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PMID: 3074013 Published · ppublish English Journal Article Review

Cloning type-II restriction and modification genes.

Gene ·Vol. 74 ·No. 1 ·1988-12-25 ·Pages 25-32

Lunnen KD, Barsomian JM, Camp RR, Card CO, Chen SZ, Croft R, Looney MC, Meda MM, Moran LS, Nwankwo DO

Abstract

We have cloned into Escherichia coli the genes for 38 type-II bacterial modification methyltransferases. The clones were isolated by selecting in vitro for protectively modified recombinants. Most of the clones modify their DNA fully but a substantial number modify only partially. In approximately one-half of the clones, the genes for the corresponding endonucleases are also present. Some of these clones restrict infecting phages and others do not. Clones carrying endonuclease genes but lacking methyltransferase genes have been found, in several instances, to be viable.

MeSH Terms
Bacterial Proteins/genetics Cloning, Molecular/methods DNA Modification Methylases/genetics DNA, Bacterial/metabolism DNA, Viral/metabolism Deoxyribonucleases, Type II Site-Specific/genetics Escherichia coli/genetics Genes, Bacterial Recombinant Proteins/genetics
Chemicals
Bacterial Proteins DNA, Bacterial DNA, Viral Recombinant Proteins DNA Modification Methylases Deoxyribonucleases, Type II Site-Specific
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Lunnen K D
New England Biolabs, Inc., Beverly, MA 01915.
Barsomian J M
Camp R R
Card C O
Chen S Z
Croft R
Looney M C
Meda M M
Moran L S
Nwankwo D O
Article Info
Journal
Gene
Abbr.
Gene
ISSN
0378-1119
Published
1988-12-25
Pages
25-32
Language
English
Region
Netherlands
NLM ID
7706761
Subset
IM
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