作物学报 ›› 2019, Vol. 45 ›› Issue (5): 792-797.doi: 10.3724/SP.J.1006.2019.84104
吴含玉1,3,肖飞1,张亚黎2,姜闯道3,*(
),张旺锋2,*(
)
Han-Yu WU1,3,Fei XIAO1,Ya-Li ZHANG2,Chuang-Dao JIANG3,*(
),Wang-Feng ZHANG2,*(
)
摘要:
除持续强光导致光合作用效率降低外, 强闪光也能够影响光合功能, 但规律和机制尚不清楚。为研究强闪光对喜光植物棉花叶片光合功能的影响, 选用陆地棉(Gossypium hirsutum L.)品种新陆早45号为材料, 于强闪光处理(20,000 μmol m -2 s -1, 300 ms, 间隔10 s, 处理时间持续30 min)前后分别测定叶绿素荧光、P700和气体交换。结果表明, 强闪光处理后不仅有活性的PSI (光系统I)反应中心含量下降, 同时PSII (光系统II)电子传递活性也受到限制。与对照相比, 强闪光处理后PSI的ΦND (PSI供体侧限制引起的非光化学量子产量)下降, ΦNA (PSI受体侧限制引起的非光化学量子产量)增加, 暗示强闪光能够抑制PSI受体侧电子传递活性。强闪光处理不仅使PSII的实际量子产量明显下降, 而且非光化学猝灭和ΦNPQ (PSII调节性能量耗散的量子产量)也降低; 但是, ΦNO (PSII非调节性能量耗散的量子产量)明显增加, 表明强闪光导致热耗散降低和PSII失活。此外, 强闪光处理后光合速率和气孔导度均降低, 但细胞间隙CO2浓度增加, 证明强闪光处理后同化能力的降低不是气孔限制导致的。因此, 本研究认为强闪光处理不仅抑制PSI活性, 而且导致PSII失活和可调节性热耗散下降; 光合电子传递活性的下降可能是强闪光下光合速率降低的重要原因。
| [1] |
Murata N, Takahashi S, Nishiyama Y, Allakhverdiev S I . Photoinhibition of photosystem II under environmental stress. Biochim Biophys Acta, 2007,1767:414-421.
doi: 10.1016/j.bbabio.2006.11.019 |
| [2] |
David J K, Zalik S . Photosystem II activity, plastoquinone A levels, and fluorescence characterization of a virescens mutant of barley. Plant Physiol, 1982,70:1026-1031.
doi: 10.1104/pp.70.4.1026 |
| [3] | Takahashi S, Murata N . Interruption of the Calvin cycle inhibits the repair of photosystem II from photodamage. Biochim Biophys Acta, 2005,1780:352-361. |
| [4] |
Nishiyama Y, Allakhverdiev S, Murata N . Inhibition of the repair of photosystem II by oxidative stress in cyanobacteria. Photosynth Res, 2005,84:1-7.
doi: 10.1007/s11120-004-6434-0 |
| [5] |
Huang W, Yang S J, Zhang S B, Zhang J L, Cao K F . Cyclic electron flow plays an important role in photoprotection for the resurrection plant Paraboea rufescens under drought stress. Planta, 2012,235:819-828.
doi: 10.1007/s00425-011-1544-3 |
| [6] | Terashima L, Funayama S, Sonoike K . The site of photoinhibition in leaves of Cucumis sativus L. at low temperatures is photosystem I, not photosystem II. Planta, 1994,193:300-306. |
| [7] |
Zhang S P, Scheller H V . Photoinhibition of photosystem I at chilling temperature and subsequent recovery in Arabidopsis thaliana. Plant Cell Physiol, 2004,45:1595-1602.
doi: 10.1093/pcp/pch180 |
| [8] |
Huang W, Zhang S B, Cao K F . The different effects of chilling stress under moderate light intensity on photosystem II compared with photosystem I and subsequent recovery in tropical tree species. Photosynth Res, 2010,103:175-182.
doi: 10.1007/s11120-010-9539-7 |
| [9] |
Tikkanen M, Mekala N R, Aro E M . Photosystem II photoinhibition-repair cycle protects photosystem I from irreversible damage. Biochim Biophys Acta, 2014,1837:210-215.
doi: 10.1016/j.bbabio.2013.10.001 |
| [10] |
Tikkanen M, Grebe S . Switching off photoprotection of photosystem I: a novel tool for gradual PSI photoinhibition. Physiol Plant, 2018,162:156-161.
doi: 10.1111/ppl.2018.162.issue-2 |
| [11] |
Li X G, Wang X M, Meng Q W, Zou Q . Factors limiting photosynthetic recovery in sweet pepper leaves after short-term chilling stress under low irradiance. Photosynthetica, 2004,42:257-262.
doi: 10.1023/B:PHOT.0000040598.48732.af |
| [12] | Zhang Z S, Jia Y J, Gao H Y, Zhang H T, Li H D, Meng Q W . Characterization of PSI recovery after chilling-induced photoinhibition in cucumber ( Cucumis stativus L.) leaves. Planta, 2011,234:883-889. |
| [13] |
Sejima T, Takagi D, Fukayama H, Makino A, Miyake C . Repetitive short-pulse light mainly inactivates photosystem I in sunflower leaves. Plant Cell Physiol, 2014,55:1184-1193.
doi: 10.1093/pcp/pcu061 |
| [14] |
Zivcak M, Brestic M, Kunderlikova K, Sytar O, Allakhverdiev S I . Repetitive light pulse-induced photoinhibition of photosystem I severely affects CO2 assimilation and photoprotection in wheat leaves. Photosynth Res, 2015,126:449-463.
doi: 10.1007/s11120-015-0121-1 |
| [15] |
Suzuki K, Ohmori Y, Ratel E . High root temperature blocks both linear and cyclic electron transport in the dark during chilling of the leaves of rice seedlings. Plant Cell Physiol, 2011,52:1697-1707.
doi: 10.1093/pcp/pcr104 |
| [16] | Kramer D M, Johnson G, Kiirats O, Edwards G E . New fluorescence parameters for the determination of QA redox state and excitation energy fluxes. Photosynth Res, 2004, 79:209-218. |
| [17] | Genty B, Briantais J M, Bake N R . The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta, 1989,1:87-92. |
| [18] | Pfündel E, Klughammer C, Schreiber U . Monitoring the effects of reduced PSII antenna size on quantum yields of photosystems I and II using the Dual-PAM-100 measuring system. PAM Appl Notes, 2008,1:21-24. |
| [19] | Schreiber U, Klughammer C . New accessory for the DUAL- PAM-100: the P515/535 module and examples of its application. PAM Appl Notes, 2008,1:1-10. |
| [20] | Klughammer C, Schreiber U . Complementary PSII quantum yields calculated from simple fluorescence parameters measured by PAM fluorometry and the saturation pulse method. PAM Appl Notes, 2008,1:27-35. |
| [21] | Suorsa M, Järvi S, Grieco M, Nurmi M, Pietrzykowska M, Rantala M, Kangasjärvi S, Paakkarinen V, Tikkanen M, Jansson S, Aro E M . PROTON GRADIENT REGULATION5 is essential for proper acclimation of Arabidopsis photosystem I to naturally and artificially fluctuating light conditions. Plant Cell, 2012,24:2934-2948. |
| [22] | Sonoike K, Terashima I . Mechanism of photosystem I photoinhibition in leaves of Cucumis sativus L. Planta, 1994,194:287-293. |
| [23] |
Sonoike K . Photoinhibition of photosystem I: its physiological significance in the chilling sensitivity of plants. Plant Cell Physiol, 1996,37:239-247.
doi: 10.1093/oxfordjournals.pcp.a028938 |
| [24] |
Takagi D, Ishizaki K, Hanawa H, Mabuchi T, Shimakawa G, Yamamoto H, Miyake C . Diversity of strategies for escaping reactive oxygen species production within photosystem I among land plants: P700 oxidation system is prerequisite for alleviating photoinhibition in photosystem I. Physiol Plant, 2017,161:56-74.
doi: 10.1111/ppl.2017.161.issue-1 |
| [25] |
Liu Y F, Qi M F, Li T L . Photosynthesis, photoinhibition, and antioxidant system in tomato leaves stressed by low night temperature and their subsequent recovery. Plant Sci, 2012,196:8-17.
doi: 10.1016/j.plantsci.2012.07.005 |
| [26] |
Sato R, Kono M, Harada K, Ohta H, Takaichi S, Masuda S . FLUCTUATING-LIGHT-ACCLIMATION PROTEIN1, conserved in oxygenic phototrophs, regulates H + homeostasis and non-photochemical quenching in chloroplasts . Plant Cell Physiol, 2017,58:1622-1630.
doi: 10.1093/pcp/pcx110 |
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