2 research outputs found
Analysis of Flavor Quality of Two Cherry Tomatoes After Refrigeration
To investigate the differences in the types and relative contents of refrigerated volatile flavor substances between 'Chitose' and 'Ji Tian No.1' cherry tomatoes, the effect of cold storage at 4 ℃ for 16 d on the flavor quality of cherry tomatoes ('Chitose' and 'Ji Tian No.1') was analyzed by using electronic nose and headspace solid-phase microextraction-gas chromatography. The results showed that electronic nose analysis results displayed, the volatile substances that undergo significant changes before and after refrigeration in two cherry tomatoes were inorganic sulfides, nitrogen oxides, and aromatic substances, a total of 93 volatile substances were detected by HS-SPME-GC-MS technique, including 27 aldehydes, 23 alcohols, 4 esters, 11 ketones, 3 furans, 9 alkanes, 12 olefins and 4 other substances. Compared to 0 d, the relative content of total volatile substances in 'Chitose' and 'Ji Tian No.1' after cold storage decreased by 7.08% and 3.68% respectively. The relative content of the main volatile compounds hexanal and trans-2-hexenal in two cherry tomatoes decreased after refrigeration, the relative content of trans 2-pentenal, heptanal, 1-pentanol, 6-methyl-5-hepten-2-one, and 1-penten-3-one increased after refrigeration. Compared with 'Chitose', 'Ji Tian No.1' could retain higher contents of main volatile substances of cherry tomato such as aldehydes, esters and ketones after cold storage. Therefore, 'Ji Tian No.1' was more suitable for post-harvest storage and transportation and low-temperature refrigeration, which would provide a theoretical basis for high-quality cherry tomato post-harvest storage and transportation technology
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Obstructive Sleep Apnea-induced Endothelial Dysfunction Is Mediated by miR-210.
Rationale: Obstructive sleep apnea (OSA)-induced endothelial cell (EC) dysfunction contributes to OSA-related cardiovascular sequelae. The mechanistic basis of endothelial impairment by OSA is unclear. Objectives: The goals of this study were to identify the mechanism of OSA-induced EC dysfunction and explore the potential therapies for OSA-accelerated cardiovascular disease. Methods: The experimental methods include data mining, bioinformatics, EC functional analyses, OSA mouse models, and assessment of OSA human subjects. Measurements and Main Results: Using mined microRNA sequencing data, we found that microRNA 210 (miR-210) conferred the greatest induction by intermittent hypoxia in ECs. Consistently, the serum concentration of miR-210 was higher in individuals with OSA from two independent cohorts. Importantly, miR-210 concentration was positively correlated with the apnea-hypopnea index. RNA sequencing data collected from ECs transfected with miR-210 or treated with OSA serum showed a set of genes commonly altered by miR-210 and OSA serum, which are largely involved in mitochondrion-related pathways. ECs transfected with miR-210 or treated with OSA serum showed reduced [Formula: see text]o2 rate, mitochondrial membrane potential, and DNA abundance. Mechanistically, intermittent hypoxia-induced SREBP2 (sterol regulatory element-binding protein 2) bound to the promoter region of miR-210, which in turn inhibited the iron-sulfur cluster assembly enzyme and led to mitochondrial dysfunction. Moreover, the SREBP2 inhibitor betulin alleviated intermittent hypoxia-increased systolic blood pressure in the OSA mouse model. Conclusions: These results identify an axis involving SREBP2, miR-210, and mitochondrial dysfunction, representing a new mechanistic link between OSA and EC dysfunction that may have important implications for treating and preventing OSA-related cardiovascular sequelae