Decolorization of methylene blue by new fungus: Trichaptum biforme and decolorization of three synthetic dyes by Trametes hirsuta and Trametes gibbosa
作者： Hossein Eshghi , Zahra Alishahi , Mahmood Zokaei , Aboulfazl Daroodi , Elahe Tabasi
DOI: 10.5155/EURJCHEM.2.4.463-468.425
关键词:
摘要: In order to screen dye decolorization by Trametes hirsuta , gibbosa and new fungus Trichaptum biforme Methylene Blue (MB), Methyl Green (MG) Reactive Black 5 (RB5) were studied in Broth culture at concentrations of 25, 50 70 ppm. Decolorization these three kind dyes T. decreased increasing concentration. RB5 was examined two different medium contains Mn 2+ or veratryl alcohol (VA), as activators. At the presence laccase activator decolorized 91% concentration ppm, MnP (Mn ), less than 50% same more ). MB, MG 80% activator. independent during 20 days did it 32 days, this is due higher potential synthetic for . MB Rate other fungi.
eurjchem.com
um.ac.ir
sci-hub.se 参考文章(24)
Geoffrey M Gadd, None, Fungi in Bioremediation ,(2001)
James Benjamin Pierce, Zaven S. Ariyan, Gaye Stuart Ovenden, Preparation and antiinflammatory activity of 2- and 4-pyridones Journal of Medicinal Chemistry. ,vol. 25, pp. 131- 136 ,(1982) , 10.1021/JM00344A008
Clive L Yeates, John F Batchelor, Edward C Capon, Neil J Cheesman, Mitch Fry, Alan T Hudson, Mary Pudney, Helen Trimming, James Woolven, José M Bueno, Jesús Chicharro, Esther Fernández, José M Fiandor, Domingo Gargallo-Viola, Federico Gomez de las Heras, Esperanza Herreros, María L León, None, Synthesis and Structure–Activity Relationships of 4-Pyridones as Potential Antimalarials Journal of Medicinal Chemistry. ,vol. 51, pp. 2845- 2852 ,(2008) , 10.1021/JM0705760
Igor V. Magedov, Madhuri Manpadi, Marcia A. Ogasawara, Adriana S. Dhawan, Snezna Rogelj, Severine Van slambrouck, Wim F. A. Steelant, Nikolai M. Evdokimov, Pavel Y. Uglinskii, Eerik M. Elias, Erica J. Knee, Paul Tongwa, Mikhail Yu. Antipin, Alexander Kornienko, Structural simplification of bioactive natural products with multicomponent synthesis. 2. Antiproliferative and antitubulin activities of pyrano[3,2-c]pyridones and pyrano[3,2-c]quinolones Journal of Medicinal Chemistry. ,vol. 51, pp. 2561- 2570 ,(2008) , 10.1021/JM701499N
J.E. Carpenter, F. Weinhold, Analysis of the geometry of the hydroxymethyl radical by the “different hybrids for different spins” natural bond orbital procedure Journal of Molecular Structure-theochem. ,vol. 169, pp. 41- 62 ,(1988) , 10.1016/0166-1280(88)80248-3
Michael W. Schmidt, Kim K. Baldridge, Jerry A. Boatz, Steven T. Elbert, Mark S. Gordon, Jan H. Jensen, Shiro Koseki, Nikita Matsunaga, Kiet A. Nguyen, Shujun Su, Theresa L. Windus, Michel Dupuis, John A. Montgomery, General atomic and molecular electronic structure system Journal of Computational Chemistry. ,vol. 14, pp. 1347- 1363 ,(1993) , 10.1002/JCC.540141112
Chengteh Lee, Weitao Yang, Robert G. Parr, Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density Physical Review B. ,vol. 37, pp. 785- 789 ,(1988) , 10.1103/PHYSREVB.37.785
Dewen Dong, Xihe Bi, Qun Liu, Fangdi Cong, [5C + 1N] annulation: a novel synthetic strategy for functionalized 2,3-dihydro-4-pyridones. Chemical Communications. pp. 3580- 3582 ,(2005) , 10.1039/B505569E
Yan-Hua Wang, Jian-Wei Zou, Bing Zhang, Yun-Xiang Lu, Hai-Xiao Jin, Qing-Sen Yu, Enone–dienol tautomerism of but-2-enal and substituent effect: A theoretical study Journal of Molecular Structure-theochem. ,vol. 755, pp. 31- 37 ,(2005) , 10.1016/J.THEOCHEM.2005.06.029
Rita S. Elias, Bahjat A. Saeed, Kawkab Y. Saour, Najim A. Al-Masoudi, Microwave-assisted synthesis of dihydropyridones from curcumin Tetrahedron Letters. ,vol. 49, pp. 3049- 3051 ,(2008) , 10.1016/J.TETLET.2008.03.064