Aspen (Populus tremuloides) and black cottonwood (Populus trichocarpa) organosolv pulps produced in a wide range of solvent composition (between 30 and 70% by volume of methanol) and catalysts (H(2)SO(4) and H(3)PO(4)) such that the cooking liquor pH = 3 are easily digested by enzymes. The total yields of hydrolysis residues (pulps) are in the 40-60% range; the acid-catalyzed delignification followed by enzyme hydrolysis can generate 70-88% of the original six-carbon sugars contained in the wood. Glucomannan and arablnogalactan are dissolved into the pulping liquor in the pH range of 2-4.5. Lower pH (=3) leads to additional solubilization of six-carbon sugars. These sugars may be fermented directly. From the insoluble hydrolysis residues, 36-41% conversions of wood into fermentable sugars were obtained after enzyme hydrolysis; the starting feedstocks contain 50.8 and 46.6% hexosans, respectively, for aspen and black cotton-wood. The kinetics of enzymatic hydrolysis of cellulose can be formally treated as two simultaneous pseudo-first-order reactions in which fast and slow hydrolyses of cellulose occur. Correlations between the glucan digestibility and the effect of the pretreatment have been made. The higher residual xylan content reduces the amount of the rapidly hydrolyzable glucan fraction and lowers the glucan digestibility. The proposed simple kinetic treatment is very helpful in assessing the effect of the pretreatment on pulp enzyme hydrolyzability.
There is a multitude of chemical and biochemical detection methods for sugars. Which ones would be most practical in an undergraduate laboratory setting? How to best detect non-reducing disaccharides? How to make such lab fun for students to perform? After trying several spectrophotometric methods, it was found that chemical detection by dinitrosalicylic acid and biochemical detection by hexokinase/glucose-6-phosphate dehydrogenase reagent are most appropriate. Sucrose, a non-reducing disaccharide was digested chemically with hydrochloric acid and biochemically with invertase. It was concluded that chemical detection and biochemical detection compliment each other. Chemical digestion method was preferred over the digestion by invertase. These methods were applied for testing the validity of sugar ingredients printed on drink labels as well as the measurement of sugar levels in ripening bananas at two different conditions. The comprehensive comparison of these methods and the detection of sugar concentrations in interesting samples might serve as a basis for an undergraduate chemistry laboratory.
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