Rational design of a Corynebacterium glutamicum pantothenate production strain and its characterization by metabolic flux analysis and genorne-wide transcriptional profiling

被引:72
作者
Hüser, AT
Chassagnole, C
Lindley, ND
Merkamm, M
Guyonvarch, A
Elisákova, V
Pátek, M
Kalinowski, J
Brune, I
Pühler, A
Tauch, A
机构
[1] Univ Bielefeld, Inst Genomforsch, D-33615 Bielefeld, Germany
[2] Univ Bielefeld, Lehrstuhl Genet, D-33615 Bielefeld, Germany
[3] CNRS, Inst Natl Sci Appl, INSA, INRA,LAb Biotechnol Bioprocedes,UMR 5504, F-31077 Toulouse, France
[4] CRITT Bioind, F-31077 Toulouse, France
[5] Univ Paris 11, Inst Genet & Microbiol, Ctr Orsay, F-91405 Orsay, France
[6] Acad Sci Czech Republ, Inst Microbiol, CZ-14220 Prague, Czech Republic
[7] Univ Bielefeld GmbH, Inst Innovationstransfer, Geschaftsbereich BioTech, D-33615 Bielefeld, Germany
关键词
D O I
10.1128/AEM.71.6.3255-3268.2005
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
A "second-generation" production strain was derived from a Corynebacterium glutamicum pantothenate producer by rational design to assess its potential to synthesize and accumulate the vitamin pantothenate by batch cultivation. The new pantothenate production strain carries a deletion of the ilvA gene to abolish isoleucine synthesis, the promoter down-mutation P-ilvEM3 to attenuate ilvE gene expression and thereby increase ketoisovalerate availability, and two compatible plasmids to overexpress the ilvBNCD genes and duplicated copies of the panBC operon. Production assays in shake flasks revealed that the P-ilvEM3 mutation and the duplication of the panBC operon had cumulative effects on pantothenate production. During pH-regulated batch cultivation, accumulation of 8 mM pantothenate was achieved, which is the highest value reported for C glutamicum. Metabolic flux analysis during the fermentation demonstrated that the P-ilvEM3 mutation successfully reoriented the carbon flux towards pantothenate biosynthesis. Despite this repartition of the carbon flux, ketoisovalerate not converted to pantothenate was excreted by the cell and dissipated as by-products (ketoisocaproate, DL-2,3,-dihydroxy-isovalerate, ketopantoate, pantoate), which are indicative of saturation of the pantothenate biosynthetic pathway. Genome-wide expression analysis of the production strain during batch cultivation was performed by whole-genome DNA microarray hybridization and agglomerative hierarchical clustering, which detected the enhanced expression of genes involved in leucine biosynthesis, in serine and glycine formation, in regeneration of methylenetetrahydrofolate, in de novo synthesis of nicotinic acid mononucleotide, and in a complete pathway of acyl coenzyme A conversion. Our strategy not only successfully improved pantothenate production by genetically modified C glutamicum strains but also revealed new constraints in attaining high productivity.
引用
收藏
页码:3255 / 3268
页数:14
相关论文
共 53 条
  • [1] BONAMY C, 1990, FEMS MICROBIOL LETT, V66, P263, DOI 10.1016/0378-1097(90)90294-Z
  • [2] Brosius J, 1988, VECTORS SURVEY MOL C, P205
  • [3] Metabolic network analysis during fed-batch cultivation of Corynebacterium glutamicum for pantothenic acid production:: first quantitative data and analysis of by-product formation
    Chassagnole, C
    Diano, A
    Létisse, F
    Lindley, ND
    [J]. JOURNAL OF BIOTECHNOLOGY, 2003, 104 (1-3) : 261 - 272
  • [4] Carbon flux analysis in a pantothenate overproducing Corynebacterium glutamicum strain.
    Chassagnole, C
    Létisse, F
    Diano, A
    Lindley, ND
    [J]. MOLECULAR BIOLOGY REPORTS, 2002, 29 (1-2) : 129 - 134
  • [5] CLONING, ORGANIZATION AND FUNCTIONAL-ANALYSIS OF ILVA, ILVB AND ILVC GENES FROM CORYNEBACTERIUM-GLUTAMICUM
    CORDES, C
    MOCKEL, B
    EGGELING, L
    SAHM, H
    [J]. GENE, 1992, 112 (01) : 113 - 116
  • [6] CLONING THE DAPA DAPB CLUSTER OF THE LYSINE-SECRETING BACTERIUM CORYNEBACTERIUM-GLUTAMICUM
    CREMER, J
    EGGELING, L
    SAHM, H
    [J]. MOLECULAR AND GENERAL GENETICS, 1990, 220 (03): : 478 - 480
  • [7] EMMA:: a platform for consistent storage and efficient analysis of microarray data
    Dondrup, M
    Goesmann, A
    Bartels, D
    Kalinowski, J
    Krause, L
    Linke, B
    Rupp, O
    Sczyrba, A
    Pühler, A
    Meyer, F
    [J]. JOURNAL OF BIOTECHNOLOGY, 2003, 106 (2-3) : 135 - 146
  • [8] Dusch N, 1999, APPL ENVIRON MICROB, V65, P1530
  • [9] GUILLOUET S, 1995, APPL MICROBIOL BIOT, V43, P315, DOI 10.1007/s002530050409
  • [10] Industrial production of amino acids by coryneform bacteria
    Hermann, T
    [J]. JOURNAL OF BIOTECHNOLOGY, 2003, 104 (1-3) : 155 - 172