Kellenberger E, Ryter A & Séchaud J. Electron microscope study of DNA-containing plasms. II. Vegetative and mature phage DNA as compared with normal bacterial nucleoids in different physiological states. J. Biophys. Biochem. Cytol. 4:671-8, 1958
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چکیده
Under specific conditions—later called the 'R.K.-conditions'—bacterial nucleoids can be fixed with OsO4 so as to contain fine fibrillar material when viewed on thin sections. Under other conditions, and —as was shown later —with aldehydes, aggregations occur. Those induced with EDTA (formerly under the trade name 'versene'} allow a practical aggregation test. The pool of vegetative ( = replicating and transcribing) T4 bacteriophage DNA is shown to be aggregation sensitive, as is the normal nucleoid. Artificial aggregation is different from physiological condensation as occurs, e.g., when T4-virions are packaged out of the DNA-pool. [The SCI indicates that this paper has been cited over 915 times since 1961.]
منابع مشابه
Electron Microscope Study of DNA-Containing Plasms II. Vegetative and Mature Phage DNA as Compared with Normal Bacterial Nucleoids in Different Physiological States*
The nucleoids of Eseherichia coil, independently of the physiological state of the bacteria, are shown to be preserved as a fine-stranded fibrillar nucleoplasm by an OsO4 fixation under defined conditions: acetate-veronal buffer pH 6, presence of Ca ++ and amino acids, stabilization with uranyl-acetate before dehydration. The same fixation procedure applied to the DNA of vegetative phage reveal...
متن کاملElectron Microscope Study of DNA-Containing Plasms
The nucleoids of Escherichia coli, independently of the physiological state of the bacteria, are shown to be preserved as a fine-stranded fibrillar nucleoplasm by an OsO(4) fixation under defined conditions: acetate-veronal buffer pH 6, presence of Ca(++) and amino acids, stabilization with uranyl-acetate before dehydration. The same fixation procedure applied to the DNA of vegetative phage rev...
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* This work was supported by grants GB-982 from the National Science Foundation and CA06927 from the U. S. Public Health Service. 1 Jacob, F., S. Brenner, and F. Cuzin, in Synthesis and Structure of Macromolecules, Cold Spring Harbor Symposia on Quantitative Biology, vol. 28 (1963), p. 329. 2 Rogers, H. J., in Function and Structure in Microorganisms, Symposium of the Society for General Microb...
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Loening, U. E. (1960). Biochem. J. 77, 20P. Lund, H. A., Vatter, A. E. & Hanson, J. B. (1958). J. biophys. biochem. Cytol. 4, 87. Palade, G. E. & Siekevitz, P. (1956). J. biophy8. biochem. Cytol. 2, 171, 671. Peterman, M. L., Hamilton, M. G., Balis, M. E., Samarth, K. & Pecora, P. (1958). In Microsomal Particles and Protein Synthesis, p. 70. Ed. by Roberts, R. B. London: Pergamon Press Ltd. Sla...
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Barker, H. A. (1956) Znd. Eng. Chem. 48,1438-1442 Clarke, F. M. & Fina, L. R. (1952) Arch. Biochem. Biophys. 36, 26-32 Dutton, P. L. & Evans, W. C. (1969) Biochem. J. 113, 525-536 Ferry, J. G. (1974) Ph.D. Thesis, University of Illinois Fina, L. R. & Fiskin, A. M. (1960) Arch. Biochem. Biophys. 91,163-165 Kellenberg, E., Ryter, A. & Sechaud, J. (1958) J. Biophys. Biochem. Cytol. 4,671-685 Notti...
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تاریخ انتشار 2004