Rocio Solis-Palacios, Graciela Espinosa-Luna, C. Peña-Montes, R. Quintana-Castro, M. Sánchez-Otero, R. Oliart-Ros
{"title":"通过硅探针从洛斯胡默洛斯地热场的元基因组中筛选推定聚酯水解酶","authors":"Rocio Solis-Palacios, Graciela Espinosa-Luna, C. Peña-Montes, R. Quintana-Castro, M. Sánchez-Otero, R. Oliart-Ros","doi":"10.3390/catal14060379","DOIUrl":null,"url":null,"abstract":"Hydrolases are the most popular enzymes, and among the most valuable in biotechnological applications. Some hydrolases, such as lipases, esterases, proteases, cellulases and amylases, are used in the food industry and the production of biopharmaceuticals, biofuels, biopolymers and detergents. Of special interest are those obtained from thermophilic microorganisms. Although there is great microbial diversity in extreme environments, the investigations aimed at detecting and isolating enzymes with potential for polyester degradation such as polyethylene terephthalate (PET) are limited. In this work, we explored the metagenomic library of an oil-enriched soil sample from the “Los Humeros” geothermal field by means of in silico probes in search for enzymes potentially able to degrade polyesters. Using conserved motifs and activity-relevant sites of reported polyester hydrolases, we designed probes that allowed us to identify 6 potential polyester hydrolases in the metagenome. Three-dimensional structure prediction revealed a canonical α/β fold and a cap covering the active site of the enzymes. The catalytic triads were composed of Ser, His and Asp. Structural comparison, substrate binding site analysis and molecular docking suggested their potential as polyester hydrolases, particularly cutinases and PETases. An enzyme, REC98271, was cloned, expressed and characterized, showing thermophilic properties and preference for short-chain substrates. These findings contribute to our understanding of enzyme diversity in “Los Humeros” metagenome and their potential applications in biodegradation and recycling processes.","PeriodicalId":505577,"journal":{"name":"Catalysts","volume":"13 7","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Selection of Putative Polyester Hydrolases from the Metagenome of Los Humeros Geothermal Field by Means of In Silico Probes\",\"authors\":\"Rocio Solis-Palacios, Graciela Espinosa-Luna, C. Peña-Montes, R. Quintana-Castro, M. Sánchez-Otero, R. Oliart-Ros\",\"doi\":\"10.3390/catal14060379\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Hydrolases are the most popular enzymes, and among the most valuable in biotechnological applications. Some hydrolases, such as lipases, esterases, proteases, cellulases and amylases, are used in the food industry and the production of biopharmaceuticals, biofuels, biopolymers and detergents. Of special interest are those obtained from thermophilic microorganisms. Although there is great microbial diversity in extreme environments, the investigations aimed at detecting and isolating enzymes with potential for polyester degradation such as polyethylene terephthalate (PET) are limited. In this work, we explored the metagenomic library of an oil-enriched soil sample from the “Los Humeros” geothermal field by means of in silico probes in search for enzymes potentially able to degrade polyesters. Using conserved motifs and activity-relevant sites of reported polyester hydrolases, we designed probes that allowed us to identify 6 potential polyester hydrolases in the metagenome. Three-dimensional structure prediction revealed a canonical α/β fold and a cap covering the active site of the enzymes. The catalytic triads were composed of Ser, His and Asp. Structural comparison, substrate binding site analysis and molecular docking suggested their potential as polyester hydrolases, particularly cutinases and PETases. An enzyme, REC98271, was cloned, expressed and characterized, showing thermophilic properties and preference for short-chain substrates. These findings contribute to our understanding of enzyme diversity in “Los Humeros” metagenome and their potential applications in biodegradation and recycling processes.\",\"PeriodicalId\":505577,\"journal\":{\"name\":\"Catalysts\",\"volume\":\"13 7\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-06-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Catalysts\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3390/catal14060379\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysts","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/catal14060379","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
水解酶是最受欢迎的酶,也是生物技术应用中最有价值的酶之一。一些水解酶,如脂肪酶、酯酶、蛋白酶、纤维素酶和淀粉酶,可用于食品工业和生物制药、生物燃料、生物聚合物和洗涤剂的生产。从嗜热微生物中获得的酶尤其令人感兴趣。虽然极端环境中的微生物种类繁多,但旨在检测和分离具有降解聚酯(如聚对苯二甲酸乙二酯)潜力的酶的研究却很有限。在这项工作中,我们通过硅探针探索了 "Los Humeros "地热田富含石油的土壤样本的元基因组库,以寻找可能降解聚酯的酶。利用已报道的聚酯水解酶的保守基团和活性相关位点,我们设计了探针,从而在元基因组中发现了 6 种潜在的聚酯水解酶。三维结构预测显示,这些酶的活性位点有一个典型的α/β折叠和一个覆盖物。催化三元组由 Ser、His 和 Asp 组成。结构比较、底物结合位点分析和分子对接表明,它们具有作为聚酯水解酶,特别是角叉菜胶酶和 PET 酶的潜力。克隆、表达和鉴定了一种名为 REC98271 的酶,该酶具有嗜热特性并偏好短链底物。这些发现有助于我们了解 "Los Humeros "元基因组中酶的多样性及其在生物降解和回收过程中的潜在应用。
Selection of Putative Polyester Hydrolases from the Metagenome of Los Humeros Geothermal Field by Means of In Silico Probes
Hydrolases are the most popular enzymes, and among the most valuable in biotechnological applications. Some hydrolases, such as lipases, esterases, proteases, cellulases and amylases, are used in the food industry and the production of biopharmaceuticals, biofuels, biopolymers and detergents. Of special interest are those obtained from thermophilic microorganisms. Although there is great microbial diversity in extreme environments, the investigations aimed at detecting and isolating enzymes with potential for polyester degradation such as polyethylene terephthalate (PET) are limited. In this work, we explored the metagenomic library of an oil-enriched soil sample from the “Los Humeros” geothermal field by means of in silico probes in search for enzymes potentially able to degrade polyesters. Using conserved motifs and activity-relevant sites of reported polyester hydrolases, we designed probes that allowed us to identify 6 potential polyester hydrolases in the metagenome. Three-dimensional structure prediction revealed a canonical α/β fold and a cap covering the active site of the enzymes. The catalytic triads were composed of Ser, His and Asp. Structural comparison, substrate binding site analysis and molecular docking suggested their potential as polyester hydrolases, particularly cutinases and PETases. An enzyme, REC98271, was cloned, expressed and characterized, showing thermophilic properties and preference for short-chain substrates. These findings contribute to our understanding of enzyme diversity in “Los Humeros” metagenome and their potential applications in biodegradation and recycling processes.