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海洋源放线菌中产角蛋白酶的综合生物信息学分析

An Integrative Bioinformatic Analysis for Keratinase Detection in Marine-Derived .

机构信息

Laboratory of Molecular Microbiology and Environmental Biotechnology, Department of Chemistry and Center for Biotechnology Daniel Alkalay Lowitt, Federico Santa María Technical University, Valparaíso 2340000, Chile.

Millennium Initiative for Collaborative Research on Bacterial Resistance (MICROB-R), Santiago 8320000, Chile.

出版信息

Mar Drugs. 2021 May 21;19(6):286. doi: 10.3390/md19060286.

Abstract

Keratinases present promising biotechnological applications, due to their ability to degrade keratin. appears as one of the main sources of these enzymes, but complete genome sequences of keratinolytic bacteria are still limited. This article reports the complete genomes of three marine-derived streptomycetes that show different levels of feather keratin degradation, with high (strain G11C), low (strain CHD11), and no (strain Vc74B-19) keratinolytic activity. A multi-step bioinformatics approach is described to explore genes encoding putative keratinases in these genomes. Despite their differential keratinolytic activity, multiplatform annotation reveals similar quantities of ORFs encoding putative proteases in strains G11C, CHD11, and Vc74B-19. Comparative genomics classified these putative proteases into 140 orthologous groups and 17 unassigned orthogroup peptidases belonging to strain G11C. Similarity network analysis revealed three network communities of putative peptidases related to known keratinases of the peptidase families S01, S08, and M04. When combined with the prediction of cellular localization and phylogenetic reconstruction, seven putative keratinases from the highly keratinolytic strain sp. G11C are identified. To our knowledge, this is the first multi-step bioinformatics analysis that complements comparative genomics with phylogeny and cellular localization prediction, for the prediction of genes encoding putative keratinases in streptomycetes.

摘要

角蛋白酶具有有前途的生物技术应用,因为它们能够降解角蛋白。羽毛是这些酶的主要来源之一,但角蛋白降解细菌的完整基因组序列仍然有限。本文报道了三种海洋来源的链霉菌的完整基因组,它们对角蛋白的降解能力不同,具有高(菌株 G11C)、低(菌株 CHD11)和无(菌株 Vc74B-19)角蛋白降解活性。描述了一种多步骤生物信息学方法来探索这些基因组中编码潜在角蛋白酶的基因。尽管它们的角蛋白降解活性不同,但多平台注释显示菌株 G11C、CHD11 和 Vc74B-19 编码潜在蛋白酶的 ORF 数量相似。比较基因组学将这些潜在的蛋白酶分为 140 个直系同源群和 17 个未分配的直系同源群肽酶,属于菌株 G11C。相似性网络分析显示,与 S01、S08 和 M04 肽酶家族的已知角蛋白酶相关的三个潜在肽酶网络社区。当与细胞定位预测和系统发育重建相结合时,从高度角蛋白降解的菌株 sp. G11C 鉴定了 7 种潜在的角蛋白酶。据我们所知,这是首次将比较基因组学与系统发育和细胞定位预测相结合,用于预测链霉菌中编码潜在角蛋白酶的基因的多步骤生物信息学分析。

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