氧化石墨对(S)-选择性胺转氨酶催化行为的影响

Nikolaos Kaloudis, P. Zygouri, Nikolaos Chalmpes, Konstantinos Spyrou, D. Gournis, Ioannis V. Pavlidis
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引用次数: 0

摘要

氧化石墨(GO)已被用于固定化几种酶,表现出非常有趣的性质作为固定化基质。然而,纳米材料对酶的影响是无法预测的。本文研究了氧化石墨烯对几种(S)选择性胺转氨酶[(S)-ATAs]的催化行为的影响。这些酶是本研究的重点,因为它们是活性位点与吡哆醛5 ' -磷酸的同二聚体,比以前研究的其他酶明显更复杂的系统。在反应介质中添加氧化石墨烯(最高0.1 mg/ml)可使所研究的大多数酶活化(活性提高50%),同时保持其温度分布(在40至45°C之间表现更好)和稳定性。然而,这种作用并不是普遍存在的,有些酶会受到纳米材料的负面影响。更深刻的是对紫色色杆菌(S)-ATA的影响,在0.1 mg/ml氧化石墨烯的存在下,它失去了近50%的活性,而稳定性明显下降,在25 μg/ml氧化石墨烯的存在下,在40°C孵育2小时后失去了活性。这种负面影响似乎是由次要结构的改变引起的;即α-螺旋的丢失和随后的随机螺旋的增加(在25 μg/ml氧化石墨烯存在下约3%)。我们假设氧化石墨烯对(S)-ATAs的影响与酶的表面化学有关;负电荷较少的酶在与氧化石墨烯的相互作用中失活。这一见解将有助于将ATA固定在碳基纳米材料上的合理化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Graphite Oxide on the Catalytic Behavior of (S)-Selective Amine Transaminases
Graphite oxide (GO) has been used for the immobilization of several classes of enzymes, exhibiting very interesting properties as an immobilization matrix. However, the effect the nanomaterial has on the enzyme cannot be predicted. Herein, the effect GO has on the catalytic behavior of several (S)-selective amine transaminases [(S)-ATAs] has been investigated. These enzymes were the focus of this work as they are homodimers with pyridoxal 5′-phosphate in their active site, significantly more complex systems than other enzymes previously studied. Addition of GO (up to 0.1 mg/ml) in the reaction medium leads to activation (up to 50% improved activity) for most enzymes studied, while they maintain their temperature profile (they perform better between 40 and 45°C) and their stability. However, the effect is not universal and there are enzymes that are negatively influenced by the presence of the nanomaterial. More profound is the effect on the (S)-ATA from Chromobacterium violaceum which loses almost 50% of its activity in the presence of 0.1 mg/ml GO, while the stability was significantly decreased, losing its activity after 2 h incubation at 40°C, in the presence of 25 μg/ml GO. This negative effect seems to rise from minor secondary structure alterations; namely, a loss of α-helices and subsequent increase in random coil (∼3% in the presence of 25 μg/ml GO). We hypothesize that the effect the GO has on (S)-ATAs is correlated to the surface chemistry of the enzymes; the less negatively-charged enzymes are deactivated from the interaction with GO. This insight will aid the rationalization of ATA immobilization onto carbon-based nanomaterials.
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