TY - JOUR
T1 - Control of the nitrile-hydrolyzing enzyme activity in Rhodococcus rhodochrous IFO 15564
T2 - Preferential action of nitrile hydratase and amidase depending on the reaction condition factors and its application to the one-pot preparation of amides from aldehydes
AU - Kashiwagi, Mieko
AU - Fuhshuku, Ken Ichi
AU - Sugai, Takeshi
N1 - Funding Information:
The authors thank Professor Hiromichi Ohta, Drs. Kenji Miyamoto and Yoichi Suzuki of Keio University, for their interest. Part of this work was accomplished as the collaborated program of “CREST: Creation of Functions of New Molecules and Molecular Assemblies” of Japan Science and Technology Corporation, and we express our sincere thanks to Professors K. Suzuki and T. Matsumoto for their discussions. This work was also supported both by a Grant-in-Aid for Scientific Research (No. 14560084) and the 21st Century COE Program (KEIO LCC) from the Ministry of Education, Culture, Sports, Science, and Technology, Japan, and acknowledged with thanks.
PY - 2004/6/21
Y1 - 2004/6/21
N2 - The reaction conditions towards the preferential action of either nitrile hydratase or amidase in the harvested whole cells of Rhodococcus rhodochrous IFO 15564 were elaborated. The amidase showed higher heat tolerance than the nitrile hydratase and, at 45°C the amidase worked exclusively. DMSO assisted the preferential action of nitrile hydratase, however, at more than 30% (v/v) addition of DMF, the nitrile hydratase activity was completely lost and only amidase worked. A one-pot chemo-enzymatic conversion of aldehydes to amides [(1) aq. NH3, I2, DMSO; (2) Na2S2O 3; (3) harvested cells of R. rhodochrous] was established. Under these reaction conditions, most of the amidase was lost, and the incubation of the firstly formed intermediates, nitriles in aq. NH3 was responsible for the selective inhibition of amidase. The freezing of harvested cells in an exhaustively deionized environment provided a long-term preservable "ready to use" for the organic chemist.
AB - The reaction conditions towards the preferential action of either nitrile hydratase or amidase in the harvested whole cells of Rhodococcus rhodochrous IFO 15564 were elaborated. The amidase showed higher heat tolerance than the nitrile hydratase and, at 45°C the amidase worked exclusively. DMSO assisted the preferential action of nitrile hydratase, however, at more than 30% (v/v) addition of DMF, the nitrile hydratase activity was completely lost and only amidase worked. A one-pot chemo-enzymatic conversion of aldehydes to amides [(1) aq. NH3, I2, DMSO; (2) Na2S2O 3; (3) harvested cells of R. rhodochrous] was established. Under these reaction conditions, most of the amidase was lost, and the incubation of the firstly formed intermediates, nitriles in aq. NH3 was responsible for the selective inhibition of amidase. The freezing of harvested cells in an exhaustively deionized environment provided a long-term preservable "ready to use" for the organic chemist.
KW - Amidase
KW - Enzyme inhibition
KW - Nitrile hydratase
KW - One-pot synthesis of amides
KW - Rhodococcus rhodochrous IFO 15564
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U2 - 10.1016/j.molcatb.2003.12.014
DO - 10.1016/j.molcatb.2003.12.014
M3 - Article
AN - SCOPUS:2442498482
SN - 1381-1177
VL - 29
SP - 249
EP - 258
JO - Journal of Molecular Catalysis B: Enzymatic
JF - Journal of Molecular Catalysis B: Enzymatic
IS - 1-6
ER -