Ectoine

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search

Script error: No such module "Unsubst". <templatestyles src="Chembox/styles.css"/>

Template:Chembox image cellTemplate:Chembox AllOtherNamesTemplate:Chembox headerbarTemplate:Chembox IndexlistTemplate:Chembox JmolTemplate:Chembox ChEMBLTemplate:Chembox ECHATemplate:Chembox E numberTemplate:Chembox IUPHAR ligandTemplate:Chembox UNIITemplate:Chembox CompToxTemplate:Chembox headerbarTemplate:Chembox SolubilityInWaterTemplate:Chembox headerbarTemplate:Chembox Datapage checkTemplate:Chembox Footer
Ectoine[1]
Template:Longitem Template:Unbulleted list
ChEBI Template:Unbulleted list
ChemSpider Template:Unbulleted list
DrugBank Template:Unbulleted list
EC Number Template:Unbulleted list
KEGG Template:Unbulleted list
Template:Longitem Template:Unbulleted list
RTECS number Template:Unbulleted list
Script error: No such module "collapsible list".
Script error: No such module "collapsible list".
Template:Longitem Template:Chembox Elements/molecular formula
Molar mass Template:Chem molar mass
Appearance White powder
Density 1.568 g/cm3
NFPA 704 (fire diamond) Template:NFPA 704 diamond

Template:Chembox Footer/trackingScript error: No such module "TemplatePar".Template:Short description

Ectoine (3,4,5,6-tetrahydro-2-methyl-4-pyrimidinecarboxylic acid) is a natural compound found in several species of bacteria. It is a compatible solute which serves as a protective substance by acting as an osmolyte and thus helps organisms survive extreme osmotic stress.[2] Furthermore it was shown to protect DNA against ionizing and ultraviolet radiation serving as a radical scavenger.[3] Ectoine is found in high concentrations in halophilic microorganisms and confers resistance towards salt and temperature stress. Ectoine was first identified in the microorganism Ectothiorhodospira halochloris,[4][5] but has since been found in a wide range of Gram-negative and Gram-positive bacteria. Other species of bacteria in which ectoine was found include:

Biosynthesis

Ectoine is synthesized in three successive enzymatic reactions starting from aspartic β-semialdehyde. The genes involved in the biosynthesis are called ectA, ectB and ectC, and they encode the enzymes L-2,4-diaminobutyric acid acetyltransferase, L-2,4-diaminobutyric acid transaminase and L-ectoine synthase, respectively.[7][6]

Use in cosmetics

Ectoine is used as an active ingredient in skin care and sun protection products.[12] It stabilizes proteins and other cellular structures and protects the skin from stresses like UV irradiation and dryness.[6]

Medical use

Due to its protein stabilizing properties, ectoine has been evaluated as a topical treatment for hay fever. Effectiveness of a nasal spray containing ectoine is comparable to cromoglycate and is reported to be well tolerated by the patients.[13] It is available over the counter in the European Union.

References

<templatestyles src="Reflist/styles.css" />

  1. ↑ Ectoine at Sigma-Aldrich
  2. ↑ Script error: No such module "Citation/CS1".
  3. ↑ Script error: No such module "Citation/CS1".
  4. ↑ a b Script error: No such module "Citation/CS1".
  5. ↑ a b Script error: No such module "Citation/CS1".
  6. ↑ a b c d Script error: No such module "Citation/CS1".
  7. ↑ a b Script error: No such module "Citation/CS1".
  8. ↑ Script error: No such module "citation/CS1".
  9. ↑ Script error: No such module "Citation/CS1".
  10. ↑ "HAMAP: Halorhodospira halophila (strain DSM 244 / SL1) (Ectothiorhodospira halophila (strain DSM 244 / SL1)) complete proteome ExPASy Proteomics Server. Swiss Institute of BioinformaticsScript error: No such module "Unsubst". http://hamap.expasy.org/proteomes/HALHL.html
  11. ↑ Script error: No such module "Citation/CS1".
  12. ↑ Script error: No such module "citation/CS1".
  13. ↑ Script error: No such module "Citation/CS1".

Script error: No such module "Check for unknown parameters".