Changes of in vivo fluxes through central metabolic pathways during the production of nystatin by Streptomyces noursei in batch culture

被引:29
作者
Jonsbu, E
Christensen, B
Nielsen, J
机构
[1] Tech Univ Denmark, Bioctr DTU, Ctr Proc Biotechnol, DK-2800 Lyngby, Denmark
[2] Norwegian Univ Sci & Technol, NTNU, Dept Biotechnol, N-7491 Trondheim, Norway
关键词
D O I
10.1007/s002530100613
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 central carbon metabolism of the nystatin-producing strain Streptomyces noursei ATCC 11455 was evaluated by C-13-labelling experiments. A batch fermentation was examined during the idiophase by GC-MS measurements of the labelling patterns of amino acids in the biomass. The labelling patterns of the amino acids and calculated fluxes of the central metabolism showed that changes in the primary and secondary metabolisms occurred simultaneously. Changes in the profiles for the integrated fluxes showed a decreased flux through the pentose phosphate pathway and an increased flux in the tricarboxylic acid cycle relative to the glucose uptake rate when the culture entered a phase with reduced specific growth rate and enhanced nystatin yield. The flux through the pentose phosphate pathway seemed to be adjusted according to the NADPH requirement during the different phases of the batch fermentation.
引用
收藏
页码:93 / 100
页数:8
相关论文
共 36 条
[1]  
BENNETT JE, 1995, PHARMACOL BASIS THER, P1175
[2]   Biosynthesis of the polyene antifungal antibiotic nystatin in Streptomyces noursei ATCC 11455:: analysis of the gene cluster and deduction of the biosynthetic pathway [J].
Brautaset, T ;
Sekurova, ON ;
Sletta, H ;
Ellingsen, TE ;
Strom, AR ;
Valla, S ;
Zotchev, SB .
CHEMISTRY & BIOLOGY, 2000, 7 (06) :395-403
[3]  
CHAMBERS HF, 1995, PHARMACOL BASIS THER, P1029
[4]  
Christensen B, 2000, Adv Biochem Eng Biotechnol, V66, P209
[5]  
Christensen B, 2000, BIOTECHNOL BIOENG, V68, P652, DOI 10.1002/(SICI)1097-0290(20000620)68:6<652::AID-BIT8>3.0.CO
[6]  
2-J
[7]   Metabolic characterization of high- and low-yielding strains of Penicillium chrysogenum [J].
Christensen, B ;
Thykær, J ;
Nielsen, J .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2000, 54 (02) :212-217
[8]   Isotopomer Analysis Using GC-MS [J].
Christensen, Bjarke ;
Nielsen, Jens .
METABOLIC ENGINEERING, 1999, 1 (04) :282-290
[9]   Classification and Sensitivity Analysis of a Proposed Primary Metabolic Reaction Network for Streptomyces Lividans [J].
Daae, Elisabeth B. ;
Ison, Andrew P. .
METABOLIC ENGINEERING, 1999, 1 (02) :153-165
[10]   Determination of full 13C isotopomer distributions for metabolic flux analysis using heteronuclear spin echo difference NMR spectroscopy [J].
de Graaf, AA ;
Mahle, M ;
Möllney, M ;
Wiechert, W ;
Stahmann, P ;
Sahm, H .
JOURNAL OF BIOTECHNOLOGY, 2000, 77 (01) :25-35