scholarly journals Optical Clearing of Plant Tissues for Fluorescence Imaging

Author(s):  
Daisuke Kurihara ◽  
Yoko Mizuta ◽  
Shiori Nagahara ◽  
Yoshikatsu Sato ◽  
Tetsuya Higashiyama
2014 ◽  
Vol 166 (4) ◽  
pp. 1684-1687 ◽  
Author(s):  
Cherish A. Warner ◽  
Meredith L. Biedrzycki ◽  
Samuel S. Jacobs ◽  
Randall J. Wisser ◽  
Jeffrey L. Caplan ◽  
...  

Author(s):  
Daisuke Kurihara ◽  
Yoko Mizuta ◽  
Shiori Nagahara ◽  
Tetsuya Higashiyama

Abstract To understand how the body of plants is made, it is essential to observe the morphology, structure, and arrangement of constituent cells. However, the opaque nature of the plant body makes it difficult to observe the internal structures directly under a microscope. To overcome this problem, we developed a reagent, ClearSee, that makes plants transparent (Kurihara et al. 2015), allowing direct observation of the inside of a plant body without inflicting damage on it, for example through physical cutting. However, because ClearSee is not effective in making some plant species and tissues transparent, in this study, we further improved its composition to prevent oxidation and have developed ClearSeeAlpha, which can be applied to a broader range of plant species and tissues. Sodium sulphite, one of the reductants, prevented brown pigmentation due to oxidation during clearing treatment. Using ClearSeeAlpha, we show that it is possible to obtain clear chrysanthemum leaves, tobacco and Torenia pistils, and fertilized Arabidopsis thaliana fruits—tissues which have hitherto been challenging to clear. Moreover, we show that the fluorescence intensity of purified fluorescent proteins emitting light of various colours was unaffected in the ClearSeeAlpha solution; only the fluorescence intensity of TagRFP was reduced by about half. ClearSeeAlpha should be useful in the discovery and analysis of biological phenomena occurring deep inside the plant tissues.


2014 ◽  
Vol 50 (62) ◽  
pp. 8547-8549 ◽  
Author(s):  
Mi-Jeong Park ◽  
Hak-Sung Jung ◽  
Young-Jae Kim ◽  
Young-Ju Kwon ◽  
Jin-Kyu Lee ◽  
...  

Fluorescence imaging of Fe ions in (a) leaf epidermal cells, (b) the stem, and (c) the root stem of Arabidopsis plants by the rapid, simple, and inexpensive photoinduced electron transfer (PET) fluorescent probing method.


Development ◽  
2015 ◽  
Vol 142 (23) ◽  
pp. 4168-4179 ◽  
Author(s):  
D. Kurihara ◽  
Y. Mizuta ◽  
Y. Sato ◽  
T. Higashiyama

Trees ◽  
2020 ◽  
Vol 34 (3) ◽  
pp. 783-790
Author(s):  
Liang Lu ◽  
Yangyang Cao ◽  
Qizouhong He ◽  
Wenchao Xu ◽  
Yan Zhang ◽  
...  

Author(s):  
John S. Gardner ◽  
W. M. Hess

Powdery mildews are characterized by the appearance of spots or patches of a white to grayish, powdery, mildewy growth on plant tissues, entire leaves or other organs. Ervsiphe cichoracearum, the powdery mildew of cucurbits is among the most serious parasites, and the most common. The conidia are formed similar to the process described for Ervsiphe graminis by Cole and Samson. Theconidial chains mature basipetally from a short, conidiophore mother-cell at the base of the fertile hypha which arises holoblastically from the conidiophore. During early development it probably elongates by polar-tip growth like a vegetative hypha. A septum forms just above the conidiophore apex. Additional septa develop in acropetal succession. However, the conidia of E. cichoracearum are more doliform than condia from E. graminis. The purpose of these investigations was to use scanning electron microscopy (SEM) to demonstrate the nature of hyphal growth and conidial formation of E. cichoracearum on field-grown squash leaves.


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