Intracellular carbon fluxes in riboflavin-producing Bacillus subtilis during growth on two-carbon substrate mixtures

被引:63
作者
Dauner, M
Sonderegger, M
Hochuli, M
Szyperski, T
Wüthrich, K
Hohmann, HP
Sauer, U [1 ]
Bailey, JE
机构
[1] Swiss Fed Inst Technol, Inst Biotechnol, CH-8093 Zurich, Switzerland
[2] Swiss Fed Inst Technol, Inst Mol Biol & Biophys, CH-8093 Zurich, Switzerland
[3] Roche Vitamins Inc, Nutley, NJ 07110 USA
关键词
D O I
10.1128/AEM.68.4.1760-1771.2002
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
Metabolic responses to cofeeding of different carbon substrates in carbon-limited chemostat cultures were investigated with riboflavin-producing Bacillus subtilis. Relative to the carbon content (or energy content) of the substrates, the biomass yield was lower in all cofeeding experiments than with glucose alone. The riboflavin yield, in contrast, was significantly increased in the acetoin- and gluconate-cofed cultures. In these two scenarios, unusually high intracellular ATP-to-ADP ratios correlated with improved riboflavin yields. Nuclear magnetic resonance spectra recorded with amino acids obtained from biosynthetically directed fractional C-13 labeling experiments were used in an isotope isomer balancing framework to estimate intracellular carbon fluxes. The glycolysis-to-pentose phosphate (PP) pathway split ratio was almost invariant at about 80% in all experiments, a result that was particularly surprising for the cosubstrate gluconate, which feeds directly into the PP pathway. The in vivo activities of the tricarboxylic acid cycle, in contrast, varied more than twofold. The malic enzyme was active with acetate, gluconate, or acetoin cofeeding but not with citrate cofeeding or with glucose alone. The in vivo activity of the gluconeogenic phosphoenolpyruvate carboxykinase was found to be relatively high in all experiments, with the sole exception of the gluconate-cofed culture.
引用
收藏
页码:1760 / 1771
页数:12
相关论文
共 66 条
[1]  
[Anonymous], CONTINUOUS CULTURE
[2]  
[Anonymous], 1985, Allgemeine Mikrobiologie
[3]  
Arbige M. V., 1993, P871
[4]  
BABEL W, 1985, J GEN MICROBIOL, V131, P39
[5]   An Overview of Evolutionary Algorithms for Parameter Optimization [J].
Baeck, Thomas ;
Schwefel, Hans-Paul .
EVOLUTIONARY COMPUTATION, 1993, 1 (01) :1-23
[6]   RELATIONSHIPS BETWEEN INTRACELLULAR CONTENTS OF NUCLEOTIDES AND 5-PHOSPHORIBOSYL 1-PYROPHOSPHATE IN ESCHERICHIA-COLI [J].
BAGNARA, AS ;
FINCH, LR .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1973, 36 (02) :422-427
[7]  
Bergmeyer H. U., 1985, METHODS ENZYMATIC AN, Viv
[8]   THE PROPERTIES OF CITRATE TRANSPORT IN MEMBRANE-VESICLES FROM BACILLUS-SUBTILIS [J].
BERGSMA, J ;
KONINGS, WN .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1983, 134 (01) :151-156
[9]  
BLANCH HW, 1996, BIOCHEMICAL ENG
[10]   Flux analysis of underdetermined metabolic networks: The quest for the missing constraints [J].
Bonarius, HPJ ;
Schmid, G ;
Tramper, J .
TRENDS IN BIOTECHNOLOGY, 1997, 15 (08) :308-314