Identification of a promoter sequence in the plasmid pUL340 of Brevibacterium lactofermentum and construction of new cloning vectors for corynebacteria containing two selectable markers
A strong promoter P1 has been found in plasmid pUL340, a cloning vector used to transform corynebacteria. This promoter is also expressed efficiently in Escherichia coli. A gene ( cat) for chloramphenicol acetyltransferase from Streptomyces acrimycini and a gene ( hyg) for hygromycin phosphotransfer...
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Published in | Gene Vol. 56; no. 2; pp. 199 - 208 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Lausanne
Elsevier B.V
1987
Amsterdam Elsevier New York, NY |
Subjects | |
Online Access | Get full text |
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Summary: | A strong promoter
P1 has been found in plasmid pUL340, a cloning vector used to transform corynebacteria. This promoter is also expressed efficiently in
Escherichia coli. A gene (
cat) for chloramphenicol acetyltransferase from
Streptomyces acrimycini and a gene (
hyg) for hygromycin phosphotransferase from
Streptomyces hygroscopicus were subcloned in different positions of the
Brevibacterium lactofermentum plasmid pUL340. Both resistance genes are expressed in
B. lactofermentum from their own promoters or from the endogenous promoter in pUL340. These genes provide useful screening markers for selecting transformants of
B. lactofermentum together with the kanamycin-resistance gene from the transposon Tn
5. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0378-1119 1879-0038 |
DOI: | 10.1016/0378-1119(87)90137-5 |