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The specificity of ParR binding determines the compatibility of conjugative plasmids in Clostridium perfringens

biorxiv. 2018; 
 View Thomas D. Watts,   View Daouda A.K. Traore,  Sarah C. Atkinson,  Carmen Lao,  Natalie Caltabiano,  Julian I. Rood,   View Vicki Adams
Products/Services Used Details Operation
Gene Synthesis The parRC gene from pCW3 was codon optimised for expression in E. coli, synthesised by GenScript and cloned into the EcoRV site of pUC57-Kan. Codon optimised parRCthen was subcloned into the NdeI/XhoI sites of pET22b(+). parRD(pJIR3118) was PCR amplified from CN1020 gDNA isolated as before (O’Connor et al., 2006) and cloned into the NdeI/Xhol site of pET22b (+) for expression. parRB(pJIR4165), parRB(pJGS1987B) parRC(pJGS1987C) and parRD(pJGS1987D) were codon optimised and synthesised before being cloned into pET22b(+) NdeI/XhoI sites by GenScript. Get A Quote

摘要

Plasmids that encode the same replication machinery are generally unable to coexist in the same bacterial cell. However, Clostridium perfringens strains often carry multiple conjugative toxin or antibiotic resistance plasmids that are closely related and encode similar Rep proteins. In many bacteria, plasmid partitioning upon cell division involves a ParMRC system and there are ~10 different ParMRC families in C. perfringens, with differences in amino acid sequences between each ParM family (15% − 54% identity). Since plasmids encoding genes belonging to the same ParMRC family are not observed in the same strain, these families appear to represent the basis for plasmid compatibility in C. perfringens. To ... More

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