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Characterization of an Extracellular Xylanase from Bacillus sp. HY-20, a Bacterium in the Gut of Apis mellifera  

Lee, Lan-Hee (Industrial Bio-materials Research Center, KRIBB)
Kim, Do-Young (Industrial Bio-materials Research Center, KRIBB)
Han, Mi-Kyoung (Industrial Bio-materials Research Center, KRIBB)
Oh, Hyun-Woo (Industrial Bio-materials Research Center, KRIBB)
Ham, Su-Jin (Industrial Bio-materials Research Center, KRIBB)
Park, Doo-Sang (Biological Resources Center, KRIBB)
Bae, Kyung-Sook (Biological Resources Center, KRIBB)
Sok, Dai-Eun (College of Phamacy, Chungnam National University)
Shin, Dong-Ha (Insect Biotech Co. Ltd.)
Son, Kwang-Hee (Industrial Bio-materials Research Center, KRIBB)
Park, Ho-Yong (Industrial Bio-materials Research Center, KRIBB)
Publication Information
Korean Journal of Microbiology / v.45, no.4, 2009 , pp. 332-338 More about this Journal
Abstract
A xylan-decomposing bacterium, HY-20, was isolated from the gut of a honeybee, Apis mellifera, and identified as Bacillus sp. The extracellular GH11 xylanase (XylP) gene (687-bp) of strain HY-20 encoded a protein of 228 amino acids with a deduced molecular mass of 25,522 Da and a calculated pI of 9.33. The primary structure of XylP was 97% identical to that of B. pumilus xylanase (GenBank accession no.: AY526092) that has not been characterized yet. The recombinant His-tagged enzyme (rXylP) overexpressed in Escherichia coli BL21 harboring pET-28a(+)/xylP was purified to electrophoretic homogeneity by cation exchange and gel permeation chromatographies. The purified enzyme exhibited the highest catalytic activity toward birchwood xylan at pH 6.5 and $50^{\circ}C$ and retained approximately 50% of its original activity when pre-incubated at $55^{\circ}C$ for 15 min. The recombinant enzyme was completely inactivated by $Hg^{2+}$ (1 mM) and N-bromosuccinimide (5 mM), while its activity was slightly stimulated by approximately 10% in the presence of $Mn^{2+}$ (1 mM), $Fe^{2+}$ (1 mM), and sodium azide (5 mM). rXylP was able to efficiently degrade various polymeric xylose-based substrates but PNP-sugar derivatives and glucose-based polymers were not susceptible to the enzyme.
Keywords
Apis mellifera; Bacillus sp. HY-20; bee; gut bacterium; xylanase;
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1 Brennan, Y., W.N. Callen, L. Christoffersen, P. Dupree, F. Goubet, S. Healey, M. Hernández, M. Keller, K. Li, N. Palackal, A. Sittenfeld, G. Tamayo, S. Wells, G.P. Hazlewood, E.J. Mathur, J.M. Short, D.E. Robertson, and B.A. Steer. 2004. Unusual microbial xylanases from insect guts. Appl. Environ. Microbiol. 70, 3609- 3617   DOI   ScienceOn
2 Brune, A. 1998. Termite guts: the world’s smallest bioreactors. Trends Biotechnol. 16, 16-21   DOI   ScienceOn
3 Chun, J. 1995. Computer-assisted classification and identification of actinomycetes. Ph. D. Thesis, University of Newcastle, UK
4 Khandeparkar, R.D.S. and N.B. Bhosle. 2006. Isolation, purification and characterization of the xylanase produced by Arthrobacter sp. MTCC 4214 when grown in solid-state fermentation. Enzyme Microb. Technol. 39, 732-742   DOI   ScienceOn
5 MacLeod, A.M., T. Lindhorst, S.G. Withers, and R.A.J. Warren. 1994. The acid/base catalyst in the exoglucanase/xylanase from Cellulomonas fimi is glutamic acid 127: evidence from detailed kinetic studies of mutants. Biochemistry 33, 6371-6376   DOI   ScienceOn
6 Shallom, D. and Y. Shoham. 2003. Microbial hemicellulases. Curr. Opin. Microbiol. 6, 219-228   DOI   ScienceOn
7 Irwin, D., E.D. Jung, and D.B. Wilson. 1994. Characterization and sequence of a Thermomonospora fusca xylanase. Appl. Environ. Microbiol. 60, 763-770   PUBMED   ScienceOn
8 Kim, H.J., D.Y. Kim, J.S. Nam, K.S. Bae, and Y.H. Rhee. 2003. Characterization of an extracellular medium-chain-length poly(3-hydroxyalkanoate) depolymerase from Streptomyces sp. KJ-72. Antonie van Leeuwenhoek 83, 183-189   DOI   ScienceOn
9 Oh, H.W., S.Y. Heo, D.Y. Kim, D.S. Park, K.S. Bae, and H.Y. Park. 2008. Biochemical characterization and sequence analysis of a xylanase produced by an exo-symbiotic bacterium of Gryllotalpa orientalis, Cellulosimicrobium sp. HY-12. Antonie van Leeuwenhoek 93, 437-442   DOI   ScienceOn
10 Kim, D.Y., M.K. Han, J.S. Lee, H.W. Oh, D.S. Park, D.H. Shin, K.H. Son, K.S. Bae, and H.Y. Park. 2009. Isolation and characterization of a cellulase-free endo-$\beta$-1,4-xylanase produced by an invertebrate-symbiotic bacterium, Cellulosimicrobium sp. HY-13. Proc. Biochem. 44, 1055-1059   DOI   ScienceOn
11 Subramaniyan, S. and P. Prema. 2000. Cellulase-free xylanases from Bacillus and other microorganisms. FEMS Microbiol. Lett. 183, 1-7   DOI   ScienceOn
12 Kulkarni, N., A. Shendye, and M. Rao. 1999. Molecular and biotechnological aspects of xylanases. FEMS Microbiol. Rev. 23, 411-456   DOI   ScienceOn
13 Heo, S.Y., J. Kwak, H.W. Oh, D.S. Park, K.S. Bae, D.H. Shin, and H.Y. Park. 2006. Characterization of an extracellular xylanase in Paenibacillus sp. HY-8 isolated from an herbivorous longicorn beetle. J. Microbiol. Biotechnol. 16, 1753-1759   ScienceOn
14 Kim, D.Y., M.K. Han, D.S. Park, J.S. Lee, H.W. Oh, D.H. Shin, T.S. Jeong, S.U. Kim, K.S. Bae, K.H. Son, and H.Y. Park. 2009. Novel GH10 xylanase, with a fibronectin type 3 domain, from Cellulosimicrobium sp. strain HY-13, a bacterium in the gut of Eisenia fetida. Appl. Environ. Microbiol. 75, 7275-7279   DOI   ScienceOn
15 Kim, D.Y., M.K. Han, H.W. Oh, D.S. Park, S.J. Kim, S.G. Lee, D.H. Shin, K.H. Son, K.S. Bae, and H.Y. Park. 2010. Catalytic properties of a GH10 endo-$\beta$-1,4-xylanase from Streptomyces thermocarboxydus HY-15 isolated from the gut of Eisenia fetida. J. Mol. Catal. B: Enzym. 62, 32-39   DOI   ScienceOn
16 Cazemier, A.E., J.C. Verdoes, A.J.J. Van Ooyen, and H.J.M. Op den Camp. 1999. Molecular and biochemical characterization of two xylanase-encoding genes from Cellulomonas pachnodae. Appl. Environ. Microbiol. 65, 4099-4107   PUBMED   ScienceOn
17 Jung, Y.J., J.K. Lee, C.G. Sung, T.K. Oh, and H.K. Kim. 2003. Nonionic detergent-induced activation of an esterase from Bacillus megaterium 20-l. J. Mol. Catal. B: Enzym. 26, 223-229   DOI   ScienceOn
18 Polizeli, M.L.T.M., A.C.S. Rizzatti, R. Monti, H.F. Terenzi, J.A. Jorge, and D.S. Amorim. 2005. Xylanases from fungi: properties and industrial applications. Appl. Microbiol. Biotechnol. 67, 577-591   DOI   ScienceOn