Physiological Characteristics of Photosynthesis in Yellow-Green, Green and Dark-Green Chinese Kale (Brassica oleracea L. var. alboglabra Musil.) under Varying Light Intensities

Plants - Tập 9 Số 8 - Trang 960
Kuan‐Hung Lin1, Feng-Chi Shih2, Mengyuan Huang2, Jen-Hsien Weng2
1Department of Horticulture and Biotechnology, Chinese Culture University, Taipei, 111, Taiwan
2Department of Life Sciences, National Chung-Hsing University, Taichung40227, Taiwan

Tóm tắt

The objective of this work was to study physiological characteristics and photosynthetic apparatus in differentially pigmented leaves of three Chinese kale cultivars. Chlorophyll (Chl) fluorescence and photochemical reflectance index (PRI) measurements in green, yellow-green, and dark-green cultivars in response to varying light intensities. As light intensity increased from 200 to 2000 photosynthetic photon flux density (PPFD), fraction of light absorbed in photosystem (PS) II and PRI values in all plants were strongly lowered, but fraction of light absorbed in PSII dissipated via thermal energy dissipation and non-photochemical quenching (NPQ) values in all plants wereremarkably elevated.When plants were exposed to 200 PPFD, the values of fraction of light absorbed in PSII, utilized in photosynthetic electron transport(p), andfraction of light absorbed excitation energy in PSII dissipated via thermal energy dissipation (D), remained stable regardless of the changes in levels of Chla + b. Under 800 and 1200 PPFD, the values of p and electron transport rate (ETR) decreased, but D and NPQ increased as Chla + bcontent decreased, suggesting that decrease inChla + bcontent led to lower PSII efficiency and it became necessary to increase dissipate excess energy. On the contrary, in 2000 PPFD, leaves with lower Chla + bcontent had relatively higher p and electron transport rate (ETR) values and lower D level, as well as tended to increase more in NPQ but decrease more in PRI values. The consistent relations between PRI and NPQ suggest that NPQ is mainly consisted ofthe xanthophyll cycle-dependentenergy quenching.Yellow-green cultivar showed lower Chla + bcontent but high carotenoids/Chla + b ratio and had high light protection ability under high PPFD. The precise management of photosynthetic parameters in response to light intensity can maximize the growth and development of Chinese kale plants.

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Tài liệu tham khảo

Demmig-Adams, B., Jared, J., Stewart, I.D., Christopher, R., and Adams, W. (2018). Optimization of Photosynthetic productivity in contrasting environments by regulons controlling plant form and function. Int. J. Mol. Sci., 19.

Montgomery, 2008, Adaptive radiation of photosynthetic physiology in the Hawaiian lobeliads:Dynamic photosynthetic responses, Oecologia, 155, 455, 10.1007/s00442-007-0936-3

Zaworska, 2018, Effect of biostimulants on chlorophyll fluorescenceparameters of broccoli (brassica oleracea var. italica)under drought stress and rewatering, Acta Sci. Pol. HortorumCultus, 17, 97, 10.24326/asphc.2018.1.9

Banks, 2017, Continuous excitation chlorophyll fluorescence parameters: A review for practitioners, Tree Physiol., 37, 1128, 10.1093/treephys/tpx059

Arellano, 2011, A protocol to assess heat tolerance in a segregating population of raspberry using chlorophyll fluorescence, Sci. Hort., 130, 524, 10.1016/j.scienta.2011.07.022

Weng, 2011, A comparison between yellow-green and green cultivars of four vegetable species in pigments, ascorbate, photosynthesis, energy dissipation, and photoinhibition, Photosynthetica, 49, 361, 10.1007/s11099-011-0046-7

Siemonsma, J.S., and Kasem, P. (1994). Brassica oleracea L. cv. group Chinese kale. Plant Resource South-East Asia No. 8: Vegetables, Pudoc Scientific Publishers.

Maxwell, 2000, Chlorophyll fluorescence—A practical guide, J. Exp. Bot., 51, 659, 10.1093/jexbot/51.345.659

Laing, 2000, Physiological impacts of magnesiumdeficiency in Pinus radiata: Growth and photosynthesis, New Phytol., 146, 47, 10.1046/j.1469-8137.2000.00616.x

Yang, 2017, Chlorophyllfluorescence tracks seasonal variations of photosynthesis from leaf tocanopy in a temperate forest, Glob. Chang. Biol., 23, 2874, 10.1111/gcb.13590

Adams, 2004, Photoprotective strategies of overwinteringevergreens, BioScience, 54, 41, 10.1641/0006-3568(2004)054[0041:PSOOE]2.0.CO;2

Osmond, 1995, Perspectives on photoinhibition and photorespiration in the field: Quintessential inefficiencies of the light and dark reactions of photosynthesis?, J. Exp. Bot., 46, 1351, 10.1093/jxb/46.special_issue.1351

Adams, 1996, Using chlorophyll fluorescence to assess the fraction of absorbed light allocated to thermal dissipation of excess excitation, Physiol. Plant, 98, 253, 10.1034/j.1399-3054.1996.980206.x

Kakani, 2008, Photosynthesis andfluorescence responses of C4 plant Andropogongerardii acclimatedto temperature and carbon dioxide, Photosynthetica, 46, 420, 10.1007/s11099-008-0074-0

Wong, 2014, Relationship between photosynthetic CO2 uptake rate and electron transport rate in two C4 perennial grasses under different nitrogen fertilization, light and temperature conditions, Acta Physiol. Plant, 36, 849, 10.1007/s11738-013-1463-y

Cheng, 2001, The relationship betweenphotosystem II efficiency and quantum yield for CO2 assimilationis not affected by nitrogen content in apple leaves, J. Exp. Bot., 52, 1865, 10.1093/jexbot/52.362.1865

Bravo, 2007, Iselectron transport to oxygen an important mechanism inphotoprotection? Contrasting responses from Antarcticvascular plants, Physiol. Plant, 130, 185, 10.1111/j.1399-3054.2007.00899.x

Lin, 2009, Identification of the phenolic components of collard greens, kale, and chinese broccoli, J. Agric. Food Chem., 57, 7401, 10.1021/jf901121v

Romeroa, 2018, Analysis of metabolic and nutritional biomarkers in Brassica oleracea L. cv. Bronco plants under alkaline stress, J. Hortic. Sci. Biotech., 93, 279, 10.1080/14620316.2017.1364979

Nichol, 2000, Remote sensing of photosynthetic-light-use efficiency of boreal forest, Agric. For. Meteorol., 101, 131, 10.1016/S0168-1923(99)00167-7

Li, 2001, Non-photochemical quenching: A response to excess light energy, Plant Physiol., 125, 1558, 10.1104/pp.125.4.1558

Schansker, 2006, Dark recovery of the Chl a fluorescence transient (OJIP) after light adaptation: The qT-component of non-photochemical quenching is related to an activated photosystem I acceptor side, Biochim. Biophys. Acta, 1757, 787, 10.1016/j.bbabio.2006.04.019

Pollastrini, 2017, Tree diversity affects chlorophyll a fluorescence andother leaf traits of tree species in a boreal forest, Tree Physiol., 37, 199

Lefsrud, 2008, Irradiance from distinct wavelength light-emitting diodes affect secondary metabolites in kale, HortScience, 43, 2243, 10.21273/HORTSCI.43.7.2243

Frank, 2010, Molecular factors controlling photosynthetic light harvesting by carotenoids, Acc. Chem. Res., 43, 1125, 10.1021/ar100030m

2012, Carotenoid biosynthesis in Arabidopsis: A colorful pathway, The Arab. Book, 10, e0158, 10.1199/tab.0158

DeEll, J.R., and Toivonen, P.M.A. (2003). The application of chlorophyll fluorescence to study light, temperature, and drought stress. Practical Applications of Chlorophyll Fluorescence in Plant Biology, Kluwer Academic Publishers.

Korhonen, 2008, A new monitoring PAM fluorometer (MONI-PAM) to study the short- and long-term acclimation of photosystem II in field conditions, Photosynth. Res., 96, 173, 10.1007/s11120-008-9292-3

Stylinski, 2002, Seasonal patterns of reflectance indices, carotenoid pigments and photosynthesis of evergreen chaparral species, Oecologia, 131, 366, 10.1007/s00442-002-0905-9

Lichtenthaler, 1987, Chlorophylls and carotenoids, the pigments of photosynthetic biomembranes, Method Enzymol., 148, 350, 10.1016/0076-6879(87)48036-1