Abstract:
:Bacterial cells containing the ner gene of phage Mu inserted into pBR322 express a binding activity with specificity for the left-end EcoRI.C fragment of Mu DNA. Crude extracts containing either Mu repressor or ner protein have been used to localize binding sites on TaqI subfragments of the EcoRI.C fragment. There are at least 3 distinct binding sites for the Mu repressor and 1 binding site for the ner protein on the EcoRI. C fragment. The possible biological function of these binding sites is discussed.
journal_name
FEBS Lettjournal_title
FEBS lettersauthors
Barlach S,Schumann Wdoi
10.1016/0014-5793(83)81128-4subject
Has Abstractpub_date
1983-06-27 00:00:00pages
119-23issue
1eissn
0014-5793issn
1873-3468pii
0014-5793(83)81128-4journal_volume
157pub_type
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