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Bacterial Membrane Transport: Organization of Membrane Activities

Etana Padan

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Abstract

Abstract Bacteria have transport systems enabling them to accumulate needed nutrients, extrude unwanted by‐products and modify their cytoplasmic content of protons and salts so as to maintain a composition conducive to growth and development. Most bacterial transport systems resemble their counterparts in eukaryotic cells, and similar principles operate in both cell types. Because bacterial transporters are often easier to deal with experimentally, they have become important models for their eukaryotic brethren. The recent determination of the crystal structure of several bacterial transporters including ones that share homology with human transporters that are important in health and disease has been a major breakthrough. It opened the way both to the understanding of the mechanism of active transport as well as to rational drug design. Key concepts Cytoplasmic membrane separates the cytoplasm from the cell‐environment and at the same time communicates between these compartments by transducing signals and transporting molecules and ions across the membrane. Channels facilitate the passive transport of molecules or ions across the membrane. Transporters couple energy to actively transport molecules or ions across the membrane. Primary transport system couples transport to chemical or light energy. Secondary transport system couples transport to chemiosmotic energy. Chemiosmotic circuit couples several secondary‐ and primary transporters in a biological membrane. A virtual proton pump emerges from combining transport and metabolism. The proton motive force or the electrochemical gradient of protons across the membrane provides a reservoir of potential energy to be used in all forms of energy‐transduction across the membrane. Crystal structure of membrane proteins are critical for understanding the mechanism of transporters and for drug design for transporters involved in human's health and disease.

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What this paper is about

Abstract Bacteria have transport systems enabling them to accumulate needed nutrients, extrude unwanted by‐products and modify their cytoplasmic content of protons and salts so as to maintain a composition conducive to growth and development. Most bacterial transport systems resemble their counterparts in eukaryotic cells, and similar principles operate in both cell types. Because bacterial transporters are often easier to deal with experimentally, they have become important models for their eukaryotic brethren. The recent determination of the crystal structure of several bacterial transporters including ones that share homology with human transporters that are important in health and disease has been a major breakthrough. It opened the way both to the understanding of the mechanism of active transport as well as to rational drug design. Key concepts Cytoplasmic membrane separates the cytoplasm from the cell‐environment and at the same time communicates between these compartments by transducing signals and transporting molecules and ions across the membrane. Channels facilitate the passive transport of molecules or ions across the membrane. Transporters couple energy to actively transport molecules or ions across the membrane. Primary transport system couples transport to chemical or light energy. Secondary transport system couples transport to chemiosmotic energy. Chemiosmotic circuit couples several secondary‐ and primary transporters in a biological membrane. A virtual proton pump emerges from combining transport and metabolism. The proton motive force or the electrochemical gradient of protons across the membrane provides a reservoir of potential energy to be used in all forms of energy‐transduction across the membrane. Crystal structure of membrane proteins are critical for understanding the mechanism of transporters and for drug design for transporters involved in human's health and disease.

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Available abstract

Abstract Bacteria have transport systems enabling them to accumulate needed nutrients, extrude unwanted by‐products and modify their cytoplasmic content of protons and salts so as to maintain a composition conducive to growth and development. Most bacterial transport systems resemble their counterparts in eukaryotic cells, and similar principles operate in both cell types. Because bacterial transporters are often easier to deal with experimentally, they have become important models for their eukaryotic brethren. The recent determination of the crystal structure of several bacterial transporters including ones that share homology with human transporters that are important in health and disease has been a major breakthrough. It opened the way both to the understanding of the mechanism of active transport as well as to rational drug design. Key concepts Cytoplasmic membrane separates the cytoplasm from the cell‐environment and at the same time communicates between these compartments by transducing signals and transporting molecules and ions across the membrane. Channels facilitate the passive transport of molecules or ions across the membrane. Transporters couple energy to actively transport molecules or ions across the membrane. Primary transport system couples transport to chemical or light energy. Secondary transport system couples transport to chemiosmotic energy. Chemiosmotic circuit couples several secondary‐ and primary transporters in a biological membrane. A virtual proton pump emerges from combining transport and metabolism. The proton motive force or the electrochemical gradient of protons across the membrane provides a reservoir of potential energy to be used in all forms of energy‐transduction across the membrane. Crystal structure of membrane proteins are critical for understanding the mechanism of transporters and for drug design for transporters involved in human's health and disease.

Key concepts: Electrochemical gradient, Chemiosmosis, Membrane transport, Membrane, Ion transporter, Cytoplasm, Transport protein, Membrane transport protein

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