期刊论文详细信息
Biology
Novel Cold-Adapted Esterase MHlip from an Antarctic Soil Metagenome
Renaud Berlemont3  Olivier Jacquin3  Maud Delsaute3  Marcello La Salla3  Jacques Georis1  Fabienne Verté2  Moreno Galleni3 
[1] Puratos Group, Rue Bourrie 12, Andenne, Belgium; E-Mail:;Puratos Group, Industrielaan 25, Groot-Bijgarden, Belgium; E-Mail:;Laboratory of Biological Macromolecules, Centre for Protein Engineering, University of Liège, Institut de Chimie B6a, Liège, Sart-Tilman (4000), Belgium; E-Mails:
关键词: α/β hydrolase;    lipolytic enzymes;    metagenomics;    p-nitrophenyl-ester;    cold-adaptation;   
DOI  :  10.3390/biology2010177
来源: mdpi
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【 摘 要 】

An Antarctic soil metagenomic library was screened for lipolytic enzymes and allowed for the isolation of a new cytosolic esterase from the α/β hydrolase family 6, named MHlip. This enzyme is related to hypothetical genes coding esterases, aryl-esterases and peroxydases, among others. MHlip was produced, purified and its activity was determined. The substrate profile of MHlip reveals a high specificity for short p-nitrophenyl-esters. The apparent optimal activity of MHlip was measured for p-nitrophenyl-acetate, at 33 °C, in the pH range of 6–9. The MHlip thermal unfolding was investigated by spectrophotometric methods, highlighting a transition (Tm) at 50 °C. The biochemical characterization of this enzyme showed its adaptation to cold temperatures, even when it did not present evident signatures associated with cold-adapted proteins. Thus, MHlip adaptation to cold probably results from many discrete structural modifications, allowing the protein to remain active at low temperatures. Functional metagenomics is a powerful approach to isolate new enzymes with tailored biophysical properties (e.g., cold adaptation). In addition, beside the ever growing amount of sequenced DNA, the functional characterization of new catalysts derived from environment is still required, especially for poorly characterized protein families like α/β hydrolases.

【 授权许可】

CC BY   
© 2013 by the authors; licensee MDPI, Basel, Switzerland.

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