Changes in sugars in organs of Phalaenopsis florets during different flowering stages of intact plant inflorescences

Authors

  • E H Hsiang National University of Kaohsiung, No. 700, Kaohsiung University Rd. Nan-Tzu district 811, Kaohsiung, Taiwan Author https://orcid.org/0009-0000-1732-1490
  • Y S Liao National University of Kaohsiung, No. 700, Kaohsiung University Rd. Nan-Tzu district 811, Kaohsiung, Taiwan Author https://orcid.org/0000-0002-6447-6097
  • J Y Chen National University of Kaohsiung, No. 700, Kaohsiung University Rd. Nan-Tzu district 811, Kaohsiung, Taiwan Author
  • Y C Chen National University of Kaohsiung, No. 700, Kaohsiung University Rd. Nan-Tzu district 811, Kaohsiung, Taiwan Author
  • H L Wang National University of Kaohsiung, No. 700, Kaohsiung University Rd. Nan-Tzu district 811, Kaohsiung, Taiwan Author https://orcid.org/0000-0001-7670-7334
  • C L Chang Food Industry Research and Development Institute, 300, Hsinchu, Taiwan Author
  • J D Chung Taiwan Forestry Research Institute, Zhongzheng district 100, Taipei, Taiwan Author

DOI:

https://doi.org/10.24154/jhs.v18i2.1204

Keywords:

floret; flowering stages; Phalaenopsis; sugars

Abstract

Phalaenopsis flowers possess extraordinary longevity. However, the changes of sugars, including glucose, fructose and sucrose, in organs of floret during different flowering stages of inflorescences attached to a plant have not been reported. To accomplish this, the sugars level in different floret organs were studied at 4 different stages (1. half open, 2. bloom 1 month, 3. bloom 2 months, and 4. wilting). Glucose and fructose were the major soluble sugars in the sepal, petal, labellum, pedicel, and remainder (including the column, anther cap, pollinia, and stigma) of a floret, but their levels decreased from stages 1 to 4. However, the amount of sucrose increased significantly at stage 4 in the sepal, petal, pedicel, and remainder, with the exception that the labellum remained constant throughout all stages. These results demonstrate that glucose and fructose are the major solutes that contribute to floret opening and blooming, and sucrose is salvaged and exported before floret senescence for opening other florets on the same inflorescence. Meanwhile, labellum possesses different sugar metabolism from other organs of Phalaenopsis floret.

References

Bieleski, R. L. (1995). Onset of phloem export from senescent petals of daylily. Plant Physiology, 109, 557–565. https://doi.org/10.1104/pp.109.2.557

Dar, R. A., Tahir, I., & Ahmad, S. S. (2015). Is the biochemical mechanism of petal senescence similar within a genus? A case study of Dianthus. Horticulture, Environment, and Biotechnology, 56, 654–661. http://dx.doi.org/10.1007/s13580-015-1068-z

Gibson, S. I. (2004). Sugar and phytohormone response pathways: Navigating a signaling network. Journal of Experimental Botany, 55, 253–264. http://dx.doi.org/10.1093/jxb/erh048

Halevy, A. H., Porat, R., Spiegelstein, H., Borochov, A., Botha, L., & Whitehead, C. S. (1996). Short-chain saturated fatty acids in the regulation of pollination-induced ethylene sensitivity of Phalaenopsis flowers. Physiologia Plantarum, 97, 469–474. http://dx .doi.org/1 0. 1111 /j.1 39 9-30 54 .1 99 6.tb00505.x

Ketsa, S., & Wongs-aree, C. (1995). The role of open florets in maximizing flower bud opening of Dendrobium held in the preservative solution. Acta Horticulturae, 405, 381–388. http://dx.doi.org/10.17660/ActaHortic.1995.405.49

Majidian, N., Naderi, R., Babalar, M., Nazeri, V., & Majidian, M. (2014). Evaluation of relation between carbohydrate with development and senescence in lilium LA hybrid cv. “CebDazzle”. Iranian Journal of Horticultural Science, 45, 103–114. https://ijhs.ut.ac.ir/a r t icle_ 5 0 9 3 8 . h t ml?l a ng= en # :~ :t ex t =20.1001.1.2008482.1393.45.1.10.2

O’Neill, S. D., Nadeau, J. A., Zhang, X. S., Bui, A. Q., & Halevy, A. H. (1993). Inter organ regulation of ethylene biosynthetic genes by pollination. Plant Cell, 5, 419–432. https://doi.org/10.1105/tpc.5.4.419

Ratchanee, P., Ketsa, S., & van Doorn, W. G. (2013). Sucrose feeding of cut Dendrobium inflorescences promotes bud opening, inhibits abscission of open flowers, and delays tepal senescence. Postharvest Biology and Technology, 77, 7–10. http://dx.doi.org/10.1016/j.postharvbio.2012.09.014

Shu, Z., Tao, Y. W., Tang, D. Q., Shi, Y. M., & Qian, H. M. (2010). Distinct respiration and physiological changes during flower development and senescence in two Freesia cultivars. HortScience, 45, 1088–1092. http://dx.doi.org/10.21273/HORTSCI.45.7.1088

Stead, A. D., & Moore, K. G. (1997). Flower development and senescence in Digitalis purpurea L., cv. Foxy. Annals Botany, 41, 283–292. http://dx.doi.org/10.1093/oxfordjournals.aob.a085290

Trivellini, A., Ferrante, A., Vernieri, P., Carmassi, G., & Serra, G. (2011). Spatial and temporal distribution of mineral nutrients and sugars throughout the lifespan of Hibiscus rosa- sinensis L. flower. Central European Journal of Biology, 6, 365–375. DOI:10.2478/s11535-011-0025-9

Wani, M., Saha, S., Bidwai, J., & Khetmalas, M. (2012). Changes in carbohydrate levels and associated enzyme activities during postharvest vase life of Gerbera jamesonii cv. Danalin flowers as influenced by mineral salts. Journal of Horticulture Letters, 2, 8–11. http://www.bioinfopublication.org/fil.

Yamane, K., Abiru, S., Fujishige, N., Sakiyama, R., & Ogata, R. (1993). Export of soluble sugars and increase membrane permeability of gladiolus florets during senescence. Journal of the Japanese Society for Horticultural Science, 62, 575–580. http://dx.doi.org/10.2503/jjshs.62.575

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Published

08-12-2023

Issue

Section

Research Notes

How to Cite

Hsiang, E. H., Liao, Y. S., Chen, J. Y., Chen, Y. C., Wang, H. L., Chang, C. L., & Chung, J. D. (2023). Changes in sugars in organs of Phalaenopsis florets during different flowering stages of intact plant inflorescences. Journal of Horticultural Sciences, 18(2). https://doi.org/10.24154/jhs.v18i2.1204

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