In situ proton-NMR analyses of Escherichia coli HB101 fermentations in 1H2O and in D2O

被引:30
作者
Brecker, L
Weber, H
Griengl, H
Ribbons, DW
机构
[1] Graz Univ Technol, Inst Organ Chem, A-8010 Graz, Austria
[2] Graz Univ Technol, Inst Biotechnol, A-8010 Graz, Austria
来源
MICROBIOLOGY-SGM | 1999年 / 145卷
关键词
proton-NMR; in situ analysis; deuterium-labelled products; Escherichia coli fermentations;
D O I
10.1099/00221287-145-12-3389
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Experiments using one-dimensional Fourier-transform proton-NMR spectrometry for non-invasive analyses of microbial fermentations in situ, in vivo and in normal aqueous buffer are described. Analyses of the 'mixed acid' fermentation during growth of Escherichia coli on glucose and citrate were performed to identify and quantitatively estimate the concentrations of the two substrates provided and of the six products formed without sampling from the NMR tube. Identification of fermentation substrates and products was achieved by coincidence of selected diagnostic proton signals of individual compounds in the same solvent. The complete time course of growth of E. coli in the NMR tube correlated well with that of the same culture grown outside the magnet, with samples taken for proton-NMR analyses. The entire course of these in situ proton measurements during growth over 16-24 h was obtained automatically, usually unattended overnight. Thus, the utilization and formation of eight substances in the fermentation were monitored simultaneously, in normal (H2O)-H-1, without sampling and individual analysis. Several metabolic changes could be readily detected during the fermentations. Additionally, the ph changes were estimated from the chemical shifts of the acetate signal as growth progressed. The effect of varying D2O concentrations in the solvent on growth rates and product yields was examined, and the increase in the complexity of signals given by these fermentations is described. This versatile and rapid method for the simultaneous, direct and automatic analysis of mixtures of many compounds has the potential to be extended to routine on-line analyses of industrial fermentations.
引用
收藏
页码:3389 / 3397
页数:9
相关论文
共 28 条
  • [1] ANAEROBIC FERMENTATION BALANCE OF ESCHERICHIA-COLI AS OBSERVED BY INVIVO NUCLEAR MAGNETIC-RESONANCE SPECTROSCOPY
    ALAM, KY
    CLARK, DP
    [J]. JOURNAL OF BACTERIOLOGY, 1989, 171 (11) : 6213 - 6217
  • [2] [Anonymous], 1996, 100 MORE BASIC NMR E
  • [3] [Anonymous], 1992, BIOCHEMISTRY-US
  • [4] Synthesis of 2,4-diketoacids and their aqueous solution structures
    Brecker, L
    Pogorevc, M
    Griengl, H
    Steiner, W
    Kappe, T
    Ribbons, DW
    [J]. NEW JOURNAL OF CHEMISTRY, 1999, 23 (04) : 437 - 446
  • [5] HUMAN ERYTHROCYTE METABOLISM STUDIES BY H-1 SPIN-ECHO NMR
    BROWN, FF
    CAMPBELL, ID
    KUCHEL, PW
    RABENSTEIN, DC
    [J]. FEBS LETTERS, 1977, 82 (01) : 12 - 16
  • [6] DISSIMILATION OF CITRIC ACID BY AEROBACTER-AEROGENES AND ESCHERICHIA-COLI
    DAGLEY, S
    [J]. JOURNAL OF GENERAL MICROBIOLOGY, 1954, 11 (02): : 218 - 227
  • [7] GADIAN DG, 1983, NUCL MAGNETIC RESONA
  • [8] Novel nuclear magnetic resonance spectroscopy methods demonstrate preferential carbon source utilization by Acinetobacter calcoaceticus
    Gaines, GL
    Smith, L
    Neidle, EL
    [J]. JOURNAL OF BACTERIOLOGY, 1996, 178 (23) : 6833 - 6841
  • [9] SOLVENT SIGNAL SUPPRESSION IN NMR
    GUERON, M
    PLATEAU, P
    DECORPS, M
    [J]. PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, 1991, 23 : 135 - 209
  • [10] Determination of the time course of an enzymatic reaction by H-1 NMR spectroscopy: Hydroxynitrile lyase catalysed transhydrocyanation
    Hickel, A
    Gradnig, G
    Griengl, H
    Schall, M
    Sterk, H
    [J]. SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 1996, 52 (01): : 93 - 96