J Gen Microbiol 1991, 137: 1511–1522 PubMed 37 Kleiner D, Paul W

J Gen AG-881 Microbiol 1991, 137: 1511–1522.PubMed 37. Kleiner D, Paul W, Merrick MJ: Construction of Multicopy Expression

Vectors for Regulated over-Production of Proteins in Klebsiella pneumoniae and Other Enteric Bacteria. J Gen Microbiol 1988, 134: 1779–1784.PubMed 38. Souza EM, Pedrosa FO, Rigo LU, Machado HB, Yates MG: Expression of the nifA gene of Herbaspirillum seropedicae : role of the NtrC and NifA binding sites and of the-24/-12 promoter element. Microbiology-Sgm 2000, 146: 1407–1418. 39. Simon R, Priefer U, Puhler A: A Broad Host Range Mobilization System for Invivo Genetic-Engineering selleck chemicals – Transposon Mutagenesis in Gram-Negative Bacteria. Bio-Technology 1983, 1 (9) : 784–791. 40. Souza EM, Funayama S, Rigo LU, Pedrosa FO: Cloning and Characterization of the nifA gene from Herbaspirillum seropedicae Strain Z78. Can J Microbiol 1991, 37 (6) : 425–429.PubMedCrossRef 41. Woodley P, Buck M, Kennedy C: Identification of sequences important for recognition of vnf genes by the VnfA transcriptional activator in Azotobacter vinelandii . FEMS Microbiol Lett 1996, 135 (2–3) : 213–221.PubMedCrossRef 42. Mead DA, Szczesna-Skorupa E, Kemper B: Single-stranded DNA ‘blue’ T7 promoter

plasmids: a versatile tandem promoter system for cloning and protein engineering. Protein Eng 1986, 1 (1) : 67–74.PubMedCrossRef Authors’ contributions LN constructed plasmids and H. seropedicae mutants, carried out physiological experiments and helped to draft the manuscript; ACB constructed plasmids and carried out immunoassays; RAM constructed plasmids and designed some of the experiments; LN, RAM and LUR helped to draft the manuscript; www.selleckchem.com/products/bay80-6946.html FOP, EMS, MBRS and LSC conceived the study, participated in its design and in writing

the manuscript, LSC also supervised the study. All authors read and approved the final manuscript.”
“Background A substantial amount of the genetic variation in bacteria is carried in plasmids [1]. Plasmids are part of the flexible genome, which is defined by the high plasticity and modularity of its genetic elements and high rates of gene acquisition and loss [2]. They are typically composed of conserved backbone modules coding for replication, Cediranib (AZD2171) maintenance and transfer functions as well as variable accessory modules. The capture of genetic modules by plasmid backbones can increase phenotypic diversity and thereby increase the chances of responding to uncertain environmental changes or of exploiting an opportunity for transient niche expansion [2, 3]. Plasmids are classified according to incompatibility (Inc) groups that are based on the inability of plasmids with the same replication or segregation mechanisms to co-exist in the same cell [4]. IncA/C plasmids have attracted the attention of the research community due to their ability to acquire antimicrobial resistance traits and to mobilize them across geographical and taxonomical borders [5].

Comments are closed.