Construction of L-lysine-overproducing strains of Brevibacterium lactofermentum by targeted disruption of the hom and thrB genes

Fernandez-Gonzalez C, Gil JA, Mateos LM, Schwarzer A, Schafer A, Kalinowski J, Pühler A, Martin JF (1996)
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 46(5-6): 554-558.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
Download
Es wurden keine Dateien hochgeladen. Nur Publikationsnachweis!
Autor*in
Fernandez-Gonzalez, C.; Gil, J.A.; Mateos, L. M.; Schwarzer, A.; Schafer, A.; Kalinowski, JörnUniBi; Pühler, AlfredUniBi ; Martin, J. F.
Abstract / Bemerkung
The mobilization of plasmids from gram-negative Escherichia coli to gram-positive Brevibacterium lactofermentum, mediated by P-type transfer functions, was used to construct disrupted mutants blocked specifically in the homoserine branch of the aspartate pathway. The mutant strain B. lactofermentum R31 showed an efficiency of conjugal transfer two to three orders of magnitude higher than that of the wild-type strain B. lactofermentum ATCC 13869. The hom- and thrB-disrupted mutants of B. lactofermentum ATCC 13869 were lysine overproducers. B. lactofermentum R31 mutants do not overproduce lysine because R31 is an alanine-overproducing strain and channels the pyruvate needed for lysine biosynthesis to the production of alanine.
Erscheinungsjahr
1996
Zeitschriftentitel
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
Band
46
Ausgabe
5-6
Seite(n)
554-558
ISSN
0175-7598
eISSN
1432-0614
Page URI
https://pub.uni-bielefeld.de/record/1637976

Zitieren

Fernandez-Gonzalez C, Gil JA, Mateos LM, et al. Construction of L-lysine-overproducing strains of Brevibacterium lactofermentum by targeted disruption of the hom and thrB genes. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY. 1996;46(5-6):554-558.
Fernandez-Gonzalez, C., Gil, J. A., Mateos, L. M., Schwarzer, A., Schafer, A., Kalinowski, J., Pühler, A., et al. (1996). Construction of L-lysine-overproducing strains of Brevibacterium lactofermentum by targeted disruption of the hom and thrB genes. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 46(5-6), 554-558. https://doi.org/10.1007/s002530050860
Fernandez-Gonzalez, C., Gil, J.A., Mateos, L. M., Schwarzer, A., Schafer, A., Kalinowski, Jörn, Pühler, Alfred, and Martin, J. F. 1996. “Construction of L-lysine-overproducing strains of Brevibacterium lactofermentum by targeted disruption of the hom and thrB genes”. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 46 (5-6): 554-558.
Fernandez-Gonzalez, C., Gil, J. A., Mateos, L. M., Schwarzer, A., Schafer, A., Kalinowski, J., Pühler, A., and Martin, J. F. (1996). Construction of L-lysine-overproducing strains of Brevibacterium lactofermentum by targeted disruption of the hom and thrB genes. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 46, 554-558.
Fernandez-Gonzalez, C., et al., 1996. Construction of L-lysine-overproducing strains of Brevibacterium lactofermentum by targeted disruption of the hom and thrB genes. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 46(5-6), p 554-558.
C. Fernandez-Gonzalez, et al., “Construction of L-lysine-overproducing strains of Brevibacterium lactofermentum by targeted disruption of the hom and thrB genes”, APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, vol. 46, 1996, pp. 554-558.
Fernandez-Gonzalez, C., Gil, J.A., Mateos, L.M., Schwarzer, A., Schafer, A., Kalinowski, J., Pühler, A., Martin, J.F.: Construction of L-lysine-overproducing strains of Brevibacterium lactofermentum by targeted disruption of the hom and thrB genes. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY. 46, 554-558 (1996).
Fernandez-Gonzalez, C., Gil, J.A., Mateos, L. M., Schwarzer, A., Schafer, A., Kalinowski, Jörn, Pühler, Alfred, and Martin, J. F. “Construction of L-lysine-overproducing strains of Brevibacterium lactofermentum by targeted disruption of the hom and thrB genes”. APPLIED MICROBIOLOGY AND BIOTECHNOLOGY 46.5-6 (1996): 554-558.

9 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Metabolic engineering of Escherichia coli for the production of phenol from glucose.
Kim B, Park H, Na D, Lee SY., Biotechnol J 9(5), 2014
PMID: 24115680
NrdH-redoxin of Mycobacterium tuberculosis and Corynebacterium glutamicum dimerizes at high protein concentration and exclusively receives electrons from thioredoxin reductase.
Van Laer K, Dziewulska AM, Fislage M, Wahni K, Hbeddou A, Collet JF, Versées W, Mateos LM, Tamu Dufe V, Messens J., J Biol Chem 288(11), 2013
PMID: 23362277
Efflux permease CgAcr3-1 of Corynebacterium glutamicum is an arsenite-specific antiporter.
Villadangos AF, Fu HL, Gil JA, Messens J, Rosen BP, Mateos LM., J Biol Chem 287(1), 2012
PMID: 22102279
Evolution of metal(loid) binding sites in transcriptional regulators.
Ordóñez E, Thiyagarajan S, Cook JD, Stemmler TL, Gil JA, Mateos LM, Rosen BP., J Biol Chem 283(37), 2008
PMID: 18591244
Characterization and chromosomal organization of the murD-murC-ftsQ region of Corynebacterium glutamicum ATCC 13869.
Ramos A, Honrubia MP, Vega D, Ayala JA, Bouhss A, Mengin-Lecreulx D, Gil JA., Res Microbiol 155(3), 2004
PMID: 15059630
Streptomyces lividans and Brevibacterium lactofermentum as heterologous hosts for the production of X22 xylanase from Aspergillus nidulans.
Díaz M, Adham SA, Ramón D, Gil JA, Santamaría RI., Appl Microbiol Biotechnol 65(4), 2004
PMID: 15168093

References

Daten bereitgestellt von Europe PubMed Central.

Export

Markieren/ Markierung löschen
Markierte Publikationen

Open Data PUB

Web of Science

Dieser Datensatz im Web of Science®
Quellen

PMID: 9008889
PubMed | Europe PMC

Suchen in

Google Scholar