Identification and characterization of novel cellulolytic and hemicellulolytic genes and enzymes derived from German grassland soil metagenomes

Autor(en): Nacke, H.
Engelhaupt, M.
Brady, S.
Fischer, C.
Tautzt, J.
Daniel, R.
Stichwörter: cellulase, 9012-54-8; xylan 1,4 beta xylosidase, 9025-53-0; Cellulases, 3.2.1.-; Xylosidases, 3.2.1.-; Activity-based screening; Carbohydrate-binding modules; Carbohydrates; Carboxy-methyl cellulose; Cellulase; Cellulase genes; Cellulose; Cellulose substrates; chemistry; Cloning, Molecular; Degradation profiles; Diagnosis; DNA sequence; E. coli; Enzyme activity; enzyme specificity; enzymology; Escherichia coli; Gene Expression; Gene Library; genetics; Germany; Glucanase; Glycoside hydrolases; Grassland soils; High activity; Hordeum; Libraries; metabolism; Metagenome; Metagenomes; Metagenomic DNA; Metagenomic libraries; microbiology; Microcrystalline cellulose; molecular cloning; molecular genetics; Molecular Sequence Data; Molecular Weight; nucleotide sequence, Cellulases; Optimal activity; Optimization; pH range; Protein domains; Recombinant enzymes; Sequence Analysis, DNA; Soil metagenome; Soil micro-organisms; Soil Microbiology; Soils, Genes, cellulase; Substrate Specificity; xylan 1,4 beta xylosidase, article; Xylanase; Xylanase activity; Xylanases, Amino acids; Xylosidases, Escherichia coli
Erscheinungsdatum: 2012
Journal: Biotechnology Letters
Volumen: 34
Ausgabe: 4
Startseite: 663
Seitenende: 675
Zusammenfassung: 
Soil metagenomes represent an unlimited resource for the discovery of novel biocatalysts from soil microorganisms. Three large-inserts metagenomic DNA libraries were constructed from different grassland soil samples and screened for genes conferring cellulase or xylanase activity. Function-driven screening identified a novel cellulase-encoding gene (cel01) and two xylanase-encoding genes (xyn01 and xyn02). From sequence and protein domain analyses, Cel01 (831 amino acids) belongs to glycoside hydrolase family 9 whereas Xyn01 (170 amino acids) and Xyn02 (255 amino acids) are members of glycoside hydrolase family 11. Cel01 harbors a family 9 carbohydrate-binding module, previously found only in xylanases. Both Xyn01 and Xyn02 were most active at 60°C with high activities from 4 to 10 and optimal at pH 7 (Xyn01) and pH 6 (Xyn02). The cellulase gene, cel01, was expressed in E. coli BL21 and the recombinant enzyme (91.9 kDa) was purified. Cel01 exhibited high activity with soluble cellulose substrates containing β-1,4-linkages. Activity with microcrystalline cellulose was not detected. These data, together with the analysis of the degradation profiles of carboxymethyl cellulose and barley glucan indicated that Cel01 is an endo 1,4-β-glucanase. Cel01 showed optimal activity at 50°C and pH 7 being highly active from pH range 5 to 9 and possesses remarkable halotolerance. © 2011 The Author(s).
ISSN: 01415492
DOI: 10.1007/s10529-011-0830-2
Externe URL: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84858009110&doi=10.1007%2fs10529-011-0830-2&partnerID=40&md5=9e324113627275ed27cc4ea977841d6a

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