Wu Ming J, Clarke Frank M, Rogers Peter J, Young Paul, Sales Narelle, O'Doherty Patrick J, Higgins Vincent J
School of Biomedical and Health Sciences, College of Health and Science, University of Western Sydney, Locked Bag 1797, Penrith South DC, New South Wales 1797, Australia; E-Mail:
Int J Mol Sci. 2011;12(9):6089-103. doi: 10.3390/ijms12096089. Epub 2011 Sep 19.
This study was carried out with fresh Australian lager beer which was sampled directly off the production line, the same samples aged for 12 weeks at 30 °C, and the vintage beer which was kept at 20 °C for 5 years. Characteristic Australian lager flavour was maintained in the fresh and vintage beers but was lost in the aged beer. Sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) and free thiol group labelling analyses of beer proteins found that this flavour stability correlated with the presence of an unknown 10 kilodaltons (kDa) protein with a higher level of free thiols. The protein was purified by size-exclusion chromatography, then peptide sequencing and database matching identified it as the barley lipid transfer protein (LTP1). Further characterisation using diphenylpicrylhydrazyl (DPPH) free radical scavenging and a Saccharomyces cerevisiae-based antioxidant screening assay demonstrated that the LTP1 protein was active in DPPH reduction and antioxidant activity. The absence of free thiol in the aged beer indicates that the thiol functional groups within the LTP1 protein were saturated and suggests that it is important in the flavour stability of beer by maintaining reduction capacity during the ageing process.
本研究使用了直接从生产线取样的新鲜澳大利亚贮藏啤酒、在30°C下陈酿12周的相同样品以及在20°C下保存5年的年份啤酒。新鲜啤酒和年份啤酒中保持了澳大利亚贮藏啤酒的特征风味,但陈酿啤酒中该风味丧失。对啤酒蛋白质进行十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)和游离巯基标记分析发现,这种风味稳定性与一种未知的10千道尔顿(kDa)蛋白质的存在相关,该蛋白质具有较高水平的游离巯基。通过尺寸排阻色谱法纯化该蛋白质,然后通过肽测序和数据库匹配将其鉴定为大麦脂质转移蛋白(LTP1)。使用二苯基苦味酰基自由基(DPPH)清除法和基于酿酒酵母的抗氧化剂筛选试验进行的进一步表征表明,LTP1蛋白在DPPH还原和抗氧化活性方面具有活性。陈酿啤酒中不存在游离巯基,这表明LTP1蛋白内的巯基官能团已饱和,并表明它通过在陈酿过程中保持还原能力对啤酒的风味稳定性很重要。