2004
DOI: 10.1016/j.carres.2004.07.005
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Structural analysis of arabinoxylans isolated from native and malted finger millet (Eleusine coracana, ragi)

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Cited by 45 publications
(19 citation statements)
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References 20 publications
(13 reference statements)
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“…A low intensity signal for C‐6 carbonyl group, pertaining to O‐Me‐a‐D‐glucuronic acid arabinose residue was noticed at 178.6 ppm which indicated the presence of XOS with lesser branching or side groups. Similar observations have been made with the 13 C NMR spectra for ragi arabinoxylans (Subba Rao & Muralikrishna, ) and enzymatically derived XOS from sugarcane bagasse (Bian et al, ). On the basis of NMR results, the major XOS derived from wheat bran hydrolysis composed of xylobiose and xylotriose.…”
Section: Resultssupporting
confidence: 82%
“…A low intensity signal for C‐6 carbonyl group, pertaining to O‐Me‐a‐D‐glucuronic acid arabinose residue was noticed at 178.6 ppm which indicated the presence of XOS with lesser branching or side groups. Similar observations have been made with the 13 C NMR spectra for ragi arabinoxylans (Subba Rao & Muralikrishna, ) and enzymatically derived XOS from sugarcane bagasse (Bian et al, ). On the basis of NMR results, the major XOS derived from wheat bran hydrolysis composed of xylobiose and xylotriose.…”
Section: Resultssupporting
confidence: 82%
“…Substitutions at C-2 and C-2/C-3 of xylose residues with arabinosfuranoses were also noted in these heavily substituted arabinoxylans (15,16). 4-(O-Me)-glucuronic acid is the other major substituent connected to C-2 of xylose residues in finger millet arabinoxylans (15).…”
Section: Introductionmentioning
confidence: 88%
“…Several methods have been developed for the isolation and characterization of water-extractable and waterunextractable arabinoxylans from major food crops such as barley (10), wheat (11), rice (12), and sorghum (13,14). However, except for a few recent papers, not many studies have been carried out on the structural features of arabinoxylans from millets such as finger millet (15) and pearl millet (16) and their malts, the major source of food in developing countries such as India and Africa. The reported structural aspects of finger millet and pearl millet arabinoxylans demonstrated the presence of a β-(1,4)-linked xylopyranoside backbone substituted primarily with arabinofuranoses at C-3 via R-(1,3) linkage.…”
Section: Introductionmentioning
confidence: 99%
“…The peak multiplicity in the 1120-1000 cm À1 , is a typical characteristic of highly substituted Table 4 Weight-average (M w ) and number-average (M n ) molecular weights and polydispersity (M w /M n ) of the hemicellulosic fractions. arabinoxylans, and the arabinose substitution at C-3 of xylose residues gives a band at 1173 cm À1 (Subba & Muralikrishna, 2004). An absorption band at 903 cm À1 is clearly visible in the spectra of H 2B , H 3B , and H 4B , indicating that the presence of dominant b-glycosidic linkages between the sugar units in these hemicellulosic fractions.…”
Section: Ft-ir Spectramentioning
confidence: 98%