[1]Finaka A, Cuendet A F, Maathuis F J H, Saidi Y, Goloubinoff P. Plasma membrane cyclic nucleotide gated calcium channels control land plant thermal sensing and acquired thermotolerance. Plant Cell, 2012, 24: 3333–3348



[2]Wang D-M(王冬梅), Xu X-Y(许向阳), Li J-F(李景富). The research progress of heat resistance in tomato. China Veg (中国蔬菜), 2003, 2: 58–60 (in Chinese)



[3]Chen T H H, Murata N. Glycinebetaine protects plants against abiotic stress: mechanisms and biotechnological applications. Plant Cell Environ, 2011, 34: 1–20



[4]Park E J, Jekni? Z, Sakamoto A, DeNoma J, Yuwansiri R, Murata N, Chen T H H. Genetic engineering of glycinebetaine synthesis in tomato protects seeds, plants, and flowers from chilling damage. Plant J, 2004, 40: 474–487



[5]Kathuria H, Giri J, Nataraja K N, Murata N, Udayakumar M, Tyagi A K. Glycinebetaine-induced water-stress tolerance in codA-expressing transgenic indica rice is associated with up-regulation of several stress responsive genes. Plant Biotechnol J, 2009, 7: 512–526



[6]Yang X H, Liang Z, Wen X G, Lu C M. Genetic engineering of the biosynthesis of glycinebetaine leads to increased tolerance of photosynthesis to salt stress in transgenic tobacco plants. Plant Mol Biol, 2008, 66: 73–86



[7]Yang X H, Liang Z, Lu C M. Genetic engineering of the biosynthesis of glycinebetaine enhances photosynthesis against high temperature stress in transgenic tobacco plants. Plant Physiol, 2005, 138: 2299–2309



[8]Yang X H, Wen X G, Gong H M, Lu Q T, Yang Z P, Tang Y L, Liang Z, Lu C M. Genetic engineering of the biosynthesis of glycinebetaine enhances thermotolerance of photosystem II in tobacco plants. Planta, 2007, 225: 719–733



[9]Li S F, Li F, Wang J W, Zhang W, Meng Q W, Chen T H H, Murata N, Yang X H. Glycinebetaine enhances the tolerance of tomato plants to high temperature during germination of seeds and growth of seedlings. Plant Cell Environ, 2011, 34: 1931–1943



[10]Park E J, Jekni? Z, Pino M T, Murata N, Chen T H H. Glycinebetaine accumulation is more effective in chloroplasts than in the cytosol for protecting transgenic tomato plants against abiotic stress. Plant Cell Environ, 2007, 30: 994–1005



[11]Rhodes D, Rich P J, Brunk D G, Ju G C, Rhodes J C, Pauly M H, Hansen L A. Development of two isogenic sweet corn hybrids differing for glycinebetaine content. Plant Physiol, 1989, 91: 1112–1121



[12]Kooten O, Snel J F H. The use of chlorophyll fluorescence nomenclature in plant stress physiology. Photosynth Res, 1990, 25: 147–150



[13]Brennan T, Frenkel C. Involvement of hydrogen peroxide in the regulation of senescence in pear. Plant Physiol, 1977, 59: 411–416



[14]Zhao S-J(赵世杰), Xu C-C(许长成), Zou Q(邹琦), Meng Q-W(孟庆伟). Improvements of method for measurement of malondialdehvde in plant tissues. Plant Physiol Commun (植物生理学通讯), 1991, 30(3): 207–210 (in Chinese)



[15]Clarke S M, Mur L A J, Wood J E, Scott I M. Salicylic acid dependent signaling promotes basal thermotolerance but is not essential for acquired thermotolerance in Arabidopsis thaliana. Plant J, 2004, 38: 432–447



[16]Aebi H. Catalase in vitro. Method Enzymol, 1984, 105:121–126



[17]Giannopolitis G N, Reis S K. Superoxide dismutase I. occurrence in higher plants. Plant Physiol, 1977, 59: 309–315



[18]Cakmak I, Marschner H. Magnesium deficiency and high light intensity enhance activities of superoxide dismutase, ascorbate peroxidase, and glutathione reductase in bean leaves. Plant Physiol, 1992, 98: 1222–1227



[19]Nakano Y, Asada K. Hydrogen peroxide is scavenged by ascorbate peroxidase in spinach chloroplasts. Plant Cell Physiol, 1981, 22: 867–880



[20]Zhang L X, Paakkarinen V, Van Wijk K J, Aro E M. Cotranslational assembly of the D1 protein into photosystem II. J Biol Chem, 1999, 274: 16062–16067



[21]Zhang Q Y, Wang L Y, Kong F Y, Deng Y S, Li B, Meng Q W. Constitutive accumulation of zeaxanthin in tomato alleviates salt stress-induced photoinhibition and photooxidation. Physiol Plant, 2012, 146: 363–373



[22]Zhao S-J(赵世杰), Zou Q(邹琦), Zheng G-S(郑国生). The study of the method of modulation determination of chloroplast pigment in tobacco. Acta Tab Sin (中国烟草), 1993, 3: 17–19 (in Chinese with English abstract)



[23]Callahan F E, Ghirardi M L, Sopory S K, Mehta A M, Edelman M, Mattoo A K. A novel metabolic from of the 32kDa-D1 protein in the grana-localized reaction center of photosystem II. J Biol Chem, 1990, 265: 15357–15360



[24]Guo J-W(郭军伟), Wei H-M(魏慧敏), Wu S-F(吴守锋), Du L-F(杜林方). Effects of low temperature on the distribution of excitation energy in photosystem and the phosphorylation of thylakoid membrane proteins in rice. Acta Biophys Sin (生物物理学报), 2006, 22(3): 197–202 (in Chinese)



[25]Chen J-M(陈建明), Yu X-P(俞晓平), Cheng J-A(程家安). The application of chlorophyll fluorescence kinetics in the study of physiological responses of plants to environmental stresses. Acta Agric Zhejiangensis (浙江农业学报), 2006, 18(1): 51–55 (in Chinese with English abstract)



[26]Apel K, Hirt H. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu Plant Biol, 2004, 55(1): 373–399



[27]McAinsh M R, Clayton H, Mansfield T A, Hetherington A M. Changes in stomatal behavior and guard cell cytosolic free calcium inresponse to oxidative stress. Plant Physiol, 1996, 111: 1031–1042



[28]Lee S, Choi H, Suh S, Doo I-S, Oh K-Y, Choi E J, Schroeder Taylor A T, Low P S, Lee Y. Oligogalacturonic acid and chitosan reduce stomatal aperture by inducing the evolution of reactive oxygen species from guard cells of tomato and Commelina communis. Plant Physiol, 1999, 121: 147–152



[29]Wang Q, Xu W, Xue Q, Su W. Transgenic Brassica chinensis plants expressing a bacterial codA gene exhibit enhanced tolerance to extreme temperature and high salinity. J Zhejiang Univ-Sci B, 2010, 11: 851–861



[30]Heber U, Bukhov N G, Shuvalov V A, Kobayashi Y, Lange O L. Protection of the photosynthetic apparatus against damage by excessive illumination in homoiohydric leaves and poikilohydric mosses and lichens. J Exp Bot, 2001, 52: 1999–2006



[31]Allakhverdiev S, Los D, Mohanty P, Nishiyama Y, Murata N. Glycinebetaine alleviates the inhibitory effect of moderate heat stress on the repair of photosystem II during photoinhibition. Biochim Biophys Acta, 2007, 1767: 1363–1371



[32]Ohnishi N, Murata N. Glycinebetaine counteracts the inhibitory effects of salt stress on the degradation and synthesis of D1 protein during photoinhibition in synechococcus sp. PCC 7942. Plant Physiol, 2006, 141: 758–765



[33]Guo Y P, Zhou H F, Zhang L C. Photosynthetic characteristics and protective mechanisms against photooxidation during high temperature stress in two citrus species. Sci Hort, 2006, 108: 260–267



[34]Alia, Kondo Y, Sakamoto A, Nonaka H, Hayashi H, Saradhi P P, Chen T H H, Murata N. Enhanced tolerance to light stress of transgenic Arabidopsis plants that express the codA gene for a bacterial choline oxidase. Plant Mol Biol, 1999, 40: 279–288



[35]Park E J, Jeknic Z, Chen T H H, Murata N. The codA transgene for glycinebetaine synthesis increases the size of flowers and fruits in tomato. Plant Biotechnol J, 2007, 5: 422–430



[36]Prasad T K, Anderson M D, Martin B A, Stewart C R. Evidence for chilling-Induced oxidative stress in maize seedlings and a regulatory role for hydrogen peroxide. Plant Cell, 1994, 6: 65–74



[37]Mittler R. Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci, 2002, 7: 405–410



[38]Miller G, Shulaev V, Mittler R. Reactive oxygen signaling and abiotic stress. Physiol Plant, 2008, 133: 481–489