Gabaculine alters plastid development and differentially affects abundance of plastid-encoded DPOR and nuclear-encoded GluTR and FLU-like proteins in spruce cotyledons

Copyright 2010 Elsevier GmbH. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Journal of plant physiology. - 1979. - 167(2010), 9 vom: 15. Juni, Seite 693-700
1. Verfasser: Demko, Viktor (VerfasserIn)
Weitere Verfasser: Pavlovic, Andrej, Hudák, Ján
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2010
Zugriff auf das übergeordnete Werk:Journal of plant physiology
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Cyclohexanecarboxylic Acids Plant Proteins gabaculine 3F3ENU341O Aldehyde Oxidoreductases EC 1.2.- glutamyl tRNA reductase EC 1.2.1.- mehr... Oxidoreductases Acting on CH-CH Group Donors EC 1.3.- protochlorophyllide reductase EC 1.3.1.33
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100 1 |a Demko, Viktor  |e verfasserin  |4 aut 
245 1 0 |a Gabaculine alters plastid development and differentially affects abundance of plastid-encoded DPOR and nuclear-encoded GluTR and FLU-like proteins in spruce cotyledons 
264 1 |c 2010 
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500 |a Date Revised 30.09.2020 
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500 |a Citation Status MEDLINE 
520 |a Copyright 2010 Elsevier GmbH. All rights reserved. 
520 |a Synthesis of 5-aminolevulinic acid (ALA) represents a rate limiting step in the tetrapyrrole biosynthetic pathway, and is regulated by metabolic feedback control of glutamyl-tRNA reductase (GluTR) activity. The FLU protein has been attributed to this regulation. Later in the biosynthetic pathway, reduction of protochlorophyllide (Pchlide), catalyzed by protochlorophyllide oxidoreductase (POR), ensures another important regulatory step in the chlorophyll biosynthesis. In the present work, we investigated the expression and cellular abundance of nuclear-encoded and plastid-encoded proteins involved in ALA synthesis and Pchlide reduction in Norway spruce (Picea abies L. Karst.) as a representative of plant species with high ability to synthesize chlorophyll in the dark. Using dark-grown, light/dark-grown and gabaculine-treated seedlings, we demonstrated that gabaculine-impaired etiochloroplast and chloroplast development has no negative effect on GluTR accumulation in the cotyledons. However, in contrast to control plants, the relative amount of GluTR was similar both in the dark-grown and light/dark-grown gabaculine-treated seedlings. We identified a partial sequence of the FLU-like gene in Norway spruce, and using antibodies against the FLU-like protein (FLP), we showed that FLP accumulated mostly in the dark-grown control seedlings and gabaculine-treated seedlings. In contrast to nuclear-encoded GluTR and FLP, accumulation of plastid-encoded light-independent POR (DPOR) was sensitive to gabaculine treatment. The levels of DPOR subunits were substantially lower in the light/dark-grown control seedlings and gabaculine-treated seedlings, although the corresponding genes chlL, chlN and chlB were expressed. Since we analyzed the samples with different plastid types, plastid ultrastructure and physiological parameters like Pchlide and chlorophyll contents, in vivo chlorophyll fluorescence and photosynthetic efficiency of the seedlings were characterized. Apart from etiochloroplast-specific accumulation of the DPOR subunits, we described, in some detail, additional specific features of chlorophyll biosynthesis in the spruce seedlings that differ from those known in angiosperms 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 7 |a Cyclohexanecarboxylic Acids  |2 NLM 
650 7 |a Plant Proteins  |2 NLM 
650 7 |a gabaculine  |2 NLM 
650 7 |a 3F3ENU341O  |2 NLM 
650 7 |a Aldehyde Oxidoreductases  |2 NLM 
650 7 |a EC 1.2.-  |2 NLM 
650 7 |a glutamyl tRNA reductase  |2 NLM 
650 7 |a EC 1.2.1.-  |2 NLM 
650 7 |a Oxidoreductases Acting on CH-CH Group Donors  |2 NLM 
650 7 |a EC 1.3.-  |2 NLM 
650 7 |a protochlorophyllide reductase  |2 NLM 
650 7 |a EC 1.3.1.33  |2 NLM 
700 1 |a Pavlovic, Andrej  |e verfasserin  |4 aut 
700 1 |a Hudák, Ján  |e verfasserin  |4 aut 
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856 4 0 |u http://dx.doi.org/10.1016/j.jplph.2009.12.008  |3 Volltext 
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