Проблемы и перспективы молекулярной генетики. Том 1 - Свердлов Е.Д.
ISBN 5-02-002753-7
Скачать (прямая ссылка):
Lomovskaya O.L., Mindlin S.Z., Gorlenko Zh.M., Khesin R.B. A nonconjugative mobilizable broad host range plasmid of Acinetobacter sp., that determines HgCl2 resistance // Mol. and Gen. Genet. 1986. Vol. 202. P. 286-290.
Lorenz M.G., Wackernagel W. Bacterial gene transfer by natural genetic transformation in the environment // Microbiol. Rev. 1994. Vol. 58. P. 563-602.
Mahler /.. Levinson H.S., Wang Y., Halvorson И.О. Cadmium- and mercury-resistant Bacillus strains from a salt marsh and from Boston Harbor// Appl. Environ. Microbiol. 1986. Vol. 52. P. 1293-1298.
Mazodier P., Davies J. Gene transfer between distantly related bacteria// Annu. Rev. Genet 1991. Vol. 25. P. 147-171.
Maynard Smith J., Dowson C.G., Spratt B.G. Localized sex in bacteria // Nature. 1991. Vol. 349. P. 29-31.
Minakhina S., Kholodii G., Mindlin S. et al. Tn5053 family transposons are res site hunters sensing plasmidal res sites occupied by cognate resolvases I I Mol. Microbiol. 1999. Vol. 33. P. 1059-1068.
Mindlin S., Kholodii G., Gorlenko Zh. et al. Mercury resistance transposons of Gram-nega-tive environmental bacteria and their classification // Res. Microbiol. 2001. Vol. 152. P. 811-822.
Misra Т.К., Brown N.L., Fritzinger D.C. et al. Mercuric ion-resistance operons of plasmid R100 and transposon Tn507: the beginning of the operon including the regulatory region and the first two structural genes //Proc. Nat. Acad. Sci. USA. 1984. Vol. 81. P. 5975-5979.
Misra Т.К., Brown N.L., Haberstroh L. et al. Mercuric reductase structural genes from plasmid R100 and transposon Tn507: functional domains of the enzyme // Gene. 1985. Vol. 34 P. 253-262.
Nakamura K., Fujisaki Т., Tamashiro H. Characteristics of Hg-resistant bacteria isolated from Minamata Bay sediment I I Environ. Res. 1986. Vol. 40. P. 58-67.
Nakamura K., Silver S. Molecular analysis of mercury-resistant Bacillus isolates from sediment of Minamata Bay, Japan // Appl. Environ. Microbiol. 1994. Vol. 60. P. 4596-4599.
Narita М., Koizumi Т., Huang C., Endo G. Broad-spectrum mercury resistance and its genetic characterization of anaerobic mercury-resistant bacterium, Clostridium butyricum Mersaru, isolated from sediment of Minamata Bay, Japan // DDBJ/EMBL/GenBank submission. 1999. Ac: AB024961.
Nelson, Clayton R.A., Gill S.R. et al.. Evidence for lateral gene transfer between Archae and teria from genome sequence of Thermotoga maritima // Nature. 1999. Vol. 399. P. 323-329.
144
Nesbo C.L., Boucher Y., Doolittle W.F. Defining the core of nontransferable prokaryotic genes: the euryarchaeal core I I J. Mol. Evol. 2001. Vol. 53. P. 340-350.
Newby D.T., Josephson K.L., Pepper I.L. Detection and characterization of plasmid pJP4 transfer to indigenous soil bacteria // Appl. Environ. Microbiol. 2000. Vol. 66. P. 290-291
Ochman H. Lateral and oblique gene transfer 11 Curr. Opin. Genet, and Develop. 2001. Vol. 11. P. 616-619.
Ochman H., Lawrence J.G., Groisman E.A. Lateral gene transfer and the nature of bacterial innovation // Nature. 2000. Vol. 405. P. 299-304.
Osborn A.M., Bruce K.D., Ritchie D.A., Strike P. The mercury resistance operon of the incJ plasmid pMERPH exhibits structural and regulatory divergence from other Gram-negative mer operons // Microbiology. 1996. Vol. 142. P. 337-345.
Osborn A.M., Bruce K.D., Strike P., Ritchie D.A. Polymerase chain reaction-restriction fragments length polymorphism analysis shows divergence among mer determinants from Gram-nega-tive soil bacteria indistinguishable by DNA-DNA hybridization I I Appl. Environ. Microbiol. 1993. Vol. 59. P. 4024-4030.
Osborn A.M., Bruce K.D.. Strike P., Ritchie D.A. Sequence conservation between regulatory mercury resistance genes in bacteria from mercury polluted and pristine environments // Syst Appl. Microbiol. 1995. Vol. 18. P. 1-6.
Osborn A.M., Bruce K.D., Strike P., Ritchie D.A. Distribution, diversity and evolution of the bacterial mercury resistance (mer) operon // FEMS Microbiol. Rev. 1997. Vol. 19. P. 239-262.
Osbourn S.E.V., Turner A.K. Grinsted J. Nucleotide sequence within Tn3926 confirms this as Tn27-like transposable element and provides evidence for the origin of the mer operon carried by plasmid pKLH2 // Plasmid. 1995. Vol. 33. P. 25-29.
Parro V., San Roman М., Galindo I. et al. A 23911 bp region of the Bacillus subtilis genome comprising genes located upstream and downstream of the lev operon // Microbiology. 1997. Vol. 143. P. 1321-1326.
Pearson A.J., Bruce K.D., Osborn A.M. et al. Distribution of class II transposase and resolvase genes in soil bacteria and their association with mer genes // Appl. Environ. Microbiol. 1996. Vol. 62. P. 2961-2965.
Radstrom P., Skod O., Swedberg G. et al. Transposon Tn5090 of plasmid R751, which carries an integron, is related to Tn7, Mu, and the retroelements // J. Bacteriol. 1994. Vol. 176. P. 3257-3268.
Reniero I)., Mozzon E., Galli E., Barbieri P. Two aberrant mercury resistance transposons in the Pseudomonas stutzery plasmid pPB // Gene. 1998. Vol. 208. P. 37—42.
