Cochineal Waxy Residues as Source of Policosanol: Chemical Hydrolysis and Enzymatic Transesterification

The aim of this study was to obtain and characterise the long-chain alcohols present in policosanol derived from waste from the production of carminic acid, a natural colouring agent widely used in the food industry. The effectiveness of different methods designed for extraction of policosanol from...

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Published in:Journal of Chemistry
Main Authors: Emilia Ramos-Zambrano, Pedro Herrera-Serrano, Jorge García-Dávila, Gabriel Ríos-Cortés, Antonio Ruperto Jiménez-Aparicio, Alma Leticia Martínez-Ayala
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2019
Subjects:
Online Access:https://doi.org/10.1155/2019/4547378
https://doaj.org/article/84e6e286994e449faae8c89c5e8e4bae
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spelling ftdoajarticles:oai:doaj.org/article:84e6e286994e449faae8c89c5e8e4bae 2024-09-15T17:48:09+00:00 Cochineal Waxy Residues as Source of Policosanol: Chemical Hydrolysis and Enzymatic Transesterification Emilia Ramos-Zambrano Pedro Herrera-Serrano Jorge García-Dávila Gabriel Ríos-Cortés Antonio Ruperto Jiménez-Aparicio Alma Leticia Martínez-Ayala 2019-01-01T00:00:00Z https://doi.org/10.1155/2019/4547378 https://doaj.org/article/84e6e286994e449faae8c89c5e8e4bae EN eng Wiley http://dx.doi.org/10.1155/2019/4547378 https://doaj.org/toc/2090-9063 https://doaj.org/toc/2090-9071 2090-9063 2090-9071 doi:10.1155/2019/4547378 https://doaj.org/article/84e6e286994e449faae8c89c5e8e4bae Journal of Chemistry, Vol 2019 (2019) Chemistry QD1-999 article 2019 ftdoajarticles https://doi.org/10.1155/2019/4547378 2024-08-05T17:48:37Z The aim of this study was to obtain and characterise the long-chain alcohols present in policosanol derived from waste from the production of carminic acid, a natural colouring agent widely used in the food industry. The effectiveness of different methods designed for extraction of policosanol from waxy waste was investigated and its content and composition was determined. Triacontanol was the main component in policosanol produced by chemical processes, and it yields up to 13% by alkaline hydrolysis in water and chloroform extraction. Regarding enzymatic transesterification, policosanol was obtained using lipase Candida antarctica recombinant in Aspergillus niger (CAL-Bn) in a reaction medium with toluene. To improve the reaction, different acyl receptors, propanol, butanol, and isopropanol, were tested and molecular sieves were employed to maintain an anhydrous reaction medium. In this case, the policosanol was made up of other long-chain alcohols, but triacontanol was obtained in yields of up to 19% using isopropanol as an acyl receptor. Triacontanol has a great commercial value due to its effect as a promoter of plant growth, and these results contribute to the use and application of this agroindustrial waste in obtaining value-added products. Article in Journal/Newspaper Antarc* Antarctica Directory of Open Access Journals: DOAJ Articles Journal of Chemistry 2019 1 10
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic Chemistry
QD1-999
spellingShingle Chemistry
QD1-999
Emilia Ramos-Zambrano
Pedro Herrera-Serrano
Jorge García-Dávila
Gabriel Ríos-Cortés
Antonio Ruperto Jiménez-Aparicio
Alma Leticia Martínez-Ayala
Cochineal Waxy Residues as Source of Policosanol: Chemical Hydrolysis and Enzymatic Transesterification
topic_facet Chemistry
QD1-999
description The aim of this study was to obtain and characterise the long-chain alcohols present in policosanol derived from waste from the production of carminic acid, a natural colouring agent widely used in the food industry. The effectiveness of different methods designed for extraction of policosanol from waxy waste was investigated and its content and composition was determined. Triacontanol was the main component in policosanol produced by chemical processes, and it yields up to 13% by alkaline hydrolysis in water and chloroform extraction. Regarding enzymatic transesterification, policosanol was obtained using lipase Candida antarctica recombinant in Aspergillus niger (CAL-Bn) in a reaction medium with toluene. To improve the reaction, different acyl receptors, propanol, butanol, and isopropanol, were tested and molecular sieves were employed to maintain an anhydrous reaction medium. In this case, the policosanol was made up of other long-chain alcohols, but triacontanol was obtained in yields of up to 19% using isopropanol as an acyl receptor. Triacontanol has a great commercial value due to its effect as a promoter of plant growth, and these results contribute to the use and application of this agroindustrial waste in obtaining value-added products.
format Article in Journal/Newspaper
author Emilia Ramos-Zambrano
Pedro Herrera-Serrano
Jorge García-Dávila
Gabriel Ríos-Cortés
Antonio Ruperto Jiménez-Aparicio
Alma Leticia Martínez-Ayala
author_facet Emilia Ramos-Zambrano
Pedro Herrera-Serrano
Jorge García-Dávila
Gabriel Ríos-Cortés
Antonio Ruperto Jiménez-Aparicio
Alma Leticia Martínez-Ayala
author_sort Emilia Ramos-Zambrano
title Cochineal Waxy Residues as Source of Policosanol: Chemical Hydrolysis and Enzymatic Transesterification
title_short Cochineal Waxy Residues as Source of Policosanol: Chemical Hydrolysis and Enzymatic Transesterification
title_full Cochineal Waxy Residues as Source of Policosanol: Chemical Hydrolysis and Enzymatic Transesterification
title_fullStr Cochineal Waxy Residues as Source of Policosanol: Chemical Hydrolysis and Enzymatic Transesterification
title_full_unstemmed Cochineal Waxy Residues as Source of Policosanol: Chemical Hydrolysis and Enzymatic Transesterification
title_sort cochineal waxy residues as source of policosanol: chemical hydrolysis and enzymatic transesterification
publisher Wiley
publishDate 2019
url https://doi.org/10.1155/2019/4547378
https://doaj.org/article/84e6e286994e449faae8c89c5e8e4bae
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_source Journal of Chemistry, Vol 2019 (2019)
op_relation http://dx.doi.org/10.1155/2019/4547378
https://doaj.org/toc/2090-9063
https://doaj.org/toc/2090-9071
2090-9063
2090-9071
doi:10.1155/2019/4547378
https://doaj.org/article/84e6e286994e449faae8c89c5e8e4bae
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container_title Journal of Chemistry
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