Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Enzyme Mechanisms for Polycyclic Triterpene Formation.

Wendt1, Schulz, Corey

  • 1Institut für Organische Chemie und Biochemie Albertstrasse 21, 79104 Freiburg (Germany).

Angewandte Chemie (International Ed. in English)
|October 12, 2000
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Echocardiography for the Diagnosis of Staphylococcus aureus Infective Endocarditis.

Current infectious disease reports·2000
Same author

Mechanistic Insights into the Factors Determining Exo-Endo Selectivity in the Lewis Acid-Catalyzed Diels-Alder Reaction of 1,3-Dienes with 2-Cycloalkenones.

Organic letters·2000
Same author

Reply

The Journal of infectious diseases·1999
Same author

Double-Resonance Spectroscopic Studies of Core-Penetrating Rydberg States of CaCl.

Journal of molecular spectroscopy·1999
Same author

The telomerase challenge - an unusual problem in drug discovery.

Drug discovery today·1999
Same author

Preparation of Polymer-Stabilized Noble Metal Colloids.

Journal of colloid and interface science·1999
Same journal

A Domino-Synthesized Dicoordinate Copper(I) Bis-imidazopyridine Complex Triggering Cuproptosis/Ferroptosis for Enhanced Cancer Immunotherapy.

Angewandte Chemie (International ed. in English)·2026
Same journal

Mirror-Symmetric Organic Two-Dimensional Crystals for Alternative Photon Transport Pathways.

Angewandte Chemie (International ed. in English)·2026
Same journal

Cobalt-Catalyzed Migratory E-Selective Asymmetric Aza-Nozaki-Hiyama-Kishi Coupling.

Angewandte Chemie (International ed. in English)·2026
Same journal

Facile Synthesis of α,ω-Dihydroxy Telechelic Macromonomers From Ethylene and α-Olefins for Recyclable Alternating Block Copolymers.

Angewandte Chemie (International ed. in English)·2026
Same journal

Multi-Atom Sub-Nanometer Assemblies on Interpenetrating Multi-Chambered N/C Nanospheres.

Angewandte Chemie (International ed. in English)·2026
Same journal

A Synergistic C<sub>2+</sub> Alcohols/Olefins-Intermediated Pathway Boosts CO<sub>2</sub> Hydrogenation to Aromatics.

Angewandte Chemie (International ed. in English)·2026
See all related articles

Triterpene cyclases are enzymes that create complex molecules. Recent studies reveal their mechanism involves protecting carbocations, enabling hydride and methyl shifts for efficient polycyclic product formation.

Area of Science:

  • Biochemistry
  • Enzymology
  • Organic Chemistry

Background:

  • Triterpene cyclases catalyze the formation of complex polycyclic molecules from olefins.
  • Understanding these enzymatic mechanisms has been a focus of research for decades.

Purpose of the Study:

  • To elucidate the enzymatic mechanism of triterpene formation.
  • To provide new insights into the function of oxidosqualene cyclases.

Main Methods:

  • Integration of recent chemical and biological studies.
  • Analysis of previous findings in the field.
  • Consideration of the first known structure of a triterpene cyclase.

Main Results:

  • Oxidosqualene cyclases protect intermediate carbocations from water or base.

Related Experiment Videos

  • This protection facilitates favorable hydride and methyl group shifts.
  • A detailed picture of the catalytic cascade has emerged.
  • Conclusions:

    • The primary role of oxidosqualene cyclases is carbocation stabilization.
    • This stabilization is crucial for the efficient synthesis of complex triterpenes.
    • Future research directions include structural biology, mutagenesis, and directed evolution.