Zur Seitenansicht
 

Titelaufnahme

Titel
Efficient recombinant expression and secretion of a thermostable GH26 mannan endo-1,4--mannosidase from Bacillus licheniformis in Escherichia coli
VerfasserSongsiriritthigul, Chomphunuch ; Buranabanyat, Bancha ; Haltrich, Dietmar ; Yamabhai, Montarop
Erschienen in
Microbial Cell Factories, 2010, Jg. 9, 20 S.
ErschienenBioMed Central (BMC), 2010
SpracheEnglisch
DokumenttypAufsatz in einer Zeitschrift
ISSN1475-2859
URNurn:nbn:at:at-ubbw:3-367 Persistent Identifier (URN)
DOIdoi:10.1186/1475-2859-9-20 
Zugriffsbeschränkung
 Das Werk ist frei verfügbar
Dateien
Efficient recombinant expression and secretion of a thermostable GH26 mannan endo-1,4--mannosidase from Bacillus licheniformis in Escherichia coli [2.55 mb]
Links
Nachweis
Klassifikation
Zusammenfassung (Englisch)

Background:

Mannans are one of the key polymers in hemicellulose, a major component of lignocellulose. The Mannan endo-1,4--mannosidase or 1,4-- D -mannanase (EC 3.2.1.78), commonly named -mannanase, is an enzyme that can catalyze random hydrolysis of -1,4-mannosidic linkages in the main chain of mannans, glucomannans and galactomannans. The enzyme has found a number of applications in different industries, including food, feed, pharmaceutical, pulp/paper industries, as well as gas well stimulation and pretreatment of lignocellulosic biomass for the production of second generation biofuel. Bacillus licheniformis is a Gram-positive endospore-forming microorganism that is generally non-pathogenic and has been used extensively for large-scale industrial production of various enzymes; however, there has been no previous report on the cloning and expression of mannan endo-1,4--mannosidase gene (manB) from B. licheniformis.

Results:

The mannan endo-1,4--mannosidase gene (manB), commonly known as -mannanase, from Bacillus licheniformis strain DSM13 was cloned and overexpressed in Escherichia coli. The enzyme can be harvested from the cell lysate, periplasmic extract, or culture supernatant when using the pFLAG expression system. A total activity of approximately 50,000 units could be obtained from 1-l shake flask cultures. The recombinant enzyme was 6 His-tagged at its C-terminus, and could be purified by one-step immobilized metal affinity chromatography (IMAC) to apparent homogeneity. The specific activity of the purified enzyme when using locust bean gum as substrate was 1672 96 units/mg. The optimal pH of the enzyme was between pH 6.0 - 7.0; whereas the optimal temperature was at 50 - 60C. The recombinant -mannanase was stable within pH 5 - 12 after incubation for 30 min at 50C, and within pH 6 - 9 after incubation at 50C for 24 h. The enzyme was stable at temperatures up to 50C with a half-life time of activity (1/2) of approximately 80 h at 50C and pH 6.0. Analysis of hydrolytic products by thin layer chromatography revealed that the main products from the bioconversion of locus bean gum and mannan were various manno-oligosaccharide products (M2 - M6) and mannose.

Conclusion:

Our study demonstrates an efficient expression and secretion system for the production of a relatively thermo- and alkali-stable recombinant -mannanase from B. licheniformis strain DSM13, suitable for various biotechnological applications.