Metabolic state of Zymomonas mobilis in glucose-, fructose-, and xylose-fed continuous cultures as analysed by 13C- and 31P-NMR spectroscopy

被引:66
作者
De Graaf, AA
Striegel, K
Wittig, RM
Laufer, B
Schmitz, G
Wiechert, W
Sprenger, GA
Sahm, H
机构
[1] Forschungszentrum Julich, Inst Biotechnol 1, D-52425 Julich, Germany
[2] Alfred Wegener Inst Polar & Marine Res, D-27515 Bremerhaven, Germany
[3] Univ Siegen, Abt Simulat Techn, IMR, D-57068 Siegen, Germany
关键词
Zymomonas mobilis; metabolic flux analysis; sugar phosphates; glucose; fructose; xylose; C-13-NMR; in vivo P-31-NMR; rate-limiting step;
D O I
10.1007/s002030050724
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The reasons for the well-known significantly different behaviour of the anaerobic, gram-negative, ethanologenic bacterium Zymomonas mobilis during growth on fructose (i.e. decreased growth and ethanol yields, increased by-product formation) as compared to that on its second natural substrate, glucose, have remained unexplained. A xylose-fermenting recombinant strain of Z. mobilis that was recently constructed in our laboratory also unexpectedly displayed an increased formation of byproducts and a strongly reduced growth rate as compared to the parent strain. Therefore, a comprehensive study employing recently developed NMR-based methods for the in vivo analysis of intracellular phosphorylated pool sizes and metabolic fluxes was undertaken to enable a global characterization of the intracellular metabolic state of Z. mobilis during growth on C-13-labelled glucose, fructose and xylose in defined continuous cultures. The C-13-NMR flux analysis indicated that ribose 5-phosphate is synthesized via the nonoxidative pentose phosphate pathway in Z. mobilis, and it identified a metabolic bottleneck in the recombinant xylose-fermenting Z. mobilis strain at the level of heterologous xylulokinase, The P-31-NMR analyses revealed a global alteration of the levels of intracellular phosphorylated metabolites during growth on fructose as compared to that on glucose. The results suggest that this is primarily caused by an elevated concentration of intracellular fructose 6-phosphate.
引用
收藏
页码:371 / 385
页数:15
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