|
|
||||||||
Genetics and Molecular Biology |
Laboratoire de Biologie Cellulaire et Moléculaire, Institut de Biologie Végétale Moléculaire, Institut National de la Recherche Agronomique and Université Victor Segalen Bordeaux 2, Domaine de la Grande Ferrade, BP 81, 33883 Villenave dOrnon cedex, France1
Author for correspondence: Frédéric Laigret. Tel: +33 5 56 84 31 50. Fax: +33 5 56 84 31 59. e-mail: laigret{at}bordeaux.inra.fr
Fructose-negative mutants of Spiroplasma citri wild-type strain GII-3 were selected by two methods. The first method is based on the selection of spontaneous xylitol-resistant mutants, xylitol being a toxic fructose analogue. Five such mutants were obtained, but only one, xyl3, was unable to use fructose and had no phosphoenolpuryvate:fructose phosphotransferase system (fructose-PTS) activity. Amplification and sequencing of the fructose permease gene of mutant xyl3 revealed the presence of an adenylic insertion leading to a truncated permease. The second method is based on inactivation of fruA and/or fruK by homologous recombination involving one crossing-over between the chromosomal genes and inactivated genes carried by replicative plasmids. Fructose-negative mutants were obtained at a frequency of about 10%. Fructose-PTS activity and 1-phosphofructokinase activity were not detected in four representative mutants that were characterized (H31, H45, E38 and E53). In strain H31, Southern blot analysis and PCR showed that the result of homologous recombination was, as expected, the presence in the chromosome of two mutated fruAfruK copies with the plasmid sequence in between. Only the mutated copy, under control of the fructose operon promoter, was transcribed. This work describes for the first time the use of two methods to obtain fructose-auxotrophic mutants of S. citri. The method involving homologous recombination is a general procedure for gene disruption in S. citri.
Keywords: Spiroplasma citri, fructose operon, xylitol, gene disruption
Abbreviations: 1-PFK, 1-phosphofructokinase; 6-PFK, 6-phosphofructokinase; fructose-PTS, phosphoenolpyruvate:fructose phosphotransferase system; XylR, xylitol resistant; wt, wild-type
The GenBank accession number for the sequence reported in this paper is AF202665.
This article has been cited by other articles:
![]() |
S. Duret, A. Andre, and J. Renaudin Specific gene targeting in Spiroplasma citri: improved vectors and production of unmarked mutations using site-specific recombination Microbiology, August 1, 2005; 151(8): 2793 - 2803. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Janis, C. Lartigue, J. Frey, H. Wroblewski, F. Thiaucourt, A. Blanchard, and P. Sirand-Pugnet Versatile Use of oriC Plasmids for Functional Genomics of Mycoplasma capricolum subsp. capricolum Appl. Envir. Microbiol., June 1, 2005; 71(6): 2888 - 2893. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Duret, N. Berho, J.-L. Danet, M. Garnier, and J. Renaudin Spiralin Is Not Essential for Helicity, Motility, or Pathogenicity but Is Required for Efficient Transmission of Spiroplasma citri by Its Leafhopper Vector Circulifer haematoceps Appl. Envir. Microbiol., October 1, 2003; 69(10): 6225 - 6234. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. M. Teachman, C. T. French, H. Yu, W. L. Simmons, and K. Dybvig Gene Transfer in Mycoplasma pulmonis J. Bacteriol., February 15, 2002; 184(4): 947 - 951. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. B. Monteiro, D. C. Teixeira, R. R. Palma, M. Garnier, J.-M. Bové, and J. Renaudin Stable Transformation of the Xylella fastidiosa Citrus Variegated Chlorosis Strain with oriC Plasmids Appl. Envir. Microbiol., May 1, 2001; 67(5): 2263 - 2269. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| INT J SYST EVOL MICROBIOL | MICROBIOLOGY | J GEN VIROL |
| J MED MICROBIOL | ALL SGM JOURNALS | |