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Polysaccharide

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Further information: Homopolysaccharide
3D structure of cellulose, a beta-glucan polysaccharide
Amylose is a linear polymer of glucose mainly linked with α(1→4) bonds. It can be made of several thousands of glucose units. It is one of the two components of starch, the other being amylopectin.

Polysaccharides (/ˌpɒliˈsækəraɪd/), or polycarbohydrates, are the most abundant carbohydrates found in food. They are long-chain polymeric carbohydrates composed of monosaccharide units bound together by glycosidic linkages. This carbohydrate can react with water (hydrolysis) using amylase enzymes as catalyst, which produces constituent sugars (monosaccharides or oligosaccharides). They range in structure from linear to highly branched. Examples include storage polysaccharides such as starch, glycogen and galactogen and structural polysaccharides such as hemicellulose and chitin.

Polysaccharides are often quite heterogeneous, containing slight modifications of the repeating unit. Depending on the structure, these macromolecules can have distinct properties from their monosaccharide building blocks. They may be amorphous or even insoluble in water.[1]

When all the monosaccharides in a polysaccharide are the same type, the polysaccharide is called a homopolysaccharide or homoglycan, but when more than one type of monosaccharide is present, it is called a heteropolysaccharide or heteroglycan.[2][3]

Natural saccharides are generally composed of simple carbohydrates called monosaccharides with general formula (CH2O)n where n is three or more. Examples of monosaccharides are glucose, fructose, and glyceraldehyde.[4] Polysaccharides, meanwhile, have a general formula of Cx(H2O)y where x and y are usually large numbers between 200 and 2500. When the repeating units in the polymer backbone are six-carbon monosaccharides, as is often the case, the general formula simplifies to (C6H10O5)n, where typically 40 ≤ n ≤ 3000.

As a rule of thumb, polysaccharides contain more than ten monosaccharide units, whereas oligosaccharides contain three to ten monosaccharide units, but the precise cutoff varies somewhat according to the convention. Polysaccharides are an important class of biological polymers. Their function in living organisms is usually either structure- or storage-related. Starch (a polymer of glucose) is used as a storage polysaccharide in plants, being found in the form of both amylose and the branched amylopectin. In animals, the structurally similar glucose polymer is the more densely branched glycogen, sometimes called "animal starch". Glycogen's properties allow it to be metabolized more quickly, which suits the active lives of moving animals. In bacteria, they play an important role in bacterial multicellularity.[5]

Cellulose and chitin are examples of structural polysaccharides. Cellulose is used in the cell walls of plants and other organisms and is said to be the most abundant organic molecule on Earth.[6] It has many uses such as a significant role in the paper and textile industries and is used as a feedstock for the production of rayon (via the viscose process), cellulose acetate, celluloid, and nitrocellulose. Chitin has a similar structure but has nitrogen-containing side branches, increasing its strength. It is found in arthropod exoskeletons and in the cell walls of some fungi. It also has multiple uses, including surgical threads. Polysaccharides also include callose or laminarin, chrysolaminarin, xylan, arabinoxylan, mannan, fucoidan, and galactomannan.

Function

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Structure

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Nutrition polysaccharides are common sources of energy. Many organisms can easily break down starches into glucose; however, most organisms cannot metabolize cellulose or other polysaccharides like cellulose, chitin, and arabinoxylans. Some bacteria and protists can metabolize these carbohydrate types. Ruminants and termites, for example, use microorganisms to process cellulose.[7]

Even though these complex polysaccharides are not very digestible, they provide important dietary elements for humans. Called dietary fiber, these carbohydrates enhance digestion. The main action of dietary fiber is to change the nature of the contents of the gastrointestinal tract and how other nutrients and chemicals are absorbed.[8][9] Soluble fiber binds to bile acids in the small intestine, making them less likely to enter the body; this, in turn, lowers cholesterol levels in the blood.[10] Soluble fiber also attenuates the absorption of sugar, reduces sugar response after eating, normalizes blood lipid levels and, once fermented in the colon, produces short-chain fatty acids as byproducts with wide-ranging physiological activities (discussion below). Although insoluble fiber is associated with reduced diabetes risk, the mechanism by which this occurs is unknown.[11]

Not yet formally proposed as an essential macronutrient (as of 2005), dietary fiber is nevertheless regarded as important for the diet, with regulatory authorities in many developed countries recommending increases in fiber intake.[8][9][12][13]

Storage polysaccharides

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Starch

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Main article: Starch

Starch is a glucose polymer in which glucopyranose units are bonded by alpha-linkages. It is made up of a mixture of amylose (15–20%) and amylopectin (80–85%). Amylose consists of a linear chain of several hundred glucose molecules, and Amylopectin is a branched molecule made of several thousand glucose units (every chain of 24–30 glucose units is one unit of Amylopectin). Starches are insoluble in water. They can be digested by breaking the alpha-linkages (glycosidic bonds). Both humans and other animals have amylases so that they can digest starches. Potato, rice, wheat, and maize are major sources of starch in the human diet. The formations of starches are the ways that plants store glucose.[14]

Glycogen

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Main article: Glycogen

Glycogen serves as the secondary long-term energy storage in animal and fungal cells, with the primary energy stores being held in adipose tissue. Glycogen is made primarily by the liver and the muscles, but can also be made by glycogenesis within the brain and stomach.[15]

Glycogen is analogous to starch, a glucose polymer in plants, and is sometimes referred to as animal starch,[16] having a similar structure to amylopectin but more extensively branched and compact than starch. Glycogen is a polymer of α(1→4) glycosidic bonds linked with α(1→6)-linked branches. Glycogen is found in the form of granules in the cytosol/cytoplasm in many cell types and plays an important role in the glucose cycle. Glycogen forms an energy reserve that can be quickly mobilized to meet a sudden need for glucose, but one that is less compact and more immediately available as an energy reserve than triglycerides (lipids).[citation needed]

In the liver hepatocytes, glycogen can compose up to 8 percent (100–120 grams in an adult) of the fresh weight soon after a meal.[17] Only the glycogen stored in the liver can be made accessible to other organs. In the muscles, glycogen is found in a low concentration of one to two percent of the muscle mass. The amount of glycogen stored in the body—especially within the muscles, liver, and red blood cells[18][19][20]—varies with physical activity, basal metabolic rate, and eating habits such as intermittent fasting. Small amounts of glycogen are found in the kidneys and even smaller amounts in certain glial cells in the brain and white blood cells. The uterus also stores glycogen during pregnancy to nourish the embryo.[17]

Glycogen is composed of a branched chain of glucose residues. It is primarily stored in the liver and muscles.[21]

  • It is an energy reserve for animals.
  • It is the chief form of carbohydrate stored in animal organisms.
  • It is insoluble in water. It turns brown-red when mixed with iodine.
  • It also yields glucose on hydrolysis.
  • Schematic 2-D cross-sectional view of glycogen. A core protein of glycogenin is surrounded by branches of glucose units. The entire globular granule may contain approximately 30,000 glucose units.[22]
    Schematic 2-D cross-sectional view of glycogen. A core protein of glycogenin is surrounded by branches of glucose units. The entire globular granule may contain approximately 30,000 glucose units.[22]
  • A view of the atomic structure of a single branched strand of glucose units in a glycogen molecule.
    A view of the atomic structure of a single branched strand of glucose units in a glycogen molecule.

Galactogen

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Galactogen is a polysaccharide of galactose that functions as energy storage in pulmonate snails and some Caenogastropoda.[23] This polysaccharide is exclusive of the reproduction and is only found in the albumen gland from the female snail reproductive system and in the perivitelline fluid of eggs.[24] Furthermore, galactogen serves as an energy reserve for developing embryos and hatchlings, which is later replaced by glycogen in juveniles and adults.[25]

Formed by crosslinking polysaccharide-based nanoparticles and functional polymers, galactogens have applications within hydrogel structures. These hydrogel structures can be designed to release particular nanoparticle pharmaceuticals and/or encapsulated therapeutics over time or in response to environmental stimuli.[26]

Galactogens are polysaccharides with binding affinity for bioanalytes. With this, by end-point attaching galactogens to other polysaccharides constituting the surface of medical devices, galactogens have use as a method of capturing bioanalytes (e.g., CTC's), a method for releasing the captured bioanalytes and an analysis method.[27]

Inulin

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Main article: Inulin

Inulin is a naturally occurring polysaccharide complex carbohydrate composed of fructose, a plant-derived food that human digestive enzymes cannot completely break down. The inulins belong to a class of dietary fibers known as fructans. Inulin is used by some plants as a means of storing energy and is typically found in roots or rhizomes. Most plants that synthesize and store inulin do not store other forms of carbohydrates such as starch. In the United States in 2018, the Food and Drug Administration approved inulin as a dietary fiber ingredient used to improve the nutritional value of manufactured food products.[28]

Structural polysaccharides

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Some important natural structural polysaccharides

Arabinoxylans

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Arabinoxylans are found in both the primary and secondary cell walls of plants and are the copolymers of two sugars: arabinose and xylose. They may also have beneficial effects on human health.[29]

Cellulose

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Main article: Cellulose

The structural components of plants are formed primarily from cellulose. Wood is largely cellulose and lignin, while paper and cotton are nearly pure cellulose. Cellulose is a polymer made with repeated glucose units bonded together by beta-linkages. Humans and many animals lack an enzyme to break the beta-linkages, so they do not digest cellulose. Certain animals, such as termites can digest cellulose, because bacteria possessing the enzyme are present in their gut. Cellulose is insoluble in water. It does not change color when mixed with iodine. On hydrolysis, it yields glucose. It is the most abundant carbohydrate in nature.[30]

Chitin

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Main article: Chitin

Chitin is one of many naturally occurring polymers. It forms a structural component of many animals, such as exoskeletons. Over time it is bio-degradable in the natural environment. Its breakdown may be catalyzed by enzymes called chitinases, secreted by microorganisms such as bacteria and fungi and produced by some plants. Some of these microorganisms have receptors to simple sugars from the decomposition of chitin. If chitin is detected, they then produce enzymes to digest it by cleaving the glycosidic bonds in order to convert it to simple sugars and ammonia.[31]

Chemically, chitin is closely related to chitosan (a more water-soluble derivative of chitin). It is also closely related to cellulose in that it is a long unbranched chain of glucose derivatives. Both materials contribute structure and strength, protecting the organism.[32]

Pectins

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Pectins are a family of complex polysaccharides that contain 1,4-linked α-D-galactosyl uronic acid residues. They are present in most primary cell walls and in the nonwoody parts of terrestrial plants.[33]

Acidic polysaccharides

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Acidic polysaccharides are polysaccharides that contain carboxyl groups, phosphate groups and/or sulfuric ester groups.[34]

Polysaccharides containing sulfate groups can be isolated from algae[35] or obtained by chemical modification.[36]

Polysaccharides are major classes of biomolecules. They are long chains of carbohydrate molecules, composed of several smaller monosaccharides. These complex bio-macromolecules functions as an important source of energy in animal cell and form a structural component of a plant cell. It can be a homopolysaccharide or a heteropolysaccharide depending upon the type of the monosaccharides.

Polysaccharides can be a straight chain of monosaccharides known as linear polysaccharides, or it can be branched known as a branched polysaccharide.

Bacterial polysaccharides

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Pathogenic bacteria commonly produce a bacterial capsule, a thick, mucus-like layer of polysaccharide. The capsule cloaks antigenic proteins on the bacterial surface that would otherwise provoke an immune response and thereby lead to the destruction of the bacteria. Capsular polysaccharides are water-soluble, commonly acidic, and have molecular weights on the order of 100,000 to 2,000,000 daltons. They are linear and consist of regularly repeating subunits of one to six monosaccharides. There is enormous structural diversity; nearly two hundred different polysaccharides are produced by E. coli alone. Mixtures of capsular polysaccharides, either conjugated or native, are used as vaccines.[37]

Bacteria and many other microbes, including fungi and algae, often secrete polysaccharides to help them adhere to surfaces and to prevent them from drying out.[38] Humans have developed some of these polysaccharides into useful products, including xanthan gum, dextran, welan gum, gellan gum, diutan gum and pullulan.

Most of these polysaccharides exhibit useful visco-elastic properties when dissolved in water at very low levels.[39] This makes various liquids used in everyday life, such as some foods, lotions, cleaners, and paints, viscous when stationary, but much more free-flowing when even slight shear is applied by stirring or shaking, pouring, wiping, or brushing. This property is named pseudoplasticity or shear thinning; the study of such matters is called rheology.[citation needed]

Viscosity of Welan gum
Shear rate (rpm) Viscosity (cP or mPa⋅s)
0.3 23330
0.5 16000
1 11000
2 5500
4 3250
5 2900
10 1700
20 900
50 520
100 310

Aqueous solutions of the polysaccharide alone have a curious behavior when stirred: after stirring ceases, the solution initially continues to swirl due to momentum, then slows to a standstill due to viscosity and reverses direction briefly before stopping. This recoil is due to the elastic effect of the polysaccharide chains, previously stretched in solution, returning to their relaxed state.

Cell-surface polysaccharides play diverse roles in bacterial ecology and physiology. They serve as a barrier between the cell wall and the environment, mediate host-pathogen interactions. Polysaccharides also play an important role in formation of biofilms and the structuring of complex life forms in bacteria like Myxococcus xanthus[5].

These polysaccharides are synthesized from nucleotide-activated precursors (called nucleotide sugars) and, in most cases, all the enzymes necessary for biosynthesis, assembly and transport of the completed polymer are encoded by genes organized in dedicated clusters within the genome of the organism. Lipopolysaccharide is one of the most important cell-surface polysaccharides, as it plays a key structural role in outer membrane integrity, as well as being an important mediator of host-pathogen interactions.

The enzymes that make the A-band (homopolymeric) and B-band (heteropolymeric) O-antigens have been identified and the metabolic pathways defined.[40] The exopolysaccharide alginate is a linear copolymer of β-1,4-linked D-mannuronic acid and L-guluronic acid residues, and is responsible for the mucoid phenotype of late-stage cystic fibrosis disease. The pel and psl loci are two recently discovered gene clusters that also encode exopolysaccharides found to be important for biofilm formation. Rhamnolipid is a biosurfactant whose production is tightly regulated at the transcriptional level, but the precise role that it plays in disease is not well understood at present. Protein glycosylation, particularly of pilin and flagellin, became a focus of research by several groups from about 2007, and has been shown to be important for adhesion and invasion during bacterial infection.[41]

Chemical identification tests for polysaccharides

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Periodic acid-Schiff stain (PAS)

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Polysaccharides with unprotected vicinal diols or amino sugars (where some hydroxyl groups are replaced with amines) give a positive periodic acid-Schiff stain (PAS). The list of polysaccharides that stain with PAS is long. Although mucins of epithelial origins stain with PAS, mucins of connective tissue origin have so many acidic substitutions that they do not have enough glycol or amino-alcohol groups left to react with PAS.[citation needed]

Derivatives

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By chemical modifications certain properties of polysaccharides can be improved. Various ligands can be covalently attached to their hydroxyl groups. Due to the covalent attachment of methyl-, hydroxyethyl- or carboxymethyl- groups on cellulose, for instance, high swelling properties in aqueous media can be introduced.[42]

Another example is thiolated polysaccharides.[43] (See thiomers.) Thiol groups are covalently attached to polysaccharides such as hyaluronic acid or chitosan.[44][45] As thiolated polysaccharides can crosslink via disulfide bond formation, they form stable three-dimensional networks. Furthermore, they can bind to cysteine subunits of proteins via disulfide bonds. Because of these bonds, polysaccharides can be covalently attached to endogenous proteins such as mucins or keratins.[43]

See also

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References

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  1. ^ Varki A, Cummings R, Esko J, Freeze H, Stanley P, Bertozzi C, Hart G, Etzler M (1999). Essentials of Glycobiology. Cold Spring Harbor Laboratory Press. ISBN 978-0-87969-560-6.
  2. ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "homopolysaccharide (homoglycan)". doi:10.1351/goldbook.H02856
  3. ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "heteropolysaccharide (heteroglycan)". doi:10.1351/goldbook.H02812
  4. ^ Matthews CE, Van Holde KE, Ahern KG (1999). Biochemistry (3rd ed.). Benjamin Cummings. ISBN 0-8053-3066-6.
  5. ^ a b Islam ST, Vergara Alvarez I, Saïdi F, Guiseppi A, Vinogradov E, Sharma G, et al. (June 2020). "Modulation of bacterial multicellularity via spatio-specific polysaccharide secretion". PLOS Biology. 18 (6): e3000728. doi:10.1371/journal.pbio.3000728. PMC 7310880. PMID 32516311.
  6. ^ Campbell NA (1996). Biology (4th ed.). NY: Benjamin Cummings. p. 23. ISBN 0-8053-1957-3.
  7. ^ "Turning Waste Into Food: Cellulose Digestion – Dartmouth Undergraduate Journal of Science". sites.dartmouth.edu. Retrieved 2021-09-18.
  8. ^ a b "Dietary Reference Intakes for Energy, Carbohydrate, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids (Macronutrients) (2005), Chapter 7: Dietary, Functional and Total fiber" (PDF). US Department of Agriculture, National Agricultural Library and National Academy of Sciences, Institute of Medicine, Food and Nutrition Board. Archived from the original (PDF) on 2011-10-27.
  9. ^ a b Eastwood M, Kritchevsky D (2005). "Dietary fiber: how did we get where we are?". Annual Review of Nutrition. 25: 1–8. doi:10.1146/annurev.nutr.25.121304.131658. PMID 16011456.
  10. ^ Anderson JW, Baird P, Davis RH, Ferreri S, Knudtson M, Koraym A, et al. (April 2009). "Health benefits of dietary fiber" (PDF). Nutrition Reviews. 67 (4): 188–205. doi:10.1111/j.1753-4887.2009.00189.x. PMID 19335713. S2CID 11762029. Archived from the original (PDF) on 2017-08-10. Retrieved 2017-10-25.
  11. ^ Weickert MO, Pfeiffer AF (March 2008). "Metabolic effects of dietary fiber consumption and prevention of diabetes". The Journal of Nutrition. 138 (3): 439–42. doi:10.1093/jn/138.3.439. PMID 18287346.
  12. ^ "Scientific Opinion on Dietary Reference Values for carbohydrates and dietary fibre". EFSA Journal. 8 (3): 1462. March 25, 2010. doi:10.2903/j.efsa.2010.1462.
  13. ^ Jones PJ, Varady KA (February 2008). "Are functional foods redefining nutritional requirements?". Applied Physiology, Nutrition, and Metabolism. 33 (1): 118–23. doi:10.1139/H07-134. PMID 18347661. Archived from the original (PDF) on 2011-10-13.
  14. ^ Pfister, Barbara; Zeeman, Samuel C. (July 2016). "Formation of starch in plant cells". Cellular and Molecular Life Sciences. 73 (14): 2781–2807. doi:10.1007/s00018-016-2250-x. ISSN 1420-682X. PMC 4919380. PMID 27166931.
  15. ^ Saladin KS (2007). Anatomy and Physiology. McGraw-Hill.
  16. ^ "Animal starch". Merriam Webster. Retrieved May 11, 2014.
  17. ^ a b Campbell NA, Williamson B, Heyden RJ (2006). Biology: Exploring Life. Boston, Massachusetts: Pearson Prentice Hall. ISBN 978-0-13-250882-7.
  18. ^ Moses SW, Bashan N, Gutman A (December 1972). "Glycogen metabolism in the normal red blood cell". Blood. 40 (6): 836–43. doi:10.1182/blood.V40.6.836.836. PMID 5083874.
  19. ^ Ingermann RL, Virgin GL (January 20, 1987). "Glycogen Content and Release of Glucose from Red blood cells of the Sipunculan Worm Themiste Dyscrita" (PDF). Journal of Experimental Biology. 129: 141–149. doi:10.1242/jeb.129.1.141. Retrieved July 21, 2017.
  20. ^ Miwa I, Suzuki S (November 2002). "An improved quantitative assay of glycogen in erythrocytes". Annals of Clinical Biochemistry. 39 (Pt 6): 612–3. doi:10.1258/000456302760413432. PMID 12564847.
  21. ^ Ørtenblad, N.; Nielsen, J. (2015). "Muscle glycogen and cell function – Location, location, location". Scandinavian Journal of Medicine & Science in Sports. 25 (S4): 34–40. doi:10.1111/sms.12599. ISSN 0905-7188.
  22. ^ McArdle WD, Katch FI, Katch VL (2006). Exercise physiology: energy, nutrition, and human performance (6th ed.). Lippincott Williams & Wilkins. p. 12. ISBN 978-0-7817-4990-9.
  23. ^ Goudsmit EM (1972). "Carbohydrates and carbohydrate metabolism in Mollusca". In Florkin M, Scheer BT (eds.). Chemical Zoology. Vol. VII Mollusca. New York: Academic Press. pp. 219–244.
  24. ^ May, F; Weinland, H (1953). "Glycogen formation in the galactogen-containing eggs of Helix pomatia during embryonal period". Zeitschrift für Biologie. 105 (5): 339–347. PMID 13078807.
  25. ^ May F (1932). "Beitrag zur Kenntnis des Glykogen und Galaktogengehaltes bei Helix pomatia". Z. Biol. 92: 319–324.
  26. ^ Hoare, Todd; Babar, Ali. "In situ gelling polysaccharide-based nanoparticle hydrogel compositions, and methods of use thereof". PubChem. 1 (1).
  27. ^ Wiegman, Peter; Mulder, Hans. "A process for applying a coating comprising one or more polysaccharides with binding affinity for bioanalytes onto the surface of a medical sampling device, and the medical sampling device for capture of bioanalytes provided with the coating". PubChem. 1 (1): 101–104.
  28. ^ "The Declaration of Certain Isolated or Synthetic Non-Digestible Carbohydrates as Dietary Fiber on Nutrition and Supplement Facts Labels: Guidance for Industry" (PDF). U.S. Food and Drug Administration. 14 June 2018.
  29. ^ Mendis M, Simsek S (15 December 2014). "Arabinoxylans and human health". Food Hydrocolloids. 42: 239–243. doi:10.1016/j.foodhyd.2013.07.022.
  30. ^ Bhardwaj, Uma; Bhardwaj, Ravindra. Biochemistry for Nurses. Pearson Education India. ISBN 978-81-317-9528-6.
  31. ^ Moussian, Bernard (2019). "Chitin: Structure, Chemistry and Biology". Advances in Experimental Medicine and Biology. 1142: 5–18. doi:10.1007/978-981-13-7318-3_2. ISSN 0065-2598. PMID 31102240.
  32. ^ Merzendorfer, Hans; Zimoch, Lars (December 2003). "Chitin metabolism in insects: structure, function and regulation of chitin synthases and chitinases". The Journal of Experimental Biology. 206 (Pt 24): 4393–4412. doi:10.1242/jeb.00709. ISSN 0022-0949. PMID 14610026. S2CID 27291096.
  33. ^ MOHNEN, D (2008). "Pectin structure and biosynthesis". Current Opinion in Plant Biology. 11 (3): 266–277. doi:10.1016/j.pbi.2008.03.006. ISSN 1369-5266. PMID 18486536.
  34. ^ Mohammed, A.S.A., Naveed, M. & Jost, N. Polysaccharides; Classification, Chemical Properties, and Future Perspective Applications in Fields of Pharmacology and Biological Medicine (A Review of Current Applications and Upcoming Potentialities). J Polym Environ 29, 2359–2371 (2021). https://doi.org/10.1007/s10924-021-02052-2
  35. ^ Cunha L, Grenha A. Sulfated Seaweed Polysaccharides as Multifunctional Materials in Drug Delivery Applications. Mar Drugs. 2016;14(3):42. doi: 10.3390/md14030042
  36. ^ Kazachenko A.S., Akman F., Malyar Y.N., ISSAOUI N., Vasilieva N.Y., Karacharov A.A. Synthesis optimization, DFT and physicochemical study of chitosan sulfates (2021) Journal of Molecular Structure, 1245, art. no. 131083. DOI: 10.1016/j.molstruc.2021.131083
  37. ^ Seeberger, Peter H. (2021-04-14). "Discovery of Semi- and Fully-Synthetic Carbohydrate Vaccines Against Bacterial Infections Using a Medicinal Chemistry Approach: Focus Review". Chemical Reviews. 121 (7): 3598–3626. doi:10.1021/acs.chemrev.0c01210. ISSN 0009-2665. PMC 8154330. PMID 33794090.
  38. ^ Misra, Swati; Sharma, Varsha; Srivastava, Ashok Kumar (2014), Ramawat, Kishan Gopal; Mérillon, Jean-Michel (eds.), "Bacterial Polysaccharides: An Overview", Polysaccharides, Cham: Springer International Publishing, pp. 1–24, doi:10.1007/978-3-319-03751-6_68-1, ISBN 978-3-319-03751-6, retrieved 2024-06-01
  39. ^ Viscosity of Welan Gum vs. Concentration in Water. "XYdatasource - Fundamental Research Data at Your Fingertips". Archived from the original on 2011-07-18. Retrieved 2009-10-02.
  40. ^ Guo H, Yi W, Song JK, Wang PG (2008). "Current understanding on biosynthesis of microbial polysaccharides". Current Topics in Medicinal Chemistry. 8 (2): 141–51. doi:10.2174/156802608783378873. PMID 18289083.
  41. ^ Cornelis P, ed. (2008). Pseudomonas: Genomics and Molecular Biology (1st ed.). Caister Academic Press. ISBN 978-1-904455-19-6.
  42. ^ Doelker, E (1990). "Swelling Behavior of Water-Soluble Cellulose Derivatives". Studies in Polymer Science. 8 (3): 125–145. doi:10.1016/B978-0-444-88654-5.50011-X. ISBN 9780444886545.
  43. ^ a b Leichner, C; Jelkmann, M; Bernkop-Schnürch, A (2019). "Thiolated polymers: Bioinspired polymers utilizing one of the most important bridging structures in nature". Adv Drug Deliv Rev. 151–152: 191–221. doi:10.1016/j.addr.2019.04.007. PMID 31028759. S2CID 135464452.
  44. ^ Griesser, J; Hetényi, G; Bernkop-Schnürch, A (2018). "Thiolated Hyaluronic Acid as Versatile Mucoadhesive Polymer: From the Chemistry Behind to Product Developments-What Are the Capabilities?". Polymers. 10 (3): 243. doi:10.3390/polym10030243. PMC 6414859. PMID 30966278.
  45. ^ Federer, C; Kurpiers, M; Bernkop-Schnürch, A (2021). "Thiolated Chitosans: A Multi-talented Class of Polymers for Various Applications". Biomacromolecules. 22 (1): 24–56. doi:10.1021/acs.biomac.0c00663. PMC 7805012. PMID 32567846.
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