Isoelectric points of spinach thylakoid membrane surfaces as determined by cross partition

1979 ◽  
Vol 552 (2) ◽  
pp. 238-246 ◽  
Author(s):  
Hans-Erik Åkerlund ◽  
Bertil Andersson ◽  
Agneta Persson ◽  
Per-Åke Albertsson
Author(s):  
Kerry K. Karukstis ◽  
Marie Y. Kao ◽  
Daniel A. Savin ◽  
Rachel A. Bittker ◽  
Karla J. Kaphengst ◽  
...  

1986 ◽  
Vol 15 (3) ◽  
pp. 497-503 ◽  
Author(s):  
P. Kicq ◽  
K.R. Temsamani ◽  
K. De Meutter ◽  
E. Goormaghtigh ◽  
J.M. Ruysschaert

1988 ◽  
Vol 91 (4) ◽  
pp. 577-586
Author(s):  
K.R. Miller ◽  
J.S. Jacob ◽  
T. Burger-Wiersma ◽  
H.C. Matthijs

Prochlorothrix hollandica is a newly described photosynthetic prokaryote, which contains chlorophylls a and b. In this paper we report the results of freeze fracture and freeze etch studies of the organization of the photosynthetic thylakoid membranes of Prochlorothrix. These membranes exhibit four distinct fracture faces in freeze fractured preparations, two of which are derived from membrane splitting in stacked regions of the thylakoid membrane, and two of which are derived from nonstacked regions. The existence of these four faces confirms that the thylakoid membranes of Prochlorothrix, like those of green plants, display true membrane stacking and have different internal composition in stacked and non-stacked regions, a phenomenon that has been given the name lateral heterogeneity. The general details of these fracture faces are similar to those of green plants, although the intramembrane particles of Prochlorothrix are generally smaller than those of green plants by as much as 30%. Freeze etched membrane surfaces have also been studied, and the results of these studies confirm freeze fracture observations. The outer surface of the thylakoid membrane displays both small (less than 8.0 nm) and large (greater than 10.0 nm) particles. The inner surface of the thylakoid membrane is covered with tetrameric particles, which are concentrated into stacked membrane regions, a situation that is similar to the inner surfaces of the thylakoid membranes of green plants. These tetramers have never before been reported in a prokaryote. The photosynthetic membranes of Prochlorothrix therefore represent a prokaryotic system that is remarkably similar, in structural terms, to the photosynthetic membranes found in chloroplasts of green plants.


eLife ◽  
2021 ◽  
Vol 10 ◽  
Author(s):  
Rosa Pipitone ◽  
Simona Eicke ◽  
Barbara Pfister ◽  
Gaetan Glauser ◽  
Denis Falconet ◽  
...  

Light triggers chloroplast differentiation whereby the etioplast transforms into a photosynthesizing chloroplast and the thylakoid rapidly emerges. However, the sequence of events during chloroplast differentiation remains poorly understood. Using Serial Block Face Scanning Electron Microscopy (SBF-SEM), we generated a series of chloroplast 3D reconstructions during differentiation, revealing chloroplast number and volume and the extent of envelope and thylakoid membrane surfaces. Furthermore, we used quantitative lipid and whole proteome data to complement the (ultra)structural data, providing a time-resolved, multi-dimensional description of chloroplast differentiation. This showed two distinct phases of chloroplast biogenesis: an initial photosynthesis-enabling ‘Structure Establishment Phase’ followed by a ‘Chloroplast Proliferation Phase’ during cell expansion. Moreover, these data detail thylakoid membrane expansion during de-etiolation at the seedling level and the relative contribution and differential regulation of proteins and lipids at each developmental stage. Altogether, we establish a roadmap for chloroplast differentiation, a critical process for plant photoautotrophic growth and survival.


1981 ◽  
Vol 642 (2) ◽  
pp. 438-442 ◽  
Author(s):  
Kenneth E. Eigenberg ◽  
William R. Croasmun ◽  
Sunney I. Chant

2020 ◽  
Author(s):  
Benedikt Junglas ◽  
Amelie Axt ◽  
Carmen Siebenaller ◽  
Hilal Sonel ◽  
Nadja Hellmann ◽  
...  

ABSTRACTThe inner membrane-associated protein of 30 kDa (IM30) is essential in chloroplasts and cyanobacteria. The spatio-temporal cellular localization of the protein appears to be highly dynamic and triggered by internal as well as external stimuli, mainly light intensity. A soluble fraction of the protein is localized in the cyanobacterial cytoplasm or the chloroplast stroma, respectively. Additionally, the protein attaches to the thylakoid membrane as well as to the chloroplast inner envelope or the cyanobacterial cytoplasmic membrane, respectively, especially under conditions of membrane stress. IM30 is involved in thylakoid membrane biogenesis and/or maintenance, where it either stabilizes membranes and/or triggers membrane-fusion processes. These apparently contradicting processes have to be tightly controlled and separated spatiotemporally in chloroplasts and cyanobacteria. The latter process depends on Mg2+-binding to IM30; yet, it still is unclear how Mg2+-loaded IM30 interacts with membranes and promotes membrane fusion. Here we show that interaction of Mg2+ with IM30 results in increased binding of IM30 to native as well as model membranes. Via Atomic Force Microscopy in liquid, IM30-induced bilayer defects were observed in solid-supported bilayers in presence of Mg2+. The observed interaction of IM30 with membrane surfaces differs dramatically from previously observed membrane-stabilizing, carpet-like structures in the absence of Mg2+. Mg2+-induced alterations of the IM30 structure switches the IM30 activity from a membrane-stabilizing to a membrane-destabilizing function, a crucial step in membrane fusion.


1978 ◽  
Vol 33 (3-4) ◽  
pp. 261-265 ◽  
Author(s):  
R. G. Binder ◽  
B. R. Selman

Conditions for washed, spinach thylakoid membranes to catalyze cyclic phosphorylation using ferredoxin as the cofactor for electron transfer have been re-examined. It was found necessary to “redox poise” the system; however, the best method to accomplish the poising seemed to be the use of a reductant (glucose-6-phosphate) and not by optimizing the rate of phosphorylation with 3- (3,4-dichlorophenyl)-1,1-dimethyl urea (DCMU). Under these conditions, ferredoxin catalyzed cyclic phosphorylation was found to be sensitive to the inhibitors antimycin A and dibromothymo- quinone (DBMIB). The inhibition of ferredoxin catalyzed cyclic phosphorylation by DBMIB, but not by antimycin A, was completely reversed by N, N, N′ N′-tetramethyl-p-phcnylenediamine (TMPD). These data are taken as further support for the function of plastoquinone in ferredoxin catalyzed cyclic phosphorylation. The effect of TMPD in reversing the DBMIB inhibition is inter­preted as the formation of a TMPD bypass on the internal side of the thylakoid membrane around the DBMIB site of inhibition.


2020 ◽  
Author(s):  
Rosa Pipitone ◽  
Simona Eicke ◽  
Barbara Pfister ◽  
Gaetan Glauser ◽  
Denis Falconet ◽  
...  

AbstractLight triggers chloroplast differentiation whereby the etioplast transforms into a photosynthesizing chloroplast and the thylakoid rapidly emerges. However, the sequence of events during chloroplast differentiation remains poorly understood. Using Serial Block Face Scanning Electron Microscopy (SBF-SEM), we generated a series of chloroplast 3D reconstructions during differentiation, revealing chloroplast number and volume and the extent of envelope and thylakoid membrane surfaces. Furthermore, we used quantitative lipid and whole proteome data to complement the (ultra)structural data, providing a time-resolved, multi-dimensional description of chloroplast differentiation. This showed two distinct phases of chloroplast biogenesis: an initial photosynthesis-enabling ‘Structure Establishment Phase’ followed by a ‘Chloroplast Proliferation Phase’ during cell expansion. Moreover, these data detail thylakoid membrane expansion during de-etiolation at the seedling level and the relative contribution and differential regulation of proteins and lipids at each developmental stage. Altogether, we establish a roadmap for chloroplast differentiation, a critical process for plant photoautotrophic growth and survival.


Author(s):  
L. Andrew Staehelin

Freeze-etched membranes usually appear as relatively smooth surfaces covered with numerous small particles and a few small holes (Fig. 1). In 1966 Branton (1“) suggested that these surfaces represent split inner mem¬brane faces and not true external membrane surfaces. His theory has now gained wide acceptance partly due to new information obtained from double replicas of freeze-cleaved specimens (2,3) and from freeze-etch experi¬ments with surface labeled membranes (4). While theses studies have fur¬ther substantiated the basic idea of membrane splitting and have shown clearly which membrane faces are complementary to each other, they have left the question open, why the replicated membrane faces usually exhibit con¬siderably fewer holes than particles. According to Branton's theory the number of holes should on the average equal the number of particles. The absence of these holes can be explained in either of two ways: a) it is possible that no holes are formed during the cleaving process e.g. due to plastic deformation (5); b) holes may arise during the cleaving process but remain undetected because of inadequate replication and microscope techniques.


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