Literature DB >> 33128766

(Hyper)Thermophilic Enzymes: Production and Purification.

Pierpaolo Falcicchio1, Mark Levisson1, Servé W M Kengen1, Sotirios Koutsopoulos2, John van der Oost1.   

Abstract

The discovery of thermophilic and hyperthermophilic microorganisms, thriving at environmental temperatures near or above 100 °C, has revolutionized our ideas about the upper temperature limit at which life can exist. The characterization of (hyper)thermostable proteins has broadened our understanding and presented new opportunities for solving one of the most challenging problems in biophysics: how are structural stability and biological function maintained at high temperatures where "normal" proteins undergo dramatic structural changes? In our laboratory, we have purified and studied many thermostable and hyperthermostable proteins in an attempt to determine the molecular basis of heat stability. Here, we present methods to express such proteins and enzymes in E. coli and provide a general protocol for overproduction and purification. The ability to produce enzymes that retain their stability and activity at elevated temperatures creates exciting opportunities for a wide range of biocatalytic applications.

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Keywords:  Biocatalysis; Heterologous production; His-tag; Immobilized metal affinity chromatography (IMAC); Protein purification; Size exclusion chromatography (SEC); Thermal stability; Thermozymes

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Year:  2021        PMID: 33128766     DOI: 10.1007/978-1-0716-0775-6_29

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  Identification, characterization and hydrolase producing performance of thermophilic bacteria: geothermal hot springs in the Eastern and Southeastern Anatolia Regions of Turkey.

Authors:  Orhan Ulucay; Arzu Gormez; Cem Ozic
Journal:  Antonie Van Leeuwenhoek       Date:  2022-01-15       Impact factor: 2.271

  1 in total

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