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具有金属-β-内酰胺酶结构的酶的来源、多样性和多种作用,来自不同的生物体。

Origin, Diversity, and Multiple Roles of Enzymes with Metallo-β-Lactamase Fold from Different Organisms.

机构信息

MEPHI, IRD, AP-HM, IHU-Méditerranée Infection, Aix Marseille University, 13005 Marseille, France.

IHU-Méditerranée Infection, 13005 Marseille, France.

出版信息

Cells. 2023 Jun 30;12(13):1752. doi: 10.3390/cells12131752.

Abstract

β-lactamase enzymes have generated significant interest due to their ability to confer resistance to the most commonly used family of antibiotics in human medicine. Among these enzymes, the class B β-lactamases are members of a superfamily of metallo-β-lactamase (MβL) fold proteins which are characterised by conserved motifs (i.e., HxHxDH) and are not only limited to bacteria. Indeed, as the result of several barriers, including low sequence similarity, default protein annotation, or untested enzymatic activity, MβL fold proteins have long been unexplored in other organisms. However, thanks to search approaches which are more sensitive compared to classical Blast analysis, such as the use of common ancestors to identify distant homologous sequences, we are now able to highlight their presence in different organisms including Bacteria, Archaea, Nanoarchaeota, Asgard, Humans, Giant viruses, and Candidate Phyla Radiation (CPR). These MβL fold proteins are multifunctional enzymes with diverse enzymatic or non-enzymatic activities of which, at least thirteen activities have been reported such as β-lactamase, ribonuclease, nuclease, glyoxalase, lactonase, phytase, ascorbic acid degradation, anti-cancer drug degradation, or membrane transport. In this review, we (i) discuss the existence of MβL fold enzymes in the different domains of life, (ii) present more suitable approaches to better investigating their homologous sequences in unsuspected sources, and (iii) report described MβL fold enzymes with demonstrated enzymatic or non-enzymatic activities.

摘要

β-内酰胺酶由于能够赋予对人类医学中最常用的抗生素家族的抗性而引起了极大的关注。在这些酶中,B 类β-内酰胺酶是金属β-内酰胺酶 (MβL) 折叠蛋白超家族的成员,其特征是保守基序(即 HxHxDH),并且不仅限于细菌。事实上,由于包括低序列相似性、默认蛋白质注释或未经测试的酶活性在内的几个障碍,MβL 折叠蛋白在其他生物体中一直未被探索。然而,由于与经典 Blast 分析相比更敏感的搜索方法,例如使用共同祖先来识别遥远的同源序列,我们现在能够在不同的生物体中突出它们的存在,包括细菌、古菌、纳米古菌、Asgard、人类、巨型病毒和候选门辐射 (CPR)。这些 MβL 折叠蛋白是多功能酶,具有多种酶或非酶活性,其中至少报道了十三种活性,如β-内酰胺酶、核糖核酸酶、核酸酶、甘油醛酶、内酯酶、植酸酶、抗坏血酸降解、抗癌药物降解或膜转运。在这篇综述中,我们 (i) 讨论了 MβL 折叠酶在不同生命领域的存在,(ii) 提出了更合适的方法来更好地研究它们在可疑来源中的同源序列,以及 (iii) 报告了具有证明的酶或非酶活性的描述的 MβL 折叠酶。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc63/10340364/7496e8fdf69d/cells-12-01752-g001.jpg

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