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1.
Biochim Biophys Acta ; 1858(11): 2940-2956, 2016 11.
Artigo em Inglês | MEDLINE | ID: mdl-27565574

RESUMO

Recent advances in lipidomic analysis in combination with various physiological experiments set the stage for deciphering the structure-function of haloarchaeal membrane lipids. Here we focused primarily on changes in lipid composition of Haloferax volcanii, but also performed a comparative analysis with four other haloarchaeal species (Halobacterium salinarum, Halorubrum lacusprofundi, Halorubrum sodomense and Haloplanus natans) all representing distinctive cell morphologies and behaviors (i.e., rod shape vs. pleomorphic behavior). Common to all five haloarchaea, our data reveal an extraordinary high level of menaquinone, reaching up to 72% of the total lipids. This ubiquity suggests that menaquinones may function beyond their ordinary role as electron and proton transporter, acting simultaneously as ion permeability barriers and as powerful shield against oxidative stress. In addition, we aimed at understanding the role of cations interacting with the characteristic negatively charged surface of haloarchaeal membranes. We propose for instance that by bridging the negative charges of adjacent anionic phospholipids, Mg2+ acts as surrogate for cardiolipin, a molecule that is known to control curvature stress of membranes. This study further provides a bioenergetic perspective as to how haloarchaea evolved following oxygenation of Earth's atmosphere. The success of the aerobic lifestyle of haloarchaea includes multiple membrane-based strategies that successfully balance the need for a robust bilayer structure with the need for high rates of electron transport - collectively representing the molecular basis to inhabit hypersaline water bodies around the planet.


Assuntos
Halobacterium salinarum/metabolismo , Haloferax volcanii/metabolismo , Halorubrum/metabolismo , Lipídeos de Membrana/metabolismo , Oxigênio/metabolismo , Fosfolipídeos/química , Adaptação Fisiológica , Aerobiose , Antioxidantes/química , Antioxidantes/metabolismo , Evolução Biológica , Cátions Bivalentes , Membrana Celular/química , Membrana Celular/metabolismo , Transporte de Elétrons , Metabolismo Energético , Halobacterium salinarum/química , Haloferax volcanii/química , Halorubrum/química , Magnésio/química , Magnésio/metabolismo , Lipídeos de Membrana/química , Fosfolipídeos/metabolismo , Salinidade , Água do Mar/química , Água do Mar/microbiologia , Eletricidade Estática , Vitamina K 2/química , Vitamina K 2/metabolismo
2.
Mil Med ; 184(Suppl 1): 374-378, 2019 03 01.
Artigo em Inglês | MEDLINE | ID: mdl-30901466

RESUMO

A recent study of all mounted vehicle underbody blast attacks found that 21% of Abbreviated Injury Scale Severity 2+ injuries in the Joint Trauma Analysis and Prevention of Injury in Combat network were injuries to the leg and ankle. To develop effective countermeasure systems for these attacks, the epidemiology and mechanisms of injury from this loading environment need to be quantified. The goal of this study was to develop a military correlate of an existing civilian case review framework, the Crash Injury Research and Engineering Network (CIREN), to consider the differences in military event types and the amount of available vehicle/attack information. Additional data fields were added to the CIREN process to cover military-specific data and "certainty" definitions in the proposed injury hypothesis were modified. To date, six group reviews have been conducted analyzing 253 injuries to the foot/ankle, tibia, femur, pelvis, and lumbar spine from 52 occupants. The familiar format and unclassified nature of the presentations allowed for the involvement of biomechanics experts from multiple disciplines.


Assuntos
Traumatismos por Explosões/classificação , Militares/estatística & dados numéricos , Terrorismo/estatística & dados numéricos , Guerra/estatística & dados numéricos , Campanha Afegã de 2001- , Traumatismos por Explosões/epidemiologia , Humanos , Escala de Gravidade do Ferimento , Guerra do Iraque 2003-2011 , Medicina Militar/métodos , Medicina Militar/tendências , Estados Unidos/epidemiologia
3.
Prog Lipid Res ; 43(5): 383-402, 2004 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-15458813

RESUMO

The Omega-3 fatty acid DHA (docosahexaenoic acid, 22:6) and its sister molecule EPA (eicosapentaenoic acid, 20:5) are highlighted here. These highly unsaturated fatty acids are widespread in nature, especially in the marine environment, and are essential in membranes ranging from deep sea bacteria to human neurons. Studies of DHA/EPA in bacteria have led to a working model on the structural roles of these molecules and are described in this review. The main points are: (a) genomic analysis shows that genes encoding the DHA/EPA pathways are similar, supporting the idea that structural roles in bacteria might be similar, (b) biochemical analysis shows that DHA and EPA are produced in bacteria by a polyketide process distinct from the pathway of plants and animals; this allows DHA and EPA to be produced in anaerobic or oxygen-limited environments, (c) regulatory systems triggered by temperature and pressure have been identified and studied, and add to the understanding of the roles of these molecules, (d) DHA/EPA bacteria are located almost exclusively in the marine environment, raising the prospect of an important linkage between membrane processes and marine conditions, (e) physiological studies of an EPA recombinant of E. coli show that EPA phospholipids contribute essential fluidity to the bilayer and that an EPA-enriched membrane supports a respiratory lifestyle dependent on proton bioenergetics; the EPA recombinant displays other physiological properties likely attributed to high levels of EPA in the bilayer, and (f) chemical studies such as chemical dynamic modeling support the idea that DHA and presumably EPA contribute hyperfluidizing properties to the membrane. We hypothesize that DHA/EPA phospholipids contribute fluidity and other properties to the bilayer which distinguish these highly unsaturated chains from monounsaturates and polyunsaturates such as 18:2 and 18:3. We further hypothesize that the structural properties of DHA/EPA functioning in bacteria are also harnessed by higher organisms for enhancing crucial membrane processes including photosynthesis and energy transduction.


Assuntos
Membrana Celular/fisiologia , Ácidos Graxos Ômega-3/fisiologia , Bactérias/metabolismo , Ácidos Docosa-Hexaenoicos/metabolismo , Ácido Eicosapentaenoico/fisiologia , Ácidos Graxos Ômega-3/genética , Humanos , Fluidez de Membrana/fisiologia , Lipídeos de Membrana/genética , Lipídeos de Membrana/fisiologia
4.
Prog Lipid Res ; 64: 1-15, 2016 10.
Artigo em Inglês | MEDLINE | ID: mdl-27448687

RESUMO

Proton bioenergetics provides the energy for growth and survival of most organisms in the biosphere ranging from unicellular marine phytoplankton to humans. Chloroplasts harvest light and generate a proton electrochemical gradient (proton motive force) that drives the production of ATP needed for carbon dioxide fixation and plant growth. Mitochondria, bacteria and archaea generate proton motive force to energize growth and other physiologies. Energy transducing membranes are at the heart of proton bioenergetics and are responsible for catalyzing the conversion of energy held in high-energy electrons→electron transport chain→proton motive force→ATP. Whereas the electron transport chain is understood in great detail there are major gaps in understanding mechanisms of proton transfer or circulation during proton bioenergetics. This paper is built on the proposition that phospho- and glyco-glycerolipids form proton transport circuitry at the membrane's surface. By this proposition, an emergent membrane property, termed the hyducton, confines active/unbound protons or hydronium ions to a region of low volume close to the membrane surface. In turn, a von Grotthuß mechanism rapidly moves proton substrate in accordance with nano-electrochemical poles on the membrane surface created by powerful proton pumps such as ATP synthase.


Assuntos
Glicolipídeos/metabolismo , Fosfolipídeos/metabolismo , Trifosfato de Adenosina/metabolismo , Archaea/metabolismo , Bactérias/metabolismo , Membrana Celular/metabolismo , Cloroplastos/metabolismo , Metabolismo Energético , Microdomínios da Membrana/metabolismo , Mitocôndrias/metabolismo , Força Próton-Motriz
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