Abstract
Wounding is a frequent, but irregular event imposed on plant life by the natural environment. Since higher plants are unable to move to better environments to escape from animal browsing or severe winds, mechanisms that overcome the wound effect are essential to survival of the individual, and the species as well. Wounding is defined herein as a mechanical process which destroys cells in a specific area of tissue. It thus breaks cell to cell continuity in a multicellular plant so that cells, or at least one side of cells which were previously in contact with other cells, are now exposed. In most cases, this will include loss of part of a tissue or organ. The reactions which occur in response to wounding are so diverse that we presently cannot integrate all of these reactions into a cogent series of physiological processes. However, the fundamental physiological outcome of the wound response is regeneration of part or all of the functions which were previously shared by the damaged or lost cells, tissues or organs (Lipetz 1970). This does not necessarily mean regeneration of the complete lost structure, however (Lipetz 1970). Thus, formation of protective materials in cells near the cut surface, initiation of cell proliferation, regeneration of vascular elements, or rooting at the base of shoot cuttings are common physiological responses to wounding. In a broad sense, one may also include in the wound response the lateral bud growth which occurs when the apical portion of the central axis is removed or damaged, a phenomenon well-known as the breaking of apical dominance.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Abeles AL, Abeles FB (1972) Biochemical pathway of stress-induced ethylene. Plant Physiol 50: 496–498
Abeles FB (1972) Biosynthesis and mechanism of action of ethylene. Ann Rev Plant Physiol 23: 259–29
Abeles FB (1973) Ethylene in plant biology. Academic Press, New York London, pp 87–108
Adams DO, Yang SF (1979) Ethylene biosynthesis: identification of 1-aminocyclopro- pane-l-carboxylic acid as an intermediate in the conversion of methionine to ethylene. Proc Nat Acad Sci USA 76: 170–174
Adams PB, Rowan KS (1970) Glycolytic control of respiration during aging of carrot root tissue. Plant Physiol 45: 490–494
Adamson D (1962) Expansion and division in auxin-treated plant cells. Can J Botany 40: 719–744
Aloni R (1976) Polarity of induction an pattern of primary phloem fiber differentiation in Coleus. Am J Botany 63: 877–889
Aloni R (1979) Role of auxin and gibberellin in differentiation of primary phloem fibers. Plant Physiol 63: 609–614
Aloni R, Jacobs WP (1977) Polarity of tracheary regeneration in young internodes of Coleus ( Labiatae ). Am J Botany 64: 395–403
Amrhein N, Schneebeck D, Skorupka H, Tophof S, Stockigt J (1981) Identification of a major metabolite of the ethylene precursor, 1-aminocyclopropane-l-carboxylic acid in higher plants. Naturwiss 68: 619–620
Amrhein N, Breuing F, Eberle J, Skorupka H, Tophof S (1982) The metabolism of 1-aminocyclopropane-l-carboxylic acid. In: Wareing PF (ed) Plant growth substances 1982. Academic Press, pp 249–258
Anderson JD, Lieberman M, Stewart RN (1979) Ethylene production by apple protoplasts. Plant Physiol 63: 931–935
Anzai T, Shibaoka H, Shimokoriyama M (1971) Increases in the number of adventitious roots caused by 2-thiouracil and 5-bromodeoxyuridine in Phaseolus mungo cuttings. Plant Cell Physiol (Tokyo) 12: 695–700
Apelbaum A, Yang SF (1981) Biosynthesis of stress ethylene induced by water deficit. Plant Physiol 68: 594–596
apRees T (1966) Evidence for the widespread occurrence of induced respiration in slices of plant tissue. Australian J Biol Sci 19: 981–990
Bacon JSD, MacDonald IR, Knight AH (1965) The development of invertase activity in slices of the root of Beta vulgaris L. washed under aseptic conditions. Biochem J 94: 175–182
Balls AK, Ryan CA (1963) Concerning a chymotryptic inhibitor from potatos and its binding capacity for the enzyme. J Biol Chem 238: 2976–2982
Behnke H-D, Schulz A (1980) Fine structure, pattern of division, and course of wound phloem in Coleus blumei. Planta 150: 357–365
Benayoun J, Aloni R, Sachs T (1975) Regeneration around wounds and the control of vascular differentiation. Ann Botany (London) 39: 447–454
Boiler T, Herner RC, Kende H (1979) Enzymatic formation of an ethylene precursor, 1-aminocyclopropane-l-carboxylic acid. Planta 145: 293–303
Borchert R (1978) Time course and spatial distribution of phenylalanine ammonia-lyase and peroxidase activity in wounded potato tuber tissue. Plant Physiol. 62: 789–793
Borchert R, McChesney JD (1973) Time course and localization of DNA synthesis during wound healing of potato tuber tissue. Develop Biol 35: 293–301
Bradford KJ, Yang SF (1980) Xylem transport of 1-aminocyclopropane-l-carboxylic 505 acid, an ethylene precursor in waterlogged tomato plants. Plant Physiol 65: 322–326
Breadshaw MJ, Edelman J (1969) Enzyme formation in higher plant tissue: The production of a gibberellin preceding invertase synthesis in aged tissue. J Exp Botany 20: 87–93
Burg SP, Clagett CO (1967) Conversion of methionine to ethylene in vegetative tissue and fruits. Biochem Biophys Res Commun 27: 125–130
Byrne H, Setterfleld G (1977) Activation of ribosomal and messenger RNA synthesis in excised Jerusalem artichoke tuber slices. Planta 136: 203–210
Cameron AC, Fenton CAK, Yu Y, Adams DO, Yang SF (1979) Increased production of ethylene by plant tissues treated with 1-aminocyclopropane-l-carboxylic acid. Hort Sci 14: 178–180
Cherry JH (1968) Regulation of invertase in washed sugar beet tissue. In: Wightman F, Setterfield G (eds) Biochemistry and physiology of plant growth substances. The Runge Press, Ottawa, pp 417–431
Clegg MD, Rappaport L (1970) Regulation of bud rest in tuber of potato, Solanum tuberosum L. VI Biochemical changes induced in excised potato buds by gibberellic acid. Plant Physiol 45: 8–13
Click RE, Hackett DP (1963) The role of protein and nucleic acid synthesis in the development of respiration in potato tuber slices. Proc Nat Acad Sci US 50: 243–250
Clutter M (1960) Hormonal induction of vascular tissue in tobacco pith in vitro. Science 132: 548–549
Comer AE (1978) Pattern of cell division and wound vessel member differentiation in Coleus pith explants. Plant Physiol 62: 354–359
Cooper WC (1938) Hormones and root formation. Botan Gaz 99: 599–614
Dalessandro G (1973) Hormonal control of xylogenesis in pith parenchyma explants of Lactuca. Ann Botany (London) 37: 375–382
Dalenssandro G, Roberts LW (1971) Induction of xylogenesis in pith parenchyma ex- plants of Lactuca. Am J Botany 58: 378–385
Davies E, Schuster A (1981) Intercellular communication in plants: Evidence for a rapidly generated, bidirectional transmitted wound signal. Proc Natl Acad Sci 78: 2422–2426
Dean BB, Kolattukudy PE (1976) Synthesis of suberin during wound-healing in jade leaves, tomato fruit, and bean pods. Plant Physiol 58: 411–416
Duda CT, Cherry JH (1971) Chromatin- and nuclei-directed ribonucleic acid synthesis in sugar beet root. Plant Physiol 47: 262–268
Edelman J, Hall MA (1964) Effect of growth hormones on the development of invertase associated with cell walls. Nature 201: 296–297
Edelman J, Hall MA (1965) Enzyme formation in higher plant tissues. Development of invertase and ascorbate oxidase activities in mature storage tissue of Helianthus tuberosus L. Biochem J 95: 403–410
Ellis RJ, MacDonald IR (1967) Activation of protein synthesis by microsomes from aging beet disks. Plant Physiol 42: 1297–1302
English J Jr, Bonner J, Haagen-Smit AJ (1939) The wound hormones of plants. II. The isolation of a crystalline active substance. Proc Natl Acad Sci USA 25: 323–329
Fosket DE, Roberts LW (1964) Induction of wound-vessel differentiation in isolated Coleus stem segments in vitro. Am J Bot 51: 19–25
Fosket DE, Torrey JG (1969) Hormonal control of cell proliferation and xylem differentiation in cultured tissues of Glycine max var. Biloxi. Plant Physiol 44: 871–880
Gahagan HE, Holm RE, Abeles FB (1968) Effect of ethylene on peroxidase activity. Physiol Plant 21: 1270–1279
Gayler KR, Glasziou KT (1964) Plant enzyme synthesis: Hormonal regulation of invertase and peroxidase synthesis in sugar cane. Planta 84: 185–194
Gersan, Lips, Sachs T (1980) Effects of wounding on transport in phloem. J Exp Bot 31: 783–789
Glasziou KT (1969) Control of enzyme formation and inactivation in plants. Annu Rev Plant Physiol 20: 63–88
Glasziou KT, Gayler KR, Waldron JC (1968) Effects of auxin and gibberellic acid on the regulation of enzyme synthesis in sugarcane stem tissue. In: Wightman F, Setterfield G (eds) Biochemistry and physiology of plant growth substances. Runge, Ottawa, pp 433–442
Green TR, Ryan CA (1972) Wound-induced proteinase inhibitor in plant leaves: A possible defense mechanism against insects. Science 175: 776–777
Green TR, Ryan CA (1973) Wound-induced proteinase inhibitor in tomato leaves. Some effects of light and temperature on the wound response. Plant Physiol 51: 19–21
Gustafson G, Ryan CA (1976) Specificity of protein turnover in tomato leaves. Accumula-tion of proteinase inhibitors, induced with the wound hormone, PIIF. J Biol Chem 251: 7004—7010
Haberlandt G (1921) Wundhormone als Erreger von Zellteilungen. Beitr Allg Bot 2: 1–53
Hackett WP (1970) The influence of auxin, catechol, and methanolic tissue extracts on root initiation in aseptically cultured shoot apices of juvenile and adult forms of Hedera helix. J Am Hortic Sci 95: 398–402
Hanson AD, Kende H (1975) Ethylene-enhanced ion and sucrose efflux in morning glory flower tissue. Plant Physiol 55: 663–669
Hanson AE, Kende H (1976) Methionine metabolism and ethylene biosynthesis in senescent flower tissue of morning glory. Plant Physiol 57: 528–537
Hanson AE, Kende H (1976) Biosynthesis of wound ethylene in morning glory flower tissue. Plant Physiol 57: 538–541
Hatanaka A, Kajiwara T, Sekiya J, Kido Y (1977) Formation of 12-oxo-trans–10-dodece- noic acid in chloroplasts from Thea sinensis leaves. Phytochemistry 16: 1827–1829
Hoffman NE, Yang SF, McKeon T (1982) Identification of l-(malonyl-amino)cyclopro- pane-l-carboxylic acid, an ethylene precursor in higher plants. Biochem Biophys Res Commun 104: 765–770
Hyodo H (1977 a) Ethylene production and respiration of Satsuma mandarin (Citrus unshiu Marc.) fruit harvested at different stages of development. J Jpn Soc Hortic Sci 45:427–432
Hyodo H (1977 b) Ethylene production by albedo tissue of Satsuma mandarin (Citrus unshiu Marc.) fruit. Plant Physiol 59:111–113
Hyodo H (1978) Ethylene production by wounded tissue of citrus fruit. Plant Cell Physiol 19: 545–551
Hyodo H, Nishino T (1981) Wound-induced ethylene formation in albedo tissue of citrus fruit. Planta Physiol 67: 421–423
Hyodo H, Yang SF (1971) Ethylene-enhanced synthesis of phenylalanine ammonia-lyase in pea seedlings. Plant Physiol 47: 765–770
Hyodo H, Yang SF (1974) The effect of ethylene on the development of phenylalanine ammonia-lyase in potato tuber disks. Z Naturforsch 71: 76–79
Hyodo H, Tanaka K, Watanabe K (1983) Wound-induced ethylene production and 1-aminocyclopropane-l-carboxylic acid synthase in winter squash fruit. Plant Cell Physiol 24: 963–969
Imaseki H (1970) Induction of peroxidase activity by ethylene in sweet potato. Plant Physiol 46: 172–174
Imaseki H, Watanabe A (1978) Inhibition of ethylene production by osmotic shock. Further evidence for membrane control of ethylene production. Plant Cell Physiol (Tokyo) 19: 345–348
Imaseki H, Asahi T, Uritani I ( 1968 a) Investigations on the possible inducers of metabolic changes in injured plant tissues. In: Hirai T, Hidaka Z, Uritani I (eds) Biochemical regulation in diseased plants and injury. Phytopathol Soc Jpn, Tokyo, pp 189–201
Imaseki H, Teranishi T, Uritani I (1968 b) Production of ethylene by sweet potato roots infected by the black rot fungus. Plant Cell Physiol 9: 769–781
Imaseki H, Uritani I, Stahmann MA (1968c) Production of ethylene by injured sweet potato root tissue. Plant Cell Physiol 9: 757–768
Imaseki H, Uchiyama M, Uritani I (1968 d) Effect of ethylene on the inductive increase in metabolic activities in sliced sweet potato roots. Agric Biol Chem 32: 387–389
Imaseki H, Yoshii H, Todaka I (1982) Regulation of auxin-induced ethylene biosynthesis in plants. In: Wareing PF (ed) Plant growth substances 1982. Academic Press, London, pp 259–268
Ishizuka M, Sato T, Watanabe A, Imaseki H (1981) Alteration of coding properties of polysome-associated messenger RNA in potato tuber slices during aging. Plant Physiol 68: 154–157
Jackson MB, Campbell DJ (1976) Production of ethylene by excised segments of plant tissue prior to the effect of wounding. Planta 129: 273–274
Jacobs WP (1952) The role of auxin in differentiation of xylem around a wound. Am J Botany 39: 301–309
Jacobs WP (1956) Internal factors controlling cell differentiation in the flowering plants. Am Naturalist 90: 163–169
Jacobs WP (1970) Regulation and differentiation of sieve tube elements. Intern Rev Cytol 28: 239–273
Jacobs WP, MacCready CC (1967) Polar transport of growth regulators in pith and vascular tissues of Coleus stems. Am J Botany 54: 1035–1040
Jeffs RA, Northcote DH (1967) The influence of indol–3-ylacetic acid and sugar on the pattern of induced differentiation in plant tissue culture. J Cell Sci 2: 77–78
Jones JF, Kende H (1979) Auxin-induced ethylene biosynthesis in subapical stem sections of etiolated seedlings of Pisum sativum L. Planta 146: 649–656
Kahl G (1971) Synthesis of rRNA, tRNA and other RNA-species concomitant with polyribosome formation in aging potato tuber slices. Z Naturforsch 26 b: 1058–1064
Kahl G (1971) Activation of protein synthesis in aging potato tuber slices. Z Naturforsch 26 b: 1064–1067
Kahl G (1973) Genetic and metabolic regulation in differentiating plant storage tissue cells. Botan Rev 39: 274–299
Kahl G (1974) Metabolism in plant storage tissue slices. Botan Rev 40: 263–314
Kahl G (1978) Biochemistry of wounded plant tissues. De Gruyter, New York, p 680 Kamisaka S, Sakurai N, Masuda Y (1973) Auxin-induced growth of tuber tissue of Jerusalem artichoke VIII. Role of cyclic AMP in the action of auxin, cytokinin and gibberellic acid. Plant Cell Physiol (Tokyo) 14:183–193 Kende H, Boiler T (1981) Wound ethylene and 1-aminocyclopropane-l-carboxylate synthase in ripening tomato fruit. Planta 151: 476–481
Kende H, Hanson AD (1976) Relationship between ethylene evolution and senescence in morning glory flower tissue. Plant Physiol 57: 523–527
Kolattukudy PE, Kronman K, Poulose AJ (1975) Determination of structure and composition of suberin from the roots of carrot, parsnip, rutabaga, turnip, red beet, and sweet potato by combined gas-liquid chromatography and mass spectrometry. Plant Physiol 55: 567–573
Komamine A, Sato M, Shimokoriyama M (1963) Physiological studies on the outgrowth of the epicotyl in Stizolobium hassjoo I. Properties of the outgrowth. Botan Mag (Tokyo) 76: 130–137
Konze JR, Kwiatkowski MK (1981) Rapidly induced ethylene formation after wounding is controlled by the regulation of 1-aminocyclopropane-l-carboxylic acid synthesis. Planta 151: 327–330
Koopowitz H, Dhys R, Fosket DE (1975) Cell membrane potentials of higher plants: Changes induced by wounding. J Exp Botany 26: 131–137
Lamotte CE, Jacobs WP (1963) A role of auxin in phloem regeneration in Coleus interno- des. Develop Biol 8: 80–98
Lange H, Rosenstock G, Kahl G (1970) Induktionsbedingungen der Suberinsynthese und Zellproliferation bei Parenchymfragmenten der Kartoffelknolle. Planta 90: 109–118
Laties GG (1962) Controlling influence of thickness on development and type of respiratory activity in potato slices. Plant Physiol 37: 679–690
Leaver CJ, Key JL (1967) Polyribosome formation and RNA synthesis during aging of carrot-root tissue. Proc Nat Acad Sci US 57: 1338–1344
Lieberman M (1979) Biosynthesis and action of ethylene. Ann Rev Plant Physiol 30: 533–591
Lieberman M, Kunishi AT, Mapson LW, Wardale DA (1965) Ethylene production from methionine. Biochem J 97: 449–459
Lieberman M, Kunishi A, Mapson LW, Wardale DA (1966) Stimulation of ethylene production in apple tissue slices by methionine. Plant Physiol 41: 376–382
Lipetz J (1970) Wound-healing in higher plants. Intern Rev Cytol 27: 1–28
Lurssen K, Naumann K, Schroder R (1979) 1-Aminocyclopropane-l-carboxylic acid - a new intermediate of ethylene biosynthesis in higher plants. Z Pflanzenphysiol 92: 285–294
Mader M, Amberg-Fischer V (1982) Role of peroxidase in lignification of tobacco cells. I. Oxidation of nicotinamide adenine dinucleotide and formation of hydrogen peroxide by cell wall peroxidases. Plant Physiol 70: 1128–1131
Mader M, Fiissl R (1982) Role of peroxidase in lignification of tobacco cells. II. Regulation by phenolic compounds. Plant Physiol 70: 1132–1134
Masuda Y (1965) Auxin-induced growth of tuber tissue of Jerusalem artichoke. I. Cell physiological studies on the expansion growth. Botan Mag (Tokyo) 78: 417–423
Masuda Y (1966) Auxin-induced growth of tuber tissue Jerusalem artichoke. II. The relation to protein and nucleic acid metabolism. Plant Cell Physiol (Tokyo) 7: 75–91
Mattoo AK, Lieberman M (1977) Localization of the ethylene-synthesizing system in apple tissue. Plant Physiol 60: 794–799
Mattoo AK, Baker JE, Chalutz E, Lieberman M (1977) Effect of temperature on the ethylene-synthesizing systems in apple, tomato and Penicillium digitatum. Plant Cell Physiol 18: 715–719
McKeon TA, Hoffman NE, Yang SF (1982) The effect of plant-hormone pretreatments on ethylene production and synthesis of 1-aminocyclopropane-l-carboxylic acid in water-stressed wheat leaves. Planta 155: 437–447
Mitsuhashi M, Shibaoka H, Shimokoriyama M (1969) Morphological and physiological characterization of IAA-less-sensitive and IAA-sensitive phases in rooting of Azukia cuttings. Plant Cell Physiol 10: 867–874
Mitsuhashi-Kato M, Shibaoka H, Shimokoriyama M (1978 a) Anatomical and physiological aspects of developmental processes of adventitious root formation in Azukia cuttings. Plant Cell Physiol 19: 393–400
Mitsuhashi-Kato M, Shibaoka H, Shimokoriyama M (1978 b) The nature of the dual effect of auxin on root formation in Azukia cutting. Plant Cell Physiol 19: 1535–1542
Mizuno K, Komamine A, Shimokoriyama M (1971) Vessel element formation in cultured carrot-root phloem slices. Plant Cell Physiol 12: 823–830
Morohashi Y, Komamine A, Shimokoriyama M (1969) Physiological studies on the outgrowth of the epicotyl in Stizolobium hassjoo VI. Changes in the IAA content and the activity of IAA destruction in the decapitated epicotyls of etiolated Stizolobium and Vicia seedlings. Bot Mag (Tokyo) 82: 110–120
Odawara S, Watanabe A, Imaseki H (1977) Involvement of cellular membrane in regulation of ethylene production. Plant Cell Physiol 18: 567–575
Palmer JM (1968) The effect of some plant growth substances on the induction of enzymic activities in thin slices of plant tubers. In: Wightman F, Setterfield G (eds) Biochemistry and physiology of plant growth substances. Runge, Ottawa, pp 401–415
Palmer JM (1970 a) The influence of growth-regulating substances on the development of enhanced metabolic rates in thin slices of beetroot storage tissue. Plant Physiol 41:1173–1178
Palmer JM (1970 b) The induction of phosphatase activity in thin slices of Jerusalem artichoke tissue by treatment with indoleacetic acid. Planta 93:53–59
Patau K, Das ND, Skoog F (1957) Induction of DNA synthesis by kinetin and indoleacetic acid in excised tobacco pith tissue. Physiol Plant 10: 949–966
Rains DW (1969) Sodium and potassium absorption by bean stem tissues. Plant physiol 44: 547–554
Rana MA, Gahan PB (1983) A quantitative cytochemical study of determination for xylem element formation in response to wounding in roots of Pisum sativum. Planta 157: 307–316
Rappaport L, Sachs M (1967) Wound-induced gibberellins. Nature 214: 1149–1150
Rhodes MJC, Wooltorton LSC (1971) The effect of ethylene on the respiration and on the activity of phenylalanine ammonia-lyase in swede and parsnip root tissue. Phytochemistry 10: 1989–1997
Rhodes MJC, Wooltorton LSC (1973) Stimulation of phenolic acid and lignin biosynthesis in swede root tissue by ethylene. Phytochemistry 12: 107–118
Riov J, Yang SF (1982) Autoinhibition of ethylene production in citrus peel discs. Plant Physiol 69: 687–690
Riov J, Monselise SP, Kahan RS (1969) Ethylene-controlled induction of phenylalanine ammonia-lyase in Citrus fruit peel. Plant Physiol 44: 631–635
Roberts LW (1969) The initiation of xylem differentiation. Botan Rev 35: 201–250
Roberts LW, Fosket DE (1966) Interaction of gibberellic acid and indoleacetic acid in the differentiation of wound vessel members. New Phytologist 65: 5–8
Robbertse PJ, McCully M (1979) Regeneration of vascular tissue in wounded pea roots. Planta 145: 167–773
Rutherford PP (1971) Inhibition by actinomycin D of water uptake and invertase and hydrolase activities induced in Jerusalem artichoke tuber tissue discs by treatment with 2,4-dichlorophenoxyacetic acid. Phytochem 10: 1469–1473
Ryan CA (1974) Assay and biochemical properties of the proteinase inhibitor-inducing factor, a wound hormone. Plant Physiol 54: 328–332
Ryan CA (1978) Proteinase inhibitors in plant leaves: A biochemical model for pest- induced natural plant protection. Trends Biochem Sci July, 148–150
Ryan CA, Bishop P, Pearce G, Darvill AG, McNeil M, Albersheim P (1981) A sycamore cell wall polysaccharide and a chemically related tomato leaf polysaccharide possess similar proteinase inhibitor-inducing activities. Plant Physiol 68: 616 — 618
Sachs T (1968 a) The role of the root in the induction of xylem differentiation in peas. Ann Botany (London) 32:389–399
Sachs T (1968 b) On the determination of the pattern of vascular tissue in peas. Ann Botany (London) 32:781–790
Sachs T (1969) Polarity and the induction of organized vascular tissues. Ann. Botany (London) 33, 263–275
Sachs T, Cohen D (1982) Circular vessels and the control of vascular differentiation in plants. Differentiation 21: 22–26
Sakai S, Imaseki H (1972) Ethylene biosynthesis: Methionine as an in vivo precursor of ethylene in auxin-treated mung bean hypocotyl segments. Planta 105: 165–173
Saltveit ME Jr, Dilley DR (1978) Rapidly induced wound ethylene from excised segments of etiolated Pisum sativum L. cv. Alaska I. Characterization of the response. Plant Physiol 61: 447–450
Saltveit ME Jr, Dilley DR (1978) Rapidly induced wound ethylene from excised segments of etiolated Pisum sativum L. cv. Alaska II. Oxygen and temperature dependency. Plant Physiol 61: 675–679
Sato T, Watanabe A, Imaseki H (1976) Effect of ethylene on DNA synthesis in potato tuber slices. Plant Cell Physiol 17: 1255–1262
Sato T, Ishizuka M, Watanabe A, Imaseki H (1980) Synthesis and properties of polysomal RNA of potato tuber slices in the early stage of aging. Plant Cell Physiol 21: 137–147
Setterfield G (1963) Growth regulation in excised slices of Jerusalem artichoke tuber tissue. Cell differentiation. Symp Soc Exp Biol 17:98–12, Univ Press, Cambridge
Shibaoka H, Anzai T, Mitsuhashi M, Shimokoriyama M (1967) Interaction between heliangine and pyrimidines in adventitious root formation of Phaseolus cutting. Plant Cell Physiol 8: 647–656
Shumway LK, Rancour JM, Ryan CA (1970) Vacuolar protein bodies in tomato leaf cells and their relationship to storage of chymotrypsin inhibitor I protein. Planta 93: 1–14
Shumway KK, Yang V, Ryan CA (1976) Evidence for the presence of proteinase inhibitor I in vacuolar protein bodies of plant cells. Planta 129: 151–165
Skoog F, Schmitz RY (1972) Cytokinins. In: Steward FC (ed) Plant physiology vol VIB. Academic Press, New York London, pp 181–213
Soekarjo R (1965) On the formation of adventitious roots in cuttings of Coleus in relation to the effect of indoleacetic acid on the epinastic curvature of isolated petioles. Acta Bot Neerl 14: 373–399
Soliday DL, Dean BB, Kolattukudy PE (1978) Suberization: Inhibition by washing and stimulation by abscisic acid in potato disks and tissue culture. Plant Physiol 61: 170–174
Sperling E, Laties GG (1963) The dependence of auxin-induced growth on auxin-independent metabolic changes in slices of storage tissue. Plant Physiol 38: 546–550
Stafford HA (1965) Factors controlling the synthesis of natural and induced lignins in Phleum and Elodea. Plant Physiol 40: 844–851
Stahmann MA, Clare BG, Woodbury W (1976) Increased disease resistance and enzyme activity induced by ethylene and ethylene production by black rot-infected sweet potato tissue. Plant Physiol 41: 1505–1512
Steward FC, Ammirato PV, Mapes MO (1970) Growth and development of totipotent cells. Some problems, procedures and perspectives. Ann Bot 34: 761–787
Tanaka Y, Uritani I (1977) Polarity of production of polyphenols and development of various enzyme activities in cut-injured sweet potato root tissue. Plant Physiol 60: 563–566
Tanaka Y, Uritani I (1979) Polar transport and content of 1–3-AA in wounded sweat potato root tissues. Plant Cell Physiol 20: 1087–1096
Theologis A, Laties GG (1981) Wound-induced membrane lipid breakdown in potato tuber. Plant Physiol 68: 530–538
Thimann KV (1972) The natural plant hormones. In: Steward FC (ed) Plant physiology. Academic Press, New York London, pp 95–100
Thimann KV (1977) Hormone action in the whole life of plants. Univ Massachusetts Press, Amherst, pp 188–203
Thimann KV, Koepfli JB (1935) Identity of the growth-promoting and root-forming substances of plants. Nature 135: 101
Thomas B, Hall MA (1975) The effect of growth regulators on wound-stimulated callose formation in Salix viminalis. Plant Sci Lett 4: 9–15
Thompson NP (1966) Vascular regeneration and long-distance transport of indole–3- acetic acid in Coleus stems. Plant Physiol 41: 1106–1112
Thompson NP, Jacobs WP (1966) Polarity of IAA effect on sieve-tube and xylem regeneration in Coleus and tomato stems. Plant Physiol 41: 673–682
Tomaszewski M (1963) The mechabism of synergistic effects between auxin and some natural phenolic substances. In: Régulateurs naturels de la croissance végétale. CNRS, Paris, pp 335–351
Treshow M (1955 a) Physiology and anatomical development of tomato fruit tumor. Am J Botany 42:198–202
Treshow M (1955 b) The etiology, development, and control of tomato fruit tumor. Phytopathol 45:132–137
Uritani I (1961) The role of plant phenolics in disease resistance and immunity. In: Johnson G, Geissman TA (eds) Proceedings of symposium on biochemistry of plant phenolic substances. Colorado State University
Uritani I (1971) Protein changes in diseased plants. Ann Rev Phytopathol 9: 211–234
Uritani I (1976) Protein metabolism. In: Heitefuss R, Williams PH (eds) Encyclopedia of plant physiology, New Series, vol 4. Springer, Berlin Heidelberg New York, pp 509 - 525
Van Overbeek J, Gregory LE (1945) A physiological separation of two factors necessary for the formation of roots on cuttings. Am J Botany 32: 336–341
Van Steveninck RFM (1961) The “lag-phase” in salt uptake of storage tissue. Nature 190: 1072–1075
Van Steveninck RFM (1972) Inhibition of the development of a cation accumulatory system and of Tris-induced uptake in storage tissues by N6-benzyladenine and kinetin. Plant Physiol 27: 43–47
Van Steveninck RFM (1975) The “washing” or “aging” phenomenon in plant tissues. Ann Rev Plant Physiol 26: 237–258
Walker-Simmons M, Ryan CA (1979 a) Immunological identification of proteinase inhibitors I and II in isolated tomato leaf vacuoles. Plant Physiol 60: 61–63
Walker-Simmons M, Ryan CA ( 1979 b) Wound-induced accumulation of trypsin inhibitor activities in plant leaves. Survey of several plant genera. Plant Physiol 59: 437-439
Wardrop AB (1971) Occurrence and formation in plants. In: Sarkanen KV, Ludwig CH (eds) Lignins, occurrence, formation structure and reactions. Wiley-Interscience, New York, pp 19–41
Hormonal Control of Wound-Induced Responses Wareing PF (1958) Interaction between indole acetic acid and gibberellic acid in cambial activity. Nature 181: 1744–1745
Warmke HE, Warmke GL (1950) Role of auxin in differentiation of root and shoot of Taraxacum and Cichorium. Am. J Bot 37: 272–280
Watanabe A, Imaseki H (1973) Induction of deoxyribonucleic acid synthesis in potato tuber tissue by cutting. Plant Physiol 51: 772–776
Watanabe A, Imaseki H (1976) Induction of deoxyribonucleic acid synthesis in potato tuber slices. Role of protein synthesis. Plant Physiol 57: 568–571
Went FW (1936) The dual effect of auxin on root formation. Am J Bot 26: 24–29
Went FW (1938) Specific factors other than auxin affecting growth and root formation. Plant Physiol 13: 55–80
Wielgat B, Kahl G (1979 a) Enhancement of polyribosome formation and RNA synthesis of gibberellic acid in wounded potato tuber tissue. Plant Physiol 64: 863–866
Wielgat B, Kahl G (1979 b) Gibberellic acid activates chromatin-bound DNA-dependent RNA polymerase in wounded potato tuber tissue. Plant Physiol 64: 867–871
Williamson CE (1950) Ethylene, a metabolic product of diseased or injured plants. Phytopathology 40: 205–208
Wright STC (1978) Phytohormones and stress phenomena. In: Letham DS, Goodwin PB, Higgins TVJ (eds) Phytohormones and related compounds - a comprehensive treatise, vol II. Elsevier/North-Holland Biomedical Press, Amsterdam New York, pp 495–536
Wright STC (1979) The effect of plant growth-regulator treatments on the levels of ethylene emanation from excised turgid and wilted wheat leaves. Planta 144: 177–188
Yang SF (1983) Mechanism and regulation of ethylene biosynthesis. In: Akazawa T, Asahi T, Imaseki H (eds) The new frontiers in plant biochemistry. Jpn Sci Soc Press and Nijhoff/Junk, pp 133–151
Yang SF, Hoffman NE, Nckeon T, Riov J, Kao CH, Yung KH (1982) Mechanism and regulation of ethylene biosynthesis. In: Wareing PF (ed) Plant growth substances 1982. Academic Press, London New York, pp 239–248
Yeoman MM (1970) Early development in callus cultures. Int Rev Cytol 29: 383–409
Yeoman MM, Evans PK (1967) Growth and differentiation of plant tissue cultures II. Synchronous cell divisions in developing callus cultures. Ann Bot 31: 323–332
Yeoman MM, Dyer AF, Roberson AI (1965) Growth and differentiation of plant tissue cultures I. Changes accompanying the growth of explants from Helianthus tuberosus tubers. Ann Bot 29: 265–276
Yeoman MM, Naik GG, Robertson AI (1968) Growth and differentiation of plant tissue cultures III. The initiation and pattern of cell division in developing callus cultures. Ann Bot 32: 301–313
Yoshii H, Imaseki H (1981) Biosynthesis of auxin-induced ethylene. Effects of indole–3- acetic acid, benzyladenine and abscisic acid on endogenous levels of 1-aminocyclopro- pane–1 -carboxylic acid ( ACC) and ACC synthase. Plant Cell Physiol 22: 369–379
Yoshii H, Imaseki H (1982) Regulation of auxin-induced ethylene biosynthesis. Repression of inductive formation of 1-amino-cyclopropane–1-carboxylate synthase by ethylene. Plant Cell Physiol 23: 639–649
Yoshii H, Watanabe A, Imaseki H (1980) Biosynthesis of auxin-induced ethylene in mung bean hypocotyls. Plant Cell Physiol 21: 279–291
Yu Y, Yang SF (1979) Auxin-induced ethylene production and its inhibition by amino- ethoxyvinylglycine and cobalt ion. Plant Physiol 64: 1074–1077
Yu Y, Yang SF (1980) Biosynthesis of wound ethylene. Plant Physiol 66: 281–285
Yu Y, Adams DO, Yang SF (1979) Regulation of auxin-induced ethylene production in mung bean hypocotyls. Role of 1-aminocyclopropane-l-carboxylic acid. Plant Physiol 63: 589–590
Yu Y, Adams DO, Yang SF (1979) 1-Aminocyclopropane-l-carboxylate synthase, a key enzyme in ethylene biosynthesis. Arch Biochem Biophys 198: 280–286
Zimmerman DC, Coudron CA (1979) Identification of traumatin, a wound hormone, as 12-oxo-trans–10-dodecenoic acid. Plant Physiol 63: 536–541
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1985 Springer-Verlag Berlin · Heidelberg
About this chapter
Cite this chapter
Imaseki, H. (1985). Hormonal Control of Wound-Induced Responses. In: Pharis, R.P., Reid, D.M. (eds) Hormonal Regulation of Development III. Encyclopedia of Plant Physiology, vol 11. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-67734-2_14
Download citation
DOI: https://doi.org/10.1007/978-3-642-67734-2_14
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-67736-6
Online ISBN: 978-3-642-67734-2
eBook Packages: Springer Book Archive