PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
2008 | 55 | 1 |

Tytuł artykułu

High light induced accumulation of two isoforms of the CF1 alpha-subunit in mesophyll and bundle sheath chloroplasts of C4 plants

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
The effect of light irradiance on the amount of ATP synthase α-subunit in mesophyll (M) and bundle sheath (BS) chloroplasts of C4 species such as maize (Zea mays L., type NADP-ME), millet (Panicum miliaceum, type NAD-ME) and guinea grass (Panicum maximum, type PEP-CK) was investigated in plants grown under high, moderate and low light intensities equal to 800, 350 and 50 μmol photons m -2 s -1, respectively. The results demonstrate that α-subunit of ATP synthase in both M and BS chloroplasts is altered by light intensity, but differently in the investigated species. Moreover, we identified two isoforms of the CF1 α-subunit, called α and ά. The CF1 α-subunit was the major isoform and was present in all light conditions, whereas ά was the minor isoform in low light. A strong increase in the level of the ά-subunit in maize mesophyll and bundle sheath thylakoids was observed after 50 h of high light treatment. The α and ά-subunits from investigated C4 species displayed apparent molecular masses of 64 and 67 kDa, respectively, on SDS/PAGE. The presence of the ά-subunit of ATPase was confirmed in isolated CF1 complex, where it was recognized by antisera to the α-subunit. The N-terminal sequence of ά-subunit is nearly identical to that of α. Our results indicate that both isoforms coexist in M and BS chloroplasts during plant growth at all irradiances. We suggest the existence in M and BS chloroplasts of C4 plants of a mechanism(s) regulating the ATPase composition in response to light irradiance. Accumulation of the ά isoform may have a protective role under high light stress against over protonation of the thylakoid lumen and photooxidative damage of PSII.

Wydawca

-

Rocznik

Tom

55

Numer

1

Opis fizyczny

p.175-182,fig.,ref.

Twórcy

  • Warsaw University, Miecznikowa 1, 02-096 Warsaw, Poland
autor
autor

Bibliografia

  • Anderson JM, Chow WS, Park YI (1995) The grand design of photosynthesis: acclimation of the photosynthetic apparatus to environmental cues. Photosynth Res 46: 129-139.
  • Andreau JM, Warth R, Munoz E (1978) Glycoprotein nature of energy-transducting ATPases. FEBS Lett 86: 1-5.
  • Arnon DI (1949) Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiol 24: 1-15.
  • Aro E-M, McCaffery S, Anderson JM (1993) Photoinhibition and Dl protein degradation in pea acclimated to different growth irradiances. Plant Physiol 103: 835-843.
  • Bailey S, Walters RG, Jansson S, Horton P (2001) Acclimation of Arabidopsis thaliana to the light environment: the existence of separate low light and high responses. Planta 213: 793-801.
  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of proteins utilizing the principle of protein-dye biding. Anal Biochem 72: 248-254.
  • Burkey KO (1992) Novel light-regulated chloroplast thylakoid membrane protein. Plant Physiol 98: 1211-1213.
  • Burkey KO, Mathis JN (1998) Identification of a novel isoform of the chloroplast-coupling factor α-subunit. Plant Physiol 116: 703-708.
  • Chow WS, Anderson JM (1987) Photosynthetic responses of Pisum sativum to an increase in irradiance during growth. II. Thylakoid membrane components. Aust J Plant Physiol 14: 9-19.
  • De la Torre WR, Burkey KO (1990) Acclimation of barley to changes in light intensity: photosynthetic electron transport activity and components. Photosynth Res 24: 127-136.
  • De Paepe R, Forchioni A, Chetrit P, Vedel F (1993) Specific mitochondrial protein in pollen: Presence of an additional ATP synthase ß subunit. Proc Natl Acad Sci USA 90: 5943-5938.
  • Drozak A, Romanowska E (2006) Acclimation of mesophyll and bundle sheath chloroplasts of maize to different irradiances during growth. Biochim Biophys Acta 1757: 1539-1546.
  • Edwards GE, Huber SC (1981) The C4 pathway. In The biochemistry of plants, a comprehensive treatise; vol. 8, Photosynthesis. Hatch MD, Boardman NI, eds, pp 237-281. Academic Press, New York.
  • Edwards GE, Franceschi VR, Ku MSB, Voznesenskaya EV, Pyankov VI, Andreo CS (2001) Compartmentation of photosynthesis in cells and tissues of C4 plants. J Exp Bot 52: 577-590.
  • Evans JR, Vogelmann TC (2003) Profiles of 14C fixation through spinach leaves in relation to light absorption and photosynthetic capacity. Plant Cell Environ 26: 547- 560.
  • Groth G, Strotmann H (2000) New results about structure, function and regulation of the chloroplast ATP synthase (CFoCF1). Physiol Plant 106: 142-148.
  • Hisabori T, Konno H, Ichimura H, Strotmann H, Bald D (2002) Molecular devices of chloroplast Fl-ATP synthase for the regulation. Biochim Biophys Acta 1555: 140-146.
  • Howe CJ, Fearnley IM, Walker JE, Dyer TA, Gray JC (1985) Nucleotide sequences of the genes for the alpha, beta, and epsilon subunits of wheat chloroplast ATP synthase. Plant Mol Biol 4: 333-345.
  • Huner NPA, Oquist G, Sarhan F (1998) Energy balance and acclimation to light and cold. Trends Plant Sci 3: 224-230.
  • Jiao S, Hilaire E, Guikema JA (2004) Identification and differential accumulation of two isoforms of the CFl-ß subunit under high light stress in Brassica rapa. Plant Physiol Biochem 42: 883-890.
  • Kim J, Mayfield SP (2002) The active side of the thiore- doxin-like domain of chloroplast protein disulfide isomerase, RB60, catalyzes the redox-regulated binding of chloroplast poly(A)-binding protein, RB47, to the 5' untranslated region of psbA mRNA. Plant Cell Physiol 43: 1238-1243.
  • Kügler M, Jänsch L, Kruft V, Schmitz UK, Braun HP (1997) Analysis of the chloroplast protein complexes by blue- native Polyacrylamide gel electrophoresis (BN-PAGE). Photosynth Res 53: 35-44.
  • Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680-685.
  • Lee WJ, Whitmarsh J (1989) Photosynthetic apparatus of pea thylakoid membranes: response to growth irradiance. Plant Physiol 89: 932-940.
  • Leegood RC, Malkin R (1986) Isolation of sub-cellular photosynthetic system. In Photosynthesis energy transduction a practical approach. Hipkins MF, Boker NR, eds, pp 9-26. IRL Press, Oxford, Washington.
  • Maier RM, Neckermann K, Igloi GL, Kossel H (1995) Complete sequence of the maize chloroplast genome : gene content, hotspots of divergence and fine tuning of genetic information by transcript editing. J Mol Biol 251: 614-628.
  • Maione TE, Jagendorf AT (1984) Partial deglycosylation of chloroplast coupling factor 1 (CFj) prevents the recon- stitution of photophosphorylation. Proc Natl Acad Sci USA 81: 3733-3736.
  • Melis A, Manodori A, Glick RE, Ghirardi ML, McCauley SW, Neale PJ (1985) The mechanism of photosynthetic membrane adaptation to environmental stress conditions: a hypothesis on the role of electron-transport capacity and of ATP/NADPH pool in the regulation of thylakoid membrane organization and function. Physiol Veg 23: 757-765.
  • Oswald O, Martin T, Dominy PJ, Graham IA (2001) Plastid redox state and sugars: interactive regulators of nucle- ar-encoded photosynthetic gene expression. Proc Natl Acad Sci USA 98: 2047-2052.
  • Perkins DN, Pappin DJ, Creasy DM, Cottrell JS (1999) Probability-based protein identification by searching sequence databases using mass spectrometry data. Electrophoresis 20: 3551-3567.
  • Pfannschmidt T (2003) Chloroplast redox signals: how photosynthesis controls its own genes. Trends Plant Sci 8: 33-41.
  • Rodermel SR, Bogorad L (1987) Molecular evolution and nucleotide sequences of the maize plastid genes for the α-subunit of CF, (atpA) and the proteolipid subunit of CF0 (atpH). Genetics 116: 127-139.
  • Romanowska E, Drożak A (2006) Comparison of photochemical activities in mesophyll and bundle sheath chloroplasts of C4 subtypes growing in moderate light. Acta Biochim Polon 53: 709-719.
  • Romanowska E, Drożak A, Pokorska B, Shiell BJ, Michalski WP (2006) Organization and activity of photosystems in the mesophyll and bundle sheath chloroplasts of maize. J Plant Physiol 163: 607-618.
  • Sailaja MV, Rama Das VS (2000) Differential photosynthetic acclimation pattern to limiting growth acclimation in two types of C4 plants. Photosynthetica 38: 267-273.
  • Sambrook J, Russel DW (2001) Molecular cloning: a laboratory manual. Cold Spring Harbor, NY Cold Spring Laboratory Press.
  • Strotmann H, Kiefer K, Altvater-Mackensen R (1986) Equilibration of the ATPase reaction of chloroplasts at transition from strong light to weak light. Biochim Biophys Acta 850: 90-96.
  • Towbin H, Staehelin T, Gordon J (1979) Electrophoretic transfer of proteins from Polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc Natl Acad Sci USA 76: 4350-4354.
  • Walters RG (2005) Towards an understanding of photo-synthetic acclimation. J Exp Bot 56: 435-447.
  • Walters RG, Horton P (1994) Acclimation of Arabidopsis thaliana to the light environment: changes in composition of the photosynthetic apparatus. Planta 195: 248- 256.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-b0503018-3a5b-482e-b631-b7ad673c4083
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.