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首页> 外文期刊>Journal of Colloid and Interface Science >Graphene oxide in cetyltrimethylammonium bromide (CTAB) reverse micelle: A befitting soft nanocomposite for improving efficiency of surface-active enzymes
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Graphene oxide in cetyltrimethylammonium bromide (CTAB) reverse micelle: A befitting soft nanocomposite for improving efficiency of surface-active enzymes

机译:十六烷基三甲基溴化铵(CTAB)反胶束中的氧化石墨烯:一种合适的软纳米复合材料,可提高表面活性酶的效率

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摘要

Herein, we report the successful inclusion of 2D allotrope of carbon, graphene oxide (GO) in cetyltrimethylammonium bromide (CTAB)/isooctane-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, k_2=433±7cm~3g~(-1)s~(-1)). In case of GO-doped CTAB reverse micelle, the observed enzyme activity (k_2=1653±11cm~3g~(-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.
机译:在此,我们报道了在十六烷基三甲基溴化铵(CTAB)/异辛烷/正己醇/反水胶束中成功包含碳,氧化石墨烯(GO)的二维同素异形体,而没有损害油包水(w / o)微乳液的稳定性。这种新开发的自组装纳米复合材料可作为表面活性酶,脂肪酶,辣根过氧化物酶(HRP)和大豆过氧化物酶(SBP)的熟练宿主。与仅在CTAB反向胶束中观察到的相比,GO掺杂的CTAB反向胶束中的脂肪酶活性显着提高了3.8倍(二级速率常数,k_2 = 433±7cm〜3g〜(-1)s〜(-1) )。在GO掺杂的CTAB反胶束的情况下,观察到的酶活性(k_2 = 1653±11cm〜3g〜(-1)s〜(-1))是迄今为止不包含微乳液的CTAB中脂肪酶的最高活性。在HRP和SBP的情况下,催化效率分别最大提高到2.6倍和2.3倍。 CTAB的阳离子头基与GO的阴离子表面之间的静电吸引以及GO的固有两亲特性可能导致该2D纳米片层限制在反胶束的界面处。 GO在界面处的整合增加了表面活性酶附近的界面空间。这种扩大的界面可能已经容纳了更高量的底物和脂肪酶,并且其构象具有灵活性,从而导致了酶活性的显着改善。 GO的界面定位通过荧光光谱法确定。另外,在2D碳同素异形体存在下,脂肪酶二级结构的变化通过圆二色性光谱法得以证实。

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