The Journal of Biochemistry
Online ISSN : 1756-2651
Print ISSN : 0021-924X
Kinetic Studies on Degradation of Nucleotides Catalyzed by Phosphodiesterase-Phosphomonoesterase from Fusarium moniliforme
Hiroshi YOSHIDATomoko WATANABEHayato ISHIDA
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1984 Volume 96 Issue 4 Pages 971-976

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Abstract
Degradation of the 2'-phosphates, 3'-phosphates, 5'-phosphates, 2':3'-cyclic phos-phates, 3':5'-cyclic phosphates, and 5'-(p-nitrophenylphosphates) of adenosine, guanosine, cytidine, and uridine catalyzed by Fusarium phosphodiesterase-phospho-monoesterase was followed by means of high performance liquid chromatography. All the nucleotides were susceptible to the enzyme to a greater or lesser degree, and the kinetic constants, Km and kcat, were determined at pH 5.3 and 37°C. These constants were affected by both the nucleoside moiety and the position of the phosphate. Judged from kcat/Km, the 3'-phosphates, 2':3'-cyclic phosphates, and 5'-(p-nitrophenylphosphates) were good substrates, whereas the 2'-phosphates, 5'-phos-phates, and 3':5'-cyclic phosphates were poor substrates except for adenosine 2'-phosphate, adenosine 5'-phosphate, and cytidine 5'-phosphate, which were hydro-lyzed relatively easily. Among the phosphodiesters, the 2':3'-cyclic phosphates of adenosine, guanosine, and cytidine; and the 3':5'-cyclic phosphates of adenosine and cytidine were degraded into nucleoside and inorganic phosphate without release of intermediary phosphomonoester into the medium. Other phosphodiesters were degraded stepwise releasing definite intermediates.
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© The Japanese Biochemical Society
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