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Salt stress is a major environmental threat influencing crop growth and yield. The plasma membrane (PM) is believed to be one facet of the cellular mechanisms of salt adaptation. Choline priming has been reported to enhance salt tolerance of the sensitive wheat cultivar used in this work. The study was, therefore, undertaken to examine whether changes in the PM lipids will participate in cholineimproved salt tolerance. The caryopses were primed in choline chloride (0, 5 and 10 mM) for 24 h. They were then germinated in sand for 10 days, watered with 1/4-strength modified Hoagland solution (MHS). The seedlings were grown in the sand, watered with MHS containing 150 mM NaCl for 3 weeks. Root PM was isolated by two-phase partitioning method and its lipid classes were determined. Choline maintained the PM total lipids, sterol and phospholipids, which were altered by NaCl. The PM sterols/ phospholipids ratio was decreased by NaCl, whereas choline retained this ratio. Salt stress reduced the PM unsaturated fatty acids while increased its saturated fatty acids. Choline alleviated PM unsaturated/saturated ratio reduction. NaCl declined the PM phosphatidylcholine (PC), phosphatidylglycerol (PG) and diphosphatidylglycerol (DPG) whereas increased phosphatidylserine (PS), phosphatidylinositol (PI) and phosphatidylethanolamine (PE). Choline decreased PS and PE, while increased PC level. The PM cholesterol, campesterol and β-sitosterol were increased while stigmasterol was declined under NaCl. Choline increased stigmasterol whereas decreased cholesterol and campesterol. The alterations in the PM lipids were discussed in relation to choline-enhanced salt tolerance.
Two contrasting maize (Zea mays L.) cultivars, i.e., Giza 2 (salt tolerant) and Trihybrid 321 (salt sensitive), were grown hydroponically to study NaCl effect (100 mM) on root plasma membrane (PM) lipid and protein alterations. The PM total sterols of Trihybrid 321 were decreased while that of Giza 2 was increased in response to salt. Salt imposition had no significant effect on PM total glycolipids and proteins of both cultivars. The PM total phospholipids were increased in Trihybrid 321 but it did not change significantly in Giza 2 after salinity stress. Molecular percentage of PM phospholipids and fatty acids of both cultivars was different in absence (0 mM) and presence (100 mM) of salt. The most abundant phospholipids in untreated Trihybrid 321 PM were phosphatidylglycerol (PG), phosphatidylcholine (PC), phosphatidylethanolamine (PE) and phosphatidylserine (PS), which changed into PG, PS, phosphatidylinositol (PI) and PC after salt treatment. However, the dominant phospholipids of the control PM of Giza 2 were PC, PE, PS and PG, which changed into PG, PE, PS and diphosphatidylglycerol (DPG) after salt imposition. Over 60% of the total fatty acids were saturated in control and salinized PM of both cultivars, which was increased after salt stress. The predominant fatty acid in the control and salinized PM of Trihybrid 321 was C18:1 and C17:0, respectively. However, in control and treated PM of Giza 2, the predominant fatty acid was C17:0 and C20:0, respectively. Qualitative and quantitative differences in PM protein patterns were found in both cultivars with and without salt. PM lipid changes enhanced membrane integrity, reflected in different ion accumulation (Mansour et al. 2005), and hence salt tolerance of Giza 2.
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