Carbohydrate Naturally Occurring Polysaccharide in Food Sea Weed Polysaccharide Sources And
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Oat Β-Glucan Lowers Total and LDL-Cholesterol
Oat β-glucan lowers total and LDL-cholesterol Sylvia Pomeroy, Richard Tupper, Marja Cehun-Aders and Paul Nestel Abstract Several soluble polysaccharides have been shown to daily, have shown to significantly lower serum cholesterol have cholesterol-lowering properties and to have a role in pre- mostly by between 5.4 and 12.8% and LDL-cholesterol by vention of heart disease. Major sources of one such between 8.5 and 12.4% in moderately hypercholesterolae- β polysaccharide ( -glucan) are oats and barley. The aim of this mic subjects. Larger reductions have been reported (8–13) study was to examine the effects on plasma lipid concentrations whereas other well executed trials have proven to be when β-glucan derived from a fractionated oat preparation was consumed by people with elevated plasma lipids. A single-blind, negative (14–18). crossover design compared plasma cholesterol, triglycerides, Two meta-analysis studies have shed more informa- high density lipoproteins and low density lipoproteins (LDLs) in β tion on this issue. One meta-analysis (19) of 23 trials 14 people; in the order of low, high and low -glucan supple- provided strong support that approximately 3 g of soluble mented diets, each of three weeks duration. For the high β- glucan diet, an average intake of 7 g per day was consumed from fibre from oat products per day can lower total cholesterol cereal, muffins and bread. The background diet remained rela- concentrations from 0.13 to 0.16 mmol/L and concluded tively constant over the three test periods. Differences during the that the reduction was greater in those with higher initial interventions were calculated by one-way repeated measures cholesterol concentrations. -
Sweeteners Georgia Jones, Extension Food Specialist
® ® KFSBOPFQVLCB?O>PH>¨ FK@LIKUQBKPFLK KPQFQRQBLCDOF@RIQROB>KA>QRO>IBPLRO@BP KLTELT KLTKLT G1458 (Revised May 2010) Sweeteners Georgia Jones, Extension Food Specialist Consumers have a choice of sweeteners, and this NebGuide helps them make the right choice. Sweeteners of one kind or another have been found in human diets since prehistoric times and are types of carbohy- drates. The role they play in the diet is constantly debated. Consumers satisfy their “sweet tooth” with a variety of sweeteners and use them in foods for several reasons other than sweetness. For example, sugar is used as a preservative in jams and jellies, it provides body and texture in ice cream and baked goods, and it aids in fermentation in breads and pickles. Sweeteners can be nutritive or non-nutritive. Nutritive sweeteners are those that provide calories or energy — about Sweeteners can be used not only in beverages like coffee, but in baking and as an ingredient in dry foods. four calories per gram or about 17 calories per tablespoon — even though they lack other nutrients essential for growth and health maintenance. Nutritive sweeteners include sucrose, high repair body tissue. When a diet lacks carbohydrates, protein fructose corn syrup, corn syrup, honey, fructose, molasses, and is used for energy. sugar alcohols such as sorbitol and xytilo. Non-nutritive sweet- Carbohydrates are found in almost all plant foods and one eners do not provide calories and are sometimes referred to as animal source — milk. The simpler forms of carbohydrates artificial sweeteners, and non-nutritive in this publication. are called sugars, and the more complex forms are either In fact, sweeteners may have a variety of terms — sugar- starches or dietary fibers.Table I illustrates the classification free, sugar alcohols, sucrose, corn sweeteners, etc. -
Structure-Function Relationships of Glucansucrase and Fructansucrase Enzymes from Lactic Acid Bacteria Sacha A
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, Mar. 2006, p. 157–176 Vol. 70, No. 1 1092-2172/06/$08.00ϩ0 doi:10.1128/MMBR.70.1.157–176.2006 Copyright © 2006, American Society for Microbiology. All Rights Reserved. Structure-Function Relationships of Glucansucrase and Fructansucrase Enzymes from Lactic Acid Bacteria Sacha A. F. T. van Hijum,1,2†* Slavko Kralj,1,2† Lukasz K. Ozimek,1,2 Lubbert Dijkhuizen,1,2 and Ineke G. H. van Geel-Schutten1,3 Centre for Carbohydrate Bioprocessing, TNO-University of Groningen,1 and Department of Microbiology, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen,2 9750 AA Haren, The Netherlands, and Innovative Ingredients and Products Department, TNO Quality of Life, Utrechtseweg 48 3704 HE Zeist, The Netherlands3 INTRODUCTION .......................................................................................................................................................157 NOMENCLATURE AND CLASSIFICATION OF SUCRASE ENZYMES ........................................................158 GLUCANSUCRASES .................................................................................................................................................158 Reactions Catalyzed and Glucan Product Synthesis .........................................................................................161 Glucan synthesis .................................................................................................................................................161 Acceptor reaction ................................................................................................................................................161 -
An Overview of Non Starch Polysaccharide
JOURNAL OF ANIMAL NUTRITION AND PHYSIOLOGY Journal homepage: www.jakraya.com/journal/janp MINI-REVIEW An Overview of Non Starch Polysaccharide Kamdev Sethy a, S.K. Mishra b, P. P. Mohanty c, J. Agarawal c, P. Meher c, D. Satapathy c, J. K. Sahoo c, S. Panda c and S. M. Nayak c aAssistant Professor, bAssociate Professor, cM.V.Sc. Scholars, Department of Animal Nutrition, College of Veterinary Science and Animal Husbandry, Orissa University of Agriculture and Technology, Bhubaneswar, India. Abstract Polysaccharides are macromolecules of monosaccharides linked by *Corresponding Author: glycosidic bonds. Polysaccharides are widespread biopolymers, which Dr. Kamdev Sethy quantitatively represent the most important group of nutrients in feed. These are major components of plant materials used in rations for E mail: [email protected] monogastrics. Non-starch polysaccharides (NSP) contain ß-glucans, cellulose, pectin and hemicellulose. NSP consist of both soluble and insoluble fractions. Soluble NSP of cereals such as wheat, barley and rye increases intestinal viscosity there by interfere with the digestive processes Received: 05/02/2015 and exert strong negative effects on net utilisation of energy. NSP cannot be degraded by endogeneous enzymes and therefore reach the colon almost Revised: 27/02/2015 indigested. Insoluble NSP make up the bulk in the diets. NSP are known to posses anti-nutritional properties by either encapsulating nutrients and/or Accepted: 02/03/2015 depressing overall nutrient digestibility through gastro-intestinal modifications. Key words: Polysaccharides, Starch, Digestibility. 1. Introduction xylans are present only in the hull and husk portion. Non starch polysaccharides (NSPs) are The cotyledon of legumes contains pectic carbohydrate fractions excluding starch and free sugars. -
Oat Beta Glucans
Oat beta glucans Oat bran is produced by removing the starchy content of the grain. It is rich in dietary fibers, especially in soluble fibers, present in the inner periphery of the kernel. Oats contain more soluble fibers than any other grain, resulting in slower digestion and an extended sensation of fullness, among other things. Oat is a rich source of the water-soluble fiber (1,3/1,4) β-glucan, and its effects on health have been extensively studied over the last 30 years. Oat β-glucans can be highly concentrated in different types of oat brans. The beta glucan content varies, from 3-5% depending on variety when it grows in the field. Rolled oat/oat flakes is about 4% and also wholemeal oat flour about 4%. With Swedish Oat Fiber’s specially developed fractionating process, we can do concentrations of beta glucans from 6% up to 32%. Beta-D-glucans, usually referred to as beta glucans, comprise a class of indigestible polysaccharides widely found in nature in sources such as grains, barley, yeast, bacteria, algae and mushrooms. In oats, they are concentrated in the bran, more precisely in the aleurone and sub-aleurone layer (see picture above). Oat beta glucan is a natural soluble fiber. It is a viscous polysaccharide made up of units of the monosaccharide D-glucose. Oat beta glucan is composed of mixed-linkage polysaccharides. This means the bonds between the D-glucose units are either beta-(1 →3) linkages or beta-(1 →4) linkages. This type of beta-glucan is also referred to as a mixed- linkage (1 →3), (1 →4)-beta-D-glucan. -
Structure and Metabolism of the Intracellular Polysaccharide of Corynebacterium. Don D
Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1969 Structure and Metabolism of the Intracellular Polysaccharide of Corynebacterium. Don D. Mickey Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Recommended Citation Mickey, Don D., "Structure and Metabolism of the Intracellular Polysaccharide of Corynebacterium." (1969). LSU Historical Dissertations and Theses. 1679. https://digitalcommons.lsu.edu/gradschool_disstheses/1679 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. This dissertation has been microfilmed exactly as received 70-9079 MICKEY, Don D., 1940- STRUCTURE AND METABOLISM OF THE INTRACELLULAR POLYSACCHARIDE OF CORYNEBACTERIUM. The Louisiana State University and Agricultural and Mechanical College, Ph.D., 1969 Microbiology University Microfilms, Inc., Ann Arbor, Michigan STRUCTURE AND METABOLISM OF THE INTRACELLULAR POLYSACCHARIDE OF CORYNEBACTERIUM A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Microbiology by Don D. Mickey B. S., Louisiana State University, 1963 August, 1969 ACKNOWLEDGMENT The author wishes to acknowledge Dr. M. D. Socolofsky for his guidance during the preparation of this dissertation. He also wishes to thank Dr. H. D. Braymer and Dr. A. D. Larson and other members of the Department of Microbiology for helpful advice given during various phases of this research. -
Carbohydrates: Disaccharides and Polysaccharides
Carbohydrates: Disaccharides and Polysaccharides Disaccharides Linkage of the anomeric carbon of one monosaccharide to the OH of another monosaccharide via a condensation reaction. The bond is termed a glycosidic bond. The end of the disaccharide that contains the anomeric carbon is referred to as the reducing end because it is capable of reducing various metal ions. Formation of a glycosidic bond between two glucose molecules. Nomenclature: To describe disaccharides you need to specify the following: 1. The names of the two monosaccharides. 2. How they are linked together (one anomeric is always used). 3. The configuration of the anomeric carbons on both monosaccharides. The Six Simple Rules for Naming Disaccharides are as follows: 1. The non-reducing end defines the first sugar. 2. Configuration of the anomeric carbon of the 1st sugar (α,β). 3. Name of 1st monosaccharide, root name followed by pyranosyl (6- ring) or furanosyl (5-ring). 4. Atoms which are linked together, 1st sugar then 2nd sugar. 5. Configuration of the anomeric carbon of the second sugar (α,β) (often omitted if the anomeric carbon is free since α and β forms are in equilibrium.) 6. Name of 2nd monosaccharide, root name followed by pyranose (6- ring) or furanose (5-ring) (If both anomeric carbons are involved, then the name ends in ‘oside”, not ‘ose’) Example: Sucrose (table sugar): The anomeric carbon of glucose forms a bridge to the anomeric carbon of fructose. Since there is no reducing end, either sugar can be used to begin the name. Sucrose, drawn in two different ways. Note that both anomeric carbons are involved in the glycosidic linkage, thus both conformations have to be specified. -
Quantitative Analysis of Polysaccharide Composition in Polyporus Umbellatus by HPLC–ESI–TOF–MS
molecules Article Quantitative Analysis of Polysaccharide Composition in Polyporus umbellatus by HPLC–ESI–TOF–MS Ning Guo 1, Zongli Bai 2, Weijuan Jia 1, Jianhua Sun 2, Wanwan Wang 1, Shizhong Chen 1,* and Hong Wang 1,* 1 School of Pharmaceutical Sciences, Peking University, Beijing 100191, China 2 Kangmei Pharmaceutical Co.Ltd, Puning 515300, China * Correspondence: [email protected] (H.W.); [email protected] (S.C.) Academic Editor: Cédric Delattre Received: 23 June 2019; Accepted: 8 July 2019; Published: 10 July 2019 Abstract: Polyporus umbellatus is a well-known and important medicinal fungus in Asia. Its polysaccharides possess interesting bioactivities such as antitumor, antioxidant, hepatoprotective and immunomodulatory effects. A qualitative and quantitative method has been established for the analysis of 12 monosaccharides comprising polysaccharides of Polyporus umbellatus based on high-performance liquid chromatography coupled with electrospray ionization–ion trap–time of flight–mass spectrometry. The hydrolysis conditions of the polysaccharides were optimized by orthogonal design. The results of optimized hydrolysis were as follows: neutral sugars and uronic acids 4 mol/L trifluoroacetic acid (TFA), 6 h, 120 ◦C; and amino sugars 3 mol/L TFA, 3 h, 100 ◦C. The resulting monosaccharides derivatized with 1-phenyl-3-methyl-5-pyrazolone have been well separated and analyzed by the established method. Identification of the monosaccharides was carried out by analyzing the mass spectral behaviors and chromatography characteristics of 1-phenyl-3-methyl-5-pyrazolone labeled monosaccharides. The results showed that polysaccharides in Polyporus umbellatus were composed of mannose, glucosamine, rhamnose, ribose, lyxose, erythrose, glucuronic acid, galacturonic acid, glucose, galactose, xylose, and fucose. -
Polysaccharides
Polysaccharides: Homopolysaccharide Heteropolysaccharide Glucose is the most common monomer Mostly homo, however, if hetero, it will be two monosaccharides in a repeating sequence Complete characterization of a polysaccharide: monomers, sequence & type of glycosidic linkage Cellulose & chitin: β-glycosidic linkages, and both are structural materials Starch and glycogen: α-glycosidic linkages, and they serve as carbohydrate storage polymers in plants and animals, respectively The major structural component of plants, especially wood and plant fibers A linear polymer of approximately 2800 D-glucose units per molecule joined by β-1,4-glycosidic bonds Extensive intra- and intermolecular hydrogen bonding between chains Cellulases, animals? Energy storage in plants A polymers of α-D-glucose units A mylose (10-20 %): continuous, unbranched chains of up to 4000 α-D-glucose units joined by α-1,4-glycosidic bonds Amylopectin (80-90 %): a highly branched polymer consisting of 24-30 units of D-glucose joined by α-1,4- glycosidic bonds and branches created by α- 1,6-glycosidic bonds Amylases catalyze hydrolysis of α-1,4-glycosidic bonds β-amylase is an exoglycosidase and cleaves from the non- reducing end of the polymer α-amylase is an endoglycosidase and hydrolyzes glycosidic linkages anywhere along the chain to produce glucose and maltose Can amylose & amylopectin be completely degraded to glucose and maltose by the two amylases? Debranching enzymes catalyze the hydrolysis of α-1,6-glycosidic bonds A branched-chain polymer of -
Bio-Based Polymer Electrolytes for Electrochemical Devices: Insight Into the Ionic Conductivity Performance
materials Review Bio-Based Polymer Electrolytes for Electrochemical Devices: Insight into the Ionic Conductivity Performance Marwah Rayung 1, Min Min Aung 1,2,* , Shah Christirani Azhar 2, Luqman Chuah Abdullah 3 , Mohd Sukor Su’ait 4, Azizan Ahmad 4,5 and Siti Nurul Ain Md Jamil 2 1 Institute of Tropical Forestry and Forest Products, Universiti Putra Malaysia, Serdang 43400, Malaysia; [email protected] 2 Unit Chemistry, Center of Foundation Studies and Agricultural Science, Universiti Putra Malaysia, Serdang 43400, Malaysia; [email protected] (S.C.A.); [email protected] (S.N.A.M.J.) 3 Department of Chemical and Environmental Engineering, Faculty of Engineering, Universiti Putra Malaysia, Serdang 43400, Malaysia; [email protected] 4 Solar Energy Research Institute (SERI), Universiti Kebangsaan Malaysia, Bangi 43600, Malaysia; [email protected] (M.S.S.); [email protected] (A.A.) 5 School of Chemical Sciences and Food Technology, Universiti Kebangsaan Malaysia, Bangi 43600, Malaysia * Correspondence: [email protected] Received: 10 October 2019; Accepted: 4 December 2019; Published: 12 February 2020 Abstract: With the continuing efforts to explore alternatives to petrochemical-based polymers and the escalating demand to minimize environmental impact, bio-based polymers have gained a massive amount of attention over the last few decades. The potential uses of these bio-based polymers are varied, from household goods to high end and advanced applications. To some extent, they can solve the depletion and sustainability issues of conventional polymers. As such, this article reviews the trends and developments of bio-based polymers for the preparation of polymer electrolytes that are intended for use in electrochemical device applications. -
Starch Cellulose
Topic 2: Molecular Biology 2.3 Carbohydrates Condensation reactions make bonds. Hydrolysis bonds break these bonds. Watch the following animation and make a generalisation about the processes: - function, roles of enzymes, roles of water http://is.gd/MaltoseGIF 2.3.U1 Monosaccharide monomers are linked together by condensation reactions to form disaccharides and polysaccharide polymers. Monosaccharide Glucose has the formula C6H12O6 #1 It forms a hexagonal ring (hexose) Glucose is the form of sugar that fuels respiration Glucose forms the base unit for many polymers 5 of the carbons form corners on the ring with the 6th corner taken by oxygen http://commons.wikimedia.org/wiki/File:Glucose_crystal.jpg 2.3.U1 Monosaccharide monomers are linked together by condensation reactions to form disaccharides and polysaccharide polymers. Monosaccharide #2 Galactose is also a hexose sugar Spot the difference It has the same formula C6H12O6 but is less sweet Most commonly found in milk, but also found in cereals http://commons.wikimedia.org/wiki/File:Galactose-3D- balls.png http://commons.wikimedia.org/wiki/File:Alpha-D-glucose-3D- balls.png 2.3.U1 Monosaccharide monomers are linked together by condensation reactions to form disaccharides and polysaccharide polymers. Fructose is another Monosaccharide #3 pentose sugar Commonly found in fruits and honey It is the sweetest naturally occurring carbohydrate 2.3.U1 Monosaccharide monomers are linked together by condensation reactions to form disaccharides and polysaccharide polymers. Monosaccharide #4 Ribose is a pentose sugar, it has a pentagonal ring It forms the backbone of RNA Deoxyribose differs as shown in the diagram, and forms the backbone of DNA N.B. -
7 | Carbohydrates and Glycobiology
7 | Carbohydrates and Glycobiology Aldoses and Ketoses; Representative monosaccharides. (a)Two trioses, an aldose and a ketose. The carbonyl group in each is shaded. • An aldose contains an aldehyde functionality • A ketose contains a ketone functionality The Glycosidic Bond • Two sugar molecules can be joined via a glycosidic bond between an anomeric carbon and a hydroxyl carbon • The glycosidic bond (an acetal) between monomers is less reactive than the hemiacetal at the second monomer – Second monomer, with the hemiacetal, is reducing – Anomeric carbon involved in the glycosidic linkage is nonreducing • The disaccharide formed upon condensation of two glucose molecules via 1 4 bond is called maltose • Formation of maltose. A disaccharide is formed from two monosaccharides (here, two molecules of D-glucose) when an —OH (alcohol) of one glucose molecule (right) condenses with the intramolecular hemiacetal of the other glucose molecule (left), with elimination of H2O and formation of a glycosidic bond. The reversal of this reaction is hydrolysis—attack by H2O on the glycosidic bond. The maltose molecule, shown here as an illustration, retains a reducing hemiacetal at the C-1 not involved in the glycosidic bond. Because mutarotation interconverts the α and β forms of the hemiacetal, the bonds at this position are sometimes depicted with wavy lines, as shown here, to indicate that the structure may be either α or β. Nonreducing Disaccharides • Two sugar molecules can be also joined via a glycosidic bond between two anomeric carbons • The product has two acetal groups and no hemiacetals • There are no reducing ends, this is a nonreducing sugar • Trehalose is a constituent of hemolymph of insects • Two common disaccharides.