Articolo in rivista, 2019, ENG, 10.1016/j.bioorg.2019.103325

Lyophilized extracts from vegetable flours as valuable alternatives to purified oxygenases for the synthesis of oxylipins

Sanfilippo C.; Paterna A.; Biondi D.M.; Patti A.

CNR - Istituto di Chimica Biomolecolare, Via Paolo Gaifami 18, Catania, I-95126, CNR - Istituto di Chimica Biomolecolare, Via Paolo Gaifami 18, I-95126 Catania, Italy, , Italy

In this work, the whole aqueous extracts of soybean flour and oat flour have been used as valuable alternatives to purified oxygenase enzymes for the preparation of oxylipins derived from (5Z,8Z,11Z,14Z,17Z)-eicosapentaenoic acid (EPA). The lipoxygenase activity in the aqueous extracts of soybean (Glycine max. L.) flour was monitored with linoleic acid as substrate and compared with the commercially available purified enzyme (LOX-1). Oat flour extracts (Avena sativa L.) were evaluated for their peroxygenase activity by comparing different enzyme preparations in the epoxidation of methyl oleate. It was found that lyophilization of the aqueous extracts from these vegetable flours offers advantages in terms of enzyme stability, reproducibility and applicability to preparative organic synthesis. The lyophilized enzyme preparations were tested for the oxyfunctionalization of EPA and the formed products were isolated in satisfactory yields. In the presence of lyophilized extract from soybean, EPA gave 15S-hydroxy-(5Z,8Z,11Z,13E,17Z)-eicosapentaenoic acid in enantiopure form as exclusive product. Peroxygenase from oat flour was less selective and catalyzed the formation of different epoxides of EPA. However, the biocatalyzed epoxidation of EPA under controlled conditions allowed to obtain optically active (17R,18S)-epoxy-(5Z,8Z,11Z,14Z)-eicosatetraenoic acid (65% ee) as the main monoepoxide, among the five possible ones.

Bioorganic chemistry (Print) 93 , pp. 103325–?

Keywords

Oxylipins Lipoxygenase Peroxygenase Lyophilization Vegetable flours EPA derivatives Stereoselective reactions

CNR authors

Paterna Angela, Sanfilippo Claudia, Biondi Daniela Maria, Patti Angela

CNR institutes

ICB – Istituto di chimica biomolecolare

ID: 408899

Year: 2019

Type: Articolo in rivista

Creation: 2019-11-05 15:55:35.000

Last update: 2022-06-06 13:13:00.000

External IDs

CNR OAI-PMH: oai:it.cnr:prodotti:408899

DOI: 10.1016/j.bioorg.2019.103325

Scopus: 2-s2.0-85072766443