He Jinhua, Liu Jie, Zhang Genyi
State Key Laboratory of Food Science and Technology and School of Food Science and Technology, Southern Yangtze University, Wuxi 214122, Jiangsu Province, People's Republic of China.
Biomacromolecules. 2008 Jan;9(1):175-84. doi: 10.1021/bm700951s. Epub 2007 Dec 8.
The mechanism and molecular structure of the slowly digestible waxy maize starch prepared by octenyl succinic anhydride (OSA) esterification and heat-moisture treatment were investigated. The in vitro Englyst test showed a proportion of 28.3% slowly digestible starch (SDS) when waxy maize starch was esterified with 3% OSA (starch weight based, and it is named OSA-starch), and a highest SDS content of 42.8% was obtained after OSA-starch (10% moisture) was further heated at 120 degrees C for 4 h (named HOSA-starch). The in vivo glycemic response of HOSA-starch, which showed a delayed appearance of blood glucose peak and a significant reduction (32.2%) of the peak glucose concentration, further confirmed its slow digestion property. Amylopectin debranching analysis revealed HOSA-starch had the highest resistance to debranching enzymes of isoamylase and pullulanase, and a simultaneous decrease of K m and V m (enzyme kinetics) was also shown when HOSA-starch was digested by either alpha-amylase or amyloglucosidase, indicating that the slow digestion of HOSA-starch resulted from an uncompetitive inhibition of enzyme activity during digestion. Size exclusion chromatography analysis of HOSA-starch showed fragmented amylopectin molecules with more nonreducing ends that are favorable for RS conversion to SDS by the action of amyloglucosidase in the Englyst test. Further solubility analysis indicates that the water-insolubility of HOSA-starch is caused by OSA-mediated cross-linking of amylopectin and the hydrophobic interaction between OSA-modified starch molecules. The water-insolubility of HOSA-starch would decrease its enzyme accessibility, and the digestion products with attached OSA molecules might also directly act as the uncompetitive inhibitor to reduce the enzyme activity leading to a slow digestion of HOSA-starch.
研究了用辛烯基琥珀酸酐(OSA)酯化和湿热处理制备的慢消化糯玉米淀粉的机制和分子结构。体外Englyst试验表明,当糯玉米淀粉用3% OSA(基于淀粉重量,命名为OSA-淀粉)酯化时,慢消化淀粉(SDS)的比例为28.3%,OSA-淀粉(10%水分)在120℃进一步加热4小时后(命名为HOSA-淀粉),SDS含量最高可达42.8%。HOSA-淀粉的体内血糖反应显示血糖峰值出现延迟,峰值葡萄糖浓度显著降低(32.2%),进一步证实了其慢消化特性。支链淀粉脱支分析表明,HOSA-淀粉对异淀粉酶和普鲁兰酶的脱支酶具有最高的抗性,并且当HOSA-淀粉被α-淀粉酶或淀粉葡萄糖苷酶消化时,Km和Vm(酶动力学)也同时降低,这表明HOSA-淀粉的慢消化是由于消化过程中酶活性的非竞争性抑制。HOSA-淀粉的尺寸排阻色谱分析表明,支链淀粉分子碎片化,具有更多的非还原端,有利于在Englyst试验中通过淀粉葡萄糖苷酶的作用将抗性淀粉(RS)转化为SDS。进一步的溶解度分析表明,HOSA-淀粉的水不溶性是由OSA介导的支链淀粉交联以及OSA改性淀粉分子之间的疏水相互作用引起的。HOSA-淀粉的水不溶性会降低其酶可及性,并且带有OSA分子的消化产物也可能直接作为非竞争性抑制剂降低酶活性,导致HOSA-淀粉消化缓慢。