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Chemical Signaling During Induced Leaf Movements

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Part of the book series: Signaling and Communication in Plants ((SIGCOMM))

Abstract

Chemical aspects of the circadian leaf movement known as nyctinasty are discussed in this chapter. Each nyctinastic plant from the five different genera examined so far contained a pair of factors, one of which induces leaf closure while the other induces leaf opening. Changes in the relative contents of the closing and opening factors correlated with nyctinastic leaf movement. The use of fluorescence-labeled and photoaffinity-labeled factors revealed that the leaf-closing factor binds to a 38-kDa membrane protein of motor cells.

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References

  • Asamitsu Y, Nakamura Y, Ueda M, Kuwahara S, Kiyota H (2006) Synthesis and Odor Descriptions of Both Enantiomers of Methyl 4,5-Didehydrojasmonate, a Component of Jasmin Absolute, Chem. Biodivers. 3: 654–659

    Article  PubMed  CAS  Google Scholar 

  • Darwin C (1875) Insectivorous plants. John Murray, London

    Book  Google Scholar 

  • Gorton H, Satter RL (1984) Extensor and flexor protoplasts from Samanea pulvini. 2. X-ray analysis of potassium, chlorine, sulfur, phosphorus, and calcium. Plant Physiol 76:680–684

    Article  PubMed  CAS  Google Scholar 

  • Kato N, Inada M, Sato H, Miyatake R, Kumagai T, Ueda M (2006) Enantio-differential approach using fluorescence-labeled phyllanthurinolactone, a leaf-closing factor of Phyllanthus urinaria L. Tetrahedron 62:7307–7318

    Article  CAS  Google Scholar 

  • Kato E, Sasaki T, Ueda M (2008) Affinity purification and characterization of a key enzyme concerning circadian rhythmic control of nyctinasty in Lespedeza cuneata L. Bioorg Med Chem 16:4600–4616

    Article  PubMed  CAS  Google Scholar 

  • Kirchner O (1874) Die botanischen Schriften des Theophrast von Eresos. Jahrb Class Philol 7:449–539

    Google Scholar 

  • Kotzyba-Hibert F, Kapfer I, Goeldner M (1995) Recent trends in photoaffinity labeling. Angew Chem Int Ed 34:1296–1312

    Article  CAS  Google Scholar 

  • Lee Y (1990) In: Satter RL, Gorton HL, Vogelmann TC (eds) The pulvinus: motor organ for leaf movement. American Society of Plant Physiologists, Rockville, MD, pp 130–141

    Google Scholar 

  • Miyoshi E, Shizuri Y, Yamamura S (1987) Isolation of potassium chelidonate as a bioactive substance concerning with circadian rhythm in nyctinastic plants. Chem Lett 16:511–514

    Article  Google Scholar 

  • Moran N (2007a) Osmoregulation of leaf motor cell. FEBS Lett 581:2337–2347

    Article  PubMed  CAS  Google Scholar 

  • Moran N (2007b) Rhythmic leaf movements: physiological and molecular aspects. In: Mancuso S, Shabala S (eds) Rhythms in plants. Springer, Berlin, pp 3–37

    Chapter  Google Scholar 

  • Moshelion M, Moran N (2000) Potassium-efflux channels in extensor and flexor cells of the motor organ of Samanea saman are not identical. Effects of cytosolic calcium. Plant Physiol 124:911–919

    Article  PubMed  CAS  Google Scholar 

  • Moshelion M, Becker D, Czempinski K, Mueller-Roeber B, Attali, B, Hedrich R, Moran N (2002) Diurnal and circadian regulation of putative potassium channels in a leaf moving organ. Plant Physiol 128:634–642

    Article  PubMed  CAS  Google Scholar 

  • Nagano H, Kato E, Yamamura S, Ueda M (2003) Fluorescence studies on nyctinasty using fluorescence labeled cis-p-coumaroylagmatine, a leaf-opening substance of Albizzia plants: Existence of genus-specific receptor for leaf-movement factor. Org Biomol Chem 1:3186–3192

    Article  PubMed  CAS  Google Scholar 

  • Nakamura Y, Miyatake R, Matsubara A, Kiyota H, Ueda M (2006a) Enantio-differential approach to identify the target cell for glucosyl jasmonate-type leaf-closing factor, by using fluorescence-labeled probe compounds. Tetrahedron 62: 8805–8813

    Article  CAS  Google Scholar 

  • Nakamura Y, Matsubara A, Okada M, Kumaga T, Ueda M (2006b) Double fluorescence-labeling study on genus Albizzia using a set of fluorecence-labeled leaf-movement factors to identify the spatial distribution of their receptors. Chem Lett 35:744–745

    Article  CAS  Google Scholar 

  • Nakamura Y, Miyatake R, Ueda M (2008) Enantiodifferential approach for the detection of the target membrane protein of the jasmonate glycoside that controls the leaf movement of Albizzia saman. Angew Chem Int Ed 47:7289–7292

    Article  CAS  Google Scholar 

  • Ohnuki T, Ueda M, Yamamura S (1998) Molecular mechanism of the control of nyctinastic leaf-movement by biological clock in Lespedeza cuneata G. Don. Tetrahedron 54:12173–12184

    Article  CAS  Google Scholar 

  • Satter RL, Galston AW(1981) Mechanisms of control of leaf movements.Annu Rev Plant Physiol 32:83–110

    Article  CAS  Google Scholar 

  • Satter RL, Gorton HL, Vogelmann TC (1990) The pulvinus: motor organ for leaf movement (Current Topics in Plant Physiology, vol 3). American Society of Plant Physiologists, Rockville, MD

    Google Scholar 

  • Schildcknecht H (1983) Turgorins, hormones of the endogeneous daily rhythms of higher organized plants—detection, isolation, structure, synthesis, and activity. Angew Chem Int Ed 22:695–710

    Article  Google Scholar 

  • Shigemori H, Sakai N, Miyoshi E, Shizuri Y, Yamamura S (1989) Potassium lespedezate and potassium isolespedezate, bioactive substances concerned with the circadian rhythm in nyctinastic plants. Tetrahedron Lett 30:3991–3994

    Article  CAS  Google Scholar 

  • Shigemori H, Sakai N, Miyoshi E, Shizuri Y, Yamamura S (1990) Bioactive substances from Lespedeza cuneata L.G. Don and their biological activities. Tetrahedron 46:383–394

    Article  CAS  Google Scholar 

  • Tamura T, Terada T, Tanaka A (2003) A quantitative analysis and chemical approach for the reduction of nonspecific binding protein on affinity resin. Bioconjugate Chem 14:1222–1230

    Article  CAS  Google Scholar 

  • Ueda M, Nakamura Y (2006) Metabolites involved in plant movement and “memory:” nyctinasty of legumes and trap movement in the Venus flytrap, Nat Prod Rep 23:548–557

    Article  PubMed  CAS  Google Scholar 

  • Ueda M, Yamamura S (1999a) Leaf-opening substance of Mimosa pudica L.; chemical studies on the other leaf-movement of Mimosa. Tetrahedron Lett 40:353–356

    Article  CAS  Google Scholar 

  • Ueda M, Yamamura S (1999b) Leaf-closing substance of Mimosa pudica L.; chemical studies on another leaf-movement of Mimosa II. Tetrahedron Lett 40:2981–2984

    Article  CAS  Google Scholar 

  • Ueda M, Yamamura S (2000) The chemistry and biology of the plant leaf-movements. Angew Chem Int Ed 39:1400–1414

    Article  CAS  Google Scholar 

  • Ueda M, Shigemori-Suzuki T, Yamamura S (1995) Phyllanthurinolactone, a leaf-closing factor of nyctinastic plant, Phyllanthus urinaria L. Tetrahedron Lett 36:6267–6270

    Article  CAS  Google Scholar 

  • Ueda M, Ohnuki T, Yamamura S (1997a) The chemical control of leaf-movement in a nyctinastic plant, Lespedeza cuneata G. Don. Tetrahedron Lett 38:2497–2500

    Article  CAS  Google Scholar 

  • Ueda M, Tashiro C, Yamamura S (1997b) cis-p-Coumaroylagmatine, the genuine leaf-opening substance of a nyctinastic plant, Albizzia julibrissin Durazz. Tetrahedron Lett 38:3253–3256

    Article  CAS  Google Scholar 

  • Ueda M, Asano M, Yamamura S (1998a) Leaf-opening substance of a nyctinastic plant, Phyllanthus urinaria L. Tetrahedron Lett 39:9731–9734

    Article  CAS  Google Scholar 

  • Ueda M, Ohnuki T, Yamamura S (1998b) Chemical substances controlling the leaf-movement of a nyctinastic plant, Cassia mimosoides L. Phytochemistry 49:633–635

    Article  CAS  Google Scholar 

  • Ueda M, Asano M, Sawai Y, Yamamura S (1999c) Leaf-movement factors of nyctinastic plant, Phyllanthus urinaria L.; the universal mechanism for the regulation of nyctinastic leaf-movement. Tetrahedron 55: 5781–5792

    Article  CAS  Google Scholar 

  • Ueda M, Okazaki M, Ueda K, Yamamura S (2000a) A leaf-closing substance of Albizzia julibrissin Durazz. Tetrahedron 56:8101–8105

    Article  CAS  Google Scholar 

  • Ueda M, Shigemori H, Sata N, Yamamura S (2000b) The diversity of chemical substances controlling the nyctinastic leaf-movement in plants. Phytochemistry 53:39–44

    Article  CAS  Google Scholar 

  • Wilchek M, Miron T, Kohn J (1984) Affinity chromatography. Methods Enzymol 104:3–55

    Article  PubMed  CAS  Google Scholar 

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Correspondence to Minoru Ueda .

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Ueda, M., Nakamura, Y. (2009). Chemical Signaling During Induced Leaf Movements. In: Balu¿ka, F. (eds) Plant-Environment Interactions. Signaling and Communication in Plants. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-89230-4_9

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