Literature DB >> 18039771

Identification of a spermidine excretion protein complex (MdtJI) in Escherichia coli.

Kyohei Higashi1, Hiroyuki Ishigure, Risa Demizu, Takeshi Uemura, Kunihiko Nishino, Akihito Yamaguchi, Keiko Kashiwagi, Kazuei Igarashi.   

Abstract

A spermidine excretion protein in Escherichia coli was looked for among 33 putative drug exporters thus far identified. Cell toxicity and inhibition of growth due to overaccumulation of spermidine were examined in an E. coli strain deficient in spermidine acetyltransferase, an enzyme that metabolizes spermidine. Toxicity and inhibition of cell growth by spermidine were recovered in cells transformed with pUCmdtJI or pMWmdtJI, encoding MdtJ and MdtI, which belong to the small multidrug resistance family of drug exporters. Both mdtJ and mdtI are necessary for recovery from the toxicity of overaccumulated spermidine. It was also found that the level of mdtJI mRNA was increased by spermidine. The spermidine content in cells cultured in the presence of 2 mM spermidine was decreased, and excretion of spermidine from cells was enhanced by MdtJI, indicating that the MdtJI complex can catalyze excretion of spermidine from cells. It was found that Tyr4, Trp5, Glu15, Tyr45, Tyr61, and Glu82 in MdtJ and Glu5, Glu19, Asp60, Trp68, and Trp81 in MdtI are involved in the excretion activity of MdtJI.

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Year:  2007        PMID: 18039771      PMCID: PMC2223573          DOI: 10.1128/JB.01505-07

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  38 in total

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6.  Effects of polyamines, polyamine analogs, and inhibitors of protein synthesis on spermidine-spermine N1-acetyltransferase gene expression.

Authors:  M Fogel-Petrovic; S Vujcic; P J Brown; M K Haddox; C W Porter
Journal:  Biochemistry       Date:  1996-11-12       Impact factor: 3.162

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10.  Crystal structure and mutational analysis of the Escherichia coli putrescine receptor. Structural basis for substrate specificity.

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4.  Surface-localized spermidine protects the Pseudomonas aeruginosa outer membrane from antibiotic treatment and oxidative stress.

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Journal:  J Bacteriol       Date:  2011-12-09       Impact factor: 3.490

5.  Short-chain diamines are the physiological substrates of PACE family efflux pumps.

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7.  Identification and characterization of a diamine exporter in colon epithelial cells.

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Review 8.  The Evolutionary Conservation of Escherichia coli Drug Efflux Pumps Supports Physiological Functions.

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9.  Involvement of polyamine binding protein D (PotD) of Synechocystis sp. PCC 6803 in spermidine uptake and excretion.

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10.  Diversity and evolution of the small multidrug resistance protein family.

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