Serveur d'exploration sur la glutarédoxine

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ydjN encodes an S-sulfocysteine transporter required by Escherichia coli for growth on S-sulfocysteine as a sulfur source.

Identifieur interne : 000399 ( Main/Exploration ); précédent : 000398; suivant : 000400

ydjN encodes an S-sulfocysteine transporter required by Escherichia coli for growth on S-sulfocysteine as a sulfur source.

Auteurs : Shunsuke Yamazaki [Japon] ; Kensuke Takei [Japon] ; Gen Nonaka [Oman]

Source :

RBID : pubmed:27481704

Descripteurs français

English descriptors

Abstract

Sulfur is an essential element for growth and many physiological functions. As sulfur sources for Escherichia coli and related bacteria, specific transporters import various sulfur-containing compounds from the environment. In this study, we identified and characterized an alternative function of the cystine transporter YdjN in E. coli as a transporter of S-sulfocysteine, a sulfur-containing intermediate in the assimilatory cysteine biosynthesis that is used as a sulfur source for the growth of E. coli We also demonstrated that the transport of S-sulfocysteine via YdjN depends on the transcriptional regulator CysB, a master regulator that controls most of the genes involved in sulfur assimilation and cysteine metabolism. We found that the use of S-sulfocysteine as a sulfur source depends on glutathione because mutations in glutathione biosynthetic genes abolish growth when S-sulfocysteine is used as a sole sulfur source, thereby supporting the previous findings that the conversion of S-sulfocysteine to cysteine is catalyzed by glutaredoxins. To the best of our knowledge, this is the first report of a functional S-sulfocysteine transporter across organisms, which strongly supports the hypothesis that S-sulfocysteine is not only a metabolic intermediate but also a physiologically significant substance in specific natural environments.

DOI: 10.1093/femsle/fnw185
PubMed: 27481704


Affiliations:


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Le document en format XML

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<term>Bacterial Proteins (genetics)</term>
<term>Cysteine (analogs & derivatives)</term>
<term>Cysteine (biosynthesis)</term>
<term>Cysteine (metabolism)</term>
<term>Cysteine (pharmacology)</term>
<term>Escherichia coli (drug effects)</term>
<term>Escherichia coli (genetics)</term>
<term>Escherichia coli (growth & development)</term>
<term>Escherichia coli (metabolism)</term>
<term>Gene Expression Regulation, Bacterial (MeSH)</term>
<term>Glutathione (metabolism)</term>
<term>Membrane Transport Proteins (genetics)</term>
<term>Membrane Transport Proteins (metabolism)</term>
<term>Sulfur (metabolism)</term>
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<term>Cystéine (biosynthèse)</term>
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<term>Cystéine (pharmacologie)</term>
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<term>Escherichia coli (effets des médicaments et des substances chimiques)</term>
<term>Escherichia coli (génétique)</term>
<term>Escherichia coli (métabolisme)</term>
<term>Glutathion (métabolisme)</term>
<term>Protéines bactériennes (génétique)</term>
<term>Protéines de transport membranaire (génétique)</term>
<term>Protéines de transport membranaire (métabolisme)</term>
<term>Régulation de l'expression des gènes bactériens (MeSH)</term>
<term>Soufre (métabolisme)</term>
<term>Systèmes de transport d'acides aminés neutres (génétique)</term>
<term>Systèmes de transport d'acides aminés neutres (métabolisme)</term>
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<term>Amino Acid Transport Systems, Neutral</term>
<term>Bacterial Proteins</term>
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<term>Cysteine</term>
<term>Glutathione</term>
<term>Membrane Transport Proteins</term>
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<div type="abstract" xml:lang="en">Sulfur is an essential element for growth and many physiological functions. As sulfur sources for Escherichia coli and related bacteria, specific transporters import various sulfur-containing compounds from the environment. In this study, we identified and characterized an alternative function of the cystine transporter YdjN in E. coli as a transporter of S-sulfocysteine, a sulfur-containing intermediate in the assimilatory cysteine biosynthesis that is used as a sulfur source for the growth of E. coli We also demonstrated that the transport of S-sulfocysteine via YdjN depends on the transcriptional regulator CysB, a master regulator that controls most of the genes involved in sulfur assimilation and cysteine metabolism. We found that the use of S-sulfocysteine as a sulfur source depends on glutathione because mutations in glutathione biosynthetic genes abolish growth when S-sulfocysteine is used as a sole sulfur source, thereby supporting the previous findings that the conversion of S-sulfocysteine to cysteine is catalyzed by glutaredoxins. To the best of our knowledge, this is the first report of a functional S-sulfocysteine transporter across organisms, which strongly supports the hypothesis that S-sulfocysteine is not only a metabolic intermediate but also a physiologically significant substance in specific natural environments.</div>
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