Unknown

Dataset Information

0

Functional and Structural Characterization of a (+)-Limonene Synthase from Citrus sinensis.


ABSTRACT: Terpenes make up the largest and most diverse class of natural compounds and have important commercial and medical applications. Limonene is a cyclic monoterpene (C10) present in nature as two enantiomers, (+) and (-), which are produced by different enzymes. The mechanism of production of the (-)-enantiomer has been studied in great detail, but to understand how enantiomeric selectivity is achieved in this class of enzymes, it is important to develop a thorough biochemical description of enzymes that generate (+)-limonene, as well. Here we report the first cloning and biochemical characterization of a (+)-limonene synthase from navel orange (Citrus sinensis). The enzyme obeys classical Michaelis-Menten kinetics and produces exclusively the (+)-enantiomer. We have determined the crystal structure of the apoprotein in an "open" conformation at 2.3 Å resolution. Comparison with the structure of (-)-limonene synthase (Mentha spicata), which is representative of a fully closed conformation (Protein Data Bank entry 2ONG ), reveals that the short H-?1 helix moves nearly 5 Å inward upon substrate binding, and a conserved Tyr flips to point its hydroxyl group into the active site.

SUBMITTER: Morehouse BR 

PROVIDER: S-EPMC5642283 | biostudies-literature | 2017 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

Functional and Structural Characterization of a (+)-Limonene Synthase from Citrus sinensis.

Morehouse Benjamin R BR   Kumar Ramasamy P RP   Matos Jason O JO   Olsen Sarah Naomi SN   Entova Sonya S   Oprian Daniel D DD  

Biochemistry 20170315 12


Terpenes make up the largest and most diverse class of natural compounds and have important commercial and medical applications. Limonene is a cyclic monoterpene (C<sub>10</sub>) present in nature as two enantiomers, (+) and (-), which are produced by different enzymes. The mechanism of production of the (-)-enantiomer has been studied in great detail, but to understand how enantiomeric selectivity is achieved in this class of enzymes, it is important to develop a thorough biochemical descriptio  ...[more]

Similar Datasets

| S-EPMC5642273 | biostudies-literature
| S-EPMC5818429 | biostudies-other
| S-EPMC5573811 | biostudies-literature
| S-EPMC10419818 | biostudies-literature
| S-EPMC4371936 | biostudies-literature
| S-EPMC7247714 | biostudies-literature
| S-EPMC3436860 | biostudies-literature
| S-EPMC4853807 | biostudies-other
2014-01-01 | GSE45680 | GEO
| S-EPMC4141690 | biostudies-literature