Hostname: page-component-76fb5796d-skm99 Total loading time: 0 Render date: 2024-04-28T15:19:01.075Z Has data issue: false hasContentIssue false

ACC-N-Malonyltransferase activity during zygotic embryogenesis and germination of chick-pea seeds

Published online by Cambridge University Press:  22 February 2007

Clemente Martin-Remesal
Affiliation:
Departament de Biologia Vegetal, Laboratorio de Fisiologia Vegetal, Facultad de Ciencias, Universidad de Granda, 18001-Granada, Spain
Maria del Carmen Gomez-Jimenez
Affiliation:
Departamenta de Biologia Vegetal, Laboratorio de Fisiologia Vegetal, Facultad de Farmacia, Universidad de Santiago de Compostela, 15706-Santiago de Compostela, La Coruna, Spain
Angel J. Matilla*
Affiliation:
Departamenta de Biologia Vegetal, Laboratorio de Fisiologia Vegetal, Facultad de Farmacia, Universidad de Santiago de Compostela, 15706-Santiago de Compostela, La Coruna, Spain
*
*Fax: +34-981-593-054 Email: bvmatilla@usc.es

Abstract

Some physiological characteristics of ACC-Nmalonyltransferase (ACC-N-MTase) have been studied in the seeds of chick-pea (Cicer arietinum L.). This enzymatic activity was detectable during all periods of zygotic embryogenesis; however, the highest values were found in the dry seed. In dry seeds, the enzymatic activity was greater in the embryonic axis than in the cotyledons. During the onset of germination, activity increased more strongly in the cotyledons than in the embryonic axis, reaching its highest values in the storage organs coinciding with radicle emergence (18 to 24 h). Removal of the cotyledons strongly diminished enzymatic activity in the embryonic axis. Low concentrations of ethrel (50 µM) stimulated the axis ACC-N-MTase. The highest specific activity was found in the apical meristem of the embryonic axis, declining over the length of the organ. The role of ACC-N-MTase activity in the germinative process is discussed, together with the regulatory effect of ethylene on this ACCconjugating enzyme.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2000

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Amrhein, N., Schonbeck, D., Skorupka, H., Tophof, S. and Stockigt, J. (1981) Identification of a major metabolite of the etylene precursor 1-aminocyclopropane-1-carboxylic acid in higher plants. Naturwissenschaften 68, 619620.Google Scholar
Benichou, .M., Martinez-Reina, G., Romojaro, F., Pech, J. C. and Latché, A. (1995) Partial purification and properties of a 36 kDa 1-aminocyclopropane-1-carboxylate N-malonyltransferase from mung bean. Physiologia Plantarum 94, 629634.CrossRefGoogle Scholar
Bradford, M.M. (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilising the principle of protein-dye binding. Analytical Biochemistry 72, 248254.CrossRefGoogle ScholarPubMed
Colorado, P., Nicolas, C., Nicolás, G. and Rodriguez, D. (1995) Expression of three ABA-regulated clones and their relationship to maturation processes during the embryogenesis of chick-pea seeds. Physiologia Plantarum 94, 16.CrossRefGoogle Scholar
Corbineau, F., Rudnicki, R.M. and Côme, D. (1989) ACC conversion to ethylene by sunflower seeds in relation to maturation, germination and thermodormancy. Plant Growth Regulation 8, 105115.CrossRefGoogle Scholar
Child, R.D., Chauvaux, N., John, K., Ulvskov, P. and Van Onklelen, H.A. (1998) Ethylene biosynthesis in oil seed rape pods in relation to pod shatter. Journal of Experimental Botany 49, 829838.CrossRefGoogle Scholar
Delgado, M.M. and Matilla, A.J. (1994) Production of ethylene, its precursors and implied enzyme activities in isolated chickpea embryonic axes during the onset of growth. Biologia Plantarum 36, 543552.CrossRefGoogle Scholar
Fluhr, R. and Mattoo, K. (1996) Ethylene-biosynthesis and perception. Critical Reviews in Plant Science 15, 479523.Google Scholar
Gallardo, M., Delgado, M.M., Sánchez-Calle, I.M. and Matilla, A.J. (1991) Ethylene production and 1- aminocyclopropane-1-carboxylic acid conjugation in thermoinhibited Cicer arietinum L. seeds. Plant Physiology 97, 122127.Google Scholar
Gallardo, M., Bueno, M., Angosto, T., Gallardo, E. and Matilla, A.J. (1992) Free polyamines in Cicer arietinum seeds during the onset of germination. Phytochemistry 31, 22832287.Google Scholar
Gallardo, M., Gallardo, M.E., Matilla, A.J., Muñoz De Rueda, P. and Sãnchez-Calle, I.M. (1994) Inhibition of polyamine synthesis by cyclohexylamine stimulates the ethylene pathway and accelereates the germination of Cicer arietinum seeds. Physiologia Plantarum 91, 916.Google Scholar
Gallardo, M., Sánchez-Calle, I.M., Muñoz De Rueda, P. and Matilla, A.J. (1996) The alleviation of thermoinhibition in chick-pea seeds by puttescine involves the ethylene pathway. Australian Journal of Plant Physiology 23, 479487.Google Scholar
Gómez-Jiménez, M.C., Matilla, A.J. and Garrido, D. (1998) Isolation and characterization of a cDNA encoding an ACC oxidase from Cicer arietinum and its expression during embryogenesis and seed germination. Australian Journal of Plant Physiology 25, 765773.Google Scholar
Guo, L., Arteca, R.N., Phillips, A.T. and Liu, Y. (1992) Purification and characterization of 1- aminocyclopropane-1-carboxylate N-malonyltransferase from etiolated mung bean hypocotyls. Plant Physiology 100, 20412045.CrossRefGoogle ScholarPubMed
Hanley, K.M., Meir, S. and Bramage, W.J. (1989) Activity of ageing carnation flower parts and the effects of 1- (malonylamino) cyclopropane-1-carboxylic acidinduced ethylene. Plant Physiology 91, 11261130.CrossRefGoogle ScholarPubMed
Johnson-Flanagan, A.M. and Spencer, M.S. (1994) Ethylene production during development of mustard (Brassica juncea) and canola (Brassica napus) seed. Plant Physiology 106, 601606.Google Scholar
Jiao, X.Z., Philosoph-Hadas, S., Su, L.Y. and Yang, S.F. (1986) The conversion of 1-(malonylamino) cyclopropane- 1-carboxylic acid to 1-aminocyclopropane-1-carboxylic acid in plant tissues. Plant Physiology 81, 637641.Google Scholar
Kende, H. (1993) Ethylene biosynthesis. Annual Review of Plant Physiology and Plant Molecular Biology 44, 283307.CrossRefGoogle Scholar
Kionka, C. and Amrhein, N. (1984) The enzymatic malonylation of 1-aminocyclopropane-1-carboxylic acid in homogenates of mung-bean hypocotyls. Planta 162, 226235.Google Scholar
Leliévre, J.M., Latché, A., Jones, B., Bouzayen, M. and Pech, J.C. (1997) Ethylene and fruit ripening. Physiologia Plantarum 101, 727739.CrossRefGoogle Scholar
Liu, Y., Su, L.Y. and Yang, S.F. (1985) Ethylene promoted the capability to malonylate 1-aminocyclopropane-1- carboxylic acid and D-amino acids in preclimateric tomato fruits. Plant Physiology 77, 891895.Google Scholar
Martin, M.N., Cohen, J.D. and Saftner, R.A. (1995) A new 1-aminocyclopropane-1-carboxylic acid-conjugating activity in tomato fruit. Plant Physiology 109, 917926.CrossRefGoogle ScholarPubMed
Martin, M.N. and Saftner, R.A. (1995) Purification and characterisation of 1-aminocyclopropane-1-carboxylic acid N-malonyltransferase from tomato fruit. Plant Physiology 108, 12411249.Google Scholar
Martínez-Reina, G., Matilla, A.J., Martín-Remesal, C., Gallardo, M. and Muñoz De Rueda, P. (1996) Biochemical properties of 1-aminocyclopropane-1- carboxylate N-malonyltransferase activity from early growing embryonic axes of chick-pea (Cicer arietinum L.) seeds. Journal of Experimental Botany 47, 17711778.CrossRefGoogle Scholar
Matilla, A.J. (1996) Polyamines and seed germination. Seed Science Research 6, 8193.Google Scholar
Matilla, A., Nicolás, G. and Sierra, J.M. (1982) Changes in messenger RNA in Cicer arietinum L. cotyledons seeds during germination. Plant Science Letters 25, 209217.CrossRefGoogle Scholar
Matilla, A. and Nicolás, G. (1983) Changes in ribonuclease activity in cotyledons of Cicer arietinum L. during the first hours of germination. Acta Physiologiae Plantarum 5, 219226.Google Scholar
Muñoz, J.L., Martín, L., Nicolás, G. and Villalobos, N. (1990) Influence of endogenous cytokinins on reverse mobilization in cotyledons of Cicer arietinum L. Plant Physiology 93, 10111016.Google Scholar
Peck, S.C. and Kende, H. (1995) Sequential induction of the ethylene biosynthetic enzymes by indole-3-acetic acid in etiolated peas. Plant Molecular Biology 28, 293301.Google Scholar
Peiser, G. and Yang, S.F. (1998) Evidence for 1- (malonylamino)cyclopropane-1-carboxylic acid being the major conjugate of aminocyclopropane-1-carboxylic acid in tomato fruit. Plant Physiology 116, 15271532.Google Scholar
Wang, T.W. and Arteca, R.N. (1995) Identification and characterization of cDNAs encoding ethylene biosynthetic enzymes from Pelargonium X hortorum cv Snow Mass leaves. Plant Physiology 109, 627636.Google Scholar