碩士 / 大同大學 / 生物工程學系(所) / 97 / D-amino acid oxidase (DAO), a flavoenzyme, using flavin adenine
dinucleotide (FAD) as its prosthetic group can catalyze the oxidative
deamination of D-amino acids to produce the corresponding keto acids,
NH3 and H2O2. It is ubiquitously present in eukaryotes and plays
important roles in metabolism, immunity and neurotransmission. In this
study, we overexpressed zebra fish DAO (ZDAO) cDNA gene in E. coli
and purify the recombinant protein by taking advantage of His-tag. When
overexpressed in TB and TB containing sorbitol and betaine at 37 oC, the
DAO activities reached the maximum 8 and 24hr after IPTG induction,
respectively. The latter was 2000 U/L, two times more than the former.
SDS PAGE analysis showed that the molecular mass for each subunit
approximately was 40 kDa, however the native PAGE analysis suggested
that ZDAO expressed with a His-tag existed as a heptamer. The optimal
temperature and Tm were 60 oC and 43 oC, respectively. The pH optimum
was at pH 10 while the best pH stability was at pH 9. The half-lives for
the oxidative resistance to 10 、20 and 30 mM H2O2 were 90, 55 and 45
min, respectively. The best substrate was D-Phe with a kcat/KM value of 9.4
s-1 mM-1.
| Identifer | oai:union.ndltd.org:TW/097TTU05106002 |
| Date | January 2009 |
| Creators | Jhen-Yang Chi, 蔡鎮陽 |
| Contributors | I-Ching Kuan, 官宜靜 |
| Source Sets | National Digital Library of Theses and Dissertations in Taiwan |
| Language | zh-TW |
| Detected Language | English |
| Type | 學位論文 ; thesis |
| Format | 106 |
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