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  • 2015-2019  (3)
  • 1
    Online Resource
    Online Resource
    Annual Reviews ; 2016
    In:  Annual Review of Plant Biology Vol. 67, No. 1 ( 2016-04-29), p. 235-259
    In: Annual Review of Plant Biology, Annual Reviews, Vol. 67, No. 1 ( 2016-04-29), p. 235-259
    Abstract: Xyloglucan (XyG) is a matrix polysaccharide that is present in the cell walls of all land plants. It consists of a β-1,4-linked glucan backbone that is further substituted with xylosyl residues. These xylosyl residues can be further substituted with other glycosyl and nonglycosyl substituents that vary depending on the plant family and specific tissue. Advances in plant mutant isolation and characterization, functional genomics, and DNA sequencing have led to the identification of nearly all transferases and synthases necessary to synthesize XyG. Thus, in terms of the molecular mechanisms of plant cell wall polysaccharide biosynthesis, XyG is the most well understood. However, much remains to be learned about the molecular mechanisms of polysaccharide assembly and the regulation of these processes. Knowledge of the XyG biosynthetic machinery allows the XyG structure to be tailored in planta to ascertain the functions of this polysaccharide and its substituents in plant growth and interactions with the environment.
    Type of Medium: Online Resource
    ISSN: 1543-5008 , 1545-2123
    URL: Issue
    Language: English
    Publisher: Annual Reviews
    Publication Date: 2016
    detail.hit.zdb_id: 2098209-4
    SSG: 12
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  • 2
    In: The Plant Journal, Wiley, Vol. 81, No. 4 ( 2015-02), p. 537-547
    Abstract: Mixed‐linkage glucan ( MLG ) is a significant cell wall carbohydrate in grasses and an important carbon source for human consumption and biofuel production. MLG biosynthesis depends on the biochemical activity of membrane spanning glucan synthases encoded by the CSLH and CSLF cellulose synthase‐like gene families. CSLF proteins are the best characterized to date but relatively little information is known about their topology with respect to the biosynthetic membranes. In this study, we report on the topology of CSLF 6 protein derived from the model grass species Brachypodium distachyon (Bd CSLF 6) when it is expressed in heterologous systems. Using live cell imaging and immuno‐electron microscopy analyses of tobacco epidermal cells expressing Bd CSLF 6 , we demonstrate that a functional yellow fluorescent protein ( YFP ) fusion of Bd CSLF 6 is localized to the Golgi apparatus and that the Golgi localization of Bd CSLF 6 is sufficient for MLG biosynthesis. By implementing protease protection assays of Bd CSLF 6 expressed in the yeast Pichia pastoris , we also demonstrate that the catalytic domain, the N‐terminus and the C‐ terminus of the protein are exposed in the cytosol. Furthermore, we found that Bd CSLF 6 is capable of producing MLG not only in tobacco cells but also in Pichia , which generally does not produce MLG . Together, these results support the conclusion that Bd CSLF 6 can produce both of the linkages present in the (1,3;1,4)‐β‐ d ‐glucan chain of MLG and that the product is channelled at the Golgi into the secretory pathway for deposition into the cell wall.
    Type of Medium: Online Resource
    ISSN: 0960-7412 , 1365-313X
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2015
    detail.hit.zdb_id: 2020961-7
    SSG: 12
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  • 3
    In: The Plant Journal, Wiley, Vol. 93, No. 6 ( 2018-03), p. 1062-1075
    Abstract: Mixed‐linkage (1,3;1,4)‐β‐glucan ( MLG ) is a glucose polymer with beneficial effects on human health and high potential for the agricultural industry. MLG is present predominantly in the cell wall of grasses and is synthesized by cellulose synthase‐like F or H families of proteins, with CSLF 6 being the best‐characterized MLG synthase. Although the function of this enzyme in MLG production has been established, the site of MLG synthesis in the cell is debated. It has been proposed that MLG is synthesized at the plasma membrane, as occurs for cellulose and callose; in contrast, it has also been proposed that MLG is synthesized in the Golgi apparatus, as occurs for other matrix polysaccharides of the cell wall. Testing these conflicting possibilities is fundamentally important in the general understanding of the biosynthesis of the plant cell wall. Using immuno‐localization analyses with MLG ‐specific antibody in Brachypodium and in barley, we found MLG present in the Golgi, in post‐Golgi structures and in the cell wall. Accordingly, analyses of a functional fluorescent protein fusion of CSLF 6 stably expressed in Brachypodium demonstrated that the enzyme is localized in the Golgi. We also established that overproduction of MLG causes developmental and growth defects in Brachypodium as also occur in barley. Our results indicated that MLG production occurs in the Golgi similarly to other cell wall matrix polysaccharides, and supports the broadly applicable model in grasses that tight mechanisms control optimal MLG accumulation in the cell wall during development and growth. This work addresses the fundamental question of where mixed linkage (1,3;1,4)‐β‐glucan (MLG) is synthesized in plant cells. By analyzing the subcellular localization of MLG and MLG synthase in an endogenous system, we demonstrated that MLG synthesis occurs at the Golgi in Brachypodium and barley. A growth inhibition due to overproduced MLG in Brachypodium supports the general applicability of the model that a tight control of the cell wall polysaccharides accumulation is needed to maintain growth homeostasis during development.
    Type of Medium: Online Resource
    ISSN: 0960-7412 , 1365-313X
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2018
    detail.hit.zdb_id: 2020961-7
    SSG: 12
    Location Call Number Limitation Availability
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