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PMID: 1312983 Published · ppublish English Journal Article

Purification and N-terminal amino acid sequences of two polypeptides encoded by the mcrB gene from Escherichia coli K-12.

Gene ·Vol. 112 ·No. 1 ·1992-03-01 ·Pages 97-100

Zheng L, Wang X, Braymer HD

Abstract

This report provides a purification method for the two proteins, 51 kDa and 33 kDa, both encoded by the same mcrB gene of the McrBC restriction system in Escherichia coli K-12. The two proteins were produced in large quantity using a T7 expression system and copurified to near homogeneity by DEAE-Sepharose and Affi-Gel blue column chromatography. The N-terminal amino acid sequences of these purified McrB proteins were the same as those predicted from the mcrB DNA sequence by Ross et al. [J. Bacteriol. 171 (1989b) 1974-1981]. The 33-kDa protein totally overlaps the C-terminal part of the 51-kDa protein.

Related Genes
MeSH Terms
Amino Acid Sequence Chromatography DNA Restriction Enzymes/chemistry,genetics,isolation & purification DNA-Cytosine Methylases/chemistry,genetics,isolation & purification Escherichia coli/genetics Escherichia coli Proteins Genetic Vectors/genetics Molecular Sequence Data T-Phages/genetics
Chemicals
Escherichia coli Proteins DNA modification methylase McrB DNA-Cytosine Methylases DNA Restriction Enzymes mcrB protein, E coli
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Zheng L
Department of Microbiology, Louisiana State University, Baton Rouge 70803.
Wang X
Braymer H D
Article Info
Journal
Gene
Abbr.
Gene
ISSN
0378-1119
Published
1992-03-01
Pages
97-100
Language
English
Region
Netherlands
NLM ID
7706761
Subset
IM
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