Halotolerant Cyanobacterium Aphanothece halophytica Contains NapA-Type Na⁺/H⁺ Antiporters with Novel Ion Specificity That Are Involved in Salt Tolerance at Alkaline pH

Aphanothece halophytica is a halotolerant alkaliphilic cyanobacterium which can grow at NaCl concentrations up to 3.0 M and at pH values up to 11. The genome sequence revealed that the cyanobacterium Synechocystis sp. strain PCC 6803 contains five putative Na⁺/H⁺ antiporters, two of which are homolo...

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Veröffentlicht in:Applied and Environmental Microbiology 2005-08, Vol.71 (8), p.4176-4184
Hauptverfasser: Wutipraditkul, Nuchanat, Waditee, Rungaroon, Incharoensakdi, Aran, Hibino, Takashi, Tanaka, Yoshito, Nakamura, Tatsunosuke, Shikata, Masamitsu, Takabe, Tetsuko, Takabe, Teruhiro
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container_issue 8
container_start_page 4176
container_title Applied and Environmental Microbiology
container_volume 71
creator Wutipraditkul, Nuchanat
Waditee, Rungaroon
Incharoensakdi, Aran
Hibino, Takashi
Tanaka, Yoshito
Nakamura, Tatsunosuke
Shikata, Masamitsu
Takabe, Tetsuko
Takabe, Teruhiro
description Aphanothece halophytica is a halotolerant alkaliphilic cyanobacterium which can grow at NaCl concentrations up to 3.0 M and at pH values up to 11. The genome sequence revealed that the cyanobacterium Synechocystis sp. strain PCC 6803 contains five putative Na⁺/H⁺ antiporters, two of which are homologous to NhaP of Pseudomonas aeruginosa and three of which are homologous to NapA of Enterococcus hirae. The physiological and functional properties of NapA-type antiporters are largely unknown. One of NapA-type antiporters in Synechocystis sp. strain PCC 6803 has been proposed to be essential for the survival of this organism. In this study, we examined the isolation and characterization of the homologous gene in Aphanothece halophytica. Two genes encoding polypeptides of the same size, designated Ap-napA1-1 and Ap-napA1-2, were isolated. Ap-NapA1-1 exhibited a higher level of homology to the Synechocystis ortholog (Syn-NapA1) than Ap-NapA1-2 exhibited. Ap-NapA1-1, Ap-NapA1-2, and Syn-NapA1 complemented the salt-sensitive phenotypes of an Escherichia coli mutant and exhibited strongly pH-dependent Na⁺/H⁺ and Li⁺/H⁺ exchange activities (the highest activities were at alkaline pH), although the activities of Ap-NapA1-2 were significantly lower than the activities of the other polypeptides. Only one these polypeptides, Ap-NapA1-2, complemented a K⁺ uptake-deficient E. coli mutant and exhibited K⁺ uptake activity. Mutagenesis experiments suggested the importance of Glu129, Asp225, and Asp226 in the putative transmembrane segment and Glu142 in the loop region for the activity. Overexpression of Ap-NapA1-1 in the freshwater cyanobacterium Synechococcus sp. strain PCC 7942 enhanced the salt tolerance of cells, especially at alkaline pH. These findings indicate that A. halophytica has two NapA1-type antiporters which exhibit different ion specificities and play an important role in salt tolerance at alkaline pH.
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The genome sequence revealed that the cyanobacterium Synechocystis sp. strain PCC 6803 contains five putative Na⁺/H⁺ antiporters, two of which are homologous to NhaP of Pseudomonas aeruginosa and three of which are homologous to NapA of Enterococcus hirae. The physiological and functional properties of NapA-type antiporters are largely unknown. One of NapA-type antiporters in Synechocystis sp. strain PCC 6803 has been proposed to be essential for the survival of this organism. In this study, we examined the isolation and characterization of the homologous gene in Aphanothece halophytica. Two genes encoding polypeptides of the same size, designated Ap-napA1-1 and Ap-napA1-2, were isolated. Ap-NapA1-1 exhibited a higher level of homology to the Synechocystis ortholog (Syn-NapA1) than Ap-NapA1-2 exhibited. Ap-NapA1-1, Ap-NapA1-2, and Syn-NapA1 complemented the salt-sensitive phenotypes of an Escherichia coli mutant and exhibited strongly pH-dependent Na⁺/H⁺ and Li⁺/H⁺ exchange activities (the highest activities were at alkaline pH), although the activities of Ap-NapA1-2 were significantly lower than the activities of the other polypeptides. Only one these polypeptides, Ap-NapA1-2, complemented a K⁺ uptake-deficient E. coli mutant and exhibited K⁺ uptake activity. Mutagenesis experiments suggested the importance of Glu129, Asp225, and Asp226 in the putative transmembrane segment and Glu142 in the loop region for the activity. Overexpression of Ap-NapA1-1 in the freshwater cyanobacterium Synechococcus sp. strain PCC 7942 enhanced the salt tolerance of cells, especially at alkaline pH. 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Psychology ; Gene Expression Regulation, Bacterial ; Hydrogen ; Hydrogen-Ion Concentration ; Ions ; Lithium Chloride - pharmacology ; Microbiology ; Molecular Sequence Data ; Mutagenesis, Site-Directed ; Permeability, membrane transport, intracellular transport ; Potassium - metabolism ; Salt ; Sodium ; Sodium Chloride - pharmacology ; Sodium-Hydrogen Exchangers - chemistry ; Sodium-Hydrogen Exchangers - genetics ; Sodium-Hydrogen Exchangers - metabolism</subject><ispartof>Applied and Environmental Microbiology, 2005-08, Vol.71 (8), p.4176-4184</ispartof><rights>2006 INIST-CNRS</rights><rights>Copyright American Society for Microbiology Aug 2005</rights><rights>Copyright © 2005, American Society for Microbiology 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c559t-d593d0cab5b9725da0877c977d072e062821af84c0b48c3d682fe2ee95612de23</citedby><cites>FETCH-LOGICAL-c559t-d593d0cab5b9725da0877c977d072e062821af84c0b48c3d682fe2ee95612de23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1183346/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1183346/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3188,3189,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17048534$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16085800$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wutipraditkul, Nuchanat</creatorcontrib><creatorcontrib>Waditee, Rungaroon</creatorcontrib><creatorcontrib>Incharoensakdi, Aran</creatorcontrib><creatorcontrib>Hibino, Takashi</creatorcontrib><creatorcontrib>Tanaka, Yoshito</creatorcontrib><creatorcontrib>Nakamura, Tatsunosuke</creatorcontrib><creatorcontrib>Shikata, Masamitsu</creatorcontrib><creatorcontrib>Takabe, Tetsuko</creatorcontrib><creatorcontrib>Takabe, Teruhiro</creatorcontrib><title>Halotolerant Cyanobacterium Aphanothece halophytica Contains NapA-Type Na⁺/H⁺ Antiporters with Novel Ion Specificity That Are Involved in Salt Tolerance at Alkaline pH</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>Aphanothece halophytica is a halotolerant alkaliphilic cyanobacterium which can grow at NaCl concentrations up to 3.0 M and at pH values up to 11. 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Ap-NapA1-1, Ap-NapA1-2, and Syn-NapA1 complemented the salt-sensitive phenotypes of an Escherichia coli mutant and exhibited strongly pH-dependent Na⁺/H⁺ and Li⁺/H⁺ exchange activities (the highest activities were at alkaline pH), although the activities of Ap-NapA1-2 were significantly lower than the activities of the other polypeptides. Only one these polypeptides, Ap-NapA1-2, complemented a K⁺ uptake-deficient E. coli mutant and exhibited K⁺ uptake activity. Mutagenesis experiments suggested the importance of Glu129, Asp225, and Asp226 in the putative transmembrane segment and Glu142 in the loop region for the activity. Overexpression of Ap-NapA1-1 in the freshwater cyanobacterium Synechococcus sp. strain PCC 7942 enhanced the salt tolerance of cells, especially at alkaline pH. 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The genome sequence revealed that the cyanobacterium Synechocystis sp. strain PCC 6803 contains five putative Na⁺/H⁺ antiporters, two of which are homologous to NhaP of Pseudomonas aeruginosa and three of which are homologous to NapA of Enterococcus hirae. The physiological and functional properties of NapA-type antiporters are largely unknown. One of NapA-type antiporters in Synechocystis sp. strain PCC 6803 has been proposed to be essential for the survival of this organism. In this study, we examined the isolation and characterization of the homologous gene in Aphanothece halophytica. Two genes encoding polypeptides of the same size, designated Ap-napA1-1 and Ap-napA1-2, were isolated. Ap-NapA1-1 exhibited a higher level of homology to the Synechocystis ortholog (Syn-NapA1) than Ap-NapA1-2 exhibited. 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These findings indicate that A. halophytica has two NapA1-type antiporters which exhibit different ion specificities and play an important role in salt tolerance at alkaline pH.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>16085800</pmid><doi>10.1128/AEM.71.8.4176-4184.2005</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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source American Society for Microbiology; MEDLINE; PubMed Central; Alma/SFX Local Collection
subjects Alkalinity
Amino Acid Sequence
Bacteria
Bacterial Proteins - chemistry
Bacterial Proteins - genetics
Bacterial Proteins - metabolism
Bacteriology
Biological and medical sciences
Culture Media
Cyanobacteria - drug effects
Cyanobacteria - metabolism
Cyanobacteria - physiology
Enzymology and Protein Engineering
Escherichia coli - genetics
Escherichia coli - metabolism
Fundamental and applied biological sciences. Psychology
Gene Expression Regulation, Bacterial
Hydrogen
Hydrogen-Ion Concentration
Ions
Lithium Chloride - pharmacology
Microbiology
Molecular Sequence Data
Mutagenesis, Site-Directed
Permeability, membrane transport, intracellular transport
Potassium - metabolism
Salt
Sodium
Sodium Chloride - pharmacology
Sodium-Hydrogen Exchangers - chemistry
Sodium-Hydrogen Exchangers - genetics
Sodium-Hydrogen Exchangers - metabolism
title Halotolerant Cyanobacterium Aphanothece halophytica Contains NapA-Type Na⁺/H⁺ Antiporters with Novel Ion Specificity That Are Involved in Salt Tolerance at Alkaline pH
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