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PMID: 6295886 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A cloning vector able to replicate in Escherichia coli and Streptococcus sanguis.

Gene ·Vol. 19 ·No. 3 ·1982-10-00 ·Pages 345-53

Macrina FL, Tobian JA, Jones KR, Evans RP, Clewell DB

Abstract

A plasmid that is able to replicate in both Escherichia coli and Streptococcus sanguis has been constructed by the in vitro joining of the pACYC184 (Cmr Tcr) and pVA749 (Emr) replicons. This plasmid, designated pVA838, is 9.2 kb in size and expresses Emr in both E. coli and S. sanguis. Its Cmr marker is expressed only in E. coli and may be inactivated by addition of DNA inserts at its internal EcoRI or PvuII sites. The pVA838 molecule also contains unique SalI, SphI, BamHI, NruI and XbaI cleavage sites suitable for molecular cloning. pVA838 may be amplified in E. coli but not in S. sanguis. We have used the pVA838 plasmid as a shuttle vector to clone streptococcal plasmid fragments in E. coli. Such chimeras isolated from E. coli were readily introduced into S. sanguis by transformation.

MeSH Terms
Base Sequence Cloning, Molecular DNA Replication DNA Restriction Enzymes Escherichia coli/genetics Phenotype Plasmids Species Specificity Streptococcus sanguis/genetics
Chemicals
DNA Restriction Enzymes
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Macrina F L
Tobian J A
Jones K R
Evans R P
Clewell D B
Article Info
Journal
Gene
Abbr.
Gene
ISSN
0378-1119
Published
1982-10-00
Pages
345-53
Language
English
Region
Netherlands
NLM ID
7706761
Subset
IM
Grants
NIAID NIH HHS · AI10318 · United States
NIDCR NIH HHS · DE02731 · United States
NIDCR NIH HHS · DE04224 · United States
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