DEVELOPMENT OF A STIRRED TANK REACTOR SYSTEM FOR THE PRODUCTION OF LIGNIN PEROXIDASES (LIGNINASES) BY PHANEROCHAETE-CHRYSOSPORIUM BKM-F-1767

被引:35
作者
MICHEL, FC [1 ]
GRULKE, EA [1 ]
REDDY, CA [1 ]
机构
[1] MICHIGAN STATE UNIV,DEPT CHEM ENGN,E LANSING,MI 48824
来源
JOURNAL OF INDUSTRIAL MICROBIOLOGY | 1990年 / 5卷 / 2-3期
关键词
Filamentous fungi; Fungal pellets; Ligninase production; Submerged culture; White-rot fungus;
D O I
10.1007/BF01573859
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Lignin peroxidases produced by Phanerochaete chrysosporium have several important potential industrial applications based on their ability to degrade lignin and lignin-like compounds. A stirred tank reactor system for the production of lignin peroxidases is described here. Included in this study is an examination of the mechanics of pellet biocatalyst formation and the optimization of an acetate buffered medium. Higher levels of lignin peroxidase were obtained with acetate buffer compared to the other buffer systems tested. Concentrations of 0.05% (w/v) Tween 80 and 0.4 mM veratryl alcohol gave optimal lignin peroxidase activity in acetate buffered medium. In shake flask cultures, mycelial fragments in the inoculum aggregated into pellets during the first eight hours of incubation and thereafter increased in size through the eighth day. The agitation rate in shake flask cultures affected pellet size, the number of pellets formed, and lignin peroxidase activity. Transfer of fungal pellets from shake flask culture to a continuously oxygenated baffled stirred tank reactor (STR) resulted in production of high lignin peroxidase titres comparable to those of shake flask cultures when the agitation rate, oxygen dispersion and foaming were closely controlled. © 1990 Society for Industrial Microbiology.
引用
收藏
页码:103 / 112
页数:10
相关论文
共 19 条
[1]  
Asther M., Corrieu G., Drapon R., Odier E., Effect of Tween 80 and oleic acid on ligninase production by Phanerochaete chrysosporium INA-12, Enzyme Microb. Technol., 9, pp. 245-249, (1987)
[2]  
Bradford M.M., A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding, Anal. Biochem., 72, pp. 248-254, (1976)
[3]  
Bumpus J.A., Tien M., Wright D., Aust S.D., Oxidation of persistent environment pollutants by a white rot fungus, Science, 228, pp. 1434-1436, (1985)
[4]  
Bumpus J.A., Aust S.D., Biodegradation of DDT pol,1,1-trichloro-2,2-bis(4-chlorophenyl)ethanel] by the white rot fungus Phanerochaete chrysosporium, Appl. Environ. Microbiol., 53, pp. 2001-2008, (1987)
[5]  
Faison B.D., Kirk T.K., Farrel R.L., Role of veratryl alcohol in regulating ligninase activity in Phanerochaete chrysosporium, Appl. Environ. Microbiol., 52, pp. 251-254, (1986)
[6]  
Fan L.T., Lee Y.H., Gharpuray M.M., The nature of lignocellulosics and their pretreatment of enzymatic hydrolysis, Adv. Biochem. Eng., 23, pp. 157-187, (1982)
[7]  
Hammerli S.D., Leisola M.S.A., Sanglard D., Fiechter A., Oxidation of benzo(a)pyrene by extracellular ligninases of Phanerochaete chrysosporium, J. Biol. Chem., 216, pp. 16900-16903, (1986)
[8]  
Irani R.R., Cullis C.F., Particle size: Measurement Interpretation and Application, (1963)
[9]  
Jager A., Croan S., Kirk T.K., Production of ligninases and degradation of lignin in agitated submerged cultures of Phanerochaete chrysosporium, Appl. Environ. Microbiol., 50, pp. 1274-1278, (1985)
[10]  
Kirk T.K., Chang H.M., Potential applications of bioligninolytic systems, Enzyme Microb. Technol., 3, pp. 189-196, (1981)