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Relevant bibliographies by topics / Catalytic studies of glycogen

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Academic literature on the topic 'Catalytic studies of glycogen'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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Journal articles on the topic "Catalytic studies of glycogen"

1

Mitchell, E. P., L. N. Johnson, Ph Ermert, A. T. Vasella, S. G. Withers, and N. G. Oikonomakos. "Crystallographic studies towards the catalytic mechanism of glycogen phosphorylase." Acta Crystallographica Section A Foundations of Crystallography 49, s1 (August 21, 1993): c87. http://dx.doi.org/10.1107/s0108767378097512.

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Papageorgiou, A. C., N. G. Oikonomakos, D. D. Leonidas, B. Bernet, D. Beer, and A. Vasella. "The binding of d-gluconohydroximo-1,5-lactone to glycogen phosphorylase. Kinetic, ultracentrifugation and crystallographic studies." Biochemical Journal 274, no. 2 (March 1, 1991): 329–38. http://dx.doi.org/10.1042/bj2740329.

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Combined kinetic, ultracentrifugation and X-ray-crystallographic studies have characterized the effect of the beta-glucosidase inhibitor gluconohydroximo-1,5-lactone on the catalytic and structural properties of glycogen phosphorylase. In the direction of glycogen synthesis, gluconohydroximo-1,5-lactone was found to competitively inhibit both the b (Ki 0.92 mM) and the alpha form of the enzyme (Ki 0.76 mM) with respect to glucose 1-phosphate in synergism with caffeine. In the direction of glycogen breakdown, gluconohydroximo-1,5-lactone was found to inhibit phosphorylase b in a non-competitive mode with respect to phosphate, and no synergism with caffeine could be demonstrated. Ultracentrifugation and crystallization experiments demonstrated that gluconohydroximo-1,5-lactone was able to induce dissociation of tetrameric phosphorylase alpha and stabilization of the dimeric T-state conformation. A crystallographic binding study with 100 mM-gluconohydroximo-1,5-lactone at 0.24 nm (2.4 A) resolution showed a major peak at the catalytic site, and no significant conformational changes were observed. Analysis of the electron-density map indicated that the ligand adopts a chair conformation. The results are discussed with reference to the ability of the catalytic site of the enzyme to distinguish between two or more conformations of the glucopyranose ring.

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3

Mavreas, Konstantinos F., Dionysios D. Neofytos, Evangelia D. Chrysina, Alessandro Venturini, and Thanasis Gimisis. "Synthesis, Kinetic and Conformational Studies of 2-Substituted-5-(β-d-glucopyranosyl)-pyrimidin-4-ones as Potential Inhibitors of Glycogen Phosphorylase." Molecules 25, no. 22 (November 22, 2020): 5463. http://dx.doi.org/10.3390/molecules25225463.

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Dysregulation of glycogen phosphorylase, an enzyme involved in glucose homeostasis, may lead to a number of pathological states such as type 2 diabetes and cancer, making it an important molecular target for the development of new forms of pharmaceutical intervention. Based on our previous work on the design and synthesis of 4-arylamino-1-(β-d-glucopyranosyl)pyrimidin-2-ones, which inhibit the activity of glycogen phosphorylase by binding at its catalytic site, we report herein a general synthesis of 2-substituted-5-(β-d-glucopyranosyl)pyrimidin-4-ones, a related class of metabolically stable, C-glucosyl-based, analogues. The synthetic development consists of a metallated heterocycle, produced from 5-bromo-2-methylthiouracil, in addition to protected d-gluconolactone, followed by organosilane reduction. The methylthio handle allowed derivatization through hydrolysis, ammonolysis and arylamine substitution, and the new compounds were found to be potent (μM) inhibitors of rabbit muscle glycogen phosphorylase. The results were interpreted with the help of density functional theory calculations and conformational analysis and were compared with previous findings.

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4

Gruppuso, P. A., and D. L. Brautigan. "Induction of hepatic glycogenesis in the fetal rat." American Journal of Physiology-Endocrinology and Metabolism 256, no. 1 (January 1, 1989): E49—E54. http://dx.doi.org/10.1152/ajpendo.1989.256.1.e49.

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We have performed an in vivo study to test the hypothesis that induction of fetal hepatic glycogenesis is stimulated by insulin and involves activation of protein phosphatase type-1. Control animals and the following two experimental groups were studied: maternal fasting for 48 h prior to term and chronic maternal hyperinsulinemia for 5 days prior to term. Maternal fasting led to decreased fetal hepatic glycogen content and fetal growth retardation. In contrast, no decrease in fetal hepatic glycogen content or fetal weight occurred with maternal hyperinsulinemia despite fetal hypoglycemia and fetal hypoinsulinemia. In neither model were fetal hepatic synthase phosphatase or phosphorylase phosphatase activities affected. In control fetuses, the appearance of hepatic glycogen from days 17 to 21 of gestation correlated with induction of glycogen synthase. Phosphorylase phosphatase and synthase phosphatase activities already were present on day 17 of gestation and changed little through term. However, phosphatase catalytic protein reactive with anti-phosphatase type-1 antibodies did increase approximately fivefold from day 18 to 21. In adult animals fasted for 48 h, 50% of hepatic glycogen synthase phosphatase activity was lost, whereas phosphorylase phosphatase activity was stimulated fourfold. The apparent size of protein phosphatase type-1 catalytic subunit as detected by Western immunoblotting was altered by fasting in the adult but not by substrate restriction (maternal fasting) in the fetus.(ABSTRACT TRUNCATED AT 250 WORDS)

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5

Acharya, K. R., J. Hajdu, D. I. Stuart, P. J. McLaughlin, D. Barford, N. G. Oikonomakos, and L. N. Johnson. "Catalysis in the crystal: synchrotron radiation studies with glycogen phosphorylaseb." Acta Crystallographica Section A Foundations of Crystallography 43, a1 (August 12, 1987): C40. http://dx.doi.org/10.1107/s0108767387084393.

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6

Tu, J., and M. Carlson. "The GLC7 type 1 protein phosphatase is required for glucose repression in Saccharomyces cerevisiae." Molecular and Cellular Biology 14, no. 10 (October 1994): 6789–96. http://dx.doi.org/10.1128/mcb.14.10.6789.

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We cloned the GLC7/DIS2S1 gene by complementation of the cid1-226 mutation, which relieves glucose repression in Saccharomyces cerevisiae. GLC7 encodes the catalytic subunit of type 1 protein phosphatase (PP1). Genetic analysis and sequencing showed that cid1-226 is an allele of GLC7, now designated glc7-T152K, which alters threonine 152 to lysine. We also show that the glc7-1 and glc7-T152K alleles cause distinct phenotypes: glc7-1 causes a severe defect in glycogen accumulation but does not relieve glucose repression, whereas glc7-T152K does not prevent glycogen accumulation. These findings are discussed in light of evidence that interaction with different regulatory or targeting subunits directs the participation of PP1 in diverse cellular regulatory mechanisms. Finally, genetic studies suggest that PP1 functions antagonistically to the SNF1 protein kinase in the regulatory response to glucose.

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7

Tu, J., and M. Carlson. "The GLC7 type 1 protein phosphatase is required for glucose repression in Saccharomyces cerevisiae." Molecular and Cellular Biology 14, no. 10 (October 1994): 6789–96. http://dx.doi.org/10.1128/mcb.14.10.6789-6796.1994.

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We cloned the GLC7/DIS2S1 gene by complementation of the cid1-226 mutation, which relieves glucose repression in Saccharomyces cerevisiae. GLC7 encodes the catalytic subunit of type 1 protein phosphatase (PP1). Genetic analysis and sequencing showed that cid1-226 is an allele of GLC7, now designated glc7-T152K, which alters threonine 152 to lysine. We also show that the glc7-1 and glc7-T152K alleles cause distinct phenotypes: glc7-1 causes a severe defect in glycogen accumulation but does not relieve glucose repression, whereas glc7-T152K does not prevent glycogen accumulation. These findings are discussed in light of evidence that interaction with different regulatory or targeting subunits directs the participation of PP1 in diverse cellular regulatory mechanisms. Finally, genetic studies suggest that PP1 functions antagonistically to the SNF1 protein kinase in the regulatory response to glucose.

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8

Hajdu, J., K. R. Acharya, D. I. Stuart, P. J. McLaughlin, D. Barford, N. G. Oikonomakos, H. Klein, and L. N. Johnson. "Catalysis in the crystal: synchrotron radiation studies with glycogen phosphorylase b." EMBO Journal 6, no. 2 (February 1987): 539–46. http://dx.doi.org/10.1002/j.1460-2075.1987.tb04786.x.

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9

Coate, Katie C., Guillaume Kraft, Masakazu Shiota, Marta S. Smith, Ben Farmer, Doss W. Neal, Phil Williams, Alan D. Cherrington, and Mary Courtney Moore. "Chronic overeating impairs hepatic glucose uptake and disposition." American Journal of Physiology-Endocrinology and Metabolism 308, no. 10 (May 15, 2015): E860—E867. http://dx.doi.org/10.1152/ajpendo.00069.2015.

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Dogs consuming a hypercaloric high-fat and -fructose diet (52 and 17% of total energy, respectively) or a diet high in either fructose or fat for 4 wk exhibited blunted net hepatic glucose uptake (NHGU) and glycogen deposition in response to hyperinsulinemia, hyperglycemia, and portal glucose delivery. The effect of a hypercaloric diet containing neither fructose nor excessive fat has not been examined. Dogs with an initial weight of ≈25 kg consumed a chow and meat diet (31% protein, 44% carbohydrate, and 26% fat) in weight-maintaining (CTR; n = 6) or excessive (Hkcal; n = 7) amounts for 4 wk (cumulative weight gain 0.0 ± 0.3 and 1.5 ± 0.5 kg, respectively, P < 0.05). They then underwent clamp studies with infusions of somatostatin and intraportal insulin (4× basal) and glucagon (basal). The hepatic glucose load was doubled with peripheral (Pe) glucose infusion for 90 min (P1) and intraportal glucose at 4 mg·kg−1·min−1 plus Pe glucose for the final 90 min (P2). NHGU was blunted ( P < 0.05) in Hkcal during both periods (mg·kg−1·min−1; P1: 1.7 ± 0.2 vs. 0.3 ± 0.4; P2: 3.6 ± 0.3 vs. 2.3 ± 0.4, CTR vs. Hkcal, respectively). Terminal hepatic glucokinase catalytic activity was reduced nearly 50% in Hkcal vs. CTR ( P < 0.05), although glucokinase protein did not differ between groups. In Hkcal vs. CTR, liver glycogen was reduced 27% ( P < 0.05), with a 91% increase in glycogen phosphorylase activity ( P < 0.05) but no significant difference in glycogen synthase activity. Thus, Hkcal impaired NHGU and glycogen synthesis compared with CTR, indicating that excessive energy intake, even if the diet is balanced and nutritious, negatively impacts hepatic glucose metabolism.

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Zographos, S. E., N. G. Oikonomakos, H. B. F. Dixon, W. G. Griffin, L. N. Johnson, and D. D. Leonidas. "Sulphate-activated phosphorylase b: the pH-dependence of catalytic activity." Biochemical Journal 310, no. 2 (September 1, 1995): 565–70. http://dx.doi.org/10.1042/bj3100565.

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The pH-dependence of sulphate-activated phosphorylase b has been studied in the direction of glycogen synthesis. The bell-shaped curve of the pH-dependence of the catalytic constant for the AMP-activated enzyme showed pK values of 6.1 and 7.3, but the curve for the enzyme activated by 0.9 M ammonium sulphate showed a drop of activity on the acid side at much higher pH values. Its bell was centred at pH 7.8 but it was too narrow to be characterized by only two pK values. The narrowness of the curve could be explained by positive co-operativity, but not its unusually steep acid side. We suggest that the fall on the acid side is due to more than one hydronation (addition of H+). The points can be fitted by a curve with two de-activating hydronations and a de-activating dehydronation having identical titration pK values of 7.5, and hence molecular values of 7.0, 7.5 and 8.0. If both 0.9 M ammonium sulphate and 5 mM AMP are added, the bell is as broad as with AMP alone, but is somewhat raised in pH optimum. The results are discussed in the light of new structural data from crystallographic studies on binary complexes of the enzyme.

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Dissertations / Theses on the topic "Catalytic studies of glycogen"

1

Martin, Jennifer Louise. "Molecular interactions involving glycogen phosphorylase." Thesis, University of Oxford, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.253306.

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Barford, D. "Crystallographic studies on glycogen phosphorylase b." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233473.

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3

McLaughlin, P. J. "Crystallographic studies on glycogen phosphorylase b." Thesis, University of Oxford, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.370290.

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4

Hu, Shu-Hong. "Crystallographic studies on activated glycogen phosphorylase." Thesis, University of Oxford, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.291283.

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Duke, Elizabeth Mary Helen. "X-ray diffraction studies on glycogen phosphorylase." Thesis, University of Oxford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.336092.

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6

Mitchell, Edward Peter. "Cryocrystallographic and mechanistic studies on glycogen phosphorylase." Thesis, University of Oxford, 1994. https://ora.ox.ac.uk/objects/uuid:d562f4f6-0a93-43a6-ad74-d480697d1b8c.

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Glycogen phosphorylase (GPb) regulates the degradation of glycogen to glucose-1-phosphate and catalyses the first step of the reaction. Many studies have provided insights into the essentials of the catalytic mechanism. Previous time resolved crystallographic work using heptenitol has revealed a putative phosphate binding site at the active site of phosphorylase. Using nojirimycin tetrazole, a transition state analogue, complexed with phosphate and both T and R state GPb crystals, this work has conclusively located the phosphate binding site and the concomitant active site conformational changes. This has confirmed the previous heptenitol results. Using R state crystals complexed with tetrazole and phosphate, data were collected to 2.5Ã resolution, higher than for the original 2.8Ã resolution native structure, and used to position water molecules in the R state model. Further to this, direct observation of the phosphate ion orientation was made possible using flash-frozen T state crystals to collect 1.7Ã resolution data at 100K. As part of this cryocrystallographic work the relationship of cryoprotectant concentration with crystal mosaicity was established, aiding the systematic search for flash-freezing cryoprotectant conditions for all protein crystals. Collection of a new native T state data set to 1.5Ã resolution was made possible using the flash-freezing technique. Refinement has produced a new higher precision native model (R factor currently 22.8%) containing additional N terminal residues (14-18) and 330 new water molecules. A molecule of glycerol, the cryoprotectant, was located at the active site. This study represents a considerable improvement over the 1.9Ã resolution room temperature native data, and is also the first time such high resolution data have been collected from such a large enzyme. In a further analysis of the phosphate binding properties, a link between structure, atomic charges and the ability of a ligand to bind phosphate at the phosphorylase active site was established. In order of phosphate binding ability, the nojirimycin tetrazole, nitroglucal, glucal and glucose complexes with T state GPb and phosphate were structurally analysed. As the charge difference between the pyranose ring oxygen (or equivalent atom) and anomeric atom becomes more negative (charges estimated using MOPAC) the tendency to bind phosphate decreases. The ligand must possess a half-chair conformation as this is essential to bind phosphate; glucose, having the most negative charge difference and a full chair conformation, does not bind phosphate significantly in the crystal. A novel surface binding site for nitroglucal (covalently linked to His 73) was also located during this work. As part of an ongoing search for potential drugs for diabetes, two gluco-hydantoin inhibitors of GPb were investigated. One proved to be the best inhibitor to date, and the inhibition was rationalised using the structural results from this work. A new improved inhibitor has been proposed on the basis of these results.

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7

Varvill, Katherine Mary. "X-ray crystallographic studies on glycogen phosphorylase b." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.352921.

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8

Watson, Kimberly Ann. "Crystallographic studies on phosphorylase : sugar recognition properties." Thesis, University of Oxford, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.259849.

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9

Khan, M. "Catalytic studies on zeolites." Thesis, City University London, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.375832.

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Maeda, Kenji. "Extended studies in catalytic hydroboration." Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.246529.

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Books on the topic "Catalytic studies of glycogen"

1

1936-, Paál Zoltán, ed. Laboratory studies of heterogeneous catalytic processes. Amsterdam: Elsevier, 1989.

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Mandani, Faisal Mohammad. Kinetic and deactivation studies during catalytic dehydrogenation. Salford: University of Salford, 1991.

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Thursfield, A. Solid state NMR studies of catalytic processes inzeolites. Manchester: UMIST, 1994.

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Lin, Yeuh-Hui. Theoretical and experimental studies of catalytic degradation of polymers. Manchester: UMIST, 1998.

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Harrison, Richard John. Studies on some niobocene derivatives and their catalytic activity. [s.l.]: typescript, 1997.

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6

Jenta, Tuah R. J. Catalytic studies of lipase in microemulsion-based reaction media. Norwich: University of East Anglia, 1993.

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7

Seal, Leonard Henry. Studies on glycogen in the nervous systems of Haemopis Sanguisuga and Planorbis Corneus. Salford: University of Salford, 1986.

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Koon, Chung Lun. Studies of coke deposition, structure and regeneration during catalytic processing. Salford: University of Salford, 1991.

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9

Kozarova, Anna. Structure-function studies between the regulatory domain of human PKCa [alpha] and the PKCa [alpha] catalytic domain. Sudbury, Ont: Laurentian University, School of Graduate Studies, 2004.

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10

Laboratory Studies of Heterogeneous Catalytic Processes. Elsevier, 1989. http://dx.doi.org/10.1016/s0167-2991(08)x6005-7.

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Book chapters on the topic "Catalytic studies of glycogen"

1

Tantillo, Dean J., Andrew G. Leach, Xiyun Zhang, and K. N. Houk. "Theoretical Studies of Antibody Catalysis." In Catalytic Antibodies, 72–117. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603662.ch3.

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Laughlin, Maren R., Douglas L. Rothman, and Robert G. Shulman. "13C NMR Studies of Heart Glycogen Metabolism." In Metabolomics by In Vivo NMR, 87–102. Chichester, UK: John Wiley & Sons, Ltd, 2005. http://dx.doi.org/10.1002/0470011505.ch7.

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Bueding, Ernest, Stanley A. Orrell, and James Sidbury. "Studies of Storage Disease Glycogens." In Ciba Foundation Symposium - Control of Glycogen Metabolism, 387–415. Chichester, UK: John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470719343.ch28.

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Burchell, A., I. D. Waddell, L. Stewart, and R. Hume. "Perinatal Diagnosis of Type 1c Glycogen Storage Disease." In Studies in Inherited Metabolic Disease, 315–17. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-1069-0_38.

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Farías, M. H. "Chemisorption Studies of Catalytic Reactions." In Springer Proceedings in Physics, 483–89. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-76376-2_71.

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Evangelopoulos, A. E. "Microenvironmental Properties and Conformational Changes in Glycogen Phosphorylase." In Recent Advances in Biological Membrane Studies, 149–63. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4684-4979-2_11.

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Cenini, Sergio, and Fabio Ragaini. "Mechanistic Studies." In Catalytic Reductive Carbonylation of Organic Nitro Compounds, 247–327. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-017-0986-6_6.

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Laughlin, Maren R. "NMR Studies of Glycogen Metabolism in the Heart." In Cardiovascular Magnetic Resonance Spectroscopy, 169–83. Boston, MA: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-3490-7_11.

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Duke, E. M. H., A. Hadfield, J. L. Martin, I. J. Clifton, J. Hajdu, L. N. Johnson, G. P. Reid, D. R. Trentham, I. Bruce, and G. W. J. Fleet. "Towards Time-Resolved Diffraction Studies with Glycogen Phosphorylase." In Ciba Foundation Symposium 161 - Protein Conformation, 75–90. Chichester, UK: John Wiley & Sons, Ltd., 2007. http://dx.doi.org/10.1002/9780470514146.ch6.

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Maire, I., G. Mandon, and M. Mathieu. "First Trimester Prenatal Diagnosis of Glycogen Storage Disease Type III." In Studies in Inherited Metabolic Disease, 292–94. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-1069-0_31.

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Conference papers on the topic "Catalytic studies of glycogen"

1

D'Netto, Geoffrey A., Peter C. Pawlicki, and Roger A. Schmitz. "Thermographic Studies Of Catalytic Reactions." In 1984 Cambridge Symposium, edited by Andronicos G. Kantsios. SPIE, 1985. http://dx.doi.org/10.1117/12.946135.

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RÉDEY, Á., Z. GAÁL, and A. KOCZKA. "CATALYTIC STUDIES ON MOLYBDENA-ALUMINA CATALYSTS." In Proceedings of the Third Asia-Pacific Conference. WORLD SCIENTIFIC, 2000. http://dx.doi.org/10.1142/9789812791924_0024.

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Inforzato, Tatiane, Liane Marcia Rossi, Tiago Venancio, and Alcindo A. Dos Santos. "Silica-Supported Proline Derivatives for Catalytic Studies." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0201-1.

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Marengo, S., and P. Comotti. "Studies of catalysts and catalytic reactions by infrared thermography." In 1994 Quantitative InfraRed Thermography. QIRT Council, 1994. http://dx.doi.org/10.21611/qirt.1994.002.

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Wang, Cheng-Xue, Lei Lv, and Xiang-Bo Wang. "Studies on Simultaneous Catalytic Removal of NOX and SO2." In 2012 International Conference on Biomedical Engineering and Biotechnology (iCBEB). IEEE, 2012. http://dx.doi.org/10.1109/icbeb.2012.370.

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MacLean, Matthew, and Michael Holden. "Catalytic Effects on Heat Transfer Measurements for Aerothermal Studies with CO2." In 44th AIAA Aerospace Sciences Meeting and Exhibit. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2006. http://dx.doi.org/10.2514/6.2006-182.

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Widdis, Stephen, Darren Hitt, Kofi Asante, Michael Cross, Walter Varhue, and Michael McDevitt. "Computational and Experimental Studies of Catalytic H2O2 Decomposition in Microscale Reactors." In 43rd AIAA Thermophysics Conference. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2012. http://dx.doi.org/10.2514/6.2012-3096.

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Guirardello, Reginaldo, and Guilherme Pessoa Nogueira. "Catalytic conversion of glucose using nano-anatase TiO2 catalyst: kinetic studies." In XXIII Congresso de Iniciação Científica da Unicamp. Campinas - SP, Brazil: Galoá, 2015. http://dx.doi.org/10.19146/pibic-2015-37330.

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Fisher, Galen B., Craig L. Dimaggio, Aleksey Yezerets, Mayfair C. Kung, Harold H. Kung, Suresh Baskaran, John G. Frye, et al. "Mechanistic Studies of the Catalytic Chemistry of NOx in Laboratory Plasma-Catalyst Reactors." In International Fuels & Lubricants Meeting & Exposition. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 2000. http://dx.doi.org/10.4271/2000-01-2965.

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Yang, L., S. C. Zhang, Y. P. Feng, Z. T. Zhu, Y. B. Song, and Y. W. Fang. "Synthesis of SAPO-34 Zeolite with Different Template Agents and DTO Catalytic Studies." In The International Workshop on Materials, Chemistry and Engineering. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0007441305450551.

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Reports on the topic "Catalytic studies of glycogen"

1

Heinemann, H., and G. A. Somorjai. Fundamental studies of catalytic gasification. Office of Scientific and Technical Information (OSTI), June 1990. http://dx.doi.org/10.2172/6410286.

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Heinemann, H., and G. A. Smorjai. Fundamental studies of catalytic gasification. Office of Scientific and Technical Information (OSTI), June 1991. http://dx.doi.org/10.2172/5146961.

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Heinemann, H., and G. A. Somorjai. Fundamental studies of catalytic gasification. Office of Scientific and Technical Information (OSTI), March 1991. http://dx.doi.org/10.2172/5240899.

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Heinemann, H., and G. A. Somorjai. Fundamental studies of catalytic gasification. Office of Scientific and Technical Information (OSTI), June 1991. http://dx.doi.org/10.2172/5240965.

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Heinemann, H., and G. Somorjai. Fundamental studies of catalytic gasification. Office of Scientific and Technical Information (OSTI), December 1989. http://dx.doi.org/10.2172/7271320.

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6

Heinemann, H., and G. Somorjai. Fundamental studies of catalytic gasification. Office of Scientific and Technical Information (OSTI), September 1989. http://dx.doi.org/10.2172/7271333.

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7

Heinemann, H., and G. A. Somorjai. Fundamental studies of catalytic gasification. Office of Scientific and Technical Information (OSTI), September 1990. http://dx.doi.org/10.2172/6224411.

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8

Heinemann, H., and G. A. Somorjai. Fundamental studies of catalytic gasification. Office of Scientific and Technical Information (OSTI), September 1991. http://dx.doi.org/10.2172/5805305.

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9

Heinemann, H., and G. A. Somorjai. Fundamental studies of catalytic gasification. Office of Scientific and Technical Information (OSTI), December 1991. http://dx.doi.org/10.2172/5877723.

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Watson, P. R. Fundamental studies of catalytic processing of synthetic liquids. Office of Scientific and Technical Information (OSTI), July 1990. http://dx.doi.org/10.2172/5066014.

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