Genome-wide analysis of the L-methionine biosynthetic pathway in Corynebacterium glutamicum by targeted gene deletion and homologous complementation

Rückert C, Pühler A, Kalinowski J (2003)
JOURNAL OF BIOTECHNOLOGY 104(1-3): 213-228.

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DOI
Autor*in
Rückert, ChristianUniBi ; Pühler, AlfredUniBi ; Kalinowski, JörnUniBi
Einrichtung
Centrum für Biotechnologie > Institut für Genomforschung und Systembiologie
Centrum für Biotechnologie > Arbeitsgruppe A. Pühler
Centrum für Biotechnologie > Arbeitsgruppe J. Kalinowski
Fakultät für Biologie
Abstract / Bemerkung
The genome sequence of Corynebacterium glutamicum. a gram-positive soil bacterium widely used as an amino acid producer, was analyzed by a similarity-based approach to elucidate the pathway for the biosynthesis Of L-methionine. The functions of candidate ORFs were derived by gene deletion and, if necessary, by homologous complementation of suitable mutants. Of nine candidate ORFs (four of which were known previously), seven ORFs (cg0754 (metX), cg0755 (met Y), cg1290 (metE), cg1702 (metH), cg2383 (metf), cg2536 (aecD), and eg2687 (metB)) were demonstrated to be part of the pathway while two others (cg0961 and cg3086) could be excluded. C glutamicum synthesizes methionine in three, respectively four steps, starting from homoserine. C glutamicum possesses two genes with similarity to homoserine acetyltransferases but only MetX can act as such while Cg0961 catalyzes a different, unknown reaction. For the incorporation of the sulfur moiety, the known functions of MetY and MetB could be confirmed and AecD was proven to be the only functional cystathionine beta-lyase in C glutamicum, while Cg3086 can act neither as cystathionine gamma-synthase nor as cystathionine beta-lyase. Finally, MetE and MetH, which catalyze the conversion of L-homocysteine to L-methionine, could be newly identified, together with MetF which provides the necessary N-5-methyltetrahydrofolate. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
Stichworte
analysis; methionine biosynthesis; Corynebacterium glutamicum; genome; met genes
Erscheinungsjahr
2003
Zeitschriftentitel
JOURNAL OF BIOTECHNOLOGY
Band
104
Ausgabe
1-3
Seite(n)
213-228
ISSN
0168-1656
Page URI
https://pub.uni-bielefeld.de/record/1610269

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Rückert C, Pühler A, Kalinowski J. Genome-wide analysis of the L-methionine biosynthetic pathway in Corynebacterium glutamicum by targeted gene deletion and homologous complementation. JOURNAL OF BIOTECHNOLOGY. 2003;104(1-3):213-228.
Rückert, C., Pühler, A., & Kalinowski, J. (2003). Genome-wide analysis of the L-methionine biosynthetic pathway in Corynebacterium glutamicum by targeted gene deletion and homologous complementation. JOURNAL OF BIOTECHNOLOGY, 104(1-3), 213-228. https://doi.org/10.1016/S0168-1656(03)00158-5
Rückert, Christian, Pühler, Alfred, and Kalinowski, Jörn. 2003. “Genome-wide analysis of the L-methionine biosynthetic pathway in Corynebacterium glutamicum by targeted gene deletion and homologous complementation”. JOURNAL OF BIOTECHNOLOGY 104 (1-3): 213-228.
Rückert, C., Pühler, A., and Kalinowski, J. (2003). Genome-wide analysis of the L-methionine biosynthetic pathway in Corynebacterium glutamicum by targeted gene deletion and homologous complementation. JOURNAL OF BIOTECHNOLOGY 104, 213-228.
Rückert, C., Pühler, A., & Kalinowski, J., 2003. Genome-wide analysis of the L-methionine biosynthetic pathway in Corynebacterium glutamicum by targeted gene deletion and homologous complementation. JOURNAL OF BIOTECHNOLOGY, 104(1-3), p 213-228.
C. Rückert, A. Pühler, and J. Kalinowski, “Genome-wide analysis of the L-methionine biosynthetic pathway in Corynebacterium glutamicum by targeted gene deletion and homologous complementation”, JOURNAL OF BIOTECHNOLOGY, vol. 104, 2003, pp. 213-228.
Rückert, C., Pühler, A., Kalinowski, J.: Genome-wide analysis of the L-methionine biosynthetic pathway in Corynebacterium glutamicum by targeted gene deletion and homologous complementation. JOURNAL OF BIOTECHNOLOGY. 104, 213-228 (2003).
Rückert, Christian, Pühler, Alfred, and Kalinowski, Jörn. “Genome-wide analysis of the L-methionine biosynthetic pathway in Corynebacterium glutamicum by targeted gene deletion and homologous complementation”. JOURNAL OF BIOTECHNOLOGY 104.1-3 (2003): 213-228.

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