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Analysis of photoenzymatic repair of UV lesions in DNA by single light flashes. IX. Excess production of photoreactivating enzyme in E. coli B s-1- 160 under different growth conditions, and its suppression by adenine
Authors:H Nishioka  W Harm
Affiliation:1. Research Laboratory of Nuclear Reactor, Tokyo Institute of Technology, Tokyo, Japan;2. Division of Biology, The University of Texas at Dallas, Tex. 75230 (U.S.A.);1. Department of Biophysics, Medical School, University of Pecs, Pecs, Hungary;2. Laboratoire d’Optique et Biosciences, Ecole Polytechnique, Palaiseau, France;3. Department of Physics, School of Physics and Materials Science, Nanchang University, Nanchang City, China;4. Department of Chemistry, Stony Brook University, New York, USA;5. School of Chemistry, University of East Anglia, Norwich, UK;1. Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto, Japan;2. Department of Life Science and Research Center for Life Science, College of Science, Rikkyo University, Tokyo, Japan;1. European XFEL GmbH, Schenefeld, Germany;2. Department of Chemistry, Universität Hamburg, Hamburg, Germany;3. Department of Chemistry and Medical School OWL, Bielefeld University, Bielefeld, Germany;4. Department of Physics, Arizona State University, Tempe, AZ 85287-1504, USA;5. Biodesign Center for Applied Structural Discovery, Arizona State University, Tempe, AZ 85287-5001, USA;6. European Molecular Biology Laboratory, Hamburg Unit, Hamburg, Germany;7. Institute for Nanostructure and Solid-State Physics, Universität Hamburg, Hamburg, Germany
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