Construction of plasmid vectors for screening replicons from gram-positive bacteria and their use as shuttle cloning vectors.

Abstract:

:Plasmids play a central role in engineering recombinant bacteria because they are the primary vehicles used to manipulate targeted sequences. In some cases, bacteria of interest are poorly provided with suitable tools for these molecular or genetic manipulations. In this context, we constructed from two shuttle cloning vectors, pUCB2871 and pUCB2872, the basic vectors pUCB30 and pUCB31, which could represent suitable tools to isolate replicons from Gram-positive bacteria. These plasmid vectors are characterized by the following after-features: (a) the pUC origin of replication is unable to replicate in Gram-positive bacteria; (b) an erythromycin-resistance encoding gene that is functional in both Gram-negative and -positive bacteria; (c) the pUC19 multiple cloning site (MCS) within the lacZalpha reporter gene; and (4) an additional multiple cloning site (MCS). Cloning replicons from Gram-positive bacteria in this additional MCS would allow the derivative vectors to function directly as shuttle cloning vectors.

journal_name

Curr Microbiol

journal_title

Current microbiology

authors

Benachour A,Auffray Y,Hartke A

doi

10.1007/s00284-006-0358-1

subject

Has Abstract

pub_date

2007-05-01 00:00:00

pages

342-7

issue

5

eissn

0343-8651

issn

1432-0991

journal_volume

54

pub_type

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