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利用基因组学和生化工具发现新型纤维小体纤维素酶的方法

Methods for Discovery of Novel Cellulosomal Cellulases Using Genomics and Biochemical Tools.

作者信息

Ben-David Yonit, Dassa Bareket, Bensoussan Lizi, Bayer Edward A, Moraïs Sarah

机构信息

Department of Biomolecular Sciences, The Weizmann Institute of Science, Rehovot, Israel.

Department of Immunology, The Weizmann Institute of Science, Rehovot, Israel.

出版信息

Methods Mol Biol. 2018;1796:67-84. doi: 10.1007/978-1-4939-7877-9_6.

Abstract

Cell wall degradation by cellulases is extensively explored owing to its potential contribution to biofuel production. The cellulosome is an extracellular multienzyme complex that can degrade the plant cell wall very efficiently, and cellulosomal enzymes are therefore of great interest. The cellulosomal cellulases are defined as enzymes that contain a dockerin module, which can interact with a cohesin module contained in multiple copies in a noncatalytic protein, termed scaffoldin. The assembly of the cellulosomal cellulases into the cellulosomal complex occurs via specific protein-protein interactions. Cellulosome systems have been described initially only in several anaerobic cellulolytic bacteria. However, owing to ongoing genome sequencing and metagenomic projects, the discovery of novel cellulosome-producing bacteria and the description of their cellulosomal genes have dramatically increased in the recent years. In this chapter, methods for discovery of novel cellulosomal cellulases from a DNA sequence by bioinformatics and biochemical tools are described. Their biochemical characterization is also described, including both the enzymatic activity of the putative cellulases and their assembly into mature designer cellulosomes.

摘要

由于纤维素酶对生物燃料生产的潜在贡献,其对细胞壁的降解作用已得到广泛研究。纤维小体是一种细胞外多酶复合物,能够非常高效地降解植物细胞壁,因此纤维小体酶备受关注。纤维小体纤维素酶被定义为含有dockerin模块的酶,该模块可与非催化蛋白(称为支架蛋白)中多个拷贝所含的cohesin模块相互作用。纤维小体纤维素酶组装成纤维小体复合物是通过特定的蛋白质 - 蛋白质相互作用实现的。最初,纤维小体系统仅在几种厌氧纤维素分解细菌中被描述。然而,由于正在进行的基因组测序和宏基因组项目,近年来新型纤维小体产生菌的发现及其纤维小体基因的描述显著增加。在本章中,将介绍通过生物信息学和生化工具从DNA序列中发现新型纤维小体纤维素酶的方法。还将描述它们的生化特性,包括推定纤维素酶的酶活性及其组装成成熟的设计纤维小体。

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