Soil salinization is a global agro-ecological problem and a major factor impeding agricultural development. Planting salt-tolerant plants to improve saline soils offers both ecological and economic benefits. Currently, there are few studies addressing the combined effects of salt and alkali stress. Quinoa is known for its salinity tolerance. However, research has predominantly focused on the effects of salinity stress on quinoa’s morphology and physiology, with its molecular mechanisms remaining unclear. To better understand quinoa’s response mechanisms to salinity and alkali stress, we employed RNA-seq technology to analyze transcriptomes under these conditions. We identified 1833 differentially expressed genes (DEGs) under salt stress and 2233 DEGs under alkali stress. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) annotations revealed that quinoa responds to salt and alkali stress through similar mechanisms. Both stresses promoted sucrose synthesis, starch synthesis and catabolism, which increased the osmotic potential of quinoa leaves. Additionally, there was a regulation of the down-regulated expression of the abscisic acid receptor PYR/PYL and the up-regulated expression of the serine/threonine protein kinase (PP2C) gene in the ABA signaling pathway. Contrasting with salt tolerance, the mechanism specific to quinoa’s alkalinity tolerance involves the up-regulation of the citric acid cycle via an active γ-aminobutyric acid (GABA) branch, enhancing quinoa’s energy metabolism. In summary, our transcriptome analysis revealed key regulatory mechanisms in quinoa’s response to saline and alkaline stress. This study deepens the understanding of quinoa’s stress response mechanisms and provides theoretical references for the biological improvement of salinized soils.

Drought stress seriously threatens human food security, and enhancing crops’ drought tolerance is an urgent problem to be solved in breeding. Quinoa is known for its high nutritional value and strong drought tolerance, but its molecular mechanism in response to drought stress is still unclear. In this study, we used drought-tolerant (D2) and drought-sensitive (ZK1) quinoa varieties, and PEG-6000 was used to simulate drought stress in quinoa seedlings. Phenotypic and physiological biochemical indicators were measured during the seedling stage, and LC-MS was used for a metabolite analysis of drought stress to explore the drought tolerance mechanism of quinoa under drought stress. With the intensification of drought stress, chlorophyll content gradually increased, and D2 reached its maximum at W4, an increase of 49.85% compared with W1. The total chlorophyll content, photosynthesis rate, and stomatal conductance of ZK1 were significantly lower than D2 under moderate and severe drought stress. Metabolomic results showed that a total of 1295 positive ion mode (pos) metabolites and 914 negative ion mode (neg) metabolites were identified. Of these, 12(R)-HETE, phosphatidylcholine, monogalactose diester (MGDG), and stachyose up-regulated expression under drought stress. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis showed that unsaturated fatty acid biosynthesis and glycerophospholipid metabolism pathways were significantly enriched. In summary, our results elucidate that quinoa responds to drought stress by accumulating chlorophyll and sugars, activating unsaturated fatty acid metabolism, and protecting the photosynthetic system. These findings provide new insights for the breeding of drought-tolerant quinoa varieties and the study of drought tolerance mechanisms.

Quinoa (Chenopodium quinoa Willd.) is an annual broadleaf plant belonging to the Amaranthaceae family. It is a nutritious food crop and is considered to be drought-tolerant, but drought is still one of the most important abiotic stress factors limiting its yield. Quinoa responses to drought are related to drought intensity and genotype. This study used two different drought-responsive quinoa cultivars, LL1 (drought-tolerant) and ZK1 (drought-sensitive), to reveal the important mechanisms of drought response in quinoa by combining physiological, transcriptomic, and metabolomic analyses. The physiological analysis indicated that Chla/Chlb might be important for drought tolerance in quinoa. A total of 1756 and 764 differentially expressed genes (DEGs) were identified in LL1 and ZK1, respectively. GO (Gene Ontology) enrichment analysis identified 52 common GO terms, but response to abscisic acid (GO:0009737) and response to osmotic stress (GO:0006970) were only enriched in LL1. KEGG (Kyoto Encyclopedia of Genes and Genomes) analysis revealed that glycerophospholipid metabolism (ko00564) and cysteine and methionine metabolism (ko00270) ranked at the top of the list in both cultivars. A total of 1844 metabolites were identified by metabolomic analysis. “Lipids and lipid-like” molecules had the highest proportions. The DEMs in LL1 and ZK1 were mainly categorized 6 and 4 Human Metabolome Database (HMDB) superclasses, respectively. KEGG analysis revealed that the ‘α-linolenic acid metabolism’ was enriched in both LL1 and ZK1. Joint KEGG analysis also revealed that the ‘α-linolenic acid metabolism’ pathway was enriched by both the DEGs and DEMs of LL1. There were 17 DEGs and 8 DEMs enriched in this pathway, and methyl jasmonate (MeJA) may play an important role in the drought response of quinoa. This study will provide information for the identification of drought resistance in quinoa, research on the molecular mechanism of drought resistance, and genetic breeding for drought resistance in quinoa.

Soil salinization and alkalization caused by global climate change have become major constraints on crop production worldwide. Quinoa (Chenopodium quinoa Willd.), owing to its exceptional adaptability to adverse environmental conditions, is considered a promising crop for saline–alkali agriculture. Successful screening and evaluation of saline–alkali-tolerant germplasm at the germination stage is essential for breeding quinoa varieties with enhanced tolerance to compound saline–alkali stress. In this study, 23 quinoa accessions originating from different regions were evaluated for saline–alkali tolerance by exposing seeds to compound saline–alkali solutions at different concentrations in a Petri dish germination assay. During the germination stage, relative vigor index, germination rate, germination energy, shoot length, root length, and fresh weight were determined, and saline–alkali tolerance was assessed using multivariate statistical analyses. The germination ability and seedling growth potential of quinoa germplasm gradually declined with increasing saline–alkali stress. Based on the comprehensive saline–alkali tolerance index at the germination stage, eight accessions were identified as highly tolerant and four accessions as highly sensitive to saline–alkali stress. Among them, LL1 and Z27 exhibited outstanding tolerance and were identified as elite saline–alkali-tolerant germplasm resources. The results indicated that vigor index and fresh weight at the germination stage can serve as key parameters for evaluating saline–alkali tolerance in quinoa germplasm. Overall, this study provides valuable germplasm resources and a practical basis for breeding new quinoa varieties with enhanced saline–alkali tolerance, as well as for the identification and utilization of stress-resistance-related genes in quinoa.