Abstract
Transposon Tn501-originated mercury resistance determinant (mer operon) located in plasmid pHP45Ω-Hg was subcloned into plasmid pJF118EH, containing the tac promoter, and was subsequently transformed into Escherichia coli VJS632QA. The resulting recombinant strain E. coli PWS1 tolerated Hg2+ concentration up to 80 mg/L and exhibited higher specific mercury reduction activity. The expression of mer operon in E. coli PWS1 was affected by inducers IPTG and mercuric ions.
Original language | English |
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Pages (from-to) | 265-274 |
Number of pages | 10 |
Journal | Journal of the Chinese Institute of Chemical Engineers |
Volume | 29 |
Issue number | 4 |
Publication status | Published - 1998 Jul |
All Science Journal Classification (ASJC) codes
- General Chemistry
- General Chemical Engineering