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The Updegraff method is the most widely used method for the cellulose estimation. The main purpose of this demonstration is to provide a detailed Updegraff protocol for estimation of cellulose content in plant biomass samples.
Cellulose is the most abundant polymer on Earth generated by photosynthesis and the main load-bearing component of cell walls. The cell wall plays a significant role in plant growth and development by providing strength, rigidity, rate and direction of cell growth, cell shape maintenance, and protection from biotic and abiotic stressors. The cell wall is primarily composed of cellulose, lignin, hemicellulose and pectin. Recently plant cell walls have been targeted for the second-generation biofuel and bioenergy production. Specifically, the cellulose component of the plant cell wall is used for the production of cellulosic ethanol. Estimation of cellulose content of biomass is critical for fundamental and applied cell wall research. The Updegraff method is simple, robust, and the most widely used method for the estimation of crystalline cellulose content of plant biomass. The alcohol insoluble crude cell wall fraction upon treatment with Updegraff reagent eliminates the hemicellulose and lignin fractions. Later, the Updegraff reagent resistant cellulose fraction is subjected to sulfuric acid treatment to hydrolyze the cellulose homopolymer into monomeric glucose units. A regression line is developed using various concentrations of glucose and used to estimate the amount of the glucose released upon cellulose hydrolysis in the experimental samples. Finally, the cellulose content is estimated based on the amount of glucose monomers by colorimetric anthrone assay.
Cellulose is the primary load-bearing component of cell walls, which is present in both primary and secondary cell walls. The cell wall is an extracellular matrix that surrounds plant cells and is primarily composed of cellulose, lignin, hemicellulose, pectin, and matrix proteins. Approximately one third of plants biomass is cellulose1 and it plays significant roles in plant growth and development by providing strength, rigidity, rate and direction of cell growth, cell shape maintenance, and protection from biotic and abiotic stressors. Cotton fiber contains 95% cellulose2 content, while trees contain 40% to 50% of cellu....
1. Experimental preparation
Cotton plants grown in the green house were selected for this study. Two different experimental lines of cotton were selected for comparative analysis of cellulose content. For each experimental line, the root tissue was collected from three biological replicates. A total of 500 mg of tissue was homogenized and 20 mg of it was used for crude cell wall extraction. Later, 5 mg of crude cell wall extract was used for Updegraff reagent treatment to remove hemicellulose and lignin from cellulose. The purified cellulose was hy.......
Cotton fibers are natural fibers produced from the cottonseed. Cotton fiber is a single cell with ~95% cellulose content2 with high crystalline cellulose content with extensive applications in textile industry31. As, cotton fiber contains ~95% cellulose, we have used cotton root tissues for demonstration of the estimation of crystalline cellulose content. Cotton root tissues are moderately rich in crystalline cellulose content and represents a commonly available plant bioma.......
We thank the Department of Plant & Soil Science and Cotton Inc. for their partial support of this study.
....Name | Company | Catalog Number | Comments |
Acetone | Fisher Chemical | A18-500 | Used in the protocol |
Anthrone | Sigma Aldrich | 90-44-8 | For colorimetric assay |
Centrifuge | Eppendorf | 5424 | For centrifugation |
Chloroform | Mallinckrodt | 67-66-3 | Used in the protocol |
Ethylenediaminetetraacetic acid (EDTA) | Sigma Aldrich | 6381-92-6 | Used in the protocol |
Ethanol | Millipore Sigma | EM-EX0276-4S | Used in the protocol |
Filter paper | Whatman | 1004-090 | Positive control |
Glacial acetic acid | Sigma | SKU A6283 | Used in the protocol |
Heat block/ ThermoMixer F1.5 | Eppendorf | 13527550 | For controlled temperatures |
Incubator | Fisherbrand | 150152633 | Used for drying plant sample |
Measuring Scale | Mettler Toledo | 30243386 | For specific quantities |
Methanol 100 % | Fisher Chemical | A412-500 | Used in the protocol |
Microplate (96 well) | Evergreen Scientific | 222-8030-01F | For anthrone assay |
Nitric acid | Sigma Aldrich | 695041 | Used in the protocol |
Polypropylene Microvials (2 mL) / screw capped tubes | BioSpec Products | 10831 | For high temperatures |
Spectrophotometer(Multimode Detector) | Beckmancoulter DTX880 | 1000814 | For measuring absorbances |
Spex SamplePrep 6870 Freezer / Mill | Spex Sample Prep | 68-701-15 | For grinding plant tissues into fine powder |
Sulphuric acid | J.T.Baker | 02-004-382 | Used in the protocol |
Sodium dodecyl sulfate (SDS) | Sigma Aldrich | 151-21-3 | Used in the PSB buffer |
Tubes (2 mL) | Fisher Scientific | 05-408-138 | Used in the protocol |
Tris Hydrochloride | Sigma Aldrich | Â 1185-53-1 | Used in the PSB buffer |
Ultrapure distilled water | Invitrogen | 10977 | Used in the protocol |
Vacuum dryer (vacufuge plus) | Eppendorf | 22820001 | For drying samples |
Vortex mixer | Fisherbrand | 14-955-151 | For mixing |
Waterbath | Thermoscientific | TSGP02PM05 | For temperature controlled conditions at specific steps |
Weighing Paper | Fisher Scientific | 09-898-12A | Used in the protocol |
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