Biochemical analysis of ‘kerosene tree’ Hymenaea courbaril L. under heat stress

References

• Lee Y, Langenheim JH. Systematics of the Genus Hymenaea L. (Leguminosae, Caesalpinioideae, Detarieae). In: University of California publications in Botany (Vol. 69). Berkeley, CA: University of California Press, 1975.
   Google Scholar
• Campos MAA, Uchida T. Influência do sombreamento no crescimento de mudas de três espécies amazônicas. Pesquisa Agropecuária Brasileira 2002; 37:281-8; http://dx.doi.org/10.1590/S0100-204X2002000300008
   Web of Science ®Google Scholar
• Cartaxo SL, Souza MM, de Albuquerque UP. Medicinal plants with bioprospecting potential used in semi-arid northeastern Brazil. J Ethnopharmacol 2010; 131:326-42; PMID:20621178; http://dx.doi.org/10.1016/j.jep.2010.07.003
   PubMed Web of Science ®Google Scholar
• Carneiro FS, Lacerda AE, Lemes MR, Gribel R, Kanashiro M, Sebbenn AM. Mendelian inheritance, linkage and genotypic disequilibrium in microsatellite loci isolated from Hymenaea courbaril (Leguminosae). Genet Mol Res 2012; 11:1942-8; PMID:22869549; http://dx.doi.org/10.4238/2012.July.19.13
   PubMed Web of Science ®Google Scholar
• Fehsenfeld F, Calvert J, Fall R, Goldan P, Guenther AB, Hewitt CN, Lamb B, Liu S, Trainer M, Westberg H, et al. Emissions of volatile organic compounds from vegetation and the implications for atmospheric chemistry. Global Biogeochem Cycles 1992; 6:389-430; http://dx.doi.org/10.1029/92GB02125
   Web of Science ®Google Scholar
• Guenther A, Hewitt CN, Erickson D, Fall R, Geron C, Graedel T, Harley P, Klinger L, Lerdau M, McKay WA, et al. A global model of natural volatile organic compound emissions. J Geophys Res: Atmospheres 1995; 100:8873-92; http://dx.doi.org/10.1029/94JD02950
   Web of Science ®Google Scholar
• Sharkey TD, Wiberley AE, Donohue AR. Isoprene emission from plants: why and how. Ann Bot 2008; 101:5-18; PMID:17921528; http://dx.doi.org/10.1093/aob/mcm240
   PubMed Web of Science ®Google Scholar
• Wahid A, Gelani S, Ashraf M, Foolad MR. Heat tolerance in plants: An overview. Environ Exp Bot 2007; 61:199-223; http://dx.doi.org/10.1016/j.envexpbot.2007.05.011
   Web of Science ®Google Scholar
• Rude MA, Schirmer A. New microbial fuels: a biotech perspective. Curr Opin Microbiol 2009; 12:274-81; PMID:19447673; http://dx.doi.org/10.1016/j.mib.2009.04.004
   PubMed Web of Science ®Google Scholar
• Harvey BG, Wright ME, Quintana RL. High-density renewable fuels based on the selective dimerization of pinenes. Energy Fuels 2009; 24:267-73; http://dx.doi.org/10.1021/ef900799c
   Web of Science ®Google Scholar
• Calvin M. Hydrocarbons from plants: Analytical methods and observations. Naturwissenschaften 1980; 67:525-33; http://dx.doi.org/10.1007/BF00450661
   Web of Science ®Google Scholar
• Meylemans HA, Quintana RL, Harvey BG. Efficient conversion of pure and mixed terpene feedstocks to high density fuels. Fuel 2012; 97:560-8; http://dx.doi.org/10.1016/j.fuel.2012.01.062
   Web of Science ®Google Scholar
• Janick J, Paull, RE (Editors). The Encyclopedia of Fruit & Nuts. Cambridge, MA: CABI Publishing, 2008.
   Google Scholar
• Holopainen JK. Can forest trees compensate for stress-generated growth losses by induced production of volatile compounds? Tree Physiol 2011; 31:1356-77; PMID:22112623; http://dx.doi.org/10.1093/treephys/tpr111
   PubMed Web of Science ®Google Scholar
• Dicke M, Gols R, Ludeking D, Posthumus M. Jasmonic Acid and Herbivory Differentially Induce Carnivore-Attracting Plant Volatiles in Lima Bean Plants. J Chem Ecol 1999; 25:1907-22; http://dx.doi.org/10.1023/A :1020942102181
   Web of Science ®Google Scholar
• Jardine K, Abrell L, Kurc SA, Huxman T, Ortega J, Guenther A. Volatile organic compound emissions from Larrea tridentata (creosotebush). Atmospheric Chem Phys 2010; 10:12191-206; http://dx.doi.org/10.5194/acp-10-12191-2010
   Web of Science ®Google Scholar
• Dudareva N, Martin D, Kish CM, Kolosova N, Gorenstein N, Fäldt J, Miller B, Bohlmann J. (E)-beta-ocimene and myrcene synthase genes of floral scent biosynthesis in snapdragon: function and expression of three terpene synthase genes of a new terpene synthase subfamily. Plant Cell 2003; 15:1227-41; PMID:12724546; http://dx.doi.org/10.1105/tpc.011015
   PubMed Web of Science ®Google Scholar
• Navia-Giné WG, Gomez SK, Yuan J, Chen F, Korth KL. Insect-induced gene expression at the core of volatile terpene release in. Plant Signal Behav 2009; 4:636-8; http://dx.doi.org/10.4161/psb.4.7.8971
   PubMedGoogle Scholar
• Harborne JB. Recent advances in the ecological chemistry of plant terpenoids. In: Harborne JB, Tomas-Barberan FA, ed. Ecological Chemistry and Biochemistry of Plant Terpenoids Clarendon Press, Oxford, UK., 1991:399-426.
   Google Scholar
• Loreto F, Sharkey TD. On the relationship between isoprene emission and photosynthetic metabolites under different environmental conditions. Planta 1993; 189:420-4; PMID:24178500; http://dx.doi.org/10.1007/BF00194440
   PubMed Web of Science ®Google Scholar
• Munné-Bosch S, Alegre L. Drought-induced changes in the redox state of alpha-tocopherol, ascorbate, and the diterpene carnosic acid in chloroplasts of Labiatae species differing in carnosic acid contents. Plant Physiol 2003; 131:1816-25; http://dx.doi.org/10.1104/pp.102.019265
   PubMed Web of Science ®Google Scholar
• Sharkey T, Loreto F. Water stress, temperature, and light effects on the capacity for isoprene emission and photosynthesis of kudzu leaves. Oecologia 1993; 95:328-33; http://dx.doi.org/10.1007/BF00320984
   PubMed Web of Science ®Google Scholar
• Tingey DT, Turner DP, Weber JA. Factors controlling the emission of monoterpenes and other volatile organic compounds. In: Sharkey TD, Holland EA, Mooney HA, ed. Trace Gas Emissions by Plants Academic Press, San Diego, CA, USA, 1991:93-119.
   Google Scholar
• Loreto F, Förster A, Dürr M, Csiky O, Seufert G. On the monoterpene emission under heat stress and on the increased thermotolerance of leaves of Quercus ilex L. fumigated with selected monoterpenes. Plant, Cell Environ 1998; 21:101-7; http://dx.doi.org/10.1046/j.1365-3040.1998.00268.x
   Web of Science ®Google Scholar
• Pateraki I, Kanellis AK. Stress and developmental responses of terpenoid biosynthetic genes in Cistus creticus subsp. creticus. Plant Cell Rep 2010; 29:629-41; PMID:20364257; http://dx.doi.org/10.1007/s00299-010-0849-1
   PubMed Web of Science ®Google Scholar
• Bokszczanin KL, Fragkostefanakis S, Consortium SPTITNS-I. Perspectives on deciphering mechanisms underlying plant heat stress response and thermotolerance. Front Plant Sci 2013; 4:315; PMID:23986766; http://dx.doi.org/10.3389/fpls.2013.00315
   PubMed Web of Science ®Google Scholar
• Weng M, Yang YUE, Feng H, Pan Z, Shen W-H, Zhu YAN, Dong A. Histone chaperone ASF1 is involved in gene transcription activation in response to heat stress in Arabidopsis thaliana. Plant, Cell Environ 2014: http://dx.doi.org/10.1111/pce.12299
   PubMed Web of Science ®Google Scholar
• Erkina TY, Erkine AM. Displacement of histones at promoters of Saccharomyces cerevisiae heat shock genes is differentially associated with histone H3 acetylation. Mol Cell Biol 2006; 26:7587-600; PMID:17015479; http://dx.doi.org/10.1128/MCB.00666-06
   PubMed Web of Science ®Google Scholar
• Kumar SV, Wigge PA. H2A.Z-containing nucleosomes mediate the thermosensory response in Arabidopsis. Cell 2010; 140:136-47.
   PubMed Web of Science ®Google Scholar
• Weng M, Yang Y, Feng H, Pan Z, Shen WH, Zhu Y, Dong A. Histone chaperone ASF1 is involved in gene transcription activation in response to heat stress in Arabidopsis thaliana. Plant Cell Environ 2014; PMID:24548003
   PubMed Web of Science ®Google Scholar
• Lang-Mladek C, Popova O, Kiok K, Berlinger M, Rakic B, Aufsatz W, Jonak C, Hauser MT, Luschnig C. Transgenerational inheritance and resetting of stress-induced loss of epigenetic gene silencing in Arabidopsis. Mol Plant 2010; 3:594-602; PMID:20410255; http://dx.doi.org/10.1093/mp/ssq014
   PubMed Web of Science ®Google Scholar
• Chinnusamy V, Zhu, J.K. Epigenetic regulation of stress responses in plants. Curr Opin Plant Biol 2009; 12:133-9; PMID:19179104; http://dx.doi.org/10.1016/j.pbi.2008.12.006
   PubMed Web of Science ®Google Scholar
• Sridhar VV, Kapoor A, Zhang K, Zhu J, Zhou T, Hasegawa PM, Bressan RA, Zhu JK. Control of DNA methylation and heterochromatic silencing by histone H2B deubiquitination. Nature 2007; 447:735-8; PMID:17554311; http://dx.doi.org/10.1038/nature05864
   PubMed Web of Science ®Google Scholar
• Zhang K, Sridhar VV, Zhu J, Kapoor A, Zhu JK. Distinctive core histone post-translational modification patterns in Arabidopsis thaliana. PLoS One 2007; 2:e1210; PMID:18030344; http://dx.doi.org/10.1371/journal.pone.0001210
   PubMedGoogle Scholar
• Drury GE, Dowle AA, Ashford DA, Waterworth WM, Thomas J, West CE. Dynamics of plant histone modifications in response to DNA damage. Biochem J 2012; 445:393-401; PMID:22574698; http://dx.doi.org/10.1042/BJ20111956
   PubMed Web of Science ®Google Scholar
• Yamane Y, Kashino Y, Koike H, Satoh K. Effects of high temperatures on the photosynthetic systems in spinach: Oxygen-evolving activities, fluorescence characteristics and the denaturation process. Photosynthesis Res 1998; 57:51-9; http://dx.doi.org/10.1023/A :1006019102619
   Web of Science ®Google Scholar
• De Ronde JA, Cress WA, Krüger GH, Strasser RJ, Van Staden J. Photosynthetic response of transgenic soybean plants, containing an Arabidopsis P5CR gene, during heat and drought stress. J Plant Physiol 2004; 161:1211-24; PMID:15602813; http://dx.doi.org/10.1016/j.jplph.2004.01.014
   PubMed Web of Science ®Google Scholar
• Mathur S, Mehta P, Jajoo A. Effects of dual stress (high salt and high temperature) on the photochemical efficiency of wheat leaves (Triticum aestivum). Physiol Mol Biol Plants 2013; 19:179-88; PMID:24431485; http://dx.doi.org/10.1007/s12298-012-0151-5
   PubMedGoogle Scholar
• Tang Y, Wen X, Lu Q, Yang Z, Cheng Z, Lu C. Heat stress induces an aggregation of the light-harvesting complex of photosystem II in spinach plants. Plant Physiol 2007; 143:629-38; PMID:17142484; http://dx.doi.org/10.1104/pp.106.090712
   PubMed Web of Science ®Google Scholar
• Heckathorn SA, Coleman JS, Hallberg RL. Recovery of net CO2 assimilation after heat stress is correlated with recovery of oxygen-evolving-complex proteins in Zea mays L. Photosynthetica 1998; 34:13-20; http://dx.doi.org/10.1023/A :1006899314677
   Web of Science ®Google Scholar
• Gazanchian A, Hajheidari M, Sima NK, Salekdeh GH. Proteome response of Elymus elongatum to severe water stress and recovery. J Exp Bot 2007; 58:291-300; PMID:17210992; http://dx.doi.org/10.1093/jxb/erl226
   PubMed Web of Science ®Google Scholar
• Tóth SZ, Schansker G, Kissimon J, Kovács L, Garab G, Strasser RJ. Biophysical studies of photosystem II-related recovery processes after a heat pulse in barley seedlings (Hordeum vulgare L.). J Plant Physiol 2005; 162:181-94.
   PubMed Web of Science ®Google Scholar
• Bukhov N, Wiese C, Neimanis S, Heber U. Heat sensitivity of chloroplasts and leaves: Leakage of protons from thylakoids and reversible activation of cyclic electron transport. Photosynthesis Res 1999; 59:81-93; http://dx.doi.org/10.1023/A :1006149317411.
   Web of Science ®Google Scholar
• Vasilikiotis C, Melis A. Photosystem II reaction center damage and repair cycle: chloroplast acclimation strategy to irradiance stress. Proc Natl Acad Sci U S A 1994; 91:7222-6; PMID:11607488; http://dx.doi.org/10.1073/pnas.91.15.7222
   PubMed Web of Science ®Google Scholar
• Crafts-Brandner SJ, Salvucci ME. Rubisco activase constrains the photosynthetic potential of leaves at high temperature and CO2. Proc Natl Acad Sci U S A 2000; 97:13430-5; PMID:11069297; http://dx.doi.org/10.1073/pnas.230451497
   PubMed Web of Science ®Google Scholar
• Crafts-Brandner SJ, Law RD. Effect of heat stress on the inhibition and recovery of the ribulose-1,5-bisphosphate carboxylase/oxygenase activation state. Planta 2000; 212:67-74; PMID:11219585; http://dx.doi.org/10.1007/s004250000364
   PubMed Web of Science ®Google Scholar
• El-Khatib RT, Hamerlynck EP, Gallardo F, Kirby EG. Transgenic poplar characterized by ectopic expression of a pine cytosolic glutamine synthetase gene exhibits enhanced tolerance to water stress. Tree Physiology 2004; 24:729-36; PMID:15123444; http://dx.doi.org/10.1093/treephys/24.7.729
   PubMed Web of Science ®Google Scholar
• Hoshida H, Tanaka Y, Hibino T, Hayashi Y, Tanaka A, Takabe T, Takabe T. Enhanced tolerance to salt stress in transgenic rice that overexpresses chloroplast glutamine synthetase. Plant Mol Biol 2000; 43:103-11; PMID:10949377; http://dx.doi.org/10.1023/A :1006408712416
   PubMed Web of Science ®Google Scholar
• Kozaki A, Takeba G. Photorespiration protects C3 plants from photooxidation. Nature 1996; 384:557-60; http://dx.doi.org/10.1038/384557a0
   Web of Science ®Google Scholar
• Weis E. Reversible heat-inactivation of the calvin cycle: A possible mechanism of the temperature regulation of photosynthesis. Planta 1981; 151:33-9; PMID:24301667; http://dx.doi.org/10.1007/BF00384234
   PubMed Web of Science ®Google Scholar
• Rodriguez P. Protein phosphatase 2C (PP2C) function in higher plants. Plant Mol Biol 1998; 38:919-27; PMID:9869399; http://dx.doi.org/10.1023/A :1006054607850
   PubMed Web of Science ®Google Scholar
• Kim SG, Kim ST, Wang Y, Kim SK, Lee CH, Kim KK, Kim JK, Lee SY, Kang KY. Overexpression of rice isoflavone reductase-like gene (OsIRL) confers tolerance to reactive oxygen species. Physiol Plant 2010; 138:1-9; PMID:19825006; http://dx.doi.org/10.1111/j.1399-3054.2009.01290.x
   PubMed Web of Science ®Google Scholar
• Jaeck E, Dumas B, Geoffroy P, Favet N, Inzé D, Van Montagu M, Fritig B, Legrand M. Regulation of enzymes involved in lignin biosynthesis: induction of O-methyltransferase mRNAs during the hypersensitive reaction of tobacco to tobacco mosaic virus. Mol Plant Microbe Interact 1992; 5:294-300; PMID:1515665; http://dx.doi.org/10.1094/MPMI-5-294
   PubMed Web of Science ®Google Scholar
• Pellegrini L, Geoffroy P, Fritig B, Legrand M. Molecular cloning and expression of a new class of ortho-diphenol-O-methyltransferases induced in tobacco (Nicotiana tabacum L.) leaves by infection or elicitor treatment. Plant Physiol 1993; 103:509-17.
   PubMed Web of Science ®Google Scholar
• Maury S, Geoffroy P, Legrand M. Tobacco O-methyltransferases involved in phenylpropanoid metabolism. The different caffeoyl-coenzyme A/5-hydroxyferuloyl-coenzyme A 3/5-O-methyltransferase and caffeic acid/5-hydroxyferulic acid 3/5-O-methyltransferase classes have distinct substrate specificities and expression patterns. Plant Physiol 1999; 121:215-24; PMID:10482677; http://dx.doi.org/10.1104/pp.121.1.215
   PubMed Web of Science ®Google Scholar
• Bligh EG, Dyer WJ. A rapid method of total lipid extraction and purification. Canadian J Biochem Physiol 1959; 37:911-7; PMID:13671378; http://dx.doi.org/10.1139/o59-099
   PubMedGoogle Scholar
• Robbins ML, Roy A, Wang P-H, Gaffoor I, Sekhon RS, de O, Buanafina MM, Rohila JS, Chopra S. Comparative proteomics analysis by DIGE and iTRAQ provides insight into the regulation of phenylpropanoids in maize. J Prot 2013; 93:254-75; PMID:23811284; http://dx.doi.org/10.1016/j.jprot.2013.06.018
   PubMed Web of Science ®Google Scholar
• Lacerda AEB, Kanashiro M, Sebbenn AM. Effects of selective logging on genetic diversity and spatial genetic structure of a Hymenaea courbaril population in the Brazilian Amazon Forest. Forest Ecol Manag 2008; 255:1034-43.
   Web of Science ®Google Scholar