Английская Википедия:Cucurbitacin
Шаблон:Short description Шаблон:Cs1 config
Cucurbitacins are a class of biochemical compounds that some plants – notably members of the pumpkin and gourd family, Cucurbitaceae – produce and which function as a defense against herbivores. Cucurbitacins and their derivatives have also been found in many other plant families (including Brassicaceae, Cucurbitaceae, Scrophulariaceae, Begoniaceae, Elaeocarpaceae, Datiscaceae, Desfontainiaceae, Polemoniaceae, Primulaceae, Rubiaceae, Sterculiaceae, Rosaceae, and Thymelaeaceae), in some mushrooms (including Russula and Hebeloma) and even in some marine mollusks.
Cucurbitacins may be a taste deterrent in plants foraged by some animals and in some edible plants preferred by humans, such as cucumbers and zucchinis.[1] In laboratory research, cucurbitacins have cytotoxic properties and are under study for their potential biological activity.[2][3]
Cucurbitacins are chemically classified as triterpenes, formally derived from cucurbitane, a triterpene hydrocarbon – specifically, from the unsaturated variant cucurbit-5-ene, or 19(10→9β)-abeo-10α-lanost-5-ene. They often occur as glycosides.[4] Most cucurbitacins are tetracyclic except some have an extra ring due to formal cyclization between C16 and C24 as in cucurbitacin S and cucurbitacin T.[5][6]
Biosynthesis
The biosynthesis of cucurbitacin C has been described. Zhang et al. (2014) identified nine cucumber genes in the pathway for biosynthesis of cucurbitacin C and elucidated four catalytic steps.[7] These authors also discovered the transcription factors Bl (Bitter leaf) and Bt (Bitter fruit) that regulate this pathway in leaves and fruits, respectively. The Bi gene confers bitterness to the entire plant and is genetically associated with an operon-like gene cluster, similar to the gene cluster involved in thalianol biosynthesis in Arabidopsis. Fruit bitterness requires both Bi and the dominant Bt (Bitter fruit) gene. Nonbitterness of cultivated cucumber fruit is conferred by bt, an allele selected during domestication. Bi is a member of the oxidosqualene cyclase (OSC) gene family. Phylogenetic analysis showed that Bi is the ortholog of cucurbitadienol synthase gene CPQ in squash (Cucurbita pepo) [7]
Variants
The cucurbitacins include:
Cucurbitacin A
- Cucurbitacin A found in some species of Cucumis [4]Шаблон:Rp
- Pentanorcucurbitacin A, or 22-hydroxy-23,24,25,26,27-pentanorcucurbit-5-en-3-one Шаблон:Chem, white powder[8]Шаблон:Rp
Cucurbitacin B
- Cucurbitacin B from Hemsleya endecaphylla (62 mg/72 g)[9]Шаблон:Rp and other plants (e.g. Cucurbita andreana);[10] anti-inflammatory, any-hepatotoxic[4]Шаблон:Rp
- Cucurbitacin B 2-O-glucoside, from Begonia heracleifolia[4]Шаблон:Rp
- 23,24-Dihydrocucurbitacin B from Hemsleya endecaphylla, 49 mg/72 g[9]Шаблон:Rp
- 23,24-Dihydrocucurbitacin B 2-O-glucoside from roots of Picrorhiza kurrooa[4]Шаблон:Rp
- Deacetoxycucurbitacin B 2-O-glucoside from roots of Picrorhiza kurrooa[4]Шаблон:Rp
- Isocucurbitacin B, from Echinocystis fabacea[4]Шаблон:Rp
- 23,24-Dihydroisocucurbitacin B 3-glucoside from Wilbrandia ebracteata[4]Шаблон:Rp
- 23,24-Dihydro-3-epi-isocucurbitacin B, from Bryonia verrucosa[4]Шаблон:Rp
- Pentanorcucurbitacin B or 3,7-dioxo-23,24,25,26,27-pentanorcucurbit-5-en-22-oic acid, Шаблон:Chem, white powder[8]Шаблон:Rp
Cucurbitacin C
- Cucurbitacin C, from Cucumis sativus (cucumber)[4]Шаблон:Rp
Cucurbitacin D
- Cucurbitacin D, from Trichosanthes kirilowii and many other plants[4] (e.g. Cucurbita andreana)[10]Шаблон:Rp
- 3-Epi-isocucurbitacin D, from species of Physocarpus[4]Шаблон:Rp and Phormium tenax[11]
- 22-Deoxocucurbitacin D from Hemsleya endecaphylla, 14 mg/72 g[9]Шаблон:Rp
- 23,24-Dihydrocucurbitacin D from Trichosanthes kirilowii[4]Шаблон:Rp also from H. endecaphylla, 80 mg/72 g[9]Шаблон:Rp
- 23,24-Dihydro-epi-isocucurbitacin D, from Acanthosicyos horridus[4]Шаблон:Rp
- 22-Deoxocucurbitacin D from Wilbrandia ebracteata[4]Шаблон:Rp
- Anhydro-22-deoxo-3-epi-isocucurbitacin D from Ecballium elaterium[4]Шаблон:Rp
- 25-O-Acetyl-2-deoxycucurbitacin D (amarinin) from Luffa amara[4]Шаблон:Rp
- 2-Deoxycucurbitacin D, from Sloanea zuliaensis[4]Шаблон:Rp
Cucurbitacin E
- Cucurbitacin E (α-Elaterin), from roots of Wilbrandia ebracteata. Strong antifeedant for the flea beetle, inhibits cell adhesion[4] (also in e.g. Cucurbita andreana)[10]Шаблон:Rp
- 22,23-Dihydrocucurbitacin E from Hemsleya endecaphylla, 9 mg/72 g,[9]Шаблон:Rp and from roots of Wilbrandia ebracteata[4]Шаблон:Rp
- 22,23-Dihydrocucurbitacin E 2-glucoside from roots of Wilbrandia ebracteata[4]Шаблон:Rp
- Isocucurbitacin E, from Cucumis prophetarum[4]Шаблон:Rp
- 23,24-Dihydroisocucurbitacin E, from Cucumis prophetarum[4]Шаблон:Rp
Cucurbitacin F
- Cucurbitacin F from Elaeocarpus dolichostylus[4]Шаблон:Rp
- Cucurbitacin F 25-acetate from Helmseya graciliflora[4]Шаблон:Rp
- 23,24-Dihydrocucurbitacin F from Helmseya amabilis[4]Шаблон:Rp
- 25-Acetoxy-23,24-dihydrocucurbitacin F from Helmseya amabilis (hemslecin A)[4]Шаблон:Rp
- 23,24-Dihydrocucurbitacin F glucoside from Helmseya amabilis[4]Шаблон:Rp
- Cucurbitacin II glucoside from Helmseya amabilis[4]Шаблон:Rp
- Hexanorcucurbitacin F from Elaeocarpus dolichostylus[4]Шаблон:Rp
- Perseapicroside A from Persea mexicana[4]Шаблон:Rp
- Scandenoside R9 from Hemsleya panacis-scandens[4]Шаблон:Rp
- 15-Oxo-cucurbitacin F from Cowania mexicana[4]Шаблон:Rp
- 15-oxo-23,24-dihydrocucurbitacin F from Cowania mexicana[4]Шаблон:Rp
- Datiscosides B, D, and H, from Datisca glomerata[4]Шаблон:Rp
Cucurbitacin G
- Cucurbitacin G from roots of Wilbrandia ebracteata[4]Шаблон:Rp
- 3-Epi-isocucurbitacin G, from roots of Wilbrandia ebracteata[4]Шаблон:Rp
Cucurbitacin H
- Cucurbitacin H, stereoisomer of cucurbitacin G, from roots of Wilbrandia ebracteata[4]Шаблон:Rp
Cucurbitacin I
- Cucurbitacin I (elatericin B) from Hemsleya endecaphylla, 10 mg/72 g,[9]Шаблон:Rp also from Ecballium elaterium[4] Citrullus colocynthis,[4] Cucurbita andreana,[10] deters feeding by flea beetle[4]Шаблон:Rp
- Hexanorcucurbitacin I from Ecballium elaterium[4]Шаблон:Rp
- 23,24-Dihydrocucurbitacin I see Cucurbitacin L
- Khekadaengosides D and K from the fruits of Trichosanthes tricuspidata[4]Шаблон:Rp
- 11-Deoxocucurbitacin I, from Desfontainia spinosa[4]Шаблон:Rp
- Spinosides A and B, from Desfontainia spinosa[4]Шаблон:Rp
- 23,24-dihydro-11-Deoxocucurbitacin I from Desfontainia spinosa[4]Шаблон:Rp
Cucurbitacin J
- Cucurbitacin J from Iberis amara[4]Шаблон:Rp
- Cucurbitacin J 2-O-β-glucopyranoside from Trichosanthes tricuspidata[4]Шаблон:Rp
Cucurbitacin K
- Cucurbitacin K, stereoisomer of cucurbitacin J,[12]Шаблон:Rp from Iberis amara[4]Шаблон:Rp
- Cucurbitacin K 2-O-β-glucopyranoside from Trichosanthes tricuspidata[4]Шаблон:Rp
Cucurbitacin L
- Cucurbitacin L, or 23,24-dihydrocucurbitacin I,[4]Шаблон:Rp[12]Шаблон:Rp
- Brydioside A from Bryonia dioica[4]Шаблон:Rp
- Bryoamaride from Bryonia dioica[4]Шаблон:Rp
- 25-O-Acetylbryoamaride from Trichosanthes tricuspidata[4]Шаблон:Rp
- Khekadaengosides A and B from Trichosanthes tricuspidata[4]Шаблон:Rp
Cucurbitacin O
- Cucurbitacin O from Brandegea bigelovii[4]Шаблон:Rp
- Cucurbitacin Q 2-O-glucoside, from Picrorhiza kurrooa[4]Шаблон:Rp
- 16-Deoxy-D-16-hexanorcucurbitacin O from Ecballium elaterium[4]Шаблон:Rp
- Deacetylpicracin from Picrorhiza scrophulariaeflora[4]Шаблон:Rp
- Deacetylpicracin 2-O-glucoside from Picrorhiza scrophulariaeflora[4]Шаблон:Rp
- 22-Deoxocucurbitacin O from Wilbrandia ebracteata[4]Шаблон:Rp
Cucurbitacin P
Cucurbitacin Q
- Cucurbitacin Q from Brandegea bigelovii[4]Шаблон:Rp
- 23,24-Dihydrodeacetylpicracin 2-O-glucoside from Picrorhiza kurrooa[4]Шаблон:Rp
- Cucurbitacin Q1 from Cucumis species, actually Cucurbitacin F 25-acetate[4]
Cucurbitacin R
- Cucurbitacin R is actually 23,24-dihydrocucurbitacin D.[4]
Cucurbitacin S
Cucurbitacin T
- Cucurbitacin T, from the fruits of Citrullus colocynthis[4]Шаблон:Rp
28/29 Norcucurbitacins
Шаблон:Expand section There are several substances that can be seen as deriving from cucurbit-5-ene skeleton by loss of one of the methyl groups (28 or 29) attached to carbon 4; often with the adjacent ring (ring A) becoming aromatic.[4]Шаблон:Rp
Other
Шаблон:Expand section Several other cucurbitacins have been found in plants.[4]Шаблон:Rp
Occurrence and bitter taste
Constituents of the colocynth fruit and leaves (Citrullus colocynthis) include cucurbitacins.[13][14][15] The 2-O-β-D-glucopyranosides of cucurbitacins K and L can be extracted with ethanol from fruits of Cucurbita pepo cv dayangua.[12] Pentanorcucurbitacins A and B can be extracted with methanol from the stems of Momordica charantia.[8] Cucurbitacins B and I, and derivatives of cucurbitacins B, D and E, can be extracted with methanol from dried tubers of Hemsleya endecaphylla.[9]
Cucurbitacins impart a bitter taste in plant foods such as cucumber, zucchini, melon and pumpkin.[16][7]
Research and toxicity
Cucurbitacins are under basic research for their biological properties, including toxicity and potential pharmacological uses in development of drugs for inflammation, cancer, cardiovascular diseases, and diabetes, among others.[4][2][3][16]
The toxicity associated with consumption of foods high in cucurbitacins is sometimes referred to as "toxic squash syndrome".[17][18] In France in 2018, two women who ate soup made from bitter pumpkins became sick, involving nausea, vomiting, and diarrhea, and had hair loss weeks later.[19] Another French study of poisoning from bitter squash consumption found similar acute illnesses and no deaths.[20] The high concentration of toxin in the plants could result from cross-pollination[21] with wild cucurbitaceae species, or from plant growth stress due to high temperature and drought.[22]
See also
- Goyaglycoside
- Hemslecin
- Mogroside
- Momordicine
- Momordicoside
- Neomogroside
- Scandenosides R1–R8, R10-R11
- Siamenoside I
References
Шаблон:Cytokine receptor modulators Шаблон:Tetracyclics
- ↑ Шаблон:Cite web
- ↑ 2,0 2,1 Шаблон:Cite journal
- ↑ 3,0 3,1 Шаблон:Cite journal
- ↑ 4,00 4,01 4,02 4,03 4,04 4,05 4,06 4,07 4,08 4,09 4,10 4,11 4,12 4,13 4,14 4,15 4,16 4,17 4,18 4,19 4,20 4,21 4,22 4,23 4,24 4,25 4,26 4,27 4,28 4,29 4,30 4,31 4,32 4,33 4,34 4,35 4,36 4,37 4,38 4,39 4,40 4,41 4,42 4,43 4,44 4,45 4,46 4,47 4,48 4,49 4,50 4,51 4,52 4,53 4,54 4,55 4,56 4,57 4,58 4,59 4,60 4,61 4,62 4,63 4,64 4,65 4,66 4,67 4,68 4,69 4,70 4,71 4,72 Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ 7,0 7,1 7,2 Шаблон:Cite journal
- ↑ 8,0 8,1 8,2 Шаблон:Cite journal
- ↑ 9,0 9,1 9,2 9,3 9,4 9,5 9,6 Шаблон:Cite journal
- ↑ 10,0 10,1 10,2 10,3 Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ 12,0 12,1 12,2 Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ 16,0 16,1 Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite web
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
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