References
- Guo J, Suo S, Wang B. Sodium chloride improves seed vigour of the euhalophyte Suaeda salsa. Seed Sci Res. 2015;25:1–9. doi:https://doi.org/10.1017/S0960258515000239.
- An J, Yao J, Xu R, You C, Wang X, Hao Y. An apple NAC transcription factor enhances salt stress tolerance by modulating the ethylene response. Physiol Planta. 2018;164:279–289. doi:https://doi.org/10.1111/ppl.12724.
- Li M, Guo S, Xu Y, Meng Q, Li G, Yang X. Glycine betaine-mediated potentiation of HSP gene expression involves calcium signaling pathways in tobacco exposed to NaCl stress. Physiol Planta. 2014;150:63–75. doi:https://doi.org/10.1111/ppl.1206.
- Sui N, Yang Z, Liu M, Wang B. Identification and transcriptomic profiling of genes involved in increasing sugar content during salt stress in sweet sorghum leaves. BMC Genomics. 2015;16:534. doi:https://doi.org/10.1186/s12864-015-1760-5.
- Feng Z, Deng Y, Fan H, Sun QJ, Sui N, Wang BS. Effects of NaCl stress on the growth and photosynthetic characteristics of Ulmus pumila L. seedlings in sand culture. Photosynthetica. 2014;52:313–320. doi:https://doi.org/10.1007/s11099-014-0032-y.
- Ma X, Wang G, Zhao W, Yang M, Ma N, Kong F, Dong X, Meng Q. SlCOR413IM1: A novel cold-regulation gene from tomato, enhances drought stress tolerance in tobacco. J Plant Physiol. 2017;216:88–99. doi:https://doi.org/10.1016/j.jplph.2017.03.016.
- You L, Song Q, Wu Y, Li S, Jiang C, Chang L, Yang X, Zhang J. Accumulation of glycine betaine in transplastomic potato plants expressing choline oxidase confers improved drought tolerance. Planta. 2019;249:1963–1975. doi:https://doi.org/10.1007/s00425-019-03132-3.
- Cui F, Sui N, Duan G, Liu Y, Han Y, Liu S, Wan S, Li G. Identification of metabolites and transcripts involved in salt stress and recovery in peanut. Front Plant Sci. 2018;9:217. doi:https://doi.org/10.3389/fpls.2018.00217.
- Tao LI, Liu R, Xinhua HE, Wang B. Enhancement of superoxide dismutase and catalase activities and salt tolerance of euhalophyte Suaeda salsa L. by mycorrhizal fungus glomus mosseae. Pedosphere. 2012;22:217–224. doi:https://doi.org/10.1016/S1002-0160(12)60008-3.
- Feng Z, Sun Q, Deng Y, Sun S, Zhang J, Wang B. Study on pathway and characteristics of ion secretion of salt glands of Limonium bicolor. Acta Physiol Planta. 2014;36:2729–2741. doi:https://doi.org/10.1007/s11738-014-1644-3.
- Guo YY, Tian SS, Liu S, Wang W, Sui N. Energy dissipation and antioxidant enzyme system protect photosystem II of sweet sorghum under drought stress. Photosynthetica. 2018;56:861–872. doi:https://doi.org/10.1007/s11099-017-0741-0.
- Liu Q, Liu R, Ma Y, Song J. Physiological and molecular evidence for Na+ and Cl− exclusion in the roots of two Suaeda salsa populations. Aquat Bot. 2018;146:1–7. doi:https://doi.org/10.1016/j.aquabot.2018.01.001.
- Zheng G, Li L, Li W. Glycerolipidome responses to freezing- and chilling-induced injuries: examples in Arabidopsis and rice. BMC Plant Biol. 2016;16:70. doi:https://doi.org/10.1186/s12870-016-0758-8.
- Feng ZT, Deng YQ, Zhang SC, Liang X, Yuan F, Hao JL, Zhang JC, Sun SF, Wang BS. K(+) accumulation in the cytoplasm and nucleus of the salt gland cells of Limonium bicolor accompanies increased rates of salt secretion under NaCl treatment using NanoSIMS. Plant Sci. 2015;238:286–296. doi:https://doi.org/10.1016/j.plantsci.2015.06.021.
- Shaheen HL, Iqbal M, Azeem M, Shahbaz M, Shehzadi M. K-priming positively modulates growth and nutrient status of salt-stressed cotton (Gossypium hirsutum) seedlings. Arch Agron Soil Sci. 2016;62:759–768. doi:https://doi.org/10.1080/03650340.2015.1095292.
- Duan M, Feng H, Wang L, Li D, Meng Q. Overexpression of thylakoidal ascorbate peroxidase shows enhanced resistance to chilling stress in tomato. J Plant Physiol. 2012;169:867–877. doi:https://doi.org/10.1016/j.plantsci.2015.06.021.
- Duan M, Ma NN, Li D, Deng YS, Kong FY, Lv W, Meng QW. Antisense-mediated suppression of tomato thylakoidal ascorbate peroxidase influences anti-oxidant network during chilling stress. Plant Physiol Biochem. 2012;58:37–45. doi:https://doi.org/10.1016/j.plaphy.2012.06.007.
- Song Y, Li J, Liu M, Meng Z, Liu K, Sui N. Nitrogen increases drought tolerance in maize seedlings. Funct Plant Biol. 2019;46:350–359. doi:https://doi.org/10.1016/j.plantsci.2015.06.021.
- Yang J, Li M, Xie X, Han G, Sui N, Wang B. Deficiency of phytochrome B alleviates chilling-induced photoinhibition in rice. Am J Bot. 2013;100:1860–1870. doi:https://doi.org/10.3732/ajb.1200574.
- Liu Z, Yue M, Yang D, Zhu S, Ma N, Meng Q. Over-expression of SlJA2 decreased heat tolerance of transgenic tobacco plants via salicylic acid pathway. Plant Cell Rep. 2017;36:529–542. doi:https://doi.org/10.1007/s00299-017-2100-9.
- Cheng S, Yang Z, Wang M, Song J, Sui N, Fan H. Salinity improves chilling resistance in Suaeda salsa. Acta Physiol Planta. 2014;36:1823–1830. doi:https://doi.org/10.1007/s11738-014-1555-3.
- Zhuang K, Gao Y, Liu Z, Diao P, Sui N, Meng Q, Meng C, Kong F. WHIRLY1 regulates HSP21.5A expression to promote thermotolerance in tomato. Plant Cell Physiol. 2020;61:169–177. doi:https://doi.org/10.1093/pcp/pcz189.
- Zhou B, Deng Y, Kong F, Li B, Meng Q. Overexpression of a tomato carotenoid ɛ-hydroxylase gene alleviates sensitivity to chilling stress in transgenic tobacco. Plant Physiol Biochem. 2013;70:235–245. doi:https://doi.org/10.1016/j.plaphy.2013.05.035.
- Kong F, Deng Y, Wang G, Wang J, Liang X, Meng Q. LeCDJ1, a chloroplast DnaJ protein, facilitates heat tolerance in transgenic tomatoes. J Integr Plant Biol. 2014;56:63–74. doi:https://doi.org/10.1111/jipb.12119.
- Liu L. Distribution and dynamics of electron transport complexes in cyanobacterial thylakoid membranes. Biochim Biophys Acta. 2016;1857:256–265. doi:https://doi.org/10.1016/j.bbabio.2015.11.010.
- Shu DF, Wang LY, Duan M, Deng YS, Meng QW. Antisense-mediated depletion of tomato chloroplast glutathione reductase enhances susceptibility to chilling stress. Plant Physiol Biochem. 2011;49:1228–1237. doi:https://doi.org/10.1016/j.plaphy.2011.04.005.
- Wang LF. Physiological and molecular responses to drought stress in rubber tree (Hevea brasiliensis Muell. Arg.) Plant Physiol Biochem. 2014;83:243–249. doi:https://doi.org/10.1016/j.plaphy.2014.08.012.
- Ivanov AG, Velitchkova MY, Allakhverdiev SI, Huner NPA. Heat stress-induced effects of photosystem I: an overview of structural and functional responses. Photosynth Res. 2017;133:17–30. doi:https://doi.org/10.1007/s11120-017-0383-x.
- Chaves MM, Flexas J, Pinheiro C. Photosynthesis under drought and salt stress: regulation mechanisms from whole plant to cell. Ann Bot. 2009;103:551–560. doi:https://doi.org/10.1093/aob/mcn125.
- Chen S, Jia H, Wang X, Shi C, Wang X, Ma P, Wang J, Ren M, Li J. Hydrogen sulfide positively regulates abscisic acid signaling through persulfidation of SnRK2.6 in guard cells. Mol Plant. 2020. doi:https://doi.org/10.1016/j.molp.2020.01.004.
- Ferreyroa GV, Lagorio MG, Trinelli MA, Lavado RS, Molina FV. Lead effects on Brassica napus photosynthetic organs. Ecotoxicol Environ Saf. 2017;140:123–130. doi:https://doi.org/10.1016/j.ecoenv.2017.02.031.
- Han H, Gao S, Li B, Dong XC, Feng HL, Meng QW. Overexpression of violaxanthin de-epoxidase gene alleviates photoinhibition of PSII and PSI in tomato during high light and chilling stress. J Plant Physiol. 2010;167:176–183. doi:https://doi.org/10.1016/j.jplph.2009.08.009.
- Peng X, Teng L, Yan X, Zhao M, Shen S. The cold responsive mechanism of the paper mulberry: decreased photosynthesis capacity and increased starch accumulation. BMC Genomics. 2015;16:898. doi:https://doi.org/10.1186/s12864-015-2047-6.
- Upchurch RG. Fatty acid unsaturation, mobilization, and regulation in the response of plants to stress. Biotechnol Lett. 2008;30:967–977. doi:https://doi.org/10.1007/s10529-008-9639-z.
- Mikami K, Murata N. Membrane fluidity and the perception of environmental signals in cyanobacteria and plants. Prog Lipid Res. 2003;42:527–543. doi:https://doi.org/10.1016/S0163-7827(03)00036-5.
- Kachroo A, Kachroo P. Fatty acid-derived signals in plant defense. Ann Rev Phytopathol. 2009;47:153–176. doi:https://doi.org/10.1146/annurev-phyto-080508-081820.
- ScottiCampos P, PhamThi A. Correlation between total lipids, linolenic acid and membrane injury under PEG-induced dehydration in leaves of Vigna genotypes differing in drought resistance. Emirates J Food Agr. 2016;28:485. doi:https://doi.org/10.9755/ejfa.2016-04-342.
- Guo Q, Liu L, Barkla BJ. Membrane lipid remodeling in response to salinity. Int J Mol Sci. 2019;20:4264. doi:https://doi.org/10.3390/ijms20174264.
- Moellering ER, Benning C. Galactoglycerolipid metabolism under stress: a time for remodeling. Trends Plant Sci. 2011;16:98–107. doi:https://doi.org/10.1016/j.tplants.2010.11.004.
- Shimojima M, Madoka Y, Fujiwara R, Murakawa M, Yoshitake Y, Ikeda K, Koizumi R, Endo K, Ozaki K, Ohta H. An engineered lipid remodeling system using a galactolipid synthase promoter during phosphate starvation enhances oil accumulation in plants. Front Plant Sci. 2015;6:664. doi:https://doi.org/10.3389/fpls.2015.00664.
- Mizusawa N, Wada H. The role of lipids in photosystem II. Biochim Biophys Acta. 2012;1817:194–208. doi:https://doi.org/10.1016/j.bbabio.2011.04.008.
- Siegenthaler PA. Molecular organization of acyl lipids in photosynthetic membranes of higher plants. Springer, Dordrecht. 1998;6:119–144. doi:https://doi.org/10.1007/0-306-48087-5_7.
- Benning C. Mechanisms of lipid transport involved in organelle biogenesis in plant cells. Annu Rev Cell Dev Biol. 2009;25:71–91. doi:https://doi.org/10.1146/annurev.cellbio.042308.113414.
- Troncosoponce MA, Nikovics K, Marchive C, Lepiniec L, Baud S. New insights on the organization and regulation of the fatty acid biosynthetic network in the model higher plant Arabidopsis thaliana. Biochimie. 2016;120:3–8. doi:https://doi.org/10.1016/j.biochi.2015.05.013.
- Libeisson Y, Shorrosh BS, Beisson F, Andersson MX, Arondel V, Bates PD, Welti R. Acyl-Lipid metabolism. The Arabidopsis Book. 2010;11:1–70. doi:https://doi.org/10.1199/tab.0161.
- Holzl G, Dormann P. Chloroplast lipids and their biosynthesis. Annu Rev Plant Biol. 2019;70:51–81. doi:https://doi.org/10.1146/annurev-arplant-050718-100202.
- Li N, Xu C, Li-Beisson Y, Philippar K. Fatty acid and lipid transport in plant cells. Trends Plant Sci. 2016;21:145–158. doi:https://doi.org/10.1016/j.tplants.2015.10.011.
- Boudiere L, Michaud M, Petroutsos D, Rebeille F, Falconet D, Bastien O, Roy S, Finazzi G, Rolland N, Jouhet J, et al. Glycerolipids in photosynthesis: composition, synthesis and trafficking. Biochim Biophys Acta. 2014;1837:470–480. doi:https://doi.org/10.1016/j.bbabio.2013.09.007.
- Joyard J, Ferro M, Masselon CD, Seigneurinberny D, Salvi D, Garin J, Rollanda N. Chloroplast proteomics highlights the subcellular compartmentation of lipid metabolism. Prog Lipid Res. 2010;49:128–158. doi:https://doi.org/10.1016/j.plipres.2009.10.003.
- Browse J, Warwick N, Somerville C, Slack CR. Fluxes through the prokaryotic and eukaryotic pathways of lipid synthesis in the ‘16:3ʹ plant Arabidopsis thaliana. Bioche J. 1986;235:25–31. doi:https://doi.org/10.1042/bj2350025.
- Awai K, Marechal E, Block MA, Brun D, Masuda T, Shimada H, Takamiya K, Ohta H, Joyard J. Two types of MGDG synthase genes, found widely in both 16:3 and 18:3 plants, differentially mediate galactolipid syntheses in photosynthetic and nonphotosynthetic tissues in Arabidopsis thaliana. Proc Natl Acad Sci USA. 2001;98:10960–10965. doi:https://doi.org/10.1073/pnas.181331498.
- Wang Z, Benning C. Chloroplast lipid synthesis and lipid trafficking through ER-plastid membrane contact sites. Biochem Soc Trans. 2012;40:457–463. doi:https://doi.org/10.1042/BST20110752.
- Frentzen M, Heinz E, Mckeon TA, Stumpf PK. Specificities and selectivities of glycerol-3-phosphate acyltransferase and monoacylglycerol-3-phosphate acyltransferase from pea and spinach chloroplasts. Febs J. 2005;129:629–636. doi:https://doi.org/10.1111/j.1432-1033.1983.tb07096.x.
- Petroutsos D, Amiar S, Abida H, Dolch L, Bastien O, Rebeille F, Jouhet J, Falconet BMA, Mcfadden GI, Bowler C, et al. Evolution of galactoglycerolipid biosynthetic pathways-From cyanobacteria to primary plastids and from primary to secondary plastids. Prog Lipid Res. 2014;54:68–85. doi:https://doi.org/10.1016/j.plipres.2014.02.001.
- Kobayashi K. Role of membrane glycerolipids in photosynthesis, thylakoid biogenesis and chloroplast development. J Plant Res. 2016;129:565–580. doi:https://doi.org/10.1007/s10265-016-0827-y.
- Hurlock AK, Roston RL, Wang K, Benning C. Lipid trafficking in plant cells. Traffic. 2014;15:915–932. doi:https://doi.org/10.1111/tra.12187.
- Li N, Zhang Y, Meng H, Li S, Wang S, Xiao Z, Chang P, Zhang X, Li Q, Guo L, et al. Characterization of fatty acid exporters involved in fatty acid transport for oil accumulation in the green alga Chlamydomonas reinhardtii. Biotechnol Biofuels. 2019;12:14. doi:https://doi.org/10.1186/s13068-018-1332-4.
- Botella C, Jouhet J, Block MA. Importance of phosphatidylcholine on the chloroplast surface. Prog Lipid Res. 2017;65:12–23. doi:https://doi.org/10.1016/j.plipres.2016.11.001.
- Li N, Gugel IL, Giavalisco P, Zeisler V, Schreiber L, Soll J, Philippar K. FAX1, a novel membrane protein mediating plastid fatty acid export. PLoS Biol. 2015;13:e1002053. doi:https://doi.org/10.1371/journal.pbio.1002053.
- Kim S, Yamaoka Y, Ono H, Kim H, Shim D, Maeshima M, Martinoia E, Cahoon EB, Nishida I, Lee Y. AtABCA9 transporter supplies fatty acids for lipid synthesis to the endoplasmic reticulum. Proc Natl Acad Sci USA. 2013;110:773–778. doi:https://doi.org/10.1073/pnas.1214159110.
- Lousa CDM, Van Roermund CWT, Postis VLG, Dietrich D, Kerr ID, Wanders RJA, Stephen A, Baldwin SA, Baker A, Theodoulou FL. Intrinsic acyl-CoA thioesterase activity of a peroxisomal ATP binding cassette transporter is required for transport and metabolism of fatty acids. Proc Natl Acad Sci USA. 2013;110:1279–1284. doi:https://doi.org/10.1073/pnas.1218034110.
- Theodoulou FL, Carrier DJ, Schaedler TA, Baldwin SA, Baker A. How to move an amphipathic molecule across a lipid bilayer: different mechanisms for different ABC transporters? Biochem Soc Trans. 2016;44:774–782. doi:https://doi.org/10.1042/BST20160040.
- LaBrant E, Barnes AC, Roston RL. Lipid transport required to make lipids of photosynthetic membranes. Photosynth Res. 2018;138:345–360. doi:https://doi.org/10.1007/s11120-018-0545-5.
- Chapman KD, Ohlrogge JB. Compartmentation of Triacylglycerol Accumulation in Plants. J Biol Chem. 2012;287:2288–2294. doi:https://doi.org/10.1074/jbc.R111.290072.
- Bates PD, Ohlrogge JB, Pollard M. Incorporation of newly synthesized fatty acids into cytosolic glycerolipids in pea leaves occurs via acyl editing. J Biological Chem. 2007;282:31206–31216. doi:https://doi.org/10.1074/jbc.M705447200.
- Xu C, Moellering ER, Muthan B, Fan J, Benning C. Lipid transport mediated by arabidopsis TGD proteins is unidirectional from the endoplasmic reticulum to the plastid. Plant Cell Physiol. 2010;51:1019–1028. doi:https://doi.org/10.1093/pcp/pcq053.
- Yang Y, Zienkiewicz A, Lavell A, Benning C. Coevolution of domain interactions in the chloroplast TGD1, 2, 3 lipid transfer complex specific to brassicaceae and poaceae plants. Plant Cell. 2017;29:1500–1515. doi:https://doi.org/10.1105/tpc.17.00182.
- Roston RL, Gao J, Murcha MW, Whelan J, Benning C. TGD1, −2, and −3 proteins involved in lipid trafficking form ATP-binding cassette (ABC) transporter with multiple substrate-binding proteins. J Biol Chem. 2012;287:21406–21415. doi:https://doi.org/10.1074/jbc.M112.370213.
- Xu C, Fan J, Cornish AJ, Benning C. Lipid trafficking between the endoplasmic reticulum and the plastid in Arabidopsis requires the extraplastidic TGD4 protein. Plant Cell. 2008;20:2190–2204. doi:https://doi.org/10.1105/tpc.108.061176.
- Fan J, Zhai Z, Yan C, Xu C. Arabidopsis TRIGALACTOSYLDIACYLGLYCEROL5 interacts with TGD1, TGD2, and TGD4 to facilitate lipid transfer from the endoplasmic reticulum to plastids. Plant Cell. 2015;27:2941–2955. doi:https://doi.org/10.1105/tpc.15.00394.
- Zhao L, Katavic V, Li F, Haughn GW, Kunst L. Insertional mutant analysis reveals that long-chain acyl-CoA synthetase 1 (LACS1), but not LACS8, functionally overlaps with LACS9 in Arabidopsis seed oil biosynthesis. Plant J. 2010;64:1048–1058. doi:https://doi.org/10.1111/j.1365-313X.2010.04396.x.
- Jessen D, Roth C, Wiermer M, Fulda M. Two activities of long-chain Acyl-Coenzyme a synthetase are involved in lipid trafficking between the endoplasmic reticulum and the plastid in Arabidopsis. Plant Physiol. 2015;167:351–366. doi:https://doi.org/10.1104/pp.114.250365.
- Gigon A, Matos AR, Laffray D, Zuilyfodil Y, Phamthi A. Effect of drought stress on lipid metabolism in the leaves of Arabidopsis thaliana (Ecotype Columbia). Ann Bot. 2004;94:345–351. doi:https://doi.org/10.1093/aob/mch150.
- Lin YT, Chen LJ, Herrfurth C, Feussner I, Li HM. Reduced biosynthesis of digalactosyldiacylglycerol, a major chloroplast membrane lipid, leads to oxylipin overproduction and phloem Cap lignification in Arabidopsis. Plant Cell. 2016;28:219–232. doi:https://doi.org/10.1105/tpc.15.01002.
- Shao RX, Xin LF, Zheng HF, Li LL, Ran WL, Mao J, Yang QH. Changes in chloroplast ultrastructure in leaves of drought-stressed maize inbred lines. Photosynthetica. 2016;54:74–80. doi:https://doi.org/10.1007/s11099-015-0158-6.
- Janik E, Bednarska J, Zubik M, Puzio M, Luchowski R, Grudzinski W, Mazur R, Garstka M, Maksymiec W, Kulik A, et al. Molecular architecture of plant thylakoids under physiological and light stress conditions: a study of lipid-light-harvesting complex ii model membranes. Plant Cell. 2013;25:2155–2170. doi:https://doi.org/10.2307/23482454.
- Varone L, Ribas-Carbo M, Cardona C, Gallé A, Medrano H, Gratani L, Flexasb J. Stomatal and non-stomatal limitations to photosynthesis in seedlings and saplings of Mediterranean species pre-conditioned and aged in nurseries: different response to water stress. Environ Exp Bot. 2012;75:235–247. doi:https://doi.org/10.1016/j.envexpbot.2011.07.007.
- Zhang FJ, Zhang KK, Du CZ, Li J, Xing YX, Yang LT, Li YR. Effect of drought stress on anatomical structure and chloroplast ultrastructure in leaves of sugarcane. Sugar Tech. 2014;17:41–48. doi:https://doi.org/10.1007/s12355-014-0337-y.
- Grigorova B, Vassileva V, Klimchuk D, Vaseva I, Demirevska K, Feller U. Drought, high temperature, and their combination affect ultrastructure of chloroplasts and mitochondria in wheat (Triticum aestivum L.) leaves. J Plant Interactions. 2012;7:204–213. doi:https://doi.org/10.1080/17429145.2011.654134.
- Kong X, Wei B, Gao Z, Zhou Y, Shi F, Zhou X, Zhou Q, Ji S. Changes in membrane lipid composition and function accompanying chilling injury in bell peppers. Plant Cell Physiol. 2018;59:167–178. doi:https://doi.org/10.1093/pcp/pcx171.
- Moellering ER, Muthan B, Benning C. Freezing tolerance in plants requires lipid remodeling at the outer chloroplast membrane. Science. 2010;330:226–228. doi:https://doi.org/10.1126/science.1191803.
- Yang S, Tang XF, Ma NN, Wang LY, Meng QW. Heterology expression of the sweet pepper CBF3 gene confers elevated tolerance to chilling stress in transgenic tobacco. J Plant Physiol. 2011;168:1804–1812. doi:https://doi.org/10.1016/j.jplph.2011.05.017.
- Zou M, Yuan L, Zhu S, Liu S, Ge J. Effects of heat stress on photosynthetic characteristics and chloroplast ultrastructure of a heat-sensitive and heat-tolerant cultivar of wucai (Brassica campestris L.). Acta Physiol Plant. 2016. doi:https://doi.org/10.1007/s11738-016-2319-z.
- Lee MH, Cho EJ, Wi SG, Bae H, Kim J, Cho J, Lee SB, Kim JH, Chung BY. Divergences in morphological changes and antioxidant responses in salt-tolerant and salt-sensitive rice seedlings after salt stress. Plant Physiol Biochem. 2013;70:325–335. doi:https://doi.org/10.1016/j.plaphy.2013.05.047.
- Feng L, Wu QY, Sun YL, Wang LY, Yang XH, Meng QW. Overexpression of chloroplastic monodehydroascorbate reductase enhanced tolerance to temperature and methyl viologen-mediated oxidative stresses. Physiologia Plantarum. 2010;139:421–434. doi:https://doi.org/10.1111/j.1399-3054.2010.01369.x.
- Velikova V, Muller C, Ghirardo A, Rock TM, Aichler M, Walch A, Schmittkopplin P, Schnitzler J. Knocking down of isoprene emission modifies the lipid matrix of thylakoid membranes and influences the chloroplast ultrastructure in poplar. Plant Physiol. 2015;168:859–870. doi:https://doi.org/10.1104/pp.15.00612.
- Tarazona P, Feussner K, Feussner I. An enhanced plant lipidomics method based on multiplexed liquid chromatography-mass spectrometry reveals additional insights into cold-and drought-induced membrane remodeling. Plant J. 2015;84:621–633. doi:https://doi.org/10.1111/tpj.13013.
- Wang G, Kong F, Zhang S, Meng X, Wang Y, Meng Q. A tomato chloroplast-targeted DnaJ protein protects rubisco activity under heat stress. J Exp Bot. 2015;66:3027–3040. doi:https://doi.org/10.1093/jxb/erv102.
- Ma X, Chen C, Yang M, Dong X, Lv W, Meng Q. Cold-regulated protein (SlCOR413IM1) confers chilling stress tolerance in tomato plants. Plant Physiol Biochem. 2018;124:29–39. doi:https://doi.org/10.1016/j.plaphy.2018.01.003.
- Thalhammer A, Hundertmark M, Popova AV, Seckler R, Hincha DK. Interaction of two intrinsically disordered plant stress proteins (COR15A and COR15B) with lipid membranes in the dry state. Biochim Biophys Acta. 2010;1798:1812–1820. doi:https://doi.org/10.1016/j.bbamem.2010.05.015.
- Shu S, Yuan L, Guo S, Sun J, Yuan Y. Effects of exogenous spermine on chlorophyll fluorescence, antioxidant system and ultrastructure of chloroplasts in Cucumis sativus L. under salt stress. Plant Physiol Biochem. 2013;63:209–216. doi:https://doi.org/10.1016/j.plaphy.2012.11.028.
- Szymanski J, Brotman Y, Willmitzer L, Cuadrosinostroza A. Linking gene expression and membrane lipid composition of Arabidopsis. Plant Cell. 2014;26:915–928. doi:https://doi.org/10.1105/tpc.113.118919.
- Fujii S, Kobayashi K, Nakamura Y, Wada H. Inducible knockdown of MONOGALACTOSYLDIACYLGLYCEROL SYNTHASE1 reveals roles of galactolipids in organelle differentiation in Arabidopsis Cotyledons. Plant Physiol. 2014;166:1436–1449. doi:https://doi.org/10.1104/pp.114.250050.
- Aronsson H, Schottler MA, Kelly AA, Sundqvist C, Dormann P, Karim S, Jarvis P. Monogalactosyldiacylglycerol deficiency in Arabidopsis affects pigment composition in the prolamellar body and impairs thylakoid membrane energization and photoprotection in leaves. Plant Physiol. 2008;148:580–592. doi:https://doi.org/10.1104/pp.108.123372.
- Testerink C, Munnik T. Molecular, cellular, and physiological responses to phosphatidic acid formation in plants. J Exp Bot. 2011;62:2349–2361. doi:https://doi.org/10.1093/jxb/err079.
- Djanaguiraman M, Prasad PVV, Kumari J, Rengel Z. Root length and root lipid composition contribute to drought tolerance of winter and spring wheat. Plant Soil. 2018;439:57–73. doi:https://doi.org/10.1007/s11104-018-3794-3.
- Sui N, Han G. Salt-induced photoinhibition of PSII is alleviated in halophyte Thellungiella halophila by increases of unsaturated fatty acids in membrane lipids. Acta Physiol Plant. 2014;36:983–992. doi:https://doi.org/10.1007/s11738-013-1477-5.
- Liu S, Wang W, Li M, Wan S, Sui N. Antioxidants and unsaturated fatty acids are involved in salt tolerance in peanut. Acta Physiol Plant. 2017:39. doi:https://doi.org/10.1007/s11738-017-2501-y.
- Sui N, Tian S, Wang W, Wang M, Fan H. Overexpression of glycerol-3-phosphate acyltransferase from suaeda salsa improves salt tolerance in Arabidopsis. Front Plant Sci. 2017;8:1337. doi:https://doi.org/10.3389/fpls.2017.01337.
- Kalisch B, Dormann P, Holzl G. DGDG and glycolipids in plants and algae. Subcell Biochem. 2016;86:51–83. doi:https://doi.org/10.1007/978-3-319-25979-6_3.
- Hernandez ML, Sicardo MD, Martinezrivas JM. Differential Contribution of endoplasmic reticulum and chloroplast ω-3 fatty acid desaturase genes to the linolenic acid content of olive (Olea europaea) fruit. Plant Cell Physiol. 2016;57:138–151. doi:https://doi.org/10.1093/pcp/pcv159.
- Cao B, Ma Q, Zhao Q, Wang L, Xu K. Effects of silicon on absorbed light allocation, antioxidant enzymes and ultrastructure of chloroplasts in tomato leaves under simulated drought stress. Scientia Horticulturae. 2015;194:53–62. doi:https://doi.org/10.1016/j.scienta.2015.07.037.
- Kobayashi K, Fujii S, Sasaki D, Baba S, Ohta H, Masuda T, Wada H. Transcriptional regulation of thylakoid galactolipid biosynthesis coordinated with chlorophyll biosynthesis during the development of chloroplasts in Arabidopsis. Front Plant Sci. 2014;5:272. doi:https://doi.org/10.3389/fpls.2014.00272.
- Kobayashi K, Endo K, Wada H. Roles of Lipids in Photosynthesis. Sub-cellular Biochemistry. 2016;86:21–49. doi:https://doi.org/10.1007/978-3-319-25979-6_2.
- Nakajima Y, Umena Y, Nagao R, Endo K, Kobayashi K, Akita F, Suga M, Wada H, Noguchi T, Shen JR. Thylakoid membrane lipid sulfoquinovosyl-diacylglycerol (SQDG) is required for full functioning of photosystem II inThermosynechococcus elongatus. J Biol Chem. 2018;293:14786–14797. doi:https://doi.org/10.1074/jbc.RA118.004304.
- Rottet S, Besagni C, Kessler F. The role of plastoglobules in thylakoid lipid remodeling during plant development. Biochim Biophys Acta. 2015;1847:889–899. doi:https://doi.org/10.1016/j.bbabio.2015.02.002.
- Sebastiana M, Duarte B, Monteiro F, Malho R, Cacador I, Matos AR. The leaf lipid composition of ectomycorrhizal oak plants shows a drought-tolerance signature. Plant Physiol Biochem. 2019;144:157–165. doi:https://doi.org/10.1016/j.plaphy.2019.09.032.
- Shimojima M, Ohta H. Critical regulation of galactolipid synthesis controls membrane differentiation and remodeling in distinct plant organs and following environmental changes. Prog Lipid Res. 2011;50:258–266. doi:https://doi.org/10.1016/j.plipres.2011.03.001.
- Hori K, Nobusawa T, Watanabe T, Madoka Y, Suzuki H, Shibata D, Shimojima M, Ohta H. Tangled evolutionary processes with commonality and diversity in plastidial glycolipid synthesis in photosynthetic organisms. Biochim Biophys Acta. 2016;1861:1294–1308. doi:https://doi.org/10.1016/j.bbalip.2016.04.015.
- Gasulla F, Vom Dorp K, Dombrink I, Zahringer U, Gisch N, Dormann P, Bartels D. The role of lipid metabolism in the acquisition of desiccation tolerance in Craterostigma plantagineum: a comparative approach. Plant J. 2013;75:726–741. doi:https://doi.org/10.1111/tpj.12241.
- Bejaoui F, Salas JJ, Nouairi I, Smaoui A, Abdelly C, Martinezforce E, Youssef NB. Changes in chloroplast lipid contents and chloroplast ultrastructure in Sulla carnosa and Sulla coronaria leaves under salt stress. J Plant Physiol. 2016;198:32–38. doi:https://doi.org/10.1016/j.jplph.2016.03.018.
- Gondor OK, Szalai G, Kovacs V, Janda T, Pal M. Impact of UV-B on drought- or cadmium-induced changes in the fatty acid composition of membrane lipid fractions in wheat. Ecotoxicol Environ Saf. 2014;108:129–134. doi:https://doi.org/10.1016/j.ecoenv.2014.07.002.
- Botella C, Sautron E, Boudiere L, Michaud M, Dubots E, Yamaryo-Botte Y, Albrieux C, Marechal E, Block MA, Jouhet J. ALA10, a phospholipid flippase, controls FAD2/FAD3 desaturation of phosphatidylcholine in the ER and affects chloroplast lipid composition in Arabidopsis thaliana. Plant Physiol. 2016;170:1300–1314. doi:https://doi.org/10.1104/pp.15.01557.
- Lim GH, Singhal R, Kachroo A, Kachroo P. Fatty acid- and lipid-mediated signaling in plant defense. Annu Rev Phytopathol. 2017;55:505–536. doi:https://doi.org/10.1146/annurev-phyto-080516-035406.
- Zhong D, Du H, Wang Z, Huang B. Genotypic variation in fatty acid composition and unsaturation levels in bermudagrass associated with leaf dehydration tolerance. J Ame Society Horticultural Sci. 2011;136:35–40. doi:https://doi.org/10.2503/jjshs1.80.113.
- Gao Q, Yu K, Xia Y, Shine MB, Wang C, Navarre DA, Kachroo A, Kachroo P. Mono-and digalactosyldiacylglycerol lipids function nonredundantly to regulate systemic acquired resistance in plants. Cell Rep. 2014;9:1681–1691. doi:https://doi.org/10.1016/j.celrep.2014.10.069.
- Karabudak T, Bor M, Ozdemir F, Turkan I. Glycine betaine protects tomato (Solanum lycopersicum) plants at low temperature by inducing fatty acid desaturase7 and lipoxygenase gene expression. Mol Biol Rep. 2014;41:1401–1410. doi:https://doi.org/10.1007/s11033-013-2984-6.
- Wang G, Cai G, Kong F, Deng Y, Ma N, Meng Q. Overexpression of tomato chloroplast-targeted DnaJ protein enhances tolerance to drought stress and resistance to Pseudomonas solanacearum in transgenic tobacco. Plant Physiol Biochem. 2014;82:95–104. doi:https://doi.org/10.1016/j.plaphy.2014.05.011.
- Avila CA, Arevalo-Soliz LM, Jia L, Navarre DA, Chen Z, Howe GA, Meng QW, Smith JE, Goggin F. Loss of function of FATTY ACID DESATURASE7 in tomato enhances basal aphid resistance in a salicylate-dependent manner. Plant Physiol. 2012;158:2028–2041. doi:https://doi.org/10.1104/pp.111.191262.
- Zhang QY, Wang LY, Kong FY, Deng YS, Li B, Meng QW. Constitutive accumulation of zeaxanthin in tomato alleviates salt stress-induced photoinhibition and photooxidation. Physiol Planta. 2012;146:363–373. doi:https://doi.org/10.1111/j.1399-3054.2012.01645.x.
- Sun X, Lin L, Sui N. Regulation mechanism of microRNA in plant response to abiotic stress and breeding. Mol Biol Rep. 2019;46:1447–1457. doi:https://doi.org/10.1007/s11033-018-4511-2.
- Sui N, Li M, Li K, Song J, Wang BS. Increase in unsaturated fatty acids in membrane lipids of Suaeda salsa L. enhances protection of photosystem II under high salinity. Photosynthetica. 2010;48:623–629. doi:https://doi.org/10.1007/s11099-010-0080-x.
- Sun XL, Yang S, Wang LY, Zhang QY, Zhao SJ, Meng QW. The unsaturation of phosphatidylglycerol in thylakoid membrane alleviates PSII photoinhibition under chilling stress. Plant Cell Rep. 2011;30:1939–1947. doi:https://doi.org/10.1007/s00299-011-1102-2.
- Li M, Ji L, Yang X, Meng Q, Guo S. The protective mechanisms of CaHSP26 in transgenic tobacco to alleviate photoinhibition of PSII during chilling stress. Plant Cell Rep. 2012;31:1969–1979. doi:https://doi.org/10.1007/s00299-012-1309-x.
- Higashi Y, Okazaki Y, Myouga F, Shinozaki K, Saito K. Landscape of the lipidome and transcriptome under heat stress in Arabidopsis thaliana. Sci Rep. 2015;5:10533. doi:https://doi.org/10.1038/srep10533.
- Allakhverdiev SI, Kinoshita M, Inaba M, Suzuki I, Murata N. Unsaturated fatty acids in membrane lipids protect the photosynthetic machinery against salt-induced damage in Synechococcus. Plant Physiol. 2001;125:1842–1853. doi:https://doi.org/10.1104/pp.125.4.1842.
- Wang HS, Yu C, Tang XF, Zhu ZJ, Ma NN, Meng QW. A tomato endoplasmic reticulum (ER)-type omega-3 fatty acid desaturase (LeFAD3) functions in early seedling tolerance to salinity stress. Plant Cell Rep. 2013;33:131–142. doi:https://doi.org/10.1007/s00299-013-1517-z.
- Yu C, Wang H, Yang S, Tang X, Duan M, Meng QW. Overexpression of endoplasmic reticulum omega-3 fatty acid desaturase gene improves chilling tolerance in tomato. Plant Physiol Biochem. 2009;47:1102–1112. doi:https://doi.org/10.1016/j.plaphy.2009.07.008.
- Wang HS, Yu C, Tang XF, Wang LY, Dong XC, Meng QW. Antisense-mediated depletion of tomato endoplasmic reticulum omega-3 fatty acid desaturase enhances thermal tolerance. J Integr Plant Biol. 2010;52:568–577. doi:https://doi.org/10.1111/j.1744-7909.2010.00957.x.
- Yurchenko O, Park S, Ilut DC, Inmon JJ, Millhollon JC, Liechty ZS, Page JT, Jenks MA, Chapman KD, Udall JA, et al. Genome-wide analysis of the omega-3 fatty acid desaturase gene family in Gossypium. BMC Plant Biol. 2014;14:312. doi:https://doi.org/10.1186/s12870-014-0312-5.
- Wang YW, Jiang DX, Chen JJHGX. Physiological characterization and thylakoid ultrastructure analysis in super high-yield hybrid rice leaves under drought stress. Photosynthetica. 2019;57:890–896. doi:https://doi.org/10.32615/ps.2019.106.
- Narayanan S, Tamura PJ, Roth MR, Prasad PV, Welti R. Wheat leaf lipids during heat stress: I. High day and night temperatures result in major lipid alterations. Plant Cell Environ. 2016;39:787–803. doi:https://doi.org/10.1111/pce.12649.
- Narayanan S, Prasad PV, Welti R. Wheat leaf lipids during heat stress: II. Lipids experiencing coordinated metabolism are detected by analysis of lipid co-occurrence. Plant Cell Environ. 2016;39:608–617. doi:https://doi.org/10.1111/pce.12648.