The dynamics of leaf litter decomposition of Quercus ilex (L.) were investigated over a 2 year period by determining the activities and isoenzyme distribution of laccases and peroxidases. The analysis of isoenzymes was performed by isoelectric focusing on high stability pH gradients with high resolving power. The preparation of zymograms was carried out using the leaf litter extract without previous concentration. During litter decomposition, laccase and peroxidase activities changed as well as the type and number of enzyme isoforms. The activities of both enzymes were low (less than or equal to0.017 and less than or equal to0.031 mmol o-tolidine oxidized h(-1) g(-1)d.w. for laccase and peroxidase, respectively) in first year and increased in October-January of the second year of litter decay. The highest activities measured after 15-18 months of litter exposure (0.37 +/- 0.03 and 0.19 +/- 0.02 mmol o-tolidine oxidized h(-1) g(-1) d.w. for laccase and peroxidase, respectively), showed that litter chemical composition affected the growth of ligninolytic microbial community. The activation energy for laccase and peroxidase reactions also changed during decomposition: the highest values (55 +/- 6 kJ mol(-1) for laccase and 60 +/- 6 kJ mol(-1) for peroxidase) occurred in autumn-winter, even if spatial changes were evidenced. Some enzyme isoforms (pI = 5.3 and 5.5 for laccase and pI=5.0 and 5.1 for peroxidase, respectively), contributed more than others to the overall laccase and peroxidase activity, suggesting that some ligninolytic species bloomed in particular seasons of the year, even if other species with similar functional activities colonized the litter.

The dynamics of leaf litter decomposition of Quercus ilex (L.) were investigated over a 2 year period by determining the activities and isoenzyme distribution of laccases and peroxidases. The analysis of isoenzymes was performed by isoelectric focusing on high stability pH gradients with high resolving power. The preparation of zymograms was carried out using the leaf litter extract without previous concentration. During litter decomposition, laccase and peroxidase activities changed as well as the type and number of enzyme isoforms. The activities of both enzymes were low (less than or equal to0.017 and less than or equal to0.031 mmol o-tolidine oxidized h(-1) g(-1)d.w. for laccase and peroxidase, respectively) in first year and increased in October-January of the second year of litter decay. The highest activities measured after 15-18 months of litter exposure (0.37 +/- 0.03 and 0.19 +/- 0.02 mmol o-tolidine oxidized h(-1) g(-1) d.w. for laccase and peroxidase, respectively), showed that litter chemical composition affected the growth of ligninolytic microbial community. The activation energy for laccase and peroxidase reactions also changed during decomposition: the highest values (55 +/- 6 kJ mol(-1) for laccase and 60 +/- 6 kJ mol(-1) for peroxidase) occurred in autumn-winter, even if spatial changes were evidenced. Some enzyme isoforms (pI = 5.3 and 5.5 for laccase and pI=5.0 and 5.1 for peroxidase, respectively), contributed more than others to the overall laccase and peroxidase activity, suggesting that some ligninolytic species bloomed in particular seasons of the year, even if other species with similar functional activities colonized the litter. (C) 2004 Elsevier Ltd. All rights reserved.

Laccase and peroxidase isoenzymes during leaf litter decomposition of Quercus ilex in a Mediterranean ecosystem

PAPA, Stefania;FUGGI, Amodio;FIORETTO, Antonietta
2004

Abstract

The dynamics of leaf litter decomposition of Quercus ilex (L.) were investigated over a 2 year period by determining the activities and isoenzyme distribution of laccases and peroxidases. The analysis of isoenzymes was performed by isoelectric focusing on high stability pH gradients with high resolving power. The preparation of zymograms was carried out using the leaf litter extract without previous concentration. During litter decomposition, laccase and peroxidase activities changed as well as the type and number of enzyme isoforms. The activities of both enzymes were low (less than or equal to0.017 and less than or equal to0.031 mmol o-tolidine oxidized h(-1) g(-1)d.w. for laccase and peroxidase, respectively) in first year and increased in October-January of the second year of litter decay. The highest activities measured after 15-18 months of litter exposure (0.37 +/- 0.03 and 0.19 +/- 0.02 mmol o-tolidine oxidized h(-1) g(-1) d.w. for laccase and peroxidase, respectively), showed that litter chemical composition affected the growth of ligninolytic microbial community. The activation energy for laccase and peroxidase reactions also changed during decomposition: the highest values (55 +/- 6 kJ mol(-1) for laccase and 60 +/- 6 kJ mol(-1) for peroxidase) occurred in autumn-winter, even if spatial changes were evidenced. Some enzyme isoforms (pI = 5.3 and 5.5 for laccase and pI=5.0 and 5.1 for peroxidase, respectively), contributed more than others to the overall laccase and peroxidase activity, suggesting that some ligninolytic species bloomed in particular seasons of the year, even if other species with similar functional activities colonized the litter. (C) 2004 Elsevier Ltd. All rights reserved.
2004
The dynamics of leaf litter decomposition of Quercus ilex (L.) were investigated over a 2 year period by determining the activities and isoenzyme distribution of laccases and peroxidases. The analysis of isoenzymes was performed by isoelectric focusing on high stability pH gradients with high resolving power. The preparation of zymograms was carried out using the leaf litter extract without previous concentration. During litter decomposition, laccase and peroxidase activities changed as well as the type and number of enzyme isoforms. The activities of both enzymes were low (less than or equal to0.017 and less than or equal to0.031 mmol o-tolidine oxidized h(-1) g(-1)d.w. for laccase and peroxidase, respectively) in first year and increased in October-January of the second year of litter decay. The highest activities measured after 15-18 months of litter exposure (0.37 +/- 0.03 and 0.19 +/- 0.02 mmol o-tolidine oxidized h(-1) g(-1) d.w. for laccase and peroxidase, respectively), showed that litter chemical composition affected the growth of ligninolytic microbial community. The activation energy for laccase and peroxidase reactions also changed during decomposition: the highest values (55 +/- 6 kJ mol(-1) for laccase and 60 +/- 6 kJ mol(-1) for peroxidase) occurred in autumn-winter, even if spatial changes were evidenced. Some enzyme isoforms (pI = 5.3 and 5.5 for laccase and pI=5.0 and 5.1 for peroxidase, respectively), contributed more than others to the overall laccase and peroxidase activity, suggesting that some ligninolytic species bloomed in particular seasons of the year, even if other species with similar functional activities colonized the litter.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11591/184890
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