Ultrastructural observations on guard cells of Vicia faba and Allium porrum

1972 ◽  
Vol 50 (6) ◽  
pp. 1405-1413 ◽  
Author(s):  
W. G. Allaway ◽  
George Setterfield

Stomata of Vicia faba and Allium porrum were examined in thin section with the electron microscope. Guard cells contained numerous mitochondria, few plastids, and relatively small vacuoles traversed by many strands of cytoplasm. Spherosomes were often observed but were variable in occurrence. Endoplasmic reticulum and dictyosomes were present, although not well developed. Scattered microtubules were present at the periphery of the cells. Microbodies were very rarely observed in guard cells and no plasmodesmata were ever seen in the guard cell walls. Plastids were small and irregular in outline in guard cells of both species. Guard cell plastids of V. faba contained abundant large starch granules. In both species thylakoids were few and grana were small in comparison with mesophyll plastids. The inner of the two bounding membranes of guard cell chloroplasts was extensively invaginated, forming a peripheral reticulum. This was not observed in mesophyll plastids of these species. Small groups of microtubule-like structures were often observed in V. faba guard cell plastids; microtubule-like structures were less frequent in A. porrum plastids, and were not in groups. The structures described are compared with those of other epidermal cells and mesophyll cells, and are discussed in relation to guard cell physiology.

2001 ◽  
Vol 44 (4) ◽  
pp. 405-410 ◽  
Author(s):  
Maria das Graças Sajo ◽  
Silvia Rodrigues Machado

The leaf ultrastructure of five Xyris species were examined using scanning electron microscope (SEM), transmission electron microscope (TEM) and histochemical methods. All studied leaves show some features in epidermis and mesophyll, which were of considerable adaptative significance to drought stress. Such features included the occurrence of a pectic layer on the stomatal guard cells and the presence of a network of pectic compounds in the cuticle. Pectic compunds were also in abundance in lamellated walls of the mesophyll cells and on the inner surface of the sclerified cell walls of the vascular bundle sheaths. There were also specialized chlorenchymatous "peg cells" in the mesophyll and drops of phenolic compounds inside the epidermal cells.


1973 ◽  
Vol 26 (2) ◽  
pp. 309 ◽  
Author(s):  
WG Allaway ◽  
TC Hsiao

A rolling technique is described with which cells in epidermal strips of V. faba were differentially broken so that only guard cells remained alive and functional. In rolled epidermis potassium was retained only in live guard cells, as judged by staining with cobaltinitrite.


2014 ◽  
Vol 37 (9) ◽  
pp. 2201-2210 ◽  
Author(s):  
SHU-WEI WANG ◽  
YING LI ◽  
XIAO-LU ZHANG ◽  
HAI-QIANG YANG ◽  
XUE-FEI HAN ◽  
...  

1988 ◽  
Vol 92 (5) ◽  
pp. 667-683 ◽  
Author(s):  
J I Schroeder

Electrical properties of the plasma membrane of guard cell protoplasts isolated from stomates of Vicia faba leaves were studied by application of the whole-cell configuration of the patch-clamp technique. The two types of K+ currents that have recently been identified in guard cells may allow efflux of K+ during stomatal closing, and uptake of K+ during stomatal opening (Schroeder et al., 1987). A detailed characterization of ion transport properties of the inward-rectifying (IK+,in) and the outward-rectifying (IK+,out) K+ conductance is presented here. The permeability ratios of IK+,in and IK+,out currents for K+ over monovalent alkali metal ions were determined. The resulting permeability sequences (PK+ greater than PRb+ greater than PNa+ greater than PLi+ much greater than PCs+) corresponded closely to the ion specificity of guard cell movements in V. faba. Neither K+ currents exhibited significant inactivation when K+ channels were activated for prolonged periods (greater than 10 min). The absence of inactivation may permit long durations of K+ fluxes, which occur during guard cell movements. Activation potentials of inward K+ currents were not shifted when external K+ concentrations were changed. This differs strongly from the behavior of inward-rectifying K+ channels in animal tissue. Blue light and fusicoccin induce hyperpolarization by stimulation of an electrogenic pump. From slow-whole-cell recordings it was concluded that electrogenic pumps require cytoplasmic substrates for full activation and that the magnitude of the pump current is sufficient to drive K+ uptake through IK+,in channels. First, direct evidence was gained for the hypothesis that IK+,in channels are a molecular pathway for K+ accumulation by the finding that IK+,in was blocked by Al3+ ions, which are known to inhibit stomatal opening but not closing. The results presented in this study strongly support a prominent role for IK+,in and IK+,out channels in K+ transport across the plasma membrane of guard cells.


2021 ◽  
Vol 22 (11) ◽  
pp. 5666
Author(s):  
Qingting Liu ◽  
Xiaoping Li ◽  
Joerg Fettke

Transitory starch granules result from complex carbon turnover and display specific situations during starch synthesis and degradation. The fundamental mechanisms that specify starch granule characteristics, such as granule size, morphology, and the number per chloroplast, are largely unknown. However, transitory starch is found in the various cells of the leaves of Arabidopsis thaliana, but comparative analyses are lacking. Here, we adopted a fast method of laser confocal scanning microscopy to analyze the starch granules in a series of Arabidopsis mutants with altered starch metabolism. This allowed us to separately analyze the starch particles in the mesophyll and in guard cells. In all mutants, the guard cells were always found to contain more but smaller plastidial starch granules than mesophyll cells. The morphological properties of the starch granules, however, were indiscernible or identical in both types of leaf cells.


2018 ◽  
Vol 115 (36) ◽  
pp. 9038-9043 ◽  
Author(s):  
Juntaro Negi ◽  
Shintaro Munemasa ◽  
Boseok Song ◽  
Ryosuke Tadakuma ◽  
Mayumi Fujita ◽  
...  

Stomatal guard cells develop unique chloroplasts in land plant species. However, the developmental mechanisms and function of chloroplasts in guard cells remain unclear. In seed plants, chloroplast membrane lipids are synthesized via two pathways: the prokaryotic and eukaryotic pathways. Here we report the central contribution of endoplasmic reticulum (ER)-derived chloroplast lipids, which are synthesized through the eukaryotic lipid metabolic pathway, in the development of functional guard cell chloroplasts. We gained insight into this pathway by isolating and examining an Arabidopsis mutant, gles1 (green less stomata 1), which had achlorophyllous stomatal guard cells and impaired stomatal responses to CO2 and light. The GLES1 gene encodes a small glycine-rich protein, which is a putative regulatory component of the trigalactosyldiacylglycerol (TGD) protein complex that mediates ER-to-chloroplast lipid transport via the eukaryotic pathway. Lipidomic analysis revealed that in the wild type, the prokaryotic pathway is dysfunctional, specifically in guard cells, whereas in gles1 guard cells, the eukaryotic pathway is also abrogated. CO2-induced stomatal closing and activation of guard cell S-type anion channels that drive stomatal closure were disrupted in gles1 guard cells. In conclusion, the eukaryotic lipid pathway plays an essential role in the development of a sensing/signaling machinery for CO2 and light in guard cell chloroplasts.


1975 ◽  
Vol 53 (16) ◽  
pp. 1698-1711 ◽  
Author(s):  
R. L. Peterson ◽  
M. S. Firminger ◽  
L. A. Dobrindt

A β-1,3-glucan which has characteristics of callose was identified as a component of the cell wall in stomatal guard cells in three species of the fern, Ophioglossum. This identification was made by the fluorochrome properties of callose when stained with aqueous solutions of aniline blue. Controls involved both the effect of solutions of different pH on autofluorescence of guard cell walls and the extraction of leaf tissues with β-1,3-glucanases before staining with aniline blue. An electron-translucent region between the plasmalemma and the cell wall proper was observed with the electron microscope and corresponded in position with the areas that fluoresced after aniline blue staining.Other components of the guard cell wall identified included cellulose, which was identified by staining techniques, polarization microscopy, and electron microscopy; and a phenolic substance identified by a number of staining reactions. The cell wall failed to stain with a number of reagents for the identification of lignin.


2003 ◽  
Vol 159 (1) ◽  
pp. 195-202 ◽  
Author(s):  
Gerhard Ritte ◽  
Klaus Raschke

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