淀粉酶
化学
酶
IC50型
猝灭(荧光)
动力学
淀粉
生物化学
餐后
基质(水族馆)
抑制性突触后电位
圆二色性
体外
荧光
食品科学
糖尿病
生物
内分泌学
物理
量子力学
生态学
作者
Hailong Zhang,Qing‐xiao Wu,Xiaoming Qin
标识
DOI:10.1016/j.procbio.2019.07.009
摘要
We optimized four addition methods for Camellia nitidissima Chi flower extracts (Cnfe). Among four methods, the first (before meals) had the greatest inhibitory effect via binding of Cnfe with starch. Cnfe bound starch, and reduced inhibition of the enzymes. The higher binding percentage of Cnfe and the substrate starch led to less free Cnfe interaction with enzymes in solution. To determine the underlying inhibitory mechanism(s), we used enzymatic inhibition kinetics, fluorescence quenching and circular dichroism spectroscopies. We found that Cnfe possessed potential inhibitory activity against α-amylase (IC50 300 μg/mL, Ki 162 μg/mL, static quenching constant KFQ 1.5 mL/mg) and α-glucosidase (45 μg/mL, 89 μg/mL and 8.5 mL/mg). Cnfe changed the microenvironment and conformation of the enzyme, making it a better digestive enzyme inhibitor. These experimental results suggest that Cnfe has the potential to control blood sugar, and that it may be used to improve diabetes by reducing postprandial hyperglycemia. Cnfe should be taken before meals and separately from foods with higher binding intensities.
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