Cell surface-engineered yeast with ability to bind, and self-aggregate in response to, copper ion

被引:69
作者
Kuroda, K [1 ]
Ueda, M [1 ]
Shibasaki, S [1 ]
Tanaka, A [1 ]
机构
[1] Kyoto Univ, Lab Appl Biol Chem, Dept Synthet Chem & Biol Chem, Grad Sch Engn,Sakyo Ku, Kyoto 6068501, Japan
关键词
D O I
10.1007/s00253-002-1014-8
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 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
In order to construct a cell surface-engineered yeast Saccharomyces cerevisiae that facilitates adsorption and recovery of heavy metal ions, we endowed it with the ability to self-aggregate in response to binding and accumulation of copper ion. A fusion gene for the expression of GTS1, which encodes a putative zinc-finger transcription factor related to occurrence of cell-aggregation, was constructed under the control of the copper ion-inducible CUP1 promoter from the yeast metallothionein gene. The multicopy plasmid carrying the fusion gene was introduced into a cell surface-engineered yeast displaying histidine hexa-peptide, which can chelate copper ion. This transformant strain aggregated in medium only in the presence of copper ion, with aggregation induced by as little as 1 mM copper ion. The copper ion-induced aggregation did not interfere with the copper ion-adsorbing function of the cell surface-engineered yeast, indicating that this transformant strain has the twin features of enhanced cell surface adsorption of copper ion and self-aggregation in response to environmental copper ion.
引用
收藏
页码:259 / 264
页数:6
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