Fucoxanthin

{{chembox

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| Watchedfields = changed

| verifiedrevid = 437956950

| ImageFile=Fucoxanthin.svg

| ImageSize=350px

| IUPACName=(3S,5R,6M,3′S,5′R,6′S)-5′,6′-Epoxy-5,3′-dihydroxy-8′-oxo-6,7-didehydro-5,6,5′,6′,7′,8′-hexahydro-β,β-caroten-3-yl acetate

| SystematicName=(1S,3R,4M)-3-Hydroxy-4-{(3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1S,4S,6R)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-3,7,12,16-tetramethyl-17-oxooctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-ylidene}-3,5,5-trimethylcyclohexyl acetate

| OtherNames=

|Section1={{Chembox Identifiers

| CASNo_Ref = {{cascite|correct|??}}

| CASNo=3351-86-8

| ChEMBL = 1575074

| ChEBI = 5186

| Beilstein = 6580822

| EINECS = 686-524-6

| KEGG = C08596

| 3DMet = B05481

| UNII_Ref = {{fdacite|correct|FDA}}

| UNII = 06O0TC0VSM

| PubChem=5281239

| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}

| ChemSpiderID = 21864745

| SMILES = CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=C=C3C(CC(CC3(C)O)OC(=O)C)(C)C

| InChI = 1/C42H58O6/c1-29(18-14-19-31(3)22-23-37-38(6,7)26-35(47-33(5)43)27-40(37,10)46)16-12-13-17-30(2)20-15-21-32(4)36(45)28-42-39(8,9)24-34(44)25-41(42,11)48-42/h12-22,34-35,44,46H,24-28H2,1-11H3/b13-12+,18-14+,20-15+,29-16+,30-17+,31-19+,32-21+/t23-,34-,35-,40+,41+,42-/m0/s1

| InChIKey = SJWWTRQNNRNTPU-XJUZQKKNBP

| StdInChI_Ref = {{stdinchicite|changed|chemspider}}

| StdInChI = 1S/C42H58O6/c1-29(18-14-19-31(3)22-23-37-38(6,7)26-35(47-33(5)43)27-40(37,10)46)16-12-13-17-30(2)20-15-21-32(4)36(45)28-42-39(8,9)24-34(44)25-41(42,11)48-42/h12-22,34-35,44,46H,24-28H2,1-11H3/b13-12+,18-14+,20-15+,29-16+,30-17+,31-19+,32-21+/t23-,34-,35-,40+,41+,42-/m0/s1

| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}

| StdInChIKey = SJWWTRQNNRNTPU-XJUZQKKNSA-N

}}

|Section2={{Chembox Properties

| C=42 | H=58 | O=6

| Appearance=

| Density=

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|Section3={{Chembox Hazards

| GHSPictograms = {{GHS07}}

| GHSSignalWord = Warning

| HPhrases = {{H-phrases|319}}

| PPhrases = {{P-phrases|264|280|305+351+338|337+313}}

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Fucoxanthin is a xanthophyll, with formula C42H58O6. It is found as an accessory pigment in the chloroplasts of brown algae and most other heterokonts, giving them a brown or olive-green color. Fucoxanthin absorbs light primarily in the blue-green to yellow-green part of the visible spectrum, peaking at around 510–525 nm by various estimates and absorbing significantly in the range of 450 to 540 nm.

Function

Carotenoids are pigments produced by plants and algae and play a role in light harvesting as part of the photosynthesis process. Xanthophylls are a subset of carotenoids, identified by the fact that they are oxygenated either as hydroxyl groups or as epoxide bridges. This makes them more water soluble than carotenes such as beta-carotene. Fucoxanthin is a xanthophyll that contributes more than 10% of the estimated total production of carotenoids in nature.{{cite journal | vauthors = Dembitsky VM, Maoka T | title = Allenic and cumulenic lipids | journal = Progress in Lipid Research | volume = 46 | issue = 6 | pages = 328–75 | date = November 2007 | pmid = 17765976 | doi = 10.1016/j.plipres.2007.07.001 }} It is an accessory pigment found in the chloroplasts of many brown macroalgae, such as Fucus {{abbr|spp.|species}}, and the golden-brown unicellular microalgae, the diatoms. It absorbs blue and green light at bandwidth 450–540 nm, imparting a brownish-olive color to algae.

Fucoxanthin has a highly unique structure that contains both an epoxide bond and hydroxyl groups along with an allenic bond (two adjacent carbon-carbon double bonds) and a conjugated carbonyl group (carbon-oxygen double bond) in the polyene chain. All of these features provide fucoxanthin with powerful antioxidant activity.{{cite journal | vauthors = Hu T, Liu D, Chen Y, Wu J, Wang S | title = Antioxidant activity of sulfated polysaccharide fractions extracted from Undaria pinnitafida in vitro | journal = International Journal of Biological Macromolecules | volume = 46 | issue = 2 | pages = 193–8 | date = March 2010 | pmid = 20025899 | doi = 10.1016/j.ijbiomac.2009.12.004 }}

In macroalgal plastids, fucoxanthin acts like an antenna for light harvesting and energy transfer in the photosystem light harvesting complexes.{{cite journal | vauthors = Owens TG, Wold ER | title = Light-Harvesting Function in the Diatom Phaeodactylum tricornutum: I. Isolation and Characterization of Pigment-Protein Complexes | journal = Plant Physiology | volume = 80 | issue = 3 | pages = 732–8 | date = March 1986 | pmid = 16664694 | pmc = 1075192 | doi=10.1104/pp.80.3.732}} In diatoms like Phaeodactylum tricornutum, fucoxanthin is protein-bound along with chlorophyll to form a light harvesting protein complex.{{cite journal | vauthors = Guglielmi G, Lavaud J, Rousseau B, Etienne AL, Houmard J, Ruban AV | title = The light-harvesting antenna of the diatom Phaeodactylum tricornutum. Evidence for a diadinoxanthin-binding subcomplex | journal = The FEBS Journal | volume = 272 | issue = 17 | pages = 4339–48 | date = September 2005 | pmid = 16128804 | doi = 10.1111/j.1742-4658.2005.04846.x | url = https://hal.archives-ouvertes.fr/hal-01094626/file/Guglielmi_FEBS-J_Modif.pdf | doi-access = free }} Fucoxanthin is the dominant carotenoid, responsible for up to 60% of the energy transfer to chlorophyll a in diatoms.{{cite journal | vauthors = Papagiannakis E, van Stokkum IH, Fey H, Büchel C, van Grondelle R | title = Spectroscopic characterization of the excitation energy transfer in the fucoxanthin-chlorophyll protein of diatoms | journal = Photosynthesis Research | volume = 86 | issue = 1–2 | pages = 241–50 | date = November 2005 | pmid = 16172942 | doi = 10.1007/s11120-005-1003-8 }} When bound to protein, the absorption spectrum of fucoxanthin expands from 450–540 nm to 390–580 nm, a range that is useful in aquatic environments.{{cite journal | vauthors = Premvardhan L, Sandberg DJ, Fey H, Birge RR, Büchel C, van Grondelle R | title = The charge-transfer properties of the S2 state of fucoxanthin in solution and in fucoxanthin chlorophyll-a/c2 protein (FCP) based on stark spectroscopy and molecular-orbital theory | journal = The Journal of Physical Chemistry B | volume = 112 | issue = 37 | pages = 11838–53 | date = September 2008 | pmid = 18722413 | pmc = 2844098 | doi = 10.1021/jp802689p }}

Sources

Fucoxanthin is present in brown seaweeds and diatoms and was first isolated from Fucus, Dictyota, and Laminaria by Willstätter and Page in 1914.{{cite journal | vauthors = Peng J, Yuan JP, Wu CF, Wang JH | title = Fucoxanthin, a marine carotenoid present in brown seaweeds and diatoms: metabolism and bioactivities relevant to human health | journal = Marine Drugs | volume = 9 | issue = 10 | pages = 1806–28 | date = 2011-10-10 | pmid = 22072997 | pmc = 3210606 | doi = 10.3390/md9101806 | doi-access = free }} Seaweeds are commonly consumed in south-east Asia and certain countries in Europe, while diatoms are single-cell planktonic microalgae characterized by a golden-brown color, due to their high content of fucoxanthin. Generally, diatoms contain up to four times more fucoxanthin than seaweed, making diatoms a viable source for fucoxanthin industrially.{{cite journal | vauthors = Wang LJ, Fan Y, Parsons RL, Hu GR, Zhang PY, Li FL | title = A Rapid Method for the Determination of Fucoxanthin in Diatom | journal = Marine Drugs | volume = 16 | issue = 1 | pages = 33 | date = January 2018 | pmid = 29361768 | pmc = 5793081 | doi = 10.3390/md16010033 | doi-access = free }} Diatoms can be grown in controlled environments (such as photobioreactors).

Bioavailability

Limited studies of fucoxanthin in humans indicate low bioavailability.

See also

References