Hg2+ reacts with different components of the NADPH:: Protochlorophyllide oxidoreductase macrodomains

被引:25
作者
Solymosi, K
Lenti, K
Mysliwa-Kurdziel, B
Fidy, J
Strzalka, K
Böddi, B
机构
[1] Eotvos Lorand Univ, Dept Plant Anat, H-1117 Budapest, Hungary
[2] Jagiellonian Univ, Dept Plant Physiol & Biochem, Krakow, Poland
[3] Semmelweis Univ, Dept Biophys & Radiat Biol, Bucharest, Romania
[4] Hungarian Acad Sci, MTS SE Res Grp Biophys, Budapest, Hungary
关键词
mercury; Hg2+; protochlorophyllide; NADPH; protopheophorbide; Shibata shift; activity loss;
D O I
10.1055/s-2004-817893
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The molecular background of Hg2+-induced inhibition of protochlorophyllide (Pchlide) photoreduction was investigated in homogenates of dark-grown wheat leaves. Our earlier work showed that 15 min incubation with 10(-2) M Hg2+ completely inhibits the activity of NADPH: Pchlide oxidoreductase (Lenti et al., 2002). Detailed analysis of spectra recorded at 10 K indicated the appearance of emission bands at 638 and 650 nm, which are characteristic for NADP(+)-Pchlide complexes. Fluorescence emission spectra recorded with different excitation wavelengths, fluorescence lifetime measurements and the analysis of acetone extractions revealed that Hg2+ can also react directly with Pchlide, resulting in protopheophorbide formation. At 10(-3) M Hg2+, the phototransformation was complete but the blue shift of the chlorophyllide emission band speeded up remarkably. This indicates oxidation of the NADPH molecules that have a structural role in keeping together the etioplast inner membrane components. We suggest a complex model for the Hg2+ effect: depending on concentration it can react with any components of the NADPH:Pchlide oxidoreductase macrodomains.
引用
收藏
页码:358 / 367
页数:10
相关论文
共 68 条
[1]   The importance of the C-terminal region and Cys residues for the membrane association of the NADPH:protochlorophyllide oxidoreductase in pea [J].
Aronsson, H ;
Sundqvist, C ;
Timko, MP ;
Dahlin, C .
FEBS LETTERS, 2001, 502 (1-2) :11-15
[2]  
Aylward G., 1974, CHEM DATA
[3]   MERCURY BINDING TO HUMAN HEMOGLOBIN [J].
BARLTROP, D ;
SMITH, AM .
EXPERIENTIA, 1973, 29 (09) :1178-1179
[4]   ANALYSIS OF THE 77-K FLUORESCENCE EMISSION AND EXCITATION-SPECTRA OF ISOLATED ETIOPLAST INNER MEMBRANES [J].
BODDI, B ;
RYBERG, M ;
SUNDQVIST, C .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1993, 21 (2-3) :125-133
[5]   Early reactions of light-induced protochlorophyllide and chlorophyllide transformations analyzed in vivo at room temperature with a diode array spectrofluorometer [J].
Böddi, B ;
Popovic, R ;
Franck, F .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2003, 69 (01) :31-39
[6]   IDENTIFICATION OF 4 UNIVERSAL PROTOCHLOROPHYLLIDE FORMS IN DARK-GROWN LEAVES BY ANALYSES OF THE 77-K FLUORESCENCE EMISSION-SPECTRA [J].
BODDI, B ;
RYBERG, M ;
SUNDQVIST, C .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1992, 12 (04) :389-401
[7]   Room temperature fluorescence spectra of protochlorophyllide and chlorophyllide forms in etiolated bean leaves [J].
Boddi, B ;
Franck, F .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1997, 41 (1-2) :73-82
[8]   ON THE AGGREGATIONAL STATES OF PROTOCHLOROPHYLLIDE AND ITS PROTEIN COMPLEXES IN WHEAT ETIOPLASTS [J].
BODDI, B ;
LINDSTEN, A ;
RYBERG, M ;
SUNDQVIST, C .
PHYSIOLOGIA PLANTARUM, 1989, 76 (02) :135-143
[9]  
BODDI B, 1991, PHOTOCHEM PHOTOBIOL, V53, P667
[10]  
BODDI B, 1995, PHOTOSYNTHETICA, V31, P411