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Appl Environ Microbiol. 1974 April; 27(4): 688-694
Copyright © 1974 American Society for Microbiology. All Rights Reserved.

Enzymatic Production of Urocanic Acid by Achromobacter liquidum

Takeji Shibatani, Noriyuki Nishimura, Koichi Nabe, Toshio Kakimoto and Ichiro Chibata

Research Laboratory of Applied Biochemistry, Tanabe Seiyaku Company, Limited, 962, Kashima-cho, Higashiyodogawa-ku, Osaka, Japan

ABSTRACT

To develop an efficient method for the production of urocanic acid, optimal conditions for the production of microbial L-histidine ammonia lyase and for the conversion of L-histidine to urocanic acid by this enzyme were studied. A number of microorganisms were screened to test their ability to form and accumulate urocanic acid from L-histidine. Achromobacter liquidum was selected as the best organism. With this organism, enzyme activity as high as 2.0 units/ml could be produced by a shaking culture at 30 C in a medium containing glucose, urea, potassium phosphate, L-histidine, yeast extract, peptone, and inorganic salts. Appropriate addition of a surface-active agent to the reaction mixture shortened the time required for the conversion. A large amount of L-histidine was converted stoichiometrically to urocanic acid in 48 h at 40 C. Accumulated urocanic acid was readily isolated in pure form by ordinary procedures with isoelectric precipitation. Yields of isolated urocanic acid of over 92% from L-histidine were easily attainable. When the culture of Achromobacter liquidum was added to DL-histidine, D-histidine and urocanic acid were simultaneously obtained in high yields.


Appl Environ Microbiol. 1974 April; 27(4): 688-694
Copyright © 1974 American Society for Microbiology. All Rights Reserved.







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Copyright © 1974 by the American Society for Microbiology. All rights reserved.