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Carotenoid-Related Volatile Compounds of Tobacco (Nicotiana tabacum L.) Essential Oils

Tobacco (Nicotiana tabacum L.) aroma is an important attribute of tobacco quality and is influenced by a variety of minor chemical components, including carotenoid degradation products. The objectives of this work were to determine the content of the most important fragrance-shaping carotenoid degra...

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Autores principales: Popova, Venelina, Ivanova, Tanya, Prokopov, Tsvetko, Nikolova, Milena, Stoyanova, Albena, Zheljazkov, Valtcho D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804150/
https://www.ncbi.nlm.nih.gov/pubmed/31547525
http://dx.doi.org/10.3390/molecules24193446
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author Popova, Venelina
Ivanova, Tanya
Prokopov, Tsvetko
Nikolova, Milena
Stoyanova, Albena
Zheljazkov, Valtcho D.
author_facet Popova, Venelina
Ivanova, Tanya
Prokopov, Tsvetko
Nikolova, Milena
Stoyanova, Albena
Zheljazkov, Valtcho D.
author_sort Popova, Venelina
collection PubMed
description Tobacco (Nicotiana tabacum L.) aroma is an important attribute of tobacco quality and is influenced by a variety of minor chemical components, including carotenoid degradation products. The objectives of this work were to determine the content of the most important fragrance-shaping carotenoid degradation products in the essential oils (EOs) of the three types of Bulgarian tobacco—Oriental (OR), flue-cured Virginia (FCV), and Burley (BU)—and to compare them with other aromatic products from tobacco. The content of total carotenoids and β-carotene was highest in BU tobacco (22.23 and 20.34 mg/100 g DW, respectively), followed by OR (13.60 and 12.09 mg/100 g DW in variety “Plovdiv 7” (Pd7); 6.27 and 5.45 mg/100 g DW in “Krumovgrad” (Kr), and FCV (5.93 and 3.73 mg/100 g DW). EOs were obtained by hydrodistillation in an acidified medium, and the main aroma-impact compounds from carotenoid degradation (identified by GC-MS) were as follows: FCV-α-ionone (0.61 mg/100 g DW), dihydro-β-ionone (0.96 mg/100 g DW), β-damascenone (1.26 mg/100 g DW); BU-α-ionone (0.73 mg/100 g DW), dihydro-β-ionone (1.19 mg/100 g DW), β-damascenone (1.35 mg/100 g DW); OR(Kr)-α-ionone (0.20 mg/100 g DW), β-ionone (1.08 mg/100 g DW), dihydro-β-ionone (1.34 mg/100 g DW), β-damascenone (0.36 mg/100 g DW); OR(Pd7)-α-ionone (1.43 mg/100 g DW), dihydro-β-ionone (1.73 mg/100 g DW), β-damascenone (1.23 mg/100 g DW). Ionone and its derivatives were not identified in the aroma extraction products concrete, resinoid, or absolute. The results suggest that temperature, pH of the medium, process duration, and possibly other unknown factors affect carotenoid transformation. The study provides insight into the composition of tobacco EOs and may be of interest to the fragrance industry.
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spelling pubmed-68041502019-11-18 Carotenoid-Related Volatile Compounds of Tobacco (Nicotiana tabacum L.) Essential Oils Popova, Venelina Ivanova, Tanya Prokopov, Tsvetko Nikolova, Milena Stoyanova, Albena Zheljazkov, Valtcho D. Molecules Communication Tobacco (Nicotiana tabacum L.) aroma is an important attribute of tobacco quality and is influenced by a variety of minor chemical components, including carotenoid degradation products. The objectives of this work were to determine the content of the most important fragrance-shaping carotenoid degradation products in the essential oils (EOs) of the three types of Bulgarian tobacco—Oriental (OR), flue-cured Virginia (FCV), and Burley (BU)—and to compare them with other aromatic products from tobacco. The content of total carotenoids and β-carotene was highest in BU tobacco (22.23 and 20.34 mg/100 g DW, respectively), followed by OR (13.60 and 12.09 mg/100 g DW in variety “Plovdiv 7” (Pd7); 6.27 and 5.45 mg/100 g DW in “Krumovgrad” (Kr), and FCV (5.93 and 3.73 mg/100 g DW). EOs were obtained by hydrodistillation in an acidified medium, and the main aroma-impact compounds from carotenoid degradation (identified by GC-MS) were as follows: FCV-α-ionone (0.61 mg/100 g DW), dihydro-β-ionone (0.96 mg/100 g DW), β-damascenone (1.26 mg/100 g DW); BU-α-ionone (0.73 mg/100 g DW), dihydro-β-ionone (1.19 mg/100 g DW), β-damascenone (1.35 mg/100 g DW); OR(Kr)-α-ionone (0.20 mg/100 g DW), β-ionone (1.08 mg/100 g DW), dihydro-β-ionone (1.34 mg/100 g DW), β-damascenone (0.36 mg/100 g DW); OR(Pd7)-α-ionone (1.43 mg/100 g DW), dihydro-β-ionone (1.73 mg/100 g DW), β-damascenone (1.23 mg/100 g DW). Ionone and its derivatives were not identified in the aroma extraction products concrete, resinoid, or absolute. The results suggest that temperature, pH of the medium, process duration, and possibly other unknown factors affect carotenoid transformation. The study provides insight into the composition of tobacco EOs and may be of interest to the fragrance industry. MDPI 2019-09-23 /pmc/articles/PMC6804150/ /pubmed/31547525 http://dx.doi.org/10.3390/molecules24193446 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Popova, Venelina
Ivanova, Tanya
Prokopov, Tsvetko
Nikolova, Milena
Stoyanova, Albena
Zheljazkov, Valtcho D.
Carotenoid-Related Volatile Compounds of Tobacco (Nicotiana tabacum L.) Essential Oils
title Carotenoid-Related Volatile Compounds of Tobacco (Nicotiana tabacum L.) Essential Oils
title_full Carotenoid-Related Volatile Compounds of Tobacco (Nicotiana tabacum L.) Essential Oils
title_fullStr Carotenoid-Related Volatile Compounds of Tobacco (Nicotiana tabacum L.) Essential Oils
title_full_unstemmed Carotenoid-Related Volatile Compounds of Tobacco (Nicotiana tabacum L.) Essential Oils
title_short Carotenoid-Related Volatile Compounds of Tobacco (Nicotiana tabacum L.) Essential Oils
title_sort carotenoid-related volatile compounds of tobacco (nicotiana tabacum l.) essential oils
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6804150/
https://www.ncbi.nlm.nih.gov/pubmed/31547525
http://dx.doi.org/10.3390/molecules24193446
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