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Applied and Environmental Microbiology, June 1999, p. 2497-2502, Vol. 65, No. 6
Technical Research Laboratories,
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.
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
*
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.
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