Enzymatic synthesis and characterization of chlorophyllide derivatives as possible internal standards for pigment chromatographic analysis
•Easy and fast enzymatic synthesis of chlorophyllides a and b esters.•Dunalliela salina provided both the enzyme chlorophyllase and chlorophyll substrates.•Chromatographic properties of esters of different alcohols and diols were studied.•Chlorophyllide a (8′-hydroxyoctyl) ester was selected and com...
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Published in | Algal research (Amsterdam) Vol. 46; p. 101688 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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01.03.2020
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Abstract | •Easy and fast enzymatic synthesis of chlorophyllides a and b esters.•Dunalliela salina provided both the enzyme chlorophyllase and chlorophyll substrates.•Chromatographic properties of esters of different alcohols and diols were studied.•Chlorophyllide a (8′-hydroxyoctyl) ester was selected and completely characterized.•The proposed internal standard showed adequate stability over time.
In this article the chlorophyllase activity of Dunaliella salina has been employed to generate different chlorophyllide a and b esters that could potentially be used as internal standards in pigment analysis. Chlorophyllide a (8’-hydroxyoctyl) ester was selected due its adequate chromatographic and spectral properties and was fully characterized by UV-Vis, ESI-MS and NMR. An easy room temperature procedure for its synthesis is described. Attachment |
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AbstractList | •Easy and fast enzymatic synthesis of chlorophyllides a and b esters.•Dunalliela salina provided both the enzyme chlorophyllase and chlorophyll substrates.•Chromatographic properties of esters of different alcohols and diols were studied.•Chlorophyllide a (8′-hydroxyoctyl) ester was selected and completely characterized.•The proposed internal standard showed adequate stability over time.
In this article the chlorophyllase activity of Dunaliella salina has been employed to generate different chlorophyllide a and b esters that could potentially be used as internal standards in pigment analysis. Chlorophyllide a (8’-hydroxyoctyl) ester was selected due its adequate chromatographic and spectral properties and was fully characterized by UV-Vis, ESI-MS and NMR. An easy room temperature procedure for its synthesis is described. Attachment |
ArticleNumber | 101688 |
Author | Sanz, Noelia Gavalás-Olea, Antonio Vaz, Belén Garrido, José Luis Riobó, Pilar |
Author_xml | – sequence: 1 givenname: Antonio surname: Gavalás-Olea fullname: Gavalás-Olea, Antonio email: gavalasolea@iim.csic.es organization: IIM-CSIC, Av. Eduardo Cabello 6, Vigo 36208, Spain – sequence: 2 givenname: Noelia surname: Sanz fullname: Sanz, Noelia organization: IIM-CSIC, Av. Eduardo Cabello 6, Vigo 36208, Spain – sequence: 3 givenname: Pilar surname: Riobó fullname: Riobó, Pilar organization: IIM-CSIC, Av. Eduardo Cabello 6, Vigo 36208, Spain – sequence: 4 givenname: José Luis surname: Garrido fullname: Garrido, José Luis organization: IIM-CSIC, Av. Eduardo Cabello 6, Vigo 36208, Spain – sequence: 5 givenname: Belén surname: Vaz fullname: Vaz, Belén organization: Department of Organic Chemistry, Biomedical Research Center (CINBIO), and Southern Galicia Institute of Health Research (IISSG), Universidade de Vigo, 36310 Vigo, Spain |
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Keywords | Internal Standard Pigment analysis Chlorophyllide sters Chromatography |
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SubjectTerms | Chlorophyllide sters Chromatography Internal Standard Pigment analysis |
Title | Enzymatic synthesis and characterization of chlorophyllide derivatives as possible internal standards for pigment chromatographic analysis |
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