Department of Biological Chemistry, Indian Association for the Cultivation of Science, Jadavpur, Kolkata, India.
J Colloid Interface Sci. 2013 Apr 1;395:111-8. doi: 10.1016/j.jcis.2012.12.064. Epub 2013 Jan 10.
Herein, we report the successful inclusion of 2D allotrope of carbon, graphene oxide (GO) in cetyltrimethylammonium bromide (CTAB)/isooctane/n-hexanol/water reverse micelle without compromising the stability of water-in-oil (w/o) microemulsion. This newly developed self-assembled nanocomposites act as proficient host for surface-active enzymes, lipase, horseradish peroxidase (HRP), and soybean peroxidase (SBP). Lipase activity within GO-doped CTAB reverse micelles remarkably improved by 3.8-fold compared to that was observed in only CTAB reverse micelle (second-order rate constant, k2=433±7 cm3 g(-1) s(-1)). In case of GO-doped CTAB reverse micelle, the observed enzyme activity (k2=1653±11 cm3 g(-1) s(-1)) is till date the highest ever activity of lipase in CTAB w/o microemulsions. In case of HRP and SBP, the catalytic efficiency maximally increased up to 2.6-fold and 2.3-fold, respectively. Electrostatic attraction between cationic head group of CTAB and anionic surface of GO as well as intrinsic amphiphilic character of GO possibly resulted in the confinement of this 2D nanosheet at the interface of reverse micelles. Integration of GO at the interface augmented the interfacial space in vicinity of surface-active enzyme. This enlarged interface might have accommodated higher amount of substrate and lipase with flexibility in its conformation resulting in marked improvement in the enzyme activity. Interfacial localization of GO was established by fluorescence spectroscopy. In addition, change in secondary structure of lipase in presence of 2D carbon allotrope was substantiated by circular dichroism spectroscopy.
在此,我们报告了将二维碳同素异形体氧化石墨烯(GO)成功纳入十六烷基三甲基溴化铵(CTAB)/异辛烷/正己醇/水反胶束中,而不会影响油包水(w/o)微乳液的稳定性。这种新开发的自组装纳米复合材料作为表面活性酶、脂肪酶、辣根过氧化物酶(HRP)和大豆过氧化物酶(SBP)的高效宿主。与仅在 CTAB 反胶束中观察到的相比,GO 掺杂 CTAB 反胶束中的脂肪酶活性显著提高了 3.8 倍(二级速率常数 k2=433±7 cm3 g(-1) s(-1))。在 GO 掺杂 CTAB 反胶束的情况下,观察到的酶活性(k2=1653±11 cm3 g(-1) s(-1))是迄今为止 CTAB w/o 微乳液中脂肪酶的最高活性。对于 HRP 和 SBP,催化效率分别最大提高了 2.6 倍和 2.3 倍。CTAB 阳离子头基与 GO 阴离子表面之间的静电吸引以及 GO 的固有两亲性可能导致这种二维纳米片在反胶束界面处被限制。GO 在界面处的集成增加了表面活性酶附近的界面空间。这种扩大的界面可能容纳了更多的底物和脂肪酶,并且其构象具有灵活性,从而导致酶活性的显著提高。荧光光谱法证实了 GO 在界面处的定位。此外,圆二色性光谱法证实了二维碳同素异形体存在时脂肪酶二级结构的变化。