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词条 Tagetitoxin
释义

  1. Chemical structure

  2. Mechanism of action

  3. References

{{Chembox
| ImageFile = Tagetitoxin.svg
| ImageSize = 200px
| ImageCaption = Proposed structure of tagetitoxin
| IUPACName =
| OtherNames =
|Section1={{Chembox Identifiers
| CASNo = 87913-21-1
| CASNo_Ref = {{cascite|correct|}}
| PubChem = 115340
| ChemSpiderID = 103185
| SMILES = O=C(N)[C@]1(O)SC[C@@]2(O[C@@H]1[C@H](OC(=O)C)[C@@H](N)[C@H]2OP(=O)(O)O)C(=O)O
| InChI = 1/C11H17N2O11PS/c1-3(14)22-5-4(12)6(24-25(19,20)21)10(9(16)17)2-26-11(18,8(13)15)7(5)23-10/h4-7,18H,2,12H2,1H3,(H2,13,15)(H,16,17)(H2,19,20,21)/t4-,5-,6-,7-,10+,11-/m1/s1
| InChIKey = UVAAUIDYGIWLMB-XJKNRETDBI
| StdInChI = 1S/C11H17N2O11PS/c1-3(14)22-5-4(12)6(24-25(19,20)21)10(9(16)17)2-26-11(18,8(13)15)7(5)23-10/h4-7,18H,2,12H2,1H3,(H2,13,15)(H,16,17)(H2,19,20,21)/t4-,5-,6-,7-,10+,11-/m1/s1
| StdInChIKey = UVAAUIDYGIWLMB-XJKNRETDSA-N
|Section2={{Chembox Properties
| C=11 | H=17 | N=2 | O=11 | P=1 | S=1
| Appearance =
| Density =
| MeltingPt =
| BoilingPt =
| Solubility =
|Section3={{Chembox Hazards
| MainHazards =
| FlashPt =
| AutoignitionPt =
}}Tagetitoxin (TGT) is a bacterial phytotoxin produced by Pseudomonas syringae pv. tagetis.[1][2]

Chemical structure

When TGT was first isolated, it was only partially characterized.[2] The first proposed chemical structure of TGT involved an eight-membered ring,[3] but this was revised shortly afterward to a bicyclic structure (shown at right) based on NMR and mass spectrometry.[4] This structure, however, has been questioned.[5] The absolute configuration remains undetermined, and attempts at confirming the structure by organic synthesis are underway.[6][7][8][9][10][11][12] Recently Porter et al. published a revised structure of TGT based on extensive 2D NMR data.[13]

Mechanism of action

TGT interferes with development of chloroplasts in young plant leaves thereby causing chlorosis.[14] The natural target of the toxin is chloroplast RNA polymerase. Chloroplast RNA polymerase belongs to ubiquitous family of multisubunit RNA polymerases (RNAP) and is most closely related to bacterial enzymes. In vitro, TGT inhibits bacterial RNAPs from Escherichia coli and Thermus thermophilus, and eukaryotic RNA polymerase III.[15] In contrast, eukaryotic RNA polymerase I and II as well as single-subunit RNA polymerases of bacteriophage T7 and SP6 are relatively insensitive to the compound. TGT binds in the RNAP active site[16] and inhibits initiation and elongation phases of transcription as well as pyrophosphorolysis of the nascent RNA.[16] However, the detailed mechanism of inhibition remains a subject of heated debate.[17][18]

It has been suggested that TGT forms a ternary RNAP-NTP-TGT complex and inhibits phosphodiester bond synthesis either by binding an inhibitory magnesium ion[16] or by trapping a flexible active site domain in an inactive conformation.[19] The third theory suggests that TGT forms predominantly a binary RNAP-TGT complex and inhibits RNAP translocation along the DNA by mimicking the transcription byproduct pyrophosphate.[20]

References

1. ^{{cite journal |doi=10.1071/AR9780831 |title=Apical chlorosis and leaf spot of Tagetes spp. Caused by Pseudomonas tagetis Hellmers |year=1978 |last1=Trimboli |first1=D |last2=Fahy |first2=PC |last3=Baker |first3=KF |journal=Australian Journal of Agricultural Research |volume=29 |issue=4 |pages=831–9}}
2. ^1 {{cite journal |last1=Mitchell |first1=R. E. |last2=Durbin |first2=R. D. |year=1981 |title=Tagetitoxin, a toxin produced by Pseudomonas syringae pv. tagetis: purification and partial characterization |journal=Physiological Plant Pathology |volume=18 |issue=2 |pages=157–68 |doi=10.1016/S0048-4059(81)80037-9 |url=http://www.sciencedirect.com/science/article/pii/S0048405981800379}}
3. ^{{Cite journal |author1=Mitchell, R. E. |author2=Durbin, R. D. | journal = Phytochemistry | year = 1983 | volume = 22 | pages = 1425–1428 | doi = 10.1016/S0031-9422(00)84028-5 | title = The structure of tagetitoxin, a phytotoxin of Pseudomonas syringae pv. Tagetis | issue = 6}}
4. ^{{Cite journal |author1=Mitchell, R. E. |author2=Coddington, J. M. |author3=Young, H. | journal = Tetrahedron Lett. | year = 1989| volume = 30 | pages = 501–504 | doi = 10.1016/S0040-4039(00)95239-0 | title = A revised structure for tagetitoxin | issue = 4}}
5. ^{{Cite journal |author1=Gronwald, J.W. |author2=Plaisance, K. L. |author3=Marimanikkuppam, S. |author4=Ostrowski, B. G. | journal = Physiol. Mol. Plant Pathol. | year = 2005 | volume = 67 | pages = 23–32 | doi = 10.1016/j.pmpp.2005.09.002 | title = Tagetitoxin purification and partial characterization}}
6. ^{{cite journal | doi = 10.1055/s-0029-1218525 | title = Thieme Chemistry Journal Awardees - Where Are They Now? Approaches to Tagetitoxin and its Decarboxy Analogue from d-Glucose | year = 2009 | last1 = Porter | first1 = Michael | last2 = Plet | first2 = Julien | last3 = Sandhu | first3 = Amandeep | last4 = Sehailia | first4 = Moussa | journal = Synlett | volume = 2009 | issue = 20 | pages = 3258–3262}}
7. ^{{cite journal | doi = 10.1021/ol802297h | title = Synthesis of the Tagetitoxin Core via Photo-Stevens Rearrangement | year = 2008 | last1 = Mortimer | first1 = Anne J. Price | last2 = Aliev | first2 = Abil E. | last3 = Tocher | first3 = Derek A. | last4 = Porter | first4 = Michael J. | journal = Organic Letters | volume = 10 | issue = 23 | pages = 5477–80 | pmid = 18973329}}
8. ^{{cite journal |author1=Sammakia, T. |author2=Hurley, T. B. |author3=Sammond, D. M. |author4=Smith, R. S. |author5=Sobolov, S. B. |author6=Oeschger, T. R. | journal = Tetrahedron Lett. | year = 1996 | volume = 37 | pages = 4427–4430 | doi = 10.1016/0040-4039(96)00879-9 | title = Dihydroxylation and oxidative cleavage of olefins in the presence of sulfur | issue = 26}}
9. ^{{cite journal |author1=Dent, B. R. |author2=Furneaux, R. H. |author3=Gainsford, G. J. |author4=Lynch, G. P. | journal = Tetrahedron | year = 1999 | volume = 55 | pages = 6977–6996 | doi = 10.1016/S0040-4020(99)00327-0 | title = Synthesis studies of structural analogues of tagetitoxin: 2-phosphate | issue = 22}}
10. ^{{cite journal |first1=Julien R. H. |last1=Plet |first2=Michael J. |last2=Porter |year=2006 |title=Synthesis of the bicyclic core of tagetitoxin |journal=Chemical Communications |volume= 44|issue=11 |pages=1197–9 |doi=10.1039/B600819D |pmid=16518489|bibcode=2008ChCom..44.5292T }}
11. ^{{cite journal |first1=Anne J. P. |last1=Mortimer |first2=Julien R. H. |last2=Plet |first3=Oluwafunsho A. |last3=Obasanjo |first4=Nikolas |last4=Kaltsoyannis |first5=Michael J. |last5=Porter |year=2012 |title=Inter- and intramolecular reactions of 1-deoxy-1-thio-1,6-anhydrosugars with α-diazoesters: synthesis of the tagetitoxin core by photochemical ylide rearrangement |journal=Org. Biomol. Chem. |pages=8616–27 |doi=10.1039/c2ob26308d |pmid=22965829 |volume=10 |issue=43}},
12. ^{{cite book |first1=Moussa |last1=Sehailia |year=2011 |title=Studies towards the total synthesis of tagetitoxin |url=http://discovery.ucl.ac.uk/1302404/ |type=Doctoral thesis |publisher=University College London}}{{page needed|date=September 2012}}
13. ^{{Cite journal|last=Aliev|first=Abil E.|last2=Karu|first2=Kersti|last3=Mitchell|first3=Robin E.|last4=Porter|first4=Michael J.|date=2015-12-15|title=The structure of tagetitoxin|url=http://pubs.rsc.org/en/content/articlelanding/2016/ob/c5ob02076j#!divAbstract|journal=Organic & Biomolecular Chemistry|language=en|volume=14|issue=1|pages=238–45|doi=10.1039/C5OB02076J|pmid=26517805|issn=1477-0539}}
14. ^{{cite journal |doi=10.1007/BF00392227 |pmid=24241135 |title=Tagetitoxin affects plastid development in seedling leaves of wheat |year=1985 |last1=Lukens |first1=J. H. |last2=Durbin |first2=R. D. |journal=Planta |volume=165 |issue=3 |pages=311–21}}
15. ^{{cite journal |pmid=2403565 |year=1990 |last1=Steinberg |first1=Thomas H. |last2=Mathews |first2=Dennis E. |last3=Durbin |first3=Richard D. |last4=Burgess |first4=Richard R. |title=Tagetitoxin: A New Inhibitor of Eukaryotic Transcription by RNA Polymerase III |volume=265 |issue=1 |pages=499–505 |journal=The Journal of Biological Chemistry |url=http://www.jbc.org/cgi/pmidlookup?view=long&pmid=2403565}}
16. ^1 2 {{cite journal |doi=10.1038/nsmb1015 |title=Structural basis for transcription inhibition by tagetitoxin |year=2005 |last1=Vassylyev |first1=Dmitry G |last2=Svetlov |first2=Vladimir |last3=Vassylyeva |first3=Marina N |last4=Perederina |first4=Anna |last5=Igarashi |first5=Noriyuki |last6=Matsugaki |first6=Naohiro |last7=Wakatsuki |first7=Soichi |last8=Artsimovitch |first8=Irina |journal=Nature Structural & Molecular Biology |volume=12 |issue=12 |pmid=16273103 |pages=1086–93 |pmc=1790907}}
17. ^{{cite journal |doi=10.4161/trns.19468 |title=The binding site and mechanism of the RNA polymerase inhibitor tagetitoxin: An issue open to debate |year=2012 |last1=Klyuyev |first1=Sergiy |last2=Vassylyev |first2=Dmitry G. |journal=Transcription |volume=3 |issue=2 |pages=46–50 |pmid=22414754 |pmc=3337825}}
18. ^{{cite journal |doi=10.4161/trns.19749 |title=Response to Klyuyev and Vassylyev: On the mechanism of tagetitoxin inhibition of transcription |year=2012 |last1=Svetlov |first1=Vladimir |last2=Artsimovitch |first2=Irina |last3=Nudler |first3=Evgeny |journal=Transcription |volume=3 |issue=2 |pages=51–5 |pmid=22414748 |pmc=3337826}}
19. ^{{cite journal |first1=Irina |last1=Artsimovitch |first2=Vladimir |last2=Svetlov |first3=Sondra Maureen |last3=Nemetski |first4=Vitaly |last4=Epshtein |first5=Timothy |last5=Cardozo |first6=Evgeny |last6=Nudler |year=2011 |title=Tagetitoxin Inhibits RNA Polymerase through Trapping of the Trigger Loop |journal=The Journal of Biological Chemistry |volume=286 |issue=46 |pages=40395–400 |doi=10.1074/jbc.M111.300889 |pmid=21976682 |pmc=3220573}}
20. ^{{cite journal |first1=Anssi M. |last1=Malinen |first2=Matti |last2=Turtola |first3=Marimuthu |last3=Parthiban |first4=Lioudmila |last4=Vainonen |first5=Mark S. |last5=Johnson |first6=Georgiy A. |last6=Belogurov |year=2012 |title=Active site opening and closure control translocation of multisubunit RNA polymerase |journal=Nucleic Acids Research |volume=40 |issue=15 |pages=7442–51 |doi=10.1093/nar/gks383 |pmid=22570421 |pmc=3424550}}

7 : Plant toxins|Acetate esters|Carboxylic acids|Organophosphates|RNA polymerase inhibitors|Carboxamides|Alcohols
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