Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/4052
Title: Molecular cloning, overexpression and characterization of thermostable esterase and lipase from thermophilic bacillus sp.
Authors: Şanlı Mohamed, Gülşah
Tekedar, Hasan Cihad
Issue Date: 2009
Publisher: Izmir Institute of Technology
Abstract: The organisms that reside in hot places called thermophiles become very useful tool for biotechnology. The natural consequence of adapting to hot environments for thermophiles is encoding thermostable enzymes which make them a target for scientists.We have aimed to use microorganisms that were previously isolated and characterized as a Bacillus sp. from Balçova Geotermal region in İzmir for their lipase and esterase activity. In order to measure esterase and lipase activity, the strains were incubated in the media that contain the detergent tween 20 and media containing rhodamin-B, respectively. Three strains out of almost 110 bacterial strains have displayed high lipase and esterase activity at the same time. Three different esterase (Est1, Est2, Est3) and two different lipase (Lip1, Lip2) from different environmental samples were cloned directly by PCR amplification using consensus degenerate primers from genomic DNA. The deduced amino acid sequence of the three types of esterase gene exhibited similar amino acid sequence identity with few amino acid differences. However sequenced lipase genes were complicated to explain so that characterization studies have been made for only esterases.For over expression in Escherichia coli, the esterase genes and lipase genes were sub-cloned in pET28a vector with a strong T7 promoter. A one step purification of the recombinant esterases and lipases was achieved using His-Select HF nickel affinity gel.Enzyme assays using variety of p-nitrophenyl (p-NP) esters with different acyl chain lengths (C2-C16) as the substrate have confirmed the esterase activity.All three esterase showed a very high specific activity toward all tested p-NP esters. Optimum pH and temperature, stability in terms of pH and temperature, the effect of several metal ions, inhibitors and detergents on activity were determined for purified Est1, Est2, Est3 separately and compared to each other.
Description: Thesis (Master)--Izmir Institute of Technology, Biotechnology, Izmir, 2009
Includes bibliographical references (leaves: 45-50)
Text in English; Abstract: Turkish and English
xi, 53 leaves
URI: http://hdl.handle.net/11147/4052
Appears in Collections:Master Degree / Yüksek Lisans Tezleri

Files in This Item:
File Description SizeFormat 
T000804.pdfMasterThesis1.98 MBAdobe PDFThumbnail
View/Open
Show full item record



CORE Recommender

Page view(s)

28
checked on Dec 11, 2023

Download(s)

18
checked on Dec 11, 2023

Google ScholarTM

Check





Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.