Information about Chitin

Chitin (C₈H₁₃O₅N)_n (IPA: [ˈkaɪtn̩]) is a long-chain polymer of beta-glucose that forms a hard, semitransparent material found throughout the natural world. It is the main component of the cell walls of fungi, the exoskeletons of arthropods, such as crustaceans (e.g. crab, lobster and shrimp) and insects (e.g. ants, beetles and butterflies), the radula of molluscs and the beaks of cephalopods (e.g. squid, and octopuses). Chitin has also proven useful for several medical and industrial purposes.

Chemistry, physical properties and biological function

Chitin is a polysaccharide; it is synthesized from units of N-acetylglucosamine (more completely, N-acetyl-D-glucos-2-amine). These units form covalent β-1,4 linkages (similar to the linkages between glucose units forming cellulose). Chitin may therefore be described as cellulose with one hydroxyl group on each monomer substituted with an acetylamine group. This allows for increased hydrogen bonding between adjacent polymers, giving the chitin-polymer matrix increased strength.

In its unmodified form, chitin is translucent, pliable, resilient and quite tough. In arthropods, however, it is often modified, becoming embedded in a hardened proteinaceous matrix, which forms much of the exoskeleton. In its pure form it's leathery, but when encrusted in calcium carbonate it becomes much harder.^[1] The difference between the unmodified and modified forms can be seen by comparing the body wall of a caterpillar (unmodified) to a beetle (modified).

Chitin is one of many naturally occurring polymers. 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.

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.

Etymology

The English word "chitin" comes from the French word "chitine", which first appeared in 1836. These words were derived from the Latin word "chitōn", meaning mollusk. That is either influenced by, or related to the Greek word khitōn, meaning "tunic" or "frock", the Central Semitic word "*kittan", the Akkadian words "kitû" or "kita’um", meaning flax or linen, and the Sumerian word "gada" or "gida".^[2]

A similar word, "chiton", refers to a marine animal with a protective shell (also known as a "sea cradle").

Uses

Industrial

Chitin is used industrially in many processes. It is used in water purification, and as an additive to thicken and stabilize foods and pharmaceuticals. It also acts as a binder in dyes, fabrics, and adhesives. Industrial separation membranes and ion-exchange resins can be made from chitin. Processes to size and strengthen paper employ chitin.

Medicine

Chitin's properties as a flexible and strong material make it favourable as surgical thread. Its biodegradibility means it wears away with time as the wound heals. Moreover, chitin has some unusual properties that accelerate healing of wounds in humans. Chitin has even been used as a stand-alone wound-healing agent. ^[3] Chitin is used to make Chitosan, a product with numerous commercial and possible biomedical uses. Its most famous use is as a weight loss product.

Agriculture

Most recent studies point out that chitin is a good inductor for defense mechanisms in plants. It was recently tested as a fertilizer that can help plants develop healthy immune responses, and have a much better yield and life expectancy.

References

External links

• Chitin Product Information from China GreatVista Chemicals
• Horseshoe Crab Chitin Research
• MeSH Chitin

•  • [ e] Major families of biochemicals
Peptides | Amino acids | Nucleic acids | Carbohydrates | Lipids | Terpenes | Carotenoids | Tetrapyrroles | Enzyme cofactors | Steroids | Flavonoids | Alkaloids | Polyketides | Glycosides
Analogues of nucleic acids:	Types of Carbohydrates	Analogues of nucleic acids:
General:	Aldose | Ketose | Pyranose | Furanose
Geometry:	Pentose | Hexose | Heptose | Cyclohexane conformation | Anomer | Mutarotation
Small/Large:	Glyceraldehyde | Dihydroxyacetone | Erythrose | Threose | Erythrulose | Sedoheptulose
Pentoses:	Arabinose | Deoxyribose | Lyxose | Ribose | Ribulose | Xylose | Xylulose
Hexoses:	Glucose | Galactose | Mannose | Gulose | Idose | Talose | Allose | Altrose | Fructose | Sorbose | Tagatose | Psicose | Fucose | Rhamnose
Disaccharides:	Sucrose | Lactose | Trehalose | Maltose
Polymers:	Glycogen | Starch (Amylose | Amylopectin) | Cellulose | Chitin | Stachyose | Inulin | Dextrin
Glycosaminoglycans:	Heparin | Chondroitin sulfate | Hyaluronan | Heparan sulfate | Dermatan sulfate | Keratan sulfate
Aminoglycosides:	Kanamycin | Streptomycin | Tobramycin | Neomycin | Paromomycin | Apramycin | Gentamicin | Netilmicin | Amikacin