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Chemoenzymatic production of 1,5-dimethyl-2-piperidone 总被引:3,自引:0,他引:3
F. B. Cooling S. K. Fager R. D. Fallon P. W. Folsom F. G. Gallagher J. E. Gavagan E. C. Hann F. E. Herkes R. L. Phillips A. Sigmund L. W. Wagner W. Wu R. DiCosimo 《Journal of Molecular Catalysis .B, Enzymatic》2001,11(4-6):295-306
A chemoenzymatic process for the preparation of 1,5-dimethyl-2-piperidone (1,5-DMPD) from 2-methylglutaronitrile (MGN) has been demonstrated. MGN was first hydrolyzed to 4-cyanopentanoic acid (4-CPA) ammonium salt using the nitrilase activity of immobilized Acidovorax facilis 72W cells. The hydrolysis reaction produced 4-CPA ammonium salt with greater than 98% regioselectivity at 100% conversion, and at concentrations of 170–210 g 4-CPA/l. Catalyst productivities of at least 1000 g 4-CPA/g dry cell weight (dcw) of immobilized cells were achieved by recycling the immobilized-cell catalyst in consecutive stirred-batch reactions. After recovery of the immobilized cell catalyst for reuse, the 4-CPA ammonium salt in the aqueous product mixture was directly converted to 1,5-DMPD by low-pressure catalytic hydrogenation in the presence of added methylamine. 相似文献
85.
Psychrophilic microorganisms and their cold-active enzymes 总被引:2,自引:0,他引:2
JE Brenchley 《Journal of industrial microbiology & biotechnology》1996,17(5-6):432-437
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Cyclins are indispensable elements of the cell cycle and derangement of their function can lead to cancer formation. Recent studies have also revealed more mechanisms through which cyclins can express their oncogenic potential. This review focuses on the aberrant expression of G1/S cyclins and especially cyclin D and cyclin E; the pathways through which they lead to tumour formation and their involvement in different types of cancer. These elements indicate the mechanisms that could act as targets for cancer therapy. 相似文献