2004
DOI: 10.1023/b:bile.0000015452.40213.bf
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Different proportions of laccase isoenzymes produced by submerged cultures of Trametes versicolor grown on lignocellulosic wastes

Abstract: The white-rot fungus Trametes versicolor grown in submerged culture produced two laccase isoenzymes, LacI and LacII. Addition of insoluble lignocellulosic materials into the culture medium increased the total laccase activity. The proportion of laccase isoenzymes also changed depending on the lignocellulosic material employed, with ratios of activity LacII/LacI from 0.9 (barley straw) to 4.4 (grape stalks). Besides, this proportion played an important role in the dye decolourisation.

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Cited by 81 publications
(65 citation statements)
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“…Then, it peaked on the day 8 (2247 U l −1 ) and hereafter it decreased. According to reports of Moldes et al (2004) barley bran cultures gave the highest lacasse activities, showing values of 2500-3200 U l −1 from the day 20 to the day 35, that of barley straw cultures exhibited values of about 300-500 U l −1 at the same days. Schlosser et al (1997) proposed the mechanism for these materials to induce the lacasse production is the presence of little quantities of phenolic soluble compounds.…”
Section: In This Study 20 Basidiomycetes Isolates Such As P Arcularmentioning
confidence: 83%
“…Then, it peaked on the day 8 (2247 U l −1 ) and hereafter it decreased. According to reports of Moldes et al (2004) barley bran cultures gave the highest lacasse activities, showing values of 2500-3200 U l −1 from the day 20 to the day 35, that of barley straw cultures exhibited values of about 300-500 U l −1 at the same days. Schlosser et al (1997) proposed the mechanism for these materials to induce the lacasse production is the presence of little quantities of phenolic soluble compounds.…”
Section: In This Study 20 Basidiomycetes Isolates Such As P Arcularmentioning
confidence: 83%
“…Additionally, it has been proposed that laccase induction stops when the glucose has been consumed and when compounds have been solvated or liberated during lignin degradation (Ha et al, 2001;Moldes et al, 2004). The results presented in Fig.…”
Section: Enzymatic Activitymentioning
confidence: 94%
“…One of the most appropriate approaches to produce low cost and efficient enzymes for biotechnological application purposes is to utilize the potential of lignocellulosic waste materials. Some such mixtures may contain significant concentrations of soluble carbohydrates and inducers of enzyme synthesis so as to allow efficient production of ligninolytic enzymes (Reddy et al 2003, Moldes et al 2004Elisashvili et al 2006;Iqbal et al 2011a,b;Asgher et al 2012c). To date, the production of various ligninolytic enzymes including lignin peroxidase (LiP), manganese peroxidase (MnP), versatile peroxidase (VP), laccases, and other lignocellulytic enzymes, mainly cellulases, have been widely studied in submerged and solid culture processes in the laboratory, ranging from shake flask to a large scale (Xia and Len 1999;Moldes et al 2004;Elisashvili et al 2006).…”
Section: Production Of Enzymesmentioning
confidence: 99%
“…Some such mixtures may contain significant concentrations of soluble carbohydrates and inducers of enzyme synthesis so as to allow efficient production of ligninolytic enzymes (Reddy et al 2003, Moldes et al 2004Elisashvili et al 2006;Iqbal et al 2011a,b;Asgher et al 2012c). To date, the production of various ligninolytic enzymes including lignin peroxidase (LiP), manganese peroxidase (MnP), versatile peroxidase (VP), laccases, and other lignocellulytic enzymes, mainly cellulases, have been widely studied in submerged and solid culture processes in the laboratory, ranging from shake flask to a large scale (Xia and Len 1999;Moldes et al 2004;Elisashvili et al 2006). Due to the lower capital investment and operating costs of solid state fermentation (SSF), that approach has been reported as an attractive alternative process to produce fungal microbial enzymes using different agro-industrial based lignocellulosic materials (Jecu 2000;Couto and Sanromán 2005;Couto and Sanromán 2006;Levin et al 2008;Oberoi et al 2010;Iqbal et al 2011a,b).…”
Section: Production Of Enzymesmentioning
confidence: 99%