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DOI: 10.1055/a-1038-6592
Metabolic Profiling and Untargeted 1H-NMR-Based Metabolomics Study of Different Iranian Pomegranate (Punica granatum) Ecotypes
Supported by: National Institute for Medical Research Development 965403Supported by: Mashhad University of Medical Sciences 951316
Publication History
received 28 July 2019
revised 26 November 2019
accepted 06 December 2019
Publication Date:
18 December 2019 (online)
Abstract
Pomegranate (Punica granatum) is an ancient fruit that is widely consumed as fresh fruit and juice. The aim of the present study was to compare the metabolic profile of pomegranate ecotypes from different geographical origins of Iran, the largest producer of pomegranates in the world. 1H-NMR and 2D NMR spectroscopy were applied to investigate the ecotypic variation. Multivariate data analyses were used to identify overall metabolic differences. Mazandaran pomegranate samples were found to be different from the other ecotypes, having a high content of citric and succinic acids. Bajestan, Ferdows, and Yazd pomegranates contained comparatively higher amounts of anthocyanins and ellagic acid derivatives than other pomegranate ecotypes. The distribution of metabolites among different ecotypes of pomegranate is discussed on the basis of these findings.
Key words
anthocyanin - 1H-NMR-based metabolomics - metabolite profiling - Iranian pomegranate - Punica granatum - LythraceaeSupporting Information
- Supporting Information
OPLS-DA score plot and loading column plot related to the discrimination of juice samples between Mazandaran and Shiraz pomegranates are described in Figs. 1S and 2S. Tight clustering among the pomegranate juice extracts of Khorasan provinces is shown in Fig. 3S. OPLS-DA score plot of pomegranate juice extracts from the mountainous areas in the West of Iran (Paveh pomegranate from Kermanshah) and semiarid regions in the East of Iran (Khorasan provinces) is available in Fig. 4S. The discrimination of the aromatic region (δ 6.5 – 10.5) between Yazd and Mazandaran pomegranate juice extracts is shown in Fig. 5S. Relative quantification of cyanidin-3,5-diglucoside based on the mean peak area of the signal at δ 9.24 is presented in Fig. 6S.
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