PMID:2007545
| Citation |
Yoshimoto, T, Higashi, H, Kanatani, A, Lin, XS, Nagai, H, Oyama, H, Kurazono, K and Tsuru, D (1991) Cloning and sequencing of the 7 alpha-hydroxysteroid dehydrogenase gene from Escherichia coli HB101 and characterization of the expressed enzyme. J. Bacteriol. 173:2173-9 |
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| Abstract |
The 7 alpha-hydroxysteroid dehydrogenase (EC 1.1.1.159) gene from Escherichia coli HB101 was cloned and expressed in E. coli DH1. The hybrid plasmid pSD1, with a 2.8-kbp insert of chromosomal DNA at the BamHI site of pBR322, was subcloned into pUC19 to construct plasmid pSD3. The entire nucleotide sequence of an inserted PstI-BamHI fragment of plasmid pSD3 was determined by the dideoxy chain-termination method. Within this sequence, the mature enzyme protein-encoding sequence was found to start at a GTG initiation codon and to comprise 765 bp, as judged by comparison with the protein sequence. The deduced amino acid sequence of the enzyme indicated that the molecular weight is 26,778. The transformant of E. coli DH1 harboring pSD3 with a 1.8-kbp fragment showed about 200-fold-higher enzyme activity than the host. The enzyme was purified by a single chromatography step on DEAE-Toyopearl and obtained as crystals, with an activity yield of 39%. The purified enzyme was homogeneous, as judged by sodium dodecyl sulfate gel electrophoresis. The enzyme was most active at pH 8.5 and stable between pH 8 and 9. The enzyme was NAD+ dependent and had a pI of 4.3. The molecular mass was estimated to be 120 kDa by the gel filtration method and 28 kDa by electrophoresis, indicating that the enzyme exists in a tetrameric form. |
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| Keywords |
Amino Acid Sequence; Base Sequence; Cloning, Molecular; Crystallography; Escherichia coli/genetics; Genes, Bacterial; Hydroxysteroid Dehydrogenases/antagonists & inhibitors; Hydroxysteroid Dehydrogenases/chemistry; Hydroxysteroid Dehydrogenases/genetics; Hydroxysteroid Dehydrogenases/metabolism; Molecular Sequence Data; Molecular Weight; Restriction Mapping; Substrate Specificity |
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