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Energizing an invertebrate embryo: bafilomycin-dependent respiration and the metabolic cost of proton pumping by the V-ATPase.

Energizing an invertebrate embryo: bafilomycin-dependent respiration and the metabolic cost of proton pumping by the V-ATPase. Research Abstract Details 

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  • Energizing an invertebrate embryo: bafilomycin-dependent respiration and the metabolic cost of proton pumping by the V-ATPase. Abstract Text:

    joseph a coviJoseph A Covi,steven c handSteven C Hand,

    We examine herein the contribution of V-ATPase activity to the energy budget of aerobically developing embryos of Artemia franciscana and discuss the results in the context of quiescence under anoxia. (31)P-NMR analysis indicates that intracellular pH and NTP levels are unaffected by acute incubation of dechorionated embryos with the V-ATPase inhibitor, bafilomycin A(1). Bafilomycin A(1) also has no significant effect on oxygen consumption by isolated mitochondria. Taken together, these data indicate that bafilomycin does not affect energy-producing pathways in the developing embryo. However, the V-ATPase inhibitor exhibits a concentration-dependent inhibition of oxygen consumption in aerobic embryos. A conservative analysis of respirometric data indicates that proton pumping by the V-ATPase, and processes immediately dependent on this activity, constitutes approximately 31% of the aerobic energy budget of the preemergent embryo. Given the complete absence of detectable Na(+)K(+)-ATPase activity during the first hours of aerobic development, it is plausible that the V-ATPase is performing a role in both the acidification of intracellular compartments and the energization of plasma membranes. Importantly, the high metabolic cost associated with maintaining these diverse proton gradients requires that V-ATPase activity be downregulated under anoxia in order to attain the almost complete metabolic depression observed in the quiescent embryo.

    Energizing an invertebrate embryo: bafilomycin-dependent respiration and the metabolic cost of proton pumping by the V-ATPase. Publishing Authors By Initials

    ja coviJA Covi,sc handSC Hand,

    For similar enzymes and coenzymes: enzymes: hydrolases: acid anhydride hydrolases: adenosine triphosphatases: proton-translocating atpases: vacuolar proton-translocating atpases research abstracts see: enzymes and coenzymes: enzymes: hydrolases: acid anhydride hydrolases: adenosine triphosphatases: proton-translocating atpases: vacuolar proton-translocating atpases research

    PUBMED ID PMID:

    MEDLINE DATE: 2007 Jul-Aug

    Energizing an invertebrate embryo: bafilomycin-dependent respiration and the metabolic cost of proton pumping by the V-ATPase. Journal Published:

    PUBLICATION TYPE: Research Support, U.S. Gov't,

    Journal: Physiological and biochemical zoology : PBZ

    VOLUME: 80

    Page Numbers: 422-32

    Journal Abbreviation: Physiol. Biochem. Zool.

    ISSN: 1522-2152

    DAY: 4

    MONTH: 05

    YEAR: 2007

    Energizing an invertebrate embryo: bafilomycin-dependent respiration and the metabolic cost of proton pumping by the V-ATPase. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 100883369

    Energizing an invertebrate embryo: bafilomycin-dependent respiration and the metabolic cost of proton pumping by the V-ATPase. Keywords Mesh Terms:

    KEYWORDS: Vacuolar Proton-Translocating ATPases

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Energizing an invertebrate embryo: bafilomycin-dependent respiration and the metabolic cost of proton pumping by the V-ATPase. Information

    Substance Name: Vacuolar Proton-Translocating ATPases

    Registry Number: EC 3.6.1.-

    Grant and Affiliation Information for Energizing an invertebrate embryo: bafilomycin-dependent respiration and the metabolic cost of proton pumping by the V-ATPase.

    AFFILIATION: Division of Cellular, Developmental, and Integrative Biology, Department of Biological Science, Louisiana State University, Baton Rouge, Louisiana 70803, USA. jcovil@lsu.edu

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIGMS

    GRANT: 1-R01-GM071345-01

    ACRONYM: GM

    MEDLINETA: Physiol Biochem Zool

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

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