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Journal articles on the topic 'Microbiological synthesis Microbiological synthesis'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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1

Utagawa, Takashi, Hirokazu Morisawa, Fumihiro Yoshinaga, Akihiro Yamazaki, Koji Mitsugi, and Yoshio Hirose. "Microbiological Synthesis of Adenine Arabinoside." Agricultural and Biological Chemistry 49, no. 4 (April 1985): 1053–58. http://dx.doi.org/10.1080/00021369.1985.10866862.

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2

Astashkina, Anna, Yuliya Kolbysheva, Alena Nikiforova, and Abdigali Bakibayev. "Microbiological synthesis of methyl ethyl ketone." MATEC Web of Conferences 85 (2016): 01022. http://dx.doi.org/10.1051/matecconf/20168501022.

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3

Mahieddine, Cherifa, Mohamed Salah Boukhechem, Said Zerkout, and Abdelghani Zitouni. "Synthesis and Microbiological Activities of Novel Acyclic Nitrones." Asian Journal of Chemistry 28, no. 5 (2016): 1027–30. http://dx.doi.org/10.14233/ajchem.2016.19576.

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4

Potaniec, Bartlomiej, Barbara Zarowska, Joanna Kozlowska, and Miroslaw Aniol. "Synthesis and anti-microbiological properties of chalcones oximes." New Biotechnology 33 (July 2016): S82. http://dx.doi.org/10.1016/j.nbt.2016.06.1003.

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5

Wagman, Allan S., Ryan Cirz, Glenn McEnroe, James Aggen, Martin S. Linsell, Adam A. Goldblum, Sara Lopez, et al. "Synthesis and Microbiological Evaluation of Novel Tetracyclic Fluoroquinolones." ChemMedChem 12, no. 20 (October 2, 2017): 1687–92. http://dx.doi.org/10.1002/cmdc.201700426.

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6

Koritala, S. "Microbiological synthesis of wax esters by euglena gracilis." Journal of the American Oil Chemists' Society 66, no. 1 (January 1989): 133–34. http://dx.doi.org/10.1007/bf02661801.

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7

Gong, Jun, ZhaoMing Zhang, HongJuan Bai, and GuanE Yang. "Microbiological synthesis of nanophase PbS by Desulfotomaculum sp." Science in China Series E: Technological Sciences 50, no. 3 (June 2007): 302–7. http://dx.doi.org/10.1007/s11431-007-0045-x.

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8

Paun, Anca, Irina Zarafu, Miron T. Caproiu, Constantin Draghici, Maria Maganu, Ani I. Cotar, Mariana C. Chifiriuc, and Petre Ionita. "Synthesis and microbiological evaluation of several benzocaine derivatives." Comptes Rendus Chimie 16, no. 7 (July 2013): 665–71. http://dx.doi.org/10.1016/j.crci.2013.03.012.

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9

Scalzo, Marcello, Mariangela Biava, Felice Cerreto, Giulo Cesare Porretta, Salvatore Panico, and Nicola Simonetti. "Synthesis and microbiological activity of new 1,5-diarylpyrroles." European Journal of Medicinal Chemistry 23, no. 6 (November 1988): 587–91. http://dx.doi.org/10.1016/0223-5234(88)90103-1.

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10

UTAGAWA, Takashi, Hirokazu MORISAWA, Fumihiro YOSHINAGA, Akihiro YAMAZAKI, Koji MITSUGI, and Yoshio HIROSE. "Enzymatic synthesis of nucleoside antibiotics. Part I. Microbiological synthesis of adenine arabinoside." Agricultural and Biological Chemistry 49, no. 4 (1985): 1053–58. http://dx.doi.org/10.1271/bbb1961.49.1053.

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11

Završnik, Davorka, Samija Muratović, Selma Špirtović, Dženita Softić, and Marica Medić-Šarić. "The Synthesis and Antimicrobial Activity of Some 4-Hydroxycoumarin Derivatives." Bosnian Journal of Basic Medical Sciences 8, no. 3 (August 20, 2008): 277–81. http://dx.doi.org/10.17305/bjbms.2008.2933.

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Due to exceptional reactivity of 4-hydroxycoumarin, the synthesis of new coumarin derivatives of dimer and tetramer type has been carried out. The synthesis was carried out from 4-hydroxycoumarin and various aromatic aldehydes. In this way, compounds of the dimer 3,3’-(benzilidene)bis (4-hydroxycoumarin) type, as well as of the tetramer 3,3,’3’,’3’’’-(1,4-dim- ethylenphenyl)tetra (4-hydroxycoumarin) type were prepared.The newly synthesized derivatives contain different functional groups, and as such they could exhibit microbiological activity. Therefore, we tested the microbiological activity of these derivatives on various species of bacteria and fungi. The tested compounds have shown different activity in terms of growth inhibition of microorganisms. Newly synthesized derivatives exhibit antibacterial activities, manifested as growth inhibition on Grampositive bacteria types (Bacillus, Staphylococcus), while the activity against Candida was much weaker. The same compound did not show any antimicrobial activity against two Gram-negative bacteria types (Escherichia coli, Pseudomonas aeruginosa). The compound 1 showed the best microbiological activity. The obtained results confirmed its good antibacterial and antimycotic activities against different microorganisms.

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12

Valadares, Rafael V., Maurício D. Costa, Júlio César L. Neves, João A. F. Vieira Netto, Ivo Ribeiro da Silva, Edemar Moro, Marcelo Rodrigo Alves, and Luiz Arnaldo Fernandes. "Rhizosphere microbiological processes and eucalypt nutrition: Synthesis and conceptualization." Science of The Total Environment 746 (December 2020): 141305. http://dx.doi.org/10.1016/j.scitotenv.2020.141305.

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13

Gong, Jun, Xiaomin Song, Yan Gao, Shiyu Gong, Yufen Wang, and Jinxian Han. "Microbiological synthesis of zinc sulfide nanoparticles using Desulfovibrio desulfuricans." Inorganic and Nano-Metal Chemistry 48, no. 2 (February 1, 2018): 96–102. http://dx.doi.org/10.1080/15533174.2016.1216451.

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14

Schiaffella, Fausto, Antonio Macchiarulo, Lara Milanese, Anna Vecchiarelli, Gabriele Costantino, Donatella Pietrella, and Renata Fringuelli. "Design, Synthesis, and Microbiological Evaluation of NewCandida albicansCYP51 Inhibitors." Journal of Medicinal Chemistry 48, no. 24 (December 2005): 7658–66. http://dx.doi.org/10.1021/jm050685j.

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15

Fraga, Braulio M., Fernando García-Tellado, Pedro González, Melchor G. Hernández, and James R. Hanson. "The chemical and microbiological synthesis of 14-hydroxy-gibberellins." Tetrahedron 48, no. 39 (September 1992): 8491–504. http://dx.doi.org/10.1016/s0040-4020(01)86597-2.

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16

Andryushina, V. A., N. V. Karpova, A. V. Druzhinina, T. S. Stytsenko, E. A. Podorozhko, A. N. Ryabev, and V. I. Lozinsky. "Novel immobilized biocatalyst for microbiological synthesis of pharmaceutical steroids." Applied Biochemistry and Microbiology 51, no. 5 (August 30, 2015): 530–38. http://dx.doi.org/10.1134/s0003683815050026.

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17

Mikhailopulo, I. A., A. I. Zinchenko, Z. Kazimierczuk, V. N. Barai, S. B. Bokut, and E. N. Kalinichenko. "Synthesis of 2-Chloro-2′-Deoxyadenosine by Microbiological Transglycosylation." Nucleosides and Nucleotides 12, no. 3-4 (March 1993): 417–22. http://dx.doi.org/10.1080/07328319308017836.

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18

Sukhodolskaya, G. V., V. V. Fokina, T. S. Savinova, A. A. Shutov, N. V. Lukashev, and M. V. Donova. "Combined chemical and microbiological synthesis of exemestane from sitosterol." Journal of Biotechnology 150 (November 2010): 189. http://dx.doi.org/10.1016/j.jbiotec.2010.08.493.

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19

Burmudžija, Adrijana, Zoran Ratković, Jovana Muškinja, Nenad Janković, Branislav Ranković, Marijana Kosanić, and Snežana Đorđević. "Ferrocenyl based pyrazoline derivatives with vanillic core: synthesis and investigation of their biological properties." RSC Advances 6, no. 94 (2016): 91420–30. http://dx.doi.org/10.1039/c6ra18977f.

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20

de Andrade Danin Barbosa, Gabriela, and Alcino Palermo de Aguiar. "Synthesis of 1,3,4-Thiadiazole Derivatives and Microbiological Activities: A Review." Revista Virtual de Química 11, no. 3 (2019): 806–48. http://dx.doi.org/10.21577/1984-6835.20190058.

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21

Rusu, Aura, Gabriel Hancu, Gergő Tóth, Szende Vancea, Felicia Toma, Anca Delia Mare, Adrian Man, George Mihai Niţulescu, and Valentina Uivarosi. "New silver complexes with levofloxacin: Synthesis, characterization and microbiological studies." Journal of Molecular Structure 1123 (November 2016): 384–93. http://dx.doi.org/10.1016/j.molstruc.2016.07.035.

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22

Augé, Claudine, and Véronique Delest. "Microbiological aldolisations. Synthesis of 2-keto-3-deoxy-D-gluconate." Tetrahedron: Asymmetry 4, no. 6 (June 1993): 1165–68. http://dx.doi.org/10.1016/s0957-4166(00)80224-4.

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23

Vetoshkin, A. G. "Methods and equipment for hydrodynamic foam quenching in microbiological synthesis." Pharmaceutical Chemistry Journal 38, no. 10 (October 2004): 554–57. http://dx.doi.org/10.1007/s11094-005-0009-z.

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24

García-Granados, Andrés, Andrés Parra, Yolanda Simeó, and Antonio L. Extremera. "Chemical, enzymatic and microbiological synthesis of 8,12-eudesmanolides: Synthesis of sivasinolide and yomogin analogues." Tetrahedron 54, no. 47 (November 1998): 14421–36. http://dx.doi.org/10.1016/s0040-4020(98)00893-x.

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25

Parshikov, I. A., L. V. Modyanova, E. V. Dovgilivich, P. B. Terent'ev, L. I. Vorob'eva, and G. V. Grishina. "Microbiological transformation of nitrogen-containing heterocyclic compounds. 3. Microbiological synthesis of hydroxy derivatives of 1-benzoylpiperidine and 1-benzoylpyrrolidine." Chemistry of Heterocyclic Compounds 28, no. 2 (February 1992): 159–62. http://dx.doi.org/10.1007/bf00473936.

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26

Galkina, Irina V., Yuliya V. Bakhtiyarova, Marina P. Shulaeva, Oskar K. Pozdeev, Svetlana N. Egorova, Rafael A. Cherkasov, and Vladimir I. Galkin. "Synthesis and Antimicrobial Activity of Carboxylate Phosphabetaines Derivatives with Alkyl Chains of Various Lengths." Journal of Chemistry 2013 (2013): 1–6. http://dx.doi.org/10.1155/2013/302937.

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The purpose of the present study was to investigate the antibacterial activity of fifteen novel nanosized alkyl esters of carboxylate phosphabetaine:β-(carboxyalkyl)ethyltriphenylphosphonium bromides4–8,β-(carboxyalkyl)-β-methylethyltriphenylphosphonium bromides9–13, andβ-(carboxyalkyl)-α-methylethyltriphenylphosphonium bromides14–18. The in vitro microbiological activity of the synthesized phosphonium bromides against gram-positive and gram-negative bacteria and the yeastCandida albicanswas determined in comparison to standard agents. Microbiological results indicate that the synthesized phosphonium salts4–18possess a broad spectrum of activity against the tested microorganisms. Every newly synthesized compound was characterized by elemental analyses, IR,1H NMR, and31P NMR spectral studies.

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27

TAKAHATA, Yusuke, Ari NISHIZAWA, Ichiro KOJIMA, Mamoru YAMANISHI, and Tetsuo TORAYA. "Synthesis, Properties and Microbiological Activity of Hydrophobic Derivatives of Vitamin B12." Journal of Nutritional Science and Vitaminology 41, no. 5 (1995): 515–26. http://dx.doi.org/10.3177/jnsv.41.515.

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28

Guanti, Giuseppe, Luca Banfi, and Enrica Narisano. "Microbiological synthesis of variously protected L-glyceraldehydes in high optical purity." Tetrahedron Letters 27, no. 30 (January 1986): 3547–50. http://dx.doi.org/10.1016/s0040-4039(00)84846-7.

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29

HUSAIN, ASIF, MOHAMMAD MAAZ, KHURSHEED AHMAD ANSARI, AUSAF AHMAD, and MOHD RASHID. "SYNTHESIS AND MICROBIOLOGICAL EVALUATION OF MANNICH BASES DERIVED FROM 4,6-DIACETYLRESORCINOL." Journal of the Chilean Chemical Society 55, no. 3 (2010): 332–34. http://dx.doi.org/10.4067/s0717-97072010000300012.

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30

Gordeeva, Yu L., and L. S. Gordeev. "Optimization of continuous microbiological synthesis processes with nonlinear microbial growth kinetics." Theoretical Foundations of Chemical Engineering 49, no. 6 (November 2015): 829–35. http://dx.doi.org/10.1134/s0040579515060044.

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31

Cherian, Philip T., Aditi Deshpande, Martin N. Cheramie, David F. Bruhn, Julian G. Hurdle, and Richard E. Lee. "Design, synthesis and microbiological evaluation of ampicillin–tetramic acid hybrid antibiotics." Journal of Antibiotics 70, no. 1 (May 18, 2016): 65–72. http://dx.doi.org/10.1038/ja.2016.52.

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32

FRAGA, B. M., F. GARCIA-TELLADO, P. GONZALEZ, M. G. HERNANDEZ, and J. R. HANSON. "ChemInform Abstract: The Chemical and Microbiological Synthesis of 14-Hydroxy-gibberellins." ChemInform 24, no. 2 (August 21, 2010): no. http://dx.doi.org/10.1002/chin.199302273.

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33

Aridoss, G., S. Balasubramanian, P. Parthiban, and S. Kabilan. "Synthesis and in vitro microbiological evaluation of imidazo(4,5-b)pyridinylethoxypiperidones." European Journal of Medicinal Chemistry 41, no. 2 (February 2006): 268–75. http://dx.doi.org/10.1016/j.ejmech.2005.10.014.

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34

García-Granados, Andrés, María C. Gutiérrez, Andrés Parra, and Francisco Rivas. "Chemical-Microbiological Synthesis of Cryptomeridiol Derivatives byGliocladiumroseum: Semisynthesis of 11-Hydroxyeudesmanolides." Journal of Natural Products 65, no. 7 (July 2002): 1011–15. http://dx.doi.org/10.1021/np010631m.

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35

El-Kady, Abeer M., Ashraf F. Ali, Rizk A. Rizk, and Manar M. Ahmed. "Synthesis, characterization and microbiological response of silver doped bioactive glass nanoparticles." Ceramics International 38, no. 1 (January 2012): 177–88. http://dx.doi.org/10.1016/j.ceramint.2011.05.158.

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36

Kim, Young-Soo, Ji-Young Lee, Junho Park, Wangtaek Hwang, Jongsung Lee, and Deokhoon Park. "Synthesis and microbiological evaluation of honokiol derivatives as new antimicrobial agents." Archives of Pharmacal Research 33, no. 1 (January 2010): 61–65. http://dx.doi.org/10.1007/s12272-010-2225-7.

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37

Parthiban, P., S. Balasubramanian, G. Aridoss, and S. Kabilan. "Synthesis and Microbiological Evaluation of Some N-Methyl Piperidone Oxime Ethers." Medicinal Chemistry Research 14, no. 8-9 (December 2005): 523–38. http://dx.doi.org/10.1007/s00044-006-0153-2.

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38

Vetoshkin, A. G., and B. A. Chagin. "Analysis of the process of dynamic foam extinguishing in microbiological synthesis." Pharmaceutical Chemistry Journal 34, no. 2 (February 2000): 87–90. http://dx.doi.org/10.1007/bf02524367.

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39

Popova, E. V., K. N. Gabinskaya, S. D. Shuvalova, S. A. Dovzhenko, and V. A. Andryushina. "ChemInform Abstract: Microbiological Synthesis of 17β-Hydroxyandrosta-1,4-dien-3-one." ChemInform 32, no. 34 (May 25, 2010): no. http://dx.doi.org/10.1002/chin.200134189.

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40

Buryakov, N., S. Shchukina, and K. Gorst. "Bacillus megaterium: amino acid producer and probiotic for farm animals (review)." Kormlenie sel'skohozjajstvennyh zhivotnyh i kormoproizvodstvo (Feeding of agricultural animals and feed production), no. 1 (January 1, 2020): 67–75. http://dx.doi.org/10.33920/sel-05-2001-07.

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Different directions of microbiological synthesis are actively used in the industry of feed and feed additives for farm animals. More than 50 years of industrial production of amino acids is carried out with the help of biotechnology and the annual growth rate of production is 5–7 %. Amino acids are produced industrially during fermentation using highly effective strains of different types of bacteria. With the progressive development of microbiological technologies and the study of the composition of animal microflora the discovery of new species of microorganisms-producers of useful substances including species Bacillus megaterium, which belong to the bacteria-polyproducts, because their cells are able to develop many substances of different chemical nature: amino acids, proteases, antibiotics, peptides, vitamins, bacteriocins and a number of other compounds. They have a highly efficient system of synthesis and transport of proteins from the cell, grow on a variety of affordable and inexpensive carbon substrates and are non-pathogenic to plants, animals and humans and do not produce alkaline proteases in the environment. Bacillus megaterium is stable in a wide range of pH and at high temperatures, and thus stably retain their properties during production cycles as well as during storage and transportation of the resulting products. The costs of growing Bacillus megaterium are relatively low and with a good yield and relatively low resource intensity of production make it economically viable. Probiotics based on Bacillus megaterium as well as strains of bacteria with increased synthesis of limiting amino acids are promising for the animal feeding industry directions of applied microbiological synthesis.

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41

Alphand, Veronique, Alain Archelas, and Roland Furstoss. "Microbiological transformations. 13. Direct synthesis of both S and R enantiomers of 5-hexadecanolide via an enantioselective microbiological Baeyer-Villiger reaction." Journal of Organic Chemistry 55, no. 1 (January 1990): 347–50. http://dx.doi.org/10.1021/jo00288a061.

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42

Garcia-Granados, Andres, Andres Parra, Yolanda Simeo, and Antonio L. Extremera. "ChemInform Abstract: Chemical, Enzymatic and Microbiological Synthesis of 8,12-Eudesmanolides: Synthesis of Sivasinolide and Yomogin Analogues." ChemInform 30, no. 10 (June 17, 2010): no. http://dx.doi.org/10.1002/chin.199910185.

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43

Bogdanowicz, Agnieszka, Henryk Foks, Anna Kędzia, Ewa Kwapisz, Zofia Zwolska, and Ewa Augustynowicz-Kopeć. "The Synthesis and Microbiological Activity of New 4-Chloropyridin-2-yl Derivatives." HETEROCYCLES 78, no. 9 (2009): 2217. http://dx.doi.org/10.3987/com-09-11696.

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44

García-Granados, Andrés, M. Belinda Jiménez, Antonio Martínez, Andrés Parra, Francisco Rivas, and José María Arias. "Chemical-microbiological synthesis of ent-13-epi-manoyl oxides with biological activities." Phytochemistry 37, no. 3 (November 1994): 741–47. http://dx.doi.org/10.1016/s0031-9422(00)90350-9.

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45

PETZOLDT, K., H. DAHL, W. SKUBALLA, and M. GOTTWALD. "ChemInform Abstract: Microbiological and Enzymatic Transformations in the Synthesis of Prostacyclin Analogues." ChemInform 22, no. 7 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199107259.

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46

AUGE, C., and V. DELEST. "ChemInform Abstract: Microbiological Aldolizations. Synthesis of 2-Keto-3-deoxy-D-gluconate." ChemInform 24, no. 41 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199341255.

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47

Pasutto, Franco M., Nikhilesh N. Singh, Fakhreddin Jamali, Ronald T. Coutts, and Syed Abuzar. "Microbiological Systems in Organic Synthesis: Preparation of Racemic Prenalterol Utilizing Cunninghamella echinulata." Journal of Pharmaceutical Sciences 76, no. 2 (February 1987): 177–79. http://dx.doi.org/10.1002/jps.2600760220.

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48

M.К. Kassymova, M.K. Nauryzbayev, А.К. Mamyrbekova, A.D. Mamitova, А.К. Mamyrbekova, and O.N. Chechina. "SYNTHESIS AND MICROBIOLOGICAL EVALUATION OF ACETYLENIC AMINO ALCOHOLS N-PHENYL CARBAMATE DERIVATIVES." SERIES CHEMISTRY AND TECHNOLOGY 4, no. 436 (August 15, 2019): 43–48. http://dx.doi.org/10.32014/2019.2518-1491.41.

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49

Box, J. A., G. Hall, J. K. Sugden, and M. B. Waghela. "SYNTHESIS AND MICROBIOLOGICAL EVALUATION OF SOME NOVEL 10H-PYRROLIZINO(1,2-b)QUINOLINES." Journal of Pharmacy and Pharmacology 37, S12 (December 1985): 135P. http://dx.doi.org/10.1111/j.2042-7158.1985.tb14206.x.

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50

Kalinichenko, E. N., V. N. Barai, S. B. Bokut, V. V. Romanova, A. I. Zinchenko, G. Herrmann, and I. A. Mikhailopulo. "Microbiological synthesis of 5-ethyl- and (E)-5-(2-bromovinyl)-2?-deoxyuridine." Biotechnology Letters 11, no. 9 (September 1989): 621–26. http://dx.doi.org/10.1007/bf01025269.

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