scholarly journals A cell wall-associated gene network shapes leaf boundary domains

2021 ◽  
Author(s):  
Nathalie Bouré ◽  
Alexis Peaucelle ◽  
Magali Goussot ◽  
Bernard Adroher ◽  
Ludivine Soubigou-Taconnat ◽  
...  
Keyword(s):  
Cell Wall ◽  
Cell Growth ◽  
Gene Network ◽  
Force Microscopy ◽  
Atomic Force ◽  
Wall Stiffness ◽  
A Cell ◽  
Wall Loosening ◽  
Building Plant ◽  
Molecular Framework

Boundary domains delimit and organize organ growth throughout plant development almost relentlessly building plant architecture and morphogenesis. Boundary domains display reduced growth and orchestrate development of adjacent tissues in a non-cell autonomous manner. How these two functions are achieved remains elusive despite the identification of several boundary-specific genes. Here, we show using morphometrics at the organ and cellular levels that leaf boundary domain development requires SPINDLY (SPY), an O-fucosyltransferase, to act as cell growth repressor. Further we show that SPY acts redundantly with the CUP-SHAPED COTYLEDON transcription factors (CUC2 and CUC3), which are major determinants of boundaries development. Accordingly at the molecular level, CUC2 and SPY repress a common set of genes involved in cell wall loosening providing a molecular framework for the growth repression associated with boundary domains. Atomic force microscopy (AFM) confirmed that young leaf boundary domain cells have stiffer cell walls than marginal outgrowth. This differential cell wall stiffness was reduced in spy mutant. Taken together our data reveal a concealed CUC2 cell wall associated gene network linking tissue patterning with cell growth and mechanics.

scholarly journals Touch-induced seedling morphological changes are determined by ethylene-regulated pectin degradation

2020 ◽  
Vol 6 (48) ◽  
pp. eabc9294
Author(s):  
Qingqing Wu ◽  
Yue Li ◽  
Mohan Lyu ◽  
Yiwen Luo ◽  
Hui Shi ◽  
...  
Keyword(s):  
Cell Wall ◽  
Morphological Changes ◽  
Mechanical Forces ◽  
Ethylene Signaling ◽  
Pectin Degradation ◽  
Force Microscopy ◽  
Mechanical Responses ◽  
Atomic Force ◽  
Wall Stiffness ◽  
Molecular Framework

How mechanical forces regulate plant growth is a fascinating and long-standing question. After germination underground, buried seedlings have to dynamically adjust their growth to respond to mechanical stimulation from soil barriers. Here, we designed a lid touch assay and used atomic force microscopy to investigate the mechanical responses of seedlings during soil emergence. Touching seedlings induced increases in cell wall stiffness and decreases in cell elongation, which were correlated with pectin degradation. We revealed that PGX3, which encodes a polygalacturonase, mediates touch-imposed alterations in the pectin matrix and the mechanics of morphogenesis. Furthermore, we found that ethylene signaling is activated by touch, and the transcription factor EIN3 directly associates with PGX3 promoter and is required for touch-repressed PGX3 expression. By uncovering the link between mechanical forces and cell wall remodeling established via the EIN3-PGX3 module, this work represents a key step in understanding the molecular framework of touch-induced morphological changes.

Motion of a Cell Wall Polysaccharide Observed by Atomic Force Microscopy

2000 ◽  
Vol 33 (15) ◽  
pp. 5680-5685 ◽  
Author(s):  
A. Patrick Gunning ◽  
Alan R. Mackie ◽  
Andrew R. Kirby ◽  
Paul Kroon ◽  
Gary Williamson ◽  
...  
Keyword(s):  
Atomic Force Microscopy ◽  
Cell Wall ◽  
Cell Wall Polysaccharide ◽  
Force Microscopy ◽  
Atomic Force ◽  
A Cell

Determining Mechanical Properties of Escherichia Coli by Nanoindentation

2012 ◽  
Vol 1424 ◽  
Author(s):  
C. A. Wright ◽  
C.J. Sullivan ◽  
B. Crawford ◽  
L.D. Britt ◽  
M.A. Mamun ◽  
...  
Keyword(s):  
Escherichia Coli ◽  
Mechanical Properties ◽  
Cell Wall ◽  
Contact Area ◽  
Solute Concentration ◽  
Force Microscopy ◽  
E Coli ◽  
Atomic Force ◽  
A Cell ◽  
Afm Cantilever

ABSTRACTEscherichia coli, like other gram-negative bacteria, is protected from the surrounding harsh environment by a cell wall consisting of the peptidoglycan and outer membrane. Whereas the cytoplasmic membrane is the selective barrier, the cell wall provides mechanical strength for the cell. As bacteria navigate various environments, osmotic pressure can change dramatically due to changes in local solute concentration. The peptidoglycan together with the cellular proteins mitigates the osmotic stress that would otherwise cause lysis. The mechanical properties of E. coli cells and its individual layers have been largely indeterminable until the recent development of probe-based measurement tools. Since their invention, scientists have reported significant data measuring elasticity, modulus, and stiffness using atomic force microscopy (AFM). Fundamentally, in order to determine these mechanical properties through probe-based techniques, the contact area and load should be well defined. The load can be precisely calculated through the AFM cantilever spring constant. However, the silicon tip contact area can only be estimated, potentially leading to compounding uncertainties. Therefore, we developed a methodology to determine nanomechanical properties of E. coli using a nanoindenter.

scholarly journals Direct Observation of Staphylococcus aureus Cell Wall Digestion by Lysostaphin

2008 ◽  
Vol 190 (24) ◽  
pp. 7904-7909 ◽  
Author(s):  
Grégory Francius ◽  
Oscar Domenech ◽  
Marie Paule Mingeot-Leclercq ◽  
Yves F. Dufrêne
Keyword(s):  
Staphylococcus Aureus ◽  
Cell Wall ◽  
Structural Changes ◽  
Time Lapse ◽  
Cell Swelling ◽  
Force Microscopy ◽  
Nanomechanical Properties ◽  
Atomic Force ◽  
Wall Stiffness ◽  
Insight Into

ABSTRACT The advent of Staphylococcus aureus strains that are resistant to virtually all antibiotics has increased the need for new antistaphylococcal agents. An example of such a potential therapeutic is lysostaphin, an enzyme that specifically cleaves the S. aureus peptidoglycan, thereby lysing the bacteria. Here we tracked over time the structural and physical dynamics of single S. aureus cells exposed to lysostaphin, using atomic force microscopy. Topographic images of native cells revealed a smooth surface morphology decorated with concentric rings attributed to newly formed peptidoglycan. Time-lapse images collected following addition of lysostaphin revealed major structural changes in the form of cell swelling, splitting of the septum, and creation of nanoscale perforations. Notably, treatment of the cells with lysostaphin was also found to decrease the bacterial spring constant and the cell wall stiffness, demonstrating that structural changes were correlated with major differences in cell wall nanomechanical properties. We interpret these modifications as resulting from the digestion of peptidoglycan by lysostaphin, eventually leading to the formation of osmotically fragile cells. This study provides new insight into the lytic activity of lysostaphin and offers promising prospects for the study of new antistaphylococcal agents.

Atomic force microscopy based analysis of cell-wall elasticity in macroalgae

2018 ◽  
pp. 335-347 ◽  
Author(s):  
Thomas Torode ◽  
Marina Linardic ◽  
J. Louis Kaplan ◽  
Siobhan A. Braybrook
Keyword(s):  
Atomic Force Microscopy ◽  
Cell Wall ◽  
Force Microscopy ◽  
Cell Wall Elasticity ◽  
Atomic Force

scholarly journals Optical, Structural and Electrical Properties of Electrochemical Synthesis of Thin Film of Polyaniline

2018 ◽  
Vol 15 (1) ◽  
pp. 73-80 ◽  
Author(s):  
Baghdad Science Journal
Keyword(s):  
X Ray Diffraction ◽  
X Ray ◽  
Force Microscopy ◽  
Morphological Studies ◽  
Atomic Force ◽  
Vis Spectroscopy ◽  
Structural And Electrical Properties ◽  
A Cell ◽  
Ft Ir ◽  
Ir And Raman

Polyaniline membranes of aniline were produced using an electrochemical method in a cell consisting of two poles. The effect of the vaccination was observed on the color of membranes of polyaniline, where analysis as of blue to olive green paints. The sanction of PANI was done by FT-IR and Raman techniques. The crystallinity of the models was studied by X-ray diffraction technique. The different electronic transitions of the PANI were determined by UV-VIS spectroscopy. The electrical conductivity of the manufactured samples was measured by using the four-probe technique at room temperature. Morphological studies have been determined by Atomic force microscopy (AFM). The structural studies have been measured by (SEM).

scholarly journals Variation of Burkholderia cenocepacia cell wall morphology and mechanical properties during cystic fibrosis lung infection, assessed by atomic force microscopy

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
A. Amir Hassan ◽  
Miguel V. Vitorino ◽  
Tiago Robalo ◽  
Mário S. Rodrigues ◽  
Isabel Sá-Correia
Keyword(s):  
Mechanical Properties ◽  
Cystic Fibrosis ◽  
Atomic Force Microscopy ◽  
Cell Wall ◽  
Adaptive Evolution ◽  
Burkholderia Cenocepacia ◽  
Force Microscopy ◽  
Atomic Force ◽  
Morphology And Mechanical Properties

Abstract The influence that Burkholderia cenocepacia adaptive evolution during long-term infection in cystic fibrosis (CF) patients has on cell wall morphology and mechanical properties is poorly understood despite their crucial role in cell physiology, persistent infection and pathogenesis. Cell wall morphology and physical properties of three B. cenocepacia isolates collected from a CF patient over a period of 3.5 years were compared using atomic force microscopy (AFM). These serial clonal variants include the first isolate retrieved from the patient and two late isolates obtained after three years of infection and before the patient’s death with cepacia syndrome. A consistent and progressive decrease of cell height and a cell shape evolution during infection, from the typical rods to morphology closer to cocci, were observed. The images of cells grown in biofilms showed an identical cell size reduction pattern. Additionally, the apparent elasticity modulus significantly decreases from the early isolate to the last clonal variant retrieved from the patient but the intermediary highly antibiotic resistant clonal isolate showed the highest elasticity values. Concerning the adhesion of bacteria surface to the AFM tip, the first isolate was found to adhere better than the late isolates whose lipopolysaccharide (LPS) structure loss the O-antigen (OAg) during CF infection. The OAg is known to influence Gram-negative bacteria adhesion and be an important factor in B. cenocepacia adaptation to chronic infection. Results reinforce the concept of the occurrence of phenotypic heterogeneity and adaptive evolution, also at the level of cell size, form, envelope topography and physical properties during long-term infection.

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