Misplaced Pages

Ethylene (CH
₂=CH
₂) is an unsaturated hydrocarbon gas (alkene) acting as a naturally occurring plant hormone. It is the simplest alkene gas and is the first gas known to act as a hormone. It acts at trace levels throughout the life of the plant by stimulating or regulating the ripening of fruit, the opening of flowers, the abscission (or shedding) of leaves and, in aquatic and semi-aquatic species, promoting the 'escape' from submergence by means of rapid elongation of stems or leaves. This escape response is particularly important in rice farming. Commercial fruit-ripening rooms use "catalytic generators" to make ethylene gas from a liquid supply of ethanol. Typically, a gassing level of 500 to 2,000 ppm is used, for 24 to 48 hours. Care must be taken to control carbon dioxide levels in ripening rooms when gassing, as high temperature ripening (20 °C; 68 °F) has been seen to produce CO₂ levels of 10% in 24 hours.

History

Ethylene has a long history of use in agriculture. Ancient Egyptians would gash figs in order to stimulate ripening (wounding stimulates ethylene production by plant tissues). The ancient Chinese would burn incense in closed rooms to enhance the ripening of pears. In the 19th century, city dwellers noticed that gas leaks from street lights led to stunting of growth, death of flowers and premature leaf fall. In 1874, it was discovered that smoke caused pineapple fields to bloom. Smoke contains ethylene, and once this was realized the smoke was replaced with ethephon or naphthalene acetic acid, which induce ethylene production.

The scientific study of ethylene as a factor in plant physiology started in the late 19th century. In 1896, Russian botanist Dimitry Neljubow studied the response pea to illuminating gas to which they showed movement. He discovered ethylene as the active component in the light source that stimulated pea behaviour. He reported his discovery in 1901. Sarah Doubt also showed in 1917 that ethylene from illuminating gas stimulated abscission. Farmers in Florida would commonly get their crops to ripen in sheds by lighting kerosene lamps, which was originally thought to induce ripening from the heat. In 1924, Frank E. Denny discovered that it was the molecule ethylene emitted by the kerosene lamps that induced the ripening. Reporting in the Botanical Gazette, he wrote:

Ethylene was very effective in bringing about the desired result, concentrations as low as one part (by volume) of ethylene in one million parts of air being sufficient to cause green lemons to turn yellow in about six to ten days... Furthermore, coloring with either ethylene or gas from the kerosene stoves caused the loss of the "buttons" (calyx, receptacle, and a portion of the peduncle)... Yellowing of the ethylene treated fruit became visible about the third or fourth day, and full yellow color was developed in six to ten days. Untreated fruit remained green during the same period of time.

The same year, Denny published the experimental details separately, and also experimentally showed that use of ethylene was more advantageous than that of kerosene. In 1934, British biologist Richard Gane discovered that the chemical constituent in ripe bananas could cause ripening of green bananas, as well as faster growth of pea. He showed that the same growth effect could be induced by ethylene. Reporting in Nature that ripe fruit (in this case Worcester Pearmain apple) produced ethylene he said:

The amount of ethylene produced is very small—perhaps of the order of 1 cubic centimetre during the whole life-history of the fruit; and the cause of its prodigious biological activity in such small concentration is a problem for further research. Its production by apple ceases or is very much reduced in the absence of oxygen.

He subsequently showed that ethylene was produced by other fruits as well, and that obtained from apple could induce seed germination and plant growth in different vegetables (but not in cereals). His conclusions were not universally accepted by other scientists. They became more convincing when William Crocker, Alfred Hitchcock, and Percy Zimmerman reported in 1935 that ethylene acts similar to auxins in causing plant growth and senescence of vegetative tissues. This established that ethylene is a plant hormone.

Ethylene biosynthesis in plants

Ethylene is produced from essentially all parts of higher plants, including leaves, stems, roots, flowers, fruits, tubers, and seeds. Ethylene production is regulated by a variety of developmental and environmental factors. During the life of the plant, ethylene production is induced during certain stages of growth such as germination, ripening of fruits, abscission of leaves, and senescence of flowers. Ethylene production can also be induced by a variety of external aspects such as mechanical wounding, environmental stresses, and certain chemicals including auxin and other regulators. The pathway for ethylene biosynthesis is named the Yang cycle after the scientist Shang Fa Yang who made key contributions to elucidating this pathway.

Ethylene is biosynthesized from the amino acid methionine to S-adenosyl-L-methionine (SAM, also called Adomet) by the enzyme Met adenosyltransferase. SAM is then converted to 1-aminocyclopropane-1-carboxylic acid (ACC) by the enzyme ACC synthase (ACS). The activity of ACS determines the rate of ethylene production, therefore regulation of this enzyme is key for the ethylene biosynthesis. The final step requires oxygen and involves the action of the enzyme ACC-oxidase (ACO), formerly known as the ethylene forming enzyme (EFE). Ethylene biosynthesis can be induced by endogenous or exogenous ethylene. ACC synthesis increases with high levels of auxins, especially indole acetic acid (IAA) and cytokinins.

Ethylene perception in plants

Ethylene is perceived by a family of five transmembrane protein dimers such as the ETR1 protein in Arabidopsis. The genes encoding ethylene gasoreceptors have been cloned in the reference plant Arabidopsis thaliana and many other plants. Ethylene gasoreceptors are encoded by multiple genes in plant genomes. Dominant missense mutations in any of the gene family, which comprises five gasoreceptors in Arabidopsis and at least six in tomato, can confer insensitivity to ethylene. Loss-of-function mutations in multiple members of the ethylene-gasoreceptor family result in a plant that exhibits constitutive ethylene responses. DNA sequences for ethylene gasoreceptors have also been identified in many other plant species and an ethylene binding protein has even been identified in Cyanobacteria.

Ethylene response to salt stress

A large portion of the soil has been affected by over salinity and it has been known to limit the growth of many plants. Globally, the total area of saline soil was 397,000,000 ha and in continents like Africa, it makes up 2 percent of the soil. The amount of soil salinization has reached 19.5% of the irrigated land and 2.1% of the dry-land agriculture around the world. Soil salinization affects the plants using osmotic potential by net solute accumulation. The osmotic pressure in the plant is what maintains water uptake and cell turgor to help with stomatal function and other cellular mechanisms. Over generations, many plant genes have adapted, allowing plants’ phenotypes to change and built distinct mechanisms to counter salinity effects.

The plant hormone ethylene is a combatant for salinity in most plants. Ethylene is known for regulating plant growth and development and adapted to stress conditions through a complex signal transduction pathway. Central membrane proteins in plants, such as ETO2, ERS1 and EIN2, are used for ethylene signaling in many plant growth processes. ETO2, Ethylene overproducer 2, is a protein that, when mutated, will gain a function to continually produce ethylene even when there is no stress condition, causing the plant to grow short and stumpy. ERS1, Ethylene response sensor 1, is activated when ethylene is present in the signaling pathway and when mutated, it loses a function and cannot bind to ethylene. This means a response is never activated and the plant will not be able to cope with the abiotic stress. EIN2, Ethylene insensitive 2, is a protein that activates the pathway and when there is a mutation here the EIN2 will block ethylene stimulation and an ethylene response gene will not be activated. Mutations in these proteins can lead to heightened salt sensitivity and limit plant growth. The effects of salinity have been studied on Arabidopsis plants that have mutated ERS1 and EIN4 proteins. These proteins are used for ethylene signaling again certain stress conditions, such as salt and the ethylene precursor ACC is allowing suppress of any sensitivity to the salt stress. Mutations in these pathways can cause lack of ethylene signaling, causing stunt in plant growth and development.

Environmental and biological triggers of ethylene

Environmental cues such as flooding, drought, chilling, wounding, and pathogen attack can induce ethylene formation in plants. In flooding, roots suffer from lack of oxygen, or anoxia, which leads to the synthesis of 1-aminocyclopropane-1-carboxylic acid (ACC). ACC is transported upwards in the plant and then oxidized in leaves. The ethylene produced causes nastic movements (epinasty) of the leaves, perhaps helping the plant to lose less water in compensation for an increase in resistance to water transport through oxygen-deficient roots.

Corolla senescence

The corolla of a plant refers to its set of petals. Corolla development in plants is broken into phases from anthesis to corolla wilting. The development of the corolla is directed in part by ethylene, though its concentration is highest when the plant is fertilized and no longer requires the production or maintenance of structures and compounds that attract pollinators. The role of ethylene in the developmental cycle is as a hormonal director of senescence in corolla tissue. This is evident as ethylene production and emission are maximized in developmental phases post-pollination, until corolla wilting. Ethylene-directed senescence of corolla tissue can be observed as color change in the corolla or the wilting/ death of corolla tissue. At the chemical level, ethylene mediates the reduction in the amount of fragrance volatiles produced. Fragrance volatiles act mostly by attracting pollinators. Ethylene's role in this developmental scenario is to move the plant away from a state of attracting pollinators, so it also aids in decreasing the production of these volatiles.

Ethylene production in corolla tissue does not directly cause the senescence of corolla tissue, but acts by releasing secondary products that are consistent with tissue ageing. While the mechanism of ethylene-mediated senescence are unclear, its role as a senescence-directing hormone can be confirmed by ethylene-sensitive petunia response to ethylene knockdown. Knockdown of ethylene biosynthesis genes was consistent with increased corolla longevity; inversely, up-regulation of ethylene biosynthesis gene transcription factors were consistent with a more rapid senescence of the corolla.

List of plant responses to ethylene

• Seedling triple response, thickening and shortening of hypocotyl with pronounced apical hook.
• Stimulation of Arabidopsis hypocotyl elongation
• In pollination, when the pollen reaches the stigma, the precursor of the ethylene, ACC, is secreted to the petal, the ACC releases ethylene with ACC oxidase.
• Stimulates leaf senescence
• Controls root growth inhibition in compacted soils
• Stimulates senescence of mature xylem cells in preparation for plant use
• Induces leaf abscission
• Induces seed germination
• Induces root hair growth — increasing the efficiency of water and mineral absorption
• Induces the growth of adventitious roots during flooding
• Stimulates survival under low-oxygen conditions (hypoxia) in submerged plant tissues
• Controls adaptive Translation (biology) dynamics during plant submergence
• Stimulates epinasty — leaf petiole grows out, leaf hangs down and curls into itself
• Stimulates fruit ripening
• Induces a climacteric rise in respiration in some fruit which causes a release of additional ethylene.
• Affects gravitropism
• Stimulates nutation
• Inhibits stem growth and stimulates stem and cell broadening and lateral branch growth outside of seedling stage (see Hyponastic response)
• Interference with auxin transport (with high auxin concentrations)
• Inhibits shoot growth and stomatal closing except in some water plants or habitually submerged species such as rice, Callitriche (e.g., C. platycarpa), and Rumex, where the opposite occurs to achieve an adaptive escape from submergence.
• Induces flowering in pineapples
• Inhibits short day induced flower initiation in Pharbitus nil and Chrysanthemum morifolium

Commercial issues

Ethylene shortens the shelf life of many fruits by hastening fruit ripening and floral senescence. Ethylene will shorten the shelf life of cut flowers and potted plants by accelerating floral senescence and floral abscission. Flowers and plants which are subjected to stress during shipping, handling, or storage produce ethylene causing a significant reduction in floral display. Flowers affected by ethylene include carnation, geranium, petunia, rose, and many others.

Ethylene can cause significant economic losses for florists, markets, suppliers, and growers. Researchers have developed several ways to inhibit ethylene, including inhibiting ethylene synthesis and inhibiting ethylene perception. Aminoethoxyvinylglycine (AVG), Aminooxyacetic acid (AOA), and silver salts are ethylene inhibitors. Inhibiting ethylene synthesis is less effective for reducing post-harvest losses since ethylene from other sources can still have an effect. By inhibiting ethylene perception, fruits, plants and flowers don't respond to ethylene produced endogenously or from exogenous sources. Inhibitors of ethylene perception include compounds that have a similar shape to ethylene, but do not elicit the ethylene response. One example of an ethylene perception inhibitor is 1-methylcyclopropene (1-MCP).

Commercial growers of bromeliads, including pineapple plants, use ethylene to induce flowering. Plants can be induced to flower either by treatment with the gas in a chamber, or by placing a banana peel next to the plant in an enclosed area.

Chrysanthemum flowering is delayed by ethylene gas, and growers have found that carbon dioxide 'burners' and the exhaust fumes from inefficient glasshouse heaters can raise the ethylene concentration to 0.05 ppmv, causing delay in flowering of commercial crops.

See also

• Gas sensor protein (Gasoreceptor).

References

1. ^ Lin Z, Zhong S, Grierson D (2009). "Recent advances in ethylene research". Journal of Experimental Botany. 60 (12): 3311–3336. doi:10.1093/jxb/erp204. PMID 19567479.
2. ^ Bakshi, Arkadipta; Shemansky, Jennifer M.; Chang, Caren; Binder, Brad M. (2015). "History of Research on the Plant Hormone Ethylene". Journal of Plant Growth Regulation. 34 (4): 809–827. doi:10.1007/s00344-015-9522-9. S2CID 14775439.
3. Jackson MB, Osborne DJ (March 1970). "Ethylene, the natural regulator of leaf abscission". Nature. 225 (5237): 1019–22. Bibcode:1970Natur.225.1019J. doi:10.1038/2251019a0. PMID 16056901. S2CID 4276844.
4. Musgrave A, Jackson MB, Ling E (1972). "Callitriche Stem Elongation is controlled by Ethylene and Gibberellin". Nature New Biology. 238 (81): 93–96. doi:10.1038/newbio238093a0. ISSN 2058-1092.
5. Jackson MB (January 2008). "Ethylene-promoted elongation: an adaptation to submergence stress". Annals of Botany. 101 (2): 229–248. doi:10.1093/aob/mcm237. PMC 2711016. PMID 17956854.
6. ^ Dahll, R.K. (2013). "Ethylene in the Post-Harvest Quality Management of Horticultural Crops: A Review". Research and Reviews: A Journal of Crop Science and Technology. 2 – via Researchgate.
7. External Link to More on Ethylene Gassing and Carbon Dioxide Control Archived 2010-09-14 at the Wayback Machine. ne-postharvest.com
8. Annual Plant Reviews, Plant Hormone Signaling. Peter Hedden, Stephen G. Thomas. John Wiley & Sons, Apr 15, 2008
9. Neljubov D (1901). "Uber die horizontale Nutation der Stengel von Pisum sativum und einiger anderen Pflanzen". Beih Bot Zentralbl. 10: 128–139.
10. Doubt SL (1917). "The Response of Plants to Illuminating Gas". Botanical Gazette. 63 (3): 209–224. doi:10.1086/332006. hdl:2027/mdp.39015068299380. JSTOR 2469142. S2CID 86383905.
11. Chamovitz D (2012). What A Plant Knows. United States of America: Scientific American. pp. 29–30. ISBN 978-0-374-28873-0.
12. Denny, F. E. (1924). "Effect of Ethylene Upon Respiration of Lemons". Botanical Gazette. 77 (3): 322–329. doi:10.1086/333319. JSTOR 2469953. S2CID 85166032.
13. Denny, F. E. (1924). "Hastening the Coloration of Lemons". Journal of Agricultural Research. 27 (10): 757–769. Archived from the original on 2021-06-10. Retrieved 2021-06-10.
14. Chace, I M.; Denny, F. E. (1924). "Use of Ethylene in the Coloring of Citrus Fruit". Industrial & Engineering Chemistry. 16 (4): 339–340. doi:10.1021/ie50172a003.
15. Gane, R (1935). "Department of Scientific and Industrial Research. Report of the Food Investigation Board for 1934". The Analyst. 60 (715): 122–123. Bibcode:1935Ana....60..687.. doi:10.1039/an9356000687. ISSN 0003-2654.
16. Gane R (1934). "Production of ethylene by some fruits". Nature. 134 (3400): 1008. Bibcode:1934Natur.134.1008G. doi:10.1038/1341008a0. S2CID 4090009.
17. Gane, R. (1935). "The Formation of Ethylene by Plant Tissues, and its Significance in the Ripening of Fruits". Journal of Pomology and Horticultural Science. 13 (4): 351–358. doi:10.1080/03683621.1935.11513459.
18. Crocker W, Hitchcock AE, Zimmerman PW (1935). "Similarities in the effects of ethlyene and the plant auxins". Contrib. Boyce Thompson Inst. Auxins Cytokinins IAA Growth substances, Ethylene. 7: 231–248.
19. Arshad, Muhammad; Frankenberger, William T. (2002), "The Plant Hormone, Ethylene", Ethylene, Boston, MA: Springer US, pp. 1–9, doi:10.1007/978-1-4615-0675-1_1, ISBN 978-1-4613-5189-4, retrieved 2021-06-10
20. Yang SF, Hoffman NE (1984). "Ethylene biosynthesis and its regulation in higher plants". Annu. Rev. Plant Physiol. 35: 155–89. doi:10.1146/annurev.pp.35.060184.001103.
21. Renziehausen, Tilo; Chaudhury, Rim; Hartman, Sjon; Mustroph, Angelika; Schmidt-Schippers, Romy (12 November 2024). "A mechanistic integration of hypoxia signaling with energy, redox and hormonal cues". Plant Physiology. doi:10.1093/plphys/kiae596.
22. Bleecker AB, Esch JJ, Hall AE, Rodríguez FI, Binder BM (September 1998). "The ethylene-receptor family from Arabidopsis: structure and function". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 353 (1374): 1405–12. doi:10.1098/rstb.1998.0295. PMC 1692356. PMID 9800203.
23. Hua J, Meyerowitz EM (July 1998). "Ethylene responses are negatively regulated by a receptor gene family in Arabidopsis thaliana". Cell. 94 (2): 261–71. doi:10.1016/S0092-8674(00)81425-7. PMID 9695954. S2CID 15437009.
24. "More information on Salt-affected soils | FAO | Food and Agriculture Organization of the United Nations". www.fao.org. Retrieved 2017-05-02.
25. ^ Azevedo Neto AD, Prisco JT, Enéas-Filho J, Lacerda CF, Silva JV, Costa PH, et al. (2004-04-01). "Effects of salt stress on plant growth, stomatal response and solute accumulation of different maize genotypes". Brazilian Journal of Plant Physiology. 16 (1): 31–38. doi:10.1590/S1677-04202004000100005. ISSN 1677-0420.
26. ^ Lei G, Shen M, Li ZG, Zhang B, Duan KX, Wang N, et al. (October 2011). "EIN2 regulates salt stress response and interacts with a MA3 domain-containing protein ECIP1 in Arabidopsis". Plant, Cell & Environment. 34 (10): 1678–92. doi:10.1111/j.1365-3040.2011.02363.x. PMID 21631530.
27. Explaining Epinasty. planthormones.inf
28. ^ Wang H, Chang X, Lin J, Chang Y, Chen JC, Reid MS, Jiang CZ (2018). "Transcriptome profiling reveals regulatory mechanisms underlying corolla senescence in petunia". Horticulture Research. 5 (16): 16. doi:10.1038/s41438-018-0018-1. PMC 5878830. PMID 29619227.
29. Underwood BA, Tieman DM, Shibuya K, Dexter RJ, Loucas HM, Simkin AJ, et al. (May 2005). "Ethylene-regulated floral volatile synthesis in petunia corollas". Plant Physiology. 138 (1): 255–66. doi:10.1104/pp.104.051144. PMC 1104180. PMID 15849311.
30. Kieber, Joseph J.; Schaller, G. Eric (2019-07-01). "Behind the Screen: How a Simple Seedling Response Helped Unravel Ethylene Signaling in Plants". The Plant Cell. 31 (7): 1402–1403. doi:10.1105/tpc.19.00342. ISSN 1040-4651. PMC 6635871. PMID 31068448.
31. Debatosh Das,"Ethylene- and shade-induced hypocotyl elongation share transcriptome patterns and functional regulators", "Plant Physiology",21-06-2016
32. Pandey, Bipin K.; Huang, Guoqiang; Bhosale, Rahul; Hartman, Sjon; Sturrock, Craig J.; Jose, Lottie; Martin, Olivier C.; Karady, Michal; Voesenek, Laurentius A. C. J.; Ljung, Karin; Lynch, Jonathan P.; Brown, Kathleen M.; Whalley, William R.; Mooney, Sacha J.; Zhang, Dabing; Bennett, Malcolm J. (15 January 2021). "Plant roots sense soil compaction through restricted ethylene diffusion". Science. 371 (6526): 276–280. Bibcode:2021Sci...371..276P. doi:10.1126/science.abf3013. PMID 33446554. S2CID 231606782.
33. Jackson MB, Osborne DJ (March 1970). "Ethylene, the natural regulator of leaf abscission". Nature. 225 (5237): 1019–22. Bibcode:1970Natur.225.1019J. doi:10.1038/2251019a0. PMID 16056901. S2CID 4276844.
34. Hartman S, Liu Z, van Veen H, Vicente J, Reinen E, Martopawiro S, et al. (September 2019). "Ethylene-mediated nitric oxide depletion pre-adapts plants to hypoxia stress". Nature Communications. 10 (1): 4020. Bibcode:2019NatCo..10.4020H. doi:10.1038/s41467-019-12045-4. PMC 6728379. PMID 31488841.
35. van Veen H, Mustroph A, Barding GA, Vergeer-van Eijk M, Welschen-Evertman RA, Pedersen O, Visser EJ, Larive CK, Pierik R, Bailey-Serres J, Voesenek LA, Sasidharan R (November 2013). "Two Rumex species from contrasting hydrological niches regulate flooding tolerance through distinct mechanisms". The Plant Cell. 25 (11): 4691–707. doi:10.1105/tpc.113.119016. PMC 3875744. PMID 24285788.
36. Hartman S, Sasidharan R, Voesenek LA (December 2019). "The role of ethylene in metabolic acclimations to low oxygen". New Phytologist. 229 (1): 64–70. doi:10.1111/nph.16378. PMC 7754284. PMID 31856295.
37. Hartman, Sjon; van Dongen, Nienke; Renneberg, Dominique M. H. J.; Welschen-Evertman, Rob A. M.; Kociemba, Johanna; Sasidharan, Rashmi; Voesenek, Laurentius A. C. J. (August 2020). "Ethylene Differentially Modulates Hypoxia Responses and Tolerance across Solanum Species". Plants. 9 (8): 1022. doi:10.3390/plants9081022. PMC 7465973. PMID 32823611.
38. Cho, Hsing-Yi; Chou, Mei-Yi; Ho, Hsiu-Yin; Chen, Wan-Chieh; Shih, Ming-Che (3 June 2022). "Ethylene modulates translation dynamics in Arabidopsis under submergence via GCN2 and EIN2". Science Advances. 8 (22): eabm7863. Bibcode:2022SciA....8M7863C. doi:10.1126/sciadv.abm7863. PMC 9166634. PMID 35658031.
39. Maric, Aida; Hartman, Sjon (17 August 2022). "Ethylene controls translational gatekeeping to overcome flooding stress in plants". The EMBO Journal. 41 (19): e112282. doi:10.15252/embj.2022112282. PMC 9531296. PMID 35975893.
40. Métraux, Jean-Pierre; Kende, Hans (1983-06-01). "The Role of Ethylene in the Growth Response of Submerged Deep Water Rice 1". Plant Physiology. 72 (2): 441–446. doi:10.1104/pp.72.2.441. ISSN 0032-0889. PMC 1066253. PMID 16663022.
41. Wilmowicz E, Kesy J, Kopcewicz J (December 2008). "Ethylene and ABA interactions in the regulation of flower induction in Pharbitis nil". Journal of Plant Physiology. 165 (18): 1917–1928. doi:10.1016/j.jplph.2008.04.009. PMID 18565620.
42. Cockshull KE, Horridge JS (1978). "2-Chloroethylphosphonic Acid and Flower Initiation by Chrysanthemum morifolium Ramat. In Short Days and in Long Days". Journal of Horticultural Science & Biotechnology. 53 (2): 85–90. doi:10.1080/00221589.1978.11514799.
43. van Doorn WG (June 2002). "Effect of ethylene on flower abscission: a survey". Annals of Botany. 89 (6): 689–93. doi:10.1093/aob/mcf124. PMC 4233834. PMID 12102524.
44. Cassells AC, Gahan PB (2006). Dictionary of plant tissue culture. Haworth Press. p. 77. ISBN 978-1-56022-919-3.
45. Constabel F, Shyluk JP (1994). "1: Initiation, Nutrition, and Maintenance of Plant Cell and Tissue Cultures". Plant Cell and Tissue Culture. Springer. p. 5. ISBN 978-0-7923-2493-5.
46. van Berkel, N. (July 1987). "Injurious effects of low ethylene concentrations on Chrysanthemum morifolium Ramat". Acta Horticulturae. 197 (197): 43–52. doi:10.17660/actahortic.1987.197.4. ISSN 0567-7572.

Further reading

• Chang C, Stadler R (July 2001). "Ethylene hormone receptor action in Arabidopsis". BioEssays. 23 (7): 619–627. doi:10.1002/bies.1087. PMID 11462215. S2CID 6640353.
• Millenaar FF, van Zanten M, Cox MC, Pierik R, Voesenek LA, Peeters AJ (2009). "Differential petiole growth in Arabidopsis thaliana: photocontrol and hormonal regulation". New Phytologist. 184 (1): 141–152. doi:10.1111/j.1469-8137.2009.02921.x. PMID 19558423.
• Schaller GE (February 2012). "Ethylene and the regulation of plant development". BMC Biology. 10 (9) (published 20 February 2012): 9. doi:10.1186/1741-7007-10-9. PMC 3282650. PMID 22348804.

External links

• International Chemical Safety Card 0475

• Aging-related substances in plants
• Monomers
• Plant hormones
• GABAA receptor positive allosteric modulators
• Gaseous signaling molecules
• Plant growth regulators