Literature DB >> 16666147

Hierarchical Response of Light Harvesting Chlorophyll-Proteins in a Light-Sensitive Chlorophyll b-Deficient Mutant of Maize.

B A Greene1, D R Allred, D T Morishige, L A Staehelin.   

Abstract

The light-sensitive chlorophyll b (Chl b)-deficient oil yellow-yellow green (OY-YG) mutant of maize (Zea mays) grown under conditions of high light exhibits differential reductions in the accumulation of the three major Chl b-containing antenna complexes and characteristic changes in thylakoid architecture. When observed by freeze-fracture electron microscopy, the most notable changes in the OY-YG thylakoid structure are: (a) a major reduction in the number of 8 nanometer particles of the protoplasmic fracture face of stacked membrane regions (PFs) paralleled by a 60% reduction in the chlorophyll-proteins (CP) associated with the peripheral light harvesting complex (LHCII) for photosystem II (PSII) and which give rise to the LHCII oligomer/monomer (CPII(*)/CPII) bands on mildly dissociated green gels; (b) a sizable decrease in the proportion of 11 to 13 nanometer particles of the protoplasmic fracture face of unstacked membrane regions (PFu) that parallels the loss of light harvesting complex I (LHCI) antennae from photosystem I (PSI) centers and a 40% reduction of the band containing CP1 and LHCI (CPI(*)) on mildly dissociating green gels; (c) an unchanged or slightly increased average size of particles of the exoplasmic fracture face of stacked (or appressed) membrane regions (EFs) along with a relative increase in CP29, the postulated bound LHC of PSII, and of CP47 and CP43, PSII core antenna complexes. This latter result sets the OY-YG mutant apart from all other Chl b-deficient mutants studied to date, all of which possess EFs particles that are substantially reduced in size. Based on these findings, we postulate that the bound LHCII associated with EFs particles consists mostly of CP29 chlorophyll proteins and very little, if any, CPII(*)/CPII chlorophyll proteins. Indeed, the CPII(*)/CPII chlorophyll proteins may be exclusively associated with the ;peripheral' LHCII units that give rise to 8 nanometer PF particles. The differential effect of the Chl b deficiency on the accumulation of the three main antenna complexes (CPII(*)/CPII>CPI(*)>CP29) suggests, furthermore, that there is a hierarchy among Chl b-binding proteins, and that this hierarchy might be an integral part of long-term photoregulation mediating Chl b partitioning in the chloroplast.

Entities:  

Year:  1988        PMID: 16666147      PMCID: PMC1054757          DOI: 10.1104/pp.87.2.357

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  15 in total

1.  COPPER ENZYMES IN ISOLATED CHLOROPLASTS. POLYPHENOLOXIDASE IN BETA VULGARIS.

Authors:  D I Arnon
Journal:  Plant Physiol       Date:  1949-01       Impact factor: 8.340

2.  Demonstration of transcriptional regulation of specific genes by phytochrome action.

Authors:  J Silverthorne; E M Tobin
Journal:  Proc Natl Acad Sci U S A       Date:  1984-02       Impact factor: 11.205

3.  Phosphorylation of spinach chlorophyll-protein complexes. CPII, but not CP29, CP27, or CP24, is phosphorylated in vitro.

Authors:  T G Dunahay; G Schuster; L A Staehelin
Journal:  FEBS Lett       Date:  1987-05-04       Impact factor: 4.124

Review 4.  Regulation of chloroplast membrane function: protein phosphorylation changes the spatial organization of membrane components.

Authors:  L A Staehelin; C J Arntzen
Journal:  J Cell Biol       Date:  1983-11       Impact factor: 10.539

5.  LR white resin and improved on-grid immunogold detection of vicilin, a pea seed storage protein.

Authors:  S Craig; C Miller
Journal:  Cell Biol Int Rep       Date:  1984-10

6.  Lateral mobility of the light-harvesting complex in chloroplast membranes controls excitation energy distribution in higher plants.

Authors:  D J Kyle; L A Staehelin; C J Arntzen
Journal:  Arch Biochem Biophys       Date:  1983-04-15       Impact factor: 4.013

7.  Fractionation of Thylakoid Membranes with the Nonionic Detergent Octyl-beta-d-glucopyranoside: RESOLUTION OF CHLOROPHYLL-PROTEIN COMPLEX II INTO TWO CHLOROPHYLL-PROTEIN COMPLEXES.

Authors:  E L Camm; B R Green
Journal:  Plant Physiol       Date:  1980-09       Impact factor: 8.340

8.  Isolation of photosystem I complexes from octyl glucoside/sodium dodecyl sulfate solubilized spinach thylakoids : characterization and reconstitution into liposomes.

Authors:  T G Dunahay; L A Staehelin
Journal:  Plant Physiol       Date:  1985-07       Impact factor: 8.340

9.  Analysis of the Light-harvesting Pigment-Protein Complex of Wild Type and a Chlorophyll-b-less Mutant of Barley.

Authors:  J J Burke; K E Steinback; C J Arntzen
Journal:  Plant Physiol       Date:  1979-02       Impact factor: 8.340

10.  Biosynthesis of the light-harvesting chlorophyll a/b protein. Polypeptide turnover in darkness.

Authors:  J Bennett
Journal:  Eur J Biochem       Date:  1981-08
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  17 in total

1.  Assembly of the Light-Harvesting Complexes (LHCs) of Photosystem II (Monomeric LHC IIb Complexes Are Intermediates in the Formation of Oligomeric LHC IIb Complexes).

Authors:  B. W. Dreyfuss; J. P. Thornber
Journal:  Plant Physiol       Date:  1994-11       Impact factor: 8.340

2.  Light-induced biogenesis of the light-harvesting complexes of Photosystems I and II : Gene expression and protein accumulation.

Authors:  D T Morishige; S Preiss
Journal:  Photosynth Res       Date:  1995-05       Impact factor: 3.573

3.  Chromatic regulation inChlamydomonas reinhardtii alters photosystem stoichiometry and improves the quantum efficiency of photosynthesis.

Authors:  A Melis; A Murakami; J A Nemson; K Aizawa; K Ohki; Y Fujita
Journal:  Photosynth Res       Date:  1996-03       Impact factor: 3.573

4.  Temperature sensitivity as a general phenomenon in a collection of chlorophyll-deficient mutants of sweetclover (Melilotus alba).

Authors:  C M Yang; J C Osterman; J Markwell
Journal:  Biochem Genet       Date:  1990-02       Impact factor: 1.890

5.  Severity of mutant phenotype in a series of chlorophyll-deficient wheat mutants depends on light intensity and the severity of the block in chlorophyll synthesis.

Authors:  T G Falbel; J B Meehl; L A Staehelin
Journal:  Plant Physiol       Date:  1996-10       Impact factor: 8.340

6.  Chlorophyll a/b binding (CAB) polypeptides of CP29, the internal chlorophyll a/b complex of PSII: characterization of the tomato gene encoding the 26 kDa (type I) polypeptide, and evidence for a second CP29 polypeptide.

Authors:  E Pichersky; R Subramaniam; M J White; J Reid; R Aebersold; B R Green
Journal:  Mol Gen Genet       Date:  1991-06

7.  Occurrence of Temperature-Sensitive Phenotypic Plasticity in Chlorophyll-Deficient Mutants of Arabidopsis thaliana.

Authors:  J Markwell; J C Osterman
Journal:  Plant Physiol       Date:  1992-01       Impact factor: 8.340

8.  Organization of the Light-Harvesting Complex of Photosystem I and Its Assembly during Plastid Development.

Authors:  B. W. Dreyfuss; J. P. Thornber
Journal:  Plant Physiol       Date:  1994-11       Impact factor: 8.340

9.  The aba Mutant of Arabidopsis thaliana (L.) Heynh. Has Reduced Chlorophyll Fluorescence Yields and Reduced Thylakoid Stacking.

Authors:  C D Rock; N R Bowlby; S Hoffmann-Benning; J A Zeevaart
Journal:  Plant Physiol       Date:  1992-12       Impact factor: 8.340

10.  Chloroplasts of Arabidopsis thaliana homozygous for the ch-1 locus lack chlorophyll b, lack stable LHCPII and have stacked thylakoids.

Authors:  D L Murray; B D Kohorn
Journal:  Plant Mol Biol       Date:  1991-01       Impact factor: 4.076

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