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Quinoa: Role and Responses Under Abiotic Stress

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Abstract

Quinoa (Chenopodium quinoa Willd.) is a hereditarily distinct Andean crop that has received remarkable interest globally owing to its nutritional and health advantages. It is extremely tolerant to harsh environmental conditions, for instance, salt- and water-deficit agroecosystems. Salinity along with drought constitute the major abiotic environmental cues examined in quinoa, whereas additional stressors like heat, frost, heavy metals, waterlogging, and UV-B light are relatively less examined. Moreover, stresses usually act in combinations of two or more. Presently, large gaps exist in our knowledge regarding quinoa’s response to several abiotic stresses, particularly at the molecular level. Even as large genetic variability exists in quinoa species, substantial exploration is necessitated to exploit this genetic diversity. With the recent publication of quinoa reference genome, categorization of genes responsible for abiotic stress tolerance would be intensely facilitated, and a genetic approach should assist in improving our knowledge of varied abiotic stress tolerance mechanisms operative in quinoa, ultimately leading to better propagation approaches. By way of these advances, quinoa has great potential for providing sustainable solutions needed for food safety issues in dry and semi-dry areas worldwide. More or less, not much research has been carried out on quinoa, and relatively lesser has been carried out to explicate the genetics supporting quinoa’s endurance to abiotic factors. With this background, the chapter aims to present (1) a brief overview of quinoa’s history, botanical features, distribution, and economic importance and (2) a recent understanding of the responses and tolerance of quinoa to different abiotic stress factors, focusing on physiological and biochemical responses, possible molecular machinery, and genetic regulation.KeywordsAbiotic stressChenopodiumDroughtHeatQuinoaSalinity

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... This characteristic has aroused the interest of researchers and a series of studies have been carried out, in recent years many researchers have shown that quinoa is a plant tolerant to salinity, being recognized for its great natural variability, these characteristics make it an attractive crop for agricultural activity in arid and semiarid zones (Ruiz et al., 2016). In addition, Kaur et al. (2022) mention experiments carried out under salinity conditions ranging from 100 to 750 mM NaCl, where different accessions have been compared, demonstrating that quinoa has a complex trait, associated with mechanisms of tolerance to salinity under multiple processes and conditions (Ruiz et al., 2016). ...
... Likewise, the highest proline content was found in 'Negra Oruro', being significantly different from the other accessions (Table 11). In addition, Table 12 also shows that the highest proline value was found with a salt concentrat ion of 400 mM, being significantly different from the other concentrations; however, at 0 and 200 mM there was nonsignificant difference, this is because metabolites such as proline have a role against salt stress, and this accumulates as salinity increases (Kaur et al., 2022). Table 10. ...
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... The significant role of ABA in plant-water balance and development is well-established [36]. Under drought stress, quinoa plants (variety 'INIA-Illpa') had elevated levels of ABA in their roots, as reported by Kaur et al. [37]. In addition, leaves of the 'Titicaca' sea-level variety had high ABA levels when grown under both water-deficient and controlled conditions [38]. ...
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Quinoa (Chenopodium quinoa Willd.) is a genetically diverse Andean crop that has earned special attention worldwide due to its nutritional and health benefits and its ability to adapt to contrasting environments, including nutrient-poor and saline soils and drought stressed marginal agroecosystems. Drought and salinity are the abiotic stresses most studied in quinoa; however, studies of other important stress factors, such as heat, cold, heavy metals, and UV-B light irradiance, are severely limited. In the last few decades, the incidence of abiotic stress has been accentuated by the increase in unpredictable weather patterns. Furthermore, stresses habitually occur as combinations of two or more. The goals of this review are to: (1) provide an in-depth description of the existing knowledge of quinoa's tolerance to different abiotic stressors; (2) summarize quinoa's physiological responses to these stressors; and (3) describe novel advances in molecular tools that can aid our understanding of the mechanisms underlying quinoa's abiotic stress tolerance.
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Quinoa (Chenopodium quinoa Willd.) is a highly resilient crop, displaying high levels of salinity and drought tolerance, although only low levels of heat tolerance. In this chapter, current knowledge of the response of quinoa to abiotic stresses is discussed, focussing on physiological responses, putative molecular mechanisms and genetic control. Relatively little research has been conducted into quinoa, and even less has been done to elucidate the genetics underpinning quinoa’s tolerance to abiotic stresses. The quinoa genes CqSOS1, CqNHX1, CqBADH, CqHSP70, CqHSP20 and CqABAs are discussed, and areas requiring further research at the genetic level are highlighted. There are currently extensive gaps in our understanding of the response of quinoa to certain abiotic stresses, with virtually no studies covering the effects of soil acidity, boron toxicity and nutrient deficiency. Whilst there is significant genetic diversity within the quinoa species, significant research is required to understand how this genetic variation can be harnessed. The recent release of a high-quality quinoa reference genome provides a useful tool to greatly facilitate the characterisation of genes involved in abiotic stress tolerance and taking a genetics-led approach should aid the rapid advancement of our understanding of quinoa’s abiotic stress tolerance mechanisms and lead to more effective improvement in engineering and breeding strategies. With these improvements, quinoa can fulfil a role urgently needed to provide food security in arid and semi-arid regions.
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Many areas of the world are affected simultaneously by salinity and heavy metal pollution. Halophytes are considered as useful candidates in remediation of such soils due to their ability to withstand both osmotic stress and ion toxicity deriving from high salt concentrations. Quinoa (Chenopodium quinoa Willd) is a halophyte with a high resistance to abiotic stresses (drought, salinity, frost), but its capacity to cope with heavy metals has not yet been fully investigated. In this pot experiment, we investigated phytoextraction capacity, effects on nutrient levels (P and Fe), and changes in gene expression in response to application of Cr(III) in quinoa plants grown on saline or non-saline soil. Plants were exposed for three weeks to 500 mg kg-1 soil of Cr(NO3)3·9H2O either in the presence or absence of 150 mM NaCl. Results show that plants were able tolerate this soil concentration of Cr(III); the metal was mainly accumulated in roots where it reached the highest concentration (ca. 2.6 mg g-1 DW) in the presence of NaCl. On saline soil, foliar Na concentration was significantly reduced by Cr(III). Phosphorus translocation to leaves was reduced in the presence of Cr(III), while Fe accumulation was enhanced by treatment with NaCl alone. A real-time RT-qPCR analysis was conducted on genes encoding for sulfate, iron, and phosphate transporters, a phytochelatin, a metallothionein, glutathione synthetase, a dehydrin, Hsp70, and enzymes responsible for the biosynthesis of proline (P5CS), glycine betaine (BADH), tocopherols (TAT), and phenolic compounds (PAL). Cr(III), and especially Cr(III)+NaCl, affected transcript levels of most of the investigated genes, indicating that tolerance to Cr is associated with changes in phosphorus and sulfur allocation, and activation of stress-protective molecules. Moderately saline conditions, in most cases, enhanced this response, suggesting that the halophytism of quinoa could contribute to prime the plants to respond to chromium stress.
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Se describen los efectos de la radiación UV-B (RUV-B) sobre algunos parámetros de crecimiento: altura de la planta (A), diámetro de tallo (DT), largo x ancho (LA), número de hojas (NH), área foliar específica (AFE) y masa foliar específica (MFE) en cinco variedades de quinoa. Los efectos de la UV-B fueron diferentes según la variedad y parámetro considerado. Así, A se incrementó en las variedades CICA (P ? 0,04) y Robura (P ? 0,02); mientras DT fue influenciado positivamente en CICA (P ? 0,0002) y Faro Roja (P ? 0,017). LA sólo mostró cambios significativos (P ? 0,05) en CICA. El NH fue la variable que experimentó cambios positivos en todas las variedades, observándose los más pronunciados en Faro Roja (P ? 0,003), CICA (P ? 0,003) y Ratuqui (P ? 0,015). La MFE cambió positivamente en Faro Roja, Kancolla y Robura (P ? 0,05). CICA fue la única variedad que experimentó incrementos significativos en todos los parámetros evaluados, seguida de Faro Roja y Robura. El menor porcentaje de cambios ocurrieron en Kancolla y Ratuqui. Las variaciones observadas se discutieron en términos de adaptación evolutiva.
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Quinoa is well known for its great ability to tolerate water stress. However, very little information is available about its potential growth under full irrigation particularly in hot and semi-arid regions. In this experiment, a newly-released quinoa (cv. Q5) bred for hot and dry regions was grown under three planting densities (PDs) of 150,000, 185,000, and 270,000 in the drainable lysimeters, south of Iran. The highest and lowest grain yields were observed in the middle and low PDs of 3.65 Mg ha −1 and 2.86 Mg ha −1 , respectively. Quinoa showed very high crop evapotranspiration (ETc) and transpiration (T) rates. ETc and T varied in the range of 1448-1687 mm, and 777-1228 mm among the PDs, respectively. These high values resulted in high single crop coefficients (Kc) that overall varied between around 1 and 2.4 during the growing season. The basal crop coefficient (Kcb) of the dual Kc (Kc = Kcb + Ke) reached about 1.9 and 1.2 in the high and low PDs, respectively, indicating high transpiration capacity. The main reasons of high Kc and Kcb were high soil evaporation rate due to very frequent irrigations of 3-4 days and soil wetting, and the prevailing regional sensible heat advection that increased transpiration. It was concluded that quinoa has a specific physiological systems that transpire continually for allowing better leaf cooling at high temperature, which results in high water use. Moreover, a vigorous root system that extended down to 1.2 m with high root length densities in the deep layers (RLD > 1 cm cm-3) helped quinoa to supply the water use. This extensive root system down to 1.2 m could help to increase irrigation interval and reducing soil evaporation. However, the effect of PD on the root length and root mass was mainly observed in the top 40 cm, below which its effect diminished and root length and root mass were nearly identical among the PDs. Overall, it is concluded that quinoa Q5 is a super crop that not only can tolerate water stress, but also can potentially grow well and produce acceptable grain yield in the hot and semi-arid areas. Adapting appropriate PD and irrigation management such as drip irrigation (surface and subsurface), mulching, increasing irrigation interval attributed to the deep rooting system, and water-saving irrigation managements would substantially reduce soil evaporation and increase water productivity.
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Hybridization and polyploidization appear to be ubiquitous in the evolution of Chenopodium s.s., but the origin and the evolutionary history of the polyploid chenopods is still poorly understood. Phylogenetic analyses of DNA sequences of nrITS, four plastid regions, and 5S rDNA spacer region (NTS) of five Eurasian hexaploid chenopods (2n = 6x = 54), C. album, C. giganteum, C. pedunculare C. formosanum and C. opulifolium, and their diploid and tetraploid relatives as well as genomic in situ hybridization (GISH) indicate their allohexaploid origin. The origin of all the analyzed hexaploids have been inferred to have involved B-genome diploid. The identity of the other parent/parents is more elusive. In the case of C. album, C. giganteum and C. pedunculare the second maternal parent seems to be similar to extant C. strictum or C. striatiforme or Asian diploids (e.g. C. acuminatum). In genomes of allohexaploid C. album, C. giganteum and C. pedunculare half of the rDNA were located in the chromosomes of B-subgenome. The remaining rDNA loci were placed in chromosomes originating from the other parent/parents. Although 35S rDNA loci inherited from two parental species seems to be present in these hexaploids, only one ribotype of nrITS was detected.
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Quinoa has been widely used as a model crop for understanding salt-tolerance in halophyte plants. However, a salt tolerance mechanism regarding the photosynthetic activity is poorly evaluated. Here we report the effects of salt stress on photosynthesis of the halophyte Chenopodium quinoa cultivated under different NaCl concentrations (0, 100, and 300 mM). Our results revealed no apparent effect of moderate salinity (100 mM NaCl) on plant growth while, a reduction of plant biomass production was detected under 300 mM NaCl without any symptom of toxicity. No significant effect on the chloroplasts ultrastructure was observed under moderate salinity. Some morphological deformations of chloroplasts such as swelling of thylakoids, disruption of envelope, accumulation of starch grains and plastoglobuli were observed following prolonged exposure to severe stress. Under moderate salinity, no considerable change was detected on the rate of primary photochemistry (fluorescence O-J phase) and the reduction of the PQ pool (J-I phase), no apparent effects on the minimal (F 0 ), the maximal fluorescence (F m ) and the maximal photochemical efficiency (Fv/Fm) showing a high stability of PSII. The high PSII efficiency was also confirmed by the donor side intactness (constant Fk/Fj ratio) and stable antenna size. The high stability of PSII efficiency was also demonstrated by enhanced communication between antenna complex and PSII reaction centre and the stability of OEC complex (PsbQ and PsbO proteins). However, high salinity (300 mM NaCl) results in a swelling of thylakoids and disappearance of grana and in a decrease of Fm and (Fv/Fm) leading to the down-regulation of PSII activity. In addition, a significant increase in F0 occurred and could be associated to the presence of some Q A⁻ in darkness in equilibrium with a partially reduced PQ pool. High salt treatment could be responsible for the thermal phase which induced an increase in chl a fluorescence (JIP rise with oxidized PQ pool).
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Soil salinity is destroying arable land and is considered to be one of the major threats to global food security in the 21st century. Therefore, the ability of naturally salt-tolerant halophyte plants to sequester large quantities of salt in external structures, such as epidermal bladder cells (EBCs), is of great interest. Using Chenopodium quinoa, a pseudo-cereal halophyte of great economic potential, we have shown previously that, upon removal of salt bladders, quinoa becomes salt sensitive. In this work, we analyzed the molecular mechanism underlying the unique salt dumping capabilities of bladder cells in quinoa. The transporters differentially expressed in the EBC transcriptome and functional electrophysiological testing of key EBC transporters in Xenopus oocytes revealed that loading of Na+ and Cl- into EBCs is mediated by a set of tailored plasma and vacuole membrane-based sodium-selective channel and chloride-permeable transporter.
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Quinoa (Chenopodium quinoa Willd.) has gained considerable attention worldwide during the past decade due to its nutritional and health benefits. However, its susceptibility to high temperatures has been reported as a serious obstacle to its global production. The objective of this study was to evaluate quinoa growth and pollen morphology in response to high temperatures. Pollen morphology and viability, plant growth and seed set, and several physiological parameters were measured at anthesis in two genotypes of quinoa subjected to day/night temperatures of 22/16°C as a control treatment and 40/24°C as the heat stress treatment. Our results showed that heat stress reduced the pollen viability between 30% and 70%. Although no visible morphological differences were observed on the surface of the pollen between the heat‐stressed and non‐heat‐stressed treatments, the pollen wall (intine and extine) thickness increased due to heat stress. High temperature did not affect seed yield, seed size and leaf greenness. On the other hand, high temperature improved the rate of photosynthesis. We found that quinoa has a high plasticity in response to high temperature, though pollen viability and pollen wall structure were affected by high temperatures in anthesis stage. This study is also the first report of quinoa pollen being trinucleate.