Abstract:
:Organophosphorus hydrolase (OPH) hydrolyzes organophosphorus esters. We constructed the yeast-displayed OPH using Flo1p anchor system. In this system, the N-terminal region of the protein was fused to Flo1p and the fusion protein was displayed on the cell surface. Hydrolytic reactions with paraoxon were carried out during 24 h of incubation of OPH-displaying cells at 30 degrees C. p-Nitrophenol produced in the reaction mixture was detected by HPLC. The strain with highest activity showed 8-fold greater OPH activity compared with cells engineered using glycosylphosphatidylinositol anchor system, and showed 20-fold greater activity than Escherichia coli using the ice nucleation protein anchor system. These results indicate that Flo1p anchor system is suitable for display of OPH in the cell surface-expression systems.
journal_name
Biotechnol Lettjournal_title
Biotechnology lettersauthors
Fukuda T,Tsuchiyama K,Makishima H,Takayama K,Mulchandani A,Kuroda K,Ueda M,Suye Sdoi
10.1007/s10529-010-0204-1subject
Has Abstractpub_date
2010-05-01 00:00:00pages
655-9issue
5eissn
0141-5492issn
1573-6776journal_volume
32pub_type
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