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A novel xylogenic suspension culture model for exploring lignification in Phyllostachys bamboo

BACKGROUND: Some prominent cultured plant cell lines, such as the BY-2 cell line of tobacco (Nicotiana tabacum cv. ‘Bright Yellow 2’) and the T87 cell line of Arabidopsis (Arabidopsis thaliana L. Heynh., ecotype Columbia) are used as model plant cells. These suspension cell culture systems are highl...

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Detalles Bibliográficos
Autores principales: Ogita, Shinjiro, Nomura, Taiji, Kishimoto, Takao, Kato, Yasuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462127/
https://www.ncbi.nlm.nih.gov/pubmed/22978662
http://dx.doi.org/10.1186/1746-4811-8-40
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author Ogita, Shinjiro
Nomura, Taiji
Kishimoto, Takao
Kato, Yasuo
author_facet Ogita, Shinjiro
Nomura, Taiji
Kishimoto, Takao
Kato, Yasuo
author_sort Ogita, Shinjiro
collection PubMed
description BACKGROUND: Some prominent cultured plant cell lines, such as the BY-2 cell line of tobacco (Nicotiana tabacum cv. ‘Bright Yellow 2’) and the T87 cell line of Arabidopsis (Arabidopsis thaliana L. Heynh., ecotype Columbia) are used as model plant cells. These suspension cell culture systems are highly applicable for investigating various aspects of plant cell biology. However, no such prominent cultured cell lines exist in bamboo species. RESULTS: We standardized a novel xylogenic suspension culture model in order to unveil the process of lignification in living bamboo cells. Initial signs of lignin deposition were able to be observed by a positive phloroglucinol-HCl reaction at day 3 to 5 under lignification conditions (LG), i.e., modified half-strength Murashige and Skoog medium (m1/2MS) containing 10 μM 6-benzyladenine (BA) and 3% sucrose. Two types of xylogenic differentiation, both fiber-like elements (FLEs) with cell wall thickening and tracheary elements (TEs) with formation of perforations in the cell wall, were observed under these conditions. The suspension cells rapidly formed secondary cell wall components that were highly lignified, making up approximately 25% of the cells on a dry weight basis within 2 weeks. Detailed features involved in cell growth, differentiation and death during lignification were characterized by laser scanning microscopic imaging. Changes in transcript levels of xylogenesis-related genes were assessed by RT-PCR, which showed that the transcription of key genes like PAL1, C4H, CCoAOMT, and CCR was induced at day 4 under LG conditions. Furthermore, interunit linkage of lignins was compared between mature bamboo culms and xylogenic suspension cells by heteronuclear single quantum coherence (HSQC) NMR spectroscopy. The presence of the most common interunit linkages, including β-aryl ether (β-O-4), phenylcoumaran (β-5) and resinol (β-β) structures was identified in the bamboo cultured cell lignin (BCCL) by HSQC NMR. In addition to these common features of lignin, several differences in lignin substructures were also found between the BCCL and the bamboo milled wood lignin (BMWL). CONCLUSIONS: Our xylogenic suspension culture model could be used for detailed characterization of physiological and molecular biological events in living bamboo cells.
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spelling pubmed-34621272012-10-02 A novel xylogenic suspension culture model for exploring lignification in Phyllostachys bamboo Ogita, Shinjiro Nomura, Taiji Kishimoto, Takao Kato, Yasuo Plant Methods Methodology BACKGROUND: Some prominent cultured plant cell lines, such as the BY-2 cell line of tobacco (Nicotiana tabacum cv. ‘Bright Yellow 2’) and the T87 cell line of Arabidopsis (Arabidopsis thaliana L. Heynh., ecotype Columbia) are used as model plant cells. These suspension cell culture systems are highly applicable for investigating various aspects of plant cell biology. However, no such prominent cultured cell lines exist in bamboo species. RESULTS: We standardized a novel xylogenic suspension culture model in order to unveil the process of lignification in living bamboo cells. Initial signs of lignin deposition were able to be observed by a positive phloroglucinol-HCl reaction at day 3 to 5 under lignification conditions (LG), i.e., modified half-strength Murashige and Skoog medium (m1/2MS) containing 10 μM 6-benzyladenine (BA) and 3% sucrose. Two types of xylogenic differentiation, both fiber-like elements (FLEs) with cell wall thickening and tracheary elements (TEs) with formation of perforations in the cell wall, were observed under these conditions. The suspension cells rapidly formed secondary cell wall components that were highly lignified, making up approximately 25% of the cells on a dry weight basis within 2 weeks. Detailed features involved in cell growth, differentiation and death during lignification were characterized by laser scanning microscopic imaging. Changes in transcript levels of xylogenesis-related genes were assessed by RT-PCR, which showed that the transcription of key genes like PAL1, C4H, CCoAOMT, and CCR was induced at day 4 under LG conditions. Furthermore, interunit linkage of lignins was compared between mature bamboo culms and xylogenic suspension cells by heteronuclear single quantum coherence (HSQC) NMR spectroscopy. The presence of the most common interunit linkages, including β-aryl ether (β-O-4), phenylcoumaran (β-5) and resinol (β-β) structures was identified in the bamboo cultured cell lignin (BCCL) by HSQC NMR. In addition to these common features of lignin, several differences in lignin substructures were also found between the BCCL and the bamboo milled wood lignin (BMWL). CONCLUSIONS: Our xylogenic suspension culture model could be used for detailed characterization of physiological and molecular biological events in living bamboo cells. BioMed Central 2012-09-14 /pmc/articles/PMC3462127/ /pubmed/22978662 http://dx.doi.org/10.1186/1746-4811-8-40 Text en Copyright ©2012 Ogita et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology
Ogita, Shinjiro
Nomura, Taiji
Kishimoto, Takao
Kato, Yasuo
A novel xylogenic suspension culture model for exploring lignification in Phyllostachys bamboo
title A novel xylogenic suspension culture model for exploring lignification in Phyllostachys bamboo
title_full A novel xylogenic suspension culture model for exploring lignification in Phyllostachys bamboo
title_fullStr A novel xylogenic suspension culture model for exploring lignification in Phyllostachys bamboo
title_full_unstemmed A novel xylogenic suspension culture model for exploring lignification in Phyllostachys bamboo
title_short A novel xylogenic suspension culture model for exploring lignification in Phyllostachys bamboo
title_sort novel xylogenic suspension culture model for exploring lignification in phyllostachys bamboo
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3462127/
https://www.ncbi.nlm.nih.gov/pubmed/22978662
http://dx.doi.org/10.1186/1746-4811-8-40
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