Sánchez-Reyez Ayixon, Batista-García Ramón Alberto, Valdés-García Gilberto, Ortiz Ernesto, Perezgasga Lucía, Zárate-Romero Andrés, Pastor Nina, Folch-Mallol Jorge Luis
Centro de Investigación en Dinámica Celular, IICBA, Universidad Autónoma del Estado de Morelos (UAEM), Colonia Chamilpa, CP, 62209, Cuernavaca, Morelos, Mexico.
Centro de Investigación en Biotecnología UAEM, CP 62209, Cuernavaca, Morelos, Mexico.
Proteins. 2017 Jul;85(7):1222-1237. doi: 10.1002/prot.25282. Epub 2017 Mar 24.
Activated sludge is produced during the treatment of sewage and industrial wastewaters. Its diverse chemical composition allows growth of a large collection of microbial phylotypes with very different physiologic and metabolic profiles. Thus, activated sludge is considered as an excellent environment to discover novel enzymes through functional metagenomics, especially activities related with degradation of environmental pollutants. Metagenomic DNA was isolated and purified from an activated sludge sample. Metagenomic libraries were subsequently constructed in Escherichia coli. Using tributyrin hydrolysis, a screening by functional analysis was conducted and a clone that showed esterase activity was isolated. Blastx analysis of the sequence of the cloned DNA revealed, among others, an ORF that encodes a putative thioesterase with 47-64% identity to GenBank CDS reported genes, similar to those in the hotdog fold thioesterase superfamily. On the basis of its amino acid similarity and its homology-modelled structure we deduced that this gene encodes an enzyme (ThYest_ar) that belongs to family TE13, with a preference for aryl-CoA substrates and a novel catalytic residue constellation. Plasmid retransformation in E. coli confirmed the clone's phenotype, and functional complementation of a paaI E. coli mutant showed preference for phenylacetate over chlorobenzene as a carbon source. This work suggests a role for TE13 family thioesterases in swimming and degradation approaches for phenyl acetic acid. Proteins 2017; 85:1222-1237. © 2017 Wiley Periodicals, Inc.
活性污泥是在污水和工业废水处理过程中产生的。其多样的化学成分使得大量具有截然不同生理和代谢特征的微生物系统型得以生长。因此,活性污泥被认为是通过功能宏基因组学发现新型酶的绝佳环境,尤其是与环境污染物降解相关的活性。从活性污泥样品中分离并纯化了宏基因组DNA。随后在大肠杆菌中构建了宏基因组文库。利用三丁酸甘油酯水解进行功能分析筛选,分离出一个显示酯酶活性的克隆。对克隆DNA序列的Blastx分析表明,除其他外,有一个开放阅读框编码一种假定的硫酯酶,与GenBank CDS报告基因的同一性为47 - 64%,类似于热狗折叠硫酯酶超家族中的那些基因。基于其氨基酸相似性和同源建模结构,我们推断该基因编码一种属于TE13家族的酶(ThYest_ar),对芳基辅酶A底物有偏好且具有新的催化残基组合。在大肠杆菌中的质粒再转化证实了该克隆的表型,并且对paaI大肠杆菌突变体的功能互补显示,作为碳源,对苯乙酸的偏好超过氯苯。这项工作表明TE13家族硫酯酶在苯乙酸的游动和降解途径中发挥作用。《蛋白质》2017年;85:1222 - 1237。©2017威利期刊公司。