Cytochemistry and ultrastructure of the dehiscence zone of almond (Prunus dulcis) fruits

1990 ◽  
Vol 68 (1) ◽  
pp. 63-72 ◽  
Author(s):  
K. Weis ◽  
V. S. Polito

At maturity, the almond pericarp dehisces along the ventral suture, a region that originates by fusion of epidermal cells and subsequently differentiates into a separation layer. We have characterized the ontogeny of the fusion–dehiscence zone with emphasis on cell wall characteristics by using cytochemical methods for detection of pectin, cutin, cellulose, and lignin to examine the middle lamellae and primary and secondary walls in dehiscence-zone cells. Carpel margins became united postgenitally along opposing epidermal layers giving rise to the suture. Fusion-zone cells host epidermal characteristics, elaborated broad pectinaceous walls, and ultimately formed a discrete band of cells that dehisced along the original line of fusion by dissolution of cell wall pectins. Treatment of treeborne fruits with 1 ppm ethylene gas or extraction of sectioned material with cell wall hydrolases resulted in cell wall changes similar to those in predehiscent fruits.

1957 ◽  
Vol 3 (2) ◽  
pp. 171-182 ◽  
Author(s):  
S. T. Bayley ◽  
J. R. Colvin ◽  
F. P. Cooper ◽  
Cecily A. Martin-Smith

The primary walls of epidermal cells in Avena coleoptiles ranging in length from 2 to 40 mm. have been studied in the electron and polarizing microscopes and by the low-angle scattering of x-rays. The outer walls of these cells are composed of multiple layers of cellulose microfibrils oriented longitudinally; initially the number of layers is between 10 and 15 but this increases to about 25 in older tissue. Where epidermal cells touch, these multiple layers fuse gradually into a primary wall of the normal type between cells. In these radial walls, the microfibrils are oriented transversely. Possible mechanisms for the growth of the multilayered outer wall during cell elongation are discussed.


2019 ◽  
Vol 55 (No. 3) ◽  
pp. 87-92
Author(s):  
Xiaobing Liu ◽  
Bingjie Tu ◽  
Qiuying Zhang ◽  
Stephen J. Herbert

Pod shattering resistance is a trait acquired by crops in the process of evolution. Manipulation of physiological and molecular processes is fundamental for the improvement of shattering resistance in crops. In this review we discuss several enzymes, key hormones and their possible roles or relationships involved in pod shattering, and highlight responsible genes, quantitative traits loci (QTLs) and their implications for increased pod shattering resistance. Cell wall degrading enzymes, particularly β-glucanases and endopolygalacturonases play an important role in the process of pod dehiscence. It is not clear how and to what extent a specific hormone regulates the dehiscence zone differentiation and the dehiscence process is not clear. Resistance to shattering is highly heritable and is not controlled by a single gene. Several QTLs associated to dehiscence have been identified in crops, while the underlying genetic functions of these QTLs deserve further investigation. Further physiological analyses of the pod wall will help to understand better the pod dehiscence.


2001 ◽  
Vol 91 (2) ◽  
pp. 149-158 ◽  
Author(s):  
P. S. Wharton ◽  
A. M. Julian ◽  
R. J. O'Connell

Ultrastructural studies of the infection of susceptible and resistant cultivars of Sorghum bicolor by Colletotrichum sublineolum were conducted. Initial penetration events were the same on both susceptible and resistant cultivars. Germ tubes originating from germinated conidia formed globose, melanized appressoria, that penetrated host epidermal cells directly. Appressoria did not produce appressorial cones, but each penetration pore was surrounded by an annular wall thickening. Inward deformation of the cuticle and localized changes in staining properties of the host cell wall around the infection peg suggests that penetration involves both mechanical force and enzymic dissolution. In compatible interactions, penetration was followed by formation of biotrophic globular infection vesicles in epidermal cells. Filamentous primary hyphae developed from the vesicles and went on to colonize many other host cells as an intracellular mycelium. Host cells initially survived penetration. The host plasma membrane invaginated around infection vesicles and primary hyphae and was appressed tightly to the fungal cell wall, with no detectable matrix layer at the interface. Necrotrophic secondary hyphae appeared after 66 h and ramified through host tissue both intercellularly and intracellularly, forming hypostromatic acervuli by 114 h. Production of secondary hyphae was accompanied by the appearance of electron-opaque material within infected cells. This was thought to represent the host phytoalexin response. In incompatible interactions, infection vesicles and primary hyphae were formed in epidermal cells by 42 h. However, they were encrusted with electron-opaque material and appeared dead. These observations are discussed in relation to the infection processes of other Colletotrichum spp. and the host phytoalexin response.


1990 ◽  
Vol 110 (4) ◽  
pp. 1111-1122 ◽  
Author(s):  
D J Flanders ◽  
D J Rawlins ◽  
P J Shaw ◽  
C W Lloyd

To investigate the spatial relationship between the nucleus and the cortical division site, epidermal cells were selected in which the separation between these two areas is large. Avoiding enzyme treatment and air drying, Datura stramonium cells were labeled with antitubulin antibodies and the three-dimensional aspect of the cytoskeletons was reconstructed using computer-aided optical sectioning. In vacuolated cells preparing for division, the nucleus migrates into the center of the cell, suspended by transvacuolar strands. These strands are now shown to contain continuous bundles of microtubules which bridge the nucleus to the cortex. These nucleus-radiating microtubules adopt different configurations in cells of different shape. In elongated cells with more or less parallel side walls, oblique strands radiating from the nucleus to the long side walls are presumably unstable, for they are progressively realigned into a transverse disc (the phragmosome) as broad, cortical, preprophase bands (PPBs) become tighter. The phragmosome and the PPB are both known predictors of the division plane and our observations indicate that they align simultaneously in elongated epidermal cells. These observations suggest another hypothesis: that the PPB may contain microtubules polymerized from the nuclear surface. In elongated cells, the majority of the radiating microtubules, therefore, come to anchor the nucleus in the transverse plane, consistent with the observed tendency of such cells to divide perpendicular to the long axis. In nonrectangular isodiametric epidermal cells, which approximate regular hexagons in section, the radial microtubular strands emanating from the nucleus tend to remain associated with the middle of each subtending cell wall. The strands are not reorganized into a single dominant transverse bar, but remain as a starlike array until mitosis. PPBs in these cells are not as tight; they may only be a sparse accumulation of microtubules, even forming along non-diametrical radii. This arrangement is consistent with the irregular division patterns observed in epidermal mosaics of isodiametric D. stramonium cells. The various conformations of the radial strands can be modeled by springs held in two-dimensional hexagonal frames, and by soap bubbles in three-dimensional hexagonal frames, suggesting that the division plane may, by analogy, be selected by minimal path criteria. Such behavior offers a cytoplasmic explanation of long-standing empirically derived "rules" which state that the new cell wall tends to meet the maternal wall at right angles. The radial premitotic strands and their analogues avoid taking the longer path to the vertex of an angle where a cross wall is already present between neighboring cells.(ABSTRACT TRUNCATED AT 400 WORDS)


1988 ◽  
Vol 36 (8) ◽  
pp. 1037-1041 ◽  
Author(s):  
K G Weis ◽  
V S Polito ◽  
J M Labavitch

We examined the middle lamella and the primary and secondary walls in almond pericarp dehiscence zone cells using a fluorescent cytochemical method which permitted specific, quantitative detection of pectic cell wall materials. Glycol methacrylate-embedded sections were stained with coriphosphine and pectin-specific fluorescent emissions at 630 nm were quantified using green excitation (546 nm). Examination of sectioned material extracted with purified pecto-lytic enzyme preparations was used to demonstrate the relative specificity of the staining reaction for pectic substances.


1987 ◽  
Vol 17 (8) ◽  
pp. 846-854 ◽  
Author(s):  
H. B. Massicotte ◽  
C. A. Ackerley ◽  
R. L. Peterson

Seedlings of Alnuscrispa (Ait.) Pursh, Alnusrubra Bong., Eucalyptuspilularis Sm., and Betulaalleghaniensis Britt. were grown in plastic pouches and subsequently inoculated with Alpovadiplophloeus (Zeller & Dodge) Trappe & Smith (two different strains), Pisolithustinctorius (Pers.) Coker & Couch, and Laccariabicolor (R. Mre) Orton, respectively, to form ectomycorrhizae insitu. Alnus seedlings were inoculated with Frankia prior to inoculation with the mycosymbiont. The interface established between A. crispa and A. diplophloeus was complex, involving wall ingrowth formation in root epidermal cells and infoldings in Hartig net hyphae. Alnusrubra – A. diplophloeus ectomycorrhizae had an interface lacking epidermal cell wall ingrowths but with infoldings in Hartig net hyphae. The interface between E. pilularis –. tinctorius consisted of branching Hartig net hyphae between radially enlarged epidermal cells lacking wall ingrowths. Ectomycorrhizae between B. alleghaniensis and L. bicolor developed unique interfaces with radially enlarged epidermal cells near the apical meristem, which synthesized dense vacuolar deposits. Very fine branchings occurred in Hartig net hyphae.


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