Abstract
Effects of root treatment with 5-aminolevulinic acid (ALA) on leaf photosynthesis in strawberry (Fragaria ananassa Duch.) plants were investigated by rapid chlorophyll fluorescence and modulated 820 nm reflection using 3-(3,4-dichlorophenyl)-1,1-dimethyl urea (DCMU) and methyl viologen (MV). Our results showed that ALA treatments increased the net photosynthetic rate and decreased the intercelluar CO2 concentration in strawberry leaves. Under DCMU treatment, trapping energy for QA reduction per PSII reaction center increased greatly, indicating DCMU inhibited electron transfer from QA −. The maximum photochemical efficiency of PSII (Fv/Fm) decreased under the DCMU treatment, while a higher Fv/Fm remained in the ALA-pretreated plants. Not only the parameters related to a photochemical phase, but also that one related to a heat phase remained lower after the ALA pretreatment, compared to the sole DCMU treatment. The MV treatment decreased PSI photochemical capacity. The results of modulated 820 nm reflection analysis showed that DCMU and MV treatments had low re-reduction of P700 and plastocyanin (PSI). However, the strawberry leaf discs pretreated with ALA exhibited high re-reduction of PSI under DCMU and MV treatments. The results of this study suggest that the improvement of photosynthesis by ALA in strawberry was not only related to PSII, but also to PSI and electron transfer chain.
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Abbreviations
- ALA:
-
5-aminolevulinic acid
- C i :
-
intercellular CO2 concentration
- Chl:
-
chlorophyll
- DCMU:
-
3-(3,4-dichlorophenyl)-1,1-dimethyl urea
- E :
-
transpiration rate
- Fj and Fi :
-
the fluorescence intensity at 2 ms (J-step) and 30 ms (I-step)
- Fm :
-
the maximum fluorescence intensity
- Fo :
-
the minimum fluorescence intensity
- Fv/Fm :
-
maximal quantum yield of PSII photochemistry
- g s :
-
stomatal conductance
- MR:
-
modulated 820 nm reflection
- MRo :
-
value of modulated 820 nm reflection at the onset of red light illumination
- MV:
-
methyl viologen
- P680:
-
PSII reaction center
- P700:
-
PSI reaction center
- P N :
-
net photosynthetic rate
- PC:
-
plastocyanin
- PQH2 :
-
plastoquinol
- RC/ABS:
-
QA reducing reaction centers per PSII antenna chlorophyll
- VJ :
-
the relative variable fluorescence intensities at the J-step
- VI :
-
the relative variable fluorescence intensities at the I-step
- VPSI :
-
maximum slope of decrease of MR/MRo
- VPSII-PSI :
-
maximum slope of increase of MR/MRo
References
Allen R.D., Webb R.P., Schake S.A.: Use of transgenic plants to study antioxidant defences. — Free Radical Biol. Med. 23: 473–479, 1997.
An Y.Y., Li J., Duan C.H. et al.: 5-aminolevulinic acid thins pear fruits by inhibiting pollen tube grown via Ca2+-ATPasemediated Ca2+ efflux. — Front. Plant Sci. 7: doi: 10.3389, 2016.
Appenroth K.J., Stöckel J., Srivastava A. et al.: Multiple effects of chromate on the photosynthetic apparatus of Spirodela polyrhiza as probed by OJIP chlorophyll a fluorescence measurements. — Environ. Pollut. 115: 49–64, 2001.
Gao J., Li P.M., Ma F.W. et al.: Photosynthetic performance during leaf expansion in Malus micromalus probed by chlorophyll a fluorescence and modulated 820 nm reflection. — J. Photoch. Photobio. B 137: 144–150, 2014.
Goltsev V., Zaharieva I., Chernev P. et al.: Drought induced modifications of photosynthetic electron transport in intact leaves: analysis and use of neural networks as a tool for a rapid non-invasive estimation. — Biochim. Biophys. Acta 1817: 1490–1498, 2012.
Han B.M., Li H., Gao X.Y. et al. [Research on photosynthetic characteristics of strawberry seedlings in vitro propagation.] — J. Fruit Sci. 4: 559–563, 2009. [In Chinese]
Hotta Y., Tanaka T., Takaoka H. et al.: New physiological effects of 5-aminolevulinic acid in plants: the increase of photosynthesis, chlorophyll content, and plant growth. — Biosci. Biotech. Bioch. 61: 2025–2028, 1997.
Jiang C.D., Shi L., Gao H.Y. et al.: Development of photosystems 2 and 1 during leaf growth in grapevine seedlings probed by chlorophyll a fluorescence transient and 820 nm transmission in vivo. — Photosynthetica 44: 454–463, 2006.
Komenda J., Koblížek M., Prášil O.: Characterization of processes responsible for the distinct effect of herbicides of DCMU and BNT on Photosystem II photoinactivation in cells of the cyanobacterium Synechococcus PCC 7942. — Photosynth. Res. 63: 135–144, 2000.
Kouřil R., Lazár D., Lee H. et al.: Moderately elevated temperature eliminates resistance of rice plants with enhanced expression of glutathione reductase to intensive photooxidative stress. — Photosynthetica 41: 571–578, 2003.
Kreslavski V.D., Kosobryukhov A.A., Shmarev A.N. et al.: Introduction of the Arabidopsis PHYB gene increases resistance of photosynthetic apparatus in transgenic Solanum tuberosum plants to UV-B radiation. — Russ. J. Plant Physl+ 62: 204–209, 2015.
Lazár D.: Modelling of light-induced chlorophyll a fluorescence rise (O-J-I-P transient) and changes in 820 nm–transmittance signal of photosynthesis. — Photosynthetica 47: 483–498, 2009.
Lazár D.: The polyphasic chlorophyll a fluorescence rise measured under high intensity of exciting light. — Funct. Plant Biology 33: 9–30, 2006.
Li P.M., Ma F.W.: Different effects of light irradiation on the photosynthetic electron transport chain during apple tree leaf dehydration. — Plant Physiol. Bioch. 55: 16–22, 2012.
Liu W.Q., Kang L., Wang L.J.: [Effect of 5-aminolevulinic acid (ALA) on photosynthesis and its relationship with antioxidant enzymes of strawberry leaves.] — Acta Bot. Boreal. Occident. Sin. 26: 57–62, 2006. [In Chinese]
Memon S.A., Hou X.L., Wang L.J. et al.: Promotion effect of 5-aminolevulinic acid on chlorophyll, antioxidant enzymes and photosynthesis of pakchoi (Brassica campestris ssp. chinensis var. communis Tsen et Lee). — Acta Physiol. Plant. 31: 51–57, 2009.
Nishihara E., Kondo K., Parvez M.M. et al.: Role of 5-aminolevulinic acid (ALA) on active oxygen-scavenging system in NaCl-treated spinach (Spinacia oleracea). — J. Plant Physiol. 160: 1085–1091, 2003.
Oukarroum A., Goltsev V., Strasser R.J.: Temperature effects on pea plants probed by simultaneous measurements of the kinetics of prompt fluorescence, delayed fluorescence and modulated 820 nm reflection. — PLoS One 8: e59433, 2013.
Panda D., Rao D.N., Sharma S.G. et al.: Submergence effects on rice genotypes during seedling stage: Probing of submergence driven changes of photosystem 2 by chlorophyll a fluorescence induction 0-J-I-P transients. — Photosynthetica 44: 69–75, 2006.
Phung T.H., Jung S.: Differential antioxidant defense and detoxification mechanisms in photodynamically stressed rice plants treated with the deregulators of porphyrin biosynthesis, 5-aminolevulinic acid and oxyfluorfen. — Biochem. Bioph. Res. Co. 459: 346–351, 2015.
Schansker G., Srivastava A., Govindjee et al.: Characterization of the 820-nm transmission signal paralleling the chlorophyll a fluorescence rise (OJIP) in pea leaves. — Funct. Plant Biol. 30: 785–796, 2003.
Schansker G., Tóth S.Z., Kovács L. et al.: Evidence for a fluorescence yield change driven by a light-induced conformational change within photosystem II during the fast chlorophyll a fluorescence rise. — Biochim. Biophys. Acta 1807: 1032–1043, 2011.
Schansker G., Tóth S.Z., Strasser R.J.: Methylviologen and dibromothymoquinone treatments pea leaves reveal the role of photosystem I in the Chl a fluorescence rise OJIP. — Biochim. Biophys. Acta 1706: 250–261, 2005.
Sowik I., Markiewicz M., Michalczuk L.: Stability of Verticillium dahliae resistance in tissue culture-derived strawberry somaclones. — HortScience 42: 141–148, 2015.
Stirbet A., Govindjee: On the relation between the Kautsky effect (chlorophyll a fluorescence induction) and photosystem II: basics and applications of the OJIP fluorescence transient. — J. Photoch. Photobio. B 104: 36–57, 2011.
Strasser B.J., Strasser R.J.: Measuring fast fluorescence transients to address environmental questions: The JIP test. — In: Mathis P. (ed).: Photosynthesis: From Light to Biosphere. Pp. 977–980. KAP Press, Dordrecht 1995.
Strasser R.J., Srivastava A., Tsimilli-Michael M.: The fluorescence transient as a tool to characterize and screen photosynthetic samples. — In: Yunus M., Pathre U., Mohanty P. (ed.): Probing Photosynthesis: Mechanism, Regulation and Adaptation. Pp. 445–483. Taylor & Francis Press, London–New York 2000.
Strasser R.J., Tsimilli-Michael M., Qiang S. et al.: Simultaneous in vivo recording of prompt and delayed fluorescence and 820 nm reflection changes during drying and after rehydration of the resurrenction plant Haberlea rhodopensis. — Biochim. Biophys. Acta 1797: 1313–1326, 2010.
Sun Y.P., Zhang Z.P., Wang L.J.: Promotion of 5-aminolevulinic acid treatment on leaf photosynthesis is related with increase of antioxidant enzyme activity in watermelon seedlings grown under shade condition. — Photosynthetica 47: 347–354, 2009.
Thiele A., Herold M., Lenk I. et al.: Heterologous expression of Arabidopsis phytochrome B in transgenic potato influences photosynthetic performance and tuber development. — Plant Physiol. 120: 73–81, 1999.
Tóth S.Z., Schansker G., Strasser R.J.: A non-invasive assay of the plastoquinone pool redox state based on the OJIP-transient. — Photosynth. Res. 93: 193–203, 2007.
von Wettstein D., Gough S., Kannangara C.G.: Chlorophyll biosynthesis. — Plant Cell 7:1039–1057, 1995.
Wang L.J., Jiang W.B., Huang B.J.: Promotion of 5-aminolevulinic acid on photosynthesis of melon (Cucumis melo) seedlings under low light and chilling stress condition. — Physiol. Plantarum 121: 258–264, 2004.
Wang L.J., Jiang W.B., Zhang Z. et al.: [Biosynthesis and physiological activities of 5-aminolevulinic acid and its potential application in agriculture.] — Plant Physiol. Comm. 39: 185–192, 2003. [In Chinese]
Yan K., Chen P., Shao H.B. et al.: Dissection of photosynthetic electron transport process in sweet sorghum under heat stress. — PLoS One 8: e62100, 2013.
Yan K., Chen P., Shao H.B. et al.: Photosynthetic characterization of Jerusalem artichoke during leaf expansion. — Acta Physiol. Plant. 34: 353–360, 2012.
Zhao Y.Y., Yan F., Hu L.P. et al.: [Effect of 5-aminolevulinic acid on photosynthetic characteristics of tomato seedlings under NaCl stress.] — Chin. J. Appl. Ecol. 25: 2919–2926, 2014. [In Chinese]
Zhao Y.Y., Yan F., Hu L.P. et al.: Effects of exogenous 5-aminolevulinic acid on photosynthesis, stomatal conductance, transpiration rate, and PIP gene expression of tomato seedlings subject to salinity stress. — Genet. Mol. Res. 14: 6401–6412, 2015.
Zushi K., Kajiwara S., Matsuzoe N.: Chlorophyll a fluorescence OJIP transient as a tool to characterize and evaluate response to heat and chilling stress in tomato leaf and fruit. — Sci. Hortic-Amsterdam 148: 39–46, 2012.
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Acknowledgements: This research was supported by Jiangsu Agriculture Science and Technology Innovation Fund (JASTIF), CX(11)4004, China.
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Sun, Y.P., Liu, J., Cao, R.X. et al. Effects of 5-aminolevulinic acid treatment on photosynthesis of strawberry. Photosynthetica 55, 276–284 (2017). https://doi.org/10.1007/s11099-016-0667-y
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DOI: https://doi.org/10.1007/s11099-016-0667-y