Article ID Journal Published Year Pages File Type
6488834 Food Bioscience 2018 35 Pages PDF
Abstract
High methoxylated citrus pectin was deesterified by alkaline or pectin methylesterase (PME) to produce pectin with various methoxylation degree (DM) from ~50% to < 10%. Alkaline deesterification (p < 0.05) was effectively achieved at pH> 10. At pH 12 pectin DM could be reduced to lower limit of 15.91 ± 2.55% under 4 ℃ after 300 min but further to 6.81 ± 1.46% under 20 ℃ within 30 min. Stronger alkaline treatment led to heavier pectin degradation, especially suggested by the statistically significant (p < 0.05) reduction of weight-average molecular weight (Mw). Namely the heavy pectin chains were disrupted by alkaline. Enzymatic deesterification using ROHAPECT MPE resulted in a DM of 28.78 ± 0.78% with 0.1% (w/w) enzyme amount and further to 14.67 ± 0.80% with 1.5% (w/w) enzyme amount within 5 h. Correspondingly, the enzymatic-deesterified pectin (DM=14.67 ± 0.80%) presented a much higher intrinsic viscosity ([η]) of ~2000 mL/mg in comparison to raw material (~1600 mL/mg) while the alkaline-treated pectin (DM=10.81 ± 1.85%) had a low [η] of ~700 mL/mg due to chain decomposition. Microscopic gelling of all the alkaline deesterified pectins was Ca2+-dependent (> 44 mg/g), but particularly the product with DM of 9.36% could gel at low Ca2+ concentration (4-8 mg/g). Enzymatic deesterified pectin produced by RAPIDASE® PEP (DM 30.83%) and ROHAPECT MPE (DM 14.67%) could gel at pH 2 in the absence of Ca2+ and their Ca2+-dependence increased with pH increase, while the product by NOVOSHAPE KEN00536 always needed > 24 mg/g Ca2+ for gelling under pH 2.0-4.0.
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Physical Sciences and Engineering Chemical Engineering Bioengineering
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