Biopolym. Cell. 1992; 8(5):48-54.
http://dx.doi.org/10.7124/bc.00033A
Gene-Engineering Biotechnology
pZE8 natural hsd plasmid replicon based cloning vectors for Escherichia coli and endorhizosphere nitrogen fixer Klebsiella oxytoca VN13
1Alexeyev M. F., 1Kovtunovich G. L., 1Kravetz A. N., 2Solonin A. S.
  1. Institute of Molecular Biology and Genetics, NAS of Ukraine
    150, Akademika Zabolotnoho Str., Kyiv, Ukraine, 03680
  2. Skryabin Institute of Biochemistry and Physiology of Microorganisms Russian Academy of Science
    5, Prospect Nauki, Puschino, Moscow reg., , Russian Federation,142290

Abstract

Natural Citobacter freundii hsd plasmid based vector plasmids for Klebstella oxytoca VN13 and Escherichia coli have been constructed. pKAS18 and pKAS19B vectors are consist of pZE8 ori, Tn903 Kmr gene and polylinkers of pUC18 or pUC19 respectively. pMG1k and pMG21k plasmids allow cloning into the unique PstI site of the EcoRV restrictase gene.
Full text: (PDF, in Russian)

References

[1] Nguyen TNH, Ton TNB, Tarasenko VA, Kozyrovskaja NA. Nitrogen-fixing bacteria colonize rice root xylema. Biopolym Cell. 1989; 5(2):97-9.
[2] Kozyrovskaya NA, Makitruk VL, Ruckdashell E. Nitrogen-fixing Klebsiella species produce indole-3-acetic acid. Biopolym Cell. 1990; 6(6):93-6.
[3] DNA cloning: a practical approach. Ed. DM Glover. Oxford, IRL Press, 1985; Vol. 1 and 2: 435 p
[4] ZaÄ­tsev EN, ZaÄ­tseva EM, Bakhlanova IV, Gorelov VN, Kuz'min NP. Cloning and characteristics of recA gene in Pseudomonas aeruginosa. Genetika. 1986;22(11):2721-7.
[5] Yanisch-Perron C, Vieira J, Messing J. Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors. Gene. 1985;33(1):103-19.
[6] Vieira J, Messing J. The pUC plasmids, an M13mp7-derived system for insertion mutagenesis and sequencing with synthetic universal primers. Gene. 1982;19(3):259-68.
[7] Gorovits RL, Solonin AS. Plasmid vectors of "insertion inactivation" of the trimethoprim resistance marker. Genetika. 1987;23(3):397-404.
[8] Fellay R, Frey J, Krisch H. Interposon mutagenesis of soil and water bacteria: a family of DNA fragments designed for in vitro insertional mutagenesis of gram-negative bacteria. Gene. 1987;52(2-3):147-54.
[9] Fomenkov AI, Kramarov VM, Andreev LV, Mochalov VV, Smolyaninov VV, Matvienko NI. Isolation and properties of a new site-specific endonuclease Bme142I from Bacillus megaterium 142. Nucleic Acids Res. 1988;16(21):10399.
[10] Maniatis T, Fritsch EF, Sambrook J. Molecular cloning: a laboratory manual. New York: Cold Spring Harbor Lab, 1982; 545 p.
[11] Alexeyev MF, Gunkovskaya NV. Method for rapid transformation of enterobacteria and some factors influencing its efficiency. Biopolym Cell. 1992; 8(3):46-50.
[12] Paton EB. Mechanisms of regulation of gene expression of ribosomal proteins L11, L7, L10 and L7/12 Escherichia coli: Author. dis. ... Dr. biol. nauk. Kyiv, 1990. 44.
[13] Miller JH. Experiments in molecular genetics. Cold Spring Harbor Laboratory, 1972, 466 p.
[14] Bougueleret L, Schwarzstein M, Tsugita A, Zabeau M. Characterization of the genes coding for the Eco RV restriction and modification system of Escherichia coli. Nucleic Acids Res. 1984;12(8):3659-76.
[15] Balbás P, Soberón X, Merino E, Zurita M, Lomeli H, Valle F, Flores N, Bolivar F. Plasmid vector pBR322 and its special-purpose derivatives--a review. Gene. 1986;50(1-3):3-40.
[16] Villa-Komaroff L, Efstratiadis A, Broome S, Lomedico P, Tizard R, Naber SP, Chick WL, Gilbert W. A bacterial clone synthesizing proinsulin. Proc Natl Acad Sci U S A. 1978;75(8):3727-31.
[17] Maloy SR, Nunn WD. Selection for loss of tetracycline resistance by Escherichia coli. J Bacteriol. 1981;145(2):1110-1.
[18] Craine BL. Novel selection for tetracycline- or chloramphenicol-sensitive Escherichia coli. J Bacteriol. 1982;151(1):487-90.