2017
DOI: 10.1016/j.carbpol.2017.03.039
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A tale of two pectins: Diverse fine structures can result from identical processive PME treatments on similar high DM substrates

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Cited by 10 publications
(3 citation statements)
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“…The total charge, as well as the distribution of carboxylic acid groups affects pectin gelling properties and block-wise rather than random de-esterification of pectin results in stronger gelling properties [23][24][25][26][27][28]. Pectin methylesterase isozymes influence the extent and pattern of de-esterification [24][25][26]29] and calcium pectate gel strength increases nonlinearly with de-esterification [28].…”
Section: Introductionmentioning
confidence: 99%
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“…The total charge, as well as the distribution of carboxylic acid groups affects pectin gelling properties and block-wise rather than random de-esterification of pectin results in stronger gelling properties [23][24][25][26][27][28]. Pectin methylesterase isozymes influence the extent and pattern of de-esterification [24][25][26]29] and calcium pectate gel strength increases nonlinearly with de-esterification [28].…”
Section: Introductionmentioning
confidence: 99%
“…The total charge, as well as the distribution of carboxylic acid groups affects pectin gelling properties and block-wise rather than random de-esterification of pectin results in stronger gelling properties [23][24][25][26][27][28]. Pectin methylesterase isozymes influence the extent and pattern of de-esterification [24][25][26]29] and calcium pectate gel strength increases nonlinearly with de-esterification [28]. Block de-esterified high methoxy pectin was a more effective encapsulant of indomethacin than randomly de-esterified pectin and under simulated gastric conditions in vitro, encapsulated indomethacin with block de-esterified pectin showed <1% release [30].…”
Section: Introductionmentioning
confidence: 99%
“…Among the constituents of the cell wall, the pectic substances are usually presented as the class of polysaccharides with the most significant modifications, marked by their depolymerisation and solubilisation, due to the action of hydrolytic enzymes such as pectinamethylesterases (PME), polygalacturonases (PG) and β‐galactosidases. Pectinamethylesterases (PME), EC 3.1.1.11, act by hydrolysing methyl ester groups in the pectin chains, promoting the formation of free carboxyl groups and methanol (Owen et al ., 2017; Salas‐Tovar et al ., 2017; Wang et al ., 2020). The PME action culminates in the formation of methylated pectins, which serve as a substrate for polygalacturonase – PG (E.C.…”
Section: Introductionmentioning
confidence: 99%