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来自[具体来源1]和[具体来源2]的新型Δ17脂肪酸去饱和酶基因的表征与分子对接

Characterization and molecular docking of new Δ17 fatty acid desaturase genes from and .

作者信息

Rong Chunchi, Chen Haiqin, Tang Xin, Gu Zhennan, Zhao Jianxin, Zhang Hao, Chen Wei, Chen Yong Q

机构信息

State Key Laboratory of Food Science and Technology, Jiangnan University Wuxi Jiangsu P. R. China

School of Food Science and Technology, Jiangnan University Wuxi Jiangsu P. R. China.

出版信息

RSC Adv. 2019 Feb 27;9(12):6871-6880. doi: 10.1039/c9ra00535h. eCollection 2019 Feb 22.

Abstract

Fatty acid desaturases are key enzymes in the biosynthesis of -3 polyunsaturated fatty acids (PUFAs) conversion of -6 polyunsaturates to their -3 counterparts. In this study, we reported the characterization and molecular docking of Δ17 desaturases from and . These two new desaturase genes were screened using the known Δ17 desaturase gene (oPaFADS17) from as a template. Analysis of their genes revealed that the sequences of oRiFADS17 and oObFADS17 contained the typical His-rich motifs (one HXXXH and two HXXHH). They were then expressed in to examine their activities and substrate preferences. Our results show that the two candidate -3 desaturases possess a strong Δ17 desaturase activity, exhibiting remarkable increase in desaturation activity on C20 fatty acids compared to C18 fatty acids. To the best of our knowledge, oRiFADS17 desaturase has greater (3-4 fold) catalytic activity for C18 substrates than other reported Δ17 desaturases and oObFADS17 is the first reported Δ17 desaturase in sea mollusks. Characterization of these two new desaturases will be of greater value for genetic engineering in industrial production of eicosapentaenoic acid (EPA, C20:5-3) and docosahexaenoic acid (DHA, C22:6-3). Due to lack of crystal structure information about -3 desaturases, for the first time, the view of their predicted structures, binding pockets and substrate tunnels was clearly observed based on molecular docking. This will contribute to strengthening our understanding of the structure-function relationships of -3 fatty acid desaturases.

摘要

脂肪酸去饱和酶是生物合成ω-3多不饱和脂肪酸(PUFAs)以及将ω-6多不饱和脂肪酸转化为ω-3对应物的关键酶。在本研究中,我们报道了来自[具体物种1]和[具体物种2]的Δ17去饱和酶的特性及分子对接情况。这两个新的去饱和酶基因是以来自[具体物种3]的已知Δ17去饱和酶基因(oPaFADS17)为模板筛选出来的。对它们的基因分析表明,oRiFADS17和oObFADS17的序列包含典型的富含组氨酸基序(一个HXXXH和两个HXXHH)。然后将它们在[具体表达宿主]中表达以检测其活性和底物偏好性。我们的结果表明,这两个候选的ω-3去饱和酶具有很强的Δ17去饱和酶活性,与C18脂肪酸相比,对C20脂肪酸的去饱和活性有显著增加。据我们所知,oRiFADS17去饱和酶对C18底物的催化活性比其他已报道的Δ17去饱和酶更高(3 - 4倍),并且oObFADS17是首次在海生软体动物中报道的Δ17去饱和酶。这两种新去饱和酶的特性对于二十碳五烯酸(EPA,C20:5ω-3)和二十二碳六烯酸(DHA,C22:6ω-3)工业生产中的基因工程具有更大价值。由于缺乏关于ω-3去饱和酶的晶体结构信息,首次基于分子对接清晰地观察到了它们预测的结构、结合口袋和底物通道。这将有助于加强我们对ω-3脂肪酸去饱和酶结构 - 功能关系的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9841/9061052/ce41a4d202d8/c9ra00535h-f1.jpg

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