Effect of different carbon sources on central metabolic fluxes and the recombinant production of a hydrolase from Thermobifida fusca in Bacillus megaterium

被引:31
作者
Fuerch, Tobias
Wittmann, Christoph
Wang, Wei
Franco-Lara, Ezequiel
Jahn, Dieter
Deckwer, Wolf-Dieter
机构
[1] Tech Univ Carolo Wilhelmina Braunschweig, HZI Helmholtz Zentrum Infekt Forsch, Inst Biochem Engn, D-38124 Braunschweig, Germany
[2] Univ Saarland, D-66123 Saarbrucken, Germany
[3] Tech Univ Carolo Wilhelmina Braunschweig, Inst Biochem Engn, D-38106 Braunschweig, Germany
[4] Tech Univ Carolo Wilhelmina Braunschweig, Inst Microbiol, D-38106 Braunschweig, Germany
关键词
Bacillus megaterium; metabolic flux analysis; central carbon pathways; recombinant protein production; energy metabolism;
D O I
10.1016/j.jbiotec.2007.08.004
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
The recombinant Bacillus megaterium strain WH323 was employed for the inducible production and secretion of recombinant Thermobifida fusca hydrolase (TFH). Continuous cultivations were carried out in a chemostat using either glucose or pyruvate as sole carbon source. A remarkable increase of produced TFH was detected for the pyruvate-dependent cultivation compared to glucose-dependent growth. Estimation of intracellular carbon fluxes through the central metabolism for both growth conditions using 13 C-labelled substrates revealed noticeable changes of the fluxes through the tricarboxylic acid cycle, the pentose phosphate pathway and around the pyruvate node when protein production was induced. With pyruvate as sole carbon source the observed alterations of the fluxes yielded an increased production of ATP and NADPH both required for the anabolism. Additionally, the analysis of the corresponding secretome revealed significantly reduced amounts of extracellular proteases in the medium compared to glucose-grown cultivations. Thus, pyruvate-dependent chemostat cultivation was identified as a favourable condition for production and secretion of recombinant TFH using B. megaterium as production host. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:385 / 394
页数:10
相关论文
共 33 条
[1]  
[Anonymous], 1990, GEL ELECTROPHORESIS
[2]  
BARG H, 2005, MICROBIAL PROCESSES, P165
[3]   Transcriptional profiling of gene expression in response to glucose in Bacillus subtilis:: regulation of the central metabolic pathways [J].
Blencke, HM ;
Homuth, G ;
Ludwig, H ;
Mäder, U ;
Hecker, M ;
Stülke, J .
METABOLIC ENGINEERING, 2003, 5 (02) :133-149
[4]   Metabolic flux analysis with a comprehensive isotopomer model in Bacillus subtilis [J].
Dauner, M ;
Bailey, JE ;
Sauer, U .
BIOTECHNOLOGY AND BIOENGINEERING, 2001, 76 (02) :144-156
[5]   Stoichiometric growth model for riboflavin-producing Bacillus subtilis [J].
Dauner, M ;
Sauer, U .
BIOTECHNOLOGY AND BIOENGINEERING, 2001, 76 (02) :132-143
[6]   Production of a recombinant polyester-cleaving hydrolase from Thermobifida fusca in Escherichia coli [J].
Dresler, Karolin ;
van den Heuvel, Joop ;
Mueller, Rolf-Joachim ;
Deckwer, Wolf-Dieter .
BIOPROCESS AND BIOSYSTEMS ENGINEERING, 2006, 29 (03) :169-183
[7]   Metabolic flux profiling of Escherichia coli mutants in central carbon metabolism using GC-MS [J].
Fischer, E ;
Sauer, U .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2003, 270 (05) :880-891
[8]   High-throughput metabolic flux analysis based on gas chromatography-mass spectrometry derived 13C constraints [J].
Fischer, E ;
Zamboni, N ;
Sauer, U .
ANALYTICAL BIOCHEMISTRY, 2004, 325 (02) :308-316
[9]   Comparative study on central metabolic fluxes of Bacillus megaterium strains in continuous culture using 13C labelled substrates [J].
Fuerch, Tobias ;
Hollmann, Rajan ;
Wittmann, Christoph ;
Wang, Wei ;
Deckwer, Wolf-Dieter .
BIOPROCESS AND BIOSYSTEMS ENGINEERING, 2007, 30 (01) :47-59
[10]   A direct comparison of approaches for increasing carbon flow to aromatic biosynthesis in Escherichia coli [J].
Gosset, G ;
YongXiao, J ;
Berry, A .
JOURNAL OF INDUSTRIAL MICROBIOLOGY, 1996, 17 (01) :47-52