| 词条 | Prymnesin-2 | |||||||||||||||||||||||||||
| 释义 |
| Name = Prymnesin 2 | ImageFile = | ImageSize = 300px | ImageAlt = | OtherNames = | IUPACName = (11S)-1-[(2R,3R,4R,5S)-6-[(2R,3S,4R,4aR,8aR)-6-[(2R,3S,4aR,8R,8aS)-6-[(2R,3R,4aR,8R,8aR)-6-[(2R,4aR,6S,7S,8aS)-6-[(1S,3R,5S,7S,10S,12R,14S,16S,21R,22R)-7-[(1Z,3Z,6R,8Z,10Z,18Z)-6-amino-19-chlorononadeca-1,3,8,10,18-pentaen-12,16-diyn-1-yl]-22-hydroxy-2,6,11,15,20-pentaoxapentacyclo[12.9.0.0^{3,12}.0^{5,10}.0^{16,21}]tricosan-19-yl]-7-methyl-octahydropyrano[3,2-b]pyran-2-yl]-3,8-dihydroxy-octahydropyrano[3,2-b]pyran-2-yl]-8-chloro-3-hydroxy-octahydropyrano[3,2-b]pyran-2-yl]-3,4-dihydroxy-octahydropyrano[3,2-b]pyran-2-yl]-3,4,5-trihydroxyoxan-2-yl]-11-chloro-3-{[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}hexadeca-13,15-diyne-2,4,6,7,8,9,10-heptol | SystematicName = | Section1 = {{Chembox Identifiers | CASNo =168180-17-4 | PubChem = 102510994 | SMILES =CC2CC1OC(CCC1OC2C7CCC6OC5CC4OC3CCC(OC3CC4OC5CC(O)C6O7)C=CC=CCC(N)CC=CC=CC#CCCC#CC=CCl)C9CC(O)C8OC(C(O)CC8O9)C%11CC(Cl)C%10OC(C(O)CC%10O%11)C%13CCC%12OC(C(O)C(O)C%12O%13)C%15OC(CC(O)C(OC%14OC(CO)C(O)C%14O)C(O)CC(O)C(O)C(O)C(O)C(O)C(Cl)CC#CC#C)C(O)C(O)C%15O }} | Section2 = {{Chembox Properties | C=96|H=136|Cl=3|N=1|O=35 | MolarMass = | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} | Section3 = {{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} | Section4 = | Section5 = | Section6 = }}Prymnesin-2 is an organic compound that is secreted by the haptophyte Prymnesium parvum. It belongs to the Prymnesin family and has potent hemolytic and ichthyotoxic properties. In a purified form it appears as a pale yellow solid.[1] P. parvum is responsible for red harmful algal blooms worldwide, causing massive fish killings. When these algal blooms occur, this compound poses a threat to the local fishing industry. This is especially true for brackish water, as the compound can reach critical concentrations more easily.[1] Structure and reactivityThe structural formula of prymnesin-2 is: C96H136Cl3NO35. The compound has two chiral centers, at the carbon atoms C14 and C85. The molecule is amphoteric, which means that it can act both as base and an acid. This is because all 16 hydroxyls, except for one at C32, are concentrated on carbons C48-84, and there is a xylose moiety at C77. This might lead to interaction with biomembranes, which is thought to be the basis of its toxicity.[1] The difference between prymnesin-1 and prymnesin-2 is the glycosidic residues: L-arabinose, D-galactose and D-ribose, yet prymnesin-2 and prymnesin-1 show comparable activities. Prymnesins also have unique features: The possession of only one methyl, but three chlorine atoms, acetylene bonds, sugars and an amino group.[2] SynthesisThere is not much known about the synthesis of prymnesin-1 and prymnesin-2 in vivo. However, its likely that both are derived from acetate-related metabolism, based on knowledge about the structure of the prymnesins. In general primary and secondary metabolites such as fatty acids, polyketides and non-ribosomal peptides are synthesised by the acetate pathway [3] Mechanism of actionThe mechanism of action of prymnesin-2 remains to be determined.[2] Prymnesin-2 and prymnesin-1 show comparable activities. Prymnesin-2 has shown multiple functionalities, such as potent hemolytic activity and diverse biological activities, such as mouse lethality, ichthyotoxicity and activity inducing Ca2+ influx into cultured cells. The hemolytic potency of prymnesin-2 exceeds that of plant saponin by 50.000 times.[4] Prymnesin-2 causes hemolysis by direct interaction between toxin and cell surface. Partly due to interaction with cellular lipids, mainly to interaction with a specific binding site on the blood cell surface. This is supported by the observation of competitive inhibition by the prymnesin-2 analogues, which assume the presence of a specific binding site on the blood cell surface. Also the process of toxin molecule aggregation may be involved in the main mechanism of the haemolytic activity.[4] ToxicityPrymnesin-2 is an ichthyotoxic compound with the ability to hemolyze blood. 2.5 nM is needed for a 50% hemolysis rate of a 1% rat blood cell suspension, and 9 nM is enough for killing freshwater fish. The hemolytic and ichthyotoxic properties increase when the pH of the solution rises from 7 to 8.[5] Prymnesin-2 causes calcium ion influx into C6 rat glioma cells at a concentration of 70 nM.[6] Besides the lytic effect on blood cells, hepatocytes, Hela cells and artificial liposomes are affected by prymnesin-2. As seen in the table below, prymnesin-2 is highly hemolytic for blood cells of different animal species, even when compared to the already highly hemolytic toxin saponin.
Effects on animalsIn the USA, the first recorded P. parvum bloom occurred in 1985 in a semi-arid region of the country (Pecos River, Texas).[7] Since then, the incidence of P. parvum blooms dramatically increased in the USA, where the organism has invaded lakes and rivers throughout southern regions and most recently into northern regions. The magnitude of P. parvum blooms are also increasing over the past decade compared to 30 years ago, with massive fish killings as result.[8][9][10] References1. ^1 2 {{cite journal|last1=Igarashi|first1=Tomoji|last2=Satake|first2=Masayuki|last3=Yasumoto|first3=Takeshi|title=Prymnesin-2: A Potent Ichthyotoxic and Hemolytic Glycoside Isolated from the Red Tide Alga Prymnesium parvum|journal=Journal of the American Chemical Society|volume=118|issue=2|pages=479–480|doi=10.1021/ja9534112|language=en|year=1996}} 2. ^1 {{Cite journal|last=Yasumoto|first=Takeshi|title=The chemistry and biological function of natural marine toxins|journal=The Chemical Record|language=en|volume=1|issue=3|pages=228–242|doi=10.1002/tcr.1010|pmid=11895121|issn=1528-0691|year=2001}} 3. ^{{Cite journal|last=Manning|first=Schonna R.|last2=La Claire|first2=John W.|date=2010-03-16|title=Prymnesins: Toxic Metabolites of the Golden Alga, Prymnesium parvum Carter (Haptophyta)|url=http://www.mdpi.com/1660-3397/8/3/678|journal=Marine Drugs|language=en|volume=8|issue=3|pages=678–704|doi=10.3390/md8030678|pmid=20411121|pmc=2857367}} 4. ^1 {{Cite journal|last=Igarashi|first=T.|last2=Aritake|first2=S.|last3=Yasumoto|first3=T.|date=1998|title=Biological activities of prymnesin-2 isolated from a red tide alga Prymnesium parvum|journal=Natural Toxins|volume=6|issue=1|pages=35–41|issn=1056-9014|pmid=9851510|doi=10.1002/(SICI)1522-7189(199802)6:1<35::AID-NT7>3.0.CO;2-7}} 5. ^{{cite journal|last1=Granéli|first1=Edna|last2=Salomon|first2=Paulo S.|title=Factors Influencing Allelopathy and Toxicity in Prymnesium parvum|journal=JAWRA Journal of the American Water Resources Association|date=1 February 2010|volume=46|issue=1|pages=108–120|doi=10.1111/j.1752-1688.2009.00395.x|language=en|issn=1752-1688}} 6. ^{{cite journal|last1=Morohashi|first1=Akio|last2=Satake|first2=Masayuki|last3=Oshima|first3=Yasukatsu|last4=Igarashi|first4=Tomoji|last5=Yasumoto|first5=Takeshi|title=Absolute configuration at C14 and C85 in prymnesin-2, a potent hemolytic and ichthyotoxic glycoside isolated from the red tide alga Prymnesium parvum|journal=Chirality|volume=13|issue=9|pages=601–605|doi=10.1002/chir.1184|pmid=11579456|language=en|issn=1520-636X|year=2001}} 7. ^James T. L., De La Cruz A.. Prymnesium parvum Carter (Chrysophyceae) as a suspect of mass mortalities of fish and shellfish communities in western Texas, Texas Journal of Science, 1989, vol. 41 (pp. 429-430). 8. ^{{Cite journal|last=Roelke|first=Daniel|last2=Augustine|first2=Sarah|last3=Buyukates|first3=Yesim|date=2003-11-01|title=Fundamental Predictability in Multispecies Competition: The Influence of Large Disturbance.|journal=The American Naturalist|volume=162|issue=5|pages=615–623|doi=10.1086/378750|issn=0003-0147}} 9. ^{{Cite journal|last=Buyukates|first=Yesim|last2=Roelke|first2=Daniel|date=2005-10-01|title=Influence of Pulsed Inflows and Nutrient Loading on Zooplankton and Phytoplankton Community Structure and Biomass in Microcosm Experiments Using Estuarine Assemblages|journal=Hydrobiologia|language=en|volume=548|issue=1|pages=233–249|doi=10.1007/s10750-005-5195-x|issn=0018-8158}} 10. ^{{Cite journal|last=Miller|first=Carrie J.|last2=Roelke|first2=Daniel L.|last3=Davis|first3=Stephen E.|last4=Li|first4=Hsiu-Ping|last5=Gable|first5=George|title=The role of inflow magnitude and frequency on plankton communities from the Guadalupe Estuary, Texas, USA: Findings from microcosm experiments|url=http://linkinghub.elsevier.com/retrieve/pii/S0272771408002722|journal=Estuarine, Coastal and Shelf Science|volume=80|issue=1|pages=67–73|doi=10.1016/j.ecss.2008.07.006|year=2008}} 10 : Phycotoxins|Polyether toxins|Polyynes|Alcohols|Alkenes|Amines|Organochlorides|Halohydrins|Halogen-containing natural products|Glycosides |
|||||||||||||||||||||||||||
| 随便看 |
|
开放百科全书收录14589846条英语、德语、日语等多语种百科知识，基本涵盖了大多数领域的百科知识，是一部内容自由、开放的电子版国际百科全书。