Literature DB >> 9208485

Investigation of refolding condition for Pseudomonas fluorescens lipase by response surface methodology.

J H Ahn1, Y P Lee, J S Rhee.   

Abstract

Response Surface Methodology (RSM) was used to investigate optimal refolding conditions of Pseudomonas fluorescens lipase which was expressed as inclusion body in E. coli. Three interacting factors, protein concentration, pH and guanidine hydrochloride (GdnHCl) concentration were selected as the variables of RSM. The protein concentration did not affect the refolding yield within the selected range (50-340 micrograms ml-1) at low temperatures of 4 and -15 degrees C, but it was a critical factor at 25 degrees C and refolding yield significantly decreased with increasing protein concentration. The pH and GdnHCl were significant factors in all experimental conditions. But there was no trends of optimal pH depending on temperature and additives, just showing the optimum at neutral pH. Glycerol shifted optimal GdnHCl concentration to higher side, while arginine to lower side. Therefore, it was concluded that glycerol and arginine deprives and supplements GdnHCl, respectively. In this study, RSM made it possible to investigate successfully the optimal conditions of in vitro refolding and to elucidate interactions between refolding factors with a minimum number of experiments. Under the optimal condition determined by RSM, approximately 90% refolding yield was obtained and it was a 30% increase over the conventional method.

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Year:  1997        PMID: 9208485     DOI: 10.1016/s0168-1656(97)01693-3

Source DB:  PubMed          Journal:  J Biotechnol        ISSN: 0168-1656            Impact factor:   3.307


  6 in total

1.  A new protein folding screen: application to the ligand binding domains of a glutamate and kainate receptor and to lysozyme and carbonic anhydrase.

Authors:  N Armstrong; A de Lencastre; E Gouaux
Journal:  Protein Sci       Date:  1999-07       Impact factor: 6.725

2.  Homologous expression of the lipase and ABC transporter gene cluster, tliDEFA, enhances lipase secretion in Pseudomonas spp.

Authors:  J H Ahn; J G Pan; J S Rhee
Journal:  Appl Environ Microbiol       Date:  2001-12       Impact factor: 4.792

3.  Studies on the refolding process of recombinant horseradish peroxidase.

Authors:  Sedigheh Asad; Bahareh Dabirmanesh; Nasser Ghaemi; Seyed Masoud Etezad; Khosro Khajeh
Journal:  Mol Biotechnol       Date:  2013-06       Impact factor: 2.695

4.  Site-specific mutational analysis of a novel cysteine motif proposed to ligate the 4Fe-4S cluster in the iron-sulfur flavoprotein of the thermophilic methanoarchaeon Methanosarcina thermophila.

Authors:  U Leartsakulpanich; M L Antonkine; J G Ferry
Journal:  J Bacteriol       Date:  2000-10       Impact factor: 3.490

5.  Identification of the tliDEF ABC transporter specific for lipase in Pseudomonas fluorescens SIK W1.

Authors:  J H Ahn; J G Pan; J S Rhee
Journal:  J Bacteriol       Date:  1999-03       Impact factor: 3.490

6.  Strategies for the recovery of active proteins through refolding of bacterial inclusion body proteins.

Authors:  Luis Felipe Vallejo; Ursula Rinas
Journal:  Microb Cell Fact       Date:  2004-09-02       Impact factor: 5.328

  6 in total

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