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  1. AU="Chatterjee, G.C"
  2. AU="Charrier, Alicia"
  3. AU="Pearson, Amelia"
  4. AU="Yang, Zhiqi"
  5. AU="Chen, John"
  6. AU="Yildirim, Sinan"
  7. AU="Percopo, Caroline"
  8. AU="Nevian, Thomas"
  9. AU="Matthias Arnold"
  10. AU="Abbonante, Francesco"
  11. AU=Cao Yongsen
  12. AU="Mei, Guoliang"
  13. AU="G.Kang, "
  14. AU="Djimdé, Abdoulaye"
  15. AU="Bone, Nathaniel"
  16. AU="Zhou, Yuewen"
  17. AU="Lynch, Stephen M"
  18. AU=Collins Jannette
  19. AU=Kim Soo-Kyoung
  20. AU=Atkinson Sarah H.
  21. AU=Ma Chunlong
  22. AU="Park, Youngjin"
  23. AU="Lakbita, Omar"
  24. AU=ElGokhy Sherin M
  25. AU="Stegmaier, Sabine"
  26. AU="Simons, Gemma N"
  27. AU="Domínguez-Zorita, Sonia"
  28. AU="Nakashima, Ayaka"
  29. AU="Skorecki, Karl"
  30. AU=Ibrahim Salwa
  31. AU=Geocadin Romergryko G
  32. AU="Leroy, J"
  33. AU="Wilson, Peter H"
  34. AU="Cunha, Carla Baroni"

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  1. Artikel: PYRITHIAMINE ADAPTATION OF STAPHYLOCOCCUS AUREUS. II. TRICARBOXYLIC ACID CYCLE AND RELATED ENZYMES.

    DAS, S K / CHATTERJEE, G C

    Journal of bacteriology

    2003  Band 86, Seite(n) 1157–1164

    Abstract: Das, S. K. (Calcutta University, Calcutta, India), and G. C. Chatterjee. Pyrithiamine adaptation of Staphylococcus aureus. II. Tricarboxylic acid cycle and related enzymes. J. Bacteriol. 86:1157-1164. 1963.-Evidence for the stimulated operation of the ... ...

    Abstract Das, S. K. (Calcutta University, Calcutta, India), and G. C. Chatterjee. Pyrithiamine adaptation of Staphylococcus aureus. II. Tricarboxylic acid cycle and related enzymes. J. Bacteriol. 86:1157-1164. 1963.-Evidence for the stimulated operation of the tricarboxylic acid cycle in Staphylococcus aureus after pyrithiamine adaptation is presented. In the cell-free extracts, isocitric, glutamic, malic, and succinic dehydrogenases and catalase were found to be stimulated after the adaptation of S. aureus to pyrithiamine. Besides such stimulation, the appearance of isocitratase and malate synthetase in the adapted strain supports the appearance of the glyoxalate bypass after such adaptation. There is little change in the activities of reduced nicotinamide adenine dinucleotide (NADH) and reduced nicotinamide adenine dinucleotide phosphate (NADPH) oxidases and diaphorase. Lactic dehydrogenase, NADH-cytochrome c reductase, and NADPH-cytochrome c reductase could not be demonstrated either in the normal or in the pyrithiamine-adapted S. aureus. These observations support the postulation that there is a stimulation in the tricarboxylic acid cycle and can account for the very marked stimulation in the utilization of acetate by the organism after adaptation.
    Mesh-Begriff(e) Acclimatization ; Antimetabolites ; Carbon Isotopes ; Catalase ; Citric Acid Cycle ; Dihydrolipoamide Dehydrogenase ; India ; Indophenol ; Metabolism ; NAD ; NADP ; Oxidoreductases ; Pyrithiamine ; Research ; Staphylococcus ; Staphylococcus aureus ; Succinate Dehydrogenase
    Chemische Substanzen Antimetabolites ; Carbon Isotopes ; NAD (0U46U6E8UK) ; Indophenol (500-85-6) ; NADP (53-59-8) ; Pyrithiamine (5JB3029BJ7) ; Oxidoreductases (EC 1.-) ; Catalase (EC 1.11.1.6) ; Succinate Dehydrogenase (EC 1.3.99.1) ; Dihydrolipoamide Dehydrogenase (EC 1.8.1.4)
    Sprache Englisch
    Erscheinungsdatum 2003-08-20
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2968-3
    ISSN 1098-5530 ; 0021-9193
    ISSN (online) 1098-5530
    ISSN 0021-9193
    DOI 10.1128/jb.86.6.1157-1164.1963
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel: Pyrithiamine adaptation of Staphylococcus aureus. I. Adaptation and carbohydrate utilization.

    DAS, S K / CHATTERJEE, G C

    Journal of bacteriology

    2003  Band 83, Seite(n) 1251–1259

    Abstract: Das, S. K. (University of Calcutta, Calcutta, India) and G. C. Chatterjee. Pyrithiamine adaptation of Staphylococcus aureus. I. Adaptation and carbohydrate utilization. J. Bacteriol. 83:1251-1259. 1962.-Staphylococcus aureus has been adapted to ... ...

    Abstract Das, S. K. (University of Calcutta, Calcutta, India) and G. C. Chatterjee. Pyrithiamine adaptation of Staphylococcus aureus. I. Adaptation and carbohydrate utilization. J. Bacteriol. 83:1251-1259. 1962.-Staphylococcus aureus has been adapted to pyrithiamine, a thiamine analogue; as a result of this adaptation, the color of the pigment of the organism changes from orange-yellow to lemon-yellow. The adaptation is reversible; the adapted strain will revert after repeated subculture in a medium containing thiamine and no pyrithiamine. Of the major biochemical alterations resulting from adaptation, severe depression in glucose utilization and simultaneous stimulation of acetate utilization have been noticed. The effect of metabolic inhibitors on the utilization of glucose and acetate has also been studied. By measuring the rate of formation of C(14)O(2) from glucose-1-C(14) and glucose-6-C(14), it has been observed that the reduction in C(14)O(2) formation from glucose-1-C(14) by the adapted organism is much more than that obtained from glucose-6-C(14), causing thereby a decreased metabolic ratio of these two substrates after such adaptation. Relative to the normal strain, the adapted strain utilizes acetate-C(14) at a much faster rate, both in the formation of C(14)O(2) and also in the incorporation of C(14) into the protein and lipid fractions; the rate of formation of C(14)O(2) from pyruvate-1-C(14) is not greatly altered. It has been postulated that there is a partial blocking of the pentose phosphate cycle, because of the lowered glucose-1-C(14) utilization, and simultaneous stimulation of the tricarboxylic acid cycle; or perhaps the initiation of some other route after pyrithiamine adaptation would account for the great increase in acetate utilization.
    Mesh-Begriff(e) Acclimatization ; Citric Acid Cycle ; Depressive Disorder, Major ; Glucose ; India ; Pyrithiamine ; Pyruvates ; Staphylococcus/metabolism ; Staphylococcus aureus ; Thiamine/antagonists & inhibitors
    Chemische Substanzen Pyruvates ; Pyrithiamine (5JB3029BJ7) ; Glucose (IY9XDZ35W2) ; Thiamine (X66NSO3N35)
    Sprache Englisch
    Erscheinungsdatum 2003-08-20
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2968-3
    ISSN 1098-5530 ; 0021-9193
    ISSN (online) 1098-5530
    ISSN 0021-9193
    DOI 10.1128/jb.83.6.1251-1259.1962
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel: Differential response of cadmium toxicity towards Mg2(+)-ATPase activity in hepatic and renal nuclear membrane in rats.

    Das, M / Chatterjee, G C

    Indian journal of biochemistry & biophysics

    1990  Band 27, Heft 3, Seite(n) 172–175

    Abstract: Treatment with cadmium chloride (40mg/kg body wt/day) for three days led to a marked inhibition of Mg2(+)-ATPase activity in rat liver nuclear membrane, whereas it stimulated the enzyme in renal nuclear membrane. On 30 days treatment (15 mg/kg body wt/ ... ...

    Abstract Treatment with cadmium chloride (40mg/kg body wt/day) for three days led to a marked inhibition of Mg2(+)-ATPase activity in rat liver nuclear membrane, whereas it stimulated the enzyme in renal nuclear membrane. On 30 days treatment (15 mg/kg body wt/day) the effect was totally different i.e. stimulation of enzyme activity in the liver and inhibition in the kidney tissue. Arrhenius plot analysis of the enzyme activity showed significant increase in phase transition temperature only in liver tissue of rats subjected to acute treatment. Lineweaver Burk plots also showed differential effect of cadmium toxicity on the enzyme activity, i.e. while both Km and Vmax were changed in the liver, there was change only in Km of enzyme from kidney.
    Mesh-Begriff(e) Animals ; Ca(2+) Mg(2+)-ATPase/metabolism ; Cadmium/toxicity ; Cadmium Chloride ; Kidney/drug effects ; Kidney/enzymology ; Liver/drug effects ; Liver/enzymology ; Male ; Nuclear Envelope/enzymology ; Organ Specificity ; Rats
    Chemische Substanzen Cadmium (00BH33GNGH) ; Ca(2+) Mg(2+)-ATPase (EC 3.6.1.-) ; Cadmium Chloride (J6K4F9V3BA)
    Sprache Englisch
    Erscheinungsdatum 1990-06
    Erscheinungsland India
    Dokumenttyp Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 121689-2
    ISSN 0975-0959 ; 0301-1208
    ISSN (online) 0975-0959
    ISSN 0301-1208
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel: Nutrient deficiencies in animals: vitamin C

    Chatterjee, G.C

    Nutritional disorders. Miloslav Rechcigl, editor-in-chief.

    1978  

    Schlagwörter noninfectious diseases ; animal health ; animal diseases
    Sprache Englisch
    Umfang v. 2 p. 149-176.
    Erscheinungsort West Palm Beach, CRC Press, 1978.
    Dokumenttyp Artikel
    Anmerkung Literature review.
    Datenquelle NAL Katalog (AGRICOLA)

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  5. Artikel: Nutritional problems of India--a developing nation

    Chatterjee, G.C

    Science and culture Jan 1976, 42 (1)

    1976  

    Schlagwörter India
    Sprache Englisch
    Erscheinungsverlauf 1976-01
    Umfang p. 3-9.
    Dokumenttyp Artikel
    ZDB-ID 2803033-3
    ISSN 0036-8156
    ISSN 0036-8156
    Datenquelle NAL Katalog (AGRICOLA)

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  6. Artikel: Effects of gamma-radiation on growth and metabolism of germinating wheat (Triticum aestivum L.)

    Chakraborti, M / Chatterjee, G.C

    Indian journal of experimental biology. Aug 1983. v. 21 (8)

    1983  

    Titelvarianten Effects of gamma-radiation on growth and metabolism of germinating wheat (Triticum aestivum L.) [India]
    Schlagwörter Triticum aestivum ; India
    Sprache Englisch
    Erscheinungsverlauf 1983-08
    Umfang p. 435-436.
    Dokumenttyp Artikel
    ZDB-ID 416061-7
    ISSN 0975-1009 ; 0019-5189
    ISSN (online) 0975-1009
    ISSN 0019-5189
    Datenquelle NAL Katalog (AGRICOLA)

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  7. Buch: Biochemical and nutritional studies on vitamin C in relation to studies on lysosomal enzymes

    Chatterjee, G. C

    final technical report

    1975  

    Körperschaft United States. / Dept. of Agriculture.
    University of Calcutta. / Dept. of Biochemistry
    Verfasserangabe G. C. Chatterjee ... [et al.]. -
    Schlagwörter Vitamin C/Metabolism. ; Lysosomes.
    Sprache Englisch
    Umfang 20 p. :, ill.
    Verlag Dept. of Biochemistry, University of Calcutta
    Erscheinungsort Calcutta
    Dokumenttyp Buch
    Anmerkung PL 480; grant no. FG-IN-467, (A7-HN-26), financed by the U.S. Dept. of Agriculture. Includes bibliographies.
    Datenquelle NAL Katalog (AGRICOLA)

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  8. Artikel: Chicken erythrocyte membrane: lipid profile and enzymatic activity under lanthanum chloride and neodymium chloride administration.

    Ghosh, N / Chattopadhyay, D / Chatterjee, G C

    Indian journal of experimental biology

    1991  Band 29, Heft 3, Seite(n) 226–229

    Abstract: Acute single dose (ip) administration of two rare earth elements like lanthanum chloride (250 mg/kg body wt) and neodymium chloride (200 mg/kg body wt) to chicks have been found to reduce the activity of certain erythrocyte membrane bound enzymes, viz. ... ...

    Abstract Acute single dose (ip) administration of two rare earth elements like lanthanum chloride (250 mg/kg body wt) and neodymium chloride (200 mg/kg body wt) to chicks have been found to reduce the activity of certain erythrocyte membrane bound enzymes, viz. acetylcholinesterase, NADH dehydrogenase, Mg(2+)-ATPase, p-nitrophenyl phosphatase. Erythrocyte membrane bound glycosidases e.g. beta-D-glucosidase, beta-D-galactosidase and beta-D-glucuronidase were also reduced. Other components such as cholesterol and phospholipid residues were reduced but their ratio (cholesterol/phospholipid) remaining unchanged. Membrane sulfhydryl groups were also significantly inhibited by these rare earth elements.
    Mesh-Begriff(e) Animals ; Chickens ; Erythrocyte Membrane/drug effects ; Erythrocyte Membrane/metabolism ; Glycoside Hydrolases/blood ; Lanthanum/toxicity ; Male ; Membrane Lipids/blood ; Neodymium/toxicity
    Chemische Substanzen Membrane Lipids ; lanthanum chloride (04M8624OXV) ; neodymium chloride (25O44EQD4O) ; Neodymium (2I87U3734A) ; Lanthanum (6I3K30563S) ; Glycoside Hydrolases (EC 3.2.1.-)
    Sprache Englisch
    Erscheinungsdatum 1991-03
    Erscheinungsland India
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 416061-7
    ISSN 0975-1009 ; 0019-5189
    ISSN (online) 0975-1009
    ISSN 0019-5189
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  9. Artikel: Antioxidant protection mechanism of chick hepatic mitochondria exposed to lanthanum chloride & neodymium chloride treatment.

    Ghosh, N / Chattopadhyay, D / Chatterjee, G C

    Indian journal of experimental biology

    1991  Band 29, Heft 5, Seite(n) 486–488

    Abstract: Acute lanthanum chloride (250 mg/kg body wt) and neodymium chloride (200 mg/kg body wt) administrations resulted in significant enhancement of glutathione level in chick hepatic mitochondria. However, glutathione-s-transferase activity was depressed. ... ...

    Abstract Acute lanthanum chloride (250 mg/kg body wt) and neodymium chloride (200 mg/kg body wt) administrations resulted in significant enhancement of glutathione level in chick hepatic mitochondria. However, glutathione-s-transferase activity was depressed. There was no alteration in the activity of glutathione reductase. Activity of glucose-6-phosphate dehydrogenase was not altered under lanthanum and neodymium treatment. There was a significant enhancement of intramitochondrial glutathione peroxidase and superoxide dismutase. Lipid peroxidation remains the same as control group of animals.
    Mesh-Begriff(e) Animals ; Antioxidants/metabolism ; Chickens ; Lanthanum/pharmacology ; Male ; Mitochondria, Liver/drug effects ; Mitochondria, Liver/metabolism ; Neodymium/pharmacology
    Chemische Substanzen Antioxidants ; lanthanum chloride (04M8624OXV) ; neodymium chloride (25O44EQD4O) ; Neodymium (2I87U3734A) ; Lanthanum (6I3K30563S)
    Sprache Englisch
    Erscheinungsdatum 1991-05
    Erscheinungsland India
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 416061-7
    ISSN 0975-1009 ; 0019-5189
    ISSN (online) 0975-1009
    ISSN 0019-5189
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel: Mode of action of iron on arylsulphatases under acute lead acetate treated conditions in rats.

    Santra, M / Basu, A / Chatterjee, G C

    Indian journal of biochemistry & biophysics

    1989  Band 26, Heft 2, Seite(n) 92–97

    Abstract: Arylsulphatases A, B and C were found to be inhibited in liver and kidney tissues under lead acetate-treated conditions (both in vivo and in vitro) in rats. When lead acetate-treated animals (in vivo) were supplemented with ferric ammonium citrate (in ... ...

    Abstract Arylsulphatases A, B and C were found to be inhibited in liver and kidney tissues under lead acetate-treated conditions (both in vivo and in vitro) in rats. When lead acetate-treated animals (in vivo) were supplemented with ferric ammonium citrate (in vivo), a remarkable recovery was found in the activities of all arylsulphatases A, B and C whereas ferric ammonium citrate itself had no effect on the activities of arylsulphatases. When both the in vivo and in vitro lead acetate-treated arylsulphatases were supplemented with the purified ferritins (in vitro) it was observed that lead-induced inhibition of the activities of arylsulphatases was successfully reversed. It was also found that ferritins were able to bind a large quantity of lead. These results indicated that ferritins were directly involved for reactivation of arylsulphatases which were inhibited by lead. It was well established that a response to iron administration in rats was an immediate de novo stimulation of ferritin biosynthesis. Iron might therefore protect the enzymatic activities of arylsulphatases by enhancing the level of ferritin in liver and kidney tissues which is known to bind a large quantity of lead thereby ameliorating their toxic effects in the living system.
    Mesh-Begriff(e) Animals ; Arylsulfatases/metabolism ; Iron/physiology ; Kidney/drug effects ; Liver/drug effects ; Male ; Organometallic Compounds/toxicity ; Rats ; Sulfatases/metabolism
    Chemische Substanzen Organometallic Compounds ; Iron (E1UOL152H7) ; Sulfatases (EC 3.1.6.-) ; Arylsulfatases (EC 3.1.6.1) ; lead acetate (RX077P88RY)
    Sprache Englisch
    Erscheinungsdatum 1989-04
    Erscheinungsland India
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 121689-2
    ISSN 0975-0959 ; 0301-1208
    ISSN (online) 0975-0959
    ISSN 0301-1208
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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