Betaine: Difference between revisions
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{{Short description|Neutral chemical compound with both a positively- and negatively-charged functional group}} |
{{Short description|Neutral chemical compound with both a positively- and negatively-charged functional group}} |
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{{About|a class of compounds|the specific chemical glycine betaine|trimethylglycine}} |
{{About|a class of compounds|the specific chemical glycine betaine|trimethylglycine}} |
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| ⚫ | A '''betaine''' ({{IPAc-en|ˈ|b|iː|t|ə|.|iː|n|,_|b|ɪ|ˈ|t|eɪ|-|,_|-|ɪ|n}}) in [[chemistry]] is any neutral [[chemical compound]] with a positively charged [[cation]]ic [[functional group]], such as a [[Quaternary ammonium cation|quaternary ammonium]] or [[phosphonium]] cation (generally: [[Onium compounds|onium]] ions) |
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[[File:Cocamidopropyl betaine2.png|thumb|400x400px|Cocamidopropyl betaine is an example of betaines]] |
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| ⚫ | 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''.<ref>{{Cite book | |
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| ⚫ | A '''betaine''' ({{IPAc-en|ˈ|b|iː|t|ə|.|iː|n|,_|b|ɪ|ˈ|t|eɪ|-|,_|-|ɪ|n}}) in [[chemistry]] is any neutral [[chemical compound]] with a positively charged [[cation]]ic [[functional group]] that bears no hydrogen atom, such as a [[Quaternary ammonium cation|quaternary ammonium]] or [[phosphonium]] cation (generally: [[Onium compounds|onium]] ions), and with a negatively charged functional group, such as a [[carboxylate]] group that may not be adjacent to the cationic site.<ref name="pubchem">{{cite web |title=Betaine |url=https://pubchem.ncbi.nlm.nih.gov/compound/247 |publisher=PubChem, US National Library of Medicine |access-date=26 August 2021 |date=21 August 2021}}</ref> Historically, the term was reserved for [[trimethylglycine]] (TMG), which is involved in [[methylation]] reactions and detoxification of [[homocysteine]].<ref name="pubchem" /> This is a modified amino acid consisting of [[glycine]] with three [[methyl group]]s serving as methyl donor for various metabolic pathways.<ref name="livertox">{{cite web |title=Betaine |url=https://www.ncbi.nlm.nih.gov/books/NBK548774/ |publisher=LiverTox, US National Library of Medicine |access-date=26 August 2021 |date=26 September 2017}}</ref> |
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| ⚫ | In biological systems, many naturally occurring betaines serve as organic [[osmolyte]]s.{{cn|date=August 2021}} These are substances synthesized or taken up from the environment by cells for protection against [[osmosis|osmotic]] stress, drought, high salinity, or high temperature. Intracellular accumulation of betaines permits water retention in cells, thus protecting from the effects of dehydration.{{cn|date=August 2021}} 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.<ref name=livertox/><ref name=pubchem/> |
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| ⚫ | In biological systems, many naturally occurring betaines serve as organic [[osmolyte]]s.{{cn|date=August 2021}} These are substances synthesized or taken up from the environment by cells for protection against [[osmosis|osmotic]] stress, drought, high salinity, or high temperature. Intracellular accumulation of betaines permits water retention in cells, thus protecting from the effects of dehydration.{{cn|date=August 2021}} 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.<ref name="livertox" /><ref name="pubchem" /> |
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== Pronunciation == |
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| ⚫ | 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''.<ref>{{Cite book |author=Alex Nickon and Ernest F. Silversmith |url=https://archive.org/details/organicchemistry0000nick |title=Organic Chemistry, the Name Game: Modern Coined Terms and Their Origins |publisher=Pergamon |year=1987 |isbn=978-0080344812 |url-access=registration}}</ref> |
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== Glycine betaine == |
== Glycine betaine == |
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[[Trimethylglycine]], a betaine, is used as a [[dietary supplement]], although there is no evidence that supplement doses are effective or safe.<ref>{{Cite journal|last1=Van Every|first1=Derrick W.|last2=Plotkin|first2=Daniel L.|last3=Delcastillo|first3=Kenneth|last4=Cholewa|first4=Jason|last5=Schoenfeld|first5=Brad J.|date=2021-08-01|title=Betaine Supplementation: A Critical Review of Its Efficacy for Improving Muscle Strength, Power, and Body Composition|url=https://journals.lww.com/10.1519/SSC.0000000000000622|journal=Strength & Conditioning Journal|language=en|volume=43|issue=4|pages=53–61|doi=10.1519/SSC.0000000000000622|s2cid=233966447 |issn=1524-1602}}</ref> Common [[side effect]]s of taking oral betaine include [[nausea]] and stomach upset.<ref name="drugs">{{cite web |title=Betaine |url=https://www.drugs.com/mtm/betaine.html |publisher=Drugs.com |access-date=26 August 2021 |date=11 November 2020}}</ref> |
[[Trimethylglycine]], a betaine, is used as a [[dietary supplement]], although there is no evidence that supplement doses are effective or safe.<ref>{{Cite journal|last1=Van Every|first1=Derrick W.|last2=Plotkin|first2=Daniel L.|last3=Delcastillo|first3=Kenneth|last4=Cholewa|first4=Jason|last5=Schoenfeld|first5=Brad J.|date=2021-08-01|title=Betaine Supplementation: A Critical Review of Its Efficacy for Improving Muscle Strength, Power, and Body Composition|url=https://journals.lww.com/10.1519/SSC.0000000000000622|journal=Strength & Conditioning Journal|language=en|volume=43|issue=4|pages=53–61|doi=10.1519/SSC.0000000000000622|s2cid=233966447 |issn=1524-1602}}</ref> Common [[side effect]]s of taking oral betaine include [[nausea]] and stomach upset.<ref name="drugs">{{cite web |title=Betaine |url=https://www.drugs.com/mtm/betaine.html |publisher=Drugs.com |access-date=26 August 2021 |date=11 November 2020}}</ref> |
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== Safety == |
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Glycine betaine is an irritant of eyes and skin.<ref name="pubchem" /> |
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==See also== |
==See also== |
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Revision as of 12:29, 11 May 2023
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]
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 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
References
- ^ a b c d e "Betaine". PubChem, US National Library of Medicine. 21 August 2021. Retrieved 26 August 2021.
- ^ a b c "Betaine". LiverTox, US National Library of Medicine. 26 September 2017. Retrieved 26 August 2021.
- ^ Alex Nickon and Ernest F. Silversmith (1987). Organic Chemistry, the Name Game: Modern Coined Terms and Their Origins. Pergamon. ISBN 978-0080344812.
- ^ DNA Methylation and Complex Human Disease, Michel Neidhart
- ^ 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.
- ^ 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. PMC 146979. PMID 9380524.
- ^ 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. PMC 7009179. PMID 32626284.
- ^ a b "Betaine". Drugs.com. 11 November 2020. Retrieved 26 August 2021.
- ^ 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". Strength & Conditioning Journal. 43 (4): 53–61. doi:10.1519/SSC.0000000000000622. ISSN 1524-1602. S2CID 233966447.
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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