Detection of singlet oxygen and superoxide with fluorescent sensors in leaves under stress by photoinhibition or UV radiation.

In order to understand the physiological functions of reactive oxygen species (ROS) generated in leaves, their direct measurement in vivo is of special importance. Here we report experiments with two dansyl-based ROS sensors, the singlet oxygen specific DanePy and HO-1889NH, which is reactive to both singlet oxygen and superoxide radicals. Here we report in vivo detection of (1)O(2) and O(2)(-*) by fluorescence quenching of two dansyl-based ROS sensors, the (1)O(2) specific DanePy and HO-1889NH, which was reactive with both (1)O(2) and O(2)(-*). The ROS sensors were administered to spinach leaves through a pinhole, and then the leaves were exposed to either excess photosynthetically active radiation or UV (280-360 nm) radiation. Microlocalization of the sensors' fluorescence and its ROS-induced quenching was followed with confocal laser scanning microscopy and with fluorescence imaging. These sensors were specifically localized in chloroplasts. Quenching analysis indicated that the leaves exposed to strong light produced (1)O(2), but hardly any O(2)(-*). On the other hand, the dominant ROS in UV-irradiated leaves was O(2)(-*), while (1)O(2) was minor.

[1]  J. McMurtrey,et al.  Laser-induced fluorescence of green plants. 1: A technique for the remote detection of plant stress and species differentiation. , 1984, Applied optics.

[2]  G. Malanga,et al.  Oxidative stress and antioxidant content in Chlorella vulgaris after exposure to ultraviolet‐B radiation , 1995 .

[3]  J. Golbeck,et al.  Superoxide contributes to the rapid inactivation of specific secondary donors of the photosystem II reaction center during photodamage of manganese-depleted photosystem II membranes. , 1995, Biochemistry.

[4]  Stephen B. Powles,et al.  Photoinhibition of Photosynthesis Induced by Visible Light , 1984 .

[5]  J. Barber,et al.  Mechanisms of Photodamage and Protein Degradation During Photoinhibition of Photosystem II , 1996 .

[6]  É. Hideg,et al.  Singlet oxygen detection with sterically hindered amine derivatives in plants under light stress. , 2000, Methods in enzymology.

[7]  É. Hideg,et al.  Do oxidative stress conditions impairing photosynthesis in the light manifest as photoinhibition? , 2000, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[8]  D. Ormrod,et al.  IMPACT OF UVB and 03 ON THE OXYGEN FREE RADICAL SCAVENGING SYSTEM IN Arabidopsis thaliana GENOTYPES DIFFERING IN FLAVONOID BIOSYNTHESIS , 1995 .

[9]  B. Halliwell,et al.  Free radicals in biology and medicine , 1985 .

[10]  K. Asada,et al.  THE WATER-WATER CYCLE IN CHLOROPLASTS: Scavenging of Active Oxygens and Dissipation of Excess Photons. , 1999, Annual review of plant physiology and plant molecular biology.

[11]  M. Edelman,et al.  Separate photosensitizers mediate degradation of the 32-kDa photosystem II reaction center protein in the visible and UV spectral regions. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[12]  Brian Thomas,et al.  Early signaling components in ultraviolet‐B responses: distinct roles for different reactive oxygen species and nitric oxide , 2001, FEBS letters.

[13]  E. Aro,et al.  Photoinhibition of Photosystem II. Inactivation, protein damage and turnover. , 1993, Biochimica et biophysica acta.

[14]  É. Hideg,et al.  UV-B induced free radical production in plant leaves and isolated thylakoid membranes , 1996 .

[15]  I. Vass,et al.  UV-B-induced inhibition of photosystem II electron transport studied by EPR and chlorophyll fluorescence. Impairment of donor and acceptor side components. , 1996, Biochemistry.

[16]  N. Baker Photosynthesis and the Environment , 1996, Advances in Photosynthesis and Respiration.

[17]  É. Hideg,et al.  Singlet oxygen production in thylakoid membranes during photoinhibition as detected by EPR spectroscopy , 1994, Photosynthesis Research.

[18]  É. Hideg,et al.  Double (fluorescent and spin) sensors for detection of reactive oxygen species in the thylakoid membrane. , 1998, Free radical biology & medicine.

[19]  K. Asada,et al.  Production and Action of Active Oxygen Species in Photosynthetic Tissues , 2019, Causes of Photooxidative Stress and Amelioration of Defense Systems in Plants.

[20]  H. Eckert,et al.  ON THE MECHANISM OF PHOTOSYSTEM II DETERIORATION BY UV‐B IRRADIATION , 1989 .

[21]  G. Kulandaivelu,et al.  Comparative study of the action of ultraviolet‐C and ultraviolet‐ B radiation on photosynthetic electron transport , 1983 .

[22]  É. Hideg,et al.  Singlet oxygen and free radical production during acceptor- and donor-side-induced photoinhibition: Studies with spin trapping EPR spectroscopy , 1994 .

[23]  J. Briantais,et al.  The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence , 1989 .

[24]  J. Barber,et al.  Too much of a good thing: light can be bad for photosynthesis. , 1992, Trends in biochemical sciences.

[25]  É. Hideg,et al.  Superoxide radicals are not the main promoters of acceptor-side-induced photoinhibitory damage in spinach thylakoids , 2004, Photosynthesis Research.

[26]  G. Friso,et al.  Degradation of Photosystem II reaction center D1-protein induced by UVB radiation in isolated thylakoids. Identification and characterization of C- and N-terminal breakdown products , 1994 .

[27]  M. Miyao Involvement of active oxygen species in degradation of the D1 protein under strong illumination in isolated subcomplexes of photosystem II. , 1994, Biochemistry.

[28]  Janet F. Bornman,et al.  New trends in photobiology: Target sites of UV-B radiation in photosynthesis of higher plants , 1989 .

[29]  B. Møller,et al.  Active oxygen produced during selective excitation of photosystem I is damaging not only to photosystem I, but also to photosystem II. , 2001, Plant physiology.

[30]  J. Pueyo,et al.  Photoinhibition of Photosystem II from Higher Plants , 1996, The Journal of Biological Chemistry.

[31]  R. Ueda,et al.  Detection of hydroxyl radical in intact cells of Chlorella vulgaris. , 1995, Free radical research.

[32]  B. Thomas,et al.  Effects of Supplementary Ultraviolet‐B Radiation on Photosynthetic Transcripts at Different Stages of Leaf Development and Light Levels in Pea (Pisum sativum L.): Role of Active Oxygen Species and Antioxidant Enzymes. , 1998 .

[33]  A. Teramura,et al.  Effects of UV-B radiation on photosynthesis and growth of terrestrial plants , 1994, Photosynthesis Research.

[34]  T. Kálai,et al.  Singlet oxygen imaging in Arabidopsis thaliana leaves under photoinhibition by excess photosynthetically active radiation. , 2001, Physiologia plantarum.

[35]  S. Green,et al.  Intramolecular quenching of excited singlet states by stable nitroxyl radicals , 1990 .

[36]  É. Hideg,et al.  SYNTHESIS AND STUDY OF DOUBLE (EPR ACTIVE AND FLUORESCENT) CHEMOSENSORS IN THE PRESENCE OF Fe3+ ION , 2001 .

[37]  É. Hideg,et al.  Synthesis and structure optimization of double (fluorescent and spin) sensor molecules , 2002 .

[38]  É. Hideg,et al.  Photoinhibition of photosynthesis in vivo results in singlet oxygen production detection via nitroxide-induced fluorescence quenching in broad bean leaves. , 1998, Biochemistry.