Research on Conditions of Solid-State Fermentation and Characters of Tannase by Aspergillus Niger B0201 with Gallnut

Article Preview

Abstract:

Study is on the solid-state fermentation of tannase with the Gallnut by Aspergillus niger B-0201.The experiments involved in the process and conditions of solid-state fermentation and factors influencing characters of tannase. The results indicated that the unpasteurized method before fermentation was in favor of the higher enzymic activity than the sterilized method. With the unpasteurized method, the tannase activity got the best level(51.2U/gds) ,when 5.0g of culture medium containing the 1g of Gallnut powder, 4g of the bran powder, 1% (w/w) of (NH4)2SO4, 0.1%(w/w) of NaCl, 0.1%(w/w) of MgSO4·7H2O, 8ml of water, 1.6:1 of the solid-to-liquid ratio and 1ml(1×108spores per milliliter)of inoculum size to a 250 ml conical flask was incubated at 30°C, initial pH6.0 for 96 hours. At the same time, the conditions of fermentation were further optimized using the Response Surface Design(RSM). The tannase activity got at 56.2U/gds with the .Gallnut(17%,w/w) and the solid-to-liquid ratio(1.5:1) in the medium under 32°C. The optimum temperature and pH of tannase was respectively 40°C and 5.0. Fe3+,Cu2+,Fe2+, Ba2+,Mn2+,Ca2+,Al3+were the inhibitor of tannase at 2.0mM concentration. The optimum concentration of propylgallate as the substrate catalyzed by Tannase was 1mM. The value of Kmwas 0.514mM and Vmax was 71.8μmol·(L·min)-1.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 236-238)

Pages:

1029-1038

Citation:

Online since:

May 2011

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2011 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] Kenji Aoki, Ryu Shlnke, Hiroshi Nishira: Agri. Biol. Chem. Vol. 40 (1976),pp.79-85

Google Scholar

[2] Makkar HPS: J. Agric. Food. Chem.Vol. 37 (1989),pp.1197-1202

Google Scholar

[3] Adachi O, Watanabe M.:Agric. Biol. Chem. Vol. 32 (1968),pp.1079-1085

Google Scholar

[4] Barthomeuf C, Regerat F, Pourrat H. Production: J. Ferment. Bioeng.Vol. 77 (1994),pp.320-323

Google Scholar

[5] Yamada H, Adachi O, Watanabe M, Sato N.: Agric. Biol. Chem. Vol. 32 (1968),pp.1070-1078.

Google Scholar

[6] Ganga PS, Nandy SC, Santappa M.: Leather. Sci. Vol. 24 (1977),P 8-16.

Google Scholar

[7] Rajakumar GS, Nandy SC.: Appl. Environ. Microbiol. Vol. 46 (1983),pp.525-537.

Google Scholar

[8] Lekha PK, Lonsane BK: Adv. Appl. Microbiol.Vol. 44 (1997),pp.215-259.

Google Scholar

[9] Bratail Kar, Rintu Banerjee and B.C. Bhattacharyya: Process Biochemistry Vol. 38 (2003),pp.1285-1293

Google Scholar

[10] Koichi Y, Tokuji T., Japanese Patent 2224100. (1972)

Google Scholar

[11] Suzuki S., Japanese Patent 73,48,668. (1973)

Google Scholar

[12] Massechelin CA, Batum MS: Proc. Cong. Eur. Brew. Conv. Vol. 18 (1981),pp.359-370

Google Scholar

[13] Canteralli C, Brenna O, Giovanelli G, Rossi M: Food Biotechnol. Vol. 3 (1989),pp.203-213

Google Scholar

[13] Giovanelli G. Enzymic: Ind Bevande Vol. 18 (1989),pp.497-502

Google Scholar

[14] Haslam E, Tanner: Phytochemistry Vol. 90 (1970),pp.05-9.

Google Scholar

[15] Sharma S, Bhat TK, Gupta MN.: Biotechnol. Appl. Biochem. Vol. 35 (2002),pp.165-179

Google Scholar

[16] Aguilar CN, Augur C, Favela-Torres E.: Microbiol. Biotechnol. Vol.26 (2001),p.296/302..

Google Scholar

[17] Aguilar, C.N., Augur, C., Favela-Torres, E., Viniegra-González, G.: Proc. Biochem. Vol. 36, (2001),pp.571-578

Google Scholar

[18] Kar B, Banerjee R, Bhattacharyya BC.: J. Ind. Microbiol. Biotechnol. Vol. 25 (2000),pp.29-38

Google Scholar

[19] Kar B, Banerjee R, Bhattacharyya BC.: J. Ind. Microbiol. Biotechnol. Vol. 23 (1999),pp.173-177

Google Scholar

[20] Lekha P K,Lonsane B K.: Process Biochemistry Vol. 29 (1994),pp.497-503

Google Scholar

[21] Shweta Sharma,Bhat T K,Dawra R K.:Analytical Biochemistry Vol. 279 (2000),pp.85-89

Google Scholar