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Liesche, J.

Publications and source records attributed to Liesche, J..

2 recordsLinked to original sources

Passive symplastic phloem loading in the duckweed Spirodela polyrhiza

The lemnoidae, commonly called duckweeds, are a group of small, rapidly growing aquatic plants that play an important role in pond ecosystems and are used in biotechnological and remediation applications. While small, duckweeds feature phloem tissue in fronds and roots. To gain insight on duckweed phloem function, we investigated how sugar is loaded into the phloem sieve elements in the giant duckweed Spirodela polyrhiza. Genomes of S. polyrhiza and three other duckweeds do not feature genes for the sucrose transporters typically associated with active apoplastic phloem loading. Neither did a sucrose transporter inhibitor affect sucrose concentration in phloem exudate. Active symplastic phloem loading was excluded based on the conventional plasmodesmata configuration and absence of oligosaccharides in S. polyrhiza phloem. Instead, uniform plasmodesmata density along the phloem loading pathway indicated a passive symplastic phloem loading type. When plasmodesmata permeability was artificially reduced by hormone treatment, the sucrose concentration in the phloem exudate was reduced, highlighting the potential role of plasmodesmata regulation in setting carbon export rates in species with passive phloem loading. Our results identify S. polyrhiza as the first monocot species with passive phloem loading. Moreover, they indicate opportunities for optimization of duckweed growth.

plant biology↗

Predicting plasmodesmata-mediated interface permeability and intercellular diffusion

Intercellular communication is essential for plant development and responses to biotic and abiotic stress. A key pathway is diffusive exchange of signal molecules and nutrients via plasmodesmata. These cell wall channels connect the cytoplasms of most cells in land plants. Their small size, with a typical diameter of about 50 nm, and complex structure have hindered the quantification plasmodesmata-mediated intercellular diffusion. This measure is essential for disentangling the contributions of diffusive and membrane transporter-mediated movement of molecules that, together, define cell interactions within and across tissues. We compared the two most promising methods to measure plasmodesmata-mediated interface permeability, live-cell microscopy with fluorescent tracer molecules and transmission electron microscopy-based mathematical modeling, to evaluate the potential for obtaining absolute quantitative values. We applied both methods to 29 cell-cell interfaces from nine angiosperm species and found a stronger association between the modelled and experimentally determined interface permeabilities than between the experimentally-determined permeability and any single structural parameter. By feeding the values into a simulation of an artificial Arabidopsis leaf, we illustrate how interface permeabilities can help to predict diffusion patterns of defense-related molecules, such as glucosinolates and transcription factors.

plant biology↗