2022
DOI: 10.1016/j.foodchem.2022.132637
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Preparation, structural characterization and antioxidant activity of water-soluble polysaccharides and purified fractions from blackened jujube by an activity-oriented approach

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Cited by 42 publications
(34 citation statements)
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“…The characteristic functional groups of BCP‐A1 and BCP‐B1 were displayed in Figure 2. The broad band at 3289 and 3433 cm −1 were O−H stretching vibration of hydrogen bonding, while 2945 cm −1 was the C−H stretching vibration, [17] which assigned to that BCP‐A1 and BCP‐B1 were carbohydrate compounds. The peak at 1747 cm −1 of BCP‐B1 indicated that it contained the carboxy groups [11] .…”
Section: Resultsmentioning
confidence: 96%
“…The characteristic functional groups of BCP‐A1 and BCP‐B1 were displayed in Figure 2. The broad band at 3289 and 3433 cm −1 were O−H stretching vibration of hydrogen bonding, while 2945 cm −1 was the C−H stretching vibration, [17] which assigned to that BCP‐A1 and BCP‐B1 were carbohydrate compounds. The peak at 1747 cm −1 of BCP‐B1 indicated that it contained the carboxy groups [11] .…”
Section: Resultsmentioning
confidence: 96%
“…Then five polysaccharides were isolated, two neutral polysaccharides (EFP-0 and EFP-1) and three acidic polysaccharides (EFP-2, EFP-3, and EFP-4), and were obtained by passing through a DEAE-52 cellulose ion-exchange column ( Figure 2A ), with recoveries of 6.74, 6.03, 5.83, 4.69, and 7.24%, respectively. Yuan et al ( 43 ) reported that five polysaccharides were also isolated and purified from blackened jujube. These five polysaccharide fractions were then further purified on a Sephadex G-100 column, and the purified five polysaccharide fractions all showed single peaks ( Figure 2B ), and the purity of polysaccharides was 77.86 ± 0.63, 81.67 ± 0.43, 90.65 ± 0.57, 81.77 ± 0.83, and 82.25 ± 0.56%, respectively, measured by phenol-sulfuric acid method.…”
Section: Resultsmentioning
confidence: 99%
“…EFP-0, EFP-1, EFP-2, EFP-3, and EFP-4 can observe a broad and intense stretching peak in all FTIR spectrum around 3,200 to 3,400 cm –1 , which was mainly caused by polysaccharide molecules or intermolecular O-H stretching vibrations, indicating the presence of intermolecular hydrogen bonds ( 49 , 50 ). The weak absorption bands around 2,900 to 2,800 cm –1 ( Figures 3A–E ) were attributed to C-H, -CH 2 -, and -CH 3 - asymmetric stretching vibrations ( 51 ), and the presence of these two absorption peaks suggests that all five components purified from elderberry polysaccharides are carbohydrates, but EFP-0 is relatively strong ( 43 ). The absorption peak near 1,400 to 1,700 cm –1 was due to the -COOH bending vibration or symmetric stretching vibration of C-O, indicating the presence of glucuronic acid in EFP and the presence of -COOH groups; in particular, EFP-2 has the largest carboxyl peak ( 52 54 ).…”
Section: Resultsmentioning
confidence: 99%
“…The peaks at 1749 cm −1 were attributed to C=O stretching vibration, indicating the presence of uronic acid in PPP. The absorptions at 1606 cm −1 and 1442 cm −1 were anti-symmetrical C=O stretching vibration and symmetrical C=O stretching vibration of ionic carboxyl groups (i.e., −COOH − ) [37]. Overall, the FT-IR spectra of PPP exhibited a typical polysaccharide structure.…”
Section: Uv-vis and Ft-ir Spectra Analysismentioning
confidence: 90%