Automatic Redirection of Carbon Flux between Glycolysis and Pentose Phosphate Pathway Using an Oxygen-Responsive Metabolic Switch in Corynebacterium glutamicum

被引:26
作者
Kobayashi, Shunsuke [1 ]
Kawaguchi, Hideo [3 ]
Shirai, Tomokazu [4 ]
Ninomiya, Kazuaki [1 ,2 ]
Takahashi, Kenji [1 ]
Kondo, Akihiko [3 ,4 ]
Tsuge, Yota [1 ,2 ]
机构
[1] Kanazawa Univ, Grad Sch Nat Sci & Technol, Kanazawa, Ishikawa 9201192, Japan
[2] Kanazawa Univ, Inst Frontier Sci Initiat, Kanazawa, Ishikawa 9201192, Japan
[3] Kobe Univ, Grad Sch Sci Technol & Innovat, Kobe, Hyogo 6578501, Japan
[4] RIKEN, Ctr Sustainable Resource Sci, Yokohama, Kanagawa 2300045, Japan
关键词
Corynebacterium glutamicum; glycolysis; pentose phosphate pathway; glucose 6-phosphate isomerase; metabolic switch; oxygen; PHOSPHOGLUCOSE ISOMERASE MUTANTS; REPEATED ETHANOL-PRODUCTION; L-LYSINE PRODUCTION; LACTATE-DEHYDROGENASE; MICROBIAL-PRODUCTION; ESCHERICHIA-COLI; EXPRESSION; SUCCINATE; CHEMICALS; AVAILABILITY;
D O I
10.1021/acssynbio.9b00493
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Controlling the carbon flux into a desired pathway is important for improving product yield in metabolic engineering. After entering a cell, glucose is channeled into glycolysis and the pentose phosphate pathway (PPP), which decreases the yield of target products whose synthesis relies on NADPH as a cofactor. Here, we demonstrate redirection of carbon flux into PPP under aerobic conditions in Corynebacterium glutamicum, achieved by replacing the promoter of glucose 6-phosphate isomerase gene (pgi) with an anaerobic-specific promoter of the lactate dehydrogenase gene (ldhA). The promoter replacement increased the split ratio of carbon flux into PPP from 39 to 83% under aerobic conditions. The titer, yield, and production rate of 1,5-diaminopentane, whose synthesis requires NADPH as a cofactor, were increased by 4.6-, 4.4-, and 2.6-fold, respectively. This is the largest improvement in the production of 1,5-diaminopentane or its precursor, lysine, reported to date. After aerobic cell growth, pgi expression was automatically induced under anaerobic conditions, altering the carbon flux from PPP to glycolysis, to produce succinate in a single metabolically engineered strain. Such an automatic redirection of metabolic pathway using an oxygen-responsive switch enables two-stage fermentation for efficient production of two different compounds by a single strain, potentially reducing the production costs and time for practical applications.
引用
收藏
页码:814 / 826
页数:13
相关论文
共 51 条
[11]   The Global Repressor SugR Controls Expression of Genes of Glycolysis and of the L-Lactate Dehydrogenase LdhA in Corynebacterium glutamicum [J].
Engels, Verena ;
Lindner, Steffen N. ;
Wendisch, Volker F. .
JOURNAL OF BACTERIOLOGY, 2008, 190 (24) :8033-8044
[12]   Potassium Transport in Corynebacterium glutamicum Is Facilitated by the Putative Channel Protein CglK, Which Is Essential for pH Homeostasis and Growth at Acidic pH [J].
Follmann, Martin ;
Becker, Markus ;
Ochrombel, Ines ;
Ott, Vera ;
Kraemer, Reinhard ;
Marin, Kay .
JOURNAL OF BACTERIOLOGY, 2009, 191 (09) :2944-2952
[13]   GLUCOSE AND GLUCONATE METABOLISM IN AN ESCHERICHIA COLI MUTANT LACKING PHOSPHOGLUCOSE ISOMERASE [J].
FRAENKEL, DG ;
LEVISOHN, SR .
JOURNAL OF BACTERIOLOGY, 1967, 93 (05) :1571-&
[14]   Metabolic analysis of Corynebacterium glutamicum during lactate and succinate productions under oxygen deprivation conditions [J].
Inui, M ;
Murakami, S ;
Okino, S ;
Kawaguchi, H ;
Vertès, AA ;
Yukawa, H .
JOURNAL OF MOLECULAR MICROBIOLOGY AND BIOTECHNOLOGY, 2004, 7 (04) :182-196
[15]   Transcriptional profiling of Corynebacterium glutamicum metabolism during organic acid production under oxygen deprivation conditions [J].
Inui, Masayuki ;
Suda, Masako ;
Okino, Shohei ;
Nonaka, Hiroshi ;
Puskas, Laszlo G. ;
Vertes, Alain A. ;
Yukawa, Hideaki .
MICROBIOLOGY-SGM, 2007, 153 :2491-2504
[16]   Regulation of the ldhA gene, encoding the fermentative lactate dehydrogenase of Escherichia coli [J].
Jiang, GRJ ;
Nikolova, S ;
Clark, DP .
MICROBIOLOGY-SGM, 2001, 147 :2437-2446
[17]   Widely targeted metabolic profiling analysis of yeast central metabolites [J].
Kato, Hiroko ;
Izumi, Yoshihiro ;
Hasunuma, Tomohisa ;
Matsuda, Fumio ;
Kondo, Akihiko .
JOURNAL OF BIOSCIENCE AND BIOENGINEERING, 2012, 113 (05) :665-673
[18]   From zero to hero - Production of bio-based nylon from renewable resources using engineered Corynebacterium glutamicum [J].
Kind, Stefanie ;
Neubauer, Steffi ;
Becker, Judith ;
Yamamoto, Motonori ;
Volkert, Martin ;
von Abendroth, Gregory ;
Zelder, Oskar ;
Wittmann, Christoph .
METABOLIC ENGINEERING, 2014, 25 :113-123
[19]   Increased lysine production by flux coupling of the tricarboxylic acid cycle and the lysine biosynthetic pathway-Metabolic engineering of the availability of succinyl-CoA in Corynebacterium glutamicum [J].
Kind, Stefanie ;
Becker, Judith ;
Wittmann, Christoph .
METABOLIC ENGINEERING, 2013, 15 :184-195
[20]   Systems-wide metabolic pathway engineering in Corynebacterium glutamicum for bio-based production of diaminopentane [J].
Kind, Stefanie ;
Jeong, Weol Kyu ;
Schroeder, Hartwig ;
Wittmann, Christoph .
METABOLIC ENGINEERING, 2010, 12 (04) :341-351