Centre for Marine Bio-Innovation and School of Biotechnology and Biomolecular Sciences, The University of New South Wales, Sydney, NSW 2052, Australia.
Colloids Surf B Biointerfaces. 2011 Feb 1;82(2):291-6. doi: 10.1016/j.colsurfb.2010.08.042. Epub 2010 Oct 30.
Confocal laser scanning microscopy (CLSM) in combination with a fluorescently labeling enzyme dye, LavaPurple™, was demonstrated as a technique for the visualization of Thermomyces (Humicola) lanuginosa lipase (LIP(HLL)) and Candida antarctica lipase A (LIP(CA)) within a transparent latex coating. Addition of Teric Surfactants (C(16) non-ionic Teric 475, 1.8% (w/w) or C(10) non-ionic Teric 460, 2.0% (w/w)) significantly increased the accumulation of both LIP(HLL) and LIP(CA) to the surface of a latex coating. An α-naphthyl acetate substrate assay was used to quantify the accumulated lipase. The results derived from the acetate assay correlated with the enzyme accumulation (at the surface) observed in the CLSM images of the latex coating. This correlation demonstrated that the increased enzyme accumulation within the top 2μm of the latex film was responsible for the increase in surface enzymatic activity. The combination of CLSM imagery and quantifiable image analysis provided a valuable tool for the optimization of surfactant concentrations for maximizing the activity of an enzyme (and potentially other additives) within a latex coating.
共聚焦激光扫描显微镜(CLSM)结合荧光标记酶染料 LavaPurple™,被证明是一种可视化嗜热真菌(毁丝霉)脂肪酶(LIP(HLL))和南极假丝酵母脂肪酶 A(LIP(CA))在透明乳胶涂层内的技术。添加 Teric 表面活性剂(C(16)非离子型 Teric 475,1.8%(w/w)或 C(10)非离子型 Teric 460,2.0%(w/w))可显著增加 LIP(HLL)和 LIP(CA)在乳胶涂层表面的积累。使用α-萘乙酸酯底物测定法定量累积的脂肪酶。从乙酸酯测定法得出的结果与乳胶涂层 CLSM 图像中观察到的酶积累(在表面)相关。这种相关性表明,乳胶膜顶层 2μm 内酶的积累增加是导致表面酶活性增加的原因。CLSM 图像和可量化的图像分析相结合,为优化表面活性剂浓度以最大程度提高乳胶涂层中酶(和潜在的其他添加剂)的活性提供了有价值的工具。