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On the bathochromic shift of the absorption by astaxanthin in crustacyanin: a quantum chemical study

机译:虾青素对虾青素吸收的红移:量子化学研究

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The structural origin of the bathochromic shift assumed by the electronic absorption spectrum of protein-bound astaxanthin, the carotenoid that upon binding to crustacyanin is responsible for the blue colouration of lobster shell, is investigated by means of quantum chemical methods. The calculations suggest that the bathochromic shift is largely due to one of the astaxanthin C4 keto groups being hydrogen-bonded to a histidine residue of the surrounding protein, and that the effect of this histidine is directly dependent on its protonation state. Out of the different methodologies (CIS, TD-DFT, and ZINDO/S) employed to calculate wavelengths of maximum absorption, the best agreement with experimental data is obtained using the semiempirical ZINDO/S method. (C) 2003 Elsevier Science B.V. All rights reserved. [References: 35]
机译:通过结合蛋白质的虾青素的电子吸收光谱推测的红移转变的结构起源是通过量子化学方法研究的,该类胡萝卜素与硬脂蓝蛋白结合后负责龙虾壳的蓝色着色。计算表明,红移主要是由于虾青素C4酮基中的一个氢键合到周围蛋白质的组氨酸残基上,该组氨酸的作用直接取决于其质子化状态。在用于计算最大吸收波长的不同方法(CIS,TD-DFT和ZINDO / S)中,使用半经验ZINDO / S方法可获得与实验数据的最佳一致性。 (C)2003 Elsevier Science B.V.保留所有权利。 [参考:35]

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