Betaine

Short description: Neutral chemical compound with both a positively- and negatively-charged functional group

Cocamidopropyl betaine is an example of a betaine

A betaine (/ˈbiːtə.iːn, bɪˈteɪ-, -ɪn/) in chemistry is any neutral chemical compound with a positively charged cationic functional group that bears no hydrogen atom, such as a quaternary ammonium or phosphonium cation (generally: onium ions), and with a negatively charged functional group, such as a carboxylate group that may not be adjacent to the cationic site.[1] Historically, the term was reserved for trimethylglycine (TMG), which is involved in methylation reactions and detoxification of homocysteine.[1] This is a modified amino acid consisting of glycine with three methyl groups serving as methyl donor for various metabolic pathways.[2]

In biological systems, many naturally occurring betaines serve as organic osmolytes.[citation needed] These are substances synthesized or taken up from the environment by cells for protection against osmotic stress, drought, high salinity, or high temperature. Intracellular accumulation of betaines permits water retention in cells, thus protecting from the effects of dehydration.[citation needed] This accumulation is non-perturbing to enzyme function, protein structure, and membrane integrity. Betaine is also a methyl donor of increasingly recognised significance in biology.[2][1]

## Contents

* 1 Pronunciation
* 2 Glycine betaine
* 3 Uses
* 3.1 Biochemistry
* 3.2 Food additive
* 3.3 Approved drug
* 3.4 Dietary supplement
* 4 Safety
* 5 See also
* 6 References
* 7 Further reading

## Pronunciation

The pronunciation of the compound reflects its origin and first isolation from sugar beets (Beta vulgaris subsp. vulgaris), and does not derive from the Greek letter beta (β). It is commonly pronounced beta-INE or BEE-tayn.[3]

## Glycine betaine

The chemical structure of trimethylglycine

Main article: Chemistry:Trimethylglycine

The original betaine, N,N,N-trimethylglycine, was named after its discovery in sugar beet (Beta vulgaris subsp. vulgaris) in the nineteenth century.[4] It is a small N-trimethylated amino acid. It is a zwitterion, which cannot isomerize because there is no labile hydrogen atom attached to the nitrogen atom. This substance may be called glycine betaine to distinguish it from other betaines.

## Uses

### Biochemistry

Phosphonium betaines are intermediates in the Wittig reaction. The addition of betaine to polymerase chain reactions improves the amplification of DNA by reducing the formation of secondary structure in GC-rich regions. The addition of betaine may enhance the specificity of the polymerase chain reaction by eliminating the base pair composition dependence of DNA melting.[5][6]

### Food additive

In 2017, the European Food Safety Authority concluded that betaine was safe "as a novel food to be used at a maximum intake level of 6 mg/kg body weight per day in addition to the intake from the background diet."[7]

### Approved drug

A prescription drug (Cystadane)[8] containing betaine has limited use for oral treatment of genetic homocystinuria to lower levels of homocysteine in circulating blood.[2][1]

### Dietary supplement

Trimethylglycine, a betaine, is used as a dietary supplement, although there is no evidence that supplement doses are effective or safe.[9] Common side effects of taking oral betaine include nausea and stomach upset.[8]

## Safety

Glycine betaine is an irritant of eyes and skin.[1]

## See also

* Cocamidopropyl betaine
* Mesoionic
* Mesomeric betaine
* Osmoprotectants
* Ylide

## References

1. ↑ 1.0 1.1 1.2 1.3 1.4 "Betaine". PubChem, US National Library of Medicine. 21 August 2021. https://pubchem.ncbi.nlm.nih.gov/compound/247.
2. ↑ 2.0 2.1 2.2 "Betaine". LiverTox, US National Library of Medicine. 26 September 2017. https://www.ncbi.nlm.nih.gov/books/NBK548774/.
3. ↑ Alex Nickon and Ernest F. Silversmith (1987). Organic Chemistry, the Name Game: Modern Coined Terms and Their Origins. Pergamon. ISBN 978-0080344812. https://archive.org/details/organicchemistry0000nick.
4. ↑ DNA Methylation and Complex Human Disease, Michel Neidhart
5. ↑ Rees, William A.; Yager, Thomas D.; Korte, John; Von Hippel, Peter H. (1993). "Betaine can eliminate the base pair composition dependence of DNA melting". Biochemistry 32 (1): 137–44. doi:10.1021/bi00052a019. PMID 8418834.
6. ↑ Henke, W; Herdel, K; Jung, K; Schnorr, D; Loening, SA (1997). "Betaine improves the PCR amplification of GC-rich DNA sequences". Nucleic Acids Research 25 (19): 3957–8. doi:10.1093/nar/25.19.3957. PMID 9380524.
7. ↑ EFSA Panel on Nutrition, Novel Foods and Food Allergens (5 April 2019). "Safety of betaine as a novel food pursuant to Regulation (EU) 2015/2283". EFSA Journal 17 (4): e05658. doi:10.2903/j.efsa.2019.5658. PMID 32626284.
8. ↑ 8.0 8.1 "Betaine". Drugs.com. 11 November 2020. https://www.drugs.com/mtm/betaine.html.
9. ↑ Van Every, Derrick W.; Plotkin, Daniel L.; Delcastillo, Kenneth; Cholewa, Jason; Schoenfeld, Brad J. (2021-08-01). "Betaine Supplementation: A Critical Review of Its Efficacy for Improving Muscle Strength, Power, and Body Composition" (in en). Strength & Conditioning Journal 43 (4): 53–61. doi:10.1519/SSC.0000000000000622. ISSN 1524-1602. https://journals.lww.com/10.1519/SSC.0000000000000622.

## Further reading

* IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006-) "betaines". doi:10.1351/goldbook.B00637

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