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Recombinant water-soluble chlorophyll protein from Brassica oleracea Var. Botrys binds various chlorophyll derivatives

Biochemistry. Bd. 42. H. 24. Washington, DC: American Chemical Society 2003 S. 7427 - 7433

Erscheinungsjahr: 2003

ISBN/ISSN: 0006-2960 ; 1520-4995

Publikationstyp: Zeitschriftenaufsatz

Sprache: Englisch

Doi/URN: 10.1021/bi034207r

Volltext über DOI/URN

Geprüft:Bibliothek

Inhaltszusammenfassung


A gene coding for water-soluble chlorophyll-binding protein (WSCP) from Brassica oleracea var. Botrys has been used to express the protein, extended by a hexahistidyl tag, in Escherichia coli. The protein has been refolded in vitro to study its pigment binding behavior. Recombinant WSCP was found to bind two chlorophylls (Chls) per tetrameric protein complex but no carotenoids in accordance with previous observations with the native protein [Satoh, H., Nakayama, K., Okada, M. (1998) J. Biol. ...A gene coding for water-soluble chlorophyll-binding protein (WSCP) from Brassica oleracea var. Botrys has been used to express the protein, extended by a hexahistidyl tag, in Escherichia coli. The protein has been refolded in vitro to study its pigment binding behavior. Recombinant WSCP was found to bind two chlorophylls (Chls) per tetrameric protein complex but no carotenoids in accordance with previous observations with the native protein [Satoh, H., Nakayama, K., Okada, M. (1998) J. Biol. Chem. 273, 30568-30575]. WSCP binds Chl a, Chl b, bacteriochlorophyll a, and the Zn derivative of Chl a but not pheophytin a, indicating that the central metal ion in Chl is essential for binding. WSCP also binds chlorophyllides a and b and even the more distant Chl precursor Mg-protoporphyrin IX; however, these pigments fail to induce oligomerization of the protein. We conclude that the phytol group in bound Chi plays a role in the formation of tetrameric WSCP complexes. If WSCP in fact binds Chi or its derivative(s) in vivo, the lack of carotenoids in pigmented WSCP raises the question of how photooxidation, mediated by triplet-excited Chl and singlet oxygen, is prohibited. We show by spin-trap electron-paramagnetic resonance that the light-induced singlet-oxygen formation of WSCP-bound Chi is lower by a factor of about 4 than that of unbound Chl. This as-yet-unknown mechanism of WSCP to protect its bound Chi against photooxidation supports the notion that WSCP may function as a transient carrier of Chi or its derivatives.» weiterlesen» einklappen

Autoren


Schmidt, Kristin (Autor)
Fufezan, Christian (Autor)
Krieger-Liszkay, Anja (Autor)
Satoh, Hiroyuki (Autor)
Paulsen, Harald (Autor)

Klassifikation


DFG Fachgebiet:
2.12 - Pflanzenwissenschaften

DDC Sachgruppe:
Pflanzen (Botanik)