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  1. Hartmut Michel (* 18. Juli 1948 in Ludwigsburg) ist ein deutscher Biochemiker. Er erhielt 1988 zusammen mit Johann Deisenhofer und Robert Huber den Nobelpreis für Chemie für die Erforschung der dreidimensionalen Molekülstruktur des Reaktionszentrums der Photosynthese im Purpurbakterium Rhodopseudomonas viridis .

  2. Prof. Dr. Dr. h.c. Hartmut Michel. Scientific member (Director) Molecular Membrane Biology. +49 69 6303 1000. +49 69 6303-1002. Hartmut.Michel@... Publication References. Curriculum Vitae. Studies of biochemistry at Tuebingen and Munich, 1969–1975. Ph. D., Biochemistry, University of Wuerzburg, 1977. Postdoc, University of Wuerzburg, 1977-1979.

  3. Hartmut Michel (German pronunciation: [ˈhaʁtmuːt ˈmɪçl̩] ⓘ; born 18 July 1948) is a German biochemist, who received the 1988 Nobel Prize in Chemistry for determination of the first crystal structure of an integral membrane protein, a membrane-bound complex of proteins and co-factors that is essential to photosynthesis.

  4. 1. Dez. 2023 · Learn more about Hartmut Michel and his findings on the 3D structure of the photosynthetic reaction center which explain how light is absorbed and converted into storable electrical charge in photosynthesis, and earned him the Nobel Prize.

  5. 27. März 2024 · Hartmut Michel (born July 18, 1948, Ludwigsburg, Germany) is a German biochemist who, along with Johann Deisenhofer and Robert Huber, received the Nobel Prize for Chemistry in 1988 for their determination of the structure of certain proteins that are essential for photosynthesis.

    • The Editors of Encyclopaedia Britannica
  6. The Nobel Prize in Chemistry 1988 was awarded jointly to Johann Deisenhofer, Robert Huber and Hartmut Michel "for the determination of the three-dimensional structure of a photosynthetic reaction centre"

  7. 3. Juli 2014 · Der in Ludwigsburg geborene Biochemiker Hartmut Michel erforscht Proteine in den Zellmembranen. Als Begrenzung nach außen sind diese halbflüssigen Lipidstrukturen für viele Funktionen der Zelle essenziell und die hier lokalisierten Enzyme wichtige Zielstrukturen für die Medikamentenentwicklung.