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本文引用的文献
1
Cloning and expression of Saccharomyces cerevisiae copper-metallothionein gene in Escherichia coli and characterization of the recombinant protein.
Eur J Biochem. 1993 Mar 1;212(2):521-8. doi: 10.1111/j.1432-1033.1993.tb17689.x.
2
The role of cysteine residues in the transport of mercuric ions by the Tn501 MerT and MerP mercury-resistance proteins.
Mol Microbiol. 1995 Jul;17(1):25-35. doi: 10.1111/j.1365-2958.1995.mmi_17010025.x.
3
Culture medium for enterobacteria.
J Bacteriol. 1974 Sep;119(3):736-47. doi: 10.1128/jb.119.3.736-747.1974.
4
Efficient expression of the yeast metallothionein gene in Escherichia coli.
J Bacteriol. 1988 Jan;170(1):21-6. doi: 10.1128/jb.170.1.21-26.1988.
5
Single-step purification of polypeptides expressed in Escherichia coli as fusions with glutathione S-transferase.
Gene. 1988 Jul 15;67(1):31-40. doi: 10.1016/0378-1119(88)90005-4.
6
High efficiency transformation of E. coli by high voltage electroporation.
Nucleic Acids Res. 1988 Jul 11;16(13):6127-45. doi: 10.1093/nar/16.13.6127.
7
Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors.
Gene. 1985;33(1):103-19. doi: 10.1016/0378-1119(85)90120-9.
8
Low copy number plasmids for regulated low-level expression of cloned genes in Escherichia coli with blue/white insert screening capability.
Nucleic Acids Res. 1990 Aug 11;18(15):4631. doi: 10.1093/nar/18.15.4631.
9
Expression of the pea gene PSMTA in E. coli. Metal-binding properties of the expressed protein.
FEBS Lett. 1991 Nov 4;292(1-2):48-52. doi: 10.1016/0014-5793(91)80831-m.
10
Purification and functional characterization of MerD. A coregulator of the mercury resistance operon in gram-negative bacteria.
J Biol Chem. 1991 Oct 5;266(28):18538-42.
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