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嗜热栖热放线菌新嗜热脂肪酶的序列鉴定及计算机模拟表征

Sequence identification and in silico characterization of novel thermophilic lipases from Geobacillus species.

作者信息

Sürmeli Yusuf, Tekedar Hasan Cihad, Şanlı-Mohamed Gülşah

机构信息

Department of Agricultural Biotechnology, Tekirdağ Namık Kemal University, Tekirdağ, Turkey.

Department of Biotechnology and Bioengineering, İzmir Institute of Technology, İzmir, Turkey.

出版信息

Biotechnol Appl Biochem. 2024 Feb;71(1):162-175. doi: 10.1002/bab.2529. Epub 2023 Nov 1.

Abstract

Microbial lipases are utilized in various biotechnological areas, including pharmaceuticals, food, biodiesel, and detergents. In this study, we cloned and sequenced Lip21 and Lip33 genes from Geobacillus sp. GS21 and Geobacillus sp. GS33, then we in silico and experimentally analyzed the encoded lipases. For this purpose, Lip21 and Lip33 were cloned, sequenced, and their amino acid sequences were investigated for determination of biophysicochemical characteristics, evolutionary relationships, and sequence similarities. 3D models were built and computationally affirmed by various bioinformatics tools, and enzyme-ligand interactions were investigated by docking analysis using six ligands. Biophysicochemical property of Lip21 and Lip33 was also determined experimentally and the results demonstrated that they had similar isoelectric point (pI) (6.21) and T (75.5°C) values as T was revealed by denatured protein analysis of the circular dichroism spectrum and pI was obtained by isoelectric focusing. Phylogeny analysis indicated that Lip21 and Lip33 were the closest to lipases from Geobacillus sp. SBS-4S and Geobacillus thermoleovorans, respectively. Alignment analysis demonstrated that S144-D348-H389 was catalytic triad residues in Lip21 and Lip33, and enzymes possessed a conserved Gly-X-Ser-X-Gly motif containing catalytic serine. 3D structure analysis indicated that Lip21 and Lip33 highly resembled each other and they were α/β hydrolase-fold enzymes with large lid domains. BANΔIT analysis results showed that Lip21 and Lip33 had higher thermal stability, compared to other thermostable Geobacillus lipases. Docking results revealed that Lip21- and Lip33-docked complexes possessed common residues (H112, K115, Q162, E163, and S141) that interacted with the substrates, except paranitrophenyl (pNP)-C10 and pNP-C12, indicating that these residues might have a significant action on medium and short-chain fatty acid esters. Thus, Lip21 and Lip33 can be potential candidates for different industrial applications.

摘要

微生物脂肪酶被应用于各种生物技术领域,包括制药、食品、生物柴油和洗涤剂。在本研究中,我们从嗜热栖热菌属GS21和嗜热栖热菌属GS33中克隆并测序了Lip21和Lip33基因,然后对编码的脂肪酶进行了电子分析和实验分析。为此,克隆并测序了Lip21和Lip33,研究了它们的氨基酸序列,以确定其生物物理化学特性、进化关系和序列相似性。利用各种生物信息学工具构建并通过计算确认了三维模型,并使用六种配体通过对接分析研究了酶-配体相互作用。还通过实验测定了Lip21和Lip33的生物物理化学性质,结果表明它们具有相似的等电点(pI)(6.21)和热变性温度(T)(75.5°C)值,其中热变性温度通过圆二色光谱的变性蛋白分析得出,等电点通过等电聚焦获得。系统发育分析表明,Lip21和Lip33分别与嗜热栖热菌属SBS-4S和嗜热栖热脂肪芽孢杆菌的脂肪酶关系最为密切。比对分析表明,S144-D348-H389是Lip21和Lip33中的催化三联体残基,并且这些酶具有包含催化丝氨酸的保守Gly-X-Ser-X-Gly基序。三维结构分析表明,Lip21和Lip33彼此高度相似,它们是具有大盖子结构域的α/β水解酶折叠酶。BANΔIT分析结果表明,与其他嗜热栖热菌属热稳定脂肪酶相比,Lip21和Lip33具有更高的热稳定性。对接结果显示,Lip21和Lip33对接复合物具有与底物相互作用的共同残基(H112、K115、Q162、E163和S141),对硝基苯基(pNP)-C10和pNP-C12除外,这表明这些残基可能对中短链脂肪酸酯具有重要作用。因此,Lip21和Lip33可能是不同工业应用的潜在候选者。

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