Comparison of Coccidioides immitis arthrospore, mycelium, and spherule cell walls, and influence of growth medium on mycelial cell wall composition.

1977 ◽  
Vol 17 (1) ◽  
pp. 91-97 ◽  
Author(s):  
R W Wheat ◽  
C Tritschler ◽  
N F Conant ◽  
E P Lowe
Keyword(s):  
Cell Wall ◽  
Growth Medium ◽  
Cell Walls ◽  
Cell Wall Composition ◽  
Coccidioides Immitis ◽  
Spherule Cell ◽  
Mycelial Cell

A relationship between cell wall composition and mutant morphology in the basidiomycete Schizophyllum commune

1968 ◽  
Vol 14 (7) ◽  
pp. 809-811 ◽  
Author(s):  
Chiu-Sheng Wang ◽  
Marvin N. Schwalb ◽  
Philip G. Miles
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Single Gene ◽  
Schizophyllum Commune ◽  
Gene Mutations ◽  
Cell Wall Composition ◽  
Statistical Analyses ◽  
Morphological Mutants ◽  
Mutant Forms ◽  
Isolated Cell

Mechanically isolated cell walls of normal homokaryons and the morphological mutants thin and puff were fractionated and hydrolyzed by chemical procedures. The yields of fractionated materials and the glucose/hexosamine ratios of acid hydrolysates were determined. Results of statistical analyses of the values obtained from these determinations indicated that single-gene mutations causing the thin and puff mutant forms of this fungus produce specific differences in the composition of cell walls.

scholarly journals Feeding the Walls: How Does Nutrient Availability Regulate Cell Wall Composition?

2018 ◽  
Vol 19 (9) ◽  
pp. 2691 ◽  
Author(s):  
Michael Ogden ◽  
Rainer Hoefgen ◽  
Ute Roessner ◽  
Staffan Persson ◽  
Ghazanfar Khan
Keyword(s):  
Cell Wall ◽  
Plant Cell ◽  
Nutrient Availability ◽  
Cell Walls ◽  
Plant Cell Wall ◽  
Nutrient Status ◽  
Cell Wall Composition ◽  
Nutrient Sensing ◽  
Tissue Type ◽  
Wall Components

Nutrients are critical for plants to grow and develop, and nutrient depletion severely affects crop yield. In order to optimize nutrient acquisition, plants adapt their growth and root architecture. Changes in growth are determined by modifications in the cell walls surrounding every plant cell. The plant cell wall, which is largely composed of complex polysaccharides, is essential for plants to attain their shape and to protect cells against the environment. Within the cell wall, cellulose strands form microfibrils that act as a framework for other wall components, including hemicelluloses, pectins, proteins, and, in some cases, callose, lignin, and suberin. Cell wall composition varies, depending on cell and tissue type. It is governed by synthesis, deposition and remodeling of wall components, and determines the physical and structural properties of the cell wall. How nutrient status affects cell wall synthesis and organization, and thus plant growth and morphology, remains poorly understood. In this review, we aim to summarize and synthesize research on the adaptation of root cell walls in response to nutrient availability and the potential role of cell walls in nutrient sensing.

PRODUCTION OF YEAST AND MOLD PROTOPLASTS BY TREATMENT WITH THE STREPZYME OF MICROMONOSPORA AS

1965 ◽  
Vol 11 (3) ◽  
pp. 573-580 ◽  
Author(s):  
S. Gascon ◽  
A. G. Ochoa ◽  
J. R. Villanueva
Keyword(s):  
Cell Wall ◽  
Growth Medium ◽  
Cell Walls ◽  
Candida Utilis ◽  
Final Concentration ◽  
Normal Cells ◽  
Prolonged Incubation ◽  
Phase Microscopy ◽  
Cell Wall Digestion ◽  
Abnormal Cells

Using phase microscopy, the authors made studies of the formation and properties of spherical protoplasts of the organisms Candida utilis, Oospora suaveolens, and Geotrichum lactis, produced by digestion of the cell walls in isotonic medium with a lytic preparation obtained from the filtrates of the growth medium of Micromonospora AS. The susceptibility of various species of yeast and molds to cell wall digestion and further liberation of protoplasts was variable. MgSO4 (0.8 to 1.0 M final concentration) was a satisfactory stabilizer for producing osmotically sensitive spherical bodies. On dilution, these fragile structures lysed immediately. The naked protoplasts were able to grow, as indicated by changes in morphology. On prolonged incubation abnormal cells were formed. Reversion to normal cells was observed but was very rare. Details of the emergence of the Oospora suaveolens protoplasts were described. Protoplasts were also prepared from a variety of bacteria.

scholarly journals The Placenta of Physcomitrium patens: Transfer Cell Wall Polymers Compared across the Three Bryophyte Groups

Diversity ◽  
2021 ◽  
Vol 13 (8) ◽  
pp. 378
Author(s):  
Jason S. Henry ◽  
Karen S. Renzaglia
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Cell Wall Composition ◽  
Transfer Cells ◽  
Primary Cell ◽  
Transfer Cell ◽  
Primary Cell Wall ◽  
Slight Variation ◽  
Wall Ingrowths ◽  
Cell Wall Polymers

Following similar studies of cell wall constituents in the placenta of Phaeoceros and Marchantia, we conducted immunogold labeling TEM studies of Physcomitrium patens to determine the composition of cell wall polymers in transfer cells on both sides of the placenta. Sixteen monoclonal antibodies were used to localize cell wall epitopes in the basal walls and wall ingrowths in this moss. In general, placental transfer cell walls of P. patens contained fewer pectins and far fewer arabinogalactan proteins AGPs than those of the hornwort and liverwort. P. patens also lacked the differential labeling that is pronounced between generations in the other bryophytes. In contrast, transfer cell walls on either side of the placenta of P. patens were relatively similar in composition, with slight variation in homogalacturonan HG pectins. Compositional similarities between wall ingrowths and primary cell walls in P. patens suggest that wall ingrowths may simply be extensions of the primary cell wall. Considerable variability in occurrence, abundance, and types of polymers among the three bryophytes and between the two generations suggested that similarity in function and morphology of cell walls does not require a common cell wall composition. We propose that the specific developmental and life history traits of these plants may provide even more important clues in understanding the basis for these differences. This study significantly builds on our knowledge of cell wall composition in bryophytes in general and in transfer cells across plants.

scholarly journals STAYMAN FRUIT CRACKING AS RELATED TO CW COMPOSITION

HortScience ◽  
1990 ◽  
Vol 25 (9) ◽  
pp. 1093G-1094
Author(s):  
Russell L. Weiser
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Cell Structure ◽  
Cell Wall Composition ◽  
Distilled Water ◽  
Fruit Cracking ◽  
Consequent Effect ◽  
The Difference ◽  
Treated Apple ◽  
Wall Extensibility

Stayman apples are predisposed to cracking. Trees whose trunks were scored and foliage sprayed with GA4+7, NAA 800, and Vapor Guard had significantly fewer apples crack than controls. The skin strength and stretch distance were the same for control and treated apples. However, slices of treated apple expanded significantly more than control apples when immersed in distilled water for 45 minutes. During this treatment the amount of water taken up was not significantly different, which may indicate the difference lies in the cell structure. Hypodermal cells of control apples appear to be more elongated and have thicker cell walls than treated apples. Cell wall sugar and amino acid components will be measured to see if this discrepancy can be attributed to cell wall structural properties. These results suggest that stayman cracking occurs when the expansion of the hypodermic cannot keep pace with expansion of the fruit. It is further hypothesized that this difference is due to a difference in cell wall composition and consequent effect on wall extensibility.

scholarly journals Cell wall composition determines handedness reversal in helicoidal cellulose architectures of Pollia condensata fruits

2021 ◽  
Vol 118 (51) ◽  
pp. e2111723118
Author(s):  
Yin Chang ◽  
Rox Middleton ◽  
Yu Ogawa ◽  
Tom Gregory ◽  
Lisa M. Steiner ◽  
...  
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Hierarchical Structures ◽  
Cell Wall Composition ◽  
Cellulose Microfibrils ◽  
Plant Cell Walls ◽  
Mechanical Responses ◽  
Structural Colors ◽  
Left Handed ◽  
Helicoidal Structure

Chiral asymmetry is important in a wide variety of disciplines and occurs across length scales. While several natural chiral biomolecules exist only with single handedness, they can produce complex hierarchical structures with opposite chiralities. Understanding how the handedness is transferred from molecular to the macroscopic scales is far from trivial. An intriguing example is the transfer of the handedness of helicoidal organizations of cellulose microfibrils in plant cell walls. These cellulose helicoids produce structural colors if their dimension is comparable to the wavelength of visible light. All previously reported examples of a helicoidal structure in plants are left-handed except, remarkably, in the Pollia condensata fruit; both left- and right-handed helicoidal cell walls are found in neighboring cells of the same tissue. By simultaneously studying optical and mechanical responses of cells with different handednesses, we propose that the chirality of helicoids results from differences in cell wall composition. In detail, here we showed statistical substantiation of three different observations: 1) light reflected from right-handed cells is red shifted compared to light reflected from left-handed cells, 2) right-handed cells occur more rarely than left-handed ones, and 3) right-handed cells are located mainly in regions corresponding to interlocular divisions. Finally, 4) right-handed cells have an average lower elastic modulus compared to left-handed cells of the same color. Our findings, combined with mechanical simulation, suggest that the different chiralities of helicoids in the cell wall may result from different chemical composition, which strengthens previous hypotheses that hemicellulose might mediate the rotations of cellulose microfibrils.

Identification and analysis of cell wall glycan epitopes and polyphenol oxidase in pawpaw (Asimina triloba [L.] Dunal) fruit pulp as affected by high pressure processing and refrigerated storage

2019 ◽  
Vol 25 (8) ◽  
pp. 711-722
Author(s):  
Robert G Brannan ◽  
Ahmed Faik ◽  
Ryan Goelz ◽  
Sivakumar Pattathil
Keyword(s):  
High Pressure ◽  
Cell Wall ◽  
Polyphenol Oxidase ◽  
Oxidase Activity ◽  
Cell Walls ◽  
High Pressure Processing ◽  
Cell Wall Composition ◽  
Refrigerated Storage ◽  
Polyphenol Oxidase Activity ◽  
Asimina Triloba

This research explores the cell wall composition and polyphenol oxidase activity of two pawpaw ( Asimina triloba) fruit varieties, Susquehanna and Green River Belle, that were subjected to high pressure processing and 45 days of refrigerated storage. We hypothesize that high pressure processing may inhibit enzymatic action responsible for pawpaw's deleterious postharvest tissue softening and browning. Glycome profiling uses mAb groupings that recognize 19 groups of glycan epitopes present in most major classes of cell wall glycans and was used to determine cell wall composition. Results show that both varieties have typical type I primary cell walls of flowering dicots. However, differences in the fine cell wall structure between the varieties can be inferred and the varieties behaved differently during refrigerated storage, likely indicating of a difference in cell wall-modifying enzymes present in the primary cell walls. High pressure processing treatment does not seem to be effective at eliminating polyphenol oxidase activity.

Cell Walls of the Phycobionts Trebouxia and Pseudotrebouxia: Constituents and Their Localization

1984 ◽  
Vol 16 (2) ◽  
pp. 129-144 ◽  
Author(s):  
J. König ◽  
E. Peveling
Keyword(s):  
Cell Wall ◽  
Cell Walls ◽  
Cell Wall Composition ◽  
Recognition Mechanism ◽  
Absorption Spectrophotometry ◽  
Species Specific ◽  
Layer Chromatography ◽  
Polysaccharide Layer ◽  
Wall Components

AbstractThe cell wall composition of several species of the lichen phycobionts Trebouxia and Pseudotrebouxia has been investigated using gas chromatography, thin layer chromatography and infrared absorption spectrophotometry. In addition cell wall components (cellulose, non-cellulosic polysaccharides, sporopollenin, protein) were localized with cytochemical methods at the EM- level. The cell walls of Trebouxia and Pseudotrebouxia consist of several layers. In Trebouxia the inner layer (Si) consists mainly of cellulose, then followed by a non-cellulosic polysaccharide layer (S2), a sporopollenin-layer (S3) and an outer layer consisting again of a non-cellulosic polysaccharide (S4). In addition Trebouxia is surrounded by a sheath (a polysaccharide with species-specific terminal residues). In Pseudotrebouxia the cell wall is similarly constructed compared to Trebouxia, however, the sheath is lacking and the S4 layer contains a polysaccharide with species-specific terminal sugar residues. The role of the different cell wall constituents for the recognition mechanism between the lichen symbionts is discussed.

scholarly journals Synchrotron FTIR and Raman spectroscopy 1 ectroscopy provide unique spectral fingerprints for Arabidopsis floral stem vascular tissues

2018 ◽  
Author(s):  
S Dinant ◽  
N Wolff ◽  
F De Marco ◽  
F Vilaine ◽  
L Gissot ◽  
...  
Keyword(s):  
Raman Spectroscopy ◽  
Cell Wall ◽  
Cell Walls ◽  
Double Mutant ◽  
Vascular Tissue ◽  
Cell Wall Composition ◽  
Specific Cell ◽  
Xylem Cell ◽  
Phloem Cell ◽  
Ftir And Raman Spectroscopy

AbstractCell walls are highly complex structures that are modified during plant growth and development. For example, the development of phloem and xylem vascular cells, which participate in the transport of sugars and water as well as support, can be influenced by cell-specific cell wall composition. Here, we used synchrotron radiation-based infrared (SR-FTIR) and Raman spectroscopy to analyze the cell wall composition of wild-type and double mutant sweet11-1sweet12-1, which impairs sugar transport, Arabidopsis floral stem vascular tissue. The SR-FTIR spectra showed that in addition to modified xylem cell wall composition, phloem cell walls in the double mutant line were characterized by modified hemicellulose composition. Moreover, combining Raman spectroscopy with a Classification and Regression Tree (CART) method identified combinations of Raman shifts that could distinguish xylem vessels and fibers. Additionally, the disruption of SWEET11 and SWEET12 genes impacts xylem cell wall composition in a cell-specific manner, with changes in hemicelluloses and cellulose observed at the xylem vessel interface. These results suggest that the facilitated transport of sugars by transporters that exist between vascular parenchyma cells and conducting cells is important to ensuring correct phloem and xylem cell wall composition.HighlightCombining vibrational spectroscopy techniques and multivariate analysis shows that the disruption of SWEET genes impacts phloem cell wall composition and that the effect on xylem cell wall composition is cell-specific.

Cell Wall Composition and Ultrastructural Immunolocalization of Pectin and Arabinogalactan Protein during Olea europaea L. Fruit Abscission

2020 ◽  
Vol 61 (4) ◽  
pp. 814-825 ◽  
Author(s):  
Ruben Parra ◽  
Miguel A Paredes ◽  
Juana Labrador ◽  
Cláudia Nunes ◽  
Manuel A Coimbra ◽  
...  
Keyword(s):  
Cell Wall ◽  
Cell Separation ◽  
Cell Walls ◽  
Cell Wall Composition ◽  
Arabinogalactan Protein ◽  
Cell Wall Polysaccharide ◽  
Ripe Fruit ◽  
Olive Fruit ◽  
Fruit Abscission ◽  
Polysaccharide Composition

Abstract Cell wall modification is integral to many plant developmental processes where cells need to separate, such as abscission. However, changes in cell wall composition during natural fruit abscission are poorly understood. In olive (Olea europaea L.), some cultivars such as ‘Picual’ undergo massive natural fruit abscission after fruit ripening. This study investigates the differences in cell wall polysaccharide composition and the localization of pectins and arabinogalactan protein (AGP) in the abscission zone (AZ) during cell separation to understand fruit abscission control in ‘Picual’ olive. To this end, immunogold labeling employing a suite of monoclonal antibodies to cell wall components (JIM13, LM5, LM6, LM19 and LM20) was investigated in olive fruit AZ. Cell wall polysaccharide extraction revealed that the AZ cell separation is related to the de-esterification and degradation of pectic polysaccharides. Moreover, ultrastructural localization showed that both esterified and unesterified homogalacturonans (HGs) localize mainly in the AZ cell walls, including the middle lamella and tricellular junction zones. Our results indicate that unesterified HGs are likely to contribute to cell separation in the olive fruit AZ. Similarly, immunogold labeling demonstrated a decrease in both galactose-rich and arabinose-rich pectins in AZ cell walls during ripe fruit abscission. In addition, AGPs were localized in the cell wall, plasma membrane and cytoplasm of AZ cells with lower levels of AGPs during ripe fruit abscission. This detailed temporal profile of the cell wall polysaccharide composition, and the pectins and AGP immunolocalization in the olive fruit AZ, offers new insights into cell wall remodeling during ripe fruit abscission.

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