scholarly journals Determining the Size Exclusion for Nanoparticles in Citrus Leaves

HortScience ◽  
2016 ◽  
Vol 51 (6) ◽  
pp. 732-737 ◽  
Author(s):  
Ed Etxeberria ◽  
Pedro Gonzalez ◽  
Priyanka Bhattacharya ◽  
Parvesh Sharma ◽  
Pu Chun Ke

Implementation of nanotechnology in agriculture is intimately dependent on the capacity of nanoparticles (NPs) to move within the plant body and reach the targeted cells. Although the fibrillar nature of the plant cell wall permits the movement of molecules through its porous matrix (apoplast), the movement of particles through the aqueous apoplastic milieu has its size limitations given the tightly knitted cellulose/hemicellulose fiber structure. In the present study, we used fluorescent NPs of different composition and sizes, and followed their movement into citrus leaves by fluorescent microscopy. Our results indicate that in citrus leaves, the size exclusion limit for NPs is of ≈5.4 nm. This conclusion was based on the capacity of PAMAM dendrimers G-4 and G-5 (4.5 and 5.4 nm, respectively) to move through the cell wall and into the phloem, but failure of similar PAMAM dendrimers G-6 (6.7 nm) to move through the apoplast. Dendrimer NPs 5.4 nm and smaller were observed to penetrate the leaf tissue, and then taken up and mobilized by the phloem elements. The current study provides evidence on the size limit for NPs use in agriculture.

Development ◽  
2002 ◽  
Vol 129 (5) ◽  
pp. 1261-1272 ◽  
Author(s):  
Insoon Kim ◽  
Frederick D. Hempel ◽  
Kyle Sha ◽  
Jennifer Pfluger ◽  
Patricia C. Zambryski

Plasmodesmata provide routes for communication and nutrient transfer between plant cells by interconnecting the cytoplasm of adjacent cells. A simple fluorescent tracer loading assay was developed to monitor patterns of cell-to-cell transport via plasmodesmata specifically during embryogenesis. A developmental transition in plasmodesmatal size exclusion limit was found to occur at the torpedo stage of embryogenesis in Arabidopsis; at this time, plasmodesmata are down-regulated, allowing transport of small (approx. 0.5 kDa) but not large (approx. 10 kDa) tracers. This assay system was used to screen for embryo-defective mutants, designated increased size exclusion limit of plasmodesmata(ise), that maintain dilated plasmodesmata at the torpedo stage. The morphology of ise1 and ise2 mutants discussed here resembled that of the wild-type during embryo development, although the rate of their embryogenesis was slower. The ISE1 gene was mapped to position 13 cM on chromosome I using PCR-based biallelic markers. ise2 was found to be allelic to the previously characterized mutant emb25 which maps to position 100 cM on chromosome I. The results presented have implications for intercellular signaling pathways that regulate embryonic development, and furthermore represent the first attempt to screen directly for mutants of Arabidopsis with altered size exclusion limit of plasmodesmata.


2015 ◽  
Vol 39 (1) ◽  
pp. 165-173 ◽  
Author(s):  
Nicolas Carlotto ◽  
Sonia Wirth ◽  
Nicolas Furman ◽  
Nazarena Ferreyra Solari ◽  
Federico Ariel ◽  
...  

2012 ◽  
Vol 66 (9) ◽  
Author(s):  
Zuzana Zemková ◽  
Soňa Garajová ◽  
Dana Flodrová ◽  
Pavel Řehulka ◽  
Ivan Zelko ◽  
...  

AbstractProtein extract of germinating nasturtium (Tropaeolum majus) seeds containing xyloglucan endotransglycosylase (xyloglucan xyloglucosyl transferase, EC 2.4.1.207, abbreviated XET) exhibited the heterotransglycosylating activity with donor/acceptor substrate pair xyloglucan/sulphorhodamine labelled pustulooligosaccharides (XG/PUOS-SR) in a dot blot assay. The heterotransglycosylating activity was confirmed by the substrate-product changes during transglycosylation by HPLC size-exclusion chromatography. Another donor substrate capable of being coupled with PUOS-SR was cellulose, probably owing to its structural similarity to xyloglucan. Surprisingly, microscopic comparison of the incorporation of the labelled xyloglucan nonasaccharide XGO9-SR (specific substrate for XET) and PUOS-SR into the cell wall structures clearly showed differences in their binding to specific cell structures: the primary cell wall and the plasma membrane. These findings indicate the existence in nasturtium of XETs with different localisation, substrate specificity and, probably, function.


Science ◽  
1989 ◽  
Vol 246 (4928) ◽  
pp. 377-379 ◽  
Author(s):  
S. WOLF ◽  
W. J. LUCAS ◽  
C. M. DEOM ◽  
R. N. BEACHY

2010 ◽  
Vol 22 (4) ◽  
pp. 1373-1387 ◽  
Author(s):  
Shengzhong Su ◽  
Zhaohui Liu ◽  
Cheng Chen ◽  
Yan Zhang ◽  
Xu Wang ◽  
...  

2010 ◽  
Vol 5 (12) ◽  
pp. 1663-1665 ◽  
Author(s):  
Cheng Chen ◽  
Yan Zhang ◽  
Lei Zhu ◽  
Ming Yuan

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