Abstract
The effects of an electric current on ethylene biosynthesis were investigated in cucumber (Cucumis sativus L.) fruit that were producing almost no ethylene. Direct currents at 0.5 to 3.0 milliamperes induced much ethylene synthesis, with a rapid continuous increase in the rate, which reached a peak within 5 to 6 hours and then decreased. The rate of production was greater with a stronger current. Ethylene production was not observed after the use of a sine-wave alternating current (60 hertz) at 3 milliamperes, the magnitude at which a direct current had the greatest effect. The activity of 1-aminocyclopropane-1-carboxylic acid (ACC) synthase and ethylene forming enzyme (EFE) increased before the rise in ethylene production. ACC synthase and EFE were activated sixfold and fourfold, respectively, by 2 hours. The concentration of ACC increased linearly up to 6 hours and then decreased. Ethylene induction by an electric current was suppressed almost completely by the infiltration of the cucumbers with 5 millimolar aminooxyacetic acid, an inhibitor of ACC synthase, and was also suppressed 70% by 5 millimolar salicylic acid, an inhibitor of EFE. The results indicate that the ethylene induced by the direct current was synthesized via the ACC-ethylene pathway as a result of electrical stress, a new kind of stress to be identified.
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Selected References
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- Bufler G. Ethylene-Enhanced 1-Aminocyclopropane-1-carboxylic Acid Synthase Activity in Ripening Apples. Plant Physiol. 1984 May;75(1):192–195. doi: 10.1104/pp.75.1.192. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bufler G. Ethylene-promoted conversion of 1-aminocyclopropane-1-carboxylic Acid to ethylene in peel of apple at various stages of fruit development. Plant Physiol. 1986 Feb;80(2):539–543. doi: 10.1104/pp.80.2.539. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Desrosiers M. F., Bandurski R. S. Effect of a longitudinally applied voltage upon the growth of Zea mays seedlings. Plant Physiol. 1988;87:874–877. doi: 10.1104/pp.87.4.874. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Leslie C. A., Romani R. J. Inhibition of ethylene biosynthesis by salicylic Acid. Plant Physiol. 1988 Nov;88(3):833–837. doi: 10.1104/pp.88.3.833. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Liu Y., Hoffman N. E., Yang S. F. Promotion by Ethylene of the Capability to Convert 1-Aminocyclopropane-1-carboxylic Acid to Ethylene in Preclimacteric Tomato and Cantaloupe Fruits. Plant Physiol. 1985 Feb;77(2):407–411. doi: 10.1104/pp.77.2.407. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lizada M. C., Yang S. F. A simple and sensitive assay for 1-aminocyclopropane-1-carboxylic acid. Anal Biochem. 1979 Nov 15;100(1):140–145. doi: 10.1016/0003-2697(79)90123-4. [DOI] [PubMed] [Google Scholar]
- Sitrit Y., Riov J., Blumenfeld A. Regulation of Ethylene Biosynthesis in Avocado Fruit during Ripening. Plant Physiol. 1986 May;81(1):130–135. doi: 10.1104/pp.81.1.130. [DOI] [PMC free article] [PubMed] [Google Scholar]
- WEBSTER W. W., Jr, SCHRANK A. R. Electrical induction of lateral transport of 3-indoleacetic acid in the Avena coleoptile. Arch Biochem Biophys. 1953 Nov;47(1):107–118. doi: 10.1016/0003-9861(53)90441-x. [DOI] [PubMed] [Google Scholar]
- Wang C. Y., Adams D. O. Chilling-Induced Ethylene Production in Cucumbers (Cucumis sativus L.). Plant Physiol. 1982 Feb;69(2):424–427. doi: 10.1104/pp.69.2.424. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yu Y. B., Adams D. O., Yang S. F. 1-Aminocyclopropanecarboxylate synthase, a key enzyme in ethylene biosynthesis. Arch Biochem Biophys. 1979 Nov;198(1):280–286. doi: 10.1016/0003-9861(79)90420-x. [DOI] [PubMed] [Google Scholar]
