| Literature DB >> 26417685 |
Munenori Takehara1, Takahiro Kuwa2, Yoshinori Inoue2, Chitoshi Kitamura2, Masaki Honda3.
Abstract
(15Z)-Lycopene was prepared by thermal isomerization of (all-E)-lycopene derived from tomatoes, and isolated by using a series of chromatographies. The fine red crystalline powder of (15Z)-lycopene was obtained from 556 mg of (all-E)-lycopene with a yield of 0.6 mg (purity: reversed-phase HPLC, 97.2%; normal-phase HPLC, ≥99.9%), and (1)H and (13)C NMR spectra of the isomer were fully assigned. More refined computational analyses that considered differences in the energy levels of the conformers involved in isomerization have also determined the stabilities of (15Z)-lycopene and other geometric isomers, along with the activation energies during isomerization from the all-E form. The fine control of conditions for HPLC separation and an advanced theoretical insight into geometric isomerization have led to the discovery of the 15Z-isomer generated from a natural source.Entities:
Keywords: Density-functional theory; Geometric isomerization; Lycopene; Purification; Spectral analysis; Tomatoes
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Year: 2015 PMID: 26417685 DOI: 10.1016/j.bbrc.2015.09.122
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575