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Selective Isolation and Screening of Actinobacteria Strains Producing Lignocellulolytic Enzymes Using Olive Pomace as Substrate
BACKGROUND: Olive pomace, as the main by-product of the olive oil industry, is recently recycled as fermentation substrate for enzyme production. OBJECTIVES: Actinobacteria isolates were separated from an Algerian soil under olive pomace cultivation and were evaluated for their lignocellulolytic enz...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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National Institute of Genetic Engineering and Biotechnology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5582256/ https://www.ncbi.nlm.nih.gov/pubmed/28959355 http://dx.doi.org/10.15171/ijb.1278 |
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author | Medouni-Haroune, Lamia Zaidi, Farid Medouni-Adrar, Sonia Roussos, Sevastianos Azzouz, Samia Desseaux, Véronique Kecha, Mouloud |
author_facet | Medouni-Haroune, Lamia Zaidi, Farid Medouni-Adrar, Sonia Roussos, Sevastianos Azzouz, Samia Desseaux, Véronique Kecha, Mouloud |
author_sort | Medouni-Haroune, Lamia |
collection | PubMed |
description | BACKGROUND: Olive pomace, as the main by-product of the olive oil industry, is recently recycled as fermentation substrate for enzyme production. OBJECTIVES: Actinobacteria isolates were separated from an Algerian soil under olive pomace cultivation and were evaluated for their lignocellulolytic enzymes production. MATERIALS AND METHODS: Isolates of Actinobacteria were separated from soils around oil mills using four isolation media, among them three were enriched by olive pomace. The isolates were screened for their cellulolytic, xylanolytic and ligninolytic activities. Isolates with potential of producing lignocellulose-degrading enzymes were selected under submerged fermentation based olive pomace. RESULTS: Ninety isolates of Actinobacteria were separated from soil samples. M3 medium (raw pomace autoclaved alone) was the best isolation medium (68 strains), whereas, the soil from oil mill with continuous system (S1) led to separation of 52 strains. Among the 90 isolates, 82 were shown promising enzyme activity, 19 isolates were presented the largest zone diameter (<30 mm). S1M3I and S1M3II isolates were exhibited the highest values. CONCLUSIONS: Olive pomace with medium low cost and high titers of enzymes can be valorized by culture of Actinobacteria to produce lignocellulolytic enzymes for industrial applications. |
format | Online Article Text |
id | pubmed-5582256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | National Institute of Genetic Engineering and Biotechnology |
record_format | MEDLINE/PubMed |
spelling | pubmed-55822562017-09-28 Selective Isolation and Screening of Actinobacteria Strains Producing Lignocellulolytic Enzymes Using Olive Pomace as Substrate Medouni-Haroune, Lamia Zaidi, Farid Medouni-Adrar, Sonia Roussos, Sevastianos Azzouz, Samia Desseaux, Véronique Kecha, Mouloud Iran J Biotechnol Brief Report BACKGROUND: Olive pomace, as the main by-product of the olive oil industry, is recently recycled as fermentation substrate for enzyme production. OBJECTIVES: Actinobacteria isolates were separated from an Algerian soil under olive pomace cultivation and were evaluated for their lignocellulolytic enzymes production. MATERIALS AND METHODS: Isolates of Actinobacteria were separated from soils around oil mills using four isolation media, among them three were enriched by olive pomace. The isolates were screened for their cellulolytic, xylanolytic and ligninolytic activities. Isolates with potential of producing lignocellulose-degrading enzymes were selected under submerged fermentation based olive pomace. RESULTS: Ninety isolates of Actinobacteria were separated from soil samples. M3 medium (raw pomace autoclaved alone) was the best isolation medium (68 strains), whereas, the soil from oil mill with continuous system (S1) led to separation of 52 strains. Among the 90 isolates, 82 were shown promising enzyme activity, 19 isolates were presented the largest zone diameter (<30 mm). S1M3I and S1M3II isolates were exhibited the highest values. CONCLUSIONS: Olive pomace with medium low cost and high titers of enzymes can be valorized by culture of Actinobacteria to produce lignocellulolytic enzymes for industrial applications. National Institute of Genetic Engineering and Biotechnology 2017-03 /pmc/articles/PMC5582256/ /pubmed/28959355 http://dx.doi.org/10.15171/ijb.1278 Text en © 2017 by National Institute of Genetic Engineering and Biotechnology https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Brief Report Medouni-Haroune, Lamia Zaidi, Farid Medouni-Adrar, Sonia Roussos, Sevastianos Azzouz, Samia Desseaux, Véronique Kecha, Mouloud Selective Isolation and Screening of Actinobacteria Strains Producing Lignocellulolytic Enzymes Using Olive Pomace as Substrate |
title | Selective Isolation and Screening of Actinobacteria Strains Producing Lignocellulolytic Enzymes Using Olive Pomace as Substrate |
title_full | Selective Isolation and Screening of Actinobacteria Strains Producing Lignocellulolytic Enzymes Using Olive Pomace as Substrate |
title_fullStr | Selective Isolation and Screening of Actinobacteria Strains Producing Lignocellulolytic Enzymes Using Olive Pomace as Substrate |
title_full_unstemmed | Selective Isolation and Screening of Actinobacteria Strains Producing Lignocellulolytic Enzymes Using Olive Pomace as Substrate |
title_short | Selective Isolation and Screening of Actinobacteria Strains Producing Lignocellulolytic Enzymes Using Olive Pomace as Substrate |
title_sort | selective isolation and screening of actinobacteria strains producing lignocellulolytic enzymes using olive pomace as substrate |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5582256/ https://www.ncbi.nlm.nih.gov/pubmed/28959355 http://dx.doi.org/10.15171/ijb.1278 |
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