In vivo NMR system for evaluating oxygen-dependent metabolic status in microbial culture

被引:12
作者
Noguchi, Y
Shimba, N
Toyosaki, H
Ebisawa, K
Kawahara, Y
Suzuki, E
Sugimoto, S
机构
[1] Ajinomoto Co Inc, Fermentat & Biotechnol Labs, Kawasaki Ku, Kawasaki, Kanagawa 2108681, Japan
[2] Ajinomoto Co Inc, Cent Res Labs, Kawasaki Ku, Kawasaki, Kanagawa 2108681, Japan
关键词
dissolved oxygen tension; in vivo NMR; energy metabolism;
D O I
10.1016/S0167-7012(02)00063-5
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
To optimize an appropriate microbial culture in a fermentor, precise control of the medium's dissolved oxygen tension (DOT) is crucial. In particular, to study the effect of DOT on cellular metabolic status by using in vivo nuclear magnetic resonance (NMR) measurements, the set-up of the experiment must be optimized to maintain DOT in the culture. In the conventional method, DOT is monitored by a sensor inside a fermentor and is controlled by changing the agitation rate. Here, we report a novel and accurate system that minimizes time lag by an automated aeration flow control device, allowing an NMR spectrometer to monitor representative metabolites in real-time. To fulfill these two objects, the fermentor was composed of a fermentation vessel and two outer tubes, through which the medium was circulated by rotary pumps. One tube monitored DOT in via a sensor, and at the same time the other tube monitored metabolites via an NMR spectrometer. In this study, we used this system to analyze the responses of Escherichia coli cells under various oxygen conditions. The results validated the use of this system in the study of microbial metabolism. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:73 / 82
页数:10
相关论文
共 19 条
[1]   Antioxidative properties of Lactobacillus sake upon exposure to elevated oxygen concentrations [J].
Amanatidou, A ;
Smid, EJ ;
Bennik, MHJ ;
Gorris, LGM .
FEMS MICROBIOLOGY LETTERS, 2001, 203 (01) :87-94
[2]  
Barrie A., 1984, SPECTROSC INT J, V3, P259
[3]   IN-SITU P-31 NUCLEAR-MAGNETIC-RESONANCE FOR OBSERVATION OF POLYPHOSPHATE AND CATABOLITE RESPONSES OF CHEMOSTAT-CULTIVATED SACCHAROMYCES-CEREVISIAE AFTER ALKALINIZATION [J].
CASTRO, CD ;
MEEHAN, AJ ;
KORETSKY, AP ;
DOMACH, MM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1995, 61 (12) :4448-4453
[4]   Performance trade-offs in in situ chemostat NMR [J].
Castro, CD ;
Koretsky, AP ;
Domach, MM .
BIOTECHNOLOGY PROGRESS, 1999, 15 (02) :185-195
[5]   Metabolic state of Zymomonas mobilis in glucose-, fructose-, and xylose-fed continuous cultures as analysed by 13C- and 31P-NMR spectroscopy [J].
De Graaf, AA ;
Striegel, K ;
Wittig, RM ;
Laufer, B ;
Schmitz, G ;
Wiechert, W ;
Sprenger, GA ;
Sahm, H .
ARCHIVES OF MICROBIOLOGY, 1999, 171 (06) :371-385
[6]   ON MULTIPLE-NUTRIENT-LIMITED GROWTH OF MICROORGANISMS, WITH SPECIAL REFERENCE TO DUAL LIMITATION BY CARBON AND NITROGEN SUBSTRATES [J].
EGLI, T .
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, 1991, 60 (3-4) :225-234
[7]   SOME REFLECTIONS ON MICROBIAL COMPETITIVENESS AMONG HETEROTROPHIC BACTERIA [J].
GOTTSCHAL, JC .
ANTONIE VAN LEEUWENHOEK JOURNAL OF MICROBIOLOGY, 1985, 51 (5-6) :473-494
[8]   PHOSPHORUS NUCLEAR-MAGNETIC-RESONANCE AND OCULAR METABOLISM [J].
GREINER, JV ;
KOPP, SJ ;
GLONEK, T .
SURVEY OF OPHTHALMOLOGY, 1985, 30 (03) :189-202
[9]   NUCLEAR-MAGNETIC-RESONANCE STUDIES OF CELLULAR-METABOLISM [J].
LUNDBERG, P ;
HARMSEN, E ;
HO, C ;
VOGEL, HJ .
ANALYTICAL BIOCHEMISTRY, 1990, 191 (02) :193-222
[10]   CULTIVATOR FOR NMR-STUDIES OF SUSPENDED CELL-CULTURES [J].
MEEHAN, AJ ;
ESKEY, CJ ;
KORETSKY, AP ;
DOMACH, MM .
BIOTECHNOLOGY AND BIOENGINEERING, 1992, 40 (11) :1359-1366