Literature DB >> 16484230

Salt tolerance of archaeal extremely halophilic lipid membranes.

Boris Tenchov1, Erin M Vescio, G Dennis Sprott, Mark L Zeidel, John C Mathai.   

Abstract

The membranes of extremely halophilic Archaea are characterized by the abundance of a diacidic phospholipid, archaetidylglycerol methylphosphate (PGP-Me), which accounts for 50-80 mol% of the polar lipids, and by the absence of phospholipids with choline, ethanolamine, inositol, and serine head groups. These membranes are stable in concentrated 3-5 m NaCl solutions, whereas membranes of non-halophilic Archaea, which do not contain PGP-Me, are unstable and leaky under such conditions. By x-ray diffraction and vesicle permeability measurements, we demonstrate that PGP-Me contributes in an essential way to membrane stability in hypersaline environments. Large unilamellar vesicles (LUV) prepared from the polar lipids of extreme halophiles, Halobacterium halobium and Halobacterium salinarum, retain entrapped carboxyfluorescein and resist aggregation in the whole range 0-4 m NaCl, similarly to LUV prepared from purified PGP-Me. By contrast, LUV made of polar lipid extracts from moderately halophilic and non-halophilic Archaea (Methanococcus jannaschii, Methanosarcina mazei, Methanobrevibacter smithii) are leaky and aggregate at high salt concentrations. However, adding PGP-Me to M. mazei lipids results in gradual enhancement of LUV stability, correlating with the PGP-Me content. The LUV data are substantiated by the x-ray results, which show that H. halobium and M. mazei lipids have dissimilar phase behavior and form different structures at high NaCl concentrations. H. halobium lipids maintain an expanded lamellar structure with spacing of 8.5-9 nm, which is stable up to at least 100 degrees C in 2 m NaCl and up to approximately 60 degrees C in 4 m NaCl. However, M. mazei lipids form non-lamellar structures, represented by the Pn3m cubic phase and the inverted hexagonal H(II) phase. From these data, the forces preventing membrane aggregation in halophilic Archaea appear to be steric repulsion, because of the large head group of PGP-Me, or possibly out-of-plane bilayer undulations, rather than electrostatic repulsion attributed to the doubly charged PGP-Me head group.

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Year:  2006        PMID: 16484230     DOI: 10.1074/jbc.M600369200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  8 in total

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Review 2.  Lipid sugar carriers at the extremes: The phosphodolichols Archaea use in N-glycosylation.

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Journal:  Biochim Biophys Acta Mol Cell Biol Lipids       Date:  2017-03-19       Impact factor: 4.698

3.  Positive and negative tandem mass spectrometric fingerprints of lipids from the halophilic Archaea Haloarcula marismortui.

Authors:  Lauro M de Souza; Marcelo Müller-Santos; Marcello Iacomini; Philip A J Gorin; Guilherme L Sassaki
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4.  Transcriptional profiling of the model Archaeon Halobacterium sp. NRC-1: responses to changes in salinity and temperature.

Authors:  James A Coker; Priya DasSarma; Jeffrey Kumar; Jochen A Müller; Shiladitya DasSarma
Journal:  Saline Systems       Date:  2007-07-25

Review 5.  On the response of halophilic archaea to space conditions.

Authors:  Stefan Leuko; Petra Rettberg; Ashleigh L Pontifex; Brendan P Burns
Journal:  Life (Basel)       Date:  2014-02-21

Review 6.  Biosynthesis of archaeal membrane ether lipids.

Authors:  Samta Jain; Antonella Caforio; Arnold J M Driessen
Journal:  Front Microbiol       Date:  2014-11-26       Impact factor: 5.640

Review 7.  Microbial diversity and biogeochemical cycling in soda lakes.

Authors:  Dimitry Y Sorokin; Tom Berben; Emily Denise Melton; Lex Overmars; Charlotte D Vavourakis; Gerard Muyzer
Journal:  Extremophiles       Date:  2014-08-26       Impact factor: 2.395

Review 8.  Lipids of archaeal viruses.

Authors:  Elina Roine; Dennis H Bamford
Journal:  Archaea       Date:  2012-09-20       Impact factor: 3.273

  8 in total

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