Cargando…

Isolation, characterization and heterologous expression of a novel chitosanase from Janthinobacterium sp. strain 4239

BACKGROUND: Chitosanases (EC 3.2.1.132) hydrolyze the polysaccharide chitosan, which is composed of partially acetylated β-(1,4)-linked glucosamine residues. In nature, chitosanases are produced by a number of Gram-positive and Gram-negative bacteria, as well as by fungi, probably with the primary r...

Descripción completa

Detalles Bibliográficos
Autores principales: Johnsen, Mads G, Hansen, Ole C, Stougaard, Peter
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2835661/
https://www.ncbi.nlm.nih.gov/pubmed/20096097
http://dx.doi.org/10.1186/1475-2859-9-5
_version_ 1782178643763527680
author Johnsen, Mads G
Hansen, Ole C
Stougaard, Peter
author_facet Johnsen, Mads G
Hansen, Ole C
Stougaard, Peter
author_sort Johnsen, Mads G
collection PubMed
description BACKGROUND: Chitosanases (EC 3.2.1.132) hydrolyze the polysaccharide chitosan, which is composed of partially acetylated β-(1,4)-linked glucosamine residues. In nature, chitosanases are produced by a number of Gram-positive and Gram-negative bacteria, as well as by fungi, probably with the primary role of degrading chitosan from fungal and yeast cell walls for carbon metabolism. Chitosanases may also be utilized in eukaryotic cell manipulation for intracellular delivery of molecules formulated with chitosan as well as for transformation of filamentous fungi by temporal modification of the cell wall structures. However, the chitosanases used so far in transformation and transfection experiments show optimal activity at high temperature, which is incompatible with most transfection and transformation protocols. Thus, there is a need for chitosanases, which display activity at lower temperatures. RESULTS: This paper describes the isolation of a chitosanase-producing, cold-active bacterium affiliated to the genus Janthinobacterium. The 876 bp chitosanase gene from the Janthinobacterium strain was isolated and characterized. The chitosanase was related to the Glycosyl Hydrolase family 46 chitosanases with Streptomyces chitosanase as the closest related (64% amino acid sequence identity). The chitosanase was expressed recombinantly as a periplasmic enzyme in Escherichia coli in amounts about 500 fold greater than in the native Janthinobacterium strain. Determination of temperature and pH optimum showed that the native and the recombinant chitosanase have maximal activity at pH 5-7 and at 45°C, but with 30-70% of the maximum activity at 10°C and 30°C, respectively. CONCLUSIONS: A novel chitosanase enzyme and its corresponding gene was isolated from Janthinobacterium and produced recombinantly in E. coli as a periplasmic enzyme. The Janthinobacterium chitosanase displayed reasonable activity at 10°C to 30°C, temperatures that are preferred in transfection and transformation experiments.
format Text
id pubmed-2835661
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-28356612010-03-10 Isolation, characterization and heterologous expression of a novel chitosanase from Janthinobacterium sp. strain 4239 Johnsen, Mads G Hansen, Ole C Stougaard, Peter Microb Cell Fact Research BACKGROUND: Chitosanases (EC 3.2.1.132) hydrolyze the polysaccharide chitosan, which is composed of partially acetylated β-(1,4)-linked glucosamine residues. In nature, chitosanases are produced by a number of Gram-positive and Gram-negative bacteria, as well as by fungi, probably with the primary role of degrading chitosan from fungal and yeast cell walls for carbon metabolism. Chitosanases may also be utilized in eukaryotic cell manipulation for intracellular delivery of molecules formulated with chitosan as well as for transformation of filamentous fungi by temporal modification of the cell wall structures. However, the chitosanases used so far in transformation and transfection experiments show optimal activity at high temperature, which is incompatible with most transfection and transformation protocols. Thus, there is a need for chitosanases, which display activity at lower temperatures. RESULTS: This paper describes the isolation of a chitosanase-producing, cold-active bacterium affiliated to the genus Janthinobacterium. The 876 bp chitosanase gene from the Janthinobacterium strain was isolated and characterized. The chitosanase was related to the Glycosyl Hydrolase family 46 chitosanases with Streptomyces chitosanase as the closest related (64% amino acid sequence identity). The chitosanase was expressed recombinantly as a periplasmic enzyme in Escherichia coli in amounts about 500 fold greater than in the native Janthinobacterium strain. Determination of temperature and pH optimum showed that the native and the recombinant chitosanase have maximal activity at pH 5-7 and at 45°C, but with 30-70% of the maximum activity at 10°C and 30°C, respectively. CONCLUSIONS: A novel chitosanase enzyme and its corresponding gene was isolated from Janthinobacterium and produced recombinantly in E. coli as a periplasmic enzyme. The Janthinobacterium chitosanase displayed reasonable activity at 10°C to 30°C, temperatures that are preferred in transfection and transformation experiments. BioMed Central 2010-01-22 /pmc/articles/PMC2835661/ /pubmed/20096097 http://dx.doi.org/10.1186/1475-2859-9-5 Text en Copyright ©2010 Johnsen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Johnsen, Mads G
Hansen, Ole C
Stougaard, Peter
Isolation, characterization and heterologous expression of a novel chitosanase from Janthinobacterium sp. strain 4239
title Isolation, characterization and heterologous expression of a novel chitosanase from Janthinobacterium sp. strain 4239
title_full Isolation, characterization and heterologous expression of a novel chitosanase from Janthinobacterium sp. strain 4239
title_fullStr Isolation, characterization and heterologous expression of a novel chitosanase from Janthinobacterium sp. strain 4239
title_full_unstemmed Isolation, characterization and heterologous expression of a novel chitosanase from Janthinobacterium sp. strain 4239
title_short Isolation, characterization and heterologous expression of a novel chitosanase from Janthinobacterium sp. strain 4239
title_sort isolation, characterization and heterologous expression of a novel chitosanase from janthinobacterium sp. strain 4239
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2835661/
https://www.ncbi.nlm.nih.gov/pubmed/20096097
http://dx.doi.org/10.1186/1475-2859-9-5
work_keys_str_mv AT johnsenmadsg isolationcharacterizationandheterologousexpressionofanovelchitosanasefromjanthinobacteriumspstrain4239
AT hansenolec isolationcharacterizationandheterologousexpressionofanovelchitosanasefromjanthinobacteriumspstrain4239
AT stougaardpeter isolationcharacterizationandheterologousexpressionofanovelchitosanasefromjanthinobacteriumspstrain4239