Putrescine distribution in Escherichia coli studied in vivo by 13C nuclear magnetic resonance

In order to study the intracellular polyamine distribution in Escherichia coli, 13C-NMR spectra of [1,4-13C]putrescine were obtained after addition of the latter to intact bacteria. The 13C-enriched methylene signal underwent line broadening. When the cells were centrifuged after 90 min the cell-bou...

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Autor principal: Frydman, B.
Otros Autores: Frydman, R.B, de Los Santos, C., Garrido, D.A, Goldemberg, S.H, Algranati, I.D
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 1984
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Acceso en línea:Registro en Scopus
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024 7 |2 cas  |a carbon, 7440-44-0; putrescine, 110-60-1, 333-93-7; transfer RNA, 9014-25-9; Carbon Isotopes; DNA, Bacterial; Putrescine, 110-60-1; RNA, Transfer, 9014-25-9 
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100 1 |a Frydman, B. 
245 1 0 |a Putrescine distribution in Escherichia coli studied in vivo by 13C nuclear magnetic resonance 
260 |c 1984 
270 1 0 |m Frydman, B.; Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín, 956 Buenos Aires, Argentina 
506 |2 openaire  |e Política editorial 
504 |a Cohen, (1971) Introduction to the Polyamines, , Prentice-Hall, Englewood Cliffs, NJ 
504 |a Bachrach, (1973) Function of Naturally Occurring Polyamines, , Academic Press, New York 
504 |a Tabor, Tabor, (1976) Annu. Rev. Biochem., 45, pp. 285-306 
504 |a Algranati, Goldemberg, (1977) Trends Biochem. Sci., 2, pp. 272-274 
504 |a Gabbay, Glaser, Gaffney, (1970) Annals of the New York Academy of Sciences, 171, pp. 810-826 
504 |a Cohen, Lichtenstein, (1960) J. Biol. Chem., 235, pp. 2112-2116 
504 |a Quigley, Teeter, Rich, (1978) Proc. Natl. Acad. Sci. USA, 75, pp. 64-68 
504 |a Tabor, Kellog, (1967) J. Biol. Chem., 242, pp. 1044-1052 
504 |a Stevens, McCann, (1970) Annals of the New York Academy of Sciences, 171, pp. 827-837 
504 |a Dion, Herbst, (1967) Proc. Natl. Acad. Sci. USA, 58, pp. 2367-2371 
504 |a Schulman, (1969) Biological Applications of Magnetic Resonance, , Academic Press, New York 
504 |a Dwek, (1975) Nuclear Magnetic Resonance in Biochemistry, , Oxford University Press, London 
504 |a Echandi, Algranati, (1975) Biochem. Biophys. Res. Commun., 62, pp. 313-319 
504 |a Murray, III, Williams, (1958) Organic Synthesis with Isotopes, p. 129. , Interscience, New York, Part I 
504 |a Murray, III, Williams, (1958) Organic Synthesis with Isotopes, p. 507. , Interscience, New York, Part I 
504 |a Levitt, Freeman, Frenkiel, (1982) J. Magn. Resonance, 47, pp. 328-330 
504 |a Canet, Levy, Peat, (1975) J. Magn. Resonance, 18, pp. 199-204 
504 |a Olsen, Schweitzer, Walkin, Hamil, Jr., Horton, Grant, (1982) Nucleic Acids Research, 10, pp. 4449-4464 
504 |a Martin, Martin, Delpuesch, (1980) Practical NMR Spectroscopy, pp. 15-18. , Heyden, London 
504 |a Martin, Martin, Delpuesch, (1980) Practical NMR Spectroscopy, pp. 22-23. , Heyden, London 
504 |a Rubin, (1977) J. Bacteriol., 129, pp. 916-925 
504 |a Gasule, Schellman, (1978) J. Mol. Biol., 121, pp. 311-326 
504 |a Pochon, Cohen, (1972) Biochem. Biophys. Res. Commun., 47, pp. 720-726 
504 |a Sakai, Cohen, (1976) Progress in Nucleic Acid Research and Molecular Biology, 17, pp. 15-42. , W.E. Cohn, Academic Press, New York 
504 |a Bolton, Kearns, (1977) Biochim. Biophys. Acta, 477, pp. 10-19 
504 |a Scraba, Bradley, Leynitz-Willis, Warren, (1983) Virology, 124, pp. 152-160 
520 3 |a In order to study the intracellular polyamine distribution in Escherichia coli, 13C-NMR spectra of [1,4-13C]putrescine were obtained after addition of the latter to intact bacteria. The 13C-enriched methylene signal underwent line broadening. When the cells were centrifuged after 90 min the cell-bound putrescine peak had a linewidth of 23 Hz, while the supernatant liquid showed an unbound putrescine signal with a linewidth smaller than 1 Hz. By using 13C-enriched internal standards it could be shown that the linewidening was not due to the heterogeneity of the medium or to an in vivo paramagnetic effect. Cell-bound putrescine was liberated by addition of trichloroacetic acid and was therefore non-covalently linked to macromolecular cell structures. Cell-bound [13C]putrescine could be displaced by addition of an excess of [12C]putrescine. When samples of membranes, soluble protein, DNA, tRNA and ribosomes from E. coli were incubated with [1,4-13C]putrescine, strong binding was detected only in the ribosomal and membrane fractions. The ribosome-putrescine complex showed properties similar to those determined with the intact cells. By measuring the nuclear Overhauser enhancements η, it was possible to estimate that only about 50% of the polyamine was linked to the macromolecules. Determination of the T1 values of free and ribosomal-bound putrescine allowed the calculation of a correlation time, τc = 4·10-7 s for the latter. T1 and τc value for the ribosome-putrescine complex were those expected for a motional regime of slowly tumbling molecules. © 1984.  |l eng 
593 |a Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junín, 956 Buenos Aires, Argentina 
593 |a Instituto de Investigaciones Bioquímicas 'Fundacion Campomar', Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Antonio Machado, 151 Buenos Aires, Argentina 
690 1 0 |a (E. COLI) 
690 1 0 |a 13C-NMR 
690 1 0 |a PUTRESCINE DISTRIBUTION 
690 1 0 |a BACTERIAL DNA 
690 1 0 |a PUTRESCINE 
690 1 0 |a TRANSFER RNA 
690 1 0 |a ARTICLE 
690 1 0 |a ESCHERICHIA COLI 
690 1 0 |a METHODOLOGY 
690 1 0 |a NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY 
690 1 0 |a RIBOSOME 
690 1 0 |a CARBON ISOTOPES 
690 1 0 |a DNA, BACTERIAL 
690 1 0 |a ESCHERICHIA COLI 
690 1 0 |a MAGNETIC RESONANCE SPECTROSCOPY 
690 1 0 |a PUTRESCINE 
690 1 0 |a RIBOSOMES 
690 1 0 |a RNA, TRANSFER 
650 1 7 |2 spines  |a CARBON 
700 1 |a Frydman, R.B. 
700 1 |a de Los Santos, C. 
700 1 |a Garrido, D.A. 
700 1 |a Goldemberg, S.H. 
700 1 |a Algranati, I.D. 
773 0 |d 1984  |g v. 805  |h pp. 337-344  |k n. 4  |p Biochim. Biophys. Acta Mol. Cell Res.  |x 01674889  |w (AR-BaUEN)CENRE-2263  |t BBA - Molecular Cell Research 
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856 4 0 |u https://doi.org/10.1016/0167-4889(84)90016-8  |y DOI 
856 4 0 |u https://hdl.handle.net/20.500.12110/paper_01674889_v805_n4_p337_Frydman  |y Handle 
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