Volume 40, Issue 11 pp. 2091-2094

Communication

Classification of Terpenoids according to the Methylerythritolphosphate or the Mevalonate Pathway with Natural ¹²C/¹³C Isotope Ratios: Dynamic Allocation of Resources in Induced Plants

Andreas Jux Dipl.-Chem.,

Andreas Jux Dipl.-Chem.

Max-Planck-Institut für Chemische Ökologie Carl-Zeiss-Promenade 10, 07745 Jena (Germany) Fax: (+49) 3641-643670

Search for more papers by this author

Gerd Gleixner Dr.,

Gerd Gleixner Dr.

Max-Planck-Institut für Biogeochemie Carl-Zeiss-Promenade 10, 07745 Jena (Germany)

Search for more papers by this author

Wilhelm Boland Prof. Dr.,

Wilhelm Boland Prof. Dr.

[email protected]

Max-Planck-Institut für Chemische Ökologie Carl-Zeiss-Promenade 10, 07745 Jena (Germany) Fax: (+49) 3641-643670

Search for more papers by this author

Andreas Jux Dipl.-Chem.,

Andreas Jux Dipl.-Chem.

Max-Planck-Institut für Chemische Ökologie Carl-Zeiss-Promenade 10, 07745 Jena (Germany) Fax: (+49) 3641-643670

Search for more papers by this author

Gerd Gleixner Dr.,

Gerd Gleixner Dr.

Max-Planck-Institut für Biogeochemie Carl-Zeiss-Promenade 10, 07745 Jena (Germany)

Search for more papers by this author

Wilhelm Boland Prof. Dr.,

Wilhelm Boland Prof. Dr.

[email protected]

Max-Planck-Institut für Chemische Ökologie Carl-Zeiss-Promenade 10, 07745 Jena (Germany) Fax: (+49) 3641-643670

Search for more papers by this author

First published: 28 May 2001

https://doi.org/10.1002/1521-3773(20010601)40:11<2091::AID-ANIE2091>3.0.CO;2-5

Citations: 48

We thank Dr. H. Bischoff (Bayer AG, Wuppertal) for cerivastatin and Steffen Rühlow for his committed technical assistance.

Share a link

Email
Wechat
Bluesky

Graphical Abstract

Plants utilize two different pathways for the biosynthesis of isopentenyl diphosphate, the universal building block of all terpenes (see scheme). Application of compound-specific isotope-ratio mass spectrometry (GC-C-IRMS) to volatile terpenoids allows distinction between the pathways on the basis of natural ¹²C/¹³C ratios.

References

1 P. W. Páre, J. H. Tumlinson, Plant Physiol. 1999, 121, 325–331.
10.1104/pp.121.2.325
CAS PubMed Web of Science® Google Scholar
2 M. Dicke, J. J. A. van Loon, Entomol. Exp. Appl. 2000, 97, 237–249.
10.1046/j.1570-7458.2000.00736.x
CAS Web of Science® Google Scholar
3 J. Bruin, M. W. Sabelis, M. Dicke, Trends Ecol. Evolut. 1995, 10, 371–371.
10.1016/S0169-5347(00)89137-5
CAS PubMed Web of Science® Google Scholar
4 M. Rohmer, Nat. Prod. Rep. 1999, 16, 565–574.
10.1039/a709175c
CAS PubMed Web of Science® Google Scholar
5 W. Eisenreich, M. Schwarz, A. Cartayrade, D. Arigoni, M. H. Zenk, A. Bacher, Chem. Biol. 1998, 5, 221–233.
10.1016/S1074-5521(98)90002-3
CAS PubMed Web of Science® Google Scholar
6 H. K. Lichtenthaler, M. Rohmer, J. Schwender, Physiol. Plant. 1997, 101, 643–652.
10.1111/j.1399-3054.1997.tb01049.x
CAS Web of Science® Google Scholar
7 J. Piel, J. Donath, K. Bandemer, W. Boland, Angew. Chem. 1998, 110, 2622–2625;
10.1002/(SICI)1521-3757(19980918)110:18<2622::AID-ANGE2622>3.0.CO;2-F
Google Scholar
Angew. Chem. Int. Ed. 1998, 37, 2478–2481.
10.1002/(SICI)1521-3773(19981002)37:18<2478::AID-ANIE2478>3.0.CO;2-Q
CAS PubMed Web of Science® Google Scholar
8 K. P. Adam, J. Zapp, Phytochemistry 1998, 48, 953–959.
10.1016/S0031-9422(97)00992-8
CAS Web of Science® Google Scholar
9 D. Arigoni, S. Sagner, C. Latzel, W. Eisenreich, A. Bacher, M. H. Zenk, Proc. Natl. Acad. Sci. USA 1997, 94, 10 600–10 605.
10.1073/pnas.94.20.10600
CAS Web of Science® Google Scholar
10 G. Gleixner, C. Scrimgeour, H. L. Schmidt, R. Viola, Planta 1998, 207, 241–245.
10.1007/s004250050479
CAS Web of Science® Google Scholar
11 W. A. Brand, J. Mass Spectrom. 1996, 31, 225–235.
10.1002/(SICI)1096-9888(199603)31:3<225::AID-JMS319>3.0.CO;2-L
CAS PubMed Web of Science® Google Scholar
12 M. H. O′Leary, Phytochemistry 1981, 20, 553–567.
10.1016/0031-9422(81)85134-5
PubMed Web of Science® Google Scholar
13 A. Mosandl in Flavor Chemistry: Thirty Years of Progress ( ), Kluwer/Plenum, New York, 1999, pp. 31–41.
10.1007/978-1-4615-4693-1_4
Web of Science® Google Scholar
14 H.-L. Schmidt, A. Roßmann, R. A. Werner in Flavourings ( ), Wiley-VCH, Weinheim, 1998, pp. 539–596.
Google Scholar
15 W. Boland, A. Gäbler, Helv. Chim. Acta 1989, 72, 247–253.
10.1002/hlca.19890720208
CAS Web of Science® Google Scholar
16 E. Melzer, H.-L. Schmidt, J. Biol. Chem. 1987, 262, 8159–8164.
10.1016/S0021-9258(18)47543-6
CAS PubMed Web of Science® Google Scholar
17 G. A. Sprenger, U. Schorken, T. Wiegert, S. Grolle, A. A. Degraaf, S. V. Taylor, T. P. Begley, S. Bringermeyer, H. Sahm, Proc. Natl. Acad. Sci. USA 1997, 94, 12 857–12 862.
10.1073/pnas.94.24.12857
CAS Web of Science® Google Scholar
18 H.-L. Schmidt, G. Gleixner in Stable Isotopes: The Integration of Biological, Ecological and Geochemical Processes ( ), BIOS Scientific, Oxford, 1998, pp. 13–25.
Google Scholar
19 S. Schouten, W. Breteler, P. Blokker, N. Schogt, W. I. C. Rijpstra, K. Grice, M. Baas, J. S. S. Sinnighe-Damstè, Geochim. Cosmochim. Acta 1998, 62, 1397–1406.
10.1016/S0016-7037(98)00076-3
CAS Web of Science® Google Scholar
20 J. Kuhlmann, W. Muck, H. Bischoff, E. von Keutz, M. Llewellyn, Cardiovasc. Drugs Rev. 1998, 16, 236–263.
10.1111/j.1527-3466.1998.tb00357.x
CAS Web of Science® Google Scholar
21 T. Kuzuyama, T. Shimizu, S. Takahashi, H. Seto, Tetrahedron Lett. 1998, 39, 7913–7916.
10.1016/S0040-4039(98)01755-9
CAS Web of Science® Google Scholar
22 J. Engelberth, T. Koch, F. Kühnemann, W. Boland, Angew. Chem. 2000, 112, 1928–1930;
10.1002/(SICI)1521-3757(20000515)112:10<1928::AID-ANGE1928>3.0.CO;2-8
Google Scholar
Angew. Chem. Int. Ed. 2000, 39, 1860–1862.
10.1002/(SICI)1521-3773(20000515)39:10<1860::AID-ANIE1860>3.0.CO;2-F
CAS PubMed Web of Science® Google Scholar
23 J. Engelberth, T. Koch, G. Schüler, N. Bachmann, J. Rechtenbach, W. Boland, Plant Physiol. 2001, 125, 369–377.
10.1104/pp.125.1.369
CAS PubMed Web of Science® Google Scholar
24 J. Donath, W. Boland, Phytochemistry 1995, 39, 785–790.
10.1016/0031-9422(95)00082-I
CAS Web of Science® Google Scholar

Citing Literature

Volume40, Issue11

June 1, 2001

Pages 2091-2094

Classification of Terpenoids according to the Methylerythritolphosphate or the Mevalonate Pathway with Natural ¹²C/¹³C Isotope Ratios: Dynamic Allocation of Resources in Induced Plants

Graphical Abstract

References

Citing Literature

References

Information

About Wiley Online Library

Help & Support

Opportunities

Connect with Wiley

Classification of Terpenoids according to the Methylerythritolphosphate or the Mevalonate Pathway with Natural 12C/13C Isotope Ratios: Dynamic Allocation of Resources in Induced Plants

Graphical Abstract

References

Citing Literature

References

Related

Information

Classification of Terpenoids according to the Methylerythritolphosphate or the Mevalonate Pathway with Natural ¹²C/¹³C Isotope Ratios: Dynamic Allocation of Resources in Induced Plants