Physiological and Metabolomic Analysis in Roots of Hordeum jubatum L. In Response to Iso-osmotic Stress
摘要
The ornamental grass Hordeum jubatum L. is noted for its tolerance to salinity, alkalinity, and drought. This study compared root physiological and metabolic responses under iso-osmotic salt, alkali, and polyethylene glycol (PEG)-simulated drought stresses (hereafter “water stress”) to clarify stress-specific tolerance mechanisms. Seedlings were exposed to iso-osmotic treatments at − 0.2, − 0.4, and − 0.8 MPa. We measured root biomass and morphology, lipid peroxidation (malondialdehyde, MDA), osmolytes (proline and soluble sugars), antioxidant enzymes (superoxide dismutase, SOD; peroxidase, POD; ascorbate peroxidase, APX; catalase, CAT; Na⁺ and K⁺ contents, and profiled root metabolites by untargeted liquid chromatography–mass spectrometry (LC–MS). Showed that all treatments reduced root biomass and activity, with the most significant declines occurring under alkali stress and the smallest under water stress. MDA increased under all stresses, particularly under alkali. Proline increased significantly only under alkali stress, while it remained similar to control under salt and water stresses. Salt and alkali stresses caused substantial Na⁺ accumulation and K⁺ loss in roots. In contrast, water-stressed roots maintained low Na⁺ and relatively higher K⁺. Antioxidant defenses (SOD, POD, APX) were upregulated — especially under alkali stress — while CAT activity declined at severe water potential. Metabolomic analysis at − 0.8 MPa revealed treatment-specific shifts: salt and alkali stresses were enriched in the tricarboxylic acid (TCA) cycle and related organic acid pathways, whereas water stress was associated with enrichment in amino acid metabolism pathways. Under iso-osmotic conditions, root physiological indicators of H. jubatum were less inhibited by PEG-simulated water stress than by salt or alkali stresses. However, salt and alkali induced broader metabolic reprogramming — notably in TCA and organic-acid metabolism — indicating stress-specific differences in ionic balance and metabolic regulation.