Back to Search
Start Over
Cloning and GST-fused expression in E. coli of mouse beta-1,4-galactosyltransferase.
- Source :
-
Journal of Zhejiang University. Science [J Zhejiang Univ Sci] 2004 Feb; Vol. 5 (2), pp. 164-72. - Publication Year :
- 2004
-
Abstract
- Beta-1,4-galactosyltransferase (beta4Gal-T) (EC 2.4.1.38) plays a multifunctional role in many aspects of normal cell physiology. By now, several dozens of beta4Gal-T genes have been cloned, separated from mouse, chick, bovine, human, etc. This paper presents the cloning and GST-fused expression of mouse beta4Gal-T gene in Escherichia coli (E. coli). The target gene was cloned by PCR, followed by identification by DNA sequencing and expression in E.coli with isopropyl-beta-D-thiogalactoside (IPTG) gradient concentrations, products of which were separated on SDS-PAGE showing that the target protein had the same molecular weight as that of mouse beta4Gal-T. The transcriptional product of beta4Gal-T gene was proved by Western hybridization analysis to be due to GST-fusion.
- Subjects :
- Amino Acid Sequence
Animals
Gene Expression Regulation, Bacterial physiology
Gene Expression Regulation, Enzymologic physiology
Mice
Molecular Sequence Data
Molecular Weight
N-Acetyllactosamine Synthase chemistry
Phylogeny
Recombinant Fusion Proteins biosynthesis
Sequence Homology, Amino Acid
Transfection methods
Cloning, Molecular methods
Escherichia coli enzymology
Escherichia coli genetics
Glutathione Transferase biosynthesis
Glutathione Transferase genetics
N-Acetyllactosamine Synthase biosynthesis
N-Acetyllactosamine Synthase genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1009-3095
- Volume :
- 5
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Journal of Zhejiang University. Science
- Publication Type :
- Academic Journal
- Accession number :
- 14674027
- Full Text :
- https://doi.org/10.1007/BF02840918