Carbohydrate

A carbohydrate (/ˌkɑːrboʊˈhaɪdreɪt/) is a sugar (saccharide) or a sugar derivative.[1] For the simplest carbohydrates, the carbon-to-hydrogen-to-oxygen atomic ratio is 1:2:1, i.e. they are often represented by the empirical formula (CH
2O)
n. Together with amino acids, fats, and nucleic acids, the carbohydrates are one of the major families of biomolecules.[2]

Carbohydrates perform numerous roles in living organisms.[3] Polysaccharides serve as an energy store (e.g., starch and glycogen) and as structural components (e.g., cellulose in plants and chitin in arthropods and fungi). The 5-carbon monosaccharide ribose is an important component of coenzymes (e.g., ATP, FAD and NAD) and the backbone of the genetic molecule known as RNA. The related deoxyribose is a component of DNA. Saccharides and their derivatives play key roles in the immune system, fertilization, preventing pathogenesis, blood clotting, and development.[4]

Carbohydrates are central to nutrition and are found in a wide variety of natural and processed foods. Starch is a polysaccharide and is abundant in cereals (wheat, maize, rice), potatoes, and processed food based on cereal flour, such as bread, pizza or pasta. Sugars appear in the human diet mainly as table sugar (sucrose, extracted from sugarcane or sugar beets), lactose (abundant in milk), glucose and fructose, both of which occur naturally in honey, many fruits, and some vegetables. Table sugar, milk, or honey is often added to drinks and many prepared foods such as jam, biscuits and cakes.

## Contents

* 1 Terminology
* 1.1 Saccharides
* 1.2 Complex carbohydrates
* 2 History
* 3 Nutrition
* 3.1 Classification
* 3.1.1 Glycemic index
* 3.2 Health effects of dietary carbohydrate restriction
* 4 Sources
* 5 Metabolism
* 5.1 Catabolism
* 6 Analytical tools
* 6.1 High-resolution mass spectrometry (MS) and high-performance liquid chromatography (HPLC)
* 6.2 Multiple reaction monitoring (MRM)
* 7 Chemical synthesis and manipulation of carbohydrates
* 8 See also
* 9 References
* 10 Further reading
* 11 External links

## Terminology

The term "carbohydrate" has many synonyms and the definition can depend on context. Terms associated with carbohydrate include "sugar", "saccharide", "glucan",[5] and "glucide".[6] In food science the term "carbohydrate" often means any food that is rich in starch (such as cereals, bread and pasta) or simple carbohydrates, or fairly simple sugars such as sucrose (found in candy, jams, and desserts). Carbohydrates can also refer to dietary fiber, like cellulose.[7][8]

### Saccharides

The starting point for the discussion of carbohydrates is the saccharides. Monosaccharides are the simplest carbohydrates in that they cannot be hydrolyzed to smaller carbohydrates. Monosaccharides usually have the formula Cm (H2O)n. Disaccharides (e.g. sucrose) are common as are polysaccharides/oligosaccharides (e.g., starch, cellulose). Saccharides are polyhydroxy aldehydes, ketones as well as derived polymers having linkages of the acetal type. They may be classified according to their degree of polymerization. Many polyols are also classified as carbohydrates. In many carbohydrates the OH groups are appended to or replaced by N-acetyl (e.g., chitin), sulfate (e.g., glycosaminoglycans), carboxylic acid and deoxy modifications (e.g., fucose and sialic acid).[6]

The major dietary carbohydrates  Class
(degree of polymerization) | Subgroup | Components

|
|

Sugars (1–2)  | Monosaccharides | Glucose, galactose, fructose, xylose
Disaccharides | Sucrose, lactose, maltose, isomaltulose, trehalose
Polyols | Sorbitol, mannitol
Oligosaccharides (3–9)  | Malto-oligosaccharides | Maltodextrins
Other oligosaccharides | Raffinose, stachyose, fructo-oligosaccharides
Polysaccharides (>9)  | Starch | Amylose, amylopectin, modified starches
Non-starch polysaccharides | Glycogen, Cellulose, Hemicellulose, Pectins, Hydrocolloids

### Complex carbohydrates

Heparin, a carbohydrate, is a blood anticoagulant.[9]

Sugars may be linked to other types of biological molecules to form glycoconjugates. The enzymatic process of glycosylation creates sugars/saccharides linked to themselves and to other molecules by the glycosidic bond, thereby producing glycans. Glycoproteins, proteoglycans and glycolipids are the most abundant glycoconjugates found in mammalian cells. They are found predominantly on the outer cell membrane and in secreted fluids. Glycoconjugates have been shown to be important in cell-cell interactions due to the presence on the cell surface of various glycan binding receptors in addition to the glycoconjugates themselves.[10][11] In addition to their function in protein folding and cellular attachment, the N-linked glycans of a protein can modulate the protein's function, in some cases acting as an on-off switch.[12]

## History

Error creating thumbnail: Emil Fischer, who elucidated the structure of glucose, with colleagues and student in their laboratory of LMU Munich in 1877.

The history of carbohydrates, to some extent, is the history of sugar cane, which was first grown in New Guinea. The mass cultivation occurred in India where techniques were developed for the isolation of crystalline sugar.[13] Cane sugar and its cultivation reached Europe around the 13th Century and then expanded to the New World, where industrialization occurred.

The chemistry and biochemistry of carbohydrates can be traced to 1811. On that year Constantin Kirchhoff discovered that grape sugar (glucose) forms when starch is boiled with acid. The starch industry started the following year. Henri Braconnot discovered in 1819 that sugar is formed through the action of sulfuric acid on cellulose. William Prout, after chemical analyses of sugar and starch by Joseph Louis Gay-Lussac and Thénard, gave this group of substances the group name "saccharine." The term "carbohydrate" was first proposed by German chemist Carl Schmidt in 1844. In 1856, glycogen, a form of carbohydrate storage in animal livers, was discovered by French physiologist Claude Bernard.[14] Emil Fischer received the 1902 Nobel Prize in Chemistry for his work on sugars and purines. For the discovery of glucose metabolism, Otto Meyerhof received the 1922 Nobel Prize in Physiology or Medicine. Hans von Euler-Chelpin, together with Arthur Harden, received the 1929 Nobel Prize in Chemistry "for their research on sugar fermentation and the role of enzymes in this process." In 1947, both Bernardo Houssay for his discovery of the role of the pituitary gland in carbohydrate metabolism and Carl and Gerty Cori for their discovery of the conversion of glycogen received the Nobel Prize in Physiology or Medicine. For the discovery of sugar nucleotides in carbohydrate biosynthesis, Luis Leloir received the 1970 Nobel Prize in Chemistry.

The term glycobiology[15] was coined in 1988 by Raymond Dwek to recognize the coming together of the traditional disciplines of carbohydrate chemistry and biochemistry.[16] This coming together was as a result of a much greater understanding of the cellular and molecular biology of glycans. "Glycoscience" is a field that explores the structures and functions of glycans.[17]

## Nutrition

Grain products: rich sources of carbohydrates

Carbohydrate consumed in food yields 3.87 kilocalories of energy per gram for simple sugars,[18] and 3.57 to 4.12 kilocalories per gram for complex carbohydrate in most other foods.[19] Relatively high levels of carbohydrate are associated with processed foods or refined foods made from plants, including sweets, cookies and candy, table sugar, honey, soft drinks, breads and crackers, jams and fruit products, pastas and breakfast cereals. Refined carbohydrates from processed foods such as white bread or rice, soft drinks, and desserts are readily digestible, and many are known to have a high glycemic index, which reflects a rapid assimilation of glucose. By contrast, the digestion of whole, unprocessed, fiber-rich foods such as beans, peas, and whole grains produces a slower and steadier release of glucose and energy into the body.[20] Animal-based foods generally have the lowest carbohydrate levels, although milk does contain a high proportion of lactose.

Organisms typically cannot metabolize all types of carbohydrate to yield energy. Glucose is a nearly universal and accessible source of energy. Many organisms also have the ability to metabolize other monosaccharides and disaccharides but glucose is often metabolized first. In Escherichia coli, for example, the lac operon will express enzymes for the digestion of lactose when it is present, but if both lactose and glucose are present, the lac operon is repressed, resulting in the glucose being used first (see: Diauxie). Polysaccharides are also common sources of energy. Many organisms can easily break down starches into glucose; most organisms, however, cannot metabolize cellulose or other polysaccharides such as chitin and arabinoxylans. These carbohydrate types can be metabolized by some bacteria and protists. Ruminants and termites, for example, use microorganisms to process cellulose, fermenting it to caloric short-chain fatty acids. Even though humans lack the enzymes to digest fiber, dietary fiber represents an important dietary element for humans. Fibers promote healthy digestion, help regulate postprandial glucose and insulin levels, reduce cholesterol levels, and promote satiety.[21]

The Institute of Medicine recommends that American and Canadian adults get between 45 and 65% of dietary energy from whole-grain carbohydrates.[22] The Food and Agriculture Organization and World Health Organization jointly recommend that national dietary guidelines set a goal of 55–75% of total energy from carbohydrates, but only 10% directly from sugars (their term for simple carbohydrates).[23] A 2017 Cochrane Systematic Review concluded that there was insufficient evidence to support the claim that whole grain diets can affect cardiovascular disease.[24]

Carbohydrates are one of the main components of insoluble dietary fiber. Although it is not digestible by humans, cellulose and insoluble dietary fiber generally help maintain a healthy digestive system by facilitating bowel movements.[7] Other polysaccharides contained in dietary fiber include resistant starch and inulin, which feed some bacteria in the microbiota of the large intestine, and are metabolized by these bacteria to yield short-chain fatty acids.[7][25][26]

### Classification

The term complex carbohydrate was first used in the U.S. Senate Select Committee on Nutrition and Human Needs publication Dietary Goals for the United States (1977) where it was intended to distinguish sugars from other carbohydrates (which were perceived to be nutritionally superior).[27] However, the report put "fruit, vegetables and whole-grains" in the complex carbohydrate column, despite the fact that these may contain sugars as well as polysaccharides. The standard usage, however, is to classify carbohydrates chemically: simple if they are sugars (monosaccharides and disaccharides) and complex if they are polysaccharides (or oligosaccharides).[7][28] Carbohydrates are sometimes divided into "available carbohydrates", which are absorbed in the small intestine and "unavailable carbohydrates", which pass to the large intestine, where they are subject to fermentation by the gastrointestinal microbiota.[7]

#### Glycemic index

The glycemic index (GI) and glycemic load concepts characterize the potential for carbohydrates in food to raise blood glucose compared to a reference food (generally pure glucose).[29] Expressed numerically as GI, carbohydrate-containing foods can be grouped as high-GI (score more than 70), moderate-GI (56–69), or low-GI (less than 55) relative to pure glucose (GI=100).[29] Consumption of carbohydrate-rich, high-GI foods causes an abrupt increase in blood glucose concentration that declines rapidly following the meal, whereas low-GI foods with lower carbohydrate content produces a lower blood glucose concentration that returns gradually after the meal.[29]

Glycemic load is a measure relating the quality of carbohydrates in a food (low- vs. high-carbohydrate content - the GI) by the amount of carbohydrates in a single serving of that food.[29]

### Health effects of dietary carbohydrate restriction

Main article: Chemistry:Low-carbohydrate diet

Low-carbohydrate diets may miss the health advantages – such as increased intake of dietary fiber and phytochemicals – afforded by high-quality plant foods such as legumes and pulses, whole grains, fruits, and vegetables.[30][31] A "meta-analysis, of moderate quality," included as adverse effects of the diet halitosis, headache and constipation.[32] Carbohydrate-restricted diets can be as effective as low-fat diets in helping achieve weight loss over the short term when overall calorie intake is reduced.[33] An Endocrine Society scientific statement said that "when calorie intake is held constant [...] body-fat accumulation does not appear to be affected by even very pronounced changes in the amount of fat vs carbohydrate in the diet."[33] In the long term, low-carbohydrate diets do not appear to confer a "metabolic advantage," and effective weight loss or maintenance depends on the level of calorie restriction,[33] not the ratio of macronutrients in a diet.[34] The reasoning of diet advocates that carbohydrates cause undue fat accumulation by increasing blood insulin levels, but a more balanced diet that restricts refined carbohydrates can also reduce serum glucose and insulin levels and may also suppress lipogenesis and promote fat oxidation.[35] However, as far as energy expenditure itself is concerned, the claim that low-carbohydrate diets have a "metabolic advantage" is not supported by clinical evidence.[33][36] Further, it is not clear how low-carbohydrate dieting affects cardiovascular health, although two reviews showed that carbohydrate restriction may improve lipid markers of cardiovascular disease risk.[37][38]

Carbohydrate-restricted diets are no more effective than a conventional healthy diet in preventing the onset of type 2 diabetes, but for people with type 2 diabetes, they are a viable option for losing weight or helping with glycemic control.[39][40][41] There is limited evidence to support routine use of low-carbohydrate dieting in managing type 1 diabetes.[42] The American Diabetes Association recommends that people with diabetes should adopt a generally healthy diet, rather than a diet focused on carbohydrate or other macronutrients.[41]

An extreme form of low-carbohydrate diet – the ketogenic diet – is established as a medical diet for treating epilepsy.[43] Through celebrity endorsement during the early 21st century, it became a fad diet as a means of weight loss, but with risks of undesirable side effects, such as low energy levels and increased hunger, insomnia, nausea, and gastrointestinal discomfort.[scientific citation needed][43] The British Dietetic Association named it one of the "top 5 worst celeb diets to avoid in 2018".[43]

## Sources

Glucose tablets

Most dietary carbohydrates contain glucose, either as their only building block (as in the polysaccharides starch and glycogen), or together with another monosaccharide (as in the hetero-polysaccharides sucrose and lactose).[44] Unbound glucose is one of the main ingredients of honey. Glucose is extremely abundant and has been isolated from a variety of natural sources across the world, including male cones of the coniferous tree Wollemia nobilis in Rome,[45] the roots of Ilex asprella plants in China,[46] and straws from rice in California.[47]

Sugar content of selected common plant foods (in grams per 100 g)[48] Food
item  | Carbohydrate,
total,A including
dietary fiber  | Total
sugars  | Free
fructose  | Free
glucose  | Sucrose  | Ratio of
fructose/
glucose  | Sucrose as
proportion of
total sugars (%)

|
|
|
|
|
|
|

Fruits
Apple | 13.8 | 10.4 | 5.9 | 2.4 | 2.1 | 2.0 | 19.9
Apricot | 11.1 | 9.2 | 0.9 | 2.4 | 5.9 | 0.7 | 63.5
Banana | 22.8 | 12.2 | 4.9 | 5.0 | 2.4 | 1.0 | 20.0
Fig, dried | 63.9 | 47.9 | 22.9 | 24.8 | 0.9 | 0.93 | 0.15
Grapes | 18.1 | 15.5 | 8.1 | 7.2 | 0.2 | 1.1 | 1
Navel orange | 12.5 | 8.5 | 2.25 | 2.0 | 4.3 | 1.1 | 50.4
Peach | 9.5 | 8.4 | 1.5 | 2.0 | 4.8 | 0.9 | 56.7
Pear | 15.5 | 9.8 | 6.2 | 2.8 | 0.8 | 2.1 | 8.0
Pineapple | 13.1 | 9.9 | 2.1 | 1.7 | 6.0 | 1.1 | 60.8
Plum | 11.4 | 9.9 | 3.1 | 5.1 | 1.6 | 0.66 | 16.2
Vegetables
Beet, red | 9.6 | 6.8 | 0.1 | 0.1 | 6.5 | 1.0 | 96.2
Carrot | 9.6 | 4.7 | 0.6 | 0.6 | 3.6 | 1.0 | 77
Red pepper, sweet | 6.0 | 4.2 | 2.3 | 1.9 | 0.0 | 1.2 | 0.0
Onion, sweet | 7.6 | 5.0 | 2.0 | 2.3 | 0.7 | 0.9 | 14.3
Sweet potato | 20.1 | 4.2 | 0.7 | 1.0 | 2.5 | 0.9 | 60.3
Yam | 27.9 | 0.5 | Traces | Traces | Traces | N/A | Traces
Cassava | 38.1 | 1.7 | Traces | Traces | Traces | N/A | Traces
Sugar cane |  | 13–18 | 0.2–1.0 | 0.2–1.0 | 11–16 | 1.0 | high
Sugar beet |  | 17–18 | 0.1–0.5 | 0.1–0.5 | 16–17 | 1.0 | high
Grains
Corn, sweet | 19.0 | 6.2 | 1.9 | 3.4 | 0.9 | 0.61 | 15.0

^A The carbohydrate value is calculated in the USDA database and does not always correspond to the sum of the sugars, the starch, and the "dietary fiber".

## Metabolism

Main article: Biology:Carbohydrate metabolism

Carbohydrate metabolism is the series of biochemical processes responsible for the formation, breakdown and interconversion of carbohydrates in living organisms.

The most important carbohydrate is glucose, a simple sugar (monosaccharide) that is metabolized by nearly all known organisms. Glucose and other carbohydrates are part of a wide variety of metabolic pathways across species: plants synthesize carbohydrates from carbon dioxide and water by photosynthesis storing the absorbed energy internally, often in the form of starch or lipids. Plant components are consumed by animals and fungi, and used as fuel for cellular respiration. Oxidation of one gram of carbohydrate yields approximately 16 kJ (4 kcal) of energy, while the oxidation of one gram of lipids yields about 38 kJ (9 kcal). The human body stores between 300 and 500 g of carbohydrates depending on body weight, with the skeletal muscle contributing to a large portion of the storage.[49] Energy obtained from metabolism (e.g., oxidation of glucose) is usually stored temporarily within cells in the form of ATP.[50] Organisms capable of anaerobic and aerobic respiration metabolize glucose and oxygen (aerobic) to release energy, with carbon dioxide and water as byproducts.

### Catabolism

Catabolism is the metabolic reaction which cells undergo to break down larger molecules, extracting energy. There are two major metabolic pathways of monosaccharide catabolism: glycolysis and the citric acid cycle.

In glycolysis, oligo- and polysaccharides are cleaved first to smaller monosaccharides by enzymes called glycoside hydrolases. The monosaccharide units can then enter into monosaccharide catabolism. A 2 ATP investment is required in the early steps of glycolysis to phosphorylate Glucose to Glucose 6-Phosphate (G6P) and Fructose 6-Phosphate (F6P) to Fructose 1,6-biphosphate (FBP), thereby pushing the reaction forward irreversibly.[49] In some cases, as with humans, not all carbohydrate types are usable as the digestive and metabolic enzymes necessary are not present.

## Analytical tools

Many techniques are used in the analysis of glycans.[51] NMR spectroscopy is common, the major challenge being spectral overlap.[52] [53]

### High-resolution mass spectrometry (MS) and high-performance liquid chromatography (HPLC)

MS and HPLC are commonly applied to glycan cleaved either enzymatically or chemically from the target.[54] In case of glycolipids, they can be analyzed directly without separation of the lipid component.

N-glycans from glycoproteins are analyzed routinely by high-performance-liquid-chromatography (reversed phase, normal phase and ion exchange HPLC) after tagging the reducing end of the sugars with a fluorescent compound (reductive labeling).[55] A large variety of different labels were introduced in the recent years, where 2-aminobenzamide (AB), anthranilic acid (AA), 2-aminopyridin (PA), 2-aminoacridone (AMAC) and 3-(acetylamino)-6-aminoacridine (AA-Ac) are just a few of them.[56] Different labels have to be used for different ESI modes and MS systems used.[57]

O-glycans are usually analysed without any tags.

Fractionated glycans from high-performance liquid chromatography (HPLC) instruments can be further analyzed by MALDI-TOF-MS(MS) to get further information about structure and purity. Sometimes glycan pools are analyzed directly by mass spectrometry without prefractionation, although a discrimination between isobaric glycan structures is more challenging or even not always possible. Anyway, direct MALDI-TOF-MS analysis can lead to a fast and straightforward illustration of the glycan pool.[58]

High performance liquid chromatography online coupled to mass spectrometry is useful. By choosing porous graphitic carbon as a stationary phase for liquid chromatography, even non derivatized glycans can be analyzed. Detection is here done by mass spectrometry, but in instead of MALDI-MS, electrospray ionisation (ESI) is more frequently used.[59][60][61]

### Multiple reaction monitoring (MRM)

Although MRM has been used extensively in metabolomics and proteomics, its high sensitivity and linear response over a wide dynamic range make it especially suited for glycan biomarker research and discovery. MRM is performed on a triple quadrupole (QqQ) instrument, which is set to detect a predetermined precursor ion in the first quadrupole, a fragmented in the collision quadrupole, and a predetermined fragment ion in the third quadrupole. It is a non-scanning technique, wherein each transition is detected individually and the detection of multiple transitions occurs concurrently in duty cycles. This technique is being used to characterize the immune glycome.[12][62]

## Chemical synthesis and manipulation of carbohydrates

Carbohydrate synthesis is a sub-field of organic chemistry concerned specifically with the generation of natural and unnatural carbohydrate structures. Carbohydrate chemistry is a large and economically important branch of organic chemistry. This can include the synthesis of monosaccharide residues or structures containing more than one monosaccharide, known as oligosaccharides. Selective formation of glycosidic linkages and selective reactions of hydroxyl groups are very important, and the usage of protecting groups is extensive.

Some of the main organic reactions that involve carbohydrates are:

* Amadori rearrangement
* Carbohydrate acetalisation
* Carbohydrate digestion
* Cyanohydrin reaction
* Koenigs–Knorr reaction
* Lobry de Bruyn–Van Ekenstein transformation
* Nef reaction
* Wohl degradation
* Tipson-Cohen reaction
* Ferrier rearrangement
* Ferrier II reaction

Related topics

* Carbohydrate NMR

## See also

* Gluconeogenesis – A process where glucose can be synthesized by non-carbohydrate sources.
* Glycobiology
* Glycogen
* Glycoinformatics
* Glycolipid
* Glycome
* Glycomics
* Glycosyl
* Macromolecule
* Saccharic acid

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2. ↑ "Essentials of Glycobiology". https://www.ncbi.nlm.nih.gov/books/NBK579927/#top.
3. ↑ Nelson, David L.; Cox, Michael M. (2005), Principles of Biochemistry (4th ed.), New York: W. H. Freeman, p. 293-324, ISBN 0-7167-4339-6
4. ↑ Human Biology and Health. Englewood Cliffs, New Jersey: Prentice Hall. 1993. pp. 52–59. ISBN 978-0-13-981176-0. https://archive.org/details/humanbiologyheal00scho/page/52.
5. ↑ "Etymology of main polysaccharide names". The European Polysaccharide Network of Excellence (EPNOE). Wien: Springer-Verlag. 2012. https://www.springer.com/cda/content/document/cda_downloaddocument/9783709104200-c1.pdf?SGWID=0-0-45-1364512-p174060193. Retrieved January 28, 2018.
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38. ↑ "Effects of carbohydrate-restricted diets on low-density lipoprotein cholesterol levels in overweight and obese adults: a systematic review and meta-analysis". Nutrition Reviews 77 (3): 161–180. March 2019. doi:10.1093/nutrit/nuy049. PMID 30544168. http://researchonline.ljmu.ac.uk/id/eprint/8898/1/nutr-rev corrected version 07072018.pdf. Retrieved April 24, 2022.
39. ↑ "Overweight and diabetes prevention: is a low-carbohydrate-high-fat diet recommendable?". European Journal of Nutrition 57 (4): 1301–1312. June 2018. doi:10.1007/s00394-018-1636-y. PMID 29541907.
40. ↑ "Efficacy of low carbohydrate diet for type 2 diabetes mellitus management: A systematic review and meta-analysis of randomized controlled trials". Diabetes Research and Clinical Practice 131: 124–131. September 2017. doi:10.1016/j.diabres.2017.07.006. PMID 28750216.
41. ↑ 41.0 41.1 "5. Lifestyle Management: Standards of Medical Care in Diabetes-2019". Diabetes Care 42 (Suppl 1): S46–S60. January 2019. doi:10.2337/dc19-S005. PMID 30559231. http://care.diabetesjournals.org/content/42/Supplement_1/S46. Retrieved April 24, 2022.
42. ↑ "The ups and downs of low-carbohydrate diets in the management of Type 1 diabetes: a review of clinical outcomes". Diabetic Medicine 36 (3): 326–334. March 2019. doi:10.1111/dme.13845. PMID 30362180.
43. ↑ 43.0 43.1 43.2 "Top 5 worst celeb diets to avoid in 2018". British Dietetic Association. 7 December 2017. https://www.bda.uk.com/resource/top-5-worst-celeb-diets-to-avoid-in-2018.html. "The British Dietetic Association (BDA) today revealed its much-anticipated annual list of celebrity diets to avoid in 2018. The line-up this year includes Raw Vegan, Alkaline, Pioppi and Ketogenic diets as well as Katie Price's Nutritional Supplements."
44. ↑ "Carbohydrates and Blood Sugar" (in en-US). The Nutrition Source. 2013-08-05. https://www.hsph.harvard.edu/nutritionsource/carbohydrates/carbohydrates-and-blood-sugar/.
45. ↑ "A syn-ent-labdadiene derivative with a rare spiro-β-lactone function from the male cones of Wollemia nobilis". Phytochemistry 158: 91–95. February 2019. doi:10.1016/j.phytochem.2018.11.012. PMID 30481664. Bibcode: 2019PChem.158...91V.
46. ↑ "Triterpene saponins from the roots of Ilex asprella". Chemistry & Biodiversity 11 (5): 767–775. May 2014. doi:10.1002/cbdv.201300155. PMID 24827686.
47. ↑ "Lignocellulosic Biomass Pretreatment Using AFEX". Biofuels. Methods in Molecular Biology. 581. Totowa, NJ: Humana Press. 2009. pp. 61–77. doi:10.1007/978-1-60761-214-8_5. ISBN 978-1-60761-213-1. Bibcode: 2009biof.book...61B.
48. ↑ "FoodData Central". https://fdc.nal.usda.gov/index.html.
49. ↑ 49.0 49.1 "Surgery Oxford". June 2013. https://onesearch.cuny.edu/primo-explore/fulldisplay?docid=TN_sciversesciencedirect_elsevierS0263-9319(13)00087-2&context=PC&vid=hc&search_scope=everything&tab=default_tab&lang=en_US.
50. ↑ "Energetics of Cellular Respiration (Glucose Metabolism)". Biochemistry Notes, Notes. 9 October 2013. http://pharmaxchange.info/press/2013/10/energetics-of-cellular-respiration-glucose-metabolism/.
51. ↑ Essentials of Glycobiology (2nd ed.). Cold Spring Harbor Laboratory Press. 2009. ISBN 978-0-87969-770-9. http://www.cshlpress.com/default.tpl?action=full&\--eqskudatarq=666.
52. ↑ Fontana, Carolina; Widmalm, Göran (2023). "Primary Structure of Glycans by NMR Spectroscopy". Chemical Reviews 123 (3): 1040–1102. doi:10.1021/acs.chemrev.2c00580. PMID 36622423.
53. ↑ Aizpurua-Olaizola, O.; Toraño, J. Sastre; Falcon-Perez, J.M.; Williams, C.; Reichardt, N.; Boons, G.-J. (2018). "Mass spectrometry for glycan biomarker discovery". TrAC Trends in Analytical Chemistry 100: 7–14. doi:10.1016/j.trac.2017.12.015.
54. ↑ "Comparison of the methods for profiling glycoprotein glycans—HUPO Human Disease Glycomics/Proteome Initiative multi-institutional study". Glycobiology 17 (4): 411–22. April 2007. doi:10.1093/glycob/cwl086. PMID 17223647.
55. ↑ "Structure analyses of oligosaccharides by tagging of the reducing end sugars with a fluorescent compound". Biochem. Biophys. Res. Commun. 85 (1): 257–63. November 1978. doi:10.1016/S0006-291X(78)80037-0. PMID 743278. Bibcode: 1978BBRC...85..257H.
56. ↑ "Comparison of fluorescent labels for oligosaccharides and introduction of a new postlabeling purification method". Anal. Biochem. 384 (2): 263–73. January 2009. doi:10.1016/j.ab.2008.09.041. PMID 18940176.
57. ↑ Šoić, Dinko; Mlinarić, Zvonimir; Lauc, Gordan; Gornik, Olga; Novokmet, Mislav; Keser, Toma (2022). "In a pursuit of optimal glycan fluorescent label for negative MS mode for high-throughput N-glycan analysis". Frontiers in Chemistry 10. doi:10.3389/fchem.2022.999770. ISSN 2296-2646. PMID 36262345. Bibcode: 2022FrCh...10.9770S.
58. ↑ "Ionisation and fragmentation of complex glycans with a quadrupole time-of-flight mass spectrometer fitted with a matrix-assisted laser desorption/ionisation ion source". Rapid Commun. Mass Spectrom. 14 (22): 2135–42. 2000. doi:10.1002/1097-0231(20001130)14:22<2135::AID-RCM143>3.0.CO;2-#. PMID 11114021. Bibcode: 2000RCMS...14.2135H.
59. ↑ Schulz, BL; Packer NH, NH; Karlsson, NG (Dec 2002). "Small-scale analysis of O-linked oligosaccharides from glycoproteins and mucins separated by gel electrophoresis.". Anal. Chem. 74 (23): 6088–97. doi:10.1021/ac025890a. PMID 12498206.
60. ↑ "Mass plus retention time equals structure: a strategy for the analysis of N-glycans by carbon LC-ESI-MS and its application to fibrin N-glycans". Anal. Chem. 79 (13): 5051–7. July 2007. doi:10.1021/ac070363i. PMID 17539604.
61. ↑ "Oligosaccharide analysis by graphitized carbon liquid chromatography-mass spectrometry". Anal Bioanal Chem 394 (1): 163–74. May 2009. doi:10.1007/s00216-009-2664-5. PMID 19247642.
62. ↑ Flowers, Sarah A.; Ali, Liaqat; Lane, Catherine S.; Olin, Magnus; Karlsson, Niclas G. (2013-04-01). "Selected reaction monitoring to differentiate and relatively quantitate isomers of sulfated and unsulfated core 1 O-glycans from salivary MUC7 protein in rheumatoid arthritis". Molecular & Cellular Proteomics 12 (4): 921–931. doi:10.1074/mcp.M113.028878. ISSN 1535-9484. PMID 23457413.

## Further reading

* "Compolition of foods raw, processed, prepared". United States Department of Agriculture. September 2015. https://www.ars.usda.gov/ARSUserFiles/80400525/Data/SR/SR28/sr28_doc.pdf.

## External links

* Carbohydrates, including interactive models and animations (Requires MDL Chime)
* IUPAC-IUBMB Joint Commission on Biochemical Nomenclature (JCBN): Carbohydrate Nomenclature
* Carbohydrates detailed
* Carbohydrates and Glycosylation – The Virtual Library of Biochemistry, Molecular Biology and Cell Biology
* Functional Glycomics Gateway, a collaboration between the Consortium for Functional Glycomics and Nature Publishing Group

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* t
* e

Metabolism, catabolism, anabolism

General|

* Metabolic pathway
* Metabolic network
* Primary nutritional groups

Energy
metabolism|

| Aerobic respiration|

* Glycolysis → Pyruvate decarboxylation → Citric acid cycle → Oxidative phosphorylation (electron transport chain \+ ATP synthase)

|

Anaerobic respiration|

* Electron acceptors are other than oxygen

Fermentation|

* Glycolysis → Substrate-level phosphorylation
* ABE
* Ethanol
* Lactic acid

Specific
paths|

| Protein metabolism|

* Protein synthesis
* Catabolism

|

Carbohydrate metabolism
(carbohydrate catabolism
and anabolism)|

| Human|

* Glycolysis ⇄ Gluconeogenesis

* Glycogenolysis ⇄ Glycogenesis

* Pentose phosphate pathway
* Fructolysis
* Galactolysis

* Glycosylation
* N-linked
* O-linked

Nonhuman|

* Photosynthesis
* Anoxygenic photosynthesis
* Chemosynthesis
* Carbon fixation

* Xylose metabolism
* Radiotrophism

Lipid metabolism
(lipolysis, lipogenesis)|

| Fatty acid metabolism|

* Fatty acid degradation (Beta oxidation)
* Fatty acid synthesis

|

Other|

* Steroid metabolism
* Sphingolipid metabolism
* Eicosanoid metabolism
* Ketosis
* Reverse cholesterol transport

Amino acid|

* Amino acid synthesis
* Urea cycle

Nucleotide
metabolism|

* Purine metabolism
* Nucleotide salvage
* Pyrimidine metabolism

Other|

* Metal metabolism
* Iron metabolism
* Ethanol metabolism

* v
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Food chemistry

* Additives
* Carbohydrates
* Coloring
* Enzymes
* Essential fatty acids
* Flavors
* Fortification
* Lipids
* "Minerals" (Chemical elements)
* Proteins
* Vitamins
* Water

* v
* t
* e

Types of carbohydrates

General|

* Aldose
* Ketose
* Furanose
* Pyranose

Geometry|

* Anomer
* Cyclohexane conformation
* Mutarotation

Monosaccharides|

| Dioses|

* Aldodiose
* Glycolaldehyde

|

Trioses|

* Aldotriose
* Glyceraldehyde
* Ketotriose
* Dihydroxyacetone

Tetroses|

* Aldotetroses
* Erythrose
* Threose
* Ketotetrose
* Erythrulose

Pentoses|

* Aldopentoses
* Arabinose
* Lyxose
* Ribose
* Xylose
* Ketopentoses
* Ribulose
* Xylulose
* Deoxy sugars
* Deoxyribose

Hexoses|

* Aldohexoses
* Allose
* Altrose
* Galactose
* Glucose
* Gulose
* Idose
* Mannose
* Talose
* Ketohexoses
* Fructose
* Psicose
* Sorbose
* Tagatose
* Deoxy sugars
* Fucose
* Fuculose
* Rhamnose

Heptoses|

* Ketoheptoses
* Mannoheptulose
* Sedoheptulose

Above 7|

* Octoses
* Nonoses
* Neuraminic acid

Multiple|

| Disaccharides|

* Cellobiose
* Isomaltose
* Isomaltulose
* Lactose
* Lactulose
* Maltose
* Sucrose
* Trehalose
* Turanose

|

Trisaccharides|

* Maltotriose
* Melezitose
* Raffinose

Tetrasaccharides|

* Stachyose

Other
oligosaccharides|

* Acarbose
* Fructooligosaccharide (FOS)
* Galactooligosaccharide (GOS)
* Isomaltooligosaccharide (IMO)
* Maltodextrin

Polysaccharides|

* Beta-glucan
* Oat beta-glucan
* Lentinan
* Sizofiran
* Zymosan
* Cellulose
* Chitin
* Chitosan
* Dextrin / Dextran
* Fructose / Fructan
* Inulin
* Galactose / Galactan
* Glucose / Glucan
* Glycogen
* Hemicellulose
* Levan beta 2→6
* Lignin
* Mannan
* Pectin
* Starch
* Amylopectin
* Amylose
* Xanthan gum

* Category

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