共 56 条
Phylogenomic analysis of Cation Diffusion Facilitator proteins uncovers Ni2+/Co2+ transporters
被引:34
作者:
Cubillas, Ciro
[1
]
Vinuesa, Pablo
[1
]
Luisa Tabche, Maria
[2
]
Garcia-de los Santos, Alejandro
[1
]
机构:
[1] Univ Nacl Autonoma Mexico, Ctr Ciencias Genom, Programa Ingn Genom, Cuernavaca 62191, Morelos, Mexico
[2] Univ Nacl Autonoma Mexico, Inst Biotecnol, Dept Mol Microbiol, Cuernavaca 62210, Morelos, Mexico
来源:
关键词:
MULTIPLE SEQUENCE ALIGNMENT;
COLI ZINC TRANSPORTER;
ESCHERICHIA-COLI;
RHIZOBIUM-ETLI;
THERMUS-THERMOPHILUS;
FUNCTIONAL-ANALYSIS;
METALLIDURANS CH34;
ANTIPORT MECHANISM;
GENOMIC ANALYSIS;
EFFLUX PROTEIN;
D O I:
10.1039/c3mt00204g
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The ubiquitous Cation Diffusion Facilitator proteins (CDF) play a key role in maintaining the cellular homeostasis of essential metal ions. Previous neighbor-joining phylogenetic analysis classified CDF proteins into three substrate-defined groups: Zn2+, Fe2+/Zn2+ and Mn2+. These studies were unable to discern substrate-defined clades for Ni2+, Co2+, Cd2+ and Cu2+ transporters, despite their existence in this family. In this study we improved the accuracy of this previous functional classification using a phylogenomic approach based on a thorough maximum-likelihood phylogeny and the inclusion of recently characterized CDF transporters. The inference of CDF protein function predicted novel clades for Zn2+, Fe2+, Cd2+ and Mn2+. The Ni2+/Co2+ and Co2+ substrate specificities of two clades containing uncharacterized proteins were defined through the functional characterization of nepA and cepA metal inducible genes which independently conferred Ni2+ and Co2+ resistances to Rhizobium etli CFN42 and increased, respectively, N-i2+/Co2+ and Co2+ resistances to Escherichia coli. Neither NepA nor CepA confer Zn2+, Fe2+ and Mn2+ resistances. The ability of NepA to confer Ni2+/Co2+ resistance is dependent on clade-specific residues Asn(88) and Arg(197) whose mutations produce a non-functional protein.
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页码:1634 / 1643
页数:10
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