2006
DOI: 10.1016/j.foodhyd.2005.09.005
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Structural elucidation of the polysaccharide from Sterculia apetala gum by a combination of chemical methods and NMR spectroscopy

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Cited by 33 publications
(8 citation statements)
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“…Based on the methylation analysis in Section 3.2 and the cross peak of d 16.9/1.24 observed in HSQC spectrum which corresponded to methyl group (Marvelys, Maritza, Lilian, Gladys, & Julio, 2006), it was concluded that residue D was a b-L-rhamnose residue. The downfield shifts of d 103.8 (C-1) and d 75.15 (C-2) from the chemical shifts of standard rhamnopyranose indicated that residue D was a 1,2-linked b-L-rhamnopyranose.…”
Section: Determination Of the Sugar Residues And Their Sequence By Nmrmentioning
confidence: 99%
“…Based on the methylation analysis in Section 3.2 and the cross peak of d 16.9/1.24 observed in HSQC spectrum which corresponded to methyl group (Marvelys, Maritza, Lilian, Gladys, & Julio, 2006), it was concluded that residue D was a b-L-rhamnose residue. The downfield shifts of d 103.8 (C-1) and d 75.15 (C-2) from the chemical shifts of standard rhamnopyranose indicated that residue D was a 1,2-linked b-L-rhamnopyranose.…”
Section: Determination Of the Sugar Residues And Their Sequence By Nmrmentioning
confidence: 99%
“…So in the polysaccharides spectra of PPQA2 and PPQA5, the signal at 52.9 ppm was assigned to methyl groups binding to carboxyl groups; the signal approximately at 100 ppm were due to the anomeric carbon of methyl galacturonate and glucuronate acids; the signal at 170.8 ppm attributed to carboxyl groups bound by methyl groups; while the signal at 174.8 ppm was derived from ionic carboxyl groups (C-6) of uronic acids [23,24]. The signal for C-5 of methyl uronic acid residues appeared approximately at 70.6 ppm [11,25]. Furthermore, the signals at ı 20.1 ppm suggested PPQA2 and PPQA5 contained O-acetyl groups [26].…”
Section: C Nmr Spectra Of Ppqa2 Ppqa4 and Ppqa5mentioning
confidence: 99%
“…Similarly, along with 1 H‐ 1 H TOCSY spectrum (Figure b), the resonances at δ H 3.76, 3.54, and 3.93 ppm were assigned to H‐4, H‐5, and H‐6 of residue A . Meantime, the large coupling constants 3 J H‐2,H‐3 and 3 J H‐3,H‐4 values of residue A supported its being D‐glucosyl moiety . Based on the 1 H NMR assignment, complete carbon signals in residue A were easily assigned from the HSQC (Figure b) spectrum as C‐1 of δ C 102.20, C‐2 of δ C 72.84, C‐3 of δ C 73.85, C‐4 of δ C 68.92, C‐5 of δ C 80.59, and C‐6 of δ C 69.45 ppm.…”
Section: Resultsmentioning
confidence: 95%