Identification and characterization of the last two unknown genes, dapC and dapF, in the succinylase branch of the L-lysine biosynthesis of Corynebacterium glutamicum

被引:38
作者
Hartmann, M
Tauch, A
Eggeling, L
Bathe, B
Möckel, B
Pühler, A
Kalinowski, J
机构
[1] Univ Bielefeld, Inst Genomforsch, D-33615 Bielefeld, Germany
[2] Univ Bielefeld, Lehrstuhl Genet, D-33615 Bielefeld, Germany
[3] Forschungszentrum Julich GmbH, Inst Biotechnol, D-52425 Julich, Germany
[4] Degussa AG, D-33788 Halle An Der Saale, Germany
关键词
Corynebacterium glutamicum; lysine biosynthesis; diaminopimelate biosynthesis; lysine production;
D O I
10.1016/S0168-1656(03)00156-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The inspection of the complete genome sequence of Corynebacterium glutamicum ATCC 13032 led to the identification of dapC and dapF, the last two unknown genes of the succinylase branch of the L-lysine biosynthesis. The deduced DapF protein of C glutamicum is characterized by a two-domain structure and a conserved diaminopimelate (DAP) epimerase signature. Overexpression of dapF resulted in an 8-fold increase of the specific epimerase activity. A defined deletion in the dapF gene led to a reduced growth of C glutamicum in a medium with excess carbon but limited ammonium availability. The predicted DapC protein of C glutamicum shared 29% identical amino acids with DapC from Bordetella pertussis, the only enzymatically characterized N-succinyl-aminoketopimelate aminotransferase. Overexpression of the dapC gene in C glutamicum resulted in a 9-fold increase of the specific aminotransferase activity. A C glutamicum mutant with deleted dapC showed normal growth characteristics with excess carbon and limited ammonium. Even a mutation of the two genes dapC and ddh, interrupting both branches of the split pathway, could be established in C glutamicum. Overexpression of the dapF or the dapC gene in an industrial C. glutamicum strain resulted in an increased L-lysine production, indicating that both genes might be relevant targets for the development of improved production strains. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:199 / 211
页数:13
相关论文
共 46 条
[1]   Exploiting the past and the future in protein secondary structure prediction [J].
Baldi, P ;
Brunak, S ;
Frasconi, P ;
Soda, G ;
Pollastri, G .
BIOINFORMATICS, 1999, 15 (11) :937-946
[2]   ASSAY OF PROTEINS IN PRESENCE OF INTERFERING MATERIALS [J].
BENSADOUN, A ;
WEINSTEIN, D .
ANALYTICAL BIOCHEMISTRY, 1976, 70 (01) :241-250
[3]   Structural symmetry:: The three-dimensional structure of Haemophilus influenzae diaminopimelate epimerase [J].
Cirilli, M ;
Zheng, RJ ;
Scapin, G ;
Blanchard, JS .
BIOCHEMISTRY, 1998, 37 (47) :16452-16458
[4]   CLONING THE DAPA DAPB CLUSTER OF THE LYSINE-SECRETING BACTERIUM CORYNEBACTERIUM-GLUTAMICUM [J].
CREMER, J ;
EGGELING, L ;
SAHM, H .
MOLECULAR AND GENERAL GENETICS, 1990, 220 (03) :478-480
[5]  
de Graaf A A, 2001, Adv Biochem Eng Biotechnol, V73, P9
[6]   Characterization of a Bordetella pertussis diaminopimelate (DAP) biosynthesis locus identifies dapC, a novel gene coding for an N-Succinyl-L,L-DAP aminotransferase [J].
Fuchs, TM ;
Schneider, B ;
Krumbach, K ;
Eggeling, L ;
Gross, R .
JOURNAL OF BACTERIOLOGY, 2000, 182 (13) :3626-3631
[7]   DIFFERENTIAL PLASMID RESCUE FROM TRANSGENIC MOUSE DNAS INTO ESCHERICHIA-COLI METHYLATION-RESTRICTION MUTANTS [J].
GRANT, SGN ;
JESSEE, J ;
BLOOM, FR ;
HANAHAN, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (12) :4645-4649
[8]   LION and Degussa apply genomics to fermentation [J].
Hodgson, J .
NATURE BIOTECHNOLOGY, 1998, 16 (08) :715-715
[9]   PCR-MEDIATED RECOMBINATION AND MUTAGENESIS [J].
HORTON, RM .
MOLECULAR BIOTECHNOLOGY, 1995, 3 (02) :93-99
[10]   NUCLEOTIDE-SEQUENCE OF THE MESO-DIAMINOPIMELATE D-DEHYDROGENASE GENE FROM CORYNEBACTERIUM-GLUTAMICUM [J].
ISHINO, S ;
MIZUKAMI, T ;
YAMAGUCHI, K ;
KATSUMATA, R ;
ARAKI, K .
NUCLEIC ACIDS RESEARCH, 1987, 15 (09) :3917-3917