Improvement in organophosphorus hydrolase activity of cell surface-engineered yeast strain using Flo1p anchor system.

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 Lett

journal_title

Biotechnology letters

authors

Fukuda T,Tsuchiyama K,Makishima H,Takayama K,Mulchandani A,Kuroda K,Ueda M,Suye S

doi

10.1007/s10529-010-0204-1

subject

Has Abstract

pub_date

2010-05-01 00:00:00

pages

655-9

issue

5

eissn

0141-5492

issn

1573-6776

journal_volume

32

pub_type

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