1994 Fiscal Year Final Research Report Summary
Determination of cofactor structure and localization of amine oxidase from Aspergillus niger
| Project/Area Number |
05660098
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
応用微生物学・応用生物化学
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| Research Institution | Yamaguchi University |
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Principal Investigator |
ADACHI Osao Yamaguchi Univ.Faculty of Agriculture, 農学部, 教授 (20027189)
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| Project Period (FY) |
1993 – 1994
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| Keywords | amine oxidase / quinoprotein / topaquinone / prosthetic group |
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| Research Abstract |
Two distinct copper-quinoprotein amine oxidases (EC 1.4.3.6) , AO-I and AO-II,were isolated from the soluble fraction of homogenized Aspergillus niger mycelia grown on butylamine medium. AO-I is a dimmer consisting of two 75 kDa subunits, while AO-II is a monomer of 80 kDa. Purified AO-I and AO-II show pink (490 nm) and yellow (420 nm) colors, respectively. The enzymes show comparable substrate specificity and sinsitivity to inhibitors. Hexylamine butylamine, benzylamine, tyramine and histamine are preferred substrates.
Both enzymes are inhibited by substrate analogs, copper chelating agents, some alkaloids and carbonyl reagents. Enzymes labeled with p-nitrophenylhydrazine showed different absroption maxima at 465 and 440 nm for AO-I and AO-II,respectively, in neutral pH.These maxima were shifted to 585 nm under alkali condition.. Absorption spectra and fluorescence spectra of synthesized model compound-topaquinone hydantoin p-nitrophenylhydrazone and labeled enzyme were in very good agreement, while PQQ p-nitrophenylhydrazone showed significant difference. After digestion by thermolysin, labeled cofactor containing peptides were purified using reverse phase HPLC and sequneced by Edman degradation, resulting typical topaquinone containing sequence, Asn-topa-Glu-Try, for AO-II and a noncofactor peptide, Val-Val-Ile-Glu-Pro, which contained topaquinone linked to gamma-carbonyl of Glu, for AO-I.Cofactor structures were confirmed by mass spectrometry. N-Terminal amino acid sequences of AO-I and II were found to be different and peptide mapping showed some distinct patterns for both enzymes. A gene encoding AO-I has been cloned already and the second gene for AO-II is now under processing.
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