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PubMed:22341919 JSONTXT 41 Projects

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Id Subject Object Predicate Lexical cue
TextSentencer_T1 0-153 Sentence denotes The diastereomers of mannosylerythritol lipids have different interfacial properties and aqueous phase behavior, reflecting the erythritol configuration.
T1 0-153 Sentence denotes The diastereomers of mannosylerythritol lipids have different interfacial properties and aqueous phase behavior, reflecting the erythritol configuration.
TextSentencer_T2 154-262 Sentence denotes Mannosylerythritol lipids (MELs) produced by yeasts are one of the most promising glycolipid biosurfactants.
T2 154-262 Sentence denotes Mannosylerythritol lipids (MELs) produced by yeasts are one of the most promising glycolipid biosurfactants.
TextSentencer_T3 263-364 Sentence denotes There are two MEL diastereomers, in which the configurations of the erythritol moieties are opposite.
T3 263-364 Sentence denotes There are two MEL diastereomers, in which the configurations of the erythritol moieties are opposite.
TextSentencer_T4 365-500 Sentence denotes The 4-O-β-D-mannopyranosyl-(2S,3R)-erythritol (S-form) or 4-O-β-D-mannopyranosyl-(2R,3S)-erythritol (R-form) is the hydrophilic domain.
T4 365-500 Sentence denotes The 4-O-β-D-mannopyranosyl-(2S,3R)-erythritol (S-form) or 4-O-β-D-mannopyranosyl-(2R,3S)-erythritol (R-form) is the hydrophilic domain.
TextSentencer_T5 501-629 Sentence denotes In this study, we prepared S- and R-form MEL homologs with similar fatty acyl groups, and compared their interfacial properties.
T5 501-629 Sentence denotes In this study, we prepared S- and R-form MEL homologs with similar fatty acyl groups, and compared their interfacial properties.
TextSentencer_T6 630-811 Sentence denotes Among the four diastereomers (S-MEL-B and -D/R-MEL-B and -D), R-form MELs showed a higher critical aggregation concentration and hydrophilicity compared to the corresponding S-form.
T6 630-811 Sentence denotes Among the four diastereomers (S-MEL-B and -D/R-MEL-B and -D), R-form MELs showed a higher critical aggregation concentration and hydrophilicity compared to the corresponding S-form.
TextSentencer_T7 812-893 Sentence denotes R-form MELs also efficiently formed relatively large vesicles compared to S-form.
T7 812-893 Sentence denotes R-form MELs also efficiently formed relatively large vesicles compared to S-form.
TextSentencer_T8 894-1035 Sentence denotes Moreover, we estimated the binary phase diagram of the MEL-water system and compared the aqueous phase behavior among the four diastereomers.
T8 894-1035 Sentence denotes Moreover, we estimated the binary phase diagram of the MEL-water system and compared the aqueous phase behavior among the four diastereomers.
TextSentencer_T9 1036-1129 Sentence denotes The present MELs self-assembled into a lamellar (L(α)) structure at all concentration ranges.
T9 1036-1129 Sentence denotes The present MELs self-assembled into a lamellar (L(α)) structure at all concentration ranges.
TextSentencer_T10 1130-1218 Sentence denotes Meanwhile, the one-phase L(α) region of R-form MELs was wider than those of S-form MELs.
T10 1130-1218 Sentence denotes Meanwhile, the one-phase L(α) region of R-form MELs was wider than those of S-form MELs.
TextSentencer_T11 1219-1338 Sentence denotes R-form MELs may maintain more water between the polar layers in accordance with an extension of the interlayer spacing.
T11 1219-1338 Sentence denotes R-form MELs may maintain more water between the polar layers in accordance with an extension of the interlayer spacing.
TextSentencer_T12 1339-1497 Sentence denotes These results suggest that the differences in MEL carbohydrate configurations significantly affect interfacial properties, self-assembly, and hydrate ability.
T12 1339-1497 Sentence denotes These results suggest that the differences in MEL carbohydrate configurations significantly affect interfacial properties, self-assembly, and hydrate ability.