Czasopismo
Tytuł artykułu
Warianty tytułu
Języki publikacji
Abstrakty
Qilian Juniper (Sabina przewalskii Kom.) and Chinese juniper [Sabina chinensis (Lin.) Ant.] are overwintering plants. S. przewalskii, a protected species in China, is distributed in subalpine and alpine area on the Qinghai-Tibet Plateau. S. chinensis is distributed in plain area. We investigated seasonal changes in photoprotective stress compounds such as anthocyanins, activities of three enzymes of ascorbate–glutathione pathway, as well as xanthophyll size and conversion in these species. Ascorbate peroxidase (APX), dehydroascorbate reductase (DHAR) and glutathione reductase (GR) levels were higher in the lowtemperature months, which was associated with changes in anthocyanins and in de-epoxidation index [(A + Z)/ (V + A + Z)]. Photochemical efficiency of PSII (Fv/Fm) was lower (<0.70) during winter and late autumn in both species. During the low-temperature months, S. przewalskii had higher levels of photoprotective stress compounds than S. chinensis. The results suggested that these two species possess cold-induced photoinhibition functions and show the inherent, season-dependent differences in the amounts of the stress-related compounds.
Słowa kluczowe
Wydawca
Czasopismo
Rocznik
Tom
Numer
Opis fizyczny
p.801-808,fig.,ref.
Twórcy
autor
- State Key Laboratory of Cryospheric Sciences, Cold and Arid Regions Environmental and Engineering Research Institute, Chinese Academy of Sciences, Lanzhou 730000, Gansu, People’s Republic of China
- College of Chemistry and Life Sciences, Leshan Teachers College, Leshan 614004, Sichuan, People’s Republic of China
- Graduate University of Chinese Academy of Sciences, Beijing 100049, People’s Republic of China
autor
- State Key Laboratory of Cryospheric Sciences, Cold and Arid Regions Environmental and Engineering Research Institute, Chinese Academy of Sciences, Lanzhou 730000, Gansu, People’s Republic of China
autor
- Department of Nature Resources and Environmental Science, Center for Forestry, Ecology, and Wildlife, Alabama A&M University, Normal, AL 35762, USA
- Ministry of Education Key Laboratory for Biodiversity Sciences and Ecological Engineering, College of Life Sciences, Beijing Normal University, Beijing 100875, People’s Republic of China
autor
- Cold and Arid Regions Environmental and Engineering Research Institute, Chinese Academy of Sciences, Lanzhou 730000, Gansu, People’s Republic of China
- Lanzhou Petrochemical College of Technology, Lanzhou 730060, Gansu, People’s Republic of China
autor
- Cold and Arid Regions Environmental and Engineering Research Institute, Chinese Academy of Sciences, Lanzhou 730000, Gansu, People’s Republic of China
autor
- Cold and Arid Regions Environmental and Engineering Research Institute, Chinese Academy of Sciences, Lanzhou 730000, Gansu, People’s Republic of China
autor
- Cold and Arid Regions Environmental and Engineering Research Institute, Chinese Academy of Sciences, Lanzhou 730000, Gansu, People’s Republic of China
- School of Life Sciences, Lanzhou University, Lanzhou 730000, Gansu, People’s Republic of China
autor
- School of Life Sciences, Lanzhou University, Lanzhou 730000, Gansu, People’s Republic of China
autor
- School of Life Sciences, Lanzhou University, Lanzhou 730000, Gansu, People’s Republic of China
Bibliografia
- Adams WW III, Barker DH (1998) Seasonal changes in xanthophyll cycle-dependent energy dissipation in Yucca glauca Nuttall. Plant Cell Environ 21:501–511
- Adams WW III, Demmig-Adams B, Verhoeven AS, Barker DH (1995) ‘Photoinhibition’ during winter stress: involvement of sustained xanthophyll cycle-dependent energy dissipation. Aust J Plant Physiol 22:261–276
- Anderson JV, Chevone BI, Hess JL (1992) Seasonal variation in the antioxidant system of eastern white pine needles: evidence for thermal dependence. Plant Physiol 98:501–508
- Asada K (1984) Chloroplasts: formation of active oxygen and its scavenging. Methods Enzymol 105:422–429
- Asada K (1999) The water–water cycle in chloroplasts: scavenging of active oxygens and dissipation of excess photons. Annu Rev Plant Physiol Plant Mol Biol 50:601–639
- Asada K (2006) Production and scavenging of reactive oxygen species in chloroplasts and their functions. Plant Physiol 141:391–396
- Aysel S, Műnevver S (2004) Seasonal changes in antioxidant activity, total phenolic and anthocyanin constituent of the stems of two Morus species (Morus alba L. and Morus nigra L.). Plant Growth Regul 44:251–256
- Björkman O, Demmig B (1987) Photon yield of O₂ evolution and chlorophyll fluorescence characteristics at 77 K among vascular plants of diverse origins. Planta 170:489–504
- Bradford MM (1976) A rapid and sensitive method for the quantisation of microgram quantities of protein utilizing the principle of protein–dye binding. Anal Biochem 72:248–254
- Christie PJ, Alfenito MR, Walbot V (1994) Impact of low-temperature stress on general phenylpropanoid and anthocyanin pathways: enhancement of transcript abundance and anthocyanin pigmentation in maize seedlings. Planta 194:541–549
- Close DC, Beadle CL (2005) Xanthophyll-cycle dynamics and rapid induction of anthocyanin synthesis in Eucalyptus nitens seedlings transferred to photoinhibitory conditions. J Plant Physiol 162:37–46
- Close DC, Beadle CL, Brown PH, Holz GK (2000) Cold-induced photoinhibition affects establishment of Eucalyptus nitens (Deane and Maiden) Maiden and Eucalyptus globulus Labill. Trees 15:32–41
- Demmig-Adams B, Adams WW III (1992) Photoprotection and other responses of plants to high light stress. Annu Rev Plant Physiol Plant Mol Biol 43:599–626
- Diaz C, Saliba-Colombani V, Loudet O, Belluomo P, Moreau L, Daniel-Vedele F, Morot-Gaudry JF, Masclaux-Daubresse C (2006) Leaf Yellowing and anthocyanin accumulation are two genetically independent strategies in response to nitrogen limitation in Arabidopsis thaliana. Plant Cell Physiol 47:74–83
- Field TS, Lee DW, Holbrook NM (2001) Why leaves turn red in autumn. The role of anthocyanins in senescing leaves of redosier dogwood. Plant Physiol 127:566–574
- Gilmore AM, Yamamoto HY (1991) Resolution of lutein and zeaxanthin using a non-end capped, lightly carbon-loaded C₁₈ high-performance liquid chromatographic column. J Chromatogr 543:137–145
- Gitelson AA, Merzlyak MN, Chivkunova OB (2001) Optical properties and non-destructive estimation of anthocyanin content in plant leaves. Photochem Photobiol 74:38–45
- Gonzaleź A, Steffen KL, Lynch JP (1998) Light and excess manganese. Implications for oxidative stress in common bean. Plant Physiol 118:493–504
- Hirotsu N, Makino A, Ushio A, Mae T (2004) Changes in the thermal dissipation and the electron flow in the water–water cycle in rice grown under conditions of physiologically low temperature. Plant Cell Physiol 45:635–644
- Hughes NM, Neufeld HS, Burkey KO (2005) Functional role of anthocyanins in high-light winter leaves of the evergreen herb Galax urceolata. New Phytol 168:575–587
- Ishii Y, Sakamoto K, Yamanaka N, Wang L, Yoshikawa K (2006) Light acclimation of needle pigment composition in Sabina vulgaris seedlings under nurse plant canopy. J Arid Environ 67:403–415
- Janda T, Szalai G, Rios-Gonzalez K, Veisz O, Pàldi E (2003) Comparative study of frost tolerance and antioxidant activity in cereals. Plant Sci 164:301–306
- Johnson GN, Young AJ, Scholes JD, Horton P (1993) The dissipation of excess excitation energy in British plant species. Plant Cell Environ 16:673–679
- Krause GH (1988) Photoinhibition of photosynthesis. An evalution of damaging and protective mechanisms. Physiol Plant 74:566–574
- Krol M, Gray GR, Hurry VM, Öquist L, Malek L, Huner NPA (1995) Low temperature stress and photoperiod effect an increased tolerance to photoinhibition in Pinus banksiana seedlings. Can J Bot 73:1119–1127
- Larbi A, Abadía A, Morales F, Abadía J (2004) Fe resupply to Fe-deficient sugar beet plants leads to rapid changes in the violaxanthin cycle and other photosynthetic characteristics without significant de novo chlorophyll synthesis. Photosynth Res 79:59–69
- Larcher W (2000) Temperature stress and survival ability of Mediterranean sclerophyllous plants. Plant Biosyst 134:279–295
- Li XG, Bi YP, Zhao SJ, Meng QW, Zou Q, He QW (2005) Cooperation of xanthophyll cycle with water-water cycle in the protection of photosystems 1 and 2 against inactivation during chilling stress under low irradiance. Photosynthetica 43:261–266
- Logan BA, Barker DH, Demmig-Adams B, Adams WW (1996) Acclimation of leaf carotenoid composition and ascorbate levels to gradients in the light environment within an Australian rainforest. Plant Cell Environ 19:1083–1090
- McKown R, Kuroki G, Warren G (1996) Cold responses of Arabidopsis mutants impaired in freezing tolerance. J Exp Bot 47:1919–1925
- Michal S, Kristina K, Jiri K, Vladimír S (2008) Dynamics of the xanthophyll cycle and non-radiative dissipation of absorbed light energy during exposure of Norway spruce to high irradiance. J Plant Physiol 165:612–622
- Nakano Y, Asada K (1981) Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant and Cell Physiol 22:867–880
- Neill SO, Gould KS (2003) Anthocyanins in leaves: light attenuators or antioxidants? Funct Plant Biol 30:865–873
- Nozzolillo C, Isabelle P, Andersen OM, Abou-Zaid M (2002) Anthocyanins of jack pine (Pinus banksiana) seedlings. Can J Bot 80:796–801
- Oberhuber W, Bauer H (1991) Photoinhibition of photosynthesis under natural conditions in ivy (Hedera helix L.) growing in an understory of deciduous trees. Planta 185:545–553
- Öquist G, Chow WS, Anderson JM (1992) Photoinhibition of photosynthesis represents a mechanism for long-term regulation of photosystem II. Planta 186:450–460
- Pietrini F, Massacci A (1998) Leaf anthocyanin content changes in Zea mays L. grown at low temperature: significance for the relationship between quantum yield of PS II and the apparent quantum yield of CO₂ assimilation. Photosynth Res 58:213–219
- Pietrini F, Iannelli MA, Massacci A (2002) Anthocyanin accumulation in the illuminated surface of maize leaves enhances protection from photo-inhibitory risks at low temperature, without further limitation to photosynthesis. Plant Cell Environ 25:1251–1259
- Pirie A, Mullins MG (1976) Changes in anthocyanin and phenolics content of grapevine leaf and fruit tissues treated with sucrose, nitrate, and abscisic acid. Plant Physiol 58:468–472
- Rada F, Rcia NC (2001) Low-temperature resistance in Polylepis tarapacana, a tree growing at the highest altitudes in the world. Plant Cell Environ 24:377–381
- Schaberg PG, Wilkinson RC, Shane JB, Donnelly JR, Cali PF (1995) Winter photosynthesis of red spruce from three Vermont seed sources. Tree Physiol 15:345–350
- Schreiber U, Berry JA (1977) Heat-induced changes of chlorophyll fluorescence in intact leaves correlated with damage of the photosynthetic apparatus. Planta 136:233–238
- Solecka D, Kacperska A (2003) Phenylpropanoid deficiency affects the course of plant acclimation to cold. Physiol Plant 119:253–262
- Taulavuori E, Taulavuori K, Laine K, Pakonen T, Saari E (1997) Winter hardening and glutathione status in the bilberry (Vaccinium myrtillus) in response to trace gases (CO₂, O₃) and nitrogen fertilization. Physiol Plant 101:192–198
- Verhoeven AS, Adams WW III, Demmig-Adams B (1998) Two forms of sustained xanthophyll cycle-dependent energy dissipation in overwintering Euonymus kiautschovicus. Plant Cell Environ 21:893–903
- Zhang YF, Zhao ZG, Zhang MX, Chen T, An LZ, Wu JM (2009) Seasonal acclimation of superoxide anion production, antioxidants, IUFA, and electron transport rates in chloroplasts of two Sabina species. Plant Sci 5:696–701
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.agro-1adaa789-8cde-4a4f-89b3-18a3987150aa