Xanthan gum was discovered by Allene Rosalind Jeanes and her research team at the United States Department of Agriculture, and brought into commercial production by CP Kelco under the trade name Kelzan in the early 1960s, CP Kelco is the only manufacuturer in the US.[2][3] It was approved for use in foods in 1968 and is accepted as a safe food additive in the US, Canada, European countries, and many other countries, with E number E415, and CAS number 11138-66-2.
Xanthan gum derives its name from the species of bacteria used during the fermentation process, Xanthomonas campestris.[4]
Uses
Xanthan gum, 1%, can produce a significant increase in the viscosity of a liquid.[5]
In foods, xanthan gum is common in salad dressings and sauces. It helps to prevent oil separation by stabilizing the emulsion, although it is not an emulsifier. Xanthan gum also helps suspend solid particles, such as spices. Xanthan gum helps create the desired texture in many ice creams. Toothpaste often contains xanthan gum as a binder to keep the product uniform. Xanthan gum also helps thicken commercial egg substitutes made from egg whites, to replace the fat and emulsifiers found in yolks. It is also a preferred method of thickening liquids for those with swallowing disorders, since it does not change the color or flavor of foods or beverages at typical use levels.[6] In gluten-free baking, xanthan gum is used to give the dough or batter the stickiness that would otherwise be achieved with gluten. In most foods, it is used at concentrations of 0.5% or less. Xanthan gum is used in a wide range of food products, such as sauces, dressings, meat and poultry products, bakery products, confectionery products, beverages, dairy products, and others.
In the oil industry, xanthan gum is used in large quantities to thicken drilling mud.[7] These fluids carry the solids cut by the drilling bit to the surface. Xanthan gum provides improved "low end"[clarification needed]rheology. When circulation stops, the solids remain suspended in the drilling fluid. The widespread use of horizontal drilling and the demand for good control of drilled solids has led to its expanded use. It has been added to concrete poured underwater, to increase its viscosity and prevent washout.
In cosmetics, xanthan gum is used to prepare water gels.[8] It is also used in oil-in-water emulsions to enhance droplet coalescence.[9] Xanthan gum is under preliminary research for its potential uses in tissue engineering to construct hydrogels and scaffolds supporting three-dimensional tissue formation.[8] Furthermore, thiolated xanthan gum (see thiomers) has shown potential for drug delivery,[10][11] since by the covalent attachment of thiol groups to this polysaccharide high mucoadhesive and permeation enhancing properties can be introduced.[12]
Shear thinning
The viscosity of xanthan gum solutions decreases with higher shear rates. This is called shear thinning or pseudoplasticity. This means that a product subjected to shear, whether from mixing, shaking or chewing, will thin. This is similar to the behaviour of tomato ketchup. When the shear forces are removed, the food will thicken again. In salad dressing, the addition of xanthan gum makes it thick enough at rest in the bottle to keep the mixture fairly homogeneous, but the shear forces generated by shaking and pouring thins it, so it can be easily poured. When it exits the bottle, the shear forces are removed and it thickens again, so it clings to the salad. The rheology of xanthan aqua solutions become visco-elastic at higher concentrations of xanthan gum in water.[13]
Concentrations used
The greater the concentration of xanthan gum in a liquid, the thicker the liquid will become. An emulsion can be formed with as little as 0.1% (by weight). Increasing the concentration of gum gives a thicker, more stable emulsion up to 1% xanthan gum. A teaspoon of xanthan gum weighs about 2.5 grams and brings one cup (250ml) of water to a 1% concentration.[6][14]
To make a foam, 0.2–0.8% xanthan gum is typically used. Larger amounts result in larger bubbles and denser foam. Egg white powder (0.2–2.0%) with 0.1–0.4% xanthan gum yields bubbles similar to soap bubbles.
Safety
According to a 2017 safety review by a scientific panel of the European Food Safety Authority (EFSA), xanthan gum (European food additive number E 415) is extensively digested during intestinalfermentation, and causes no adverse effects, even at high intake amounts.[15] The EFSA panel found no concern about genotoxicity from long-term consumption.[15] The EFSA concluded that there is no safety concern for the general population when xanthan gum is consumed as a food additive.[15]
Preparation
Xanthan gum is produced by the fermentation of glucose and sucrose.[4] The medium is well-aerated and stirred, and the xanthan polymer is produced extracellularly into the medium. After one to four days, the polymer is precipitated from the medium by the addition of isopropyl alcohol, and the precipitate is dried and milled to give a powder that is readily soluble in water or brine.[15]
A strain of X. campestris that will grow on lactose has been developed – which allows it to be used to process whey, a waste product of cheese production. This can produce 30 g/L of xanthan gum for every 40 g/L of whey powder. Whey-derived xanthan gum is commonly used in many commercial products, such as shampoos and salad dressings.[17]
Detail of the biosynthesis
Synthesis originates from glucose as substrate for synthesis of the sugar nucleotides precursors UDP-glucose, UDP-glucuronate, and GDP-mannose that are required for building the pentasaccharide repeat unit.[15] This links the synthesis of xanthan to carbohydrate metabolism. The repeat units are built up at undecaprenylphosphate lipid carriers that are anchored in the cytoplasmic membrane.[citation needed]
Specific glycosyltransferases sequentially transfer the sugar moieties of the nucleotide sugar xanthan precursors to the lipid carriers. Acetyl and pyruvyl residues are added as non-carbohydrate decorations. Mature repeat units are polymerized and exported in a way resembling the Wzy-dependent polysaccharide synthesis mechanism of Enterobacteriaceae. Products of the gum gene cluster drive synthesis, polymerization, and export of the repeat unit.[18]
^Whistler RL, BeMiller JN (1973). Industrial gums, polysaccharides and their derivatives (2nd ed.). New York: Academic Press. ISBN978-0-12-746252-3.
^"KELZAN Xanthan Gum - CP Kelco". cpkelco.com. CP Kelco. Feb 18, 2019. Retrieved Feb 18, 2019. CP Kelco offers a range of biopolymers to thicken, suspend and stabilize emulsions and other water-based systems. The KELZAN xanthan gum line of industrial products can be used to modify the texture of industrial products and to stabilize household cleaners, fabric care products, suspensions, oil-in-water emulsions and foams against separation.
^ abBarrere GC, Barber CE, Daniels MJ (December 1986). "Molecular cloning of genes involved in the production of the extracellular polysaccharide xanthan by Xanthomonas campestris pv. campestris". International Journal of Biological Macromolecules. 8 (6): 372–374. doi:10.1016/0141-8130(86)90058-9.
^Davidson RL (1980). Handbook of Water-soluble Gums and Resins. McGraw Hill. ISBN978-0-07-015471-1.
^ abcuisine, m. (2014). Xanthan Gum. Retrieved from modernist cuisine: "Xanthan Gum". 2012-11-27. Archived from the original on 2014-06-18. Retrieved 2014-06-21.
^ abKumar A, Rao KM, Han SS (January 2018). "Application of xanthan gum as polysaccharide in tissue engineering: A review". Carbohydrate Polymers. 180: 128–144. doi:10.1016/j.carbpol.2017.10.009. PMID29103488.
^Ye A, Hemar Y, Singh H (August 2004). "Influence of polysaccharides on the rate of coalescence in oil-in-water emulsions formed with highly hydrolyzed whey proteins". Journal of Agricultural and Food Chemistry. 52 (17): 5491–5498. Bibcode:2004JAFC...52.5491Y. doi:10.1021/jf030762o. PMID15315390.
^Bhatia M, Ahuja M, Mehta H (October 2015). "Thiol derivatization of Xanthan gum and its evaluation as a mucoadhesive polymer". Carbohydrate Polymers. 131: 119–124. doi:10.1016/j.carbpol.2015.05.049. PMID26256167.
^Leichner C, Jelkmann M, Bernkop-Schnürch A (2019). "Thiolated polymers: Bioinspired polymers utilizing one of the most important bridging structures in nature". Advanced Drug Delivery Reviews. 151–152: 191–221. doi:10.1016/j.addr.2019.04.007. PMID31028759. S2CID135464452.
^García-Ochoa F, Santos VE, Casas JA, Gómez E (November 2000). "Xanthan gum: production, recovery, and properties". Biotechnology Advances. 18 (7): 549–579. doi:10.1016/S0734-9750(00)00050-1. PMID14538095.
^Tortora GJ, Funke BR, Case CL (2010). Microbiology: An Introduction (10th ed.). San Francisco: Benjamin Cummings. p. 801.
^Becker A, Vorhölter FJ (2009). "Xanthan Biosynthesis by Xanthomonas Bacteria: An Overview of the Current Biochemical and Genomic Data". In Rehm BH (ed.). Microbial Production of Biopolymers and Polymer Precursors. Caister Academic Press. ISBN978-1-904455-36-3.