Cargando…

Isomers of the Tomato Glycoalkaloids α-Tomatine and Dehydrotomatine: Relationship to Health Benefits

High-performance liquid chromatography (HPLC) analysis of three commercial tomatine samples and another isolated from green tomatoes revealed the presence of two small peaks in addition to those associated with the glycoalkaloids dehydrotomatine and α-tomatine. The present study investigated the pos...

Descripción completa

Detalles Bibliográficos
Autores principales: Kozukue, Nobuyuki, Kim, Dong-Seok, Choi, Suk-Hyun, Mizuno, Masashi, Friedman, Mendel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142774/
https://www.ncbi.nlm.nih.gov/pubmed/37110854
http://dx.doi.org/10.3390/molecules28083621
_version_ 1785033693200384000
author Kozukue, Nobuyuki
Kim, Dong-Seok
Choi, Suk-Hyun
Mizuno, Masashi
Friedman, Mendel
author_facet Kozukue, Nobuyuki
Kim, Dong-Seok
Choi, Suk-Hyun
Mizuno, Masashi
Friedman, Mendel
author_sort Kozukue, Nobuyuki
collection PubMed
description High-performance liquid chromatography (HPLC) analysis of three commercial tomatine samples and another isolated from green tomatoes revealed the presence of two small peaks in addition to those associated with the glycoalkaloids dehydrotomatine and α-tomatine. The present study investigated the possible structures of the compounds associated with the two small peaks using HPLC–mass spectrophotometric (MS) methods. Although the two peaks elute much earlier on chromatographic columns than the elution times of the known tomato glycoalkaloids dehydrotomatine and α-tomatine, isolation of the two compounds by preparative chromatography and subsequent analysis by MS shows the two compounds have identical molecular weights, tetrasaccharide side chains, and MS and MS/MS fragmentation patterns to dehydrotomatine and α-tomatine. We suggest the two isolated compounds are isomeric forms of dehydrotomatine and α-tomatine. The analytical data indicate that widely used commercial tomatine preparations and those extracted from green tomatoes and tomato leaves consist of a mixture of α-tomatine, dehydrotomatine, an α-tomatine isomer, and a dehydrotomatine isomer in an approximate ratio of 81:15:4:1, respectively. The significance of the reported health benefits of tomatine and tomatidine is mentioned.
format Online
Article
Text
id pubmed-10142774
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-101427742023-04-29 Isomers of the Tomato Glycoalkaloids α-Tomatine and Dehydrotomatine: Relationship to Health Benefits Kozukue, Nobuyuki Kim, Dong-Seok Choi, Suk-Hyun Mizuno, Masashi Friedman, Mendel Molecules Article High-performance liquid chromatography (HPLC) analysis of three commercial tomatine samples and another isolated from green tomatoes revealed the presence of two small peaks in addition to those associated with the glycoalkaloids dehydrotomatine and α-tomatine. The present study investigated the possible structures of the compounds associated with the two small peaks using HPLC–mass spectrophotometric (MS) methods. Although the two peaks elute much earlier on chromatographic columns than the elution times of the known tomato glycoalkaloids dehydrotomatine and α-tomatine, isolation of the two compounds by preparative chromatography and subsequent analysis by MS shows the two compounds have identical molecular weights, tetrasaccharide side chains, and MS and MS/MS fragmentation patterns to dehydrotomatine and α-tomatine. We suggest the two isolated compounds are isomeric forms of dehydrotomatine and α-tomatine. The analytical data indicate that widely used commercial tomatine preparations and those extracted from green tomatoes and tomato leaves consist of a mixture of α-tomatine, dehydrotomatine, an α-tomatine isomer, and a dehydrotomatine isomer in an approximate ratio of 81:15:4:1, respectively. The significance of the reported health benefits of tomatine and tomatidine is mentioned. MDPI 2023-04-21 /pmc/articles/PMC10142774/ /pubmed/37110854 http://dx.doi.org/10.3390/molecules28083621 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kozukue, Nobuyuki
Kim, Dong-Seok
Choi, Suk-Hyun
Mizuno, Masashi
Friedman, Mendel
Isomers of the Tomato Glycoalkaloids α-Tomatine and Dehydrotomatine: Relationship to Health Benefits
title Isomers of the Tomato Glycoalkaloids α-Tomatine and Dehydrotomatine: Relationship to Health Benefits
title_full Isomers of the Tomato Glycoalkaloids α-Tomatine and Dehydrotomatine: Relationship to Health Benefits
title_fullStr Isomers of the Tomato Glycoalkaloids α-Tomatine and Dehydrotomatine: Relationship to Health Benefits
title_full_unstemmed Isomers of the Tomato Glycoalkaloids α-Tomatine and Dehydrotomatine: Relationship to Health Benefits
title_short Isomers of the Tomato Glycoalkaloids α-Tomatine and Dehydrotomatine: Relationship to Health Benefits
title_sort isomers of the tomato glycoalkaloids α-tomatine and dehydrotomatine: relationship to health benefits
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10142774/
https://www.ncbi.nlm.nih.gov/pubmed/37110854
http://dx.doi.org/10.3390/molecules28083621
work_keys_str_mv AT kozukuenobuyuki isomersofthetomatoglycoalkaloidsatomatineanddehydrotomatinerelationshiptohealthbenefits
AT kimdongseok isomersofthetomatoglycoalkaloidsatomatineanddehydrotomatinerelationshiptohealthbenefits
AT choisukhyun isomersofthetomatoglycoalkaloidsatomatineanddehydrotomatinerelationshiptohealthbenefits
AT mizunomasashi isomersofthetomatoglycoalkaloidsatomatineanddehydrotomatinerelationshiptohealthbenefits
AT friedmanmendel isomersofthetomatoglycoalkaloidsatomatineanddehydrotomatinerelationshiptohealthbenefits