. Fedtsch. have complex physiological dormancy that can be released by 15 weeks stratification. The present study revealed that cold stratification enhanced content of H2O2, O2 -· and application of GA3 and ROS donors (Fenton reagent, H2O2, methylviologen and menadione) did not affect or only slightly promoted the germination of non-stratified, fully dormant seeds. Dormancy was markedly decreased by ROS-generating reagents, GA3 and fluridone (an inhibitor of ABA biosynthesis) and was enhanced by ROS-decreasing compounds (DMTU, Tiron, SB and DPI), diniconazole (Dinc, an inhibitor of ABA catabolism) and paclobutrazol (PAC, an inhibitor of GA biosynthesis) when dormancy was partially removed by cold stratification. The response to these compounds reduced with increasing time of stratification. ABA inhibited germination by repressing of NADPH oxidase activity and ROS accumulation and conversely, GA triggered germination by promoting an increase of NADPH oxidase activity and ROS levels. Data in this study, for the first time suggest releasing deep complex physiological dormancy by cold stratification is associated with interplay between ROS and ABA/GA.

The present study was undertaken to investigate the mechanism underlying NaCl-alleviated Fe (iron) deficiency in Arabidopsis thaliana Col-0 (Columbia ecotype). Six-week-old Col-0 with rosettes of similar diameters was grown in full-strength nutrient solution lacking Fe (Fe-deficient) or full-strength nutrient solution (Fe-sufficient) with or without 10 mM NaCl for 7 days. Roots were then harvested for analysis of total Fe content, soluble Fe concentration, and abscisic acid (ABA) content as well as for cell wall and RNA extraction, while shoots were harvested for total Fe content and soluble Fe concentration measurements. The total Fe content and the soluble Fe concentration were higher in roots and shoots of −Fe + NaCl-treated plants than −Fe-treated plants, whereas Fe retention in the cell wall was reduced, suggesting the presence of a cell wall Fe-reutilization mechanism. This conclusion was confirmed by the observation that less hemicelluloses Fe was found in plants under −Fe + NaCl treatment. In addition, associated to the upregulation of genes related to the long-distance transport of Fe, such as FRD3 (FERRIC REDUCTASE DEFECTIVE3), YSL2 (YELLOW STRIPE-LIKE), and NAS1 (NICOTIANAMINE SYNTHASE1) under −Fe + NaCl treatment, more Fe was available in shoots. Furthermore, endogenous ABA is involved in NaCl-alleviated Fe deficiency, as the addition of Flu (fluridone), an inhibitor of ABA biosynthesis, abolished the positive effect of NaCl on Fe deficiency. Under −Fe condition, NaCl not only is involved in the reutilization of cell wall Fe but also participates in the translocation of Fe from root to shoot in Arabidopsis, partially through its effect on ABA contents.

Despite the intensive study of xyloglucan endotransglucosylases/hydrolases, their multifaceted role in plant growth regulation in changing environmental conditions is not yet clarified. The functional role of the large number of genes encoding this group of enzymes is also still unclear. NtEXGT gene encodes one of xyloglucan endotransglucosylases/hydrolases (XTHs) of Nicotiana tabacum L. The highest level of NtEXGT gene expression was detected in young flowers and leaves near the shoot apex. Expression of the NtEXGT gene in leaves was induced by cytokinins, auxins, brassinosteroids and gibberellins. NtEXGT gene was also up-regulated by salinity, drought, cold, cadmium and 10 μM abscisic acid treatments and down-regulated in response to 0 °C and 100 μM abscisic acid. Pretreatment of leaves with fluridone contributed to smaller increase in the level of NtEXGT transcripts in response to drought stress. These data suggest that NtEXGT gene is ABA-regulated and probably implicated in ABA-dependent signaling in response to stress factors. 35S::NtEXGT plants of tobacco showed higher rate of root growth under salt-stress conditions, greater frost and heat tolerance as compared with the wild type tobacco plants.

In order to improve the problem of poor coloring caused by high fruit nitrogen in apple production, we studied the effects of different concentrations of abscisic acid (ABA: 0, 50, 100, and 150 mg/L) and fluridone (ABA biosynthesis inhibitor) on the fruit of 'Red Fuji' apple (Malus Domestica Borkh.) in the late stage of apple development (135 days after blooming) in 2017 and 2018. The effects of these treatments on the distribution of 13C and 15N and anthocyanin synthesis in fruit were studied. The results showed that the expression levels of ABA synthesis and receptor genes in the peel and flesh were upregulated by exogenous ABA treatment. An appropriate concentration of ABA significantly increased the expression of anthocyanin synthesis genes and transcription factors and increased the content of anthocyanin in the peel. The results of 13C and 15N double isotope labeling showed that exogenous ABA coordinated the carbon-nitrogen nutrient of apple fruit in the late stage of the development, reduced the accumulation of fruit nitrogen, increased the accumulation of fruit carbon and sugar, provided a substrate for anthocyanin synthesis, or promoted anthocyanin synthesis through the sugar signal regulation mechanism. Comprehensive analysis showed that the application of 100 mg/L ABA effectively improved the problem of poor coloring caused by high fruit nitrogen in the late stage of apple development and is beneficial to the accumulation of carbon in fruit and the formation of color.

The herbicides glyphosate, imazamox and fluridone are herbicides, with low toxicity towards fish and invertebrates, which are applied to waterways to control invasive aquatic weeds. However, the effects of these herbicides on natural isolates of phytoplankton and cyanobacteria are unknown. Three species of microalgae found in the San Francisco Estuary (SFE)/Sacramento-San Joaquin River Delta (Delta) (

Roots are important plant organs. Lateral root (LR) initiation (LRI) and development play a central role in environmental adaptation. The mechanism of LR development has been well investigated in Arabidopsis. When we evaluated the distribution of auxin and abscisic acid (ABA) in maize, we found that the mechanism differed from that in Arabidopsis. The distribution of ABA and auxin within the primary roots (PRs) and LRs was independent of each other. Auxin localization was observed below the quiescent center of the root tips, while ABA localized at the top of the quiescent center. Furthermore, NaCl inhibited LRI by increasing ABA accumulation, which mainly regulates auxin distribution, while auxin biosynthesis was inhibited by ABA in Arabidopsis. The polar localization of ZmPIN1 in maize was disrupted by NaCl and exogenous ABA. An inhibitor of ABA biosynthesis, fluridone (FLU), and the ABA biosynthesis mutant vp14 rescued the phenotype under NaCl treatment. Together, all the evidence suggested that NaCl promoted ABA accumulation in LRs and that ABA altered the polar localization of ZmPIN1, disrupted the distribution of auxin and inhibited LRI and development.

Fluridone is widely used as a herbicide for controlling invasive aquatic plants such as hydrilla in surface water bodies. When applied on surface waters fluridone can attach to bed sediment, requiring rigorous extraction methods prior to analysis. Currently, very limited information exists in terms of fluridone residue detection in delta sediment. In this study, we researched fluridone detection in both water and sediment. To extract fluridone from sediment, here we have tested two extraction methods: (1) a rotavapor method (RM); and (2) a quick, easy, cheap, effective, rugged and safe (QuEChERS) method (QM). The extraction results of RM were compared with those of QM. To quantify fluridone concentrations in extracts, a high-performance liquid chromatography (HPLC)-UV detector was used. HPLC separation was achieved using an Allure C18 5µm 150 × 4.6mm column with a mobile phase composed of acetonitrile and water (60:40, v/v). The UV detector was operated at 237nm. The method was tested and validated using a series of water and sediment samples taken from Sacramento-San Joaquin Delta in California. The average recovery of fluridone was 73% and 78% using RM and QM respectively. The proposed method can be used for testing fluridone in water and sediment samples.

Purpose: In recreational water bodies, herbicides are widely used for controlling unwanted weeds, and impacts of herbicide residues on health risks to aquatic ecosystem is a serious concern. This study was aimed to improve the existing understanding of the deposition of herbicides from water column to bed sediment and leachate of herbicides from bed sediment to water column. We investigated the attachment of two herbicides with sediment and release from sediment: (1) Glyphosate; and (2) Fluridone. The goal of this study was to determine the deposition and release of Glyphosate and Fluridone in bed sediment of the Sacramento–San Joaquin River Delta.Materials and Methods: Field sampling was performed to collect water and sediment samples from Sacramento–San Joaquin River Delta. Bottom dredge sampler was used for collecting sediment samples and horizontal water bottle sampler was used for collecting water samples. A series of experiments were conducted to determine the attachment and release of Fluridone and Glyphosate from sediment at a different level of initial concentrations. For analyzing Fluridone and Glyphosate in sediment leachate and water, samples were processed using enzyme-linked immunosorbent assay (ELISA) based method.Results and Discussion: Observations showed that proportions of Glyphosate concentrations in water were higher than Fluridone concentrations in water, when both herbicides were inoculated in water in same quantity. On the contrary, the concentrations of Fluridone in sediment-bound leachate were higher than Glyphosate concentrations in sediment-bound leachate, regardless of the initial concentrations. Fluridone and Glyphosate concentrations in water column samples differed significantly (p < 0.05) over the time even initial concentrations of these herbicides were kept similar, which indicates that Fluridone interaction with water column was considerably different than the interaction of Glyphosate with the water column.Conclusions: Bed sediment can be an important sink and source for release of Fluridone and Glyphosate from bed sediment to the water column of an ambient water body. Significant concentrations of herbicides were deposited in bed sediment of Sacramento-San Joaquin Delta, and eventually the high concentrations of herbicides were observed in sediment leachate. Improved understanding of this important release pathway can provide much needed information to adequately address the impacts of particle attached herbicides on aquatic and ecological environment of a water body.

In plants, sugar acts as an essential signaling molecule that modulates various aspects of metabolism, growth and development, which are also controlled by phytohormones. However, the molecular mechanism of cross-talk between sugar and phytohormones still remains to be elucidated. We have identified gsm1 (glucose-hypersensitive mutant 1) as a mutant with impaired cotyledon development that shows sensitivity to exogenous abscisic acid (ABA). The addition of fluridone can reverse the glucose (Glc) inhibitory effect in gsm1, implying that endogenous ABA is involved in the Glc response of gsm1. In 4.5% Glc, the expression of Glc-induced ABA-responsive genes in gsm1-1 was nearly two times higher than that in the wild type. Compared to gsm1-1, the gsm1-1 abi4-1 double mutant exhibited reduced sensitivity to Glc and ABA, which was similar to the Glc and ABA insensitive phenotype of abi4-1, suggesting that ABI4 is epistatic to GSM1. In the treatment with 4.5% Glc, the GSM1 transcript level was greatly increased in abi4-1 by almost 4-fold of that in the wild type. These data suggest that GSM1 plays an important role in the ABI4-regulated Glc-ABA signaling cascade during Arabidopsis early seedling growth.

We elucidated the effect of increased planting density (single and grouped competing plants) on concentrations of auxin, abscisic acid, and cytokinins in normal lettuce plants and in those with ethylene perception inhibited by 1-methylcyclopropene (1-MCP). An attempt was made to relate the changes in hormone concentration induced by competition and inhibition of ethylene sensitivity to growth responses of lettuce planting. The results showed changes in concentrations of auxins, cytokinins, and ABA in the response of lettuce to crowding. Accumulation of ABA in shoots was likely to contribute to inhibition of transpiration of the plants grown in the presence of neighbors. This assumption was supported by the results of application of an inhibitor of ABA synthesis (fluridone and carotenoid biosynthesis herbicide) resulting in increased transpiration of grouped, but not single plants. Increased planting density led to the decline in root auxins paralleled by inhibition of root growth. This effect was likely to be due to decreased auxin transport to the roots from the shoots suggested by accumulation of auxins in the shoots and inhibition of root growth by application of the auxin transport inhibitor [N-(1-naphtyl)phtalamic acid (NPA)]. Importance of the changes in hormone concentrations was confirmed by data showing that disturbance of auxin and cytokinin distribution detected in MCP-treated plants was accompanied by corresponding modification of the growth response.

In the root exudate and root extracts of maize hybrid cv NK Falkone seven putative strigolactones were detected using UPLC-TQ-MS-MS. All seven compounds displayed MS-MS-fragmentation common for strigolactones and particularly the presence of a fragment of m/z 97 Da, which may indicate the presence of the so-called D-ring, suggests they are strigolactones. The levels of all these putative strigolactones increased upon phosphate starvation and decreased upon fluridone (carotenoid biosynthesis inhibitor) treatment, both of which are a common response for strigolactones. All seven compounds were subsequently isolated with prep-HPLC-MS. They all exhibited Striga hermonthica seed germination inducing activity just as the synthetic strigolactone analog GR24. The structure of two of the seven compounds was elucidated by NMR spectroscopy as: methyl (2E,3E)-4-(3,3-dimethyl-5-oxo-2-(prop-1-en-2-yl)tetrahydrofuran-2-yl)-2-(((4-methyl-5-oxo-2,5-dihydrofuran-2-yl)oxy)methylene)but-3-enoate (two diastereomers 1a and 1b). Strigolactones (1a/b) are closely related to the methyl ester of carlactonoic acid (MeCLA) and heliolactone. However, they contain a unique 4,4-dimethyltetrahydrofuran-2-one motif as the “A-ring” instead of the classical (di)methylcyclohexene. Because these compounds were isolated from maize (Zea mays) we called them “zealactone 1a and 1b”. The implications of this discovery for our view on strigolactones and their biosynthesis are discussed.

Flumioxazin and fomesafen are commonly used to control glyphosate-resistant Palmer amaranth in cotton and other crops, thus increasing risk to select for Palmer amaranth biotypes resistant to protoporphyrinogen oxidase (PPO) inhibitors. A field experiment was conducted to determine the potential for fluridone and acetochlor to substitute for soil-applied PPO inhibitors in a Palmer amaranth management system with glufosinate applied twice POST and diuron plus MSMA POST-directed in conservation tillage cotton. Fluridone and flumioxazin applied preplant 23 to 34 d prior to planting were similarly effective. Fluridone and acetochlor plus diuron applied PRE controlled Palmer amaranth as well as fomesafen plus diuron PRE. All systems with preplant and PRE herbicides followed by glufosinate POST and diuron plus MSMA layby controlled Palmer amaranth well. Cotton yield did not differ among herbicide treatments. This research demonstrates that fluridone and acetochlor can substitute for soil-applied PPO-inhibiting herbicides in management systems for Palmer amaranth.

Potassium (K+) plays an important role in the regulation of plant growth and development. However, how potassium works in K+ channels in strawberry fruit development is yet unknown. Here, a 2205 bp potassium channel cDNA encoding 734 amino acids, named FaKAT1, was cloned from strawberry fruits. Bioinformatics analysis showed that the cis-element ABRE responsive to ABA and conserved domains characteristic to the KAT1 superfamily were found in the promoter and encoding protein of FaKAT1. Transcription analysis revealed that FaKAT1 was expressed higher in stems and leaves, followed by fruits, but was less in roots and flowers, and that coupled with the fruit red-coloring, its transcripts increased rapidly, suggesting that FaKAT1 might play a role in ripening. Using tobacco rattle virus-induced gene silencing, downregulation of the FaKAT1 transcripts resulted in significant unripening of fruits, which is consistent with changes of the ripening-related events and genes, such as fruit firmness, contents of titratable acid, sugar, anthocyanin, and abscisic acid (ABA), as well as transcripts of PYR1, ABI1, SnRK2, GAL6, PE5, EXP2, XYL2, CA4H, CHS, CHI, DFR, and 4CL. Furthermore, ABA and the ABA inhibitor, fluridone, promoted and inhibited the mRNA expression levels of FaKAT1, respectively. Importantly, a K+ channel blocker, tetraethylammonium, also inhibited FaKAT1 expression and fruit red coloring. In conclusion, FaKAT1 is an ABA-induced K+ channel, which regulates strawberry fruit ripening.

In this study, we performed a comparative analysis of the physiological and biochemical parameters of wheat cultivars with contrasting drought resistance, drought-resistant Omskaya 35 (O-35) and less drought-resistant Salavat Yulaev (SYu), during 7-day germination under drought stress simulated by 5% mannitol. In addition, we evaluated the effectiveness of pre-sowing seed treatment with 0.4 μM 24-epibrassinolide (EBR) used to increase the resistance of plants of both cultivars to drought stress. It was revealed that mannitol has caused significant changes in the hormonal balance of the plants of both cultivars, associated with abscisic acid (ABA) accumulation and decrease in the contents of indoleacetic acid (IAA) and cytokinins (CKs). It should be noted that more dramatic changes in the content of phytohormones were characteristic for seedlings of SYu cultivar, which was reflected in a stronger growth inhibition of these plants. Pretreatment with EBR mitigated the negative effect of drought on the hormonal status and growth of seedlings during their germination. Furthermore, we found that drought caused accumulation of dehydrin (DHN) proteins, especially of low molecular weight DHNs, whose abundance was 2.5 times greater in O-35 cultivar than in SYu plants. EBR-pretreated plants of both cultivars were characterized by the additional accumulation of DHNs, indicating their involvement in the development of the EBR-induced wheat drought resistance. The use of fluridone allowed us to demonstrate ABA-dependent and ABA-independent pathways of regulation of low molecular mass dehydrins accumulation by EBR in wheat plants of both cultivars under drought conditions.

Some organisms have retained plastids even after they have lost the ability to photosynthesize. Several studies of nonphotosynthetic plastids in apicomplexan parasites have shown that the isopentenyl pyrophosphate biosynthesis pathway in the organelle is essential for their survival. A phytohormone, abscisic acid, one of several compounds biosynthesized from isopentenyl pyrophosphate, regulates the parasite cell cycle. Thus, it is possible that the phytohormone is universally crucial, even in nonphotosynthetic plastids. Here, we examined this possibility using the oyster parasite Perkinsus marinus, which is a plastid‐harboring cousin of apicomplexan parasites and has independently lost photosynthetic ability. Fluridone, an inhibitor of abscisic acid biosynthesis, blocked parasite growth and induced cell clustering. Nevertheless, abscisic acid and its intermediate carotenoids did not affect parasite growth or rescue the parasite from inhibition. Moreover, abscisic acid was not detected from the parasite using liquid chromatography mass spectrometry. Our findings show that abscisic acid does not play any significant roles in P. marinus.

The relationship between the phytohormones, gibberellin (GA) and abscisic acid (ABA) and light and temperature on seed germination is still not well understood. We aimed to investigate the role of the ABA and GA on seed germination of Vellozia caruncularis, V. intermedia and V. alutacea in response to light/dark conditions on different temperature. Seeds were incubated in GA (GA3 or GA4) or ABA and their respective biosynthesis inhibitors (paclobutrazol – PAC, and fluridone – FLU) solutions at two contrasting temperatures (25 and 40 °C). Furthermore, endogenous concentrations of active GAs and those of ABA were measured in seeds of V. intermedia and V. alutacea during imbibition/germination. Exogenous ABA inhibited the germination of Vellozia species under all conditions tested. GA, FLU and FLU + GA3 stimulated germination in the dark at 25 °C (GA4 being more effective than GA3). PAC reduced seed germination in V. caruncularis and V. alutacea, but did not affect germination of V. intermedia at 40 °C either under light or dark conditions. During imbibition in the dark, levels of active GAs decreased in the seeds of V. intermedia, but were not altered in those of V. alutacea. Incubation at 40 °C decreased ABA levels during imbibition in both V. caruncularis and V. alutacea. We conclude that the seeds of Vellozia species studied here require light or high temperature to germinate and ABA has a major role in the regulation of Vellozia seed germination in response to light and temperature.

Summary Protein farnesylation is a post-translational modification known to regulate abscisic acid (ABA)-mediated drought tolerance in plants. However, it is unclear whether and to what extent protein farnesylation affects plant tolerance to high-temperature conditions. The Arabidopsis heat-intolerant 5 (hit5) mutant was isolated because it was thermosensitive to prolonged heat incubation at 37°C for 4 d but thermotolerant to sudden heat shock at 44°C for 40 min. Map-based cloning revealed that HIT5 encodes the β-subunit of the protein farnesyltransferase. hit5 was crossed with the aba-insensitive 3 (abi3) mutant, the aba-deficient 3 (aba3) mutant, and the heat shock protein 101 (hsp101) mutant, to characterize the HIT5-mediated heat stress response. hit5/abi3 and hit5/aba3 double mutants had the same temperature-dependent phenotypes as hit5. Additionally, exogenous supplementation of neither ABA nor the ABA synthesis inhibitor fluridone altered the temperature-dependent phenotypes of hit5. The hit5/hsp101 double mutant was still sensitive to prolonged heat incubation, yet its ability to tolerate sudden heat shock was lost. The results suggest that protein farnesylation either positively or negatively affects the ability of plants to survive heat stress, depending on the intensity and duration of high-temperature exposure, in an ABA-independent manner. HSP101 is involved in the hit5-derived heat shock tolerance phenotype.