期刊
FOOD CHEMISTRY
卷 270, 期 -, 页码 429-435出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.foodchem.2018.07.135
关键词
Lactic acid isomers; Human serum albumin; Fluorescence spectroscopy; Circular dichroism; Docking simulation
资金
- National Key Research and Development Program of China [2017YFC1601700]
- National Natural Science Foundation of China, China [31601540, 31771939]
- Natural Science Foundation of Guangdong Province, China
- Guangdong and Guangzhou ST Plan [2016A030310304, S2013030013338, 2017B020207010, 2016201604030004]
- Provincial Key Platform and Major Research Projects of Guangdong Universities [2015KQNCX106]
- Doctoral Research Project of Guangdong University of Education [2014ARF02]
Lactic acid enantiomers, normally found in fermented food, are absorbed into the blood and interact with plasma carrier protein human serum albumin (HSA). Unveiling the effect on the function and structure of HSA during chiral interaction can give a better understanding of the different distribution activities of the two enantiomers. Multi-spectroscopic methods and molecular modelling techniques are used to study the interactions between lactic acid enantiomers and HSA. Time-resolved and steady-state fluorescence spectra manifest that the fluorescence quenching mechanism is mainly static in type, due to complex formation. Binding interactions, deduced by thermodynamic calculation, agree with the docking prediction. Docking results and kinetic constants represent chiral-recognizing discriminations consistently. The bindings of lactic acid enantiomers lead to some microenvironmental and slight conformational changes of HSA as shown by circular dichroism (CD), synchronous and three-dimensional fluorescence spectra. This investigation may yield useful information about the possible toxicity risk of lactic acid enantiomers to human health.
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