Bioprocess development of the production of the mutant P-219-L human D-amino acid oxidase for high soluble fraction expression in recombinant Escherichia coli
被引:5
作者:
Abou El-Magd, Rabab M.
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Univ Tokushima, Inst Enzyme Res, Div Enzyme Pathophysiol, Tokushima 7708503, JapanUniv Tokushima, Inst Enzyme Res, Div Enzyme Pathophysiol, Tokushima 7708503, Japan
Abou El-Magd, Rabab M.
[1
]
Sasaki, Chizuru
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Univ Tokushima, Dept Biol Sci & Technol, Div Biol React Engn, Tokushima 7708506, JapanUniv Tokushima, Inst Enzyme Res, Div Enzyme Pathophysiol, Tokushima 7708503, Japan
Sasaki, Chizuru
[2
]
Kawazoe, Tomoya
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Univ Tokushima, Inst Enzyme Res, Div Enzyme Pathophysiol, Tokushima 7708503, JapanUniv Tokushima, Inst Enzyme Res, Div Enzyme Pathophysiol, Tokushima 7708503, Japan
Kawazoe, Tomoya
[1
]
El-Sayed, Salah M.
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Univ Tokushima, Inst Enzyme Res, Div Enzyme Pathophysiol, Tokushima 7708503, JapanUniv Tokushima, Inst Enzyme Res, Div Enzyme Pathophysiol, Tokushima 7708503, Japan
El-Sayed, Salah M.
[1
]
Yorita, Kazuko
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Univ Tokushima, Inst Enzyme Res, Div Enzyme Pathophysiol, Tokushima 7708503, JapanUniv Tokushima, Inst Enzyme Res, Div Enzyme Pathophysiol, Tokushima 7708503, Japan
Yorita, Kazuko
[1
]
Shishido, Yuji
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Univ Tokushima, Inst Enzyme Res, Div Enzyme Pathophysiol, Tokushima 7708503, JapanUniv Tokushima, Inst Enzyme Res, Div Enzyme Pathophysiol, Tokushima 7708503, Japan
Shishido, Yuji
[1
]
Sakai, Takashi
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Univ Tokushima, Inst Enzyme Res, Div Enzyme Pathophysiol, Tokushima 7708503, JapanUniv Tokushima, Inst Enzyme Res, Div Enzyme Pathophysiol, Tokushima 7708503, Japan
Sakai, Takashi
[1
]
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Nakamura, Yoshitoshi
[2
]
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机构:
Fukui, Kiyoshi
[1
]
机构:
[1] Univ Tokushima, Inst Enzyme Res, Div Enzyme Pathophysiol, Tokushima 7708503, Japan
[2] Univ Tokushima, Dept Biol Sci & Technol, Div Biol React Engn, Tokushima 7708506, Japan
Human D amino acid oxidase;
Structure-activity relationship;
Bioprocess development;
Fed batch culture;
Chaperon inducer;
HIGH-CELL-DENSITY;
METHYL-D-ASPARTATE;
MOLECULAR-CLONING;
TUMOR-CELLS;
D-SERINE;
CATABOLITE REPRESSION;
PROTEIN EXPRESSION;
SEQUENCE-ANALYSIS;
GENE;
GROWTH;
D O I:
10.1016/j.bej.2010.08.016
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
In order to examine the structure-activity relationship and the substrate specificity of human D-amino acid oxidase (h DAO) a single amino acid mutation had been established as proline-219-luecine (P-219-L) The gene encoding mutant h DAO has been cloned and expressed in Escherichia coli BL21 (DE3) It was observed that the host cell was negatively affected by the expressed mutant h DAO resulting in a remarkable decrease in the cell growth and consequently the amount of the produced enzyme To overcome this problem we Investigated several factors that may affect the cell growth rate and the mutant h DAO production such as optimization of the glucose concentration as a main carbon source and the yeast extract concentration as a main nitrogen source optimization of dissolved oxygen (DO%) concentration and the addition of benzyl alcohol (BA which can artificially induce a strong heat shock response at low temperature) to enhance the production of natively folded soluble fraction of the recombinant protein These parameters were tested on both shake flask level and fed-batch bioreactor level The Western blot analysis and the enzyme activity assay indicated the higher level of the mutant expression towards enhancement of the conditions by using our designed approach The specific activity (which was used as an indicator for the level of the desired protein produced = U/mg protein) and the OD600nm of the host cells (which was used as an indicator for the cell growth) reached to be 0 061 U/mg protein and 3 44 respectively upon using fed-batch culture system containing the optimized medium composition (15 g/l glucose and 5 g/l yeast extract) While upon using the shake flask level these values were 0 032 and 11 respectively Enhancement of the cell growth and the enzyme production was noticed after DO% optimization upon using 500 rpm agitation speed and 1 8 v v m (volume volume minute) aeration The specific activity for the mutant enzyme and the OD600nm of the host cells reached to be 0 14 U/mg protein and 7 1 respectively Finally upon using the optimized culture composition (15 g/l glucose and 5 g/l yeast extract) optimized DO% (using 500 rpm agitation speed and 1 8 v v m) and 0 1 mM BA at the fed-batch bioreactor level the specific activity and the OD600nm of the host cells increased significantly to be 0 21 U/mg protein and 11 3 respectively at 24 h culture These results indicate the importance of our approaches to overproducing mutant h DAO in soluble form in E coli (C) 2010 Published by Elsevier B V
机构:
Genentech Inc, Cell Culture & Fermentat Res & Dev, San Francisco, CA 94080 USAGenentech Inc, Cell Culture & Fermentat Res & Dev, San Francisco, CA 94080 USA
Andersen, DC
;
Krummen, L
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机构:
Genentech Inc, Cell Culture & Fermentat Res & Dev, San Francisco, CA 94080 USAGenentech Inc, Cell Culture & Fermentat Res & Dev, San Francisco, CA 94080 USA
机构:
Genentech Inc, Cell Culture & Fermentat Res & Dev, San Francisco, CA 94080 USAGenentech Inc, Cell Culture & Fermentat Res & Dev, San Francisco, CA 94080 USA
Andersen, DC
;
Krummen, L
论文数: 0引用数: 0
h-index: 0
机构:
Genentech Inc, Cell Culture & Fermentat Res & Dev, San Francisco, CA 94080 USAGenentech Inc, Cell Culture & Fermentat Res & Dev, San Francisco, CA 94080 USA