This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ikeda, M.
Right arrow Articles by Katsumata, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ikeda, M.
Right arrow Articles by Katsumata, R.
Agricola
Right arrow Articles by Ikeda, M.
Right arrow Articles by Katsumata, R.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, June 1999, p. 2497-2502, Vol. 65, No. 6
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Hyperproduction of Tryptophan by Corynebacterium glutamicum with the Modified Pentose Phosphate Pathway

Masato Ikeda1,* and Ryoichi Katsumata2

Technical Research Laboratories, Kyowa Hakko Kogyo Co., Ltd., Hofu, Yamaguchi 747-8522,1 and Laboratory of Animal Microbiology, Faculty of Agriculture, Tohoku University, Aobaku, Sendai 981-0914,2 Japan

Received 11 January 1999/Accepted 16 March 1999

A classically derived tryptophan-producing Corynebacterium glutamicum strain was recently significantly improved both by plasmid-mediated amplification of the genes for the rate-limiting enzymes in the terminal pathways and by construction of a plasmid stabilization system so that it produced more tryptophan. This engineered strain, KY9218 carrying pKW9901, produced 50 g of tryptophan per liter from sucrose after 80 h in fed-batch cultivation without antibiotic pressure. Analysis of carbon balances showed that at the late stage of the fermentation, tryptophan yield decreased with a concomitant increase in CO2 yield, suggesting a transition in the distribution of carbon flow from aromatic biosynthesis toward the tricarboxylic acid cycle via glycolysis. To circumvent this transition by increasing the supply of erythrose 4-phosphate, a direct precursor of aromatic biosynthesis, the transketolase gene of C. glutamicum was coamplified in the engineered strain by using low- and high-copy-number plasmids which were compatible with the resident plasmid pKW9901. The presence of the gene in low copy numbers contributed to improvement of tryptophan yield, especially at the late stage, and led to accumulation of more tryptophan (57 g/liter) than did its absence, while high-copy-number amplification of the gene resulted in a tryptophan production level even lower than that resulting from the absence of the gene due to reduced growth and sugar consumption. In order to assemble all the cloned genes onto a low-copy-number plasmid, the high-copy-number origin of pKW9901 was replaced with the low-copy-number one, generating low-copy-number plasmid pSW9911, and the transketolase gene was inserted to yield pIK9960. The pSW9911-carrying producer showed almost the same fermentation profiles as the pKW9901 carrier in fed-batch cultivation without antibiotic pressure. Under the same culture conditions, however, the pIK9960 carrier achieved a final tryptophan titer of 58 g/liter, which represented a 15% enhancement over the titers achieved by the pKW9901 and pSW9911 carriers.


* Corresponding author. Mailing address: Technical Research Laboratories, Kyowa Hakko Kogyo Co., Ltd., Kyowa-machi, Hofu, Yamaguchi 747-8522, Japan. Phone: 0835-22-2518. Fax: 0835-22-2466. E-mail: m.ikeda{at}kyowa.co.jp.


Applied and Environmental Microbiology, June 1999, p. 2497-2502, Vol. 65, No. 6
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Brune, I., Jochmann, N., Brinkrolf, K., Huser, A. T., Gerstmeir, R., Eikmanns, B. J., Kalinowski, J., Puhler, A., Tauch, A. (2007). The IclR-Type Transcriptional Repressor LtbR Regulates the Expression of Leucine and Tryptophan Biosynthesis Genes in the Amino Acid Producer Corynebacterium glutamicum. J. Bacteriol. 189: 2720-2733 [Abstract] [Full Text]  
  • Becker, J., Klopprogge, C., Zelder, O., Heinzle, E., Wittmann, C. (2005). Amplified Expression of Fructose 1,6-Bisphosphatase in Corynebacterium glutamicum Increases In Vivo Flux through the Pentose Phosphate Pathway and Lysine Production on Different Carbon Sources. Appl. Environ. Microbiol. 71: 8587-8596 [Abstract] [Full Text]  
  • Wittmann, C., Kiefer, P., Zelder, O. (2004). Metabolic Fluxes in Corynebacterium glutamicum during Lysine Production with Sucrose as Carbon Source. Appl. Environ. Microbiol. 70: 7277-7287 [Abstract] [Full Text]  
  • Simic, P., Willuhn, J., Sahm, H., Eggeling, L. (2002). Identification of glyA (Encoding Serine Hydroxymethyltransferase) and Its Use Together with the Exporter ThrE To Increase L-Threonine Accumulation by Corynebacterium glutamicum. Appl. Environ. Microbiol. 68: 3321-3327 [Abstract] [Full Text]