2006
DOI: 10.1016/j.carbpol.2006.03.019
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Structural and stoichiometric studies of complexes between aroma compounds and amylose. Polymorphic transitions and quantification in amorphous and crystalline areas

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Cited by 125 publications
(88 citation statements)
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“…3a and b) suggesting the presence of uncomplexed stearic acid. V-amylose diffraction patterns with such an additional peak that indicated the presence of non-complexed (or non-specifically bound) fatty acids were demonstrated by Biais, Le Bail, Robert, Pontoire & Bule´on (2006). In the present study, after the short pasting time (11.5 min), the stearic acid is probably not entirely complexed with the amylose molecules.…”
Section: Waxs Of Teff and Maize Starch From The First And Second Peakmentioning
confidence: 60%
“…3a and b) suggesting the presence of uncomplexed stearic acid. V-amylose diffraction patterns with such an additional peak that indicated the presence of non-complexed (or non-specifically bound) fatty acids were demonstrated by Biais, Le Bail, Robert, Pontoire & Bule´on (2006). In the present study, after the short pasting time (11.5 min), the stearic acid is probably not entirely complexed with the amylose molecules.…”
Section: Waxs Of Teff and Maize Starch From The First And Second Peakmentioning
confidence: 60%
“…Considering that each platelet is a polycrystalline assembly, its size could readily vary according to the physical environmental conditions. Because the crystalline complexes have high resistance to enzymatic hydrolysis, whereas amorphous matrices are easily hydrolyzed (Biais, Bail, Robert, Pontoire, & Buléon, 2006;Cui & Oates, 1999;Godet et al, 1996), the crystalline complexes could be recovered by enzymatic hydrolysis. The hydrolysis pattern of the complex has been reported by several researches (Cui & Oates, 1999;Gelders et al, 2005), but the maximum degree of hydrolysis of the complex in this study was higher than those in the literature (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…FTIR has been previously used to quantify the amount of complexed compounds that contain a carbonyl group (Biais et al, 2006;Fanta, Shogren & Salch, 1999;Uchino et al, 2002). For RP and PE samples, the carbonyl peak in the complexes and physical mixture (used to generate the calibration curve) resembled that of the pure compound.…”
Section: Inclusion Complexes With Amylose and Amylopectinmentioning
confidence: 99%
“…In the presence of these molecules, amylose forms a left-handed single helix stabilized by hydrogen bonds (Conde-Petit, Escher & Nuessli, 2006), with a hydrophilic outside surface and a hydrophobic inside helical channel (Immel & Lichtenthaler, 2000). Amylose single helices can arrange forming a crystalline structure known as V-type (Biais, Le Bail, Robert, Pontoire & Buléon, 2006). Guest molecules are usually included within the helix, but can also be trapped between helices (Rondeau-Mouro et al, 2004).…”
Section: Introductionmentioning
confidence: 98%