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Hormonal Control of Wound-Induced Responses

  • Chapter
Hormonal Regulation of Development III

Part of the book series: Encyclopedia of Plant Physiology ((PLANT,volume 11))

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.

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References

  1. Abeles AL, Abeles FB (1972) Biochemical pathway of stress-induced ethylene. Plant Physiol 50: 496–498

    PubMed  CAS  Google Scholar 

  2. Abeles FB (1972) Biosynthesis and mechanism of action of ethylene. Ann Rev Plant Physiol 23: 259–29

    CAS  Google Scholar 

  3. Abeles FB (1973) Ethylene in plant biology. Academic Press, New York London, pp 87–108

    Google Scholar 

  4. 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

    PubMed  CAS  Google Scholar 

  5. Adams PB, Rowan KS (1970) Glycolytic control of respiration during aging of carrot root tissue. Plant Physiol 45: 490–494

    PubMed  CAS  Google Scholar 

  6. Adamson D (1962) Expansion and division in auxin-treated plant cells. Can J Botany 40: 719–744

    CAS  Google Scholar 

  7. Aloni R (1976) Polarity of induction an pattern of primary phloem fiber differentiation in Coleus. Am J Botany 63: 877–889

    Google Scholar 

  8. Aloni R (1979) Role of auxin and gibberellin in differentiation of primary phloem fibers. Plant Physiol 63: 609–614

    PubMed  CAS  Google Scholar 

  9. Aloni R, Jacobs WP (1977) Polarity of tracheary regeneration in young internodes of Coleus ( Labiatae ). Am J Botany 64: 395–403

    Google Scholar 

  10. 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

    CAS  Google Scholar 

  11. 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

    Google Scholar 

  12. Anderson JD, Lieberman M, Stewart RN (1979) Ethylene production by apple protoplasts. Plant Physiol 63: 931–935

    PubMed  CAS  Google Scholar 

  13. 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

    CAS  Google Scholar 

  14. Apelbaum A, Yang SF (1981) Biosynthesis of stress ethylene induced by water deficit. Plant Physiol 68: 594–596

    PubMed  CAS  Google Scholar 

  15. apRees T (1966) Evidence for the widespread occurrence of induced respiration in slices of plant tissue. Australian J Biol Sci 19: 981–990

    CAS  Google Scholar 

  16. 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

    PubMed  CAS  Google Scholar 

  17. Balls AK, Ryan CA (1963) Concerning a chymotryptic inhibitor from potatos and its binding capacity for the enzyme. J Biol Chem 238: 2976–2982

    PubMed  CAS  Google Scholar 

  18. Behnke H-D, Schulz A (1980) Fine structure, pattern of division, and course of wound phloem in Coleus blumei. Planta 150: 357–365

    Google Scholar 

  19. Benayoun J, Aloni R, Sachs T (1975) Regeneration around wounds and the control of vascular differentiation. Ann Botany (London) 39: 447–454

    Google Scholar 

  20. Boiler T, Herner RC, Kende H (1979) Enzymatic formation of an ethylene precursor, 1-aminocyclopropane-l-carboxylic acid. Planta 145: 293–303

    Google Scholar 

  21. 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

    PubMed  CAS  Google Scholar 

  22. Borchert R, McChesney JD (1973) Time course and localization of DNA synthesis during wound healing of potato tuber tissue. Develop Biol 35: 293–301

    PubMed  CAS  Google Scholar 

  23. 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

    PubMed  CAS  Google Scholar 

  24. 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

    Google Scholar 

  25. Burg SP, Clagett CO (1967) Conversion of methionine to ethylene in vegetative tissue and fruits. Biochem Biophys Res Commun 27: 125–130

    PubMed  CAS  Google Scholar 

  26. Byrne H, Setterfleld G (1977) Activation of ribosomal and messenger RNA synthesis in excised Jerusalem artichoke tuber slices. Planta 136: 203–210

    CAS  Google Scholar 

  27. 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

    CAS  Google Scholar 

  28. 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

    Google Scholar 

  29. 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

    Google Scholar 

  30. 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

    CAS  Google Scholar 

  31. Clutter M (1960) Hormonal induction of vascular tissue in tobacco pith in vitro. Science 132: 548–549

    PubMed  CAS  Google Scholar 

  32. Comer AE (1978) Pattern of cell division and wound vessel member differentiation in Coleus pith explants. Plant Physiol 62: 354–359

    PubMed  CAS  Google Scholar 

  33. Cooper WC (1938) Hormones and root formation. Botan Gaz 99: 599–614

    CAS  Google Scholar 

  34. Dalessandro G (1973) Hormonal control of xylogenesis in pith parenchyma explants of Lactuca. Ann Botany (London) 37: 375–382

    CAS  Google Scholar 

  35. Dalenssandro G, Roberts LW (1971) Induction of xylogenesis in pith parenchyma ex- plants of Lactuca. Am J Botany 58: 378–385

    Google Scholar 

  36. 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

    Google Scholar 

  37. Dean BB, Kolattukudy PE (1976) Synthesis of suberin during wound-healing in jade leaves, tomato fruit, and bean pods. Plant Physiol 58: 411–416

    PubMed  CAS  Google Scholar 

  38. Duda CT, Cherry JH (1971) Chromatin- and nuclei-directed ribonucleic acid synthesis in sugar beet root. Plant Physiol 47: 262–268

    PubMed  CAS  Google Scholar 

  39. Edelman J, Hall MA (1964) Effect of growth hormones on the development of invertase associated with cell walls. Nature 201: 296–297

    PubMed  CAS  Google Scholar 

  40. 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

    Google Scholar 

  41. Ellis RJ, MacDonald IR (1967) Activation of protein synthesis by microsomes from aging beet disks. Plant Physiol 42: 1297–1302

    PubMed  CAS  Google Scholar 

  42. 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

    Google Scholar 

  43. Fosket DE, Roberts LW (1964) Induction of wound-vessel differentiation in isolated Coleus stem segments in vitro. Am J Bot 51: 19–25

    CAS  Google Scholar 

  44. 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

    Google Scholar 

  45. Gahagan HE, Holm RE, Abeles FB (1968) Effect of ethylene on peroxidase activity. Physiol Plant 21: 1270–1279

    CAS  Google Scholar 

  46. Gayler KR, Glasziou KT (1964) Plant enzyme synthesis: Hormonal regulation of invertase and peroxidase synthesis in sugar cane. Planta 84: 185–194

    Google Scholar 

  47. Gersan, Lips, Sachs T (1980) Effects of wounding on transport in phloem. J Exp Bot 31: 783–789

    Google Scholar 

  48. Glasziou KT (1969) Control of enzyme formation and inactivation in plants. Annu Rev Plant Physiol 20: 63–88

    CAS  Google Scholar 

  49. 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

    Google Scholar 

  50. Green TR, Ryan CA (1972) Wound-induced proteinase inhibitor in plant leaves: A possible defense mechanism against insects. Science 175: 776–777

    Google Scholar 

  51. 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

    Google Scholar 

  52. 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

    Google Scholar 

  53. Haberlandt G (1921) Wundhormone als Erreger von Zellteilungen. Beitr Allg Bot 2: 1–53

    Google Scholar 

  54. 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

    CAS  Google Scholar 

  55. Hanson AD, Kende H (1975) Ethylene-enhanced ion and sucrose efflux in morning glory flower tissue. Plant Physiol 55: 663–669

    PubMed  CAS  Google Scholar 

  56. Hanson AE, Kende H (1976) Methionine metabolism and ethylene biosynthesis in senescent flower tissue of morning glory. Plant Physiol 57: 528–537

    PubMed  CAS  Google Scholar 

  57. Hanson AE, Kende H (1976) Biosynthesis of wound ethylene in morning glory flower tissue. Plant Physiol 57: 538–541

    PubMed  CAS  Google Scholar 

  58. 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

    Google Scholar 

  59. 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

    PubMed  CAS  Google Scholar 

  60. 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

    Google Scholar 

  61. Hyodo H (1977 b) Ethylene production by albedo tissue of Satsuma mandarin (Citrus unshiu Marc.) fruit. Plant Physiol 59:111–113

    Google Scholar 

  62. Hyodo H (1978) Ethylene production by wounded tissue of citrus fruit. Plant Cell Physiol 19: 545–551

    CAS  Google Scholar 

  63. Hyodo H, Nishino T (1981) Wound-induced ethylene formation in albedo tissue of citrus fruit. Planta Physiol 67: 421–423

    CAS  Google Scholar 

  64. Hyodo H, Yang SF (1971) Ethylene-enhanced synthesis of phenylalanine ammonia-lyase in pea seedlings. Plant Physiol 47: 765–770

    PubMed  CAS  Google Scholar 

  65. 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

    CAS  Google Scholar 

  66. 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

    CAS  Google Scholar 

  67. Imaseki H (1970) Induction of peroxidase activity by ethylene in sweet potato. Plant Physiol 46: 172–174

    PubMed  CAS  Google Scholar 

  68. 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

    Google Scholar 

  69. 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

    Google Scholar 

  70. 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

    Google Scholar 

  71. Imaseki H, Uritani I, Stahmann MA (1968c) Production of ethylene by injured sweet potato root tissue. Plant Cell Physiol 9: 757–768

    CAS  Google Scholar 

  72. 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

    Google Scholar 

  73. 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

    Google Scholar 

  74. 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

    PubMed  CAS  Google Scholar 

  75. Jackson MB, Campbell DJ (1976) Production of ethylene by excised segments of plant tissue prior to the effect of wounding. Planta 129: 273–274

    CAS  Google Scholar 

  76. Jacobs WP (1952) The role of auxin in differentiation of xylem around a wound. Am J Botany 39: 301–309

    CAS  Google Scholar 

  77. Jacobs WP (1956) Internal factors controlling cell differentiation in the flowering plants. Am Naturalist 90: 163–169

    Google Scholar 

  78. Jacobs WP (1970) Regulation and differentiation of sieve tube elements. Intern Rev Cytol 28: 239–273

    CAS  Google Scholar 

  79. Jacobs WP, MacCready CC (1967) Polar transport of growth regulators in pith and vascular tissues of Coleus stems. Am J Botany 54: 1035–1040

    CAS  Google Scholar 

  80. 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

    PubMed  CAS  Google Scholar 

  81. Jones JF, Kende H (1979) Auxin-induced ethylene biosynthesis in subapical stem sections of etiolated seedlings of Pisum sativum L. Planta 146: 649–656

    CAS  Google Scholar 

  82. 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

    Google Scholar 

  83. Kahl G (1971) Activation of protein synthesis in aging potato tuber slices. Z Naturforsch 26 b: 1064–1067

    Google Scholar 

  84. Kahl G (1973) Genetic and metabolic regulation in differentiating plant storage tissue cells. Botan Rev 39: 274–299

    CAS  Google Scholar 

  85. Kahl G (1974) Metabolism in plant storage tissue slices. Botan Rev 40: 263–314

    CAS  Google Scholar 

  86. 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

    Google Scholar 

  87. Kende H, Hanson AD (1976) Relationship between ethylene evolution and senescence in morning glory flower tissue. Plant Physiol 57: 523–527

    PubMed  CAS  Google Scholar 

  88. 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

    PubMed  CAS  Google Scholar 

  89. 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

    Google Scholar 

  90. 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

    CAS  Google Scholar 

  91. Koopowitz H, Dhys R, Fosket DE (1975) Cell membrane potentials of higher plants: Changes induced by wounding. J Exp Botany 26: 131–137

    Google Scholar 

  92. Lamotte CE, Jacobs WP (1963) A role of auxin in phloem regeneration in Coleus interno- des. Develop Biol 8: 80–98

    CAS  Google Scholar 

  93. Lange H, Rosenstock G, Kahl G (1970) Induktionsbedingungen der Suberinsynthese und Zellproliferation bei Parenchymfragmenten der Kartoffelknolle. Planta 90: 109–118

    CAS  Google Scholar 

  94. Laties GG (1962) Controlling influence of thickness on development and type of respiratory activity in potato slices. Plant Physiol 37: 679–690

    PubMed  CAS  Google Scholar 

  95. Leaver CJ, Key JL (1967) Polyribosome formation and RNA synthesis during aging of carrot-root tissue. Proc Nat Acad Sci US 57: 1338–1344

    CAS  Google Scholar 

  96. Lieberman M (1979) Biosynthesis and action of ethylene. Ann Rev Plant Physiol 30: 533–591

    CAS  Google Scholar 

  97. Lieberman M, Kunishi AT, Mapson LW, Wardale DA (1965) Ethylene production from methionine. Biochem J 97: 449–459

    PubMed  CAS  Google Scholar 

  98. Lieberman M, Kunishi A, Mapson LW, Wardale DA (1966) Stimulation of ethylene production in apple tissue slices by methionine. Plant Physiol 41: 376–382

    PubMed  CAS  Google Scholar 

  99. Lipetz J (1970) Wound-healing in higher plants. Intern Rev Cytol 27: 1–28

    CAS  Google Scholar 

  100. 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

    Google Scholar 

  101. 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

    Google Scholar 

  102. Mader M, Fiissl R (1982) Role of peroxidase in lignification of tobacco cells. II. Regulation by phenolic compounds. Plant Physiol 70: 1132–1134

    Google Scholar 

  103. 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

    CAS  Google Scholar 

  104. 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

    CAS  Google Scholar 

  105. Mattoo AK, Lieberman M (1977) Localization of the ethylene-synthesizing system in apple tissue. Plant Physiol 60: 794–799

    PubMed  CAS  Google Scholar 

  106. 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

    CAS  Google Scholar 

  107. 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

    CAS  Google Scholar 

  108. 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

    CAS  Google Scholar 

  109. 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

    Google Scholar 

  110. 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

    Google Scholar 

  111. Mizuno K, Komamine A, Shimokoriyama M (1971) Vessel element formation in cultured carrot-root phloem slices. Plant Cell Physiol 12: 823–830

    CAS  Google Scholar 

  112. 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

    Google Scholar 

  113. Odawara S, Watanabe A, Imaseki H (1977) Involvement of cellular membrane in regulation of ethylene production. Plant Cell Physiol 18: 567–575

    Google Scholar 

  114. 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

    Google Scholar 

  115. 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

    Google Scholar 

  116. 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

    Google Scholar 

  117. 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

    CAS  Google Scholar 

  118. Rains DW (1969) Sodium and potassium absorption by bean stem tissues. Plant physiol 44: 547–554

    PubMed  CAS  Google Scholar 

  119. 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

    CAS  Google Scholar 

  120. Rappaport L, Sachs M (1967) Wound-induced gibberellins. Nature 214: 1149–1150

    CAS  Google Scholar 

  121. 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

    CAS  Google Scholar 

  122. Rhodes MJC, Wooltorton LSC (1973) Stimulation of phenolic acid and lignin biosynthesis in swede root tissue by ethylene. Phytochemistry 12: 107–118

    CAS  Google Scholar 

  123. Riov J, Yang SF (1982) Autoinhibition of ethylene production in citrus peel discs. Plant Physiol 69: 687–690

    PubMed  CAS  Google Scholar 

  124. Riov J, Monselise SP, Kahan RS (1969) Ethylene-controlled induction of phenylalanine ammonia-lyase in Citrus fruit peel. Plant Physiol 44: 631–635

    PubMed  CAS  Google Scholar 

  125. Roberts LW (1969) The initiation of xylem differentiation. Botan Rev 35: 201–250

    CAS  Google Scholar 

  126. Roberts LW, Fosket DE (1966) Interaction of gibberellic acid and indoleacetic acid in the differentiation of wound vessel members. New Phytologist 65: 5–8

    CAS  Google Scholar 

  127. Robbertse PJ, McCully M (1979) Regeneration of vascular tissue in wounded pea roots. Planta 145: 167–773

    Google Scholar 

  128. 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

    CAS  Google Scholar 

  129. Ryan CA (1974) Assay and biochemical properties of the proteinase inhibitor-inducing factor, a wound hormone. Plant Physiol 54: 328–332

    PubMed  CAS  Google Scholar 

  130. Ryan CA (1978) Proteinase inhibitors in plant leaves: A biochemical model for pest- induced natural plant protection. Trends Biochem Sci July, 148–150

    Google Scholar 

  131. 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

    PubMed  CAS  Google Scholar 

  132. Sachs T (1968 a) The role of the root in the induction of xylem differentiation in peas. Ann Botany (London) 32:389–399

    Google Scholar 

  133. Sachs T (1968 b) On the determination of the pattern of vascular tissue in peas. Ann Botany (London) 32:781–790

    Google Scholar 

  134. Sachs T (1969) Polarity and the induction of organized vascular tissues. Ann. Botany (London) 33, 263–275

    Google Scholar 

  135. Sachs T, Cohen D (1982) Circular vessels and the control of vascular differentiation in plants. Differentiation 21: 22–26

    Google Scholar 

  136. 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

    Google Scholar 

  137. 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

    Google Scholar 

  138. 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

    Google Scholar 

  139. Sato T, Watanabe A, Imaseki H (1976) Effect of ethylene on DNA synthesis in potato tuber slices. Plant Cell Physiol 17: 1255–1262

    CAS  Google Scholar 

  140. 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

    CAS  Google Scholar 

  141. 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

    Google Scholar 

  142. 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

    CAS  Google Scholar 

  143. 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

    CAS  Google Scholar 

  144. 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

    Google Scholar 

  145. Skoog F, Schmitz RY (1972) Cytokinins. In: Steward FC (ed) Plant physiology vol VIB. Academic Press, New York London, pp 181–213

    Google Scholar 

  146. 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

    CAS  Google Scholar 

  147. 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

    Google Scholar 

  148. 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

    PubMed  CAS  Google Scholar 

  149. Stafford HA (1965) Factors controlling the synthesis of natural and induced lignins in Phleum and Elodea. Plant Physiol 40: 844–851

    PubMed  CAS  Google Scholar 

  150. 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

    Google Scholar 

  151. Steward FC, Ammirato PV, Mapes MO (1970) Growth and development of totipotent cells. Some problems, procedures and perspectives. Ann Bot 34: 761–787

    Google Scholar 

  152. 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

    PubMed  CAS  Google Scholar 

  153. 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

    CAS  Google Scholar 

  154. Theologis A, Laties GG (1981) Wound-induced membrane lipid breakdown in potato tuber. Plant Physiol 68: 530–538

    Google Scholar 

  155. Thimann KV (1972) The natural plant hormones. In: Steward FC (ed) Plant physiology. Academic Press, New York London, pp 95–100

    Google Scholar 

  156. Thimann KV (1977) Hormone action in the whole life of plants. Univ Massachusetts Press, Amherst, pp 188–203

    Google Scholar 

  157. Thimann KV, Koepfli JB (1935) Identity of the growth-promoting and root-forming substances of plants. Nature 135: 101

    CAS  Google Scholar 

  158. Thomas B, Hall MA (1975) The effect of growth regulators on wound-stimulated callose formation in Salix viminalis. Plant Sci Lett 4: 9–15

    CAS  Google Scholar 

  159. Thompson NP (1966) Vascular regeneration and long-distance transport of indole–3- acetic acid in Coleus stems. Plant Physiol 41: 1106–1112

    PubMed  CAS  Google Scholar 

  160. 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

    PubMed  CAS  Google Scholar 

  161. 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

    Google Scholar 

  162. Treshow M (1955 a) Physiology and anatomical development of tomato fruit tumor. Am J Botany 42:198–202

    Google Scholar 

  163. Treshow M (1955 b) The etiology, development, and control of tomato fruit tumor. Phytopathol 45:132–137

    Google Scholar 

  164. 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

    Google Scholar 

  165. Uritani I (1971) Protein changes in diseased plants. Ann Rev Phytopathol 9: 211–234

    CAS  Google Scholar 

  166. 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

    Google Scholar 

  167. 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

    Google Scholar 

  168. Van Steveninck RFM (1961) The “lag-phase” in salt uptake of storage tissue. Nature 190: 1072–1075

    Google Scholar 

  169. 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

    Google Scholar 

  170. Van Steveninck RFM (1975) The “washing” or “aging” phenomenon in plant tissues. Ann Rev Plant Physiol 26: 237–258

    Google Scholar 

  171. 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

    Google Scholar 

  172. 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

    Google Scholar 

  173. 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

    Google Scholar 

  174. Hormonal Control of Wound-Induced Responses Wareing PF (1958) Interaction between indole acetic acid and gibberellic acid in cambial activity. Nature 181: 1744–1745

    Google Scholar 

  175. Warmke HE, Warmke GL (1950) Role of auxin in differentiation of root and shoot of Taraxacum and Cichorium. Am. J Bot 37: 272–280

    Google Scholar 

  176. Watanabe A, Imaseki H (1973) Induction of deoxyribonucleic acid synthesis in potato tuber tissue by cutting. Plant Physiol 51: 772–776

    PubMed  CAS  Google Scholar 

  177. Watanabe A, Imaseki H (1976) Induction of deoxyribonucleic acid synthesis in potato tuber slices. Role of protein synthesis. Plant Physiol 57: 568–571

    Google Scholar 

  178. Went FW (1936) The dual effect of auxin on root formation. Am J Bot 26: 24–29

    Google Scholar 

  179. Went FW (1938) Specific factors other than auxin affecting growth and root formation. Plant Physiol 13: 55–80

    PubMed  CAS  Google Scholar 

  180. 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

    Google Scholar 

  181. 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

    Google Scholar 

  182. Williamson CE (1950) Ethylene, a metabolic product of diseased or injured plants. Phytopathology 40: 205–208

    CAS  Google Scholar 

  183. 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

    Google Scholar 

  184. 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

    Google Scholar 

  185. 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

    Google Scholar 

  186. 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

    Google Scholar 

  187. Yeoman MM (1970) Early development in callus cultures. Int Rev Cytol 29: 383–409

    CAS  Google Scholar 

  188. 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

    Google Scholar 

  189. 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

    Google Scholar 

  190. 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

    Google Scholar 

  191. 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

    Google Scholar 

  192. 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

    CAS  Google Scholar 

  193. Yoshii H, Watanabe A, Imaseki H (1980) Biosynthesis of auxin-induced ethylene in mung bean hypocotyls. Plant Cell Physiol 21: 279–291

    CAS  Google Scholar 

  194. Yu Y, Yang SF (1979) Auxin-induced ethylene production and its inhibition by amino- ethoxyvinylglycine and cobalt ion. Plant Physiol 64: 1074–1077

    PubMed  CAS  Google Scholar 

  195. Yu Y, Yang SF (1980) Biosynthesis of wound ethylene. Plant Physiol 66: 281–285

    PubMed  CAS  Google Scholar 

  196. 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

    PubMed  CAS  Google Scholar 

  197. Yu Y, Adams DO, Yang SF (1979) 1-Aminocyclopropane-l-carboxylate synthase, a key enzyme in ethylene biosynthesis. Arch Biochem Biophys 198: 280–286

    Google Scholar 

  198. Zimmerman DC, Coudron CA (1979) Identification of traumatin, a wound hormone, as 12-oxo-trans–10-dodecenoic acid. Plant Physiol 63: 536–541

    PubMed  CAS  Google Scholar 

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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

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