Skip to main content
Log in

Effect of 1-aminocyclopropane-1-carboxylic acid on maize kernel development in vitro

  • Published:
Journal of Plant Growth Regulation Aims and scope Submit manuscript

Abstract

Pollination stimulates ethylene production in maize ears, and the application of ethephon during the pollination period can cause kernel abortion. The objective of this study was to determine if kernel abortion could be induced in vitro by the ethylene precursor 1-aminocyclopropane-1-carboxylic acid (ACC). Adding ACC to the culture medium resulted in the evolution of ethylene which caused abortion and reduced mature kernel mass. The effect of ethylene on kernel abortion and dry matter accumulation was partially negated by the addition of the ethylene-binding site inhibitor, 2,5-norbornadiene (NBD). The effect of ethylene on kernel abortion was greatest during the early stage of kernel development and was intensified by an increase in media sucrose concentration. These data suggest that ethylene could regulate kernel abortion in maize.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Abeles FB (1973) Ethylene in plant biology. Academic Press, New York, pp 153–178

    Google Scholar 

  • Daynard TB, Duncan WD (1969) The black layer and grain maturity in corn. Crop Sci 9:473–476

    Google Scholar 

  • Dill G, Maxwell C, McLaren JS (1987) The presence of 1-aminocyclopropane-1-carboxylic acid in corn pollen and the evolution of ethylene during pollination (Abstract no. 576). Plant Physiol 83:S-96

    Google Scholar 

  • Gengenbach BG (1977) Development of maize caryopses resulting fromin vitro pollination. Planta 134:91–93

    Article  Google Scholar 

  • Guinn G (1982) Fruit age and changes in abscisic acid content, ethylene production, and abscission rate of cotton fruits. Plant Physiol 69:349–352

    PubMed  CAS  Google Scholar 

  • Halevy AH, Whitehead CS, Kofranek AM (1984) Does pollination induce corolla abscission of cyclamen by promoting ethylene production? Plant Physiol 75:1090–1093

    PubMed  CAS  Google Scholar 

  • Hanft JM, Jones RJ (1986a) Kernel abortion in maize. I. Carbohydrate concentration patterns and acid invertase activity of kernels induced to abortin vitro. Plant Physiol 81:503–510

    PubMed  CAS  Google Scholar 

  • Hanft JM, Jones RJ (1986b) Kernel abortion in maize. II. Distribution of14C among kernel carbohydrates. Plant Physiol 81:511–516

    PubMed  CAS  Google Scholar 

  • Hanft JM, Jones RJ, Stumme AB (1986) Dry matter accumulation and carbohydrate concentration patterns of field-grown andin vitro cultured maize kernels from the tip and middle ear positions. Crop Sci 26:568–572

    Google Scholar 

  • Hirai M (1982) Acceleration of sugar accumulation and ripening of loquat fruit by exogenously applied ethylene. J Japan Soc Hort Sci 51:159–164

    Article  CAS  Google Scholar 

  • Hoffman NE, Yang SF (1980) Changes of 1-aminocyclopropane-1-carboxylic acid content in ripening fruits in relation to their ethylene production rates. J Amer Soc Hort Sci 105:321–326

    Google Scholar 

  • Jones RJ, Gengenbach BG, Cardwell VB (1981) Temperature effects onin vitro kernel development in maize. Crop Sci 21:761–766

    Google Scholar 

  • Jones RJ, Roessler JA, Outtar S (1985) Thermal environment during endosperm cell division: Effect on kernel sink potential. Crop Sci 25:830–834

    Google Scholar 

  • Lipe JA, Morgan PM (1973) Ethylene, a regulator of young fruit abscission. Plant Physiol 51:949–953

    PubMed  CAS  Google Scholar 

  • Nichols R (1976) Cell enlargement and sugar accumulation in the gynoecium of the glasshouse carnation (Dianthus caryophyllus L.) induced by ethylene. Planta 130:47–52

    Article  CAS  Google Scholar 

  • Nichols R (1977) Sites of ethylene production in the pollinated and unpollinated senescing carnation (Dianthus caryophyllus) inflorescence. Planta 135:155–159

    Article  CAS  Google Scholar 

  • Nichols R, Ho LC (1975) Effects of ethylene and sucrose on the translocation of dry matter and 14C-sucrose in the cut flower of the glasshouse carnationDianthus (caryophyllus) during senescence. Ann Bot 39:287–296

    CAS  Google Scholar 

  • Nunez-Elisea R, Davenport TL (1986) Abscission of mango fruitlets as influenced by enhanced ethylene biosynthesis. Plant Physiol 82:991–994

    PubMed  CAS  Google Scholar 

  • Philosoph-Hadas S, Meir S, Aharoni N (1985) Carbohydrates stimulate ethylene production in tobacco leaf discs. II. Sites of stimulation in the ethylene biosynthesis pathway. Plant Physiol 78:139–143

    PubMed  CAS  Google Scholar 

  • Reed AJ, Singletary GW, Schussler JR, Williamson DR, Christy AL (1988) Shading effects on dry matter and nitrogen partitioning, kernel number, and yield of maize. Crop Sci 28:819–825

    Google Scholar 

  • Sisler EC, Goren R, Huberman M (1985) Effect of 2,5-norbornadiene on abscission and ethylene production in citrus leaf explants. Physiol Plant 63:114–120

    Article  CAS  Google Scholar 

  • Stead AD, Moore KG (1983) Studies on flower longevity in Digitalis. The role of ethylene in corolla abscission. Planta 157:15–21

    Article  CAS  Google Scholar 

  • Urwiler MJ, Stutte CA (1986) Influence of ethephon on soybean reproductive development. Crop Sci 26:976–979

    CAS  Google Scholar 

  • Veen H, Kwakkenbos AAM (1984) Role of ethylene in the distribution of assimilates in cut carnations. J Plant Physiol 115:389–397

    CAS  Google Scholar 

  • Westgate ME, Boyer JS (1986) Reproduction at low silk and pollen water potentials in maize. Crop Sci 26:951–956

    Google Scholar 

  • Woodson WR, Hanchey SH, Chisholm DN (1985) Role of ethylene in the senescence of isolated hibiscus petals. Plant Physiol 79:679–683

    Article  PubMed  CAS  Google Scholar 

  • Yang SF, Hoffman NE (1984) Ethylene biosynthesis and its regulation in higher plants. Ann Rev Plant Physiol 35:155–189

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Contribution of the Department of Agronomy and Plant Genetics, University of Minnesota, St. Paul, MN 55108. Paper No. 17,088, Scientific Journal Series, Minnesota Agriculture Experimental Station.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hanft, J.M., Reed, A.J., Jones, R.J. et al. Effect of 1-aminocyclopropane-1-carboxylic acid on maize kernel development in vitro. J Plant Growth Regul 9, 89–94 (1990). https://doi.org/10.1007/BF02041947

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02041947

Keywords

Navigation