Abstract
The McrC protein, encoded by one of the two genes involved in the McrB restriction system, was produced in Escherichia coli cells by using a T7 expression system. Following sequential DEAE-Sepharose and hydroxylapatite column chromatography, the protein was purified to apparent homogeneity as judged by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The N-terminal amino acid sequence of the purified McrC protein agreed exactly with the one deduced from the DNA sequence by Ross et al. (J. Bacteriol. 171:1974-1981, 1989).
MeSH Terms
Autoradiography
Bacterial Proteins/biosynthesis,isolation & purification
DNA Restriction Enzymes
DNA-Cytosine Methylases/genetics
Electrophoresis, Polyacrylamide Gel
Escherichia coli/metabolism
Escherichia coli Proteins
Open Reading Frames
Plasmids
Restriction Mapping
Chemicals
Bacterial Proteins
Escherichia coli Proteins
mcrC protein, E coli
DNA modification methylase McrB
DNA-Cytosine Methylases
DNA Restriction Enzymes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Zheng L
Department of Microbiology, Louisiana State University, Baton Rouge 70803.
Braymer H D
References (11)
11 references, click to expand
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