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Inferring the role of pit membranes in solute transport from solute exclusion studies in living conifer stems

The functional role of pits between living and dead cells has been inferred from anatomical studies but amassing physiological evidence has been challenging. Centrifugation methods were used to strip water from xylem conduits, permitting a more quantitative gravimetric determination of the water and...

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Autores principales: Yang, Dongmei, Wei, Kailu, Li, Junhui, Peng, Guoquan, Tyree, Melvin T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7210765/
https://www.ncbi.nlm.nih.gov/pubmed/32020191
http://dx.doi.org/10.1093/jxb/eraa058
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author Yang, Dongmei
Wei, Kailu
Li, Junhui
Peng, Guoquan
Tyree, Melvin T
author_facet Yang, Dongmei
Wei, Kailu
Li, Junhui
Peng, Guoquan
Tyree, Melvin T
author_sort Yang, Dongmei
collection PubMed
description The functional role of pits between living and dead cells has been inferred from anatomical studies but amassing physiological evidence has been challenging. Centrifugation methods were used to strip water from xylem conduits, permitting a more quantitative gravimetric determination of the water and solid contents of cell walls than is possible by more traditional methods. Quantitative anatomical evidence was used to evaluate the water volume in xylem conduits and the water content of living cells. Quantitative perfusion of stems with polyethylene glycol of different molecular weight was used to determine the solute-free space. We measured the portioning of water and solute-free space among anatomical components in stems and demonstrated that lignin impeded the free movement of solutes with molecular weight >300. Hence, movement of large solutes from living cells to xylem conduits is necessarily confined to pit structures that permit transmembrane solute transport via primary walls without lignin. The functional role of pits was additionally indicated by combining data in this paper with previous studies of unusual osmotic relationships in woody species that lack pits between dead wood fibers and vessels. The absence of pits, combined with the evidence of exclusion of solutes of molecular weight >300, explains the unexpected osmotic properties.
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spelling pubmed-72107652020-05-14 Inferring the role of pit membranes in solute transport from solute exclusion studies in living conifer stems Yang, Dongmei Wei, Kailu Li, Junhui Peng, Guoquan Tyree, Melvin T J Exp Bot Research Papers The functional role of pits between living and dead cells has been inferred from anatomical studies but amassing physiological evidence has been challenging. Centrifugation methods were used to strip water from xylem conduits, permitting a more quantitative gravimetric determination of the water and solid contents of cell walls than is possible by more traditional methods. Quantitative anatomical evidence was used to evaluate the water volume in xylem conduits and the water content of living cells. Quantitative perfusion of stems with polyethylene glycol of different molecular weight was used to determine the solute-free space. We measured the portioning of water and solute-free space among anatomical components in stems and demonstrated that lignin impeded the free movement of solutes with molecular weight >300. Hence, movement of large solutes from living cells to xylem conduits is necessarily confined to pit structures that permit transmembrane solute transport via primary walls without lignin. The functional role of pits was additionally indicated by combining data in this paper with previous studies of unusual osmotic relationships in woody species that lack pits between dead wood fibers and vessels. The absence of pits, combined with the evidence of exclusion of solutes of molecular weight >300, explains the unexpected osmotic properties. Oxford University Press 2020-05-09 2020-02-05 /pmc/articles/PMC7210765/ /pubmed/32020191 http://dx.doi.org/10.1093/jxb/eraa058 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Yang, Dongmei
Wei, Kailu
Li, Junhui
Peng, Guoquan
Tyree, Melvin T
Inferring the role of pit membranes in solute transport from solute exclusion studies in living conifer stems
title Inferring the role of pit membranes in solute transport from solute exclusion studies in living conifer stems
title_full Inferring the role of pit membranes in solute transport from solute exclusion studies in living conifer stems
title_fullStr Inferring the role of pit membranes in solute transport from solute exclusion studies in living conifer stems
title_full_unstemmed Inferring the role of pit membranes in solute transport from solute exclusion studies in living conifer stems
title_short Inferring the role of pit membranes in solute transport from solute exclusion studies in living conifer stems
title_sort inferring the role of pit membranes in solute transport from solute exclusion studies in living conifer stems
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7210765/
https://www.ncbi.nlm.nih.gov/pubmed/32020191
http://dx.doi.org/10.1093/jxb/eraa058
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