| [1] WHO. Worl Health Organization Report 2010, Global tuberculosis control. 2010.[2] Machowski EE, Dawes S, Mizrahi V. TB tools to tell the tale-molecular genetic methods for mycobacterial research. Int J Biochem Cell Biol, 2005, 37(1): 54-68.[3] Muttucumaru DG, Parish T. The molecular biology of recombination in Mycobacteria: what do we know and how can we use it? Curr Issues Mol Biol, 2004, 6(2): 145-157.[4] Bardarov S, Kriakov J, Carriere C, Yu SW, Vaamonde C, McAdam RA, Bloom BR, Hatfull GF, Jacobs WR Jr. Conditionally replicating mycobacteriophages: a system for transposon delivery to Mycobacterium tuberculosis. Proc Natl Acad Sci USA, 1997, 94(20): 10961-10966.[5] Guilhot C, Gicquel B, Martín C. Temperature-sensitive mutants of the mycobacterium plasmid pAL5000. FEMS Microbiol Lett, 1992, 77(1-3): 181-186.[6] Pelicic V, Reyrat JM, Gicquel B. Generation of unmarked directed mutations in mycobacteria, using sucrose counter- selectable suicide vectors. Mol Microbiol, 1996, 20(5): 919-925.[7] Pelicic V, Reyrat JM, Gicquel B. Positive selection of allelic exchange mutants in Mycobacterium bovis BCG. FEMS Microbiol Lett, 1996, 144(2-3): 161-166.[8] Pelicic V, Reyrat JM, Gicquel B. Genetic advances for studying Mycobacterium tuberculosis pathogenicity. Mol Microbiol, 1998, 28(3): 413-420.[9] Reyrat JM, Berthet FX, Gicquel B. The urease locus of Mycobacterium tuberculosis and its utilization for the demonstration of allelic exchange in Mycobacterium bovis bacillus Calmette-Guérin. Proc Natl Acad Sci USA, 1995, 92(19): 8768-8772.[10] Parish T, Stoker NG. Use of a flexible cassette method to generate a double unmarked Mycobacterium tuberculosis tlyA plcABC mutant by gene replacement. Microbiology, 2000, 146(Pt 8): 1969-1975.[11] Parish T, Gordhan BG, McAdam RA, Duncan K, Mizrahi V, Stoker NG. Production of mutants in amino acid biosynthesis genes of Mycobacterium tuberculosis by homologous recombination. Microbiology, 1999, 145(Pt 12): 3497-3503.[12] Balhana R, Stoker NG, Sikder MH, Chauviac FX, Kendall SL. Rapid construction of mycobacterial mutagenesis vectors using ligation-independent cloning. J Microbiol Methods, 2010, 83(1): 34-41.[13] Hasan N, Koob M, Szybalski W. Escherichia coli genome targeting, I. Cre-lox-mediated in vitro generation of ori plasmids and their in vivo chromosomal integration and retrieval. Gene, 1994, 150(1): 51-56.[14] Tsuda M. Use of a transposon-encoded site-specific resolution system for construction of large and defined deletion mutations in bacterial chromosome. Gene, 1998, 207(1): 33-41.[15] Merlin C, McAteer S, Masters M. Tools for characterization of Escherichia coli genes of unknown function. J Bacteriol, 2002, 184(16): 4573-4581.[16] Reed RR. Transposon-mediated site-specific recombination: a defined in vitro system. Cell, 1981, 25(3): 713-719.[17] Stephan J, Stemmer V, Niederweis M. Consecutive gene deletions in Mycobacterium smegmatis using the yeast FLP recombinase. Gene, 2004, 343(1): 181-190.[18] Song HH, Niederweis M. Functional expression of the Flp recombinase in Mycobacterium bovis BCG. Gene, 2007, 399(2): 112-119.[19] Malaga W, Perez E, Guilhot C. Production of unmarked mutations in mycobacteria using site-specific recombination. FEMS Microbiol Lett, 2003, 219(2): 261-268.[20] Bloor AE, Cranenburgh RM. An efficient method of selectable marker gene excision by Xer recombination for gene replacement in bacterial chromosomes. Appl Environ Microbiol, 2006, 72(4): 2520-2525.[21] Hendrickson H, Lawrence JG. Mutational bias suggests that replication termination occurs near the dif site, not at Ter sites. Mol M |
