scholarly journals Chloroplast Membrane Remodeling during Freezing Stress Is Accompanied by Cytoplasmic Acidification Activating SENSITIVE TO FREEZING2

2016 ◽  
Vol 171 (3) ◽  
pp. 2140-2149 ◽  
Author(s):  
Allison C. Barnes ◽  
Christoph Benning ◽  
Rebecca L. Roston
Keyword(s):  
Freezing Stress ◽  
Membrane Remodeling ◽  
Chloroplast Membrane ◽  
Cytoplasmic Acidification

The structure of membranes and membrane proteins embedded in amorphous ice

1992 ◽  
Vol 50 (1) ◽  
pp. 432-433
Author(s):  
Uwe Lücken ◽  
Joachim Jäger
Keyword(s):  
Phase Transition ◽  
Transition Temperature ◽  
Membrane Proteins ◽  
Phase Transition Temperature ◽  
Lipid Vesicles ◽  
Freezing Stress ◽  
Amorphous Ice ◽  
Different Temperatures ◽  
Band Pass ◽  
Lipid Polymorphism

TEM imaging of frozen-hydrated lipid vesicles has been done by several groups Thermotrophic and lyotrophic polymorphism has been reported. By using image processing, computer simulation and tilt experiments, we tried to learn about the influence of freezing-stress and defocus artifacts on the lipid polymorphism and fine structure of the bilayer profile. We show integrated membrane proteins do modulate the bilayer structure and the morphology of the vesicles.Phase transitions of DMPC vesicles were visualized after freezing under equilibrium conditions at different temperatures in a controlled-environment vitrification system. Below the main phase transition temperature of 24°C (Fig. 1), vesicles show a facetted appearance due to the quasicrystalline areas. A gradual increase in temperature leads to melting processes with different morphology in the bilayer profile. Far above the phase transition temperature the bilayer profile is still present. In the band-pass-filtered images (Fig. 2) no significant change in the width of the bilayer profile is visible.

TaPK-R1 Overexpressing Transgenic Wheat Lines Enhance Resistance to Sharp Eyespot and Freezing Stress

2016 ◽  
Vol 42 (11) ◽  
pp. 1601
Author(s):  
Mei-Ying LUO ◽  
Wei RONG ◽  
Xue-Ning WEI ◽  
Kun YANG ◽  
Hui-Jun XU ◽  
...  
Keyword(s):  
Transgenic Wheat ◽  
Freezing Stress ◽  
Sharp Eyespot ◽  
Wheat Lines

Cytoplasmic pH regulation in phorbol ester-activated human neutrophils

1986 ◽  
Vol 251 (1) ◽  
pp. C55-C65 ◽  
Author(s):  
S. Grinstein ◽  
W. Furuya
Keyword(s):  
Metabolic Pathways ◽  
Phorbol Esters ◽  
Ph Regulation ◽  
Human Neutrophils ◽  
Hexose Monophosphate ◽  
Cytoplasmic Ph ◽  
Extracellular Acidification ◽  
Hexose Monophosphate Shunt ◽  
Activated Neutrophils ◽  
Cytoplasmic Acidification

Activation of neutrophils by 12-O-tetradecanoylphorbol-13-acetate (TPA) is accompanied by an initial cytoplasmic acidification, followed by an alkalinizing phase due to Na+-H+ countertransport. The source of the acidification, which is fully expressed by activation with TPA in Na+-free or amiloride-containing media, was investigated. The acidification phase was detected also in degranulated and enucleated cytoplasts, ruling out a major contribution by the nucleus or secretory vesicles. Cytoplasmic acidification was found to be associated with an extracellular acidification, suggesting metabolic generation of H+. Two principal metabolic pathways are stimulated in activated neutrophils: the reduction of O2 by NADPH-oxidase and the hexose monophosphate shunt. A good correlation was found between the activity of these pathways and the changes in cytoplasmic pH. Inhibition of superoxide synthesis prevented the TPA-induced cytoplasmic acidification. Moreover, activation of the hexose monophosphate shunt with permeable NADPH-oxidizing agents (in the absence of TPA) also produced a cytoplasmic acidification. Cytoplasmic acidification was also elicited by exogenous diacylglycerol and by other beta-phorbol diesters, which are activators of the kinase, but not by unesterified phorbol or by alpha-phorbol diesters, which are biologically inactive. The results suggest that the cytoplasmic acidification induced by phorbol esters in neutrophils reflects accumulation of H+ liberated during the metabolic burst that follows activation.

scholarly journals Correlative AFM and fluorescence imaging demonstrate nanoscale membrane remodeling and ring-like and tubular structure formation by septins

Nanoscale ◽  
2021 ◽  
Author(s):  
Anthony Vial ◽  
Cyntia Taveneau ◽  
Luca Costa ◽  
brieuc chauvin ◽  
hussein nasrallah ◽  
...  
Keyword(s):  
Plasma Membrane ◽  
Cell Division ◽  
Structure Formation ◽  
Fluorescence Imaging ◽  
Tubular Structure ◽  
Membrane Remodeling

Septins are ubiquitous cytoskeletal filaments that interact with the inner plasma membrane and are essential for cell division in eukaryotes. In cellular contexts, septins are often localized at micrometric gaussian...

scholarly journals The role of VPS4 in ESCRT-III polymer remodeling

2019 ◽  
Vol 47 (1) ◽  
pp. 441-448 ◽  
Author(s):  
Christophe Caillat ◽  
Sourav Maity ◽  
Nolwenn Miguet ◽  
Wouter H. Roos ◽  
Winfried Weissenhorn
Keyword(s):  
Active Role ◽  
Mechanistic Models ◽  
Membrane Remodeling ◽  
Filament Formation ◽  
Enveloped Viruses ◽  
Endosomal Sorting ◽  
Membrane Fission ◽  
Dynamic Assembly ◽  
Inside Out

Abstract The endosomal sorting complex required for transport-III (ESCRT-III) and VPS4 catalyze a variety of membrane-remodeling processes in eukaryotes and archaea. Common to these processes is the dynamic recruitment of ESCRT-III proteins from the cytosol to the inner face of a membrane neck structure, their activation and filament formation inside or at the membrane neck and the subsequent or concomitant recruitment of the AAA-type ATPase VPS4. The dynamic assembly of ESCRT-III filaments and VPS4 on cellular membranes induces constriction of membrane necks with large diameters such as the cytokinetic midbody and necks with small diameters such as those of intraluminal vesicles or enveloped viruses. The two processes seem to use different sets of ESCRT-III filaments. Constriction is then thought to set the stage for membrane fission. Here, we review recent progress in understanding the structural transitions of ESCRT-III proteins required for filament formation, the functional role of VPS4 in dynamic ESCRT-III assembly and its active role in filament constriction. The recent data will be discussed in the context of different mechanistic models for inside-out membrane fission.

Fluorescence as a tool in photosynthesis research: application in studies of photoinhibition, cold acclimation and freezing stress

1989 ◽  
Vol 323 (1216) ◽  
pp. 281-293 ◽  
Keyword(s):  
Quantum Yield ◽  
Cold Acclimation ◽  
Spinacia Oleracea ◽  
Photosynthetic Apparatus ◽  
Fluorescence Induction ◽  
High Light ◽  
Thermal Dissipation ◽  
Freezing Stress ◽  
Chlorophyll Fluorescence Induction ◽  
Freezing And Thawing

Chlorophyll fluorescence induction (at 20 °C and 77 K) and quenching were analysed in relation to effects of environmental stresses imposed by chilling in high light and by freezing and thawing of spinach ( Spinacia oleracea L.) leaves. The data indicate that cold acclimation of spinach plants, which leads to increased frost tolerance of the leaves, results in decreased susceptibility to photoinhibition of photosynthesis at chilling temperatures. When plants acclimated to 18 °C and 260-300 µmol quanta m -2 s -1 were exposed to higher light (550 µmol quanta m -2 s -1 ) at 4 °C, they developed strong photoinhibition, as characterized by decreased quantum yield of O 2 evolution and decreased ratio of variable: maximum fluorescence (F V /F M ) of photosystem II. The decrease in F V /F M resulted from a decline in F V and an increase in F 0 . The F V /F M ratio was lowered to a significantly greater extent when induction was recorded at 20 °C, as compared with 77 K. The effects related to photoinhibition were fully reversible at 18 °C in dim light. Plants that had been cold-acclimated for 10 days exhibited slightly decreased quantum yield and lowered F V /F M ratio. However, they did not show further photoinhibition on exposure to 550 µmol quanta m -2 s -1 at 4 °C. The reversible photoinhibition is discussed as a protective pathway serving for thermal dissipation of excessive light energy. It is hypothesized that such a mechanism prevents destruction of the photosynthetic apparatus, until other means of protection become effective during long-term acclimation to high light. Inhibition of photosynthetic carbon assimilation caused by freezing and thawing of leaves in the dark was closely correlated with inhibition of photochemical fluorescence quenching (q Q ). As a sensitive response of the thylakoid membranes to freezing stress, the energy-dependent quenching, q E , was inhibited. Only more severe impact of freezing caused a significant decline in the F V /F M ratio. It is concluded that measurements of fluorescence induction signals ( F V /F M ratios) provide a sensitive tool with which to investigate photoinhibition, whereas freezing damage to the photosynthetic system can be detected more readily by the quenching coefficients q Q and q E than by F V /F M ratios.

scholarly journals Correction to: Transcriptome profiling of fully open flowers in a frost‑tolerant almond genotype in response to freezing stress

2017 ◽  
Vol 293 (1) ◽  
pp. 165-165
Author(s):  
Batool Hosseinpour ◽  
Sadegh Sepahvand ◽  
Kazem Kamali Aliabad ◽  
MohammadReza Bakhtiarizadeh ◽  
Ali Imani ◽  
...  
Keyword(s):  
Transcriptome Profiling ◽  
Freezing Stress

The eyespot of Chlamydomonas eugametos: a freeze-etch study

1973 ◽  
Vol 51 (4) ◽  
pp. 817-819 ◽  
Author(s):  
Kazuo Nakamura ◽  
D. F. Bray ◽  
J. W. Costerton ◽  
E. B. Wagenaar
Keyword(s):  
Cleavage Plane ◽  
Chloroplast Membrane ◽  
Ordered Arrays ◽  
Chlamydomonas Eugametos

The ultrastructure of the eyespot region of Chlamydomonas eugametos was studied with the freeze-etch technique. In the region of the eyespot the outer chloroplast membrane, when fractured medially, showed the presence of bulgings which appeared as either depressions or bumps depending on the cleavage plane. These deformations of the outer chloroplast membrane produced by the granules of the eyespot are about 80 mμ in diameter and form ordered arrays of 800 or more particles.

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