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Article

Barley Plants Overexpressing Ferrochelatases (HvFC1 and HvFC2) Show Improved Photosynthetic Rates and Have Reduced Photo-Oxidative Damage under Drought Stress than Non-Transgenic Controls

by
Dilrukshi S. K. Nagahatenna
1,
Boris Parent
2,
Everard J. Edwards
3,
Peter Langridge
1,4,* and
Ryan Whitford
1
1
School of Agriculture, Food and Wine, University of Adelaide, Waite Campus, PMB1, Glen Osmond SA 5064, Australia
2
Unité Mixte de Recherche 759 Laboratoire d’Ecophysiologie des Plantes sous Stress Environnementaux, INRAE, F–34060 Montpellier, France
3
CSIRO Agriculture & Food, Locked Bag 2, Glen Osmond SA 5064, Australia
4
Wheat Initiative, Julius-Kühn-Institute, Königin-Luise-Str 19, 14195 Berlin, Germany
*
Author to whom correspondence should be addressed.
Agronomy 2020, 10(9), 1351; https://doi.org/10.3390/agronomy10091351
Submission received: 14 August 2020 / Revised: 30 August 2020 / Accepted: 3 September 2020 / Published: 8 September 2020
(This article belongs to the Special Issue GMO, New Breeding Techniques and Novel Technologies for Abiotic Stress Tolerance in Crop Plants)
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Abstract

:
We investigated the roles of two Ferrochelatases (FCs), which encode the terminal enzyme for heme biosynthesis, in drought and oxidative stress tolerance in model cereal plant barley (Hordeum vulgare). Three independent transgenic lines ectopically overexpressing either barley FC1 or FC2 were selected and evaluated under well-watered, drought, and oxidative stress conditions. Both HvFC1 and HvFC2 overexpressing transgenics showed delayed wilting and maintained higher photosynthetic performance relative to controls, after exposure to soil dehydration. In each case, HvFC overexpression significantly upregulated the nuclear genes associated with detoxification of reactive oxygen species (ROS) upon drought stress. Overexpression of HvFCs, also suppressed photo-oxidative damage induced by the deregulated tetrapyrrole biosynthesis mutant tigrinad12. Previous studies suggest that only FC1 is implicated in stress defense responses, however, our study demonstrated that both FC1 and FC2 affect drought stress tolerance. As FC-derived free heme was proposed as a chloroplast-to-nuclear signal, heme could act as an important signal, stimulating drought responsive nuclear gene expression. This study also highlighted tetrapyrrole biosynthetic enzymes as potential targets for engineering improved crop performance, both in well-watered and water-limited environments.

1. Introduction

Drought is one of the major abiotic stress factors that adversely affects plant growth and limits crop yield [1]. Therefore, improving drought tolerance of major crops such as cereals is a primary objective for plant breeding. Improved crop performance under water-limited conditions is necessary to satisfy food demands that are a consequence of a growing world population. The incidence and severity of drought events in many rain-fed cereal growing areas is likely to increase in the face of a changing climate. Photosynthesis is a primary cellular process that is directly affected by cellular water status [2]. Drought stress and the consequent reduction in cellular water status significantly reduces photosynthetic rate, by limiting CO2 diffusion through the stomata, and potentially induces secondary effects like oxidative stress, which can damage the photosynthetic machinery [3]. Ultimately, this leads to substantial yield losses. Drought-tolerant C3 plants evolved efficient strategies to avoid or respond to drought stress, for example, acclimation mechanisms allow plants to minimize water loss from transpiration. This can occur as a result of stomatal closure, adjusted leaf architecture, reduced leaf growth, and by shedding older leaves [3]. Plants can also avoid dehydration by maximizing water uptake as a result of favored root, relative to shoot growth [4]. Plants exhibiting developmental plasticity can also escape drought by completing their life cycle before the drought stress becomes lethal. Increased levels of osmoprotectants such as proline, glycine, betaine, and polyols, allow plants to maintain turgor and protect cells from plasmolysis [3]. Similarly, high levels of antioxidants can mitigate ROS damage [5]. Drought tolerance is a complex phenotype under complex genetic control [6,7], as evidenced by the multitude of gene expression changes upon exposure to stress. Such transcriptional changes are necessary for ‘reprogramming’ whole plant performance upon stress. Understanding the physiological basis for drought tolerance as well as the underlying genes and biochemical mechanisms is a prerequisite towards developing superior crop varieties.
The tetrapyrrole biosynthesis pathway supplies essential compounds, chlorophyll, and heme, for photosynthesis [8] (Figure 1). Chlorophyll is the most abundant pigment in plants and is necessary for photochemical energy conversion, which drives photosynthesis. Heme, on the other hand, is an integral component of photosynthetic and respiratory cytochromes that is involved in electron transport [9,10]. Unlike chlorophyll, heme is important for many cellular functions, including acting as a co-factor for enzymes that are able to detoxify ROS [11]. Recently, it was proposed that a sub-pool of heme might serve as a retrograde signal, triggering photosynthesis-associated nuclear gene expression [12,13,14]. Both chlorophyll and heme are produced in the chloroplast. For their synthesis, 5-aminolevulinic acid (ALA), the initial common tetrapyrrole precursor is converted, through a series of reactions, into protoporphyrin IX (Proto IX). Insertion of Mg2+ into Proto IX, through the action of Mg-chelatase, leads to the production of chlorophyll, whereas the insertion of Fe2+ by Ferrochelatase (FC), results in the production of heme [15] (Figure 1).
In all plant species investigated so far, FC, the terminal enzyme for heme biosynthesis, is encoded by two genes [16,17]. Both FC isoforms have similar catalytic properties, substrate affinity, and specificity [18], but seem to have different expression profiles and subcellular localization. For instance, FC1 is ubiquitously expressed in all plant tissues, including roots, whereas FC2 is only found in aerial portions of the plant [16,19,20,21,22]. Transcriptional reporter gene fusions showed that Arabidopsis FC1 is induced in response to wounding, oxidative stress, and viral infection. In contrast, FC2 is repressed or remains unchanged under these stress conditions [16,21]. Furthermore, FC2 is strictly confined to the chloroplast, but FC1 is transported to both chloroplast and mitochondria [19,23,24,25,26]. These findings led the authors to propose that two physiologically distinct heme pools are synthesized by each of these FCs, with only FC1-derived heme being implicated in stress response. However, there is still disagreement regarding these proposed distinct roles for FC isoforms, as outlined in subsequent studies. For example, Lister et al. (2001) [27] were unable to detect FC1 in Arabidopsis mitochondria, whilst in cucumber, both FC1 and FC2 were found to be solely targeted to chloroplasts [28]. Therefore, it is now timely that their respective roles are being investigated more broadly. Gaining this knowledge in monocots is crucial for determining whether these genes are ideal targets for engineering stress tolerance in economically important cereals.
Several genetic and biochemical studies proposed that increased flux through the heme branch of the pathway improves tolerance to drought stress [29,30,31,32,33,34]. To understand the roles for these genes in drought and oxidative stress responses, we used barley, a major global crop but also a model for wheat. Two FCs were identified and cloned from barley cultivar Golden Promise (GP) [35]. Transgenic lines ectopically overexpressing either HvFC1 or HvFC2 were generated with three independent lines selected for each FC isoform [35]. Intriguingly, we found that overexpression of either HvFC1 or HvFC2 improves photosynthetic performance under non-stressed conditions, implying that both FCs play crucial roles in photosynthesis [35]. Transgenic lines were then evaluated under drought and oxidative stress. Oxidative stress was induced either by herbicide (Paraquat) application or genetically via the exposure of a deregulated tetrapyrrole biosynthetic mutant, tigrinad12, to a dark to light shift. Here, we report that ectopic overexpression of either HvFC1 or HvFC2, improves photosynthetic capacity, both under well-watered and drought conditions, with this being a likely consequence of increased tolerance to photo-oxidative damage.

2. Materials and Methods

2.1. Genetic Materials

Barley transgenic lines (cv. Golden Promise (GP)) ectopically overexpressing either HvFC1 or HvFC2 were generated by Agrobacterium-mediated delivery of pMDC32-HvFC1 and pMDC32-HvFC2 constructs (Figure S1), as described by Tingay et al. (1997) and Matthews et al. (2001) [36,37]. Twenty-nine T0 transformants were successfully generated and their transgene integrity was confirmed by PCR, using primers specific for hygromycin resistance gene (Hyg) and transgenes (Table S1). Transgene copy number and total HvFC1 and HvFC2 expression levels were analyzed by Southern hybridization and quantitative RT–PCR, respectively [35]. T1 and T2 plants originating from each independent transformation event was screened for transgene copy number and expression. Eventually, three single-copy, stable overexpression lines were selected for each FC isoform from T2 generation [35] and evaluated for stress tolerance. For detailed information on the experimental procedure please refer to Nagahatenna et al. (2020) [35].

2.2. Plant Growth and Stress Conditions

For HvFC gene expression analysis under oxidative stress, barley (Hordeum vulgare L.cv. Golden promise) plants were grown in pots containing coco-peat and field soil (50:50, v/v), supplemented with slow-release fertilizer pellets (Mini Osmocote; Smoult Horticultural Suppliers, Adelaide, Australia), at 2 g per liter soil volume. All replicates were randomly allocated in the controlled environment growth chamber to minimize positional effect, and growth conditions were maintained at 20–18 °C day/night temperature, 50–60% relative humidity, 460 μmolm−2s−1, and a 12:12 h photoperiod. In all drought assays, control plants were grown under the conditions as outlined above.
For evaluating performance of barley transgenics that ectopically overexpressed HvFCs upon drought stress, one untransformed control, null segregant, and transgenic seed was planted together in a single pot (25.5 cm in diameter and 23.5 cm in height), therefore, exposing all plants to the same soil conditions. A total of five pot replicates were analyzed per time point and per treatment. Each pot was lined with a polythene sheet to ensure no water added to the pot was lost due to drainage, so that all plants within the pot had access to the same soil water moisture. All plants were grown under conditions as outlined above.
For gene expression analysis involving tigrinad12, plants were grown under 24 h continuous light. To investigate the role of HvFC overexpression on tetrapyrrole-mediated oxidative stress, control barley (Hordeum vulgare L. cv. Golden promise and cv. Bonus), transgenic lines (T2), non-transgenic and transgenic tigrinad12 overexpressing either HvFC1 or HvFC2, were also grown under 24 h continuous light, with all other conditions controlled as outlined above.

2.3. Drought Assay

Each pot was watered equally to maintain similar pot weight for six weeks and then water was withheld. In order to identify variation of soil water potential in each pot upon drought stress, a calibration experiment was conducted concurrently. In this calibration experiment, control (cv. Golden Promise) plants were planted in similar polythene lined pots containing the same amount of soil and were grown under the same growth conditions, as outlined above. Predawn leaf water potential was measured daily, using a plant water status console (Model 3000, Soil moisture Equipment Corp., P.O. Box 30025, Santa Barbara, CA 93105, USA), until the plants wilted. This predawn leaf water potential was considered to be equivalent to the soil water potential in each pot [38]. Furthermore, pot weight was measured daily to determine the soil moisture corresponding to the respective soil water potential. Based on the soil humidity and soil water potential, a water release curve of this soil mixture was constructed (Figure S2). In the drought assay, pot weights were monitored daily upon drought stress to identify corresponding soil water potential, as indicated by the water release curve. A soil water potential of −0.6 MPa was maintained for 1 week and then plants were rewatered (Figure 2). Measurements were taken before stress, 2, 5, 8, and 15 days post water-withholding as well as after rewatering (18 days post water-withholding; Figure 2). These time-points represent fully irrigated (0), −0.1, −0.3, −0.6, and −0.6 MPa, and fully rewatered soil water potentials.

2.4. Paraquat Treatment

The second leaf from the top of the primary tiller of the 3-week-old control and transgenic lines were dipped in a 20 μM Paraquat solution (Sigma, NSW, Australia) for 1 min under dark, and re-exposed to 24 h continuous light of constant intensity. The degree of necrosis in transgenics, relative to the controls was evaluated following herbicide treatment. Transcriptional responses of HvFC1 and HvFC2 to Paraquat-induced oxidative stress was analyzed in the leaves of the control plants through quantitative RT–PCR.

2.5. Screening and Evaluating Tigrinad12 Mutants Overexpressing HvFC1 and HvFC2 Under Tetrapyrrole-Mediated Oxidative Stress

To investigate the role of the HvFC under tetrapyrrole-mediated oxidative stress, a representative transgenic line for HvFC1 and HvFC2 was crossed with tigrinad12. Seeds from non-transgenic and transgenic tigrinad12 mutants (F2), HvFC overexpressing lines (T2) and control barley (Hordeum vulgare L.cv. Golden promise and cv. Bonus) were grown on a wet petri plate for 5 days, under continuous darkness. Cotyledons were removed under a safe green light and were illuminated under UV light to identify homozygous mutants in F2 segregating population. Photographs were taken with a Canon 60D digital camera. Images were analyzed for red fluorescence intensity, using the ImageJ software (1.33 version; http://imagej.nih.gov/ij/).
Homozygous F2 tigrinad12 mutant phenotypes were confirmed using a cleaved amplified polymorphic sequence (CAPS) marker, designed to the causative mutation in the FLU gene [39]. PCR analysis was conducted with FLU and transgene specific primers. For the analysis using the CAPS markers, the PCR product was digested with Hae III restriction endonuclease (NEB, Victoria, Australia) at 37 °C for 2 h, and 65 °C for 10 min. PCR products before and after digestion were analyzed in 2% agarose gel and visualized by staining with ethidium bromide.
Mutant seedlings, which contain HvFC transgenes, were identified by using a dominant transgene-specific PCR marker. The primer sequences used are described in Supplementary Materials (Table S1). In order to investigate the effect of HvFC overexpression on tetrapyrrole-mediated oxidative stress, 3-week-old transgenic tigrinad12 mutants with all of the above-mentioned controls were grown under 24 h continuous light with 450 µmol m−2s−1 photosynthetically active radiation. Then, the plants were subjected to 24 h dark period and re-illuminated, before measuring chlorophyll fluorescence, and sampling for chlorophyll content.

2.6. Chlorophyll Content

Chlorophyll was extracted from leaf tissues using dimethyl sulfoxide (DMSO; Sigma, NSW, Australia) and determined spectrophotometrically, according to Hiscox and Israelstam (1979) [40]. The total chlorophyll content was calculated using the following equation. Total chlorophyll (g L−1) = 0.0202 A645 + 0.00802 A663 (A645 and A663 are absorbance at 645 and 663 nm).

2.7. Chlorophyll Fluorescence

Chlorophyll fluorescence parameters were measured using a pulse-amplitude-modulated photosynthesis yield analyzer (Mini-PAM, Walz, Effeltrich, Germany), with a dark leaf clip, to ensure all measurements were taken at the same distance from the leaf. Maximum quantum yield of PSII photochemistry (calculated as ratio Fv/Fm = (Fm − Fo)/Fm) was determined by applying an 800 ms saturating light pulse to leaves, under predawn conditions.

2.8. Measurements of Relative Water Content (RWC)

For leaf RWC measurement, leaves were excised between 09.00 h and 10.00 h, and their fresh weight was measured immediately. Rehydrated weight was determined by floating them in deionized water at 4 °C overnight. Leaf dry weight was measured by oven-drying at 80 °C for 48 h. The RWC was calculated as follows: RWC (%) = (fresh weight − dry weight)/(rehydrated weight − dry weight) × 100.

2.9. Photosynthetic Measurements

In vivo gas exchange parameters were measured in developmentally equivalent, fully expanded leaves, in 4- to 6-weeks old plants using a LI-6400 portable photosynthesis system (Licor inc, Lincoln, NE, USA). The conditions of the leaf cuvette were set to a light intensity of 2000 μmol m−2 s−1, humidity of 50–60%, temperature 25 °C, and reference air CO2 concentration of 400 μmols−1. The measurement period was from 09.00 h to 17.00 h. Leaf area in the cuvette was measured and gas exchange parameters per unit leaf area were recalculated. Instantaneous WUE and carboxylation efficiency (CE) were calculated based on the gas exchange parameters. Instantaneous WUE = photosynthesis rate under saturated light/transpiration rate, CE = Asat/intracellular CO2 concentration.

2.10. Gene Expression Analysis

Total RNA was extracted from leaf tissues of 3-weeks old control and transgenic plants before and during drought stress, as well as post oxidative stress, using an RNeasy plant extraction kit (Qiagen, VIC, Australia). cDNAs were prepared using SuperScript III reverse transcriptase (Invitrogen, Carlsbad, CA, USA). Gene expression was analyzed by quantitative RT–PCR, using primers from the coding regions of HvFC1, HvFC2, Catalase (Cat), and Superoxide dismutase (Sod), as described by Burton et al., (2004) [41]. mRNA copy number for each tested gene was normalized against four control genes (GAPDH, HSP70, cyclophilin, and tubulin), as described by Burton et al., (2004) [41]. Primer sequences used in these experiments are described in the Supplementary Materials (Table S1). Relative expression was calculated using the 2−ΔΔCT method, as described by Schmittgen and Livak (2008) [42], and fold change in target gene expression was normalized to endogenous reference genes and to the untreated wild-type control.

2.11. Statistical Analysis

All data were statistically analyzed by either one-way or two-way ANOVA, using GenStat 12.1 software (England, UK), and mean differences were compared through LSD test. Differences were considered to be statistically significant when p < 0.05.

3. Results

3.1. Overexpression of HvFC1 and HvFC2 Maintained Higher Leaf Water Status and Water Use Efficiency Under Drought Stress, Independent of Stomatal Closure

As an initial step towards understanding the role of FCs in drought stress responses, two FCs were identified in barley [35]. Our bioinformatics analysis revealed that two FCs are localized on separate chromosomes; HvFC1 on 5H and HvFC2 on 1H. Barley transgenic lines (cv. GP) ectopically overexpressing HvFC1 and HvFC2 were generated by cloning the coding regions of FC into the pMDC32 vector, under the control of the 2 × 35SCaMV promoter [35]. Twenty-nine independent T0 transgenic lines were screened for transgene copy number and expression. Three single copy, independent transgenic events, each ectopically overexpressing either HvFC1 or HvFC2, were selected [35] and evaluated upon drought stress. The gradual reduction in soil water potential over the period of the drought stress (Figure 2) was inferred by using a standardized drying curve (Figure S2).
This drying curve was previously determined to represent the relationship between predawn leaf water potential, pot weight, and the particular soil characteristics used in this experiment. We first made qualitative observations on the relative time to wilting. Visual inspection revealed controls reversibly wilted at −0.6 MPa soil water potential (8 days post water-withholding), whereas neither HvFC1 nor HvFC2 overexpressing transgenics exhibited wilting symptoms. This can be seen in Figure 3 in the day 8 image (b,e), where the representative transgenic line for either HvFC1 or HvFC2 at the rear of the pot remain erect, while those at the front were wilted (untransformed controls (WT) and null segregants).
Given that a plant’s wilting point is in part governed by leaf water content, we measured leaf relative water content (RWC) before, during, and after water deficit stress. No significant difference in leaf RWC was observed between the transgenics and controls before drought stress and after rewatering. However, results revealed that both HvFC1 and HvFC2 transgenics (calculated as an average of data from three transgenic events per construct) had a higher leaf RWC during drought stress, than the controls (Figure 4a). At −0.6 MPa soil water potential (day 8), transgenics on average had 10–12% higher leaf RWC, compared to controls.
Water is continually lost to the atmosphere via transpiration and one of the mechanisms that protects plants from excessive water loss is the stomatal closure. Therefore, we investigated whether HvFC transgenics had a higher leaf RWC, as a consequence of lower stomatal conductance (gs), relative to controls. However, HvFC1 transgenics showed greater gs, before and during the early phases of drought stress (2 and 5 days post water-withholding) relative to controls (Figure 4b). This observed difference ceased at a soil water potential of −0.6 MPa (8 days), and increased once more, post rewatering. A similar trend, albeit not statistically significant, was observed between HvFC2 transgenics and controls. These findings indicated that the higher leaf RWC was unlikely to be a consequence of reduced gs for HvFC1 and HvFC2 overexpressing transgenics. Collectively, these findings indicate that both HvFC transgenics improved leaf water status during drought stress, when compared to controls. The observed differences in gs between HvFC1 and HvFC2 transgenics might be a consequence of the alternate modes of action for FC isoforms.

3.2. HvFC1 and HvFC2 Overexpressing Transgenics Maintained Higher Photosynthetic Activity in the Well-Watered Conditions and Upon Dehydration

Water and CO2 are essential substrates for photosynthesis. Therefore, we investigated whether the observed positive water status and enhanced gs in HvFC transgenics has the capacity to improve photosynthesis. Measurements of CE revealed that both HvFC1 and HvFC2 transgenics had a significantly higher photosynthetic capacity, relative to wild-type controls, before and during the early phases (2–5 days post water-withholding) of drought stress, and even after 1 week, at −0.6 MPa soil water potential (15 days post water-withholding) (Figure 4c). This finding extended to the photosynthesis rate under saturated light, whereby both HvFC1 and HvFC2 transgenics showed a significantly higher Asat, before and 2 to 5 days post water-withholding, relative to the controls (Figure 4d). The improvement in Asat was between 3 and 4 µmol m−2s−1 in both transgenics, relative to wild-type (Figure 4d).
The amount of photosynthetic pigment was also important for photosynthesis, considering they were responsible for light energy absorption. Both HvFC1 and HvFC2 overexpressing transgenics exhibited a significantly higher chlorophyll content before stress, at −0.1 and at −0.3 MPa soil water potential (2 to 5 days after post water-withholding), as well as after rewatering, relative to the controls (Figure 4e). Importantly, in HvFC1 transgenics (calculated as an average of data from three transgenic events per construct), the instantaneous WUE was unchanged, before and up to 5 days post water-withholding, as well as after rewatering (Figure 4f). Only marginal increases in WUE were observed from 8 to 15 days post water-withholding. In contrast, HvFC2 transgenics exhibited significantly higher WUE, 5 to 8 days post water-withholding. These findings suggest that HvFC1 and HvFC2 differentially affect WUE. However, collectively these results suggest that the overexpression of both HvFC’s have the capacity to maintain higher photosynthetic activity relative to controls, under both well-watered and drought stress conditions.

3.3. Overexpression of HvFCs Invokes Expression of ROS Detoxification Markers

Impairment of photosynthetic electron transport and increased photorespiration lead to photo-oxidative damage, upon dehydration [3]. The ability to minimize cellular oxidative damage is an important protective strategy. To investigate whether both types of transgenics have the ability to prevent drought-mediated oxidative stress, transcriptional responses of genes associated with ROS detoxification were analyzed in controls versus a representative transgenic line for HvFC1 and HvFC2, before, during, and after water-deficit stress. Transcripts targeted for analysis included Cat and Sod, as they were previously shown to be transcriptionally responsive to drought and encode proteins that are important for ROS detoxification [43]. Cat expression in HvFC1 transgenics was significantly repressed (p < 0.05) as compared to the control plants, both before stress and up to 8 days post exposure to drought (Figure 5a). As stress progressed up to 15 days, this trend reversed, whereby Cat was significantly upregulated (p < 0.05) in the transgenic, relative to the control. However, this observation was not statistically significant when comparing plants overexpressing HvFC2 to control plants, both before stress and up to 8 days post exposure to drought (Figure 5c). Analysis of Sod mRNA levels in HvFC1 transgenics revealed that Sod is transcriptionally upregulated, both at 8 and 15 days post water-withholding, with no significant difference observed in transcriptional activity before the onset of stress (Figure 5b). This contrasted with Sod transcription in HvFC2 transgenics, which showed a significant downregulation (p < 0.05), when compared to control plants before stress (Figure 5c). Similar to HvFC1 transgenics, Sod was transcriptionally upregulated in HvFC2 transgenics, after 8 days of exposure to drought stress. These findings showed that both FC isoforms had the capacity to modulate nuclear encoded transcription of ROS detoxification enzymes, upon drought stress.

3.4. HvFC Overexpression Protects Plants from Tetrapyrrole-Induced Photo-Oxidation

The apparent ability of both HvFC transgenics to improve ROS detoxification upon drought stress, prompted us to investigate whether ectopic overexpression of HvFCs improved oxidative stress tolerance. This was tested by exposing HvFC transgenic leaves to 20 μM paraquat and visually assessing leaf photo-bleaching, relative to wild-type and null controls. Qualitative observations of leaf photo-bleaching as a time-course, post-paraquat treatment, revealed no significant differences in leaf photo-bleaching between both HvFC1 and HvFC2 transgenics, relative to their respective controls (data not shown). This would indicate that these transgenics did not improve tolerance to paraquat-induced oxidative stress, although visual differences between transgenics and controls might be observed if lower concentrations of paraquat were used.
Under stress, plants also undergo oxidative stress, generated by photo-sensitizing tetrapyrrole intermediate accumulation [44,45]. In order to investigate whether ectopic overexpression of HvFCs contribute to tetrapyrrole-induced oxidative stress tolerance, we used the tigrinad12 mutant. In tigrinad12, tetrapyrrole biosynthesis is deregulated and consequently these plants accumulate the highly photo-sensitizing chlorophyll branch intermediate, Pchlide, under darkness. Etiolated mutant seedlings display strong red fluorescence at 655 nm through UV excitation, due to Pchlide accumulation [39]. When these plants are re-exposed to light, photosensitizing Pchlide generates 1O2 and causes extensive photo-oxidative damage [39]. A representative transgenic line for HvFC1 and HvFC2 was crossed with tigrinad12. Homozygous tigrinad12 plants were detected within a segregating F2 population, using a CAPS marker, designed to the causative mutation in the FLU gene [39] (Figure 6, 1st and 2nd panel). Lines containing HvFC transgenes were additionally identified by using a dominant transgene specific PCR marker (Figure 6, 3rd panel).
Seedlings identified to be both homozygous for tigrinad12 and containing either the HvFC1 or HvFC2 transgenes were compared to non-transgenic (cv. Golden Promise, cv. Bonus, tigrinad12, Golden Promise × Bonus F2 progenies) and transgenic controls (2 × 35S::FC1, 2 × 35S::FC2), for both Pchlide accumulation upon darkness and subsequent photo-oxidative damage induced by a continuous light treatment. Indeed, etiolated tigrinad12 seedlings displayed a strong red fluorescence (Figure 7a). However, tigrinad12 seedlings overexpressing either HvFC1 or HvFC2, exhibited significantly less red fluorescence at 655 nm (p < 0.05), when compared to non-transgenic tigrinad12 controls (Figure 7a). Fluorescence levels were similar between the non-transgenic controls (data not presented). These findings implied that ectopic overexpression of HvFC1 and HvFC2 can suppress Pchlide accumulation that is normally observed in etiolated tigrinad12 seedlings.
Potential photo-toxic effects were evaluated in these plants, upon re-exposure to light, by analyzing the total chlorophyll content and the chlorophyll fluorescence parameter Fv/Fm. Total chlorophyll content was significantly reduced (p < 0.05) in tigrinad12 mutants, 24 h post re-illumination (Figure 7b). However, the chlorophyll content remained unchanged in transgenic tigrinad12 overexpressing either HvFC1 or HvFC2, suggesting that overexpression of HvFCs suppress the potential photo-bleaching effects of tigrinad12. Similarly, tigrinad12 exhibited a significant reduction in chlorophyll fluorescence, 24 h after re-illumination (Figure 7c). Such an effect was not observed in the tigrinad12 overexpressing HvFC1. In the tigrinad12 overexpressing HvFC2, Fv/Fm was reduced 24 h after re-illumination, relative to the before-dark treatment, but it was not as strong as tigrinad12. Taken together, these results indicate that both HvFC1 and HvFC2 have the capacity to suppress the photo-toxic effects caused by tetrapyrrole deregulation in tigrinad12.

3.5. Barley FC1 and FC2 are Differentially Responsive to Drought Stress and Oxidative Stress

Our results indicated that both HvFC1 and HvFC2 play roles in drought and oxidative stress tolerance, while previous studies reported that only FC1 is involved in the stress defense responses [14,20,21,22,23,24,25,26,27,28]. Therefore, we investigated HvFCs stress responsive expression patterns. For this purpose, we compared well-watered control plants to plants under drought stress. Dehydrated plants were visually assessed for wilting and transcript abundance of drought responsive Cat and Sod were analyzed to ensure that the plants were successfully drought stressed. Expression of HvFC1 and HvFC2 was analyzed in leaves of well-watered and drought-stressed plants.
Control plants wilted 8 days post water-withholding (Figure 8a). Cat expression was significantly upregulated 5 days post water-withholding, relative to the well-watered plants (Figure 8b). Transcript levels of Sod was also significantly increased 2 to 5 days post water-withholding (Figure 8b). In-line with previous studies [16,20,21,29,30,31,32,33,34], HvFC1 was significantly upregulated, whereas HvFC2 was downregulated, 2 to 5 days post water-withholding, relative to the well-watered plants (Figure 8c).
To investigate the transcriptional responses of HvFCs to oxidative stress, wild-type control plants were exposed to Paraquat-induced and tetrapyrrole-mediated oxidative stress. Paraquat treated leaves were severely photo-bleached, 24 h after the treatment (Figure 9a). Even though, expression of HvFC1 and HvFC2 did not change 1.5 h post paraquat treatment, HvFC1 was significantly upregulated and HvFC2 was markedly downregulated, 24 h after paraquat application (Figure 9c). When etiolated tigrinad12 mutants were illuminated, the leaves were severely photo-bleached (Figure 9b) in response to tetrapyrrole-induced oxidative stress. Transcript levels of HvFC1 and HvFC2 did not significantly change 1.5 h post illumination. However, both HvFC1 and HvFC2 were significantly downregulated, 24 h post-illumination (Figure 9c). It is important to note that, HvFC1 expression was less affected by severe oxidative stress than HvFC2, 24 h post re-illumination.
Collectively, these results demonstrate that the two HvFCs were differentially responsive to drought and oxidative stresses.

4. Discussion

4.1. Both FC1 and FC2 are Implicated in Maintaining Higher Leaf Water Status and Photosynthetic Activity Upon Drought Stress

Transgenic plants ectopically overexpressing either HvFC1 or HvFC2 showed several beneficial traits, which enabled them to perform better under water-limited conditions. Even though the control plants wilted at −0.6 MPa soil water potential (8 days post water-withholding), neither HvFC1 nor HvFC2 overexpressing transgenics exhibited wilting symptoms (Figure 3). The leaf RWC of both types of transgenics was similar to the controls, prior to stress, but they were able to maintain a higher RWC, as the soil dehydrated (Figure 4a). This finding was in agreement with Allen et al., (2015) [31] who reported that Arabidopsis plants overexpressing either FC1 or FC2 were less wilted under terminal drought. As drought stress progressed, water uptake from the soil became more difficult, because of the reducing soil water potential. This, in turn, caused a reduction in the intercellular plant water potential and therefore the overall plant water status. One of the very early responses to water deficit was stomatal closure, which facilitated water retention by restricting transpiration. Even though we speculated that increased leaf RWC for both HvFC transgenics might be due to a lower gs, HvFC1 transgenics displayed significantly higher gs, whereas HvFC2 transgenics showed no significant increase in gs relative to the controls (Figure 4b). Therefore, it is probable that HvFC transgenics express a more effective mechanism for water uptake.
HvFC ectopically overexpressing transgenics are expected to have a higher heme content. Several studies report that heme oxygenase (HO), which breaks down heme into an antioxidative compound, Biliverdin IX, is implicated in lateral root development [46,47,48]. Therefore, HvFC transgenics might have a higher amount of heme and HO activity in roots, which could facilitate root development, therefore, allowing plants to access deep-water resources, as the drought stress progresses. This hypothesis was supported by the fact that HO activity was significantly enhanced in root tissues, during drought stress [32]. Furthermore, rice transgenics ectopically overexpressing Protoporphyrinogen IX oxidase (PPO), produced more of the branch point intermediate, Proto IX, and increased FC activity, heme content, and HO activity in roots, upon drought [32]. Plants in this study were also able to maintain a higher RWC upon drought stress, relative to the non-transgenic controls. This would indicate that the heme branch intermediates might regulate mechanisms that aid in water acquisition, at low soil water potentials.
Transgenics ectopically overexpressing either HvFC1 or HvFC2 also exhibited a significantly higher photosynthetic capacity under both non-stressed and drought stress conditions, relative to controls (Figure 4c). This observation implied that before initiation of the drought stress, higher gs of HvFC overexpressing transgenics was more likely to be a consequence of increased photosynthetic capacity. As stomata are highly responsive to intracellular CO2 concentration [49,50], we assumed that the transgenics have a higher gradient in the partial pressure of CO2 between the surrounding atmosphere and the inside of the leaf, as a result of an inherent higher carboxylation efficiency, thus, promoting higher gs. However, as the drought stress progressed, even though the photosynthetic capacity remained high relative to controls, gs progressively declined in both transgenics. Given that under drought stress, the stomata are more responsive to stress signals than intracellular CO2 concentration [51,52,53], this reduction in gs is most likely explained as a normal stress response.
As ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) is the primary enzyme involved in carboxylation, improved photosynthetic capacity of the transgenics could be due to either an increased Rubisco content or its activity. It was reported that ectopic overexpression of Arabidopsis FC1 transcriptionally upregulated the expression of photosynthesis-associated nuclear genes (PhANG), such as Rubisco and light-harvesting complex b protein (LHCB), under non-stressed conditions [12,13,14]. In contrast, Arabidopsis plants overexpressing FC2, failed to display transcriptional upregulation of the same nuclear genes. These findings led the authors of these studies to propose that only the FC1-derived heme sub-pool might act as a plastid-to-nuclear signal. Subsequent studies revealed that chloroplasts also transmit such retrograde signals under stress conditions, therefore, modulating nuclear gene expression associated with stress acclimation [14,54,55,56]. This signal has since been termed an “operational signal” [57,58]. Whether heme is a causal agent in such a retrograde signaling process during drought exposure, is yet to be determined.
Our study goes someway to support a putative role for heme in retrograde signaling, given that overexpression of either HvFC1 or HvFC2, significantly upregulates the expression of nuclear genes Cat and Sod, which each encode proteins necessary for ROS detoxification, upon prolonged drought conditions (Figure 5). Future investigations are required to determine whether these observations are a direct or indirect consequence of heme accumulation and signaling. If heme is deemed a bona fide retrograde signal, then our data would suggest that both FC-derived heme sub-pools could potentially act as operational signals to protect plants from drought-mediated cellular damage. In this context, we would anticipate transcriptional upregulation of photosynthesis-associated nuclear genes in HvFC transgenics, which could in part explain the observed higher photosynthetic capacity both under well-watered and drought stress conditions. Two likely downstream targets for this signaling are Rubisco and LHCB, with Rubisco being a major target for improving photosynthetic capacity [59], and LHCB, encoding apoproteins required for binding major light harvesting pigments, such as chlorophylls and xanthophylls in photosystem II (PSII) [60,61]. It is also important to note that LHCB is involved in modulating gs under drought stress and preventing oxidative damage [62,63], which could explain the improvement in photo-oxidative damage protection of HvFC transgenics, relative to controls.
Carbon assimilation depends on a number of factors such as the amount of light harvesting pigments, capacity for CO2 diffusion from ambient air to the site of carboxylation and carboxylation efficiency [64,65]. HvFC transgenics maintained higher Asat, relative to controls, under both non-stressed conditions as well as at 2 and 5 days post water-withholding (Figure 4d). This observation correlated well with the higher photosynthetic capacity and chlorophyll content for both HvFC transgenics (Figure 4c,e) and the higher gs in HvFC1 overexpressing transgenics (Figure 4b). Higher Asat in the transgenics could partly be attributed to the higher chlorophyll content, which allowed more light perception for photosynthesis. In line with our results, Fan et al., [28] also found an increased chlorophyll accumulation in AtFC1 ectopic overexpression line. Another possible reason could be due to a likely increase in heme content, resulting from FC overexpression. Heme being an integral component of the cytochrome b6f complex, is important for the photosynthetic electron transport [9,10]. Lack of cytochrome b6f-bound heme in FC2 knock out Arabidopsis mutants, display impaired electron transport and PSII efficiency [16]. Therefore, HvFC2 overexpressing transgenics might contain a higher cytochrome b6f-bound heme, therefore, improving photosynthetic electron transport capacity and PSII efficiency. FC1 knock out Arabidopsis mutants, on the other hand, do not display such a reduction in photosynthetic performance, implying that FC1-derived heme might not necessarily be as important for photosynthesis [16]. This contrasts with our previous report showing that both HvFC1 and HvFC2 overexpressing transgenics improved the photosynthetic rate and photosynthetic capacity under non-stressed conditions [35]. We, therefore, expect that both FC-derived heme pools, were likely to contribute to photosynthetic performance, as a consequence of improved electron transport and PSII efficiency. Since both types of HvFC transgenics also significantly improved photosynthetic performance under drought stress, this would support the proposal that both FCs play an important role in adapting photosynthesis to water stress.

4.2. Both FC1 and FC2 Prevent Tetrapyrrole-Mediated Oxidative Stress

Under stress, photosensitizing tetrapyrrole intermediates accumulate, leading to an oxidative burst [44,45]. A study by Sobotka et al., (2011) [66] indicates that FC2 plays an important role in preventing toxic intermediate accumulation. This evidence prompted us to investigate whether two HvFCs have distinct regulatory functions in preventing potential photo-oxidative damage upon stress. Here, we used the tigrinad12 mutant, which is defective in the FLU-based negative regulation of chlorophyll biosynthesis. Consequently, the etiolated mutant displayed a strong red fluorescence, which is an indicator of Pchlide accumulation (Figure 7a). Notably, overexpression of either HvFC1 or HvFC2, significantly reduced toxic intermediate accumulation (Figure 7a). When etiolated mutants are illuminated, they exhibited severe photo-bleaching, indicating a significant damage to PSII, upon illumination (Figure 7b,c). However, tigrinad12 ectopically overexpressing either HvFC1 or HvFC2, showed reduced photo-bleaching, indicating a suppression of photo-oxidative damage. This data suggest that both FC1 and FC2 play roles in preventing photo-oxidative damage caused by tetrapyrrole accumulation.
In line with these observations, the Arabidopsis flu mutant, an ortholog of barley tigrinad12 also shows suppressed Pchlide accumulation, when introduced into heme accumulating hy1 or ulf3 [67]. Therefore, a reason for the reduced intermediate levels in HvFC overexpressing tigrinad12 could be the increased heme content. Heme serves as a negative regulator of the tetrapyrrole biosynthesis, by inhibiting the activity of the first rate-limiting enzyme, glutamyl-tRNA reductase (GluTR), by binding to its C-terminal end [59]. Taken together, our results indicate that a likely heme-based negative feedback mechanism protects plants from potential photo-oxidative damage under stress. This proposed role for heme is further supported by a more recent study by Kim et al. (2014) [33], who showed that ectopic overexpression of Bradyrhizobium japonicum cytosol-targeted FC in rice, substantially increased FC activity, total heme content, and tolerance to oxidative and polyethylene glycol-induced drought stress.

4.3. FC1 and FC2 are Differentially Responsive to Drought Stress and Oxidative Stress

Even though our study indicated that both FC1 and FC2 are good candidate genes for improving drought and oxidative stress tolerance, previous studies proposed that only FC1 is implicated in stress defense responses [29,30,31,32,33,34]. This was proposed solely based on HvFC’s differential transcriptional responses to distinct stress stimuli. In order to investigate whether the two HvFC’s had contrasting stress responsive expression profiles, we analyzed transcriptional abundance in the leaves of wild-type plants, before and after exposure to drought and oxidative stress. In line with previous observations, HvFC1 was significantly upregulated upon drought stress, whereas HvFC2 was markedly downregulated at the early stage of the drought stress (2 and 5 days post water-withholding) (Figure 8c).
Similar differential expression profiles of HvFC were observed in response to Paraquat-induced oxidative stress (Figure 9c). Paraquat disrupts the electron transport system of PSI, leading to generation of superoxide radical (O2−), which subsequently reduces into hydrogen peroxide (H2O2) and the hydroxyl radical (OH–). In contrast, when etiolated tigrinad12 was illuminated, both genes were severely downregulated (Figure 9c). Severe suppression of both HvFCs might be due to the elevated toxicity of 1O2 relative to H2O2 [5]. It is important to note that HvFC1 expression was less affected by the photo-toxicity of 1O2 compared to HvFC2 (Figure 9c). Data in this study showed that FC1 and FC2 were differentially responsive to drought and oxidative stress.
Collectively, these findings suggest that, despite distinct stress responsive expression of FC1 and FC2, increasing heme biosynthesis generally improved the plant photosynthetic capacity and also allowed plants to cope better when exposed to drought and oxidative stress. Both FCs are good candidates as targets for metabolic engineering towards improved crop performance, both under non-stressed and water-limited environments. Both heme pools were likely to play important roles in triggering the regulatory machinery involved in photosynthesis per se, as well as responses to drought and oxidative stress.

5. Patent

The authors declare that a patent was filed and granted for this work (WO20160544624A1).

Supplementary Materials

The following are available online at https://www.mdpi.com/2073-4395/10/9/1351/s1. Figure S1: A schematic illustration of the pMDC32 constitutive expression vector used for barley transformation, which harbours a dual 35S promoter, and either HvFC1 or HvFC2; Figure S2: Standardized drying curve used in the drought assay for evaluating the physiological performance of transgenics and control plants. In order to maintain −6 MPa soil water potential for one week, the pot weight was maintained at 4150g by adding small amount of water; Table S1: Primers used in this study.

Author Contributions

Conceptualization, D.S.K.N., B.P., E.J.E., R.W., and P.L.; Methodology and Validation, D.S.K.N.; Data Curation and Analysis, D.S.K.N.; Manuscript preparation, D.S.K.N., R.W., and P.L. Funding Acquisition, R.W. and P.L. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the Australian Research Council, the Grains Research and Development Corporation, the Government of South Australia, the University of Adelaide and DuPont Agricultural Biotechnology, USA.

Acknowledgments

We thank Bernhard Grimm of the Institute of Biology, Humboldt University, Berlin for kindly supplying tigrinad12, Alison Hay for generating transgenic vectors, Rohan Singh for the barley transformation, and Yuan Lee for the quantitative RT–PCR analysis. We would also like to thank Julie Hayes, Penny Tricker, and Robyn Grove for the critical comments on the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Boyer, J.S. Plant productivity and environment. Science 1982, 218, 443–448. [Google Scholar] [CrossRef] [PubMed]
  2. Chaves, M.M. Effects of water deficits on carbon assimilation. J. Exp. Bot. 1991, 42, 1–16. [Google Scholar] [CrossRef]
  3. Chaves, M.M.; Flexas, J.; Pinheiro, C. Photosynthesis under drought and salt stress: Regulation mechanisms from whole plant to cell. Ann. Bot. 2008, 103, 551–560. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Sagadevan, G.M.; Bienyameen, B.; Shaheen, M.; Shaun, P.; Saberi, M.; Clare, V.; Er, W.; Kershini, G.; Alice, M.; Samson, M.; et al. Physiological and molecular insights into drought tolerance. Afr. J. Biotechnol. 2002, 1, 28–38. [Google Scholar] [CrossRef]
  5. De Carvalho, M.H.C. Drought stress and reactive oxygen species: Production, scavenging and signaling. Plant Signal. Behav. 2008, 3, 156–165. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Mcwilliam, J. The dimensions of drought. In Drought Resistance in Cereals; Baker, F.W.G., Ed.; CAB International: Wallingford, UK, 1989; pp. 1–11. [Google Scholar]
  7. Fleury, D.; Jefferies, S.; Kuchel, H.; Langridge, P. Genetic and genomic tools to improve drought tolerance in wheat. J. Exp. Bot. 2010, 61, 3211–3222. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Tanaka, R.; Tanaka, A. Tetrapyrrole biosynthesis in higher plants. Annu. Rev. Plant Boil. 2007, 58, 321–346. [Google Scholar] [CrossRef]
  9. Cramer, W.A.; Soriano, G.M.; Ponomarev, M.; Huang, D.; Zhang, H.; Martinez, S.E.; Smith, J.L. Some new structural aspects and old controversies concerning the cytochromeb6fcomplex of oxygenic photosynthesis. Annu. Rev. Plant Boil. 1996, 47, 477–508. [Google Scholar] [CrossRef]
  10. Kurisu, G.; Zhang, H.; Smith, J.L.; Cramer, W.A. Structure of the cytochrome b6f complex of oxygenic photosynthesis: Tuning the cavity. Science 2003, 302, 1009–1014. [Google Scholar] [CrossRef] [Green Version]
  11. Del Río, L.A. ROS and RNS in plant physiology: An overview. J. Exp. Bot. 2015, 66, 2827–2837. [Google Scholar] [CrossRef] [Green Version]
  12. Woodson, J.D.; Pérez-Ruiz, J.M.; Chory, J. Heme synthesis by plastid ferrochelatase I regulates nuclear gene expression in plants. Curr. Boil. 2011, 21, 897–903. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Woodson, J.D.; Pérez-Ruiz, J.M.; Schmitz, R.J.; Ecker, J.R.; Chory, J. Sigma factor-mediated plastid retrograde signals control nuclear gene expression. Plant J. 2012, 73, 1–13. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Page, M.T.; Garcia-Becerra, T.; Smith, A.G.; Terry, M.J. Overexpression of chloroplast-targeted ferrochelatase 1 results in a genomes uncoupled chloroplast-to-nucleus retrograde signalling phenotype. Philos. Trans. R. Soc. B Boil. Sci. 2020, 375, 20190401. [Google Scholar] [CrossRef]
  15. Moulin, M.; Smith, A.G. Regulation of tetrapyrrole biosynthesis in higher plants. Biochem. Soc. Trans. 2005, 33, 737–742. [Google Scholar] [CrossRef]
  16. Scharfenberg, M.; Mittermayr, L.; Von Roepenack-Lahaye, A.; Schlicke, H.; Grimm, B.; Leister, D.; Kleine, T.; Roepenack-Lahaye, E. Functional characterization of the two ferrochelatases in Arabidopsis thaliana. Plant Cell Environ. 2014, 38, 280–298. [Google Scholar] [CrossRef] [PubMed]
  17. Zhao, W.T.; Feng, S.J.; Li, H.; Faust, F.; Kleine, T.; Li, L.-N.; Yang, Z.M. Salt stress-induced ferrochelatase 1 improves resistance to salt stress by limiting sodium accumulation in Arabidopsis thaliana. Sci. Rep. 2017, 7, 14737. [Google Scholar] [CrossRef] [Green Version]
  18. Little, H.N.; Jones, O.T.G. The subcellular loclization and properties of the ferrochelatase of etiolated barley. Biochem. J. 1976, 156, 309–314. [Google Scholar] [CrossRef]
  19. Chow, K.S.; Singh, D.P.; Walker, A.R.; Smith, A.G. Two different genes encode ferrochelatase in Arabidopsis: Mapping, expression and subcellular targeting of the precursor proteins. Plant J. 1998, 15, 531–541. [Google Scholar] [CrossRef]
  20. Nagai, S.; Koide, M.; Takahashi, S.; Kikuta, A.; Aono, M.; Sasaki-Sekimoto, Y.; Ohta, H.; Takamiya, K.-I.; Masuda, T. Induction of isoforms of tetrapyrrole biosynthetic enzymes, AtHEMA2 and AtFC1, under stress conditions and their physiological functions in arabidopsis. Plant Physiol. 2007, 144, 1039–1051. [Google Scholar] [CrossRef] [Green Version]
  21. Singh, D.P.; Cornah, J.E.; Hadingham, S.; Smith, A.G. Expression analysis of the two ferrochelatase genes in Arabidopsis in different tissues and under stress conditions reveals their different roles in haem biosynthesis. Plant Mol. Boil. 2002, 50, 773–788. [Google Scholar] [CrossRef]
  22. Smith, A.G.; Santana, M.A.; Wallace-Cook, A.D.; Roper, J.M.; Labbe-Bois, R. Isolation of a cDNA encoding chloroplast ferrochelatase from Arabidopsis thaliana by functional complementation of a yeast mutant. J. Boil. Chem. 1994, 269, 13405–13413. [Google Scholar]
  23. Papenbrock, J.; Mishra, S.; Mock, H.-P.; Kruse, E.; Schmidt, E.-K.; Petersmann, A.; Braun, H.-P.; Grimm, B. Impaired expression of the plastidic ferrochelatase by antisense RNA synthesis leads to a necrotic phenotype of transformed tobacco plants. Plant J. 2001, 28, 41–50. [Google Scholar] [CrossRef] [PubMed]
  24. Chow, K.S.; Singh, D.P.; Roper, J.M.; Smith, A.G. A single precursor protein for ferrochelatase-I from Arabidopsis is imported In Vitro into both chloroplasts and mitochondria. J. Boil. Chem. 1997, 272, 27565–27571. [Google Scholar] [CrossRef] [Green Version]
  25. Suzuki, T.; Masuda, T.; Singh, D.P.; Tan, F.-C.; Tsuchiya, T.; Shimada, H.; Ohta, H.; Amith, A.G.; Takamiya, K. Two types of ferrochelatase in photosynthetic and nonphotosynthetic tissues of cucumber: Their difference in phylogeny, gene expression, and localization. J. Biol. Chem. 2002, 277, 4731–4737. [Google Scholar] [CrossRef] [Green Version]
  26. Hey, D.; Ortega-Rodés, P.; Fan, T.; Schnurrer, F.; Brings, L.; Hedtke, B.; Grimm, B. Transgenic tobacco lines expressing sense or antisense Ferrochelatase 1RNA show modified ferrochelatase activity in roots and provide experimental evidence for dual localization of ferrochelatase 1. Plant Cell Physiol. 2016, 57, 2576–2585. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Lister, R.; Chew, O.; Rudhe, C.; Lee, M.-N.; Whelan, J. Arabidopsis thaliana ferrochelatase-I and II are not imported into Arabidopsis mitochondria. FEBS Lett. 2001, 506, 291–295. [Google Scholar] [CrossRef] [Green Version]
  28. Masuda, T.; Suzuki, T.; Shimada, H.; Ohta, H.; Takamiya, K. Subcellular localization of two types of ferrochelatase in cucumber. Planta 2003, 217, 602–609. [Google Scholar] [CrossRef]
  29. Nagahatenna, D.S.K.; Langridge, P.; Whitford, R. Tetrapyrrole-based drought stress signalling. Plant Biotechnol. J. 2015, 13, 447–459. [Google Scholar] [CrossRef] [Green Version]
  30. Nagahatenna, D.S.K.; Whitford, R. Ferrochelatase Compositions and Methods to Increase Agronomic Performance of Plants. U.S. Patent WO2016054462A1, 7 April 2016. [Google Scholar]
  31. Allen, S.M.; Luck, S.; Mullen, J.; Sakai, H.; Sivasanker, S.; Tingey, S.V.; Williams, R.W. Drought Tolerant Plants and Related Constructs and Methods Involving Genes Encoding Ferrochelatases. U.S. Patent US 2015/0284739 A1, 8 October 2015. [Google Scholar]
  32. Phung, T.-H.; Jung, H.-I.; Park, J.-H.; Kim, J.-G.; Back, K.; Jung, S. porphyrin biosynthesis control under water stress: Sustained porphyrin status correlates with drought tolerance in transgenic rice. Plant Physiol. 2011, 157, 1746–1764. [Google Scholar] [CrossRef] [Green Version]
  33. Kim, J.-G.; Back, K.; Lee, H.Y.; Lee, H.-J.; Phung, T.-H.; Grimm, B.; Jung, S. Increased expression of Fe-chelatase leads to increased metabolic flux into heme and confers protection against photodynamically induced oxidative stress. Plant Mol. Boil. 2014, 86, 271–287. [Google Scholar] [CrossRef]
  34. Espinas, N.A.; Kobayashi, K.; Sato, Y.; Mochizuki, N.; Takahashi, K.; Tanaka, R.; Masuda, T. Allocation of heme is differentially regulated by ferrochelatase isoforms in arabidopsis cells. Front. Plant Sci. 2016, 7, 1326. [Google Scholar] [CrossRef] [Green Version]
  35. Nagahatenna, D.S.K.; Tiong, J.; Edwards, E.J.; Langridge, P.; Whitford, R. Altering tetrapyrrole biosynthesis by overexpressing Ferrochelatases (FC1 and FC2), improves photosynthesis in transgenic barley. J. MDPI Agron. 2020. (submitted). [Google Scholar]
  36. Tingay, S.; McElroy, D.; Kalla, R.; Fieg, S.; Wang, M.; Thornton, S.; Brettell, R. Agrobacterium tumefaciens-mediated barley transformation. Plant J. 1997, 11, 1369–1376. [Google Scholar] [CrossRef]
  37. Matthews, P.R.; Wang, M.; Waterhouse, P.M.; Thornton, S.; Fieg, S.J.; Gubler, F.; Jacobsen, J.V. Marker gene elimination from transgenic barley, using co-transformation with adjacenttwin T-DNAs’ on a standard Agrobacterium transformation vector. Mol. Breed. 2001, 7, 195–202. [Google Scholar] [CrossRef]
  38. Améglio, T.; Archer, P.; Cohen, M.; Valancogne, C.; Daudet, F.-A.; Dayau, S.; Cruiziat, P. Significance and limits in the use of predawn leaf water potential for tree irrigation. Plant Soil 1998, 207, 155–167. [Google Scholar] [CrossRef]
  39. Lee, K.P.; Kim, C.; Lee, D.W.; Apel, K. TIGRINA d, required for regulating the biosynthesis of tetrapyrroles in barley, is an ortholog of the FLU gene of Arabidopsis thaliana. FEBS Lett. 2003, 553, 119–124. [Google Scholar] [CrossRef] [Green Version]
  40. Hiscox, J.D.; Israelstam, G.F. A method for the extraction of chlorophyll from leaf tissue without maceration. Can. J. Bot. 1979, 57, 1332–1334. [Google Scholar] [CrossRef]
  41. Burton, R.A.; Jobling, S.A.; Harvey, A.J.; Shirley, N.J.; Mather, D.E.; Bacic, A.; Fincher, G.B. The genetics and transcriptional profiles of the cellulose synthase-like HvCslF Gene Family in Barley. Plant Physiol. 2008, 146, 1821–1833. [Google Scholar] [CrossRef] [Green Version]
  42. Schmittgen, T.D.; Livak, K.J. Analyzing real-time PCR data by the comparative CT method. Nat. Protoc. 2008, 3, 1101–1108. [Google Scholar] [CrossRef]
  43. Zhang, J.; Kirkham, M. Drought-stress-induced changes in activities of superoxide dismutase, catalase, and peroxidase in wheat species. Plant Cell Physiol. 1994, 35, 785–791. [Google Scholar] [CrossRef]
  44. Mock, H.-P.; Heller, W.; Molina, A.; Neubohn, B.; Sandermann, H.; Grimm, B. Expression of uroporphyrinogen decarboxylase or coproporphyrinogen oxidase antisense RNA in tobacco induces pathogen defense responses conferring increased resistance to tobacco mosaic virus. J. Boil. Chem. 1999, 274, 4231–4238. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  45. Mock, H.-P.; Keetman, U.; Kruse, E.; Rank, B.; Grimm, B. Defense responses to tetrapyrrole-induced oxidative stress in transgenic plants with reduced uroporphyrinogen decarboxylase or coproporphyrinogen oxidase activity. Plant Physiol. 1998, 116, 107–116. [Google Scholar] [CrossRef] [Green Version]
  46. Chen, Y.-H.; Chao, Y.-Y.; Hsu, Y.Y.; Hong, C.-Y.; Kao, C.H. Heme oxygenase is involved in nitric oxide- and auxin-induced lateral root formation in rice. Plant Cell Rep. 2012, 31, 1085–1091. [Google Scholar] [CrossRef]
  47. Xuan, W.; Zhu, F.-Y.; Xu, S.; Huang, B.-K.; Ling, T.-F.; Qi, J.-Y.; Ye, M.-B.; Shen, W.-B. The heme oxygenase/carbon monoxide system is involved in the auxin-induced cucumber adventitious rooting process. Plant Physiol. 2008, 148, 881–893. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. Xu, S.; Zhang, B.; Cao, Z.-Y.; Ling, T.-F.; Shen, W.-B. Heme oxygenase is involved in cobalt chloride-induced lateral root development in tomato. BioMetals 2010, 24, 181–191. [Google Scholar] [CrossRef] [PubMed]
  49. Farquhar, G.D.; Sharkey, T.D. Stomatal conductance and photosynthesis. Annu. Rev. Plant Physiol. 1982, 33, 317–345. [Google Scholar] [CrossRef]
  50. Mott, K.A. Do stomata respond to CO2 concentrations other than intercellular? Plant Physiol. 1988, 86, 200–203. [Google Scholar] [CrossRef] [Green Version]
  51. Chaves, M.M.; Maroco, J.P.; Pereira, J.S. Understanding plant responses to drought—From genes to the whole plant. Funct. Plant Biol. 2003, 30, 239–264. [Google Scholar] [CrossRef]
  52. Flexas, J.; Medrano, H. Drought-inhibition of Photosynthesis in C3 Plants: Stomatal and non-stomatal limitations revisited. Ann. Bot. 2002, 89, 183–189. [Google Scholar] [CrossRef] [Green Version]
  53. Flexas, J.; Bota, J.; Loreto, F.; Cornic, G.; Sharkey, T.D. Diffusive and metabolic limitations to photosynthesis under drought and salinity in C 3 plants. Plant Boil. 2004, 6, 269–279. [Google Scholar] [CrossRef]
  54. Pogson, B.; Woo, N.S.; Förster, B.; Small, I. Plastid signalling to the nucleus and beyond. Trends Plant Sci. 2008, 13, 602–609. [Google Scholar] [CrossRef] [PubMed]
  55. Pfannschmidt, T. Plastidial retrograde signalling—A true “plastid factor” or just metabolite signatures? Trends Plant Sci. 2010, 15, 427–435. [Google Scholar] [CrossRef] [PubMed]
  56. Zhao, C.; Haigh, A.M.; Holford, P.; Chen, Z.-H. Roles of chloroplast retrograde signals and ion transport in plant drought tolerance. Int. J. Mol. Sci. 2018, 19, 963. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Xiao, Y.; Savchenko, T.; Baidoo, E.E.; Chehab, W.E.; Hayden, D.M.; Tolstikov, V.; Corwin, J.A.; Kliebenstein, D.J.; Keasling, J.D.; Dehesh, K. Retrograde signaling by the plastidial metabolite MEcPP regulates expression of nuclear stress-response genes. Cell 2012, 149, 1525–1535. [Google Scholar] [CrossRef] [Green Version]
  58. Woodson, J.D.; Chory, J. Organelle signaling: How stressed chloroplasts communicate with the nucleus. Curr. Boil. 2012, 22, R690–R692. [Google Scholar] [CrossRef] [Green Version]
  59. Galmes, J.; Andralojc, P.J.; Kapralov, M.V.; Flexas, J.; Keys, A.J.; Molins, A.; Parry, M.A.J.; Conesa, M.A. Environmentally driven evolution of R ubisco and improved photosynthesis and growth within the C 3 genus L imonium (P lumbaginaceae). N. Phytol. 2014, 203, 989–999. [Google Scholar] [CrossRef] [Green Version]
  60. Jansson, S. The light-harvesting chlorophyll ab-binding proteins. Biochim. Biophys. Acta (BBA) Bioenerg. 1994, 1184, 1–19. [Google Scholar] [CrossRef]
  61. Liu, X.-G.; Xu, H.; Zhang, J.-Y.; Liang, G.-W.; Liu, Y.-T.; Guo, A.-G. Effect of low temperature on chlorophyll biosynthesis in albinism line of wheat (Triticum aestivum) FA85. Physiol. Plant. 2012, 145, 384–394. [Google Scholar] [CrossRef]
  62. Xu, Y.-H.; Liu, R.; Yan, L.; Liu, Z.-Q.; Jiang, S.-C.; Shen, Y.-Y.; Wang, X.-F.; Zhang, D.-P. Light-harvesting chlorophyll a/b-binding proteins are required for stomatal response to abscisic acid in Arabidopsis. J. Exp. Bot. 2011, 63, 1095–1106. [Google Scholar] [CrossRef] [Green Version]
  63. De Bianchi, S.; Betterle, N.; Kouril, R.; Cazzaniga, S.; Boekema, E.; Bassi, R.; Dall’Osto, L. Arabidopsis mutants deleted in the light-harvesting protein Lhcb4 have a disrupted photosystem II macrostructure and are defective in photoprotection. Plant Cell 2011, 23, 2659–2679. [Google Scholar] [CrossRef] [Green Version]
  64. Flexas, J.; Niinemets, Ü.; Gallé, A.; Barbour, M.M.; Centritto, M.; Diaz-Espejo, A.; Douthe, C.; Galmés, J.; Ribas-Carbo, M.; Rodriguez, P.; et al. Diffusional conductances to CO2 as a target for increasing photosynthesis and photosynthetic water-use efficiency. Photosynth. Res. 2013, 117, 45–59. [Google Scholar] [CrossRef] [PubMed]
  65. Austin, R.B. Genetic variation in photosynthesis. J. Agric. Sci. 1989, 112, 287–294. [Google Scholar] [CrossRef]
  66. Sobotka, R.; Tichy, M.; Wilde, A.; Hunter, C.N. Functional assignments for the carboxyl-terminal domains of the ferrochelatase from synechocystis PCC 6803: The CAB domain plays a regulatory role, and region II is essential for catalysis. Plant Physiol. 2010, 155, 1735–1747. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  67. Goslings, D.; Meskauskiene, R.; Kim, C.; Lee, K.P.; Nater, M.; Apel, K. Concurrent interactions of heme and FLU with Glu tRNA reductase (HEMA1), the target of metabolic feedback inhibition of tetrapyrrole biosynthesis, in dark and light-grown Arabidopsis plants. Plant J. 2004, 40, 957–967. [Google Scholar] [CrossRef] [PubMed]
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Figure 1. The tetrapyrrole biosynthesis pathway with the major end-products (bold text) and some catalytic enzymes. GluTR—glutamyl-tRNA reductase and Protogen IX oxidase—Protoporphyrinogen IX oxidase.
Figure 1. The tetrapyrrole biosynthesis pathway with the major end-products (bold text) and some catalytic enzymes. GluTR—glutamyl-tRNA reductase and Protogen IX oxidase—Protoporphyrinogen IX oxidase.
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Figure 2. Variation of the soil water potential before, during, and after drought stress. Four weeks after planting, watering was withheld. Minus 6 MPa soil water potential was maintained for a week, and then plants were rewatered to initial soil water potential. Arrows indicate different time-points where measurements were taken.
Figure 2. Variation of the soil water potential before, during, and after drought stress. Four weeks after planting, watering was withheld. Minus 6 MPa soil water potential was maintained for a week, and then plants were rewatered to initial soil water potential. Arrows indicate different time-points where measurements were taken.
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Figure 3. Phenotypes of the representative control plants and transgenic lines (T2) grown under controlled environmental conditions in the absence of stress (a,d), 8 days post water-withholding (b,e), and after re-watering (c,f). The control plants were reversibly wilted, 8 days after withholding water, whereas both types of transgenics did not wilt.
Figure 3. Phenotypes of the representative control plants and transgenic lines (T2) grown under controlled environmental conditions in the absence of stress (a,d), 8 days post water-withholding (b,e), and after re-watering (c,f). The control plants were reversibly wilted, 8 days after withholding water, whereas both types of transgenics did not wilt.
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Figure 4. HvFC overexpressing transgenics maintained higher leaf water status and photosynthetic performance relative to controls upon drought. Physiological traits measured include—(a) leaf relative water content (RWC), (b) stomatal conductance, (c) instantaneous carboxylation efficiency, (d) carbon assimilation rate, (e) total chlorophyll content, and (f) instantaneous water use efficiency (WUE) relative to wild-type (WT) control plants upon drought stress. The data are shown as mean ± standard error (SE) of five plants for each of the three independent transgenic lines, per construct and WT. Asterisks indicate a statistically significant difference between the transgenics and controls, at * p < 0.05 based on two-way ANOVA.
Figure 4. HvFC overexpressing transgenics maintained higher leaf water status and photosynthetic performance relative to controls upon drought. Physiological traits measured include—(a) leaf relative water content (RWC), (b) stomatal conductance, (c) instantaneous carboxylation efficiency, (d) carbon assimilation rate, (e) total chlorophyll content, and (f) instantaneous water use efficiency (WUE) relative to wild-type (WT) control plants upon drought stress. The data are shown as mean ± standard error (SE) of five plants for each of the three independent transgenic lines, per construct and WT. Asterisks indicate a statistically significant difference between the transgenics and controls, at * p < 0.05 based on two-way ANOVA.
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Figure 5. Transcriptional responses of ROS detoxification enzymes, catalase, and superoxide dismutase, in a representative transgenic line, each ectopically overexpressing HvFC1 (a,b) or HvFC2 (c) under drought stress, relative to WT control. The data are shown as mean ± standard error (SE) of 3 different plants. Asterisks indicate statistically significant expression difference between transgenics and WT control, at * p < 0.05, based on two-way ANOVA.
Figure 5. Transcriptional responses of ROS detoxification enzymes, catalase, and superoxide dismutase, in a representative transgenic line, each ectopically overexpressing HvFC1 (a,b) or HvFC2 (c) under drought stress, relative to WT control. The data are shown as mean ± standard error (SE) of 3 different plants. Asterisks indicate statistically significant expression difference between transgenics and WT control, at * p < 0.05, based on two-way ANOVA.
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Figure 6. Molecular characterization of tigrinad12 mutants overexpressing HvFC1 or HvFC2 using CAPS markers and transgene specific primers. PCR was conducted using FLU specific primers (top panel). The PCR amplicons were cleaved using HaeIII restriction enzyme, and tigrinad12 mutants could be differentiated from other plants based on the cleaved fragment sizes (middle panel). The presence or absence of the transgenes was detected by using the transgene specific primers (bottom panel). Lane (-) is the negative control.
Figure 6. Molecular characterization of tigrinad12 mutants overexpressing HvFC1 or HvFC2 using CAPS markers and transgene specific primers. PCR was conducted using FLU specific primers (top panel). The PCR amplicons were cleaved using HaeIII restriction enzyme, and tigrinad12 mutants could be differentiated from other plants based on the cleaved fragment sizes (middle panel). The presence or absence of the transgenes was detected by using the transgene specific primers (bottom panel). Lane (-) is the negative control.
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Figure 7. Ectopic overexpression of HvFC1 and HvFC2 suppresses tigrinad12 mutant phenotypes. (a) Red fluorescence of dark grown seedlings, which is an indication of the level of Pchlide accumulation. The data are shown as mean ± standard error of 5 different plants. Means with the same letter are not significantly different at * p < 0.05 based on one-way ANOVA. (b) Total chlorophyll content and (c) Chlorophyll fluorescence (Fv/Fm) before dark treatment and upon 24 h after re-exposure to light. The data are shown as mean ± standard error of 5 different plants. Asterisks indicate a statistically significant difference relative to before treatment, at * p < 0.05 based on two-way ANOVA. tig- tigrinad12 mutant. FC1, FC2- representative transgenic lines ectopically overexpressing either HvFC1 or HvFC2. tig × FC1or tig × FC1- tigrinad12 mutants ectopically overexpressing either HvFC1 or HvFC2.
Figure 7. Ectopic overexpression of HvFC1 and HvFC2 suppresses tigrinad12 mutant phenotypes. (a) Red fluorescence of dark grown seedlings, which is an indication of the level of Pchlide accumulation. The data are shown as mean ± standard error of 5 different plants. Means with the same letter are not significantly different at * p < 0.05 based on one-way ANOVA. (b) Total chlorophyll content and (c) Chlorophyll fluorescence (Fv/Fm) before dark treatment and upon 24 h after re-exposure to light. The data are shown as mean ± standard error of 5 different plants. Asterisks indicate a statistically significant difference relative to before treatment, at * p < 0.05 based on two-way ANOVA. tig- tigrinad12 mutant. FC1, FC2- representative transgenic lines ectopically overexpressing either HvFC1 or HvFC2. tig × FC1or tig × FC1- tigrinad12 mutants ectopically overexpressing either HvFC1 or HvFC2.
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Figure 8. Transcript abundance of ROS detoxification markers (Cat and SOD) and HvFCs in control plants upon drought stress. (a) Phenotypes of control plants before stress and after exposure to drought stress. (b) Expression of Cat and Sod and, (c) HvFC1 and HvFC2 in drought-treated plants, relative to the well-watered plants. The data are shown as mean ± standard error (SE) of 3 different plants. Asterisks indicate a statistically significant expression difference relative to the well-watered plants, at * p < 0.05, based on one-way ANOVA.
Figure 8. Transcript abundance of ROS detoxification markers (Cat and SOD) and HvFCs in control plants upon drought stress. (a) Phenotypes of control plants before stress and after exposure to drought stress. (b) Expression of Cat and Sod and, (c) HvFC1 and HvFC2 in drought-treated plants, relative to the well-watered plants. The data are shown as mean ± standard error (SE) of 3 different plants. Asterisks indicate a statistically significant expression difference relative to the well-watered plants, at * p < 0.05, based on one-way ANOVA.
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Figure 9. Phenotypes of control barley leaves and HvFC transcript abundance upon exposure to Paraquat-induced and tetrapyrrole-mediated oxidative stress. Leaves of control plants before and 24 h after exposure to (a) Paraquat-induced oxidative stress, and (b) tetrapyrrole-mediated oxidative stress in tigrinad12 mutants. (c) Relative expression of HvFC1 and HvFC2, upon oxidative stress relative to before stress. The data are shown as mean ± standard error (SE) of 3 different plants. Asterisks indicate a statistically significant expression difference, relative to before treatment, at * p < 0.05 using one-way ANOVA.
Figure 9. Phenotypes of control barley leaves and HvFC transcript abundance upon exposure to Paraquat-induced and tetrapyrrole-mediated oxidative stress. Leaves of control plants before and 24 h after exposure to (a) Paraquat-induced oxidative stress, and (b) tetrapyrrole-mediated oxidative stress in tigrinad12 mutants. (c) Relative expression of HvFC1 and HvFC2, upon oxidative stress relative to before stress. The data are shown as mean ± standard error (SE) of 3 different plants. Asterisks indicate a statistically significant expression difference, relative to before treatment, at * p < 0.05 using one-way ANOVA.
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MDPI and ACS Style

Nagahatenna, D.S.K.; Parent, B.; Edwards, E.J.; Langridge, P.; Whitford, R. Barley Plants Overexpressing Ferrochelatases (HvFC1 and HvFC2) Show Improved Photosynthetic Rates and Have Reduced Photo-Oxidative Damage under Drought Stress than Non-Transgenic Controls. Agronomy 2020, 10, 1351. https://doi.org/10.3390/agronomy10091351

AMA Style

Nagahatenna DSK, Parent B, Edwards EJ, Langridge P, Whitford R. Barley Plants Overexpressing Ferrochelatases (HvFC1 and HvFC2) Show Improved Photosynthetic Rates and Have Reduced Photo-Oxidative Damage under Drought Stress than Non-Transgenic Controls. Agronomy. 2020; 10(9):1351. https://doi.org/10.3390/agronomy10091351

Chicago/Turabian Style

Nagahatenna, Dilrukshi S. K., Boris Parent, Everard J. Edwards, Peter Langridge, and Ryan Whitford. 2020. "Barley Plants Overexpressing Ferrochelatases (HvFC1 and HvFC2) Show Improved Photosynthetic Rates and Have Reduced Photo-Oxidative Damage under Drought Stress than Non-Transgenic Controls" Agronomy 10, no. 9: 1351. https://doi.org/10.3390/agronomy10091351

APA Style

Nagahatenna, D. S. K., Parent, B., Edwards, E. J., Langridge, P., & Whitford, R. (2020). Barley Plants Overexpressing Ferrochelatases (HvFC1 and HvFC2) Show Improved Photosynthetic Rates and Have Reduced Photo-Oxidative Damage under Drought Stress than Non-Transgenic Controls. Agronomy, 10(9), 1351. https://doi.org/10.3390/agronomy10091351

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