Abstract
Ethylene is biosynthesized from methionine by S-adenosyl-l-methionine (SAM) synthetase, 1-aminocyclopropane-1-carboxylic acid (ACC) synthase (ACS), and ACC oxidase (ACO) and plays a crucial role in ripening and senescence of horticultural crops. Ethylene first binds with ethylene receptors (ETR/ERS) localized on the endoplasmic reticulum (ER) membrane, and the signal is transmitted through a pathway involving CTR1 → EIN2 → EIN3/EIL → ERFs and then to ethylene-responsive genes, leading to ethylene response. Aminoethoxyvinylglycine (AVG) and 1-methylcyclopropene (1-MCP) are potent inhibitors of ACS activity and ethylene perception, respectively, and are commercially utilized for the control of ethylene in horticultural crops. Temperature is the most influential environmental factor for postharvest control of crops because low temperature suppresses most metabolic process, including respiration, thereby dramatically extending storage and shelf life. In chilling-susceptible crops such as bananas, pineapples, and avocados, exposure to temperatures below a critical limit imposes stress and results in chilling injury, with symptoms of pitting and browning of tissues. In pears and kiwifruit, low temperature modulates fruit ripening in an ethylene-dependent and -independent manner, respectively. Elevated CO2 and reduced O2 atmospheres have both beneficial and harmful effects on physiology and quality of crops, depending on concentration, duration, temperature, species, and other factors. Low O2 conditions reduce rates of respiration and ethylene production in crops and extend storage life. When O2 concentration drops to a certain limit, anaerobic respiration is induced, resulting in physiological damage. The respiratory response of horticultural crops to elevated CO2 differs among species and may be mediated by the effect of CO2 on the synthesis or action of ethylene. Excessive exposure to high CO2 atmosphere induces a stress response, including a shift from aerobic to anaerobic metabolism in sensitive crops, resulting in CO2 disorder.
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References
Adams-Phillips L, Barry C, Giovannoni J (2004) Signal transduction systems regulating fruit ripening. Trends Plant Sci 7:331–338
Barry CS, Givannoni JJ (2007) Ethylene and fruit ripening. J Plant Growth Regul 26:143–159
Barry CS, Llop-Tous MI, Grierson D (2000) The regulation of 1-aminocyclopropane-1-carboxylic acid synthase gene expression during the transition from system-1 to system-2 ethylene synthesis in tomato. Plant Physiol 123:979–986
Biale JB (1960) The postharvest biochemistry of tropical and subtropical fruit. Adv Food Res 10:293–354
Burg SP, Burg EA (1967) Molecular requirements for the biological activity of ethylene. Plant Physiol 42:144–152
Fujimoto SY, Ohta M, Usui A, Shinshi H, Ohme-Takagi M (2000) Arabidopsis ethylene-responsive element binding factor act as transcriptional activator or repressors of GCC box-mediated gene expression. Plant Cell 12:393–404
Gapper NE, McQuinn RP, Givannoni JJ (2013) Molecular and genetic regulation of fruit ripening. Plant Mol Biol 82(6):575–591. doi:10.1007/s11103-013-0050-3
Hiwasa K, Kinugasa Y, Amamo S, Hashimoto A, Nakano R, Inaba A, Kubo Y (2003) Ethylene is required for both the initiation and progression of softening in pear (Pyrus communis L.) fruit. J Exp Bot 54:771–779
Kader AA (1986) Biochemical and physiological basis for effects of controlled and modified atmospheres on fruits and vegetables. Food Technol 40:99–105
Kader AA (2002) Postharvest technology of horticultural crops. University of California Division of Agriculture and Natural Resources Communication Service Publications, Davis
Kamiyoshihara Y, Tieman DM, Huber DJ, Klee HJ (2012) Ligand-induced alterations in the phosphorylation state of ethylene receptors in tomato fruit. Plant Physiol 160:488–497
Kerbel EL, Kader AA, Romani RJ (1988) Effects of elevated CO2 concentration on glycolysis in intact ‘Bartlett’ pear fruit. Plant Physiol 86:1205–1209
Kevany B, Tieman DM, Taylor M, Dal Cin V, Klee H (2007) Ethylene receptor degradation controls the timing of ripening in tomato fruit. Plant J 51:458–467
Kubo Y (1993) Controlled atmosphere (CA) storage. (b) Effects on fruit and vegetables. In: Encyclopaedia of food science, food technology and nutrition. Academic Press, London, pp 1219–1223
Kubo Y, Inaba A, Nakamura R (1989) Effects of high CO2 on respiration in various horticultural crops. J Jpn Soc Hortic Sci 58:731–736
Kubo Y, Inaba A, Nakamura R (1990) Respiration and C2H4 production in various harvested crops in CO2-enriched atmosphere. J Am Soc Hortic Sci 115:975–978
Lelièvre JM, Tichit L, Dao P, Fillion L, Nam YW, Pech JC, Latché A (1997) Effects of chilling on the expression of ethylene biosynthetic genes in Passe-Crassan pear (Pyrus communis L.) fruits. Plant Mol Biol 33:847–855
Lin Z, Zhong S, Grierson D (2009) Recent advances in ethylene research. J Exp Bot 60:3311–3336
Mitchell EG (1992) Postharvest handling systems: temperate zone tree fruits (pome fruits and stone fruits). In: Kader AA (ed) Postharvest technology of horticultural crops. University of California Division of Agriculture and Natural Resources Communication Service Publications, Davis, pp 215–221
Mworia EG, Yoshikawa T, Salikon N, Oda C, Asiche WO, Yokotani N, Abe D, Ushijima K, Nakano R, Kubo Y (2012) Low-temperature-modulated fruit ripening is independent of ethylene in ‘Sanuki Gold’ kiwifruit. J Exp Bot 63:963–971
Nakano R, Inoue S, Kubo Y, Inaba A (2002) Water stress-induced ethylene in the calyx triggers autocatalytic ethylene production and fruit softening in ‘Tonewase’ persimmon grown in a heated plastic-house. Postharvest Biol Technol 25:293–300
Nakano R, Ogura E, Kubo Y, Inaba A (2003) Ethylene biosynthesis in detached young persimmon fruit is initiated in calyx and modulated by water loss from the fruit. Plant Physiol 131:276–286
Nakatsuka A, Murachi S, Okunishi H, Shiomi S, Nakano R, Kubo Y, Inaba A (1998) Differential expression and internal feedback regulation of 1-aminocyclopropane-1-carboxylate synthase, 1-aminocyclopropane-1- carboxylate oxidase, and ethylene receptor genes in tomato fruit during development and ripening. Plant Physiol 118:1295–1305
Qiao H, Chang KN, Yazaki J, Ecker JR (2009) Interplay between ethylene, ETP1/ETP2 F-box proteins, and degradation of EIN2 triggers ethylene responses in Arabidopsis. Genes Dev 23:512–521
Seymour GB, Chapman NH, Chew BL, Rose JKC (2013) Regulation of ripening and opportunities for control in tomato and other fruits. Plant Biotechnol J 11:269–278
Shipway MR, Bramlage WJ (1973) Effects of carbon dioxide on activity of apple mitochondria. Plant Physiol 51:1095–1098
Tieman DM, Taylor MG, Ciardi JA, Klee HJ (2000) The tomato ethylene receptors NR and LeETR4 are negative regulators of ethylene response and exhibit functional compensation within a multigene family. Proc Natl Acad Sci USA 97:5663–5668
Tieman DM, Ciardi JA, Taylor MG, Klee HJ (2001) Members of the tomato LeEIL (EIN3-like) gene family are functionally redundant and regulate ethylene responses throughout plant development. Plant J 26:47–58
Wang KLC, Li H, Ecker JR (2002) Ethylene biosynthesis and signaling networks. Plant Cell 14:S131–S151
Wills R, McGlasson B, Graham D, Joyce D (1998) Postharvest: an introduction to the physiology & handling of fruit, vegetables and ornamentals. University of New South Wales Press, Wallingford
Yang SF, Hoffman NE (1984) Ethylene biosynthesis and its regulation in higher plants. Annu Rev Plant Physiol 35:155–190
Yokotani N, Tamura S, Nakano R, Inaba A, Kubo Y (2003) Characterization of a novel tomato EIN3-like gene (LeEIL4). J Exp Bot 393:2775–2776
Yokotani N, Nakano R, Imanishi S, Nagata M, Inaba A, Kubo Y (2009) Ripening-associated ethylene biosynthesis in tomato fruit is autocatalytically and developmentally regulated. J Exp Bot 60:3433–3442
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Kubo, Y. (2015). Ethylene, Oxygen, Carbon Dioxide, and Temperature in Postharvest Physiology. In: Kanayama, Y., Kochetov, A. (eds) Abiotic Stress Biology in Horticultural Plants. Springer, Tokyo. https://doi.org/10.1007/978-4-431-55251-2_2
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DOI: https://doi.org/10.1007/978-4-431-55251-2_2
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