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J Bacteriol, May 1998, p. 2280-2284, Vol. 180, No. 9
Centro Nacional de Biotecnología,
CSIC, 28049 Madrid, Spain,1 and
Department of Biochemistry and Microbiology, Institute of
Chemical Technology, 166 28 Prague, Czech Republic2
Received 18 November 1997/Accepted 23 February 1998
Yeast (CUP1) and mammalian (HMT-1A) metallothioneins (MTs) have
been efficiently expressed in Escherichia coli as fusions to the outer membrane protein LamB. A 65-amino-acid sequence from the
CUP1 protein of Saccharomyces cerevisiae (yeast [Y] MT)
was genetically inserted in permissive site 153 of the LamB
sequence, which faces the outer medium. A second LamB fusion at
position 153 was created with 66 amino acids recruited from the form of human (H) MT that is predominant in the adipose tissue, HMT-1A. Both LamB153-YMT and LamB153-HMT
hybrids were produced in vivo as full-length proteins, without any
indication of instability or proteolytic degradation.
Each of the two fusion proteins was functional as the port of
entry of lambda phage variants, suggesting maintenance of
the overall topology of the wild-type LamB. Expression of the hybrid
proteins in vivo multiplied the natural ability of E. coli
cells to bind Cd2+ 15- to 20-fold, in good
correlation with the number of metal-binding centers contributed by
the MT moiety of the fusions.
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Metalloadsorption by Escherichia coli
Cells Displaying Yeast and Mammalian Metallothioneins Anchored to
the Outer Membrane Protein LamB

and
*
Corresponding author. Mailing address: Centro Nacional
de Biotecnología (CSIC), Campus de Cantoblanco, 28049 Madrid,
Spain. Phone: (341) 5854536. Fax: (341) 5854506. E-mail:
VDLORENZO{at}CNB.UAM.ES.
Present address: Centre National de la Recherche Scientifique,
Institut des Sciences Végétales, 91198 Gif-sur-Yvette,
France.
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