scholarly journals Radial Movement of Minerals in the Trunks of Standing Japanese Cedar (Cryptomeria Japonica D. Don) Trees in Summer by Tracer Analysis

Forests ◽  
2020 ◽  
Vol 11 (5) ◽  
pp. 562
Author(s):  
Katsushi Kuroda ◽  
Kenichi Yamane ◽  
Yuko Itoh

The radial movement of minerals in tree trunks is a widely accepted function of ray parenchyma cells, but there is little experimental evidence for this. We previously obtained experimental data showing that the parenchyma cells were the site of the radial mineral movement in Japanese cedar (Cryptomeria japonica D. Don) trunks in winter. Therefore, the aim of this study was to answer two remaining questions: do parenchyma cells move minerals via active transport or passive diffusion and how do seasonality and the injection duration affect the radial movement of minerals. To analyze this, we compared mineral movement in living standing Japanese cedar trees with heartwood in which the trunk had been left untreated or freeze–thawed with liquid nitrogen to kill the living cells. A solution of a stable isotope of cesium (Cs), as a tracer of mineral movement, was continuously injected into the outer sapwood of these normal and freeze–thaw-treated trees for an objective period, following which the trunk was freeze-fixed with liquid nitrogen. The Cs distribution in frozen samples was then analyzed by cryo-scanning electron microscopy/energy-dispersive X-ray spectroscopy. After 1 and 5 days of injection, the Cs detection area was almost the same among parenchyma cells and tracheid cell walls in the freeze–thaw-treated samples (without living cells) but was further toward the inner xylem in the parenchyma cells than the tracheids in the normal samples (with living cells), indicating that living parenchyma cells move Cs. Furthermore, after 5 days of injection, Cs in the tracheid cell walls was detected further toward the inner xylem in the normal samples than in the freeze–thaw-treated samples, indicating that Cs is exuded from the parenchyma cells into the tracheid cell walls. Together, these results suggest that the radial movement of minerals in standing Japanese cedar trees occurs through a combination of active transport by parenchyma cells and diffusion in the cell walls.


Forests ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 251
Author(s):  
Katsushi Kuroda ◽  
Kenichi Yamane ◽  
Yuko Itoh

Although the radial movement of minerals in tree trunks is a widely accepted phenomenon, experimental evidence of their movement in standing trees and underlying mechanisms is very limited. Previously, we clarified that cesium (Cs) artificially injected into the outer part of the sapwood of standing Japanese cedar (Cryptomeria japonica D. Don) trunks moved to the inner part of the sapwood, including the intermediate wood, via active transport by xylem parenchyma cells and diffusion through cell walls and then moved into the heartwood by diffusion. To understand the mechanism underlying the radial movement of minerals in the standing tree trunk, it is necessary to clarify their movement in the opposite direction. Therefore, the present study aimed to determine the radial movement of minerals from inside to outside in the trunks of standing trees at the cellular level. For this, a long hole across the center part of the trunk, which reached the heartwood, intermediate wood, and sapwood, was made in standing Japanese cedar trunks, and a solution of stable isotope Cs was continuously injected into the hole for several days as a tracer. The injected part of the trunk was collected after being freeze-fixed with liquid nitrogen, and the frozen sample was subjected to analysis of Cs distribution at the cellular level using cryo-scanning electron microscopy/energy-dispersive X-ray spectroscopy. The Cs injected into the inner sapwood or intermediate wood rapidly moved toward the outer sapwood via xylem ray parenchyma cells together with diffusion through the cell walls. In contrast, the Cs injected into the heartwood barely moved to the sapwood, although it reached a part of the inner intermediate wood. These results suggest that minerals in xylem ray parenchyma cells in the sapwood are bidirectionally supplied to each other; however, the minerals accumulated in the heartwood may not be supplied to living cells.





2011 ◽  
Vol 57 (5) ◽  
pp. 421-428 ◽  
Author(s):  
Naoki Okada ◽  
Yasuhiko Hirakawa ◽  
Yukio Katayama


Holzforschung ◽  
2015 ◽  
Vol 69 (3) ◽  
pp. 273-279 ◽  
Author(s):  
Toru Kanbayashi ◽  
Hisashi Miyafuji

Abstract Japanese cedar (Cryptomeria japonica) was treated with the ionic liquid (IL) 1-ethyl-3-methylimidazolium chloride ([C2mim][Cl]), which is a solvent for cellulose, and the changes in the chemical components and their distribution in wood cell walls have been investigated by Raman microscopy. Raman spectra, recorded from various areas of the cell walls, showed that lignin in the compound middle lamellae (CML) and cell corners (CC) was resistant to the reaction with [C2mim][Cl], but its molecular structure changed partially. The reactivity of cellulose and hemicelluloses with [C2mim][Cl] was higher than that of lignin in the cell wall, and the cell wall structure was maintained even in an advanced state of the reactions. The effects of [C2mim]-[Cl] on cellulose and hemicelluloses in the cell wall were homogeneous, whereas that of lignin was inhomogeneous.



Fuel ◽  
2021 ◽  
Vol 292 ◽  
pp. 120287
Author(s):  
Weibo Han ◽  
Gang Zhou ◽  
Junpeng Wang ◽  
Wenjing Jiang ◽  
Qian Zhang ◽  
...  


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Yoshihiko Nanasato ◽  
Masafumi Mikami ◽  
Norihiro Futamura ◽  
Masaki Endo ◽  
Mitsuru Nishiguchi ◽  
...  

AbstractCryptomeria japonica (Japanese cedar or sugi) is one of the most important coniferous tree species in Japan and breeding programs for this species have been launched since 1950s. Genome editing technology can be used to shorten the breeding period. In this study, we performed targeted mutagenesis using the CRISPR/Cas9 system in C. japonica. First, the CRISPR/Cas9 system was tested using green fluorescent protein (GFP)-expressing transgenic embryogenic tissue lines. Knock-out efficiency of GFP ranged from 3.1 to 41.4% depending on U6 promoters and target sequences. The GFP knock-out region was mottled in many lines, indicating genome editing in individual cells. However, in 101 of 102 mutated individuals (> 99%) from 6 GFP knock-out lines, embryos had a single mutation pattern. Next, we knocked out the endogenous C. japonica magnesium chelatase subunit I (CjChlI) gene using two guide RNA targets. Green, pale green, and albino phenotypes were obtained in the gene-edited cell lines. Sequence analysis revealed random deletions, insertions, and replacements in the target region. Thus, targeted mutagenesis using the CRISPR/Cas9 system can be used to modify the C. japonica genome.



2018 ◽  
Vol 74 (3) ◽  
pp. 123-127 ◽  
Author(s):  
Shin NAGAI ◽  
Taku M. SAITOH ◽  
Koji KAJIWARA ◽  
Shinpei YOSHITAKE ◽  
Yoshiaki HONDA


2006 ◽  
Vol 61 (5-6) ◽  
pp. 347-350 ◽  
Author(s):  
Rilka M. Taskova ◽  
Holger Zorn ◽  
Ulrich Krings ◽  
Henning Bouws ◽  
Ralf G. Berger

Different techniques were compared for their effectiveness in the disruption of the rigid cell walls of Basidiomycetes. Grinding under liquid nitrogen, stirred glass bead milling and enzymatic cell lysis were applied to the mycelia of Pleurotus sapidus and Lepista irina grown submerged. Each of the disruption procedures was evaluated by testing the quantity and quality of released intracellular metabolites: DNA, RNA, enzymes, and secondary metabolites. The most suitable method for nucleic acid isolation was grinding under liquid nitrogen, while bead mill homogenization was the superior technique for isolation of active enzymes. A new effective method is proposed for isolation of secondary metabolites with the aid of bead milling of fungal mycelia.



1994 ◽  
Vol 105 (2) ◽  
pp. 198-202 ◽  
Author(s):  
Ako Hijikata ◽  
Isamu Matsumoto ◽  
Kyoko Kojima ◽  
Haruko Ogawa


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