Parameter Optimization for Production of Ligninolytic Enzymes Using Agro-industrial Wastes by Response Surface Method

被引:39
|
作者
Gassara, Fatma [1 ]
Brar, Satinder Kaur [1 ]
Tyagi, R. D. [1 ]
John, Rojan P. [1 ]
Verma, M. [2 ]
Valero, J. R. [1 ]
机构
[1] Univ Quebec, INRS ETE, Quebec City, PQ G1K 9A9, Canada
[2] Inst Rech & Dev Agroenvironnem Inc IRDA, Quebec City, PQ G1P 3W8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
ligninolytic enzyme; Phanerocheate chrysosporium; response surface; moisture; inducers; WHITE-ROT FUNGI; SOLID-STATE FERMENTATION; PHANEROCHAETE-CHRYSOSPORIUM; BIOTECHNOLOGICAL APPLICATIONS; DEGRADING BASIDIOMYCETE; TRAMETES-VERSICOLOR; VERATRYL ALCOHOL; LACCASE; PEROXIDASE; CULTURE;
D O I
10.1007/s12257-010-0264-z
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 and manganese peroxidase (LiP, MnP) and laccase production by Phanerocheate chrysosporium was optimized by response surface methodology for brewery waste and apple pomace. The effect of moisture, copper sulphate, and veratryl alcohol (VA) concentrations on enzyme production was studied. Moisture and VA had significant positive effect on MnP and LiP production and the viability of P chrysosporium (p < 0.05) and copper sulphate produced a negative effect. However, moisture and copper sulphate had a significant positive (p < 0.05) effect on laccase production, but VA had an insignificant positive effect (p < 0.05). Higher values of MnP, LiP and viability of P chrysosporium on apple pomace (1287.5 U MnP/gds (units/gram dry substrate), 305 U LiP/gds, and 10.38 Log 10 viability) and brewery waste (792 U MnP/gds and 9.83 Log 10 viability) were obtained with 80% moisture, 3 mmol/kg VA, and 0.5 mmol/kg copper. LiP production in brewery waste (7.87 U/gds) was maximal at 70% moisture, 2 mmol/kg VA, and 1 mmol/kg copper. Higher production of laccase in apple pomace (789 U/gds) and brewery waste (841 U/gds) were obtained with 80% moisture, 3 mmol/kg VA, and 1.5 mmol/kg copper. Thus, moisture along with VA and copper sulphate was pertinent for the production of ligninolytic enzymes and increased cell viability.
引用
收藏
页码:343 / 351
页数:9
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