The chemical composition of glochids from Opuntia

1976 ◽  
Vol 54 (1-2) ◽  
pp. 173-176 ◽  
Author(s):  
Hayden N. Pritchard ◽  
James A. Hall

Glochids of two species of cactus were analyzed using infrared spectrophotometry and x-ray diffraction to determine their chemical constituency. The results were compared with calcium oxalate, a known constituent of many plant crystals, and with pure cellulose, the major component of plant cell walls. The analysis showed the glochids to be pure crystalline cellulose.

2020 ◽  
Author(s):  
Huimin Xu ◽  
Yuanyuan Zhao ◽  
Yuanzhen Suo ◽  
Yayu Guo ◽  
Yi Man ◽  
...  

Abstract Background: Cell wall imaging can considerably permit direct visualization of the molecular architecture of cell walls and provide the detailed chemical information on wall polymers, which is imperative to better exploit and use the biomass polymers; however, detailed imaging and quantifying of the native composition and architecture in the cell wall remains challenging.Results: Here, we describe a label-free imaging technology, coherent Raman scattering microscopy (CRS), including coherent anti-Stokes Raman scattering (CARS) microscopy and stimulated Raman scattering (SRS) microscopy, which images the major structures and chemical composition of plant cell walls. The major steps of the procedure are demonstrated, including sample preparation, setting the mapping parameters, analysis of spectral data, and image generation. Applying this rapid approach, which will help researchers understand the highly heterogeneous structures and organization of plant cell walls.Conclusions: This method can potentially be incorporated into label-free microanalyses of plant cell wall chemical composition based on the in situ vibrations of molecules.


2018 ◽  
Vol 24 (S2) ◽  
pp. 358-359
Author(s):  
Hayato Hiraki ◽  
Na Liu ◽  
Jian Wang ◽  
Jarvis Stobbs ◽  
Chithra Karunakaran ◽  
...  

2012 ◽  
Vol 442 (2) ◽  
pp. 241-252 ◽  
Author(s):  
Douglas B. Jordan ◽  
Michael J. Bowman ◽  
Jay D. Braker ◽  
Bruce S. Dien ◽  
Ronald E. Hector ◽  
...  

Conversion of plant cell walls to ethanol constitutes second generation bioethanol production. The process consists of several steps: biomass selection/genetic modification, physiochemical pretreatment, enzymatic saccharification, fermentation and separation. Ultimately, it is desirable to combine as many of the biochemical steps as possible in a single organism to achieve CBP (consolidated bioprocessing). A commercially ready CBP organism is currently unreported. Production of second generation bioethanol is hindered by economics, particularly in the cost of pretreatment (including waste management and solvent recovery), the cost of saccharification enzymes (particularly exocellulases and endocellulases displaying kcat ~1 s−1 on crystalline cellulose), and the inefficiency of co-fermentation of 5- and 6-carbon monosaccharides (owing in part to redox cofactor imbalances in Saccharomyces cerevisiae).


Plant Methods ◽  
2021 ◽  
Vol 17 (1) ◽  
Author(s):  
Huimin Xu ◽  
Yuanyuan Zhao ◽  
Yuanzhen Suo ◽  
Yayu Guo ◽  
Yi Man ◽  
...  

Abstract Background New cell wall imaging tools permit direct visualization of the molecular architecture of cell walls and provide detailed chemical information on wall polymers, which will aid efforts to use these polymers in multiple applications; however, detailed imaging and quantification of the native composition and architecture in the cell wall remains challenging. Results Here, we describe a label-free imaging technology, coherent Raman scattering (CRS) microscopy, including coherent anti-Stokes Raman scattering (CARS) microscopy and stimulated Raman scattering (SRS) microscopy, which can be used to visualize the major structures and chemical composition of plant cell walls. We outline the major steps of the procedure, including sample preparation, setting the mapping parameters, analysis of spectral data, and image generation. Applying this rapid approach will help researchers understand the highly heterogeneous structures and organization of plant cell walls. Conclusions This method can potentially be incorporated into label-free microanalyses of plant cell wall chemical composition based on the in situ vibrations of molecules.


2011 ◽  
Vol 12 (7) ◽  
pp. 2434-2439 ◽  
Author(s):  
Anna L. Barnette ◽  
Laura C. Bradley ◽  
Brandon D. Veres ◽  
Edward P. Schreiner ◽  
Yong Bum Park ◽  
...  

1976 ◽  
Vol 22 (4) ◽  
pp. 486-494 ◽  
Author(s):  
D. R. Letourneau ◽  
J. M. Deven ◽  
M. S. Manocha

Mechanically isolated, cytoplasm-free cell walls of Choanephora cucurbitarum were analyzed qualitatively and quantitatively by use of microchemical methods, infrared spectrophotometry, and X-ray diffraction. Chemical analysis of cell wall revealed the presence of chitin (17%), chitosan (28.4%), neutral sugars (7.2%), uronic acid (2.4%), proteins (8.2%), and lipids (13.8%). The structure of hyphal wall, investigated by electron microscopy of shadowed replicas before and after alkali-acid hydrolysis, showed two distinct regions: microfibrillar and amorphous. The microfibrils, which were composed of mainly chitin, were organized into two distinct layers; an outer, thicker layer of randomly oriented microfibrils, and an inner, thin layer of parallel microfibrils. In its structure and chemical composition the cell wall of C. cucurbitarum resembles those of other zygomycetous fungi.


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