Ultrastructure des parois de cerises Bigarreau Burlat de textures différentes au cours de la maturation

1996 ◽  
Vol 74 (12) ◽  
pp. 1974-1981 ◽  
Author(s):  
C. Batisse ◽  
P. J. Coulomb ◽  
C. Coulomb ◽  
M. Buret
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Middle Lamella ◽  
Primary Cell ◽  
Wall Material ◽  
Cell Wall Degradation ◽  
Composition And Structure ◽  
Cell Wall Texture ◽  
Synthesis And Degradation ◽  
Soft Fruits

The changes in texture of fruits during ripening are linked to cell wall degradation involving synthesis and degradation of polymers. An increase in pectin solubility leads to cell sliding and an elastic aspect of tissues. The biochemical cell wall process differs between soft and crisp fruits originating from a same cultivar but cultivated under different agroclimatic conditions. Although the proportions of cell wall material are similar, the composition and structure of the two cell walls are very different at maturity. A solubilization of the middle lamella and a restructuration of the primary cell walls arising from the cells separation is observed in crisp fruits. In contrast, the middle lamella of the soft fruits is better preserved and the primary cell walls are thin and show degradation bags delimited by residual membrane formations. In addition, the macroendocytosis process by endosome individualization is more important in soft fruits. In conclusion, the fruit texture depends on the extent of the links between cell wall polymers. Keywords: cherry, cell wall, texture, ultrastructural study.

scholarly journals Relative Contributions of Bacteria, Protozoa, and Fungi to In Vitro Degradation of Orchard Grass Cell Walls and Their Interactions

2000 ◽  
Vol 66 (9) ◽  
pp. 3807-3813 ◽  
Author(s):  
S. S. Lee ◽  
J. K. Ha ◽  
K.-J. Cheng
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Rumen Fluid ◽  
Wall Material ◽  
P System ◽  
Cell Wall Material ◽  
Cell Wall Degradation ◽  
Chemical Treatments ◽  
System A ◽  
Microbial Groups

ABSTRACT To assess the relative contributions of microbial groups (bacteria, protozoa, and fungi) in rumen fluids to the overall process of plant cell wall digestion in the rumen, representatives of these groups were selected by physical and chemical treatments of whole rumen fluid and used to construct an artificial rumen ecosystem. Physical treatments involved homogenization, centrifugation, filtration, and heat sterilization. Chemical treatments involved the addition of antibiotics and various chemicals to rumen fluid. To evaluate the potential activity and relative contribution to degradation of cell walls by specific microbial groups, the following fractions were prepared: a positive system (whole ruminal fluid), a bacterial (B) system, a protozoal (P) system, a fungal (F) system, and a negative system (cell-free rumen fluid). To assess the interactions between specific microbial fractions, mixed cultures (B+P, B+F, and P+F systems) were also assigned. Patterns of degradation due to the various treatments resulted in three distinct groups of data based on the degradation rate of cell wall material and on cell wall-degrading enzyme activities. The order of degradation was as follows: positive and F systems > B system > negative and P systems. Therefore, fungal activity was responsible for most of the cell wall degradation. Cell wall degradation by the anaerobic bacterial fraction was significantly less than by the fungal fraction, and the protozoal fraction failed to grow under the conditions used. In general, in the mixed culture systems the coculture systems demonstrated a decrease in cellulolysis compared with that of the monoculture systems. When one microbial fraction was associated with another microbial fraction, two types of results were obtained. The protozoal fraction inhibited cellulolysis of cell wall material by both the bacterial and the fungal fractions, while in the coculture between the bacterial fraction and the fungal fraction a synergistic interaction was detected.

Ultrastructural and biochemical effects of endopectate lyase on cell walls from cell suspension cultures of bean and rice

1980 ◽  
Vol 58 (8) ◽  
pp. 867-880 ◽  
Author(s):  
Con J. Baker ◽  
James R. Aist ◽  
Durward F. Bateman
Keyword(s):  
Cell Wall ◽  
Cell Suspension ◽  
Cell Walls ◽  
Plant Cell Wall ◽  
Middle Lamella ◽  
Cell Suspension Cultures ◽  
Suspension Cultures ◽  
Cell Wall Integrity ◽  
Wall Material ◽  
Wall Structure

Cell walls prepared from suspension cell cultures of bean and rice in log-phase growth were used to examine the effects of endopectate lyase (PL) on the solubilization of cell wall carbohydrates and concomitant ultrastructural alterations. Cell wall preparations from both plant sources were heterogeneous and contained a range of wall types from primary walls to xylem elements with spiral, secondary wall thickenings. Marked differences in wall thickness and number of wall laminations typified both preparations.Bean cell walls were more susceptible to degradation by PL than were those of rice. Upon treatment of the former with 2.3 × 10−3 units/mL of PL (1 unit released 1 μmol of unsaturated uronide/min at 30 °C from polygalacturonic acid at pH 8.5), 27% of the noncellulosic wall carbohydrate was solubilized in 1 h. This represented 50% of the PL susceptible carbohydrate in the preparation. Only 3% of the noncellulosic carbohydrate was released from rice cell walls in 1 h when treated with 115 × 10−3 units of PL/mL. This accounted for 60% of the PL susceptible wall fractions. Only uronic acid, rhamnose, galactose, and arabinose were solubilized from both preparations by PL.Cell walls in the bean and rice preparations were affected differentially by the PL. Those walls with secondary thickenings did not appear to be degraded, while the distinct fibrillar appearance of both bean and rice walls tended to fade or disappear. The middle lamella tended to dissolve to varying degrees in the presence of PL. Bean walls were more severely degraded than were the rice walls and many exhibited swelling, separation of wall layers, markedly reduced staining intensity, and (or) a granular ultrastructure.This study has demonstrated that as PL acts on susceptible cell walls there are major changes evoked in cell wall structure which suggest that the rhamnogalacturonan fraction of the higher plant cell wall contributes significantly to cell wall integrity. This study also emphasizes the need for cell wall material of proven uniformity for investigations of both cell wall composition and effects of specific polysaccharide degrading enzymes on cell wall integrity. Preliminary studies indicate that tobacco pith may provide more uniform cell walls than do cell suspension cultures.

Silicification of wood-cell walls

1994 ◽  
Vol 52 ◽  
pp. 428-429
Author(s):  
S. E. Keckler ◽  
D. M. Dabbs ◽  
N. Yao ◽  
I. A. Aksay
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Cell Walls ◽  
Lignin Content ◽  
Resin Composite ◽  
Middle Lamella ◽  
Cellulose Fibers ◽  
Complex Structures ◽  
Rich Region ◽  
Inorganic Precursors

Cellular organic structures such as wood can be used as scaffolds for the synthesis of complex structures of organic/ceramic nanocomposites. The wood cell is a fiber-reinforced resin composite of cellulose fibers in a lignin matrix. A single cell wall, containing several layers of different fiber orientations and lignin content, is separated from its neighboring wall by the middle lamella, a lignin-rich region. In order to achieve total mineralization, deposition on and in the cell wall must be achieved. Geological fossilization of wood occurs as permineralization (filling the void spaces with mineral) and petrifaction (mineralizing the cell wall as the organic component decays) through infiltration of wood with inorganics after growth. Conversely, living plants can incorporate inorganics into their cells and in some cases into the cell walls during growth. In a recent study, we mimicked geological fossilization by infiltrating inorganic precursors into wood cells in order to enhance the properties of wood. In the current work, we use electron microscopy to examine the structure of silica formed in the cell walls after infiltration of tetraethoxysilane (TEOS).

Synchrotron infrared microspectroscopy reveals the response of Sphagnum cell wall material to its aqueous chemical environment

2018 ◽  
Vol 15 (8) ◽  
pp. 513
Author(s):  
Ewen Silvester ◽  
Annaleise R. Klein ◽  
Kerry L. Whitworth ◽  
Ljiljana Puskar ◽  
Mark J. Tobin
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Chemical Environment ◽  
Wall Material ◽  
Organic Soils ◽  
Cell Wall Material ◽  
Acid Base ◽  
Widespread Species ◽  
Flowing Liquid ◽  
Infrared Microspectroscopy

Environmental contextSphagnum moss is a widespread species in peatlands globally and responsible for a large fraction of carbon storage in these systems. We used synchrotron infrared microspectroscopy to characterise the acid-base properties of Sphagnum moss and the conditions under which calcium uptake can occur (essential for plant tissue integrity). The work allows a chemical model for Sphagnum distribution in the landscape to be proposed. AbstractSphagnum is one the major moss types responsible for the deposition of organic soils in peatland systems. The cell walls of this moss have a high proportion of carboxylated polysaccharides (polygalacturonic acids), which act as ion exchangers and are likely to be important for the structural integrity of the cell walls. We used synchrotron light source infrared microspectroscopy to characterise the acid-base and calcium complexation properties of the cell walls of Sphagnum cristatum stems, using freshly sectioned tissue confined in a flowing liquid cell with both normal water and D2O media. The Fourier transform infrared spectra of acid and base forms are consistent with those expected for protonated and deprotonated aliphatic carboxylic acids (such as uronic acids). Spectral deconvolution shows that the dominant aliphatic carboxylic groups in this material behave as a monoprotic acid (pKa=4.97–6.04). The cell wall material shows a high affinity for calcium, with a binding constant (K) in the range 103.9–104.7 (1:1 complex). The chemical complexation model developed here allows for the prediction of the chemical environment (e.g. pH, ionic content) under which Ca2+ uptake can occur, and provides an improved understanding for the observed distribution of Sphagnum in the landscape.

scholarly journals Requirement of Autolytic Activity for Bacteriocin-Induced Lysis

2000 ◽  
Vol 66 (8) ◽  
pp. 3174-3179 ◽  
Author(s):  
M. Carmen Martínez-Cuesta ◽  
Jan Kok ◽  
Elisabet Herranz ◽  
Carmen Peláez ◽  
Teresa Requena ◽  
...  
Keyword(s):  
Cell Wall ◽  
Sodium Dodecyl Sulfate ◽  
Growth Phase ◽  
Cell Walls ◽  
Cell Damage ◽  
Sodium Dodecyl ◽  
Exponential Growth Phase ◽  
Cell Wall Degradation ◽  
Intracellular Proteins ◽  
Autolytic Activity

ABSTRACT The bacteriocin produced by Lactococcus lactis IFPL105 is bactericidal against several Lactococcus andLactobacillus strains. Addition of the bacteriocin to exponential-growth-phase cells resulted in all cases in bacteriolysis. The bacteriolytic response of the strains was not related to differences in sensitivity to the bacteriocin and was strongly reduced in the presence of autolysin inhibitors (Co2+ and sodium dodecyl sulfate). When L. lactis MG1363 and its derivative deficient in the production of the major autolysin AcmA (MG1363acmAΔ1) were incubated with the bacteriocin, the latter did not lyse and no intracellular proteins were released into the medium. Incubation of cell wall fragments of L. lactisMG1363, or of L. lactis MG1363acmAΔ1 to which extracellular AcmA was added, in the presence or absence of the bacteriocin had no effect on the speed of cell wall degradation. This result indicates that the bacteriocin does not degrade cell walls, nor does it directly activate the autolysin AcmA. The autolysin was also responsible for the observed lysis of L. lactis MG1363 cells during incubation with nisin or the mixture of lactococcins A, B, and M. The results presented here show that lysis of L. lactis after addition of the bacteriocins is caused by the resulting cell damage, which promotes uncontrolled degradation of the cell walls by AcmA.

scholarly journals Cell fusion in yeast is negatively regulated by components of the cell wall integrity pathway

2019 ◽  
Vol 30 (4) ◽  
pp. 441-452 ◽  
Author(s):  
Allison E. Hall ◽  
Mark D. Rose
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Cell Death ◽  
Cell Wall ◽  
Yeast Cell ◽  
Cell Fusion ◽  
Cell Walls ◽  
Cell Wall Integrity ◽  
Fusion Genes ◽  
Cell Wall Degradation ◽  
Cell Wall Integrity Pathway

During mating, Saccharomyces cerevisiae cells must degrade the intervening cell wall to allow fusion of the partners. Because improper timing or location of cell wall degradation would cause lysis, the initiation of cell fusion must be highly regulated. Here, we find that yeast cell fusion is negatively regulated by components of the cell wall integrity (CWI) pathway. Loss of the cell wall sensor, MID2, specifically causes “mating-induced death” after pheromone exposure. Mating-induced death is suppressed by mutations in cell fusion genes ( FUS1, FUS2, RVS161, CDC42), implying that mid2Δ cells die from premature fusion without a partner. Consistent with premature fusion, mid2Δ shmoos had thinner cell walls and lysed at the shmoo tip. Normally, Cdc42p colocalizes with Fus2p to form a focus only when mating cells are in contact (prezygotes) and colocalization is required for cell fusion. However, Cdc42p was aberrantly colocalized with Fus2p to form a focus in mid2Δ shmoos. A hyperactive allele of the CWI kinase Pkc1p ( PKC1*) caused decreased cell fusion and Cdc42p localization in prezygotes. In shmoos, PKC1* increased Cdc42p localization; however, it was not colocalized with Fus2p or associated with cell death. We conclude that Mid2p and Pkc1p negatively regulate cell fusion via Cdc42p and Fus2p.

Étude cytochimique ultrastructurale de la dégradation des lignines dans les résidus pariétaux de bois d'épicéa et de peuplier par le Reticulitermes lucifugus var. santonensis (Rhinotermitidae, Isoptera)

1992 ◽  
Vol 70 (5) ◽  
pp. 933-941 ◽  
Author(s):  
E. Garnier-Sillam ◽  
I. Grech ◽  
Y. Czaninski ◽  
M.-T. Tollier ◽  
B. Monties
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Periodic Acid ◽  
Mechanical Action ◽  
Free Cell ◽  
Uranyl Acetate ◽  
Picea Sitchensis ◽  
Wall Material ◽  
Before And After ◽  
Acetate Lead

Free cell-wall residues were prepared by extracting wood samples of spruce (Populus euramericana cv. Fidzi Pauley) and poplar (Picea sitchensis). These species were chosen for their lignin types: guaiacyl in spruce and guaiacyl–syringyl in poplar. The parietal residues obtained were used as the sole food for the xylophagous termite Reticulitermes lucifugus var. santonensis and were compared before and after ingestion and transit in the digestive tracts. Differences due to the mechanical action of the gizzard were found in association with chemical changes. Polysaccharides were unmasked after digestion and could clearly be observed after reaction with periodic acid – thiocarbohydrazide – silver proteinate. A fibrillary meshwork was also observed inside the lignified cell walls. Biodegradation of cell wall material was particularly clear in poplar where granules formed an electron-dense plasma when uranyl acetate – lead citrate or periodic acid – thiocarbohydrazide – silver proteinate was used as a contrast medium. A selective biodegradation of syringyl monomers in poplar parietal residues was indicated by thioacidolysis but requires confirmation. Breakdown of lignified cell walls begins with a biodegradation of the lignin network associated with or followed by the digestion of polysaccharides. Syringyl-rich lignin fractions seemed to break down faster. Whether the enzymic pathway leading to ligninolysis originates from the termite digestive cells or from the endosymbionts present in their digestive tract lumen remains to be defined. Key words: Isoptera, Reticulitermes lucifugus var. santonensis, wood, lignin, spruce, poplar.

Ultrastructural Changes in the Cell Walls of Cambial Derivatives During Wood Formation in Indian ELM (Holoptelea Integrifolia)

IAWA Journal ◽  
2012 ◽  
Vol 33 (4) ◽  
pp. 403-416 ◽  
Author(s):  
Karumanchi S. Rao ◽  
Yoon Soo Kim ◽  
Pramod Sivan
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Middle Lamella ◽  
Ultrastructural Changes ◽  
Cell Wall Polysaccharides ◽  
Lignin Distribution ◽  
Parenchyma Cells ◽  
Ray Cells ◽  
Xylem Elements ◽  
S2 Layer

Sequential changes occurring in cell walls during expansion, secondary wall (SW) deposition and lignification have been studied in the differentiating xylem elements of Holoptelea integrifolia using transmission electron microscopy. The PATAg staining revealed that loosening of the cell wall starts at the cell corner middle lamella (CCML) and spreads to radial and tangential walls in the zone of cell expansion (EZ). Lignification started at the CCML region between vessels and associated parenchyma during the final stages of S2 layer formation. The S2 layer in the vessel appeared as two sublayers,an inner one and outer one.The contact ray cells showed SW deposition soon after axial paratracheal parenchyma had completed it, whereas noncontact ray cells underwent SW deposition and lignification following apotracheal parenchyma cells. The paratracheal and apotracheal parenchyma cells differed noticeably in terms of proportion of SW layers and lignin distribution pattern. Fibres were found to be the last xylem elements to complete SW deposition and lignification with differential polymerization of cell wall polysaccharides. It appears that the SW deposition started much earlier in the middle region of the fibres while their tips were still undergoing elongation. In homogeneous lignin distribution was noticed in the CCML region of fibres.

scholarly journals Domain-specific and cell type-specific localization of two types of cell wall matrix polysaccharides in the clover root tip.

1992 ◽  
Vol 118 (2) ◽  
pp. 467-479 ◽  
Author(s):  
M A Lynch ◽  
L A Staehelin
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Cellular Differentiation ◽  
Cortical Cell ◽  
Middle Lamella ◽  
Root Cap ◽  
Root Tip ◽  
Cortical Cells ◽  
Peripheral Cell ◽  
Clover Root

Using immunocytochemical techniques and antibodies that specifically recognize xyloglucan (anti-XG), polygalacturonic acid/rhamnogalacturonan I (anti-PGA/RG-I), and methylesterified pectins (JIM 7), we have shown that these polysaccharides are differentially synthesized and localized during cell development and differentiation in the clover root tip. In cortical cells XG epitopes are present at a threefold greater density in the newly formed cross walls than in the older longitudinal walls, and PGA/RG-I epitopes are detected solely in the expanded middle lamella of cortical cell corners, even after pretreatment of sections with pectinmethylesterase to uncover masked epitopes. These results suggest that in cortical cells XG and PGA/RG-I are differentially localized not only to particular wall domains, but also to particular cell walls. In contrast to their nonoverlapping distribution in cortical cells, XG epitopes and PGA/RG-I epitopes largely colocalize in the epidermal cell walls. The results also demonstrate that the middle lamella of the longitudinal walls shared by epidermal cells and by epidermal and cortical cells constitutes a barrier to the diffusion of cell wall and mucilage molecules. Synthesis of XG and PGA/RG-I epitope-containing polysaccharides also varies during cellular differentiation in the root cap. The differentiation of gravitropic columella cells into mucilage-secreting peripheral cells is marked by a dramatic increase in the synthesis and secretion of molecules containing XG and PGA/RG-I epitopes. In contrast, JIM 7 epitopes are present at abundant levels in columella cell walls, but are not detectable in peripheral cell walls or in secreted mucilage. There were also changes in the cisternal labeling of the Golgi stacks during cellular differentiation in the root tip. Whereas PGA/RG-I epitopes are detected primarily in cis- and medial Golgi cisternae in cortical cells (Moore, P. J., K. M. M. Swords, M. A. Lynch, and L. A. Staehelin. 1991. J. Cell Biol. 112:589-602), they are localized predominantly in the trans-Golgi cisternae and the trans-Golgi network in epidermal and peripheral root cap cells. These observations suggest that during cellular differentiation the plant Golgi apparatus can be both structurally and functionally reorganized.

Sign in / Sign up

Export Citation Format

Share Document