Cargando…
Differential Expression of Laccase Genes in Pleurotus ostreatus and Biochemical Characterization of Laccase Isozymes Produced in Pichia pastoris
In this study, transcriptome analysis of twelve laccase genes in Pleurotus ostreatus revealed that their expression was differentially regulated at different developmental stages. Lacc5 and Lacc12 were specifically expressed in fruiting bodies and primordia, respectively, whereas Lacc6 was expressed...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Mycology
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630434/ https://www.ncbi.nlm.nih.gov/pubmed/26539044 http://dx.doi.org/10.5941/MYCO.2015.43.3.280 |
_version_ | 1782398703664889856 |
---|---|
author | Park, Minsa Kim, Minseek Kim, Sinil Ha, Byeongsuk Ro, Hyeon-Su |
author_facet | Park, Minsa Kim, Minseek Kim, Sinil Ha, Byeongsuk Ro, Hyeon-Su |
author_sort | Park, Minsa |
collection | PubMed |
description | In this study, transcriptome analysis of twelve laccase genes in Pleurotus ostreatus revealed that their expression was differentially regulated at different developmental stages. Lacc5 and Lacc12 were specifically expressed in fruiting bodies and primordia, respectively, whereas Lacc6 was expressed at all developmental stages. Lacc1 and Lacc3 were specific to the mycelial stage in solid medium. In order to investigate their biochemical characteristics, these laccases were heterologously expressed in Pichia pastoris using the pPICHOLI-2 expression vector. Expression of the laccases was facilitated by intermittent addition of methanol as an inducer and sole carbon source, in order to reduce the toxic effects associated with high methanol concentration. The highest expression was observed when the recombinant yeast cells were grown for 5 days at 15℃ with intermittent addition of 1% methanol at a 12-hr interval. Investigation of enzyme kinetics using 2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid (ABTS) as a substrate revealed that the primordium-specific laccase Lacc12 was 5.4-fold less active than Lacc6 at low substrate concentration with respect to ABTS oxidation activity. The optimal pH and temperature of Lacc12 were 0.5 pH units and 5℃ higher than those of Lacc6. Lacc12 showed maximal activity at pH 3.5 and 50℃, which may reflect the physiological conditions at the primordiation stage. |
format | Online Article Text |
id | pubmed-4630434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Korean Society of Mycology |
record_format | MEDLINE/PubMed |
spelling | pubmed-46304342015-11-04 Differential Expression of Laccase Genes in Pleurotus ostreatus and Biochemical Characterization of Laccase Isozymes Produced in Pichia pastoris Park, Minsa Kim, Minseek Kim, Sinil Ha, Byeongsuk Ro, Hyeon-Su Mycobiology Research Article In this study, transcriptome analysis of twelve laccase genes in Pleurotus ostreatus revealed that their expression was differentially regulated at different developmental stages. Lacc5 and Lacc12 were specifically expressed in fruiting bodies and primordia, respectively, whereas Lacc6 was expressed at all developmental stages. Lacc1 and Lacc3 were specific to the mycelial stage in solid medium. In order to investigate their biochemical characteristics, these laccases were heterologously expressed in Pichia pastoris using the pPICHOLI-2 expression vector. Expression of the laccases was facilitated by intermittent addition of methanol as an inducer and sole carbon source, in order to reduce the toxic effects associated with high methanol concentration. The highest expression was observed when the recombinant yeast cells were grown for 5 days at 15℃ with intermittent addition of 1% methanol at a 12-hr interval. Investigation of enzyme kinetics using 2,2-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid (ABTS) as a substrate revealed that the primordium-specific laccase Lacc12 was 5.4-fold less active than Lacc6 at low substrate concentration with respect to ABTS oxidation activity. The optimal pH and temperature of Lacc12 were 0.5 pH units and 5℃ higher than those of Lacc6. Lacc12 showed maximal activity at pH 3.5 and 50℃, which may reflect the physiological conditions at the primordiation stage. The Korean Society of Mycology 2015-09 2015-09-30 /pmc/articles/PMC4630434/ /pubmed/26539044 http://dx.doi.org/10.5941/MYCO.2015.43.3.280 Text en © The Korean Society of Mycology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Park, Minsa Kim, Minseek Kim, Sinil Ha, Byeongsuk Ro, Hyeon-Su Differential Expression of Laccase Genes in Pleurotus ostreatus and Biochemical Characterization of Laccase Isozymes Produced in Pichia pastoris |
title | Differential Expression of Laccase Genes in Pleurotus ostreatus and Biochemical Characterization of Laccase Isozymes Produced in Pichia pastoris |
title_full | Differential Expression of Laccase Genes in Pleurotus ostreatus and Biochemical Characterization of Laccase Isozymes Produced in Pichia pastoris |
title_fullStr | Differential Expression of Laccase Genes in Pleurotus ostreatus and Biochemical Characterization of Laccase Isozymes Produced in Pichia pastoris |
title_full_unstemmed | Differential Expression of Laccase Genes in Pleurotus ostreatus and Biochemical Characterization of Laccase Isozymes Produced in Pichia pastoris |
title_short | Differential Expression of Laccase Genes in Pleurotus ostreatus and Biochemical Characterization of Laccase Isozymes Produced in Pichia pastoris |
title_sort | differential expression of laccase genes in pleurotus ostreatus and biochemical characterization of laccase isozymes produced in pichia pastoris |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630434/ https://www.ncbi.nlm.nih.gov/pubmed/26539044 http://dx.doi.org/10.5941/MYCO.2015.43.3.280 |
work_keys_str_mv | AT parkminsa differentialexpressionoflaccasegenesinpleurotusostreatusandbiochemicalcharacterizationoflaccaseisozymesproducedinpichiapastoris AT kimminseek differentialexpressionoflaccasegenesinpleurotusostreatusandbiochemicalcharacterizationoflaccaseisozymesproducedinpichiapastoris AT kimsinil differentialexpressionoflaccasegenesinpleurotusostreatusandbiochemicalcharacterizationoflaccaseisozymesproducedinpichiapastoris AT habyeongsuk differentialexpressionoflaccasegenesinpleurotusostreatusandbiochemicalcharacterizationoflaccaseisozymesproducedinpichiapastoris AT rohyeonsu differentialexpressionoflaccasegenesinpleurotusostreatusandbiochemicalcharacterizationoflaccaseisozymesproducedinpichiapastoris |