Literature DB >> 28696278

Outer Membrane Permeability of Cyanobacterium Synechocystis sp. Strain PCC 6803: Studies of Passive Diffusion of Small Organic Nutrients Reveal the Absence of Classical Porins and Intrinsically Low Permeability.

Hikaru Kowata1, Saeko Tochigi2, Hideyuki Takahashi1, Seiji Kojima3,2.   

Abstract

The outer membrane of heterotrophic Gram-negative bacteria plays the role of a selective permeability barrier that prevents the influx of toxic compounds while allowing the nonspecific passage of small hydrophilic nutrients through porin channels. Compared with heterotrophic Gram-negative bacteria, the outer membrane properties of cyanobacteria, which are Gram-negative photoautotrophs, are not clearly understood. In this study, using small carbohydrates, amino acids, and inorganic ions as permeation probes, we determined the outer membrane permeability of Synechocystis sp. strain PCC 6803 in intact cells and in proteoliposomes reconstituted with outer membrane proteins. The permeability of this cyanobacterium was >20-fold lower than that of Escherichia coli The predominant outer membrane proteins Slr1841, Slr1908, and Slr0042 were not permeable to organic nutrients and allowed only the passage of inorganic ions. Only the less abundant outer membrane protein Slr1270, a homolog of the E. coli export channel TolC, was permeable to organic solutes. The activity of Slr1270 as a channel was verified in a recombinant Slr1270-producing E. coli outer membrane. The lack of putative porins and the low outer membrane permeability appear to suit the cyanobacterial autotrophic lifestyle; the highly impermeable outer membrane would be advantageous to cellular survival by protecting the cell from toxic compounds, especially when the cellular physiology is not dependent on the uptake of organic nutrients.IMPORTANCE Because the outer membrane of Gram-negative bacteria affects the flux rates for various substances into and out of the cell, its permeability is closely associated with cellular physiology. The outer membrane properties of cyanobacteria, which are photoautotrophic Gram-negative bacteria, are not clearly understood. Here, we examined the outer membrane of Synechocystis sp. strain PCC 6803. We revealed that it is relatively permeable to inorganic ions but is markedly less permeable to organic nutrients, with >20-fold lower permeability than the outer membrane of Escherichia coli Such permeability appears to fit the cyanobacterial lifestyle, in which the diffusion pathway for inorganic solutes may suffice to sustain the autotrophic physiology, illustrating a link between outer membrane permeability and the cellular lifestyle.
Copyright © 2017 American Society for Microbiology.

Entities:  

Keywords:  Gram-negative bacteria; cyanobacteria; outer membrane; permeability; porins

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Year:  2017        PMID: 28696278      PMCID: PMC5585710          DOI: 10.1128/JB.00371-17

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


  27 in total

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Authors:  Hiroshi Nikaido
Journal:  Microbiol Mol Biol Rev       Date:  2003-12       Impact factor: 11.056

Review 2.  Structure and function of TolC: the bacterial exit duct for proteins and drugs.

Authors:  Vassilis Koronakis; Jeyanthy Eswaran; Colin Hughes
Journal:  Annu Rev Biochem       Date:  2004       Impact factor: 23.643

3.  Structural and functional characterization of OmpF porin mutants selected for larger pore size. II. Functional characterization.

Authors:  N Saint; K L Lou; C Widmer; M Luckey; T Schirmer; J P Rosenbusch
Journal:  J Biol Chem       Date:  1996-08-23       Impact factor: 5.157

4.  The TolC-like protein HgdD of the cyanobacterium Anabaena sp. PCC 7120 is involved in secondary metabolite export and antibiotic resistance.

Authors:  Alexander Hahn; Mara Stevanovic; Oliver Mirus; Enrico Schleiff
Journal:  J Biol Chem       Date:  2012-10-15       Impact factor: 5.157

5.  The outer membrane TolC-like channel HgdD is part of tripartite resistance-nodulation-cell division (RND) efflux systems conferring multiple-drug resistance in the Cyanobacterium Anabaena sp. PCC7120.

Authors:  Alexander Hahn; Mara Stevanovic; Oliver Mirus; Iryna Lytvynenko; Klaas Martinus Pos; Enrico Schleiff
Journal:  J Biol Chem       Date:  2013-09-06       Impact factor: 5.157

6.  Cadaverine covalently linked to peptidoglycan is required for interaction between the peptidoglycan and the periplasm-exposed S-layer-homologous domain of major outer membrane protein Mep45 in Selenomonas ruminantium.

Authors:  Seiji Kojima; Kyong-Cheol Ko; Yumiko Takatsuka; Naoki Abe; Jun Kaneko; Yoshifumi Itoh; Yoshiyuki Kamio
Journal:  J Bacteriol       Date:  2010-09-17       Impact factor: 3.490

7.  Identification and characterization of porins in Pseudomonas aeruginosa.

Authors:  H Nikaido; K Nikaido; S Harayama
Journal:  J Biol Chem       Date:  1991-01-15       Impact factor: 5.157

8.  Outer membrane of gram-negative bacteria. XII. Molecular-sieving function of cell wall.

Authors:  G M Decad; H Nikaido
Journal:  J Bacteriol       Date:  1976-10       Impact factor: 3.490

9.  Outer Membrane Proteins Derived from Non-cyanobacterial Lineage Cover the Peptidoglycan of Cyanophora paradoxa Cyanelles and Serve as a Cyanelle Diffusion Channel.

Authors:  Seiji Kojima; Koji Muramoto; Tomonobu Kusano
Journal:  J Biol Chem       Date:  2016-08-08       Impact factor: 5.157

10.  Structure-function of cyanobacterial outer-membrane protein, Slr1270: homolog of Escherichia coli drug export/colicin import protein, TolC.

Authors:  Rachna Agarwal; Stanislav Zakharov; S Saif Hasan; Christopher M Ryan; Julian P Whitelegge; William A Cramer
Journal:  FEBS Lett       Date:  2014-09-13       Impact factor: 4.124

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Journal:  Curr Microbiol       Date:  2021-05-13       Impact factor: 2.188

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4.  Development of a Highly Sensitive Luciferase-Based Reporter System To Study Two-Step Protein Secretion in Cyanobacteria.

Authors:  David A Russo; Julie A Z Zedler; Fabian D Conradi; Nils Schuergers; Poul Erik Jensen; Conrad W Mullineaux; Annegret Wilde; Georg Pohnert
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5.  Order-of-magnitude enhancement in photocurrent generation of Synechocystis sp. PCC 6803 by outer membrane deprivation.

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6.  The Role of Outer Membrane Protein(s) Harboring SLH/OprB-Domains in Extracellular Vesicles' Production in Synechocystis sp. PCC 6803.

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8.  Reciprocal Effect of Copper and Iron Regulation on the Proteome of Synechocystis sp. PCC 6803.

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