Yoo Sang-Ho, Fishman Marshall L, Savary Brett J, Hotchkiss Arland T
Crop Conversion Science and Engineering, Eastern Regional Research Center, Agricultural Research Service, U.S. Department of Agriculture, 600 East Mermaid Lane, Wyndmoor, Pennsylvania 19038.
J Agric Food Chem. 2003 Dec 3;51(25):7410-7. doi: 10.1021/jf030152o.
Pectin gels were induced by monovalent salts (0.2 M) concurrently with deesterification of high methoxy pectin using a salt-independent orange pectin methylesterase (PME). Constant pH was maintained during deesterification and gelation. If salt or PME was absent, the pectin did not form a gel. The gel strength was influenced by both pH and species of monovalent cation. At pH 5.0, the pectin gel induced by KCl was significantly stronger than the NaCl-induced gel. In contrast, a much stronger gel was produced in the presence of NaCl as compared to KCl at pH 7.0. LiCl did not induce pectin gelation at either pH. Molecular weights of pectins increased from 1.38 x 10(5) to 2.26 x 10(5) during NaCl-induced gelation at pH 7. One proposal to explain these pectin molecular weight changes is a hypothetical PME transacylation mechanism. However, these pectin molecular weight changes can also be explained by metastable aggregation of the enzymatically deesterified low methoxy pectin. We postulate that gelation was induced by a slow deesterification of pectin under conditions that would normally salt out (precipitate) low methoxy pectin in the absence of PME.
单价盐(0.2 M)在使用不依赖盐的橙果胶甲酯酶(PME)使高甲氧基果胶脱酯的同时诱导果胶凝胶形成。在脱酯和凝胶化过程中保持恒定的pH值。如果没有盐或PME,果胶不会形成凝胶。凝胶强度受pH值和单价阳离子种类的影响。在pH 5.0时,由KCl诱导的果胶凝胶明显比NaCl诱导的凝胶更强。相反,在pH 7.0时,与KCl相比,在NaCl存在下产生的凝胶要强得多。LiCl在任何一个pH值下都不会诱导果胶凝胶化。在pH 7的NaCl诱导凝胶化过程中,果胶的分子量从1.38×10⁵增加到2.26×10⁵。一种解释这些果胶分子量变化的假说是一种假设的PME转酰基化机制。然而,这些果胶分子量的变化也可以用酶促脱酯的低甲氧基果胶的亚稳聚集来解释。我们推测,凝胶化是由果胶在通常会使低甲氧基果胶盐析(沉淀)的条件下缓慢脱酯诱导的,而在没有PME的情况下。