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Microbiology 151 (2005), 2793-2803; DOI  10.1099/mic.0.28123-0
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Microbiology 151 (2005), 2793-2803; DOI  10.1099/mic.0.28123-0
© 2005 Society for General Microbiology

Specific gene targeting in Spiroplasma citri: improved vectors and production of unmarked mutations using site-specific recombination

Sybille Duret, Aurélie André and Joël Renaudin

UMR 1090 Génomique Développement et Pouvoir Pathogène, INRA, Université de Bordeaux 2, Centre INRA de Bordeaux, 71 avenue Edouard Bourlaux, BP 81, 33883 Villenave d'Ornon Cedex, France

Correspondence
Joël Renaudin
renaudin{at}bordeaux.inra.fr

In Spiroplasma citri, where homologous recombination is inefficient, specific gene targeting could only be achieved by using replicative, oriC plasmids. To improve the probability of selecting rare recombination events without fastidious, extensive passaging of the transformants, a new targeting vector was constructed, which was used to inactivate the crr gene encoding the IIA component of the glucose phosphotransferase system (PTS) permease. Selection of recombinants was based on a two-step strategy using two distinct selection markers, one of which could only be expressed once recombination had occurred through one single crossover at the target gene. According to this strategy, spiroplasmal transformants were screened and multiplied in the presence of gentamicin before the crr recombinants were selected for their resistance to tetracycline. In contrast to the wild-type strain GII-3, the crr-disrupted mutant GII3-gt1 used neither glucose nor trehalose, indicating that in S. citri the glucose and trehalose PTS permeases function with a single IIA component. In addition, the feasibility of using the transposon {gamma}{delta} TnpR/res recombination system to produce unmarked mutations in S. citri was demonstrated. In an arginine deiminase (arcA-disrupted) mutant, the tetM gene flanked by the res sequences was efficiently excised from the chromosome through expression of the TnpR resolvase from a replicative oriC plasmid. Due to oriC incompatibility, plasmid loss occurred spontaneously when selection pressure was removed. This approach will be helpful for constructing unmarked mutations and generating multiple mutants with the same selection marker in S. citri. It should also be relevant to other species of mollicutes.


Abbreviations: ADI, arginine deiminase; CK, carbamate kinase; CDS, coding sequences; HNPP, 2-hydroxy-3-naphthoic acid-2'-phenylanilide phosphate; OTC, ornithine carbamoyltransferase; PPLO, pleuropneumonia-like organisms; PTS, phosphotransferase system




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