Статті в журналах з теми "Penicillina G Amidas"
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Ознайомтеся з топ-35 статей у журналах для дослідження на тему "Penicillina G Amidas".
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Wang, Jianguo, Qingqing Chen, Jie Wu, Wenping Zhu, Yongquan Wu, Xiaolin Fan, Guanxin Zhang, Yibao Li, and Guoyu Jiang. "A highly selective and light-up red emissive fluorescent probe for imaging of penicillin G amidase inBacillus cereus." New Journal of Chemistry 43, no. 16 (2019): 6429–34. http://dx.doi.org/10.1039/c9nj00890j.
Повний текст джерелаEVO, M., G. DEGRASSI, N. SKOKO, V. VENTURI, and G. LJUBIJANKI. "Production of glycosylated thermostable penicillin G amidase in." FEMS Yeast Research 1, no. 4 (January 2002): 271–77. http://dx.doi.org/10.1016/s1567-1356(01)00040-x.
Повний текст джерелаBrand, U., T. Scheper, and K. Schügerl. "Penicillin G sensor based on penicillin amidase coupled to a field effect transistor." Analytica Chimica Acta 226, no. 1 (January 1989): 87–97. http://dx.doi.org/10.1016/s0003-2670(00)80906-x.
Повний текст джерелаLjubijankić, Goran, Miroslav Konstantinović, and Vladimir Glišin. "The primary structure of Providencia rettgeri penicillin G amidase gene and its relationship to other gram negative amidases." DNA Sequence 3, no. 3 (January 1992): 195–200. http://dx.doi.org/10.3109/10425179209034017.
Повний текст джерелаSánchez, Juan, José Luis Marrugo Negrete, and Iván Urango. "Biosorción simultanea de plomo y cadmio en solución acuosa por biomasa de hongos penicillium sp." Temas Agrarios 19, no. 1 (August 19, 2016): 63–72. http://dx.doi.org/10.21897/rta.v19i1.725.
Повний текст джерелаPiotraschke, Elke, Allan Nurk, Boris Galunsky, and Volker Kasche. "Genetic construction of catalytically active cross-species heterodimer penicillin G amidase." Biotechnology Letters 16, no. 2 (February 1994): 119–24. http://dx.doi.org/10.1007/bf01021656.
Повний текст джерелаBraiuca, Paolo, Luca Boscarol, Cynthia Ebert, Paolo Linda, and Lucia Gardossi. "3D-QSAR Applied to the Quantitative Prediction of Penicillin G Amidase Selectivity." Advanced Synthesis & Catalysis 348, no. 6 (April 2006): 773–80. http://dx.doi.org/10.1002/adsc.200505346.
Повний текст джерелаGou, Bin-Quan, Ju Chu, Si-Liang Zhang, Yong-Hong Wang, Ying-Ping Zhuang, Hua Huang, Zhen Li, and Zhong-Yi Yuan. "Production of penicillin G amidase from Alcaligenes faecalis in a recombinant Escherichia coli." Journal of the Taiwan Institute of Chemical Engineers 40, no. 2 (March 2009): 233–36. http://dx.doi.org/10.1016/j.jtice.2008.09.004.
Повний текст джерелаQuratulain, S., B. Nasira, and M. A. Kashmiri. "Development and characterization of a potent producer of penicillin G amidase by mutagenization." World Journal of Microbiology and Biotechnology 22, no. 3 (November 25, 2005): 213–18. http://dx.doi.org/10.1007/s11274-005-9023-2.
Повний текст джерелаLee, C. K., and S. K. Chang. "Plate and frame filter as a recirculated batch reactor for penicillin-G amidase." Bioprocess Engineering 16, no. 2 (1997): 87. http://dx.doi.org/10.1007/s004490050293.
Повний текст джерелаBasso, Alessandra, Sara Cantone, Paolo Linda, and Cynthia Ebert. "Stability and activity of immobilised penicillin G amidase in ionic liquids at controlled aw." Green Chemistry 7, no. 9 (2005): 671. http://dx.doi.org/10.1039/b506230f.
Повний текст джерелаRobas, Nathalie, and Christiane Branlant. "The expression of the penicillin G amidase gene ofEscherichia coli by primer extension analysis." Current Microbiology 29, no. 5 (November 1994): 263–68. http://dx.doi.org/10.1007/bf01577438.
Повний текст джерелаNupur, Neh, Bentham Science Publisher Ashish, and Mira Debnath (Das). "Preparation and Biochemical Property of Penicillin G Amidase-Loaded Alginate and Alginate/Chitosan Hydrogel Beads." Recent Patents on Biotechnology 10, no. 1 (September 29, 2016): 121–32. http://dx.doi.org/10.2174/1872208310666160805112515.
Повний текст джерелаBasso, Alessandra, Beatrice A. Maltman, Sabine L. Flitsch, Graham Margetts, Ian Brazendale, Cynthia Ebert, Paolo Linda, Silvia Verdelli, and Lucia Gardossi. "Optimized polymer–enzyme electrostatic interactions significantly improve penicillin G amidase efficiency in charged PEGA polymers." Tetrahedron 61, no. 4 (January 2005): 971–76. http://dx.doi.org/10.1016/j.tet.2004.11.015.
Повний текст джерелаMönster, Andrea, Louis Villain, Thomas Scheper, and Sascha Beutel. "One-step-purification of penicillin G amidase from cell lysate using ion-exchange membrane adsorbers." Journal of Membrane Science 444 (October 2013): 359–64. http://dx.doi.org/10.1016/j.memsci.2013.05.054.
Повний текст джерелаScherrer, S., N. Robas, H. Zouheiry, G. Branlant, and C. Branlant. "Periplasmic aggregation limits the proteolytic maturation of the Escherichia coli Penicillin G amidase precursor polypeptide." Applied Microbiology and Biotechnology 42, no. 1 (November 1, 1994): 85–91. http://dx.doi.org/10.1007/s002530050221.
Повний текст джерелаScherrer, S., N. Robas, H. Zouheiry, G. Branlant, and C. Branlant. "Periplasmic aggregation limits the proteolytic maturation of the Escherichia coli Penicillin G amidase precursor polypeptide." Applied Microbiology and Biotechnology 42, no. 1 (October 1994): 85–91. http://dx.doi.org/10.1007/bf00170229.
Повний текст джерелаVrudhula, Vivekananda M., Peter D. Senter, Keith J. Fischer, and Philip M. Wallace. "Prodrugs of doxorubicin and melphalan and their activation by a monoclonal antibody-penicillin-G amidase conjugate." Journal of Medicinal Chemistry 36, no. 7 (April 1993): 919–23. http://dx.doi.org/10.1021/jm00059a018.
Повний текст джерелаZmijewski, Milton J., Barbara S. Briggs, Allen R. Thompson, and Ian G. Wright. "Enantioselective acylation of a beta-lactam intermediate in the synthesis of loracarbef using penicillin G amidase." Tetrahedron Letters 32, no. 13 (March 1991): 1621–22. http://dx.doi.org/10.1016/s0040-4039(00)74287-0.
Повний текст джерелаStankovic, Nada, Branka Vasiljevic та Goran Ljubijankic. "Effect of the kanamycin resistance marker on stability of 2μ-based expression plasmids". Archives of Biological Sciences 59, № 1 (2007): 1P—12P. http://dx.doi.org/10.2298/abs0701001s.
Повний текст джерелаGalaction, Anca-Irina, Ramona Mihaela Matran, Marius Turnea, Alexandra Cristina Blaga, and Dan Caşcaval. "ENGINEERING ASPECTS OF PENICILLIN G TRANSFER AND CONVERSION TO 6-AMINOPENICILLANIC ACID IN A BIOREACTOR WITH A MOBILE BED OF IMMOBILIZED PENICILLIN AMIDASE." Chemical Engineering Communications 201, no. 12 (June 17, 2014): 1568–81. http://dx.doi.org/10.1080/00986445.2013.819801.
Повний текст джерелаBegley, Máire, Roy D. Sleator, Cormac G. M. Gahan, and Colin Hill. "Contribution of Three Bile-Associated Loci, bsh, pva, and btlB, to Gastrointestinal Persistence and Bile Tolerance of Listeria monocytogenes." Infection and Immunity 73, no. 2 (February 2005): 894–904. http://dx.doi.org/10.1128/iai.73.2.894-904.2005.
Повний текст джерелаDe Martin, Luigi, Cynthia Ebert, Gianpiero Garau, Lucia Gardossi, and Paolo Linda. "Penicillin G amidase in low-water media: immobilisation and control of water activity by means of celite rods." Journal of Molecular Catalysis B: Enzymatic 6, no. 4 (April 1999): 437–45. http://dx.doi.org/10.1016/s1381-1177(99)00011-9.
Повний текст джерелаSitnikov, Nikolay S., Yingchun Li, Danfeng Zhang, Benito Yard, and Hans-Günther Schmalz. "Design, Synthese und funktionelle Evaluierung von CO-freisetzenden Molekülen, die durch Penicillin-G-Amidase als Modellprotease aktiviert werden." Angewandte Chemie 127, no. 42 (June 2, 2015): 12489–93. http://dx.doi.org/10.1002/ange.201502445.
Повний текст джерелаCardoso, J. P. "Purification of Penicillin G Amidase using Quaternary Ammonium Salts and effect on the activity of the immobilised enzymes." Bioprocess Engineering 16, no. 4 (1997): 209. http://dx.doi.org/10.1007/s004490050310.
Повний текст джерелаSitnikov, Nikolay S., Yingchun Li, Danfeng Zhang, Benito Yard, and Hans-Günther Schmalz. "Design, Synthesis, and Functional Evaluation of CO-Releasing Molecules Triggered by Penicillin G Amidase as a Model Protease." Angewandte Chemie International Edition 54, no. 42 (June 2, 2015): 12314–18. http://dx.doi.org/10.1002/anie.201502445.
Повний текст джерелаCascaval, Dan, Ramona Mihaela Matran, Anca-Irina Galaction, Alexandra Cristina Blaga, and Marius Turnea. "GREEN TECHNOLOGY FOR 6-AMINOPENICILLANIC ACID PRODUCTION - STUDY OF PENICILLIN G HYDROLYSIS IN A BIOREACTOR WITH MOBILE BED OF IMMOBILIZED PENICILLIN AMIDASE UNDER SUBSTRATE INHIBITION." Environmental Engineering and Management Journal 12, no. 11 (2013): 2261–66. http://dx.doi.org/10.30638/eemj.2013.278.
Повний текст джерелаGalunsky, Boris, Karsten Lummer, and Volker Kasche. "Comparative Study of Substrate- and Stereospecificity of Penicillin G Amidases from Different Sources and Hybrid Isoenzymes." Monatshefte fuer Chemie/Chemical Monthly 131, no. 6 (June 15, 2000): 623–32. http://dx.doi.org/10.1007/s007060070090.
Повний текст джерелаCaşcaval, Dan, Marius Turnea, Anca-Irina Galaction, and Alexandra Cristina Blaga. "6-Aminopenicillanic acid production in stationary basket bioreactor with packed bed of immobilized penicillin amidase—Penicillin G mass transfer and consumption rate under internal diffusion limitation." Biochemical Engineering Journal 69 (December 2012): 113–22. http://dx.doi.org/10.1016/j.bej.2012.09.004.
Повний текст джерелаBasso, Alessandra, Cynthia Ebert, Lucia Gardossi, Paolo Linda, Thao Tran Phuong, Mingzhao Zhu, and Ludger Wessjohann. "Penicillin G Amidase-Catalysed Hydrolysis of Phenylacetic Hydrazides on a Solid Phase: A New Route to Enzyme-Cleavable Linkers." Advanced Synthesis & Catalysis 347, no. 7-8 (June 2005): 963–66. http://dx.doi.org/10.1002/adsc.200505038.
Повний текст джерелаBasso, Alessandra, Luigi De Martin, Cynthia Ebert, Lucia Gardossi, and Paolo Linda. "Controlling the hydration of covalently immobilised penicillin G amidase in low-water medium: properties and use of Celite R-640." Journal of Molecular Catalysis B: Enzymatic 8, no. 4-6 (February 2000): 245–53. http://dx.doi.org/10.1016/s1381-1177(99)00075-2.
Повний текст джерелаCarboni, Chiara, Peter J. L. M. Quaedflieg, Quirinus B. Broxterman, Paolo Linda, and Lucia Gardossi. "Quantitative enzymatic protection of d-amino acid methyl esters by exploiting ‘relaxed’ enantioselectivity of penicillin-G amidase in organic solvent." Tetrahedron Letters 45, no. 52 (December 2004): 9649–52. http://dx.doi.org/10.1016/j.tetlet.2004.10.153.
Повний текст джерелаNi, Zhong, Huayou Chen, Xianfu Lin, and Rongzhong Jin. "Insight into molecular mechanism underlying the transesterification catalysed by penicillin G amidase (PGA) using a combination protocol of experimental assay and theoretical analysis." Molecular Simulation 40, no. 14 (January 13, 2014): 1125–30. http://dx.doi.org/10.1080/08927022.2013.850500.
Повний текст джерелаSambyal, Krishika, та Rahul Vikram Singh. "Exploitation of E. coli for the production of penicillin G amidase: a tool for the synthesis of semisynthetic β-lactam antibiotics". Journal of Genetic Engineering and Biotechnology 19, № 1 (15 жовтня 2021). http://dx.doi.org/10.1186/s43141-021-00263-7.
Повний текст джерелаZhao, Chao, Wanlu Sun, Baojin Tan, Dan Su, and Yi Liu. "Penicillin G amidase-activatable near-infrared imaging guiding PDT of bacterial infections." Sensors and Actuators B: Chemical, February 2023, 133502. http://dx.doi.org/10.1016/j.snb.2023.133502.
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