Composition of the cell wall in the stem and leaf sheath of wheat straw

2007 ◽  
Vol 104 (2) ◽  
pp. 1236-1240 ◽  
Author(s):  
Hui Yu ◽  
Ruigang Liu ◽  
Limei Qiu ◽  
Yong Huang
Keyword(s):  
IAWA Journal ◽  
2014 ◽  
Vol 35 (2) ◽  
pp. 127-137 ◽  
Author(s):  
Shengcheng Zhai ◽  
Yoshiki Horikawa ◽  
Tomoya Imai ◽  
Junji Sugiyama

The cell wall organization of leaf sheath fibers in different palm species was studied with polarized light microscopy (PLM) and transmission electron microscopy (TEM). The secondary wall of the fibers consisted of only two layers, S1 and S2. The thickness of the S1 layer in leaf sheath fibers from the different palm species ranged from 0.31 to 0.90 μm, with a mean value of 0.57 μm, which was thicker than that of tracheids and fibers in secondary xylem of conifers and dicotyledons. The thickness of the S2 layer ranged from 0.44 to 3.43 μm, with a mean value of 1.86 μm. The ratio of S1 thickness to the whole cell wall thickness in palm fibers appears to be higher than in secondary xylem fibers and tracheids. The lignin in the fiber walls is very electron dense which makes it difficult to obtain high contrast of the different layers in the secondary wall. To clarify the cell wall layering with cellulose microfibrils in different orientations, the fibrovascular bundles of the windmill palm (Trachycarpus fortunei) were delignified with different reaction time intervals. The treated fibers were surveyed using attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy analysis and TEM. The secondary fiber walls of windmill palm clearly showed only two layers at different reaction intervals with different lignin contents, even after almost all lignin was removed. We suggest that the two-layered structure in the secondary wall of palm leaf fibers, which presumably also applies to the homologous fibers in palm stems, is a specific character different from the fibers in other monocotyledons (such as bamboo and rattan) and dicot wood.


1990 ◽  
Vol 94 (2) ◽  
pp. 411-416 ◽  
Author(s):  
D M Gibeaut ◽  
N Karuppiah ◽  
Chang S-R ◽  
T G Brock ◽  
B Vadlamudi ◽  
...  

1989 ◽  
Vol 61 (1-2) ◽  
pp. 159-164 ◽  
Author(s):  
A. Schiesser ◽  
C. Filippi ◽  
A.A. Lepidi
Keyword(s):  

2014 ◽  
Vol 70 ◽  
pp. 347-355 ◽  
Author(s):  
Zhiliang Wu ◽  
Huanhuan Hao ◽  
Zahoor ◽  
Yuanyuan Tu ◽  
Zheng Hu ◽  
...  

2014 ◽  
Vol 55 ◽  
pp. 63-69 ◽  
Author(s):  
Mads A.T. Hansen ◽  
Louise I. Ahl ◽  
Henriette L. Pedersen ◽  
Bjørge Westereng ◽  
William G.T. Willats ◽  
...  

2018 ◽  
Vol 21 (1) ◽  
pp. 1303-1310 ◽  
Author(s):  
Tabussam Tufail ◽  
Farhan Saeed ◽  
Muhammad Imran ◽  
Muhammad Umair Arshad ◽  
Faqir Muhammad Anjum ◽  
...  

mBio ◽  
2011 ◽  
Vol 2 (6) ◽  
Author(s):  
Sarah Moraïs ◽  
Yoav Barak ◽  
Yitzhak Hadar ◽  
David B. Wilson ◽  
Yuval Shoham ◽  
...  

ABSTRACTIn nature, the complex composition and structure of the plant cell wall pose a barrier to enzymatic degradation. Nevertheless, some anaerobic bacteria have evolved for this purpose an intriguing, highly efficient multienzyme complex, the cellulosome, which contains numerous cellulases and hemicellulases. The rod-like cellulose component of the plant cell wall is embedded in a colloidal blend of hemicelluloses, a major component of which is xylan. In order to enhance enzymatic degradation of the xylan component of a natural complex substrate (wheat straw) and to study the synergistic action among different xylanases, we have employed a variation of the designer cellulosome approach by fabricating a tetravalent complex that includes the three endoxylanases ofThermobifida fusca(Xyn10A, Xyn10B, and Xyn11A) and an Xyl43A β-xylosidase from the same bacterium. Here, we describe the conversion of Xyn10A and Xyl43A to the cellulosomal mode. The incorporation of the Xyl43A enzyme together with the three endoxylanases into a common designer cellulosome served to enhance the level of reducing sugars produced during wheat straw degradation. The enhanced synergistic action of the four xylanases reflected their immediate juxtaposition in the complex, and these tetravalent xylanolytic designer cellulosomes succeeded in degrading significant (~25%) levels of the total xylan component of the wheat straw substrate. The results suggest that the incorporation of xylanases into cellulosome complexes is advantageous for efficient decomposition of recalcitrant cellulosic substrates—a distinction previously reserved for cellulose-degrading enzymes.IMPORTANCEXylanases are important enzymes for our society, due to their variety of industrial applications. Together with cellulases and other glycoside hydrolases, xylanases may also provide cost-effective conversion of plant-derived cellulosic biomass into soluble sugars en route to biofuels as an alternative to fossil fuels. Xylanases are commonly found in multienzyme cellulosome complexes, produced by anaerobic bacteria, which are considered to be among the most efficient systems for degradation of cellulosic biomass. Using a designer cellulosome approach, we have incorporated the entire xylanolytic system of the bacteriumThermobifida fuscainto defined artificial cellulosome complexes. The combined action of these designer cellulosomes versus that of the wild-type free xylanase system was then compared. Our data demonstrated that xylanolytic designer cellulosomes displayed enhanced synergistic activities on a natural recalcitrant wheat straw substrate and could thus serve in the development of advanced systems for improved degradation of lignocellulosic material.


2019 ◽  
Vol 272 ◽  
pp. 288-299 ◽  
Author(s):  
Thibaut M.B. Mouthier ◽  
Bake de Rink ◽  
Gijs van Erven ◽  
Peter de Gijsel ◽  
Henk A. Schols ◽  
...  

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