Academic literature on the topic 'Sucrose hydrolysis'

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Journal articles on the topic "Sucrose hydrolysis"

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Li, Dongmei, Chaofan Weng, Yi Ruan, et al. "An Optical Chiral Sensor Based on Weak Measurement for the Real-Time Monitoring of Sucrose Hydrolysis." Sensors 21, no. 3 (2021): 1003. http://dx.doi.org/10.3390/s21031003.

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A chiral sensor with optical rotation detection based on weak measurement for the kinetic study of sucrose hydrolysis is presented. Based on the polarization modulation to the pre-selection state, the optical rotation of chiral sample was accurately determined through the central wavelength shift of the output spectrum. With this approach, the concentration response curves of sucrose and its hydrolysis products, i.e., fructose and glucose, were experimentally obtained for the hydrolysis analysis. By collecting the output spectrum with a frequency of 100 Hz and fitting the central wavelength sh
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Radovanovic, Mirjana, Branimir Racic, Snezana Tanaskovic, Goran Markovic, Dalibor Tomic, and Jelena Pantovic. "The catalytic effect of honey on formation of reducing sugars during sucrose hydrolysis." Chemical Industry 71, no. 2 (2017): 105–10. http://dx.doi.org/10.2298/hemind140313068r.

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In commercial apiculture, beekepers usually remove honey from hives and replenish food reserves with sugar syrup. When honeybees use sugar syrup (sucrose solution), they break down sucrose into glucose and fructose. These processes exhaust and weaken bees. In order to prevent bee exhaustion resulting from this processing, bees should preferably be supplied with ready made food before winter, i.e., with syrup in which sucrose has already been inverted. Feeding with inverted syrups is the most popular way of honeybee feeding. Beekeepers usually prepare inverted syrups by adding a weak organic ac
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Goldberg, R. N., Y. B. Tewari, and J. C. Ahluwalia. "Thermodynamics of the hydrolysis of sucrose." Journal of Biological Chemistry 264, no. 17 (1989): 9901–4. http://dx.doi.org/10.1016/s0021-9258(18)81744-6.

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Nagamune, Teruyuki, Takashi Nakamura, Isao Endo, and Ichiro Inoue. "Simulation of Sucrose Hydrolysis by Yeast." KAGAKU KOGAKU RONBUNSHU 17, no. 3 (1991): 462–69. http://dx.doi.org/10.1252/kakoronbunshu.17.462.

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Iloukhani, H., S. Azizian, and N. Samadani. "Hydrolysis of Sucrose by Heterogeneous Catalysis." Physics and Chemistry of Liquids 40, no. 2 (2002): 159–65. http://dx.doi.org/10.1080/00319100208086658.

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Pito, D. S., I. M. Fonseca, A. M. Ramos, J. Vital, and J. E. Castanheiro. "Hydrolysis of sucrose over composite catalysts." Chemical Engineering Journal 184 (March 2012): 347–51. http://dx.doi.org/10.1016/j.cej.2012.01.033.

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Catana, R., B. S. Ferreira, J. M. S. Cabral, and P. Fernandes. "Immobilization of inulinase for sucrose hydrolysis." Food Chemistry 91, no. 3 (2005): 517–20. http://dx.doi.org/10.1016/j.foodchem.2004.04.041.

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Romanov, Vasilly I., and Esperanza Martínez-Romero. "Sucrose transport and hydrolysis inRhizobium tropici." Plant and Soil 161, no. 1 (1994): 91–96. http://dx.doi.org/10.1007/bf02183088.

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Jones, B. J. M., B. E. Higgins, and D. B. A. Silk. "Glucose absorption from maltotriose and glucose oligomers in the human jejunum." Clinical Science 72, no. 4 (1987): 409–14. http://dx.doi.org/10.1042/cs0720409.

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1. The jejunal absorption of glucose from (1–4)-linked glucose oligomers including maltotriose has been compared with that from free glucose and sucrose in normal subjects. 2. A steady-state perfusion technique in vivo was used to study proximal jejunal assimilation of isotonic sugar-saline solutions isocaloric with 140 mmol/l glucose. Endogenous α-amylase was excluded from the test segment by proximal balloon occlusion. The glucose oligomer mixture consisted mainly of maltotriose, maltotetraose, maltopentaose and maltoheptaose. 3. Glucose absorption was significantly faster from maltotriose a
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Schebor, Carolina, Maria del Pilar Buera, Jorge Chirife, and Marcus Karel. "Sucrose hydrolysis in a glassy starch matrix." LWT - Food Science and Technology 28, no. 2 (1995): 245–48. http://dx.doi.org/10.1016/s0023-6438(95)91684-9.

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Dissertations / Theses on the topic "Sucrose hydrolysis"

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Rose, Susan 1977. "Sucrose accumulation and the expression of neutral invertase in sugarcane." Thesis, Stellenbosch : Stellenbosch University, 2001. http://hdl.handle.net/10019.1/52468.

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Thesis (MSc)--University of Stellenbosch, 2001.<br>ENGLISH ABSTRACT: The goals of this project were to (i) determine maximum extractable neutral invertase (NI) activity in the sugarcane culm, (ii) sequence a cDNA encoding for the sugarcane NI (SNI), (iii) determine SNI copy number in the genome, (iv) describe SNI transcript and protein expression patterns throughout the plant, and (v) attempt to determine the contribution of hydrolysis to sucrose accumulation. SNI and sugars were extracted from the developing culm tissues of sugarcane, commercial variety N19. Tissues were divided accord
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Demnitz-King, Antje Charlotte. "Sucrose metabolism in relation to import and compartmentation of carbohydrates in developing tomato fruit (Lycopersicon Spp.)." Thesis, Imperial College London, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.295594.

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Mrůzková, Karolína. "Využití polarimetrie a refraktometrie ke stanovení koncentrace invertního cukru v invertních sirupech." Master's thesis, Vysoké učení technické v Brně. Fakulta chemická, 2021. http://www.nusl.cz/ntk/nusl-449740.

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Invert syrup is a liquid sweetener, which is produced by sucrose hydrolysis to form fructose and glucose. Important qualitative parameter of invert syrup is the sucrose inversion – weight percentage of invert sugar (sum of fructose and glucose) in invert syrup dry mass. This diploma thesis presents a possibility of sucrose inversion determination by polarimetry in combination with refractometry in invert syrups of 70–78 % dry mass produced at 80 °C and pH 2,4. New relationship describing the sucrose inversion as a function of polarization and refractometric dry mass was determined. The results
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Seabra, Joaquim Eugênio Abel 1981. "Avaliação tecnico-economica de opções para o aproveitamento integral da biomassa de cana no Brasil." [s.n.], 2008. http://repositorio.unicamp.br/jspui/handle/REPOSIP/265245.

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Orientador: Isaias de Carvalho Macedo<br>Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Engenharia Mecanica<br>Made available in DSpace on 2018-08-11T15:17:55Z (GMT). No. of bitstreams: 1 Seabra_JoaquimEugenioAbel_D.pdf: 2147529 bytes, checksum: e9ebd63f7d029f2346cd2c026285a2cf (MD5) Previous issue date: 2008<br>Resumo: O objetivo deste trabalho foi investigar, no cenário prospectivo, as opções tecnológicas que deverão permitir o melhor aproveitamento da biomassa da cana e suas possíveis implicações no contexto das usinas. Além das possibilidades envolvendo o uso mais div
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Nolasco, Junior Jonas. "Desenvolvimento de processo termico otimizado para mosto de caldo de cana na fermentação alcoolica." [s.n.], 2005. http://repositorio.unicamp.br/jspui/handle/REPOSIP/255406.

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Orientador: Pilar Rodriguez de Massaguer<br>Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Engenharia de Alimentos<br>Made available in DSpace on 2018-08-04T02:36:41Z (GMT). No. of bitstreams: 1 NolascoJunior_Jonas_M.pdf: 917952 bytes, checksum: 1c082a25920f5c8390a73425551d86ef (MD5) Previous issue date: 2005<br>Resumo: Nesta pesquisa é proposto um processo de tratamento térmico do mosto, com máxima preservação do conteúdo em açúcares fermentescíveis (sacarose, glicose e frutose), a fim de promover a inativação térmica de seus contaminantes bacterianos e por extensã
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Derrien, Elie. "Valorisation des sucres dérivés des hémicelluloses." Thesis, Lyon 1, 2015. http://www.theses.fr/2015LYO10185.

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Meline, Thomas. "Synthèse enzymatique d’esters de sucres à partir du son de blé et applications." Thesis, Reims, 2017. http://www.theses.fr/2017REIMS026.

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La biomasse lignocellulosique est au cœur du développement de la bioraffinerie de par l’intérêt de fractionner ses composants avec divers procédés pour la production de biocarburants, de molécules d’intérêt et de matériaux agro-sourcés. L’objectif de cette thèse visait à étudier la transformation des xylanes du son de blé en molécules tensio-actives (esters de pentoses). Cette transformation a été envisagée en deux étapes : une première étape d’hydrolyse du son de blé par des hémicellulases pour la production de xylose et d’arabinose, suivie d’une seconde étape d’acylation de ces glucides par
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Trollope, Kim Mary. "Engineering a fungal β-fructofuranosidase". Thesis, Stellenbosch : Stellenbosch University, 2015. http://hdl.handle.net/10019.1/96757.

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Thesis (PhD)--Stellenbosch University, 2015.<br>ENGLISH ABSTRACT: β-fructofuranosidases are hydrolytic enzymes that act on sucrose to yield the products glucose and fructose. Under high substrate conditions these enzymes display fructosyltransferase activity which results in the synthesis of fructooligosaccharides (FOS). Some enzymes display higher propensities for FOS synthesis than others, with the determinants of this activity remaining unclear. The consumption of FOS produces a prebiotic effect that positively alters the composition of the colonic microflora, and as a result is linked to i
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Epoune, lingome Cédric. "Nouveaux agrotensioactifs glycolipidiques : synthèse, propriétés physico-chimiques et application en polymérisation." Thesis, Lyon, INSA, 2011. http://www.theses.fr/2011ISAL0150/document.

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Conscients de la raréfaction progressive et l’augmentation continue du coût du pétrole et aussi des volumes importants des tensioactifs produits et éliminés chaque année, l’industrie chimique s’intéresse de plus en plus aux ressources issues de la biomasse. Cependant, dans le marché européen des tensioactifs, la part des produits d’origine végétale par rapport aux dérivés pétrochimiques est estimée à seulement 20%. Compte-tenu de ces enjeux, de nouvelles stratégies de synthèse pour produire des tensioactifs ayant des structures originales issus d’agro-ressources sont nécessaires. Dans le cadre
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Galindo, Sabine. "Production simultanée de sucres et d'éthanol à partir de biomasse végétale." Montpellier 2, 1996. http://www.theses.fr/1996MON20067.

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Les tubercules de topinambour possedent une reserve glucidique essentiellement composee par des polyfructosanes de type inuline dont le degre de polymerisation moyen depend de la date de recolte des tubercules. La production simultanee d'ethanol et de sirops d'inuline enrichis en fructose est realisable par fermentation selective d'extraits de topinambour par la souche saccharomyces diastaticus ncyc 625 a faible activite inulinasique. Les extraits provenant de recoltes tardives sont plus fermentescibles que ceux issus de recoltes precoces contenant de l'inuline plus polymerisee: l'hydrolyse de
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Book chapters on the topic "Sucrose hydrolysis"

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Romanov, Vasilly I., and Esperanza Martínez-Romero. "Sucrose transport and hydrolysis in Rhizobium tropici." In Symbiotic Nitrogen Fixation. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-1088-4_9.

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Compton, Robert N., and Michael A. Duncan. "Inversion of Sucrose by Acid-Catalyzed Hydrolysis." In Laser Experiments for Chemistry and Physics. Oxford University Press, 2015. http://dx.doi.org/10.1093/acprof:oso/9780198742975.003.0031.

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Morrow, Gary W. "Biosynthesis of Carbohydrates and Amino Acids." In Bioorganic Synthesis. Oxford University Press, 2016. http://dx.doi.org/10.1093/oso/9780199860531.003.0006.

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We have already seen that some of the basic building blocks used in the biosynthesis of natural products are amino acids such as phenylalanine, tyrosine, and others. These and other crucial construction materials such as the acyl group in acetyl-CoA are all ultimately derived from carbohydrates. In this chapter, we will present an abbreviated overview of the components of carbohydrate structure and metabolism sufficient for our purposes going forward, with a schematic flowchart showing how carbohydrates and amino acids are modified, combined, and branched off in various ways to yield the distinct set of biosynthetic pathways that will form the core of the remainder of the text. We will finish the chapter with a brief, general review of amino acid nomenclature and structure with emphasis on the key amino acids that will be used throughout the remainder of the text. We know that plants make glucose (C6H12O6) by photosynthesis using light, water (H2O), and carbon dioxide (CO2). Another way of looking at the formula for glucose is C6(H2O)6, that is, six carbon atoms and six water molecules. Thus, glucose was originally referred to as a hydrated form of carbon—a carbohydrate. But this is a very general term since there are many different types of carbohydrate compounds. One way to broadly classify carbohydrates is to identify them as either mono- (one), di- (two), oligo- (a few) or poly- (many) saccharides. For example, glucose (C6H12O6) cannot be broken down into simpler carbohydrates by simple hydrolysis, so it is classified as a monosaccharide, that is, a single, discrete carbohydrate compound. On the other hand, the carbohydrate sucrose (C12H22O11) is classified as a disaccharide since when it is subjected to aqueous hydrolysis, it yields two different monosaccharide carbohydrates, namely glucose (C6H12O6) and fructose (C6H12O6). Noting that glucose and fructose are different compounds but with the same molecular formula, they must be related to one another either as stereoisomers or as constitutional isomers, so further refinement of classification is needed. Structurally speaking, most monosaccharide carbohydrates are simply polyhydroxyaldehydes (aldoses) or polyhydroxyketones (ketoses) which can be further classified using a combination of aldo- or keto- prefixes along with suffixes such as triose, tetrose, pentose, or hexose to designate the number of carbon atoms.
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"nose family of sugars [178]. Total free sugar content of rye from tubers and roots, particularly potato, sweet potato, and was reported as 3.2%, with sucrose (1.9%), raffinose tapioca (cassava). Isolated starch can be modified physical-(0.4%), fructose (0.1%), and glucose (0.08%) [120]. ly and/or chemically to alter its functional properties. Starches and modified starches have an enormous number Ill. STARCH of food uses, including adhesive, binding, clouding, dust-ing, film forming, and thickening applications [20]. Starch is found in a number of plant sources, and the plant relies on starch for its energy requirements for growth and reproduction. For humans, starch is extremely important as A. Starch Content of Cereals a macronutrient, because it is a complex carbohydrate and The most important sources of starch are cereal grains an important energy source in our diet. (40-90% of their dry weight), pulses (30-70%), and tubers The commercial and technological uses of starch are (65-85%). Of the common starches, regular corn, waxy numerous; this arises from its unique character, because it corn, and high-amylose corn are by far the most important can be used directly as intact granules, in the dispersed sources. The starch content of corn may vary from about form, as a film dried from a dispersion, as an extruded 54% in sweet corn to 64-78% in dent [194]. Corn is large-powder, or after conversion to a mixture of oligosaccha-ly used as stock feed but nevertheless supplies the bulk, by rides or via hydrolysis and isomerization. far, of the world's starch production. Corn starch is manu-When starch is heated in water, it absorbs water and factured by traditional wet-milling process. Only about 5% swells. This is the process of gelatinization, a process that of the annual world maize crop is used for the manufacture cause a tremendous change in rheological properties of the of maize starch. About 70% of the maize starch produced starch suspension. The crystalline structure is destroyed is converted into corn syrups, high-fructose corn syrup, during gelatinization. The ability of starch molecules to and dextrose. Corn starch has a wide variety of industrial crystallize after gelatinization is described by the term of applications, with uses ranging from thickening and retrogradation. Although some retrogradation of amylose gelling agents in puddings and fillings to molding for con-seems to be a prerequisite for the formation of a normal fections [72]. bread crumb, long-term retrogradation usually causes Potato starch is a variable commodity, sensitive to vari-gradual deterioration of bread quality during the products' ety, climate, and agricultural procedure. Potato starch, shelf life [55]. however, is presently second only to corn and comparable Starch occurs as discrete granules in higher plants. Two to wheat in terms of quantity produced and especially pop-major polymers, amylose and amylopectin, are contained in ular in Europe. About 3% of the world crop of potatoes is the granule. Cereal starch granules may also contain small used for the production of potato starch. Potato starch is amounts of proteins, lipids, and minerals [118]. Cereal used in food, paper, textile, and adhesive industries. starches are widely used in foods, where they are important The starch content of wheat has been reported to be in functionally and nutritionally. Commercial starches are ob-the range of 63-72% [147] (Table 2). Wheat starch, found tained from cereal grain seeds, particularly from corn, waxy in the endosperm of the wheat kernel, constitutes approxi-corn, high-amylose corn, wheat, and various rites, and mately 75-80% of the endosperm on a dry basis. The TABLE 2 Carbohydrate Composition of Some Cereal Grains' Sample Starch (%) Amylose (%) Pentosan (%) P-Glucan (%) Total dietary fiber Wheat 63-72 (147) 23.4-27.6 (133) 6.6 (81) 1.4 (151) 14.6 (32) Barley 57.6-59.5 (87) 22-26 (27) 5.9 (82) 3-7 (139) 19.3-22.6 (87) Brown rice 66.4 (104) 16-33 (124) 1.2 (81) 0.11 (102) 3.9 (32) Milled rice 77.6 (104) 7-33 (102) 0.5-1.4 (104) 0.11 (104) 2.4 (32) Sorghum 60-77 (194) 21-28 (127) 1.8-4.9 (127) 1.0 (151) 10.1 (160) Pearl Millet 63 (123) 17 (11) 2-3 (12) 8.5 (32) Corn 64-78 (194) 24 (132) 5.8-6.6 (194) 13.4 (32) Oats 43-61 (143) 16-27 (120) 7.7 (81) 3.9-6.8 (198) 9.6 (32) Rye 69 (168) 24-31 (168) 8.5 (81) 1.9-2.9 (151) 14.6 (32) Triticale 53 (22) 24-26 (40) 7.1 (81) 1.2 (151) 18.1 (32) aSources shown in parentheses." In Handbook of Cereal Science and Technology, Revised and Expanded. CRC Press, 2000. http://dx.doi.org/10.1201/9781420027228-40.

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Conference papers on the topic "Sucrose hydrolysis"

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Casu, S., A. Fanti, N. Djuric, F. Desogus, and G. Mazzarella. "Microwave resonant cavity as a reactor for the enzymatic hydrolysis of sucrose." In 2015 IEEE 15th Mediterranean Microwave Symposium (MMS). IEEE, 2015. http://dx.doi.org/10.1109/mms.2015.7375499.

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Steiner, B., and D. R. Phillips. "CA2+-INDUCED STRUCTURAL TRANSITIONS OF THE PLATELET GP IIb-IIIa COMPLEX." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643956.

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Previous studies have shown that the membrane glycoprotein (GP) IIb-IIIa complex can be reversibly dissociated by incubating platelets for 5 min at 37°C in an EDTA-containing buffer. Prolonged incubations (30 min) with EDTA, however, result in the formation of high molecular weight aggregates of GP IIb and GP IIIa. These aggregates of individual GP's neither bind fibrinogen nor support platelet aggregation, indicating that chelation of Ca2+ can affect the functional activity of GP IIb-IIIa. The present study was designed to identify conditions for the generation of functionally active GP IIb a
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