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Cloning, expression, and characterization of Aureobasidium melanogenum lipase in Pichia pastoris
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Document Title
Cloning, expression, and characterization of Aureobasidium melanogenum lipase in Pichia pastoris
Author
Wongwatanapaiboon J, Klinbunga S, Ruangchainikom C, Thummadetsak G, Chulalaksananukul S, Marty A, Chulalaksananukul W
Name from Authors Collection
Affiliations
Chulalongkorn University; Chulalongkorn University; National Science & Technology Development Agency - Thailand; National Center Genetic Engineering & Biotechnology (BIOTEC); Chulalongkorn University; PTT Public Company Limited; Mahidol University; Centre National de la Recherche Scientifique (CNRS); CNRS - Institute of Physics (INP); Universite de Toulouse; Universite Federale Toulouse Midi-Pyrenees (ComUE); Institut National des Sciences Appliquees de Toulouse; Universite Toulouse III - Paul Sabatier; Institut National Polytechnique de Toulouse; Centre National de la Recherche Scientifique (CNRS); CNRS - Institute for Engineering & Systems Sciences (INSIS); Universite de Toulouse; Universite Federale Toulouse Midi-Pyrenees (ComUE); Institut National des Sciences Appliquees de Toulouse; INRAE; Universite de Toulouse; Universite Federale Toulouse Midi-Pyrenees (ComUE); Institut National des Sciences Appliquees de Toulouse; Centre National de la Recherche Scientifique (CNRS); Chulalongkorn University; Chulalongkorn University
Type
Article
Source Title
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
Year
2016
Volume
80
Issue
11
Page
2231-2240
Open Access
Bronze
Publisher
TAYLOR & FRANCIS LTD
DOI
10.1080/09168451.2016.1206809
Format
Abstract
cDNA of Aureobasidium melanogenum lipase comprises 1254bp encoding 417 amino acids, whereas genomic DNA of lipase comprises 1311bp with one intron (57bp). The lipase gene contains a putative signal peptide encoding 26 amino acids. The A. melanogenum lipase gene was successfully expressed in Pichia pastoris. Recombinant lipase in an inducible expression system showed the highest lipase activity of 3.8 U/mL after six days of 2% v/v methanol induction. The molecular mass of purified recombinant lipase was estimated as 39kDa using SDS-PAGE. Optimal lipase activity was observed at 35-37 degrees C and pH 7.0 using p-nitrophenyl laurate as the substrate. Lipase activity was enhanced by Mg2+, Mn2+, Li+, Ca2+, Ni2+, CHAPS, DTT, and EDTA and inhibited by Hg2+, Ag+, SDS, Tween 20, and Triton X-100. The addition of 10% v/v acetone, DMSO, p-xylene, and octanol increased lipase activity, whereas that of propanol and butanol strongly inhibited it.
Keyword
Aureobasidium melanogenum | Expression | Lipase | Pichia pastoris
Industrial Classification
Knowledge Taxonomy Level 1
Knowledge Taxonomy Level 2
Knowledge Taxonomy Level 3
Funding Sponsor
Development and Promotion of Science and Technology Talents Project (DPST); Institute for the Promotion of Teaching Science and Technology (IPST)
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Copyright
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Publication Source
WOS