scholarly journals Are diurnal patterns of stomatal movement the result of alternating metabolism of endogenous guard cell ABA and accumulation of ABA delivered to the apoplast around guard cells by transpiration?

2004 ◽  
Vol 55 (405) ◽  
pp. 1963-1976 ◽  
Author(s):  
G. Tallman
2019 ◽  
Vol 20 (11) ◽  
pp. 2753
Author(s):  
Xin Li ◽  
Min Diao ◽  
Yanan Zhang ◽  
Guanlin Chen ◽  
Shanjin Huang ◽  
...  

The actin cytoskeleton is involved in regulating stomatal movement, which forms distinct actin arrays within guard cells of stomata with different apertures. How those actin arrays are formed and maintained remains largely unexplored. Elucidation of the dynamic behavior of differently oriented actin filaments in guard cells will enhance our understanding in this regard. Here, we initially developed a program called ‘guard cell microfilament analyzer’ (GCMA) that enables the selection of individual actin filaments and analysis of their orientations semiautomatically in guard cells. We next traced the dynamics of individual actin filaments and performed careful quantification in open and closed stomata. We found that de novo nucleation of actin filaments occurs at both dorsal and ventral sides of guard cells from open and closed stomata. Interestingly, most of the nucleated actin filaments elongate radially and longitudinally in open and closed stomata, respectively. Strikingly, radial filaments tend to form bundles whereas longitudinal filaments tend to be removed by severing and depolymerization in open stomata. By contrast, longitudinal filaments tend to form bundles that are severed less frequently in closed stomata. These observations provide insights into the formation and maintenance of distinct actin arrays in guard cells in stomata of different apertures.


2021 ◽  
Vol 12 ◽  
Author(s):  
Li-Na Yang ◽  
Hao Liu ◽  
Yan-Ping Wang ◽  
Jenifer Seematti ◽  
Laura J. Grenville-Briggs ◽  
...  

Phytophthora infestans, the most damaging oomycete pathogen of potato, is specialized to grow sporangiophore through opened stomata for secondary inoculum production. However, it is still unclear which metabolic pathways in potato are manipulated by P. infestans in the guard cell–pathogen interactions to open the stomata. Here microscopic observations and cell biology were used to investigate antagonistic interactions between guard cells and the oomycete pathogen. We observed that the antagonistic interactions started at the very beginning of infection. Stomatal movement is an important part of the immune response of potato to P. infestans infection and this occurs through guard cell death and stomatal closure. We observed that P. infestans appeared to manipulate metabolic processes in guard cells, such as triacylglycerol (TAG) breakdown, starch degradation, H2O2 scavenging, and NO catabolism, which are involved in stomatal movement, to evade these stomatal defense responses. The signal transduction pathway of P. infestans-induced stomatal opening likely starts from H2O2 and NO scavenging, along with TAG breakdown while the subsequent starch degradation reinforces the opening process by strengthening guard cell turgor and opening the stomata to their maximum aperture. These results suggest that stomata are a barrier stopping P. infestans from completing its life cycle, but this host defense system can be bypassed through the manipulation of diverse metabolic pathways that may be induced by P. infestans effector proteins.


2020 ◽  
Vol 22 ◽  
Author(s):  
Suren Jeevaratnam ◽  
Chuwei Lin ◽  
Sixue Chen

The primary goal of this study was to determine the effect of sonication on stomatal movement. A minor goal was to determine the best time interval at which sonication is the most effective at removing mesophyll cells and enriching guard cells. For this study, abaxial leaf peels of Arabidopsis thaliana were sonicated for 1, 3, 5, and 7-minute intervals at a set amplitude to analyze the removal of mesophyll cells. To juxtapose the leaves and to determine guard cell enrichment, microscopic images were taken prior to and after sonication. Furthermore, to establish that the stomata are alive, neutral red staining was used in conjunct with 40x magnification. It was hypothesized that sonication is an effective method for the removal of mesophyll cells and the enrichment of guard cells. The results of this study suggest that sonication is in fact an effective protocol for guard cell enrichment; however, it is not as effective for guard cell purification. This is due to the presence of mesophyll cells and epidermal layers present after sonication. Previous research dealing with sonication is very prevalent; however, research on sonication dealing with the removal of mesophyll cells in Arabidopsis thaliana is not widely studied. Thus, previous information to support this study could not be attained. Results from the first part of the experiment were then extended to determine how sonication affects stomatal movement. It was determined that in the experimental group, the average stomatal aperture decreased over a two-hour period.


2009 ◽  
Vol 35 (8) ◽  
pp. 1491-1499 ◽  
Author(s):  
Lin ZHANG ◽  
Xiang ZHAO ◽  
Ya-Jing WANG ◽  
Xiao ZHANG

1993 ◽  
Vol 44 (10) ◽  
pp. 1569-1577 ◽  
Author(s):  
WILFRIED DIEKMANN ◽  
RAINER HEDRICH ◽  
KLAUS RASCHKE ◽  
DAVID G. ROBINSON

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.


2015 ◽  
Vol 208 (2) ◽  
pp. 342-353 ◽  
Author(s):  
Kai Shi ◽  
Xin Li ◽  
Huan Zhang ◽  
Guanqun Zhang ◽  
Yaru Liu ◽  
...  

2015 ◽  
Vol 6 ◽  
Author(s):  
Biswapriya B. Misra ◽  
Biswa R. Acharya ◽  
David Granot ◽  
Sarah M. Assmann ◽  
Sixue Chen

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