REGULATION OF CARBON METABOLISM IN CHEMOSTAT CULTURES OF SACCHAROMYCES-CEREVISIAE GROWN ON MIXTURES OF GLUCOSE AND ETHANOL

被引:123
作者
DEJONGGUBBELS, P [1 ]
VANROLLEGHEM, P [1 ]
HEIJNEN, S [1 ]
VANDIJKEN, JP [1 ]
PRONK, JT [1 ]
机构
[1] DELFT UNIV TECHNOL, DEPT BIOPROC ENGN, KLYYVER LAB BIOTECHNOL, 2628 BC DELFT, NETHERLANDS
关键词
CHEMOSTAT; MIXED SUBSTRATES; GLUCONEOGENESIS; GLYOXYLATE CYCLE; SACCHAROMYCES CEREVISIAE;
D O I
10.1002/yea.320110503
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Growth efficiency and regulation of key enzyme activities were studied in carbon- and energy-limited chemostat cultures of Saccharomyces cerevisiae grown on mixtures of glucose and ethanol at a fixed dilution rate. Biomass yields on substrate carbon and oxygen could be adequately described as the net result of growth on the single substrates. Activities of isocitrate lyase and malate synthase were not detected in cell-free extracts of glucose-limited cultures. However, both enzymes were present when the ethanol fraction in the reservoir medium exceeded the theoretical minimum above which the glyoxylate cycle is required for anabolic reactions. Fructose-1,6-bisphosphatase activity was only detectable at high ethanol fractions in the feed, when activity of this enzyme was required for synthesis of hexose phosphates. Phospho-enol-pyruvate-carboxykinase activity was not detectable in extracts from glucose-grown cultures and increased with the ethanol fraction in the feed. It is concluded that, during carbon-limited growth of S. cerevisiae on mixtures of glucose and ethanol, biosynthetic intermediates with-three or more carbon atoms are preferentially synthesized from glucose. Synthesis of the key enzymes of gluconeogenesis and the glyoxylate cycle is adapted to the cells' requirement for these intermediates. The gluconeogenic enzymes and their physiological antagonists (pyruvate kinase, pyruvate carboxylase and phosphofructokinase) were expressed simultaneously at high ethanol fractions in the feed. If futile cycling is prevented under these conditions, this is not primarily achieved by tight control of enzyme synthesis.
引用
收藏
页码:407 / 418
页数:12
相关论文
共 50 条
[21]   Regulation of central carbon metabolism in Saccharomyces cerevisiae by metabolic inhibitors [J].
Matsuda, Fumio ;
Shirai, Tomokazu ;
Ishii, Jun ;
Kondo, Akihiko .
JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 2013, 116 (01) :59-64
[22]   OSCILLATORY METABOLISM OF SACCHAROMYCES-CEREVISIAE IN CONTINUOUS CULTURE [J].
SATROUTDINOV, AD ;
KURIYAMA, H ;
KOBAYASHI, H .
FEMS MICROBIOLOGY LETTERS, 1992, 98 (1-3) :261-267
[23]   Catabolite repression mutants of Saccharomyces cerevisiae show altered fermentative metabolism as well as cell cycle behavior in glucose-limited chemostat cultures [J].
Aon, MA ;
Cortassa, S .
BIOTECHNOLOGY AND BIOENGINEERING, 1998, 59 (02) :203-213
[24]   TRANSCRIPTIONAL REGULATION OF FLOCCULATION GENES IN SACCHAROMYCES-CEREVISIAE [J].
TEUNISSEN, AWRH ;
VANDENBERG, JA ;
STEENSMA, HY .
YEAST, 1995, 11 (05) :435-446
[25]   DIFFERENTIAL REGULATION OF STA GENES OF SACCHAROMYCES-CEREVISIAE [J].
PUGH, TA ;
CLANCY, MJ .
MOLECULAR & GENERAL GENETICS, 1990, 222 (01) :87-96
[26]   REACTORS IN SERIES FOR THE COMPLETE CONVERSION OF GLUCOSE XYLOSE MIXTURES BY PICHIA-STIPITIS AND SACCHAROMYCES-CEREVISIAE [J].
GROOTJEN, DRJ ;
JANSEN, ML ;
VANDERLANS, RGJM ;
LUYBEN, KCAM .
ENZYME AND MICROBIAL TECHNOLOGY, 1991, 13 (10) :828-833
[27]   Polyamine metabolism in Saccharomyces cerevisiae exposed to ethanol [J].
Walters, D ;
Cowley, T .
MICROBIOLOGICAL RESEARCH, 1998, 153 (02) :179-184
[28]   METABOLISM OF ANAEROBIC FORMATION OF SUCCINIC ACID BY SACCHAROMYCES-CEREVISIAE [J].
HEERDE, E ;
RADLER, F .
ARCHIVES OF MICROBIOLOGY, 1978, 117 (03) :269-276
[29]   PROPIONATE METABOLISM IN SACCHAROMYCES-CEREVISIAE - IMPLICATIONS FOR THE METABOLON HYPOTHESIS [J].
PRONK, JT ;
VANDERLINDENBEUMAN, A ;
VERDUYN, C ;
SCHEFFERS, WA ;
VANDIJKEN, JP .
MICROBIOLOGY-UK, 1994, 140 :717-722
[30]   The effect of growth factors on anoxic chemostat cultures of two Saccharomyces cerevisiae strains [J].
S.H. de Kock ;
J.C. du Preez ;
S.G. Kilian .
Biotechnology Letters, 2001, 23 :957-962