Non-targeted metabolomic analysis of orange (Citrus sinensis [L.] Osbeck) wild type and bud mutant fruits by direct analysis in real-time and HPLC-electrospray mass spectrometry

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TitleNon-targeted metabolomic analysis of orange (Citrus sinensis [L.] Osbeck) wild type and bud mutant fruits by direct analysis in real-time and HPLC-electrospray mass spectrometry
Publication TypeJournal Article
Year of Publication2014
AuthorsPan, Z, Li, Y, Deng, X, Xiao, S
JournalMetabolomics
Volume10
Issue3
Pagination508-523
Date PublishedJun 2014
ISSN1573-3882
KeywordsBud mutation, Citrus, Direct analysis in real-time, LC-ESI, Mass Spectrometry, Metabolomics
Abstract

The direct analysis in real-time (DART) ion source and HPLC-electrospray mass spectrometry were applied in non-targeted metabolomic analyses of fruits of an orange bud mutant, ‘Hong Anliu’ along with its parental wild-type, ‘Anliu’. Fruits of the two isogenic cultivars were sampled at three different ripening stages, i.e. 120, 170 and 220 days after flowering. More than 130 metabolites were tentatively identified, including acids, sugars, flavonoids, alkaloids, limonoids, coumarins, amino acids, and plant hormones. Metabolomic analyses revealed that, compared to its wild type, the bud mutant fruit is characterized by higher levels of monosaccharides and disaccharides and lower levels of organic acids such as citric acid, malic acid and quinic acid, which agrees well with the anticipated fruit quality benefits of the mutation. In addition, many secondary metabolites, such as flavonoids, showed significant differences between the two genotypes, indicating that the whole fruit metabolome is significantly changed due to the bud mutation. This study provided a comprehensive assessment of metabolites in orange fruits, and revealed metabolomic differences in fruits between two isogenic orange genotypes. The results are helpful for understanding how the bud mutation in ‘Hong Anliu’ impacts the physiological and biochemical processes of orange fruits.

URLhttp://dx.doi.org/10.1007/s11306-013-0597-7
DOI10.1007/s11306-013-0597-7