Efficient electrotransformation of Corynebacterium diphtheriae with a mini-replicon derived from the Corynebacterium glutamicum plasmid pGA1

Tauch A, Kirchner O, Löffler B, Götker S, Pühler A, Kalinowski J (2002)
CURRENT MICROBIOLOGY 45(5): 362-367.

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Zeitschriftenaufsatz | Veröffentlicht | Englisch
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Abstract / Bemerkung
Efficient transformation of the human pathogen Corynebacterium diphtheriae was achieved with novel cloning vectors consisting of a mini-replicon from the cryptic C. glutamicum plasmid pGA1 as well as of the aph(3')-IIa or tetA(Z) antibiotic resistance genes. Plasmid-containing transformants of C. diphtheriae were recovered at frequencies ranging from 1.3 x 10(5) to 4.8 x 10(6) colony forming units (cfu)/mug of plasmid DNA. Vector DNA was directly transferred from Escherichia coli into C. diphtheriae with frequencies up to 5.6 x 10(5) cfu/mug of plasmid DNA. On the basis of the pGA1 mini-replicon, an expression vector system was established for C. diphtheriae by means of the P-tac promoter and the green fluorescent reporter protein. In addition, other commonly used vector systems from C. glutamicum, including the pBL1 and pHM1519 replicons, and the sacB conditionally lethal selection market from Bacillus subtilis, were shown to be functional in C. diphtheriae. Thus, the ability to apply the standard methods of C. glutamicum recombinant DNA technology will greatly facilitate the functional analysis of the recently completed C. diphtheriae genome sequence.
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Zeitschriftentitel
CURRENT MICROBIOLOGY
Band
45
Zeitschriftennummer
5
Seite
362-367
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Tauch A, Kirchner O, Löffler B, Götker S, Pühler A, Kalinowski J. Efficient electrotransformation of Corynebacterium diphtheriae with a mini-replicon derived from the Corynebacterium glutamicum plasmid pGA1. CURRENT MICROBIOLOGY. 2002;45(5):362-367.
Tauch, A., Kirchner, O., Löffler, B., Götker, S., Pühler, A., & Kalinowski, J. (2002). Efficient electrotransformation of Corynebacterium diphtheriae with a mini-replicon derived from the Corynebacterium glutamicum plasmid pGA1. CURRENT MICROBIOLOGY, 45(5), 362-367. doi:10.1007/s00284-002-3728-3
Tauch, A., Kirchner, O., Löffler, B., Götker, S., Pühler, A., and Kalinowski, J. (2002). Efficient electrotransformation of Corynebacterium diphtheriae with a mini-replicon derived from the Corynebacterium glutamicum plasmid pGA1. CURRENT MICROBIOLOGY 45, 362-367.
Tauch, A., et al., 2002. Efficient electrotransformation of Corynebacterium diphtheriae with a mini-replicon derived from the Corynebacterium glutamicum plasmid pGA1. CURRENT MICROBIOLOGY, 45(5), p 362-367.
A. Tauch, et al., “Efficient electrotransformation of Corynebacterium diphtheriae with a mini-replicon derived from the Corynebacterium glutamicum plasmid pGA1”, CURRENT MICROBIOLOGY, vol. 45, 2002, pp. 362-367.
Tauch, A., Kirchner, O., Löffler, B., Götker, S., Pühler, A., Kalinowski, J.: Efficient electrotransformation of Corynebacterium diphtheriae with a mini-replicon derived from the Corynebacterium glutamicum plasmid pGA1. CURRENT MICROBIOLOGY. 45, 362-367 (2002).
Tauch, Andreas, Kirchner, O, Löffler, B, Götker, S, Pühler, Alfred, and Kalinowski, Jörn. “Efficient electrotransformation of Corynebacterium diphtheriae with a mini-replicon derived from the Corynebacterium glutamicum plasmid pGA1”. CURRENT MICROBIOLOGY 45.5 (2002): 362-367.

133 Zitationen in Europe PMC

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McHardy AC, Tauch A, Rückert C, Pühler A, Kalinowski J., J Biotechnol 104(1-3), 2003
PMID: 12948641
Development of a Corynebacterium glutamicum DNA microarray and validation by genome-wide expression profiling during growth with propionate as carbon source.
Hüser AT, Becker A, Brune I, Dondrup M, Kalinowski J, Plassmeier J, Pühler A, Wiegräbe I, Tauch A., J Biotechnol 106(2-3), 2003
PMID: 14651867

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