A method for site-directed transplacement of in vitro altered DNA sequences in Rhizobium

Abstract

A method that directs transplacement of in vitro altered DNA sequences to substitute the corresponding wild-type DNA sequences at the original location in the Rhizobium genome is described. The NPTII gene of transposon Tn5 which confers resistance to several antibiotics in a wide variety of organisms is used as a selectable marker on the vector. To generate DNA fragment substitution, it is not essential to place a selectable genetic marker directly linked to the in vitro altered region of the DNA fragment. The method utilizes the vector pSUP201 that replicates in E. coli but neither in Rhizobium nor in many other host systems. DNA transplacement occurs by the integration of the in vitro altered DNA fragment at its homologous site in the chromosome along with the vector. A duplicated target sequence is generated, which is then followed by a homologous recombination event between the duplicated DNA sequences leading to the excision of the vector carrying the selectable marker together with one of the duplicated copies of DNA. The excised DNA fragment is subsequently lost due to the inability of the vector pSUP201 to replicate in Rhizobium. Using this method, we have transplaced a nif DNA fragment containing a large deletion of approximately 9 Kb into its homologous site in the genome of cowpea Rhizobium IRc78. The IRc78 strain carrying the deletion forms nodules on host-plants but is unable to reduce atmospheric nitrogen. The method allows precise alterations of the genomic DNA in an organism that is genetically not well characterized, provided a vector carrying a selectable marker can be transferred.